Arginine, scurvy and Cartier's "tree of life"
Journal of Ethnobiology and Ethnomedicine volume 5, Article number: 5 (2009)
Several conifers have been considered as candidates for "Annedda", which was the source for a miraculous cure for scurvy in Jacques Cartier's critically ill crew in 1536. Vitamin C was responsible for the cure of scurvy and was obtained as an Iroquois decoction from the bark and leaves from this "tree of life", now commonly referred to as arborvitae. Based on seasonal and diurnal amino acid analyses of candidate "trees of life", high levels of arginine, proline, and guanidino compounds were also probably present in decoctions prepared in the severe winter.
The semi-essential arginine, proline and all the essential amino acids, would have provided additional nutritional benefits for the rapid recovery from scurvy by vitamin C when food supply was limited. The value of arginine, especially in the recovery of the critically ill sailors, is postulated as a source of nitric oxide, and the arginine-derived guanidino compounds as controlling factors for the activities of different nitric oxide synthases. This review provides further insights into the use of the candidate "trees of life" by indigenous peoples in eastern Canada. It raises hypotheses on the nutritional and synergistic roles of arginine, its metabolites, and other biofactors complementing the role of vitamin C especially in treating Cartier's critically ill sailors.
One of the first documented uses of indigenous medicine in North America was the cure in the winter of 1536 of Jacques Cartier's crew from a disease he called "Scorbut"(scurvy) [1, 2]. Cartier's second voyage (1535–1536) was undertaken at the command of King François 1er to complete the discovery of the western lands under the same climate and parallels as in France. At Stadaconna, now Quebec City, Cartier's crew was cured from scurvy by ascorbic acid (vitamin C) obtained as a decoction from the Iroquois. It was prepared by boiling winter leaves and the bark from an evergreen tree. The tree, identified as "Annedda", became known as the "tree of life" or "arbre de vie" because of its remarkable curative effects. In the winter, scurvy was the most prevalent disease among the Iroquois. This was due to the lack of food and vitamin C .
The cure for scurvy was significant for future naval explorations and for the introduction of the tree into France during the Reformation when the Age of Reason began (1558–1648) . The medicinal value of the tree of life contributed to the resurrection of botany, which at that time struggled to free itself from pharmacy when medical men were still its masters. By the eighteenth century, the French naturalists at the Jardin du Roi in Paris knew of Thuja occidentalis as the tree of life and planted an avenue of it in the Jardin itself .
The Iroquois referred to the tree as Annedda (l'Annedda, Aneda, Anneda, Hanneda) . Other tribal names for conifers were "ohnehta" for white pine, "onita" and "onnetta" for white spruce (Mohawk, Onandaga). These names represent the evergreen nature characteristic of coniferous trees. Regarding the transmission of the tree of life to France, the earlier one goes, the sparser are the available manuscripts. The pre-Linnaeus terminology for conifers made their precise identity impossible to make. Based on collections by French explorers and the ethnomedicine of indigenous peoples in eastern Canada, the true identity of the tree of life became controversial . The identity of Anneda was narrowed down to eastern white cedar or arborvitae (Thuja occidentalis L.), white spruce (Picea glauca (Moench) Voss), black spruce (Picea mariana (Mill.)), eastern white pine (Pinus strobus L.), red pine (Pinus resinosa Aiton), balsam fir (Abies balsamea (L.) Mill.), eastern hemlock (Tsuga canadensis (L.)), and juniper (Juniperus communis L.) [2, 6].
We now know that during late a severe winter and at a similar latitude to Quebec City, the candidate trees of life are a rich nutritional source of arginine, proline and other amino acids [7–9]. Their physiological fluids and proteins contain amino acids which are essential in the human diet because the body does not synthesize them (viz., phenylalanine, valine, threonine, tryptophan, isoleucine, methionine, leucine, and lysine). Arginine, cysteine, glycine, glutamine, histidine, proline, serine and tyrosine are conditionally essential, meaning they are not normally required in the diet, but must be supplied to specific populations that do not synthesize these amino acids in adequate amounts . Today, these amino acids are used as nutritional support for the recovery of critically ill patients [11–14]. In the recovery from scurvy they would help to promote vitamin C-dependent collagen biosynthesis, promote wound healing, reduce susceptibility to sepsis, and contribute to weight gain [10, 15–17].
The importance of arginine as a source of the free radical nitric oxide (NO) was recognized by the Nobel Prize in Physiology or Medicine in 1998 given to R. Furchgott, J. Ignarro and F. Murad. They identified NO as a signalling molecule in the cardiovascular system. Derived from arginine and oxygen, NO maintains blood pressure by dilating blood vessels, helps kill invaders in the immune response, and is needed for wound repair [18–21]. It can pass through biological membranes, oxidize foreign substances, and acts as a secondary biological messenger which affects diverse metabolic pathways. Unexpectedly, the candidate trees of life can produce NO from arginine, and contain guanidino compounds that may regulate the enzyme, nitric oxide synthase (NOS), which is responsible for the formation of NO [8, 22, 23]. The arginine-derived guanidino compounds are potential therapeutic agents for the regulation of various nitric oxide synthases (NOSs) when the overproduction of NO becomes associated with septic shock, neurodegeneration, and inflammation .
My review deals with the nitrogenous compounds in the physiological fluids of candidate trees of life in a severe winter, and theorizes as to how these nutrients could have helped to improve the recovery of the critically ill sailors in 1536. The availability of arginine, the essential amino acids, and biofactors in decoctions, obtained from the trees of life, are discussed in terms of their contributions to the recovery of the critically ill crew at Stadaconna, the ethnnobotany and ethnomedicine of the indigenous peoples in eastern Canada during food shortages, and in the vitamin C-dependent cure for scurvy. This is meant to generate hypotheses, not to confirm them.
The recovery from scurvy in Jacques Cartier's crew in 1536
Scurvy is an acute chronic illness caused by a dietary deficiency of ascorbic acid (vitamin C). Humans are not able to synthesize vitamin C from glucose because they lack a gluconolactone oxidase . There are two active forms of vitamin C: L-ascorbic acid and dehydroascorbic acid. Ascorbic acid is absorbed by the small intestine and requires an energy-dependent active transport system. It is stored in all tissues. Exposure to long periods of cold temperatures can lead to ascorbic-acid insufficiency.
The first symptoms of scurvy occur when the total-body pool of vitamin C falls below five grams. The body requires vitamin C to efficiently use carbohydrates, fats, and protein. It binds and neutralizes the tissue-damaging effects of free radicals. It is an essential cofactor for the formation of collagen, the body's major building protein, and is essential to the proper functioning of all internal organs.
Scurvy is characterized principally by anemia, hemorrhagic manifestations in the skin (ecchymoses and perifollicular haemorrhage), and in the musculoskeletal system (haemorrhage into periosteum and muscles). The gums start to bleed. Teeth are loosened . With no vitamin C intake, the symptoms of scurvy would occur after one to three months. Unless treated, scurvy is fatal.
At Stadaconna (46° 49' N, 71° 13' N) and in November1535, Canada's cold struck with its entire rigor, and ice thickened to two fathoms. In December, over 50 of the Iroquois died from an unknown sickness (scurvy). The sickness began to spread to Cartier's crews in all three of his ships. By mid-February 1536, of the 110 member crews, 8 were already dead and more than 50 past all hope of recovery. Excerpts from Burrage [1, p. 73] reveal that the unknown sickness in Cartier's crew "spread itselfe amongst us after the strangest sort that ever was eyther heard of or seene, insomuch as some did lose all their strength, and could not stand on their feete, then did their legges swel, their sinnowes shrinke as blacke as any cole. Others also had all their skins spotted with spots of blood of a purple colour: then did it ascend up to their ankels, knees, thighes, shoulders, armes and necke: their mouth became stincking, their gummes so rotten, that all the flesh did fall off, even to the rootes of teeth, which did also almost fall out".
"Our Captaine seeing this our misery, and that the sicknesse was gone to farre, ordained and commanded, that every one should devoutly prepare himselfe to prayer, and in remembrance of Christ, caused his Image to be set upon a tree, about a flight shot from the fort amidst the yce and snow, giving all men to understand, that on the Sunday following, service should be said there, and that whosoever could goe, sicke or whole, should go thither in Procession, singing the seven Psalmes of David, with other Letanies, praying most heartily that it would please the said our Christ to have compassion upon us ... That day Philip Rougemont...being 22 yeeres olde, and because the sicknesse was to us unknown, our Captaine caused him to be ripped to see if by any meanes possible we might know what it was...he was found to have his heart white, but rotten, and more than a quart of red water about it: his liver was indifferent faire, but his lungs blacke and mortified, his blood was altogither shrunke about the heart, so that when he was opened great quantitie of rotten blood issued out from about his heart...Moreover, because one of his thighs was very blacke without, it was opened, but within it was whole and sound." Scurvy continued to spread until not more than three sound men remained in the ships. None were able to go under the hatches to "draw drink for himselfe, nor for his fellowes."
At Stadaconna, Cartier encountered the native Domagaia, who "not passing ten or twelve dayes afore, had bene very sike with that disease, and had his knees swolne as bigge as a childe of two yeres old, all his sinews shrunke together, his teeth spoyled, his gummes rotten, and stinking. Our Captaine seeing him whole and sound, was therat marvelous glad, hoping to understand and know of him how he had healed himselfe...He answered, that he had taken the juice and sappe of the leaves of a certain Tree, and therewith had healed himselfe: For it is a singular remedy against that disease."
Domagaia "sent two women to fetch some of it, which brought ten or twelve branches of it, and therewithall shewed the way how to use it... to take the barke and leaves of the sayd tree, and boile them togither, then to drinke of the sayd decoction every other day, and to put the dregs of it upon his legs that is sicke: moreover, they told us, that the vertue of that tree was, to heale any other disease: the tree in their language called Ameda or Hanneda..." Other translations refer to the tree as "Annedda", "Anneda" or "Hanneda" . This sickness was treated with a boiled decoction from the bark and leaves of "a tree as big as any oak in France".
Cook  translates that "The Captain at once ordered a drink to be prepared for the sick men but none of them would taste it. At length one or two thought they would risk a trial. As soon as they had drunk it they felt better, which must clearly be ascribed to miraculous causes; for after drinking it two or three times they recovered health and strength and were cured of all the diseases they had ever had. And some of the sailors who had been suffering for five or six years from the French pox [syphilis] were by this medicine cured completely. When this became known, there was such a press for the medicine that they almost killed each other to have it first; so that in less than eight days a whole tree as large and as tall as any I ever saw was used up, and produced such a result that had all the doctors of Louvain and Montpellier been there, with all the drugs of Alexandria, they could not have done so much in a year as did this tree in eight days; for it benefitted us so much that all who were willing to use it recovered health and strength, thanks be to God." We do not know how much ascorbic acid was lost during the boiling of the decoction and in the recovery of the "dregs", but it is clear that sufficient vitamin C was available to initiate a cure.
In today's healthy men, the body is estimated to store 1,500 mg of ascorbic acid. It is used at an average rate of 3% of the existing pool per day . After three months of vitamin C deprivation, the stores become largely depleted. The earliest signs of depletion begin during the first month of deprivation. Bleeding gums are not the most characteristic feature of scurvy and are a late manifestation. Except in the most severe cases, vitamin C would stop spontaneous bleeding within 24 hours and bleeding of the gums would stop in two to three days. Muscle and bone pain would quickly fade .
In advanced scurvy another group of symptoms becomes identifiable [15, 24]. They include ocular haemorrhages, loss of secretion of salivary and lachrymal glands, swelling of the parotid and submaxillary glands, loss of hair, femoral neuropathy, oliguria with edema of the lower extremities, psychological disturbances, impaired vascular activity, poor responses to stimuli that normally activate vasomotor adaptive mechanisms, and scorbutic arthritis, which is clinically similar to rheumatoid arthritis with pain, swelling, joint effusions, and limited motion. All of the above would respond completely to therapy with ascorbic acid given the added nutritional benefits of the conditionally and essential amino acids and other biofactors in the decoction.
Identities of Annedda and the trees of life
Before 1547 and during the reign of François 1er, seeds of Annedda were delivered to the Royal Garden (Jardin du Roi) at Fontainbleau and presented to the King. Apparently seeds were collected from a tree or trees similar to Annedda . In 1553, Belon wrote in the Bulletin Dendrologique that Annedda was growing in the Royal Gardens at Fontainbleau. Nearby was another small tree, a five-needled pine, referred to as the second tree of life. Wood from these trees were used as medicine.
In Hickel's translation  of Belon's book, we read that "...à cette époque, les seules espèces exotiques introduites étaient l'Arborvitae (Thuya occidentalis) et Pinus strobus, et que, d'autre part l'auteur confond plus ou moins diverses espèces de pins." When Belon visited Turkey, he found a tree similar to the one at Fontainebleau, which was brought from Canada and called "Arbre de Vie". Moore  citing the works of Bolle  and Annon. , who both reexamined Belon's records, proposed that the identity of the Annedda was not eastern white cedar, but a five-needled white pine (Pinus strobus). It is now evident that two trees of life were introduced from North America as exotic species [2, 6]. "The fate of the pine at Fontainbleau is not known" . Bolle "could not find any further record of eastern white pine growing in Europe until 150 years later when it was introduced into England".
In 1632, the botanical garden, established in Paris in 1632 by King Louis XIII of France, was intended for the cultivation of medicinal plants . Landowners and naturalists were engaged in testing the effects of climate upon growing new exotic species arriving in France. A Bridgeman Art Library archive shows a "burgeoning bower" resembling eastern white pine in the botanical garden (Nature 2001, 410, 303). The King's garden survived the French Revolution (1796–1798) and its nurseries were used to provide patriotic 'trees of liberty'. They were planted in front of public buildings. The first trees of liberty were actually maypoles planted by peasants as a symbol of revolt against local lords in the winter of 1790.
Today, Annedda is commonly referred to as eastern white cedar or arborvitae (Thuja occidentalis L.). This appellation was based on botanical evaluations, historical documents, naval and folklore medicine, notes of Cartier's contemporaries, and on the estimates of biochemical content of vitamin C . The anti-scorbutic benefits of the candidate trees of life are abundant in the records and reviews of indigenous Maritime medicine [2, 3, 30–33].
Conifers, native along the travel routes of Jacques Cartier, and with known high levels of vitamin C are Picea rubens, Pinus resinosa, Pinus nigra, and Pinus banksiana. In the "Native Trees of Canada", Canada Forest Service Bulletin 1919, No. 61 the botanical names of conifers had popular names. Thuja occidentalis was called cedar, and referred to as white cedar, and arborvitae. Pinus strobus was called white pine, and sometimes referred to as Weymouth pine, pattern pine, eastern white, yellow, and Quebec pine. Picea canadensis was called white spruce, and sometimes northern, skunk, cat spruce, and pine. Pinus banksiana was called jack pine and sometimes grey pine, cypress, juniper, and Banksian pine.
Today, the eastern white cedar (Thuja occidentalis L.) has the largest number of cultivars, and many do not resemble the species type . Mature trees will reach 30 to 40 feet tall with a spread of 15 feet. The upright cultivars are much shorter. The latter would unlikely be "as big as any oak in France". In eastern Canada, white pine was reported to reach a height of 250 feet and a diameter of 6 to 15 feet .
Conifer decoctions for the treatment of scurvy
Domagaia cured himself with the "the juice and sappe of the leaves of a certain tree". Adult scurvy is now treated with 300–1000 mg of ascorbic acid per day . In clinical dermatology, ascorbic acid is recommended three times a day, 100 mg is given until 4 g is reached, and then 100 mg/d becomes curative in days to weeks . Repletion studies demonstrated recovery from daily doses of only 6.5 . Larger doses gave more rapid improvement and increased ascorbic acid storage in the body. The plasma levels of ascorbic acid attained depended on body weight (dose per kg of body weight) and on whether or not any prior depletion had been adequately repleted .
In early explorers, a deficiency of vitamin C repeatedly caused morbidity and death [36, 37]. Teas, brews, and beers, prepared from the needles of spruces and pines, were used to treat the symptoms of scurvy [38, 39]. Scurvy remedies were being made, sold and used under the name of "sapinette"."According to the physician Gardane, in Des maladies des créoles (Paris 1784), this was a decoction of "sapin du Nord", or Picea abies . In Canada sapinette was made from the buds of the "Prussian fir", a name which was used indiscriminately for Abies alba , A. balsamea , and Picea abiesby Cartier. Sapinette was widely used in Canada, but the recipe seems to have come originally from the Baltic coast and sapinette was being used by the Russian navy long before the French took interest in it. The Russians in fact did use fermented pine buds with their fir decoction, though the species here is not specified. But it seems the French used fir, even in Canada" (Spary, personal communication ).
Spary writes, "The French were experimenting with sapinette on their long-distance voyages during the 1780s, and it was stocked on board the Laperouse expedition vessels"..." sapinette was bought ready-made from London. All things considered, this does not suggest that there was a direct connection between Pinus strobusin particular and the antiscorbutic programme, though it is entirely possible that this species was brought to Paris to be investigated for its virtues in that regard". The British knew of the anti-scorbutic benefits of sapinette and of lemons and oranges in a cure for scurvy . In 1753 scurvy was recognized by the British medical community as directly related to dietary deficiency.
Spruce beer was used as an anti-scorbuticum by James Cook in his second Pacific voyages in Western Canada (1772–1775) . Cook obtained this recipe for spruce beer from Joseph Banks who had visited Newfoundland before Cook . The beer was prepared from fresh needles of a spruce tree, which in New Zealand was Dacrydium cupressinum . On Cook's third voyage near Alaska, Sitka spruce (Picea sitchensis) was used but it was not as acceptable as the brew from Dacrydium. . A similar drink called "Kallebogas" was used in Newfoundland. Variations involved the addition of rum and maple sugar .
Vitamin C was first isolated from paprika, chemically identified, and its metabolic role worked out by Albert Szent-Györgyi. He found that vitamin C also required cofactors to function properly. These cofactors are now known to be flavonoids. He was awarded the Nobel Prize in Physiology or Medicine in 1937 for his discoveries in biological combustion with special reference to vitamin C and for the catalysis of fumaric acid, an intermediate in the citric acid cycle. These factors, taken together, were probably available in the decoction used to cure scurvy.
Eastern hemlock (Tsuga canadensis) and black spruce (Picea mariana) served as ascorbutica [32, 44]. The indigenous peoples of the Maritime Provinces of Canada used roots, twigs, leaves, and bark, but rarely strobili or seeds in decoctions taken as a cupful in the morning . Teas, prepared by steeping or boiling leaves from conifers, served as refreshing drinks and a tonic of medicinal value . Green tissues offer high moisture content, vitamin C, folic acid, minerals and other biofactors. Roots are a good source of minerals but provide only small amounts of vitamins in a 100-gram portion . The bark was usually collected from the east side of the tree. The selected root or branch ran to the east . The reason was that these collections benefited from having more potency obtained from sunlight.
The vitamin C in lemon and oranges (50 mg/100 g) are exceeded in the needles and bark of several conifer spp. . Reduced ascorbic acid in 100 g of fresh needles and shoots was reported in Abies balsamea (270 mg), Picea rubens (169 mg), Pinus strobus (32 mg, bark contained 200 mg), Thuja occidentalis (45 mg) . R. B. Thomson at the University of Toronto found a content of 20–80 mg reduced ascorbate in 100 g of white spruce bark . For the treatment of scurvy, spruce (white and black) was considered as a likely candidate for the tree of life based on the ethnobotanical literature. Spruce is frequently recorded as being antiscorbutric and common in Quebec City. White pine was also widely used.
The extracts from Cartier's tree of life raised considerable interest as a cure for all diseases. In 1494 King Charles VIII of France had already invaded Italy. Within months, his army collapsed and was routed not by the Italian army but by a mysterious new disease . The disease was spread through sex and killed many of Charles's solders. European physicians were already aware of the root of sarsaparilla (Smilax officinalis) as a tonic, blood purifier, diuretic, and sweat promoter. Cartier's claim for the Iroquois decoction as a cure of all diseases may have been overstated to impress King François 1er (1515–1547). It is unlikely that vitamin C and other components from the trees of life would have cured syphilis in Cartier's crew at Stadaconna.
Food sources and medicines used by indigenous peoples in Canada
Twenty-five conifer species are identified as a traditional food source by indigenous peoples of Canada. Kuhnlein and Turner  have described the distribution, occurrence, food values and warnings for the Cypress family (Cupressacae), the Pine family (Pinaceae), and the Yew family (Taxaceae). The Canadian indigenous peoples are recognized for their ingenuity in processing foods to remove toxins by heating, leaching, fermenting, adsorption, drying, physical processing, and changing the acid-base ratio. Arnason et al.  have produced a compendium of the various uses of plants, which would have been accessible to Cartier before winter, and used by indigenous peoples of eastern Canada.
Land-based scurvy is well documented as occurring during times of food shortages . Late springs and low levels of vitamin C in stored grain contributed to endemics of sub-clinical scurvy. As for the candidate trees of life, food would include seeds, buds, inner bark, cambium and sap of trees. The inner bark of trees was eaten at any time of the year as an emergency food. The inner bark of hemlock was not an adequate famine food on its own if harvested outside the spring season .
Needles of Abies, Picea, and Pinus spp. have protein content from 2.5 to 8.8 mg/100 g fresh weight . Arginine, a dominant amino acid in protein and the physiological fluids of conifers, was first isolated in Switzerland by Schulze  using seedlings of Picea, Pinus, and Abies spp.. In seeds, arginine can represent 10% of the N in conifer protein . The sugar, amino acids, and protein content of Pinus banksiana seeds from different geographic sources across Canada correlates significantly with climate variables at the seed source . Expanding spruce buds and germinating jack pine seedlings would provide a rich source of amino acids, proteins and nucleic acids [50–56].
Given the statement that "in less than eight days a whole tree as large and as tall as any I ever saw was used up", lichens, commonly found on tree trunks and branches, and probably added many biofactors to the nutrients and vitamins in the Iroquois decoction. The main edible tree lichen is Bryoria fremontii . Lichens comprise two types of plants, an alga and a fungus growing together in a symbiotic relationship. Lichens are difficult to digest because of their complex polysaccharides, which do not break down during cooking. Some lichens were boiled for 24 h and eaten only in times of food scarcity and to remove toxic substances .
In general, tree bark only contains traces (0.04 to 0.17%) of nitrogenous extractives [57, 58]. The inner bark of loblolly pine, felled in December at Gulfport, Mississippi in a much warmer climate than Quebec City, was dominated by the amides (glutamine and asparagine), their dicarboxylic acids, and alanine . As for compounds not containing nitrogen in conifer bark, the bioflavonoids and proanthocyanidins are constituents that have been commonly found in medicines. The Algonquin in Quebec used decoctions from Pinus strobus to treat breathing disorders, rheumatism, and kidney disorders . Picea spp. were used by the Iroquois to treat respiratory ailments, urinary problems as a poultice for blood poisoning .
The boiled decoction that cured scurvy was prepared from the bark and leaves of ten or twelve branches. The dregs, which were put on legs, would contain many factors as a salve. In a 20 kg bulk extract from white spruce, the boiled extractives contained at least nine compounds which were weakly reactive with the Sakaguchi reagent for the guanidino group (unpublished data). A total ion chromatogram, mass spectral data, the molecular weight of species in the extract, and a list of their putative elemental composition, revealed several yet unidentified N-containing compounds and polymers having very high molecular weights, one of which had 220 Da subunits.
During a sabbatical at the University of Quebec, Dr. J. Masquelier read Jacques Cartier's account and this turned his attention to the antioxidant proanthocyanidins of conifer bark . He referred to proanthocyanidins as pycnogenols. Pycnogenol® is now a patented trade name for a water extract of the bark of the maritime pine (Pinus pinaster) commonly grown in the coastal southwest of France. The trade name refers to a specific proprietary pine bark extract with proanthrocyanidins (procyanidins) from Pinus maritima. The procyanidins scavenge free radicals and modulate NO metabolism . They are capable of preventing the oxidation of vitamin C and are more effective than vitamin E in scavenging damaging free radicals. Considerable literature now exists on the health benefits of the procyanidins when taken as supplements. As of 2008, the National Institutes of Health in the USA were carrying out clinical trials of pycnogenol for the treatment of lymphedema, endothelial function in coronary heart disease, hypertension and diabetes.
Herbal remedies from eastern Canadian conifers contain salicylates, astringent tannins, polyacetylenes, antibacterial alkaloids, anti-inflammatory terpenes [33, 62, 63]. Recognizing Thuja occidentalis as the "tree of life", Felter  described its medicinal uses in American therapy. He recommended extractives in the form of aqueous, non-alcoholic, ointment and oil preparations.
Indigenous peoples have employed Taxus spp. for their utility, wood quality, mythology and medicines . Decoctions were used to treat fever, scurvy, and to bring out clots and alleviate pain after childbirth.Taxus spp. contain more than 300 taxanes (taxoids) some of which are poisons, and others have significant physiological effects . Today, the most well known taxane is paclitaxel (Taxol®). It blocks cellular growth by binding to microtubules. This property makes it useful for the treatment of various cancers, but with side effects. Taxane-like compounds were detected in spruce and other conifers using antibodies to the taxane ring [23, 67, 68]. The recovery of paclitaxel and the taxanes from Taxus biomass was increased by mechanical stresses which elicit NO production from arginine [22, 23]. Product recovery was reduced by adding a synthetic guanidino inhibitor of NOS. We now return to arginine and other amino acids, which are important in human nutrition and serve as substrates required for the vitamin C-dependent synthesis of collagen in the cure for scurvy.
Arginine and amino acids in overwintering conifers
The seasonal changes in the amino acid composition of conifers represent a tropistic adaptation to environmental changes which prepare trees for dormancy and survival over long and severe winters. Winter decoctions, used by the Iroquois, would have contained the conditionally essential arginine and the essential amino acids required in the human diet. The physiological fluids of Picea glauca buds and shoots during a severe winter at Petawawa (45° 08' N, 81° 27' W) and similar in latitude to Quebec City were found to contain between150 to 200 mg amino acid N per 100 g fresh weight .
When the first snow appeared in November, the percent contribution of arginine N to the total soluble amino acid N increased from 20 to 45%. It was 40–53% in December. In January and February the shoots became ice-covered and the temperatures averaged -16 C. Arginine N now comprised 30–43% and 12–18% of the total soluble amino acid N, respectively. Levels of glutamine N always remained low, but increased significantly when buds expanded in spring. Proline N, which is derived from arginine, varied between 3 to 5% (November), 4 to 6% (December), 4 to 7% (January), and 8–13% (February).
From November to February, the concentrations in mg of the nine amino acids, essential in human nutrition, and recovered from the physiological fluids of 100 g fresh needles from shoots at 4 to 5 feet were: phenylalanine (0.5–1.5), leucine (0.4–1.6), isoleucine (0.4–1.0), valine (0.5–1.5), lysine (0.7–1.5), threonine (0.9–1.3), methionine, tryptophan, and histidine (each 0.01). Arginine, ranged between 16.0–21.0 mg/100 g fresh weight. The seasonal trends in amino acid content were reaffirmed with excised dormant buds forced to sprout under aseptic conditions in the laboratory . Tissue and bark compositions can vary due to differences in age of tissues in trees, environmental stresses, time of day, and the availability of N from the environment [7, 52, 53, 69–71]. With white spruce saplings, when ammonium is the sole source of N in sand cultures, arginine and guanidino compounds are major components of the total soluble N but not when nitrate is the sole source of N [72, 73].
Isotopic tracers are phenotyping tools in metabolism and a cornerstone in nutritional science. In white spruce, [UL-14C]-L-arginine serves as a precursor for proline via ornithine [8, 9]. Feeding [UL-C14]-L-proline and [UL-14C]-L-glutamine to winter dormant buds revealed traces of 14C-glutamic-γ-semialdehyde and 14C-Δ1-pyrroline-5-carboxylic acid . These intermediates are highly transient precursors for the synthesis of proline, glutamic acid and glutamine. Free hydroxyproline is not found in the physiological fluids unless the tissues are pathological. 14C-Proline and 14C-hydroxyproline residues were recovered from protein hydrolysate indicating that proline was hydroxylated to hydroxyproline in spruce protein. L-Proline-4-3H incorporation into protein was also observed with seedlings of Pinus banksiana . In humans, proline and hydroxyproline obtained from conifer buds and seedlings would be available for the vitamin C-dependent synthesis of collagen.
The metabolic pathways, cycles, and enzymes responsible for arginine metabolism in conifers are summarized in Figure 1. [UL-14C]-L-arginine and [carbamoyl-14C]-L-citrulline fed to pines and spruces revealed that arginine was synthesized via the intermediate steps of the urea (ornithine) cycle [74–80]. Arginine serves as a pivotal departure point from the urea cycle for the synthesis of urea and ornithine via arginase, and for proline, glutamate and glutamine. It is a substrate for the formation of NO and citrulline via NOS, and for the guanidino compounds and in protein synthesis. Arginase has been purified from conifers .
During rapid growth, the fates of 14C-urea and tritiated water in white spruce and jack pine tissues were a function of light availability [78, 79]. In light and darkness, urea was degraded by urease to ammonia and carbon dioxide. In light, the 14C-carbon dioxide, derived from urea, was reassimilated by photosynthesis and incorporated initially into alanine and glutamic acid. In darkness, ammonia and 14C-carbon dioxide contributed to the formation of carbamoyl phosphate for the biosynthesis of arginine and other metabolites . In winter dormant tissues, these metabolic steps were latent and difficult to detect. Most of the N in the physiological fluids was stored in arginine and the guanidino compounds.
Amino acids are water soluble at high temperatures  and most would be stable in boiled decoctions. Depending on pH, boiling may reduce the levels of glutamic acid due to its conversion to pyroglutamic acid. Vitamin C is readily available in fresh tissues even in winter. Its concentration usually increases during the spring growing season .
The food processing industry has demonstrated that the largest losses of vitamin C in foods occur during heating . We do not know if the "juice and sappe of the leaves" from Annedda were obtained without boiling and taken by Domagaia. Fresh conifer leaves can be chewed right off a branch provided that scurvy would prevent him from doing this. Chewing or crushing the leaves would release NO from the conifer cells (Figure 2). The decoction from Annedda, took every other day, provided the needed warmth as a protection from cold, sufficient vitamin C, various biofactors, the essential amino acids, and the conditionally essential arginine, which would provide N for the synthesis of NO in the wasting sailors.
Arginine as a source of nitric oxide in conifers
The first report of NO production from arginine in a conifer was provided by Magalhaes et al. . Using a dye (Figure 2), bursts of NO were visually detected when cells were wounded or exposed to a variety of and biotic and abiotic stresses [22, 23]. NO is synthesized by NOS in the L-arginine-NO pathway. The pathway comprises a citrulline/NO cycle (Figure 1). A citric acid cycle, not shown in Figure 1, provides aspartate N via fumarate, malate, and oxaloacetate for the synthesis of L-argininosuccinate from citrulline.
Plants and animals synthesize NO and citrulline from arginine and oxygen as substrates [22, 23, 84, 85]. The amidine N of the guanidino moiety of arginine is the source of the N in NO. Citrulline is recycled back to arginine via argininosuccinate. Plant NOS remains incompletely characterized and is a different enzyme from the NOSs in humans [84, 85]. Atypical of most conifers, the shoots of seedlings of Cryptomeria japonica have high levels of citrulline rather than arginine .
In conifers, low and protective levels of NO are rapidly produced in response to mechanical forces, environmental stresses, wounding, and as a protective measure against insects and diseases [22, 23, 85, 87–90]. NO activates second messengers which participate in protein phosphorylation, nitrosylation, gene expression, development, and in expressions of adaptive plasticity. NO contributes to developmentally programmed cell death (apoptosis) and autophagy. This is demonstrated in the death of one of the four megaspore cells after meiosis, and again in monozygotic cleavage polyembryony of early embryos found in developing seeds [91, 92]. High levels of NO damage DNA and lead to the nitration of the tyrosine residues in cell regulatory proteins [88, 89]. NO bursts are produced before the release of ethylene, a plant hormone which is associated with senescence and fruit ripening .
NO production from arginine represents a significant evolutionary advance in gymnosperms before angiosperms and humans evolved. Recognition of the natural and synthetic guanidino compounds as inhibitors of NOS was facilitated by the availability of authentic standards, isotopic tracers, and by the development of new analytical instrumentation [94–96].
Guanidino compounds derived from arginine in conifers
An important physiological property of the guanidino group is its ability to form a bond of high energy with phosphate. This phosphate can be transferred, without the loss of bond energy, to couple and provide energy for biochemical and mechanical processes . Guanidines with the high energy bond are called phosphagens, e.g., N-phosphorylarginine. Phosphagens are vital for the sustained action of muscles in many invertebrates and some vertebrates. N-phosphorylarginine was reported in jack pine cell cultures [97, 98] and in developmental stages in the eastern spruce budworm which feeds on conifer needles [99, 100].
In humans, a guanidino-amino acid, creatine is the precursor for phosphocreatine, which serves as the phosphagen and energy buffer . Creatine is synthesized from glycine and receives its guanidino group from arginine. I could find no evidence in spruce buds for the synthesis of creatine from 14C-glycine and [1-14C]-guanidinoacetic acid. Guanidinoacetic acid inhibited oxygen uptake and yielded 14CO2, 14C-glycine and 14C-serine. The transamidination of [1-14C]-guanidinoacetic acid with glycine yielded guanidinoacetic acid and 14C-glycine. This transamidination occurred as arginine-rich storage proteins in spruce buds were being turned over with a respiratory quotient less than one.
In spruce and pine, γ-guanidinobutyric acid is commonly reported as a product of arginine metabolism [8, 9, 42, 101, 102]. The detection of α-keto-δ-guanidinovaleric acid in white spruce suggested that the transamination of arginine with a keto acid followed by decarboxylation would account for the formation of γ-guanidinobutyric acid . In general, the naturally occurring guanidino compounds are derived by decarboxylation, transamidination, transamination, condensation, methylation, phosphorylation, cyclization, and by dehydrogenase activity [104, 105].
In the Petawawa forest and after four years of growth in continuous full, 45, 25, and 13% natural light, shade-tolerant white spruce saplings redistributed their biomass before the onset of winter dormancy . A spruce sapling requires at least 20% light to survive. Increased shading diverted soluble N from glutamate, glutamine, and aspartic acid to arginine N mainly in roots and to a lesser extent in stems, buds, and needles. γ-Guandinobutyric acid and several unidentified guanidino compounds accumulated mostly in roots of saplings at 25 and 13% light [unpublished data]. Arginine and the guanidino compounds comprise a N-rich metabolic pathway that helps to account for the ability of conifers to adapt and survive under limiting environmental conditions. Their importance in the food and medicinal practices and as markers of the inappropriate release of NO of the indigenous peoples, requires further investigation. Their role as regulators of NOS would depend on being closely related to the structure of arginine and their ability to bind to NOS.
Nutritional support in treating scurvy and critical illness
The purpose of nutritional support is to save life, preserve and improve cellular function, and to speed recovery. Critical illness is generally characterized by a combination of starvation and stress. Critical illness can be viewed in four stages : 1. Acute critical illness in response to a stressor. 2. Prolonged acute critical illness. 3. Chronic critical illness. 4. Recovery.
In the first stage, substrates are shunted away from anabolism and toward vital organ support and inflammatory proteins. Nutritional support at this stage remains unproven and may ultimately become detrimental. At stage 2, nutrition and metabolic support to prevent and treat multiple organ dysfunction syndromes become very important. This must be maintained to prevent the deficiency of water-soluble vitamins. Care must be taken not to do harm by inappropriate overfeeding. At Stadaconna, the prescribed remedy of taking the Iroquois decoction "every other day" was consistent with this purpose.
The best-understood function of vitamin C is in the synthesis of collagen . Ascorbate is required for the hydroxylation of proline residues in procollagen. Procollagen is secreted by fibroblasts as a complex of three cross-linked polypeptide chains. Cross-linking requires the formation of covalent bonds between lysine residues. The hydroxylation of proline to hydroxyproline stabilizes the triple helix structure of collagen. This contributes to the formation of fibers, which can take several months, followed by scar formation, wound contraction and healing .
Collagen subunits contain a prolyl 4-hydroxylase with one atom of non-heme iron . This enzyme requires α-ketoglutarate and oxygen as substrates. The α-ketoglutarate is oxidatively decarboxylated to carbon dioxide and succinate. A remaining oxygen atom is used to hydroxylate the proline residue in collagen. Heme iron is now oxidized to inactivate the enzyme.
Vitamin C deficiency leads to decreased collagen secretion due to capillary fragility. This is associated with defective connective tissues, poor wound healing, and susceptibility to sepsis.
The synthesis of NO by a heme-containing NOS would increase the circulation of oxygen supply in blood. The lack of vitamin C reduces the hydroxylation reactions needed for the synthesis of carnitine from lysine, and for the hydroxylation of dopamine to norepinephrine. The oxidation of tetrahydrofolic acid, which maintains adequate levels of folic acid and keeps iron in its reduced state, would be prevented .
Vitamin C has nutritional value as a co-antioxidant by interacting with vitamin E . In the prevention of disease, intervention studies with vitamin C as an antioxidant have shown no clinical benefit . Arginine supplementation and the availability of other amino acids, such as proline and glutamate, would spare the energy costs in ATP equivalents for their synthesis as substrates for collagen, and other proteins in the body .
In the winter, the Iroquois hunted a 'number of wild animals such as fawns, stags, and bears, hares, martens, foxes, otters, and others" but they were stingy and brought Cartier's crew very few. The ice was extremely thick and the sailors were too weak to fish. They would not be seriously deficient in arginine as long as some meat and fish were available. Proteins are graded by "quality" on the basis of their content of essential amino acids , and arginine is conditionally essential. Intakes of 1 to 1.5 g protein (0.16 to 0.24 g N)/dg per d are common practice and usually advised.
In healthy adults, arginine is derived from the diet, endogenous synthesis, and turnover of body proteins. Arginine is usually ingested in diets at a rate of 3 to 5 g/d . A common supplemental dose for arginine is 3 g which is taken by mouth three times a day [13, 14]
A kilogram of fresh spruce needles would contain 120 to 160 mg of free arginine N. More arginine would be available if the arginine-rich storage proteins of conifers were digested. Protein, ingested in amounts exceeding those needed to replace body losses, is deaminated. Its nitrogen is excreted as urea in urine .
In cases of catabolic stress or conditions involving a dysfunction of the kidneys or small intestine, the endogenous synthesis of arginine may not meet metabolic demands . The availability of arginine for metabolic functions is determined by its transporters in the plasma and mitochondrial membranes. During critical illness, gastric emptying would be delayed and small intestinal and colonic motility reduced . The rate-controlling enzymes in arginine synthesis and catabolism are argininosuccinate synthase, arginase isozymes, NOS, arginine decarboxylase . Control is expressed according to cell type, age developmental stage, diet, and state of health and disease.
Four enzymes use arginine as a substrate: arginine decarboxylase, arginine:glycine amidinotransferase, arginase and its isoforms, and NOS [19–21]. The main products of the four enzymes are agmatine, guanidinoacetate and ornithine, ornithine and urea, and NO and citrulline. Arginine-derived guanidinoacetate is the immediate precursor for creatine, which maintains the energy metabolism of muscle, nerve and testis . Creatine breaks down to creatinine at a constant rate and is cleared from the body by the kidneys.
In severe scurvy and in syndromes having pathological consequences, the correction of arginine deficiency could become a clinical priority. In critically ill patients, arginine maintains body homeostasis, muscle mass and function, and catabolic states [13, 20]. It triggers the body to make protein, prevents the wasting, and is used in the management of wounds in the lower extremities . Infectious complications become a serious problem [113, 114]. Host invasion triggers an intense inflammatory response, which is then amplified by further pro-inflammatory cascades . Severe cases are characterized by the rapid development of multiple organ failure resulting in mortality in excess of 40%. Dietary arginine supplementation helps to restore its plasma concentrations, boosts the immune system and helps to reduce neuropathy.
Clinical trials have used immune-enhancing enteral feeds that combine arginine with anti-inflammatory fatty acids, antioxidants, glutamine, and nucleotides. Glutamine has a potential beneficial metabolic effect in the critically ill , and in the treatment of infections in trauma patients . Glutamine is the principal fuel of enterocytes and lymphocytes. While doubt has been raised as to the value of arginine supplementation , due to the lack of its exact role in the regulation of immune functions , the European Society of Parenteral and Enteral Nutrition has published guidelines recommending the routine use of arginine-containing diets in surgical patients . An analysis of clinical studies using enteral formulas supplemented with arginine has suggested benefits upon outcomes from chronic and critical illness with little or no evidence of significant detrimental effects .
Today, vitamin and amino acid supplements have gained popularity as preventive or therapeutic agents. The excessive intake of high levels of a single amino acid or biofactor may be hazardous because of its potential for toxicity and control over genetic expressions. The effects of nutrients on gene expression are referred to as "nutrigenomics'. The study of the selective effects of arginine on gene expression is called 'argenomics'.
Did nitric oxide aid in the recovery from scurvy?
While we may never know the answer to this question, the discovery of the significance of NO in the human body remains as one of the most important developments in recent medical history. In 1987, NO production from arginine was first identified in endothelial cells . NO is a gas that transmits signals that are produced by one cell, penetrates through membranes, and regulates the function of another cell in humans and conifers (Figure 2). A recovery from scurvy involving NO occurs as a series of events over time. No model yet exists which integrates nutrition with vitamin C and NO in the Iroquois cure for scurvy.
In the severe winter at Stadaconna, the exposure of Cartier's crew to cold, poor diet, and insufficient vitamin C, would have benefited from the nutritional values of supplemental arginine, amino acids, and antioxidants. Boreal conifers lack nitrate because acid forest soils are poor in N and tissues contain little nitrate in the absence of fertilizers . Nitrates and nitrites in the decoction would not have been available for their conversion to NO by the acidic gastric juice in the stomach. Readily available free arginine remains the main N source for NO which would kill almost all bacteria that were swallowed with food.
In clinical medicine and pharmacology, NO is a factor in treating intensive care patients [11–13, 15, 18, 110, 111]. In tissues, it regulates oxygen release from red blood cells. NO protects the heart, stimulates the brain, and regulates inflammation. It improves blood circulation for the provision of essential amino acids, antioxidants and vitamins to tissues. NO is important for olfactory function and memory. White blood cells use NO to kill infectious bacteria, fungi and parasites. It defends against tumors by inducing apoptosis. Dosage is critical since NO can be toxic at high concentrations.
Levels of vitamin C were depleted during the severely cold winter. The mitochondria, being the responsible subcellular organelles for the oxidation of dietary and remaining stored fat, would generate almost all of the energy needed by humans. The oxidation of arginine to NO and citrulline is exothermic and occurs in mitochondria. Shivering generates body heat from muscles. Mitochondria generate most of the ATP that provides the energy for metabolism to occur.
In tissues that consume ATP rapidly, such as brain, and skeletal and smooth muscle, phosphocreatine serves as an energy reservoir for the rapid regeneration of ATP . Mitochondrial creatine kinase produces ATP from ADP by converting creatine phosphate to creatine in the mitochondrial intermembrane space. Creatine kinase is routinely determined in emergency patients because its elevated activity is an indication of damage to muscles, renal failure, and myocardial infarction. The oxidative reactions in mitochondria are also a major source of potentially damaging oxygen free radicals. Reactions with NO can remove these radicals, and stimulate the formation of new and larger mitochondria , which in turn would improve body bioenergetics.
Arginine is metabolized via mitochondria and in the cytosol via the urea cycle  (Figure 1). The cytosol makes up the cytoplasm of cells. It contains thousands of enzymes. Some act synergistically with vitamin C to provide a cure for scurvy and others aid in the recovery to health. NO, formed by the turnover of body proteins and supplemented by arginine from the decoction would reduce excessive stress, provide a targeted redistribution of energy resources to the vital organs, and activate a series of early and late-expressing genes as the body recovers. At the recovery stage, NO would participate in the maintenance of long-term health.
Arginine, amino acids and vitamin C are absorbed into circulation by the small intestine, and carried to collagen-rich cells throughout the body. Endothelial cells, which make up the capillaries and line blood vessels and the lymph ducts, use arginine to make NO. NO diffuses into the smooth muscle cells that surround the endothelial lining of blood vessels. This leads to muscle relaxation resulting in more blood flow to tissues, brain, lungs, kidneys, liver and other vital organs. Blood pressure is lowered. Blood flow and blood vessel diameter are improved, and the formation of blood clots would be reduced and repaired. The improvement of heart function would allow more oxygen, nutrients, vitamins, and amino acids to aid in the recovery from scurvy.
Improved circulation would relieve tension, sore muscles, the pain caused by swelling, and the accumulation of excess fluids in Cartier's crew and in Domagaia's legs. Wound healing would increase and mineral depletion would be reduced. NO is an important regulator in immune cells which fight infections and viruses. It aids in the killing of bacteria and engulfed pathogens found within the lysosomes of macrophages, which remove harmful cellular debris and dead cells. NO is a scavenger for cytotoxic free radicals that contribute to aging. NO, being involved in the transmission of messages between nerve cells connected with memory, sleeping and learning would support the wellness of sailors for their return to France.
Human NOS has three distinct isoforms having a multitude of organ-specific regulatory functions [18, 19, 21]. A constitutive form (nNOS) is found in neural tissue, and a second constitutive form (eNOS) is found in the vascular endothelium. Both are regulated by calcium and calmodulin. A third calcium-independent form (iNOS) occurs in a variety of cells after induction with inflammatory mediators and bacterial products. During inflammation, arginine transport increases . The activation of iNOS or arginase, or both, reflects the type of inflammatory response in the development of specific diseases . Sepsis, which occurred in Cartier's critically ill crew, probably involved a predominant role for arginine and iNOS . Septic shock is a life threatening complication that can have a mortality rate of 50 to 80%. Trauma exhibits a preferential induction of arginase . Arginase would reduce the arginine available as a substrate for NOS.
The formation of S-nitrosothiols provides a different mode of transporting NO, offers a buffering system that regulates the bioavailability of NO, and increases the range of NO action . In plants and humans, glutamine serves as an antioxidant by enhancing the levels of glutathione resulting in the formation of S-nitrosoglutathione [11, 22, 121]. Some S-nitrosothiols (S-nitrosocysteine, S-nitrosohomocysteine) are taken up into cells via the amino acid transport system. S-Nitrosothiols are being considered as exogenous sources of NO for the treatment of NO-deficient pathological states. They are cleared to ameliorate nitrosative stress. They regulate innate immune and vascular function. S-nitrosylation may also contribute to the posttranslational modification of proteins involved in the regulation of NO action and in the recovery from scurvy. The nitrosylation of cysteine thiols is recognized as critical for the mechanism of NO function in health and disease.
Without clinical trials, it is not clear how quickly Cartier's crew would have recovered if given only vitamin C. It is evident that the decoction with vitamin C, arginine, the essential amino acids, antioxidants and other unidentified biofactors integrated with NO production in the body and aided in the recovery from scurvy.
Guanidino compounds as NOS regulators and metabolic markers
The inappropriate release of NO is linked to the pathogenesis of a number of disease states. High levels of NO interact with molecular oxygen and superoxide radicals to produce damaging peroxynitrite that modifies proteins, lipids, and nucleic acids with harmful effects [122, 123]. The need to regulate NO production has led to the development of modulators and inhibitors of NOS activity [18, 21, 122–125]. L-arginine analogues have the advantage of being closely related to the substrate itself and may be taken up by amino acid transporters. The guanidino compounds that interfere with the binding of arginine to NOS have been the most extensively researched as drugs .
In general, guanidino-substituted L-arginine molecules are effective but they show little selectivity for the NOS isoforms. Nω-Methylations of the guanidino moiety of L-arginine have yielded potent NOS inhibitors . Their use in treating septic shock provided hemodynamic stabilization in a large number of patients. While Nω-methylated guanidino compounds have not yet been identified in conifers, they effectively inhibit NOS activity when fed to a variety of conifers [22, 23, 83, 88, 89]. L-arginine analogues with substitutions on their carbon chains, and lacking the α-amino group or α-carboxyl groups are inactive as inhibitors and as substrates for NOS. These include guanidinoacetic and γ-guanidobutyric acid.
Reviews of the physiological effects of natural and synthetic guanidino compounds in research and clinical practice are available in several books [126–128]. Among the known guanidino compounds in conifers, α-keto-δ-guanidinobutyric acid and γ-guanidinobutyric acid are found in nerve tissues  and in the urine of hyperarginemic patients . Agmatine, a decarboxylation product of arginine, which occurs in conifers, has various pharmacological effects, but little is known about its metabolism and human physiology [19, 20].
Guanidino compounds have been used as respiratory inhibitors, antibiotics, markers for metabolic disorders, and in studies of cardiovascular diseases, diabetes, and microbial activity [102, 126–128]. Markers carry information about the sites and pathological cause. In uremia, guanidine, guanidinosuccinic acid and creatinine are greatly increased in biological fluids and tissues . Guanidino compounds are implicated in hypertension, anaesthesia, hemorrhagic shock, seizure, renal dysfunction, and immersion stress . γ-Guanidinobutyric acid reacts with hydroxyl radicals and induces epileptic discharges . Its transamidination precursors are γ-aminobutyric acid and arginine .
Guanidine and the guanidino compounds have been used to treat botulism, viral diseases, diabetes, and paraneoplastic syndromes . Evidence for mechanisms of action, dosing, pharmokinetics, cautions, interactions and clinical applications remains preliminary. Synthetic guanidino compounds are used in the treatment of diabetes . Type II diabetes is one of the most serious health problems for Native Americans in the USA . Pharmacogenetic differences, which diminish or enhance the predicted response, would indicate an inherited defect . The surprisingly wide and natural diversity of chemically identified guanidino compounds in nature  may yet offer new biofactors and drugs in understanding ethnomedicine, in treating diseases, and for their contribution to regimens for human wellness.
The history of the native indigenous peoples of eastern Canada has provided evidence of a culture strong enough to withstand the most difficult hardships. Their coniferous forests have had a pervasive influence on offering a source of food, fibre, protection, and medicinal products for human survival. In the absence of forensic evidence and apart from being a source of vitamin C, the formulary nature of the decoctions from Annedda to cure scurvy and hasten the recovery of the sailors is a story that may never be completely solved nor will it end here. We do not really know the true identity of Annedda. This tree, known today as arborvitae, has subsequently been represented by many candidate coniferous trees of life.
When food was short and the winter most severe, the candidate trees of life in eastern Canada provided a source of vitamins, arginine, proline, other conditionally and essential amino acids, antioxidants, and other biofactors, which aided in the recovery from of scurvy. The discovery of vitamins and amino acids played an important role in understanding human nutrition. For the discovery of the importance of arginine-derived NO in clinical nutrition we are indebted to the investigators who were honoured by the Nobel Prize in 1998.
After the transfer of the tree of life to France, old principles were now viewed in new ways. Jean Fernel (1497–1558), a foremost figure in the French Renaissance of science and medicine, broke away from the irrationality of occultism and magic that had dominated medieval natural philosophy and medicine . His treatises on "Physiologia", first published in 1542, created debate in Europe for the next 100 years, and laid the "seeds of systems biology". To learn from history, we must transform it into a science.
Clinical nutrition is now faced with a vast amount of data from the ethnobotanical and ethnomedical literature. The detailed interdisciplinary and systematic understanding of the complex interactions among anatomy, histology, pathology, neurology, nutrition, and metabolism represents a modern-day challenge. The genetic loci of many controlling quantitative traits have been identified and are being compared in ill and healthy individuals [137–139]. Through genomics, argenomics, nutrigenomics, and other "omics" technologies, we expect to have a better understanding of how the control of complex traits would aid the recovery from sickness and diseases . Integrated databases are being developed to describe the toxological, pharmaceutical, nutritional and environmental effects of diets and drugs on disease [140–143].
The history of medicine and clinical practice has involved a succession of blind alleys and detours, mountains of often uninterpretable observations, and a great leap forward as in the discovery of vitamin C as a cure for scurvy. This review takes us centuries back, and turns our attention to the combined values of arginine, NO, proline, other conditionally and essential amino acids, guanidino compounds, and antioxidants as added factors in the food and medicines of indigenous Canadian peoples.
Burrage HS, Ed: Early English and French Voyages, from Hakluyt 1534–1608. 1906, New York: Barnes and Noble
Rousseau J: L'Annedda et l'arbre de vie. Revue d'Histoire L'Amerique Française. 1954, VIII (2): 171-212.
Van Wart AF: The Indians of the Maritime provinces, their diseases and native cures. Canadian Medical Association Journal. 1948, 59: 573-577.
Durant W, Durant A: The Story of Civilization. 1961, New York: Simon and Schuster, Part VI The Reformation. Part VII. The Age of Reason Begins. New York: Simon and Schuster;
Spary EC: Utopia's Garden. French Natural History From Old Regime to Revolution. 2000, Chicago: University of Chicago Press
Moore MI: Eastern white pine and eastern white cedar. Forestry Chronicle. 1978, 54: 222-223.
Durzan DJ, Steward FC: Nitrogen metabolism. Plant Physiology: An Advanced Treatise. Edited by: Steward FC, Bidwell RGS. 1983, New York; Academic Press, VIII: 255-265.
Durzan DJ: Nitrogen metabolism of Picea glauca. I. Seasonal changes of free amino acids in buds, shoot apices and leaves, and the metabolism of uniformly labeled 14C-L-arginine by buds during the onset of dormancy. Canadian Journal Botany. 1968, 46: 909-919.
Durzan DJ: Nitrogen metabolism of Picea glauca. IV. Metabolism of uniformly labeled 14C-L-arginine, [carbamyl-14C]-L-citrulline, and [1,2,3,4-14C]-γ-guanidinobutyric acid during diurnal changes in the soluble and protein nitrogen associated with the onset of expansion of spruce buds. Canadian Journal Biochemistry. 1969, 47: 771-783.
Nelson DL, Cox MM: Principles of Biochemistry. 2008, New York: WH Freeman, 5
Powell-Tuck J: Nutritional interventions in critical illness. Proceedings Nutrition Society. 2007, 66: 16-24.
Hollander JM, Mechanick JI: Nutrition support and the chronic illness syndrome. Nutrition in Clinical Practice. 2006, 21: 587-604.
Appleton J: Arginine: clinical potential of a semi-essential amino acid. Alternative Medicine Review. 2002, 7: 512-222.
MayoClinic: Drugs and Supplements. 2008, [http://www.mayoclinic.com/health/1-arginine/NS-patient-arginine]
McPhee SJ, Papadakis MA: Current Medical Diagnosis and Treatment. 2007, New York: McGraw-Hill, 1301-
Block G, Manels AR, Patterson BH, Levander OA, Norkus EP, Taylor PR: Body weight and prior depletion affect plasma ascorbate levels attained on identical vitamin C intake: a controlled diet study. Journal American College Nutrition. 1999, 8: 628-637.
Tannenbaum SR, Young VR: Vitamins and Minerals. Food Chemistry. Edited by: Fennema OR. 1985, New York: Marcel Dekker Inc, 477-544.
Moncada S, Higgs A: The L-arginine-nitric oxide pathway. New England Journal of Medicine. 1993, 329: 2002-2012.
Morris SM: Arginine: beyond protein. American Journal Clinical Nutrition. 2006, 83: 5085-5125.
Morris SM: Arginine metabolism: Boundaries of our knowledge. Journal of Nutrition. 2007, 137: 1620S-1609S.
Hobbs AH, Higgs A, Moncada S: Inhibition of nitric oxide synthase as a potential therapeutic agent. Annual Review Pharmacology and Toxicology. 1999, 39: 191-220.
Durzan DJ, Pedroso MC: Nitric oxide and reactive nitrogen oxide species in plants. Biotechnology and Genetic Engineering Reviews. 2002, 19: 293-337.
Durzan DJ: Nitric oxide, cell death and increased taxol recovery. Cell biology and Instrumentation: UV Radiation, Nitric Oxide, and Cell Death in Plants. Edited by: Blume Y, Durzan DJ, Smertenko P. 2006, Amsterdam: NATO Advanced Research Workshop, Yalta, Ukraine, IOS Press, 234-252. Sept 8–11, 2004
Fitzpatrick TB, Johnson A, Wolff K, Suurmond D: Color Atlas and Synopsis of Clinical Dermatology. Common and Serious Diseases. 2001, New York: McGraw-Hill
Cook R, Ed: The Voyages of Jacques Cartier. 1993, Toronto: University of Toronto Press, cf., National Humanities Center, [http://www.nhc.rtrp.nc.us/pds/pds.htm]
Hodges RE: What's new about scurvy?. American Journal Clinical Nutrition. 1971, 24: 383-384.
Hickel R: Un précurseur en dendrologie, Pierre Belon (1517–1564). Bulletin de la Société Dendrologique de France. 1924, 51: 3-75.
Bolle C: Wann erscheint die Weymouthskiefer zuerst in Europa?. Gartenflora. 1890, 39: 434-438.
Anon: A bit of forgotten history (A review of C. Bolle's articles). Garden and Forest. A Journal of Horticulture, Landscape Art and Forestry. 1890, III: 536-(Cited by ).
Houston CS: Notes et dossiers de recherche. Scurvy and Canadian exploration. Canadian Bulletin Medical History. 1990, 7: 161-167.
Moerman DE: Native American Ethnobotany. 1998, Portland OR: Timber Press Inc
Kuhnlein HV, Turner NJ: Traditional plant foods of Canadian Indigenous Peoples. 1991, Philadelphia: Gordon and Breach Sci Pub
Arnason T, Hebda R, Johns T: Use of plants for food and medicine by Native peoples of eastern Canada. Canadian Journal of Botany. 1981, 59: 2189-2325.
Hasselkus E, West C, Zampardo M: Thuja thrills. American Nurseryman. 1999, 189: 40-46.
Lower ARM: The North American Assault on the Canadian Forest. A History of the Lumber Trade between Canada and the United States. 1938, Toronto: Ryerson Press
Carpenter KJ: The History of Scurvy and Vitamin C. 1987, Cambridge: Cambridge University Press
Watt J, Freeman EJ, Bynum WF, Eds: Starving Sailors. 1981, Greenwich: National Maritime Museum, 131-162.
Schick B: A tea prepared from needles of pine trees against scurvy. Science. 1943, 98: 241-242.
Macnamara C: Vitamin C in Evergreen-Tree Needles. Science. 1943, 98: 242-
Kodicek EH, Young FG: Captain Cook and scurvy. Notes and Records of the Royal Society of London. 1969, 24: 43-63.
Parrish CC, Turner N, Solberg SM, Eds: Resetting the Kitchen Table: Food Security, Culture, Health and Resilience in Coastal Communities. 2006, Hauppague, New York: Nova Science Publ
Beaglehole JC, Ed: The Journals of Captain James Cook on his Voyages of Discovery. II. The Voyage of the Resolution and Adventure. 1772–1775. 1961, Cambridge: Cambridge University Press
Beaglehole JC, Ed: The Journals of Captain James Cook on his Voyages of Discovery. III. The Voyage of the Resolution and Adventure. 1776–1780. 1967, Cambridge: Cambridge University Press
Blouin G: Medicinal uses of forest trees and shrubs by indigenous people of northeastern North America. Proceedings XII World Forestry Congress, Quebec City, Canada. 2003, 21-28.
Zimmer C: Isolated tribe gives clues to the origins of syphilis. Science. 2008, 319: 272-
Koon HEC, Collins MJ: Scurvy, the scourge of guinea pigs and man. Proceedings of the 3rd International Symposium on Biomolecular Archeology: 14–16. 2008, University of York, Session 2, (Cf. Old bones reveal new signs of scurvy. Science 2008, 322:368–369)., September ; Rpt 1
Schulze E: Über die beim Umsatz der Proteinstoffe in den Keimpflanzen einiger Coniferen Arten entstehanden Stickstoffverbindungen. Zeitschrift physiologische Chemie. 896 (22): 435-448.
Klein G, Tauböck K: Argininstoffewechsel und Harnstoffgenese bei höheren Pflanzen. Biochemische Zeitschrift. 1932, 251: 10-50.
Durzan DJ, Chalupa V: Free sugars, amino acids, and soluble proteins in the embryo and female gametophyte of jack pine as related to climate at the seed source. Canadian Journal of Botany. 1968, 46: 417-428.
Durzan DJ, Mia AJ, Ramaiah PK: The metabolism and subcellular organization of jack pine embryo (Pinus banksiana) during germination. Canadian Journal of Botany. 1971, 49: 927-938.
Durzan DJ, Mia AJ, Wang BSP: Effects of tritiated water on the metabolism and germination of jack pine seeds. Canadian Journal of Botany. 1971, 49: 2139-2149.
Durzan DJ: Nitrogen metabolism of Picea glauca. III. Diurnal changes of amino acids, amides, protein, and chlorophyll in leaves of expanding buds. Canadian Journal of Botany. 1968, 46: 929-937.
Ramaiah PK, Durzan DJ, Mia AJ: Amino acids, soluble proteins and isoenzyme patterns of peroxidase during the germination of jack pine. Canadian Journal of Botany. 1971, 49: 2151-2161.
Durzan DJ, Ramaiah PK: The metabolism of L-proline by jack pine Seedlings. Canadian Journal of Botany. 1971, 49: 2163-2173.
Durzan DJ, Pitel J, Ramaiah PK: Acid soluble nucleotides and ribonucleic acids from germinating jack pine seeds. Canadian Journal of Forest Research. 1972, 2: 206-216.
Durzan DJ, Pitel J, Mia AJ, Ramaiah PK: Metabolism of uracil by germinating jack pine seedlings. Canadian Journal of Forest Research. 1973, 3: 209-221.
Rowe JW: Natural Products of Woody Plants. I. Chemicals Extraneous to the Lignocellulosic Cell Wall. 1989, New York, Springer Verlag
Durzan DJ: Nitrogenous extractives. Amino acids, proteins, and nucleic acids. Natural Products of Woody Plants. 1. Chemicals Extraneous to the Lignocellulosic Cell Wall. Edited by: Rowe JW. 1989, New York, Springer Verlag, 179-200.
Hodges JD, Barras SJ, Mauldin JK: Free and protein-bound amino acids in the inner bark of loblolly pine. Forest Science. 1968, 14: 330-333.
Passwater RA, Kandaswami C: Pycnogenol: The Super Protector Nutrient. 1994, Connecticut: Keats Publications Inc
Virgili F, Kobuchi H, Packer L: Procyanidins extracted from Pinus maritima (Pycnogenol®): scavengers of free radical species and modulators of nitrogen monoxide metabolism in activated murine RAW 264.7 macrophages. Free Radical Biology and Medicine. 1998, 24: 1120-1129.
Chandler RF: Vindication of Maritime Indian herbal remedies. Journal of Ethnopharmacology. 1983, 9: 323-327.
Jones NP, Arnason JT, Abou-Zaid M, Akpagana K, Sanchez-Vindas P, Smith ML: Antifungal activity of extracts from medicinal plants used by First Nations Peoples of eastern Canada. Journal of Ethnopharmacology. 2000, 73: 191-198.
Felter WH: A Treatise on Thuya occidentalis. Drug Treatise No. 1. 1904, Cincinnati Ohio: Lloyd Bros
Hartzell H: The Yew Tree: A Thousand Whispers: Biography of a Species. 1991, Eugene OR: Hulogosi
Appendino G: The phytochemistry of the yew tree. Natural Product Reports. 1995, 12: 349-360.
Durzan DJ, Ventimiglia F: Free taxanes and the release of bound compounds having taxane antibody reactivity by xylanase in female, haploid-derived cell suspension cultures of Taxus brevifolia. In Vitro Plant Cell and Developmental Biology. 1994, 30P: 219-227.
Choi H-K, Kim S-I, Song J-Y, Son J-S, Hong S-S, Durzan DJ, Lee H-J: Localization of paclitaxel in suspension cultures of Taxus chinensis. Journal Applied Microbiology & Biotechnology. 2001, 11: 458-462.
Chalupa V, Durzan DJ: Growth and development of resting buds of conifers in vitro. Canadian Journal of Forest Research. 1973, 3: 196-208.
Durzan DJ: Nitrogen metabolism of Picea glauca. II. Diurnal changes of free amino acids, amides, and guanidino compounds in roots, buds, and leaves during the onset of dormancy of white spruce saplings. Canadian Journal of Botany. 1968, 46: 921-928.
Durzan DJ: Free amino acids as affected by light intensity and the relation of responses to the shade tolerance of white spruce and shade intolerance of jack pine. Canadian Journal of Forest Research. 1971, 1: 131-140.
Durzan DJ, Steward FC: The nitrogen metabolism of Picea glauca (Moench) Voss and Pinus banksiana Lamb. as influenced by mineral nutrition. Canadian Journal of Botany. 1967, 45: 695-710.
Durzan DJ: Nitrogen metabolism of Picea glauca. V. Metabolism of uniformly labeled 14C-L-proline and 14C-L-glutamine by dormant buds in late fall. Canadian Journal of Botany. 1973, 51: 359-369.
Buchanan BB, Gruissem W, Jones RL: Biochemistry and Molecular Biology of Plants. 2000, Rockville MD: American Society of Plant Physiologists
Naylor AW: Interrelations of ornithine, citrulline and arginine in plants. Symposium Society of Experimental Biology. 1959, 13: 193-209.
Barnes RL, Naylor AW: Studies on the ornithine cycle in roots and callus tissue of Pinus serotina and Pinus clausa. Botanical Gazette. 1959, 121: 63-69.
Guitton Y: Métabolisme de l'arginine dans le premiers stades de développement de Pinus pinea L. Physiologie Végétale. 1964, 2: 95-156.
Durzan DJ: The incorporation of tritiated water into amino acids in the presence of urea by white spruce seedlings in light and darkness. Canadian Journal of Botany. 1973, 51: 351-358.
Durzan DJ: The metabolism of 14C-urea by white spruce seedlings in light and darkness. Canadian Journal of Botany. 1973, 51: 1197-1211.
Durzan DJ: The fate of carbon during the assimilation of carbamoyl phosphate in white spruce seedlings as revealed by [14C]-carbamoyl phosphate, [14C]-cyanate, and [14C]-bicarbonate labeling patterns. Physiology Plantarum. 1983, 59: 233-241.
Todd CD, Cooke JEK, Gifford DJ: Purification and properties of Pinus taeda arginase from germinated seedlings. Plant Physiology & Biochemistry. 2001, 39: 1037-1045.
Greenstein JP, Winitz M: Chemistry of the Amino Acids. 1961, New York: John Wiley & Sons, 1:
Magalhaes JR, Pedroso MC, Durzan DJ: Nitric oxide, apoptosis and plant stresses. Physiology & Plant Molecular Biology. 1999, 5: 115-125.
Crawford NM: Mechanisms for nitric oxide synthesis in plants. Journal Experimental Botany. 2005, 57: 471-478.
Bard-Besson A, Pugin A, Wendehenne D: New insights into Nitric Oxide signaling in plants. Annual Review of Plant Biol. 2008, 59: 21-39.
Mori T: Effect of nitrogen nutrition on citrulline accumulation in Cryptomeria japonica shoots. Journal Japanese Forest Society. 1976, 58: 15-19.
Garcês H, Durzan DJ, Pedroso MC: Mechanical stress elicits nitric oxide formation and DNA fragmentation in Arabidopsis thaliana. Annals of Botany. 2001, 87: 567-574.
Pedroso MC, Magalhaes JR, Durzan DJ: A nitric oxide burst precedes apoptosis in an angiosperm and a gymnosperm. Journal Experimental Botany. 2000, 51: 1027-1036.
Pedroso MC, Magalhaes JR, Durzan DJ: Nitric oxide induces cell death in Taxus cells. Plant Science. 2000, 157: 173-181.
Durzan DJ: Stress-induced nitric oxide and adaptive plasticity in conifers. Journal of Forest Science. 2002, 48: 281-291.
Havel L, Durzan DJ: Apoptosis in plants. Botanica Acta. 1996, 109: 268-277.
Durzan DJ: Monozygotic cleavage polyembryogenesis. Cytology and Genetics. 2008, 42: 159-173.
Magalhaes JR, Monte DC, Durzan DJ: Nitric oxide and ethylene emission in Arabidopsis thaliana. Physiology and Plant Molecular Biology. 2000, 6: 117-127.
Durzan DJ: Automated chromatographic analysis of free monosubstituted guanidines in physiological fluids. Canadian Journal of Biochemistry. 1969, 47: 657-664.
Durzan DJ: Column chromatographic separation of guanidines. Journal of Chromatography. 1972, 74: D146-D149.
Ventimiglia FV, Durzan DJ: The determination of monosubstituted guanidines using a dedicated amino acid analyzer. Liquid Chromatography/Gas Chromatography. 1986, 4: 1121-1124.
Durzan DJ, Chalupa V: Growth and metabolism of cells and tissue of jack pine (Pinus banksiana). 4. Changes in amino acids of callus and in seedlings of similar genetic origin. Canadian Journal of Botany. 1976, 54: 468-482.
Durzan DJ, Chalupa V: Growth and metabolism of cells and tissue of jack pine (Pinus banksiana). 5. Changes in free arginine and Sakaguchi-reactive compounds during callus growth and in germinating seedlings of similar genetic origin. Canadian Journal of Botany. 1976, 54: 483-495.
Durzan DJ, Pitel JA: Occurrence of N -phosphoryl-arginine in the spruce budworm (Choristoneura fumiferana). Journal of Insect Biochemistry. 1977, 7: 11-13.
Durzan DJ, Lopushanski SM: Free and bound amino acids of spruce budworm larvae feeding on balsam fir and red and white spruce. Journal of Insect Physiology. 1968, 14: 1485-1497.
Barnes RL: Formation of γ-guanidinobutyric acid in pine tissue. Nature. 1962, 193: 781-
Bidwell RGS, Durzan DJ: Some recent aspects of nitrogen metabolism. Historical and Recent Aspects of Plant Physiology: A Symposium Honoring F. Steward. Edited by: Davies PJ. 1975, Ithaca New York: Cornell University Press, College of Agriculture and Life Sciences, 162-227.
Durzan DJ, Richardson RG: The occurrence and role of α-keto-δ-guanidinovaleric acid in white spruce Picea glauca (Moench) Voss. Canadian Journal of Biochemistry. 1966, 44: 141-143.
van Thoai N: Nitrogen bases. Comprehensive Biochemistry: Lipids and Amino Acids and Related Compounds. Edited by: Florkin M, Stotz EH. 1965, Amsterdam: Elsevier, 6: 208-253.
Matsuda H, Suzuki Y: γ-Guanidinobutyraldehyde dehydrogenase of Vicia faba leaves. Plant Physiology. 1984, 76: 654-657.
McChance KL, Huether SE: Pathophysiology. The Biological Basis for Disease in Adults and Children. 1998, St. Louis: Mosby
Fürst P: The role of antioxidants in nutritional support. Proceedings of Nutrition Society. 1996, 55: 945-961.
Padayhatty SJ, Katz A, Wang Y, Eck P, Kwon O, Lee J-H, Chen S, Corpe C, Dutta A, Dutta SK, Levine M: Vitamin C as an antioxidant: Evaluation of its role in disease prevention. Journal American College of Nutrition. 2003, 22: 18-35.
Atkinson D: Cellular energy metabolism and its regulation. 1977, New York: Academic Press
Brody TM, Larner J, Minneman KP: Human Pharmacology. Molecular to Clinical. 1998, St. Louis: Mosby, 3
Popovic PJ, Zeh HJ, Ochoa JB: Arginine and immunity. Journal Nutrition. 2007, 137: 1681S-1686S.
Wyss M, Kaddurah-Daouk R: Creatine and creatinine metabolism. Physiological Reviews. 2000, 80: 1107-1213.
Patel GK: The role of nutrition in the management of lower extremity wounds. International Journal of Lower Extremity Wounds. 2005, 4: 12-22.
Baudouin S: Critical illness: an overview of the physiological and metabolic changes. Endocrine Abstracts. 2008, 14: S28-
Boelens PG, Houdijk APJ, Fonk JCM, Nijveldt RJ, Ferwerda CC, Von Blomberg-Van der Flier , Thijs LG, Haarman HJT, Puyana JC, Van Leeuwen PAM: Glutamine-enriched enteral nutrition increases HLA-DR expression on monocytes of trauma patients. Journal of Nutrition. 2002, 132: 2580-2586. 112
Schutz T, Valentini I, Herbst B, Lochs H: European Society for Clinical Nutrition and Metabolism. ESPEN guidelines on enteral nutrition: summary. Zeitschrift Gastroenterologie. 2006, 44: 683-684.
Zaloga GP, Siddiqui R, Terry C, Marik PE: Arginine: mediator or modulator of sepsis. Nutrition in Clinical Practice. 2004, 19: 201-215.
Ignarro IJ, Buga GM, Wood KS, Byrns RE, Chaudhuri G: Endothelium-derived relaxing factor produced and released from artery and vein is nitric oxide. Proceedings National Academy Sciences USA. 1987, 84: 9265-9269.
Nisoli E, Clementi E, Paolucci C, Cozzi V, Tonello C, Sciorati C, Bracale R, Valerio A, Francolini M, Moncada S, Carruba MO: Mitochondrial biogenesis in mammals: The role of endogenous nitric oxide. Science. 2003, 299: 896-899.
Zhang Y, Hogg N: S-Nitrosothiols: cellular formation and transport. Free Radical Biology and Medicine. 2005, 7: 831-838.
Corpas FJ, Carreras A, Esteban FJ, Chaki M, Valerrama R, del Rio LA, Barroso JB: Localization of S-nitrosothiols and assay of nitric oxide synthase and S-nitrosoglutathione reductase activity in plants. Methods in Enzymol. 2008, 427: 561-573.
Pryor WA, Squadrito GL: The chemistry of peroxynitrite: a product from the reaction of nitric oxide with superoxide. American Journal Physiology – Lung Cellular and Molecular Physiology. 1995, 268: L699-L722.
Pryor WA, Houk KN, Foote CS, Fukuto JM, Ignarro LJ, Squadrito , Davies KJA: Free radical biology and medicine: it's a gas, man!. American Journal Physiology – Regulatory, Integrative and Comparative Physiology. 2006, 291: R491-R511.
Alderton WK, Cooper CE, Knowles RG: Nitric oxide synthases: structure, function and inhibition. Biochemical Journal. 2001, 357: 593-615.
Lefèvre-Groboillot D, Boucher J-L, Stuehr DJ, Mansuy D: Relationship between the structure of guanidines and N-hydroxyguanidines, their binding to inductible nitric oxide synthase (iNOS) and their iNOS-catalyzed oxidation to NO. Federation of Experimental and Biological Sciences Journal. 2005, 272: 3172-3183.
Clark JF, Ed: Guanidino compounds in Biology and Medicine. Molecular and Cellular Biochemistry. 2003, 244 (1 and 2): 204-
Mori A, Cohen BD, Koide H, Eds: Guanidines 2. Further Explorations of the Biological and Clinical Significance of Guanidino Compounds. 1989, New York: Plenum Press
Mori A, Ishida M, Clark JF, Eds: Guanidino compounds in Biology and Medicine. 1999, London: Blackwell, 5
Pisano JJ, Chozo M, Udenfriend S: Biosynthesis of γ-guanidinobutyric acid from γ-aminobutyric acid and arginine. Nature. 1957, 180: 1125-1126.
De Deyn P, Macdonald R, Marescau R, Lowenthal A: α-Keto-δ-guanidinobutyric acid, a compound isolated from hyperargininemic patients, displays epileptogenic activities. Guanidines 2. Further Explorations of the Biological and Clinical Significance of Guanidino Compounds. Edited by: Mori A, Cohen BD, Koide H. 1989, New York, Plenum Press, 251-257.
Vanholder R, Schepers E, Meert N, Lameire N: What is uremia? Retention versus oxidation. Blood Purification. 2006, 24: 33-38.
Beers MH, Ed: The Merck Manual of Diagnosis and Therapy. 2006, Whitehouse Station New Jersey: Merck Research Laboratories, 1152-1153. 18
Oubré AY, Carlson TJ, King SR, Reaven GM: From plant to patient: an ethnomedical approach to the identification of new drugs for the treatment of NIDDM. Diabetologia. 1997, 40: 614-617.
Berlinck RGS, Kossuga MH: Natural guanidine derivatives. Natural Product Reports. 2005, 22: 516-550.
Forrester JM: The Physiologia of Jean Fernel. 2003, Darby PA: American Philosophical Society and Diane Publishing Co
Welch GR: In Retrospect: Fernel's Physiologia. Nature. 2008, 456: 446-447.
Hampton JR: Evidence-based medicine, opinion-based medicine, and real-world medicine. Perspectives in Biology and Medicine. 2002, 45: 549-568.
Morley M, Molony CM, Weber T, Devlin J, Ewens KG, Spielman RS, Cheung VG: Genetic analysis of genome-wide variations in human gene expression. Nature. 2004, 430: 743-747.
Flint J, Mott R: Finding the molecular basis of quantitative traits. Successes and pitfalls. Nature Reviews Genetics. 2001, 2: 437-445.
Dunn WB, Ellis DI: Metabolomics: current analytical platforms and methodologies. Trends in Analytical Chemistry. 2005, 24: 285-294.
Fiehn O: Combining genomics, metabolome analysis, and biochemical modeling to understand metabolic networks. Comparative Functional Genetics. 2001, 2: 155-168.
Watkins SM, German B: Toward the implementation of metabolomic assessments of human health and nutrition. Current Opinions Biotechnology. 2002, 13: 512-516.
Nicholson JK, Lindon JC: Metabonomics. Nature. 2008, 455: 1054-1056.
The author in indebted to Mary Moore (1978) at Petawawa regarding the identity of Annedda. W. B. Stewart (1976) at Fredricton NB, G. DuLong (1977) at Quebec, and Kat Anderson at Davis (2008) provided manuscripts and references on food sources, medicines and cures used by indigenous peoples in eastern Canada. Research cited in this review was supported by the Canadian Forestry Service (1966 to 1972) at Petawawa and Ottawa, by the University of California's McIntyre-Stennis funds (1990 to 1993) for analytical work with guanidino compounds, and NASA (NG 9–825) (1996–1998) for the research on NO and paclitaxel in simulated microgravity.
The author declares that they have no competing interests.
About this article
Cite this article
Durzan, D.J. Arginine, scurvy and Cartier's "tree of life". J Ethnobiology Ethnomedicine 5, 5 (2009). https://doi.org/10.1186/1746-4269-5-5
- Nitric Oxide
- Indigenous People
- Essential Amino Acid