Open Access

Ethnomedicinal plant knowledge and practice of the Oromo ethnic group in southwestern Ethiopia

Journal of Ethnobiology and Ethnomedicine20084:11

DOI: 10.1186/1746-4269-4-11

Received: 17 December 2007

Accepted: 29 April 2008

Published: 29 April 2008

Abstract

An ethnomedicinal study was conducted to document the indigenous medicinal plant knowledge and use by traditional healers in southwestern Ethiopia from December 2005 to November 2006. Data were collected from 45 randomly selected traditional healers using semi-structured interviews and observations. Sixty-seven ethnomedicinal plant species used by traditional healers to manage 51 different human ailments were identified and documented. Healers' indigenous knowledge was positively correlated with their reported age but not with their educational level. High degree of consensus was observed among traditional healers in treating tumor (locally known as Tanacha), rabies (Dhukuba Seree) and insect bite (Hadhaa). The use of more than one species was significantly cited for remedy preparations. The reported abundance of the ethnomedicinal plant species varied significantly with respect to the presence of multiple uses of the reported species. Our results showed that ethnomedicinal plant species used by healers are under serious threat due to several factors, which indicates the need for urgent attention towards their conservation and sustainable utilization.

Background

Ethnomedicinal plants have been used since ancient time for human healthcare and still remain the most widely used medication system in developing and least developed nations like Ethiopia where over 80% of the population is dependent on traditional medicines [1]. The reliance of people on ethnomedicine has been for reasons of cost-effectiveness, acceptability, biomedical benefits and accessibility. There has been a continuous growth of demand for herbal medicines globally [2]. The demand has been increasing as a result of growth of human populations and the frequently inadequate provision of modern medicine [3]. Numerous species of ethnomedicinal plants are threatened in most of developing nations mainly due to overexploitation, overgrazing, habitat loss and alteration, destructive harvesting techniques, unsustainable trade and deforestation [4]. The loss of medicinal plant species has also been aggravated by the erosion of the age old accumulated indigenous knowledge on traditional use and management of these plants as its transfer system is widely known to be poor [1, 5, 6].

In Ethiopia, ethnomedicinal plant knowledge and use is underreported and most of the studies made so far are not focused on specific ethnic group or agro ecological zone of the country. Therefore, the main objective of this study was to document the ethnomedicinal plant species used to manage human ailments and the associated indigenous knowledge in and around Gilgel Gibe Hydropower Reservoir, southwestern Ethiopia.

Materials and methods

Study area and population

The study was carried out in nine Kebeles (the smallest administrative units in Ethiopia) belonging to three districts (Omo Nada, Kersa and Tiro Afeta) around Gilgel Gibe Hydropower Reservoir, Jimma Zone, southwestern Ethiopia. Jimma Zone is one of the administrative zones in Oromia Region of Ethiopia. It is one of the major coffee growing areas of the country contributing much to the economy of the nation. The population of Omo Nada, Kersa and Tiro Afeta is 254417, 329629 and 130554, respectively [7]. The study Kebeles under the aforementioned districts were Siba, Degoso, Asandabo, Burqaa, Waqtolaa, Gudeta Bula, Qajaloo, Ayino and Dacha Nadhii (Figure 1). The study area is located at about 265 km southwest of the capital Addis Ababa and 65 km Northeast of Jimma town at 07°42'37" – 07°53'50" N and 037°11'22" – 037°20'36" E. It has an altitudinal range of 1675 to 2094 m, a mean annual temperature of 19.2°C and receives an annual rainfall ranging from 1200 – 2800 mm. Evergreen montane thickets and shrubs are typical vegetation types of the area. Cultivating crops (maize, teff, sorghum, barley, pulses and false banana) and rearing of livestock are the major socioeconomic activities of the local people.
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Figure 1

Location of the study Kebeles in the three selected districts of Jimma Zone, Ethiopia.

The people of the study area belong to the Oromo ethnic group, which is the largest ethnic group in Ethiopia [8], consisting about 40% of the population of the nation [9]. The people of Oromo speak Afaan Oromo, which is one of the Kushitic language families of the Afro-Asiatic language group [10]. The Oromo people living in different parts of the country were engaged in different socio-economic activities as pastoralists and sedentary agriculturalists for centuries. Currently, the dominant socioeconomic activity of the Oromo people is mixed farming. The major religions of the Oromos are now Islam and Christianity [11]. The people have a long tradition of social organization, the Gada System, by which they maintain their social, political and cultural systems. Moreover, traditional healers of the Oromo people are well known in treating many illnesses with medicines made from local medicinal plant species and individuals also were known to use plants for home remedies for minor illnesses.

Data collection

Ethnobotanical data were collected from December 2005 to November 2006. Ethical clearance was obtained from Jimma University Ethics and Review Committee and written consent to undertake the study was sought from district leaders of Omo Nada, Kersa and Tiro Afeta. The full names and residential addresses of traditional healers residing in the nine selected Kebeles within 20 Km distance from Gilgel Gibe Dam were exhaustively identified and registered with the help of local administrators, local people, translators and field assistants. Individuals who were indicated to know and practice at least one medicinal plant species were considered as traditional healers in this study. A total of 90 healers were identified and registered. From this list, 45 healers were selected randomly and considered as the study subjects. Semi-structured interviews were then employed and observations [12] made to collect ethnomedicinal data with the help of local language translators and field assistants. Some of the events during data collection are shown in Additional file 1.

Data on age, sex, level of education, occupation, religion, ethnicity, human diseases treated, local names of plants used, degree of management (wild/cultivated), abundance, parts used, condition of plant part used (fresh/dried), methods of remedy preparations, remedy preservation (storage), dosage prescriptions, routes of remedy administration, noticeable adverse effects of remedies, use of antidotes for adverse effects, indigenous knowledge transfer, other uses of the ethnomedicinal plant species, existing threats to these species and traditional conservation practices were gathered during the interviews. The authors also made observations in the field on the general habitats and the ethnomedicinal plants collected by accompanying traditional healers, translators and field assistants. The collected voucher specimens were pressed, numbered, dried, identified and deposited at Jimma University Regional Herbarium and The National Herbarium (ETH) in Addis Ababa University. Identification of specimens was made with the help of herbarium materials, experts and taxonomic keys in the Flora of Ethiopia and Eritrea [1320]. The local names of diseases are included in the following text within brackets.

Data analyses

Facilities in MS Excel spread sheet were utilized to make simple calculations, determine proportions and draw bar graphs. Informant consensus factor (ICF) values were determined following [21] to evaluate the consensus among traditional healers. These values were calculated as: ICF = nuc – ns/nuc – 1, where nuc = number of use citations, ns = number of species used for each use citation. Moreover, the level of fidelity (Fl) was computed to determine the most important species used by the healers according to [22] as: Fl (%) = (SF/TF)100, where SF = frequency of citation of a species for a specific ailment and TF = total number of citations of that species.

Chi-square (X2), Spearman Rank Correlation and Binomial Tests were also employed to analyze ethnomedicinal data using SPSS 12.0.1 software package. Chi-square test was used to determine if there was a significant difference (p < 0.05) on i) the mean number of medicinal plant species reported by each healer versus district; and ii) the abundance of medicinal plant species with respect to plant part used, condition of plant part used (fresh/dried), marketability, and added values of the medicinal species.

The Spearman Rank Correlation Test was employed to evaluate whether there was significant (p < 0.05) correlation between i) the diversity of medicinal plant species recorded and altitude; ii) the age of traditional healers and the number of ethnomedicinal plant species reported; and iii) the educational level of healers and the number of species reported.

The Binomial Test was used to evaluate whether i) the indigenous knowledge was transferred to generations; ii) modernization had any influence on the transfer of the indigenous knowledge; iii) taboos were present during collection and processing of remedies, iv) mixtures of species were used more frequently, v) healers were preserving (storing) remedies, vi) dosage prescriptions were similar for different age groups, vii) remedies were devoid of adverse effects after administration, viii) healers were using antidotes for noticeable adverse effects, ix) the reported species were mainly marketable, x) the species reported were threatened in the study area, xi) the medicinal species had added values; and xii) most healers were practicing conservation of the reported species.

Results

Particulars of traditional healers

All of the traditional healers involved in the study were male, married, Muslims and farmers, except one, who was a self-employed traditional medicine practitioner. The traditional healers belonged to the Oromo ethnic group. Their reported ages ranged from 25 to 87, and each traditional healer had a mean family number of eight. The majority (53%) were illiterate and those who could read and write constituted 33% while 13% attended grades one to four.

Reported human ailments and consensus of healers

Fifty one different human ailments were treated by the traditional healers using various ethnomedicinal plant species. High degree of consensus (ICF = 0.50) was observed among the traditional healers in treating tumor (Tanacha) and that this disease was treated by employing Tapinanthus globiferus (A. Rich.) Tieghem, Gloriosa superba L. and Plumbago zeylanica L. (Table 1).
Table 1

Healers' consensus factor and fidelity levels

Ailment

ICF

Species

Fidelity level (%)

Tumor

0.50

Gloriosa superba L.

66.67

  

Plumbago zeylanica L.

40.00

Rabies

0.33

Ricinus communis L.

100.00

  

Salix subserrata Willd.

50.00

  

Afrocarpus falcatus (Thunb.) C. N. Page

50.00

Insect bite

0.33

Alysicarpus quartinianus A. Rich.

33.33

  

Cassia arereh Del.

50.00

Rheumatism

0.29

Croton macrostachyus Del.

42.86

  

Plumbago zeylanica L.

20.00

  

Justicia schimperiana (Hochst. ex Nees) T. Anders.

50.00

  

Momordica foetida Schumach.

33.33

  

Calpurnia aurea (Ait.) Benth.

25.00

  

Clausena anisata (Willd.) Benth.

33.33

Rissaa

0.25

Croton macrostachyus Del.

14.29

  

Cyathula uncinulata (Shrad.) Schinz

50.00

  

Clerodendrum myricoides (Hochst.) Vatke

40.00

Rabies (Dhukuba Seree) and insect bite (Hadhaa) shared the second highest degree of consensus (ICF = 0.33) (Table 1). Freshly pounded and squeezed leaves of Ricinus communis L. were reported to be used along with milk in treating patients of rabies (Dhukuba Seree). Crushed leaves of Salix subserrata Willd. and Afrocarpus falcatus (Thunb.) C. N. Page were also used in fresh form, mixed with water and milk, to treat the same disease.

On the other hand, traditional healers treat insect bite (Hadhaa) by applying leaf poultices of Alysicarpus quartinianus A. Rich. and Canavalia africana Dunn. Leaves or roots of A. quartinianus were also crushed while fresh and bandaged over infected sites with a clean piece of cotton cloth. The stem bark of Cassia arereh Del. was also pounded either in fresh or dried conditions and dressed on infected sites with a piece of cotton cloth to treat this ailment.

The consensus factor among traditional healers for rheumatism was 0.29. Eleven ethnomedicinal plant species were effective to treat this ailment: Dregea schimperi (Decne.) Bullock, Croton macrostachyus Del., P. zeylanica, Justicia schimperiana (Hochst. ex Nees) T. Anders., Clutia abyssinica Jaub. & Spach., Celtis africana Burm. f., Momordica foetida Schumach., Ocimum gratissimum L., Calpurnia aurea (Ait.) Benth., Bersama abyssinica Fresen. and Clausena anisata (Willd.) Benth.

Rissaa was still another ailment reported with considerable consensus among the traditional healers with an ICF value of 0.25. Leaves of C. macrostachyus and Cyathula uncinulata (Shrad.) Schinz were crushed in fresh, mixed with water and very small amount of it (only base of a cup) was reported to be drunk to treat this ailment. The roots of Clerodendrum myricoides (Hochst.) Vatke were also reported to be crushed in fresh, squeezed and the juice mixed with milk and eventually administered orally in very small amount while leaves of Desmodium repandum (Vahl) DC. were crushed in fresh and pasted over the body.

Indigenous knowledge and diversity of medicinal plant species

The correlation between the age of traditional healers and the number of medicinal species reported by each healer was highly significant. The statistical details are presented in Table 2. Older traditional healers mentioned more number of medicinal plant species than younger healers. Cross tabulation of the result on the mean number of species reported by each traditional healer versus district also showed highly significant difference. However, no significant correlation was observed between the educational level of traditional healers and the number of species reported by each healer.
Table 2

Statistical tests of significance

Type of test

Variables tested

r

χ2

df

p-value

Chi-square

Mean no spp Vs District

 

286.401*

27

0.0001

 

Spp abundance Vs Parts used

 

232.134*

76

0.0001

 

Spp abundance Vs Condition used (Fresh/Dried)

 

167.170*

12

0.0001

 

Spp abundance Vs Marketability

 

167.538*

8

0.0001

 

Spp abundance Vs Added values

 

17.343*

4

0.0002

Spearman Rank Correlation

Diversity of spp Vs Altitude

-0.290**

  

0.0001

 

Age of healers Vs No spp

0.446**

  

0.0001

 

Educational level of healers Vs No spp

0.055*

  

0.483

* Significant at 0.05 level (two tailed); ** Correlation is significant at the 0.01 level (two tailed).

High diversity of medicinal plant species was recorded with a total of 67 species, 65 genera and 35 botanical families (see Additional file 2). Highly significant negative correlation was observed between altitude where medicinal plants were collected and the number of medicinal plant species recorded. Fabaceae was represented with the highest number of species (10). This was followed by Euphorbiaceae (6 species), Asteraceae (5 species), Lamiaceae (4 species) and Solanaceae (3 species). Acanthaceae, Asclepiadaceae, Cucurbitaceae, Loranthaceae, Malvaceae, Myrsinaceae, Ranunculaceae, Rubiaceae and Rutaceae were represented with two species each while the other 21 families were represented with one species each (Table 3). The majority (76%) of these medicinal plant species were wild while few (13%) were both wild and cultivated and the remaining (12%) were cultivated.
Table 3

Medicinal plant families in the study area with the corresponding numbers of species

Families

Species

Proportion (%)

Fabaceae

10

14.93

Euphorbiaceae

6

8.96

Asteraceae

5

7.46

Lamiaceae

4

5.97

Solanaceae

3

4.48

Rutaceae

2

2.99

Rubiaceae

2

2.99

Ranunculaceae

2

2.99

Myrsinaceae

2

2.99

Malvaceae

2

2.99

Loranthaceae

2

2.99

Cucurbitaceae

2

2.99

Asclepiadaceae

2

2.99

Acanthaceae

2

2.99

Vitaceae

1

1.49

Ulmaceae

1

1.49

Salicaceae

1

1.49

Podocarpaceae

1

1.49

Poaceae

1

1.49

Plumbaginaceae

1

1.49

Phytolaccaceae

1

1.49

Oxalidaceae

1

1.49

Oleaceae

1

1.49

Myricaceae

1

1.49

Moraceae

1

1.49

Menispermaceae

1

1.49

Melianthaceae

1

1.49

Hypericaceae

1

1.49

Flacourtiaceae

1

1.49

Dioscoriaceae

1

1.49

Colchicaceae

1

1.49

Boraginaceae

1

1.49

Apocynaceae

1

1.49

Amaranthaceae

1

1.49

Verbenaceae

1

1.49

Woody species (21 shrub species, 32% and 16 tree species, 24%) were more frequently used for traditional medicine preparations than other life forms. Herbs, climbers and lianas accounted for 14%, 12%, and 9%, respectively (Figure 2).
https://static-content.springer.com/image/art%3A10.1186%2F1746-4269-4-11/MediaObjects/13002_2007_Article_115_Fig2_HTML.jpg
Figure 2

Medicinal plant habits and proportion of human ailments treated.

According to traditional healers, extensive indigenous plant use knowledge was retained and transferred orally to a selected family member. Most of the traditional healers reported that modernization had no effect on the transfer of the indigenous knowledge to generations. The majority of traditional healers also reported that there were no taboos associated with medicinal plant collection and uses in the study area.

Plant parts used, methods of preparation and application

Leaves (48 species, 50%), roots (15 species, 16%) and stem bark (8 species, 8%) were the most cited plant parts for remedy preparations. Considerable numbers of species were also sought for their fruits (5 species, 5%) (Figure 3). The various plant parts were mostly (56 species, 72%) processed fresh while some (16 species, 21%) were used dried and others (6 species, 8%) either fresh or dried.
https://static-content.springer.com/image/art%3A10.1186%2F1746-4269-4-11/MediaObjects/13002_2007_Article_115_Fig3_HTML.jpg
Figure 3

Medicinal plant parts used to the treatment of human ailments.

Medicinal plant parts were reported mostly to be crushed (35%), squeezed (27%) and powdered (12%) during preparation of remedies (Table 4). Mixtures of different species were used to treat most of the reported ailments than the use of a single species. About 65%, 41% and 27% of the reported ailments were treated with remedies prepared by crushing, squeezing and powdering, respectively. Most of the traditional healers were not preserving or storing traditional medicinal preparations for use at another time.
Table 4

Reported methods of preparation of traditional medicine

Methods of preparation

Frequency

Proportion (%)

Crushed

60

35.09

Squeezed

46

26.90

Powdered

20

11.70

Pounded

13

7.60

Concocted

12

7.02

Extracted with cold water

11

6.43

Decocted

4

2.34

Warmed

2

1.17

Smoked

1

0.58

Extracted by boiling stem

1

0.58

Enclosed in a piece of close

1

0.58

The administration of remedial preparations were mainly oral (42 species, 44%) and on top of the body (32 species, 34%) (Figure 4). According to healers, preparations were prescribed to patients differently for different age groups. The dosage prescription for children was mostly lower than for adults. Dosages were estimated using lids, spoons, cups, glasses, pinches or handfuls. The amounts of remedy and prescription rates were generally dependent on the degree and duration of the ailment. Treatment durations varied between 1 and 7 days.
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Figure 4

Administration routes of traditional medicine.

Traditional healers also indicated that their remedies were devoid of any adverse effects. However, some mild adverse effects like abdominal pain, diarrhoea, inflammation, vomiting, unconsciousness and high rate of breathing were reported for some of the remedial preparations. Almost all of the informants were not using antidotes for noticeable adverse effects of traditional medicines applied.

Threats to medicinal plants and their conservation

The ethnomedicinal plant species were mainly reported as rare (36 species, 40%) and abundant (27 species, 30%) while others as very abundant (17 species, 19%) and very rare (10 species, 11%). Highly significant difference was observed between the plant parts used for medicinal purposes and the abundance of the medicinal species in the study area. The use of plant remedy in fresh or dried conditions also showed highly significant variation on the abundance of the medicinal plant species. Non-marketable ethnomedicinal plants were more frequently reported. The abundance of medicinal species also varied significantly with regard to the marketability of the medicinal plant species.

The number of ethnomedicinal plant species threatened in the study area was significantly higher. The most cited threats to ethnomedicinal plants of the area were deforestation (25 species, 23%), drought (22 species, 20.56%), fire (16 species, 15%), overgrazing/over browsing (11 species, 10%) and agricultural expansion (8 species, 7%). Twenty one species (20%) were reported to have no apparent threat (Figure 5). Moreover, the absence of practice by traditional healers to conserve or recuperate ethnomedicinal plants of the area was highly significant.
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Figure 5

Threats to medicinal plant species of human importance.

Ethnomedicinal plant species having other than medicinal values were significantly greater than those without any added values. A significant difference was also observed between the reported abundance and presence of added values of the ethnomedicinal plant species. The majority of ethnomedicinal plant species were used for firewood (25 species, 26%), forage (21 species, 22%), construction (14 species, 14%), food and fencing (3 species each, 3%), as well as timber, toothbrush and live fencing (2 species each, 2%) by the local people. However, many species (22 species, 23%) were indicated to have no added values other than their medicinal use (Figure 6).
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Figure 6

Other uses of medicinal plant species.

Discussion and conclusion

A remarkable traditional medicinal plant knowledge and practice was documented from the study area. Older traditional healers had greater knowledge and use of ethnomedicinal plant species than younger traditional healers. This may indicate that the indigenous medicinal plant use knowledge was declining among the younger generation, which could be attributed to the low interest of the younger generation to inherit and use ethnomedicinal knowledge. Another study by [23] also showed that medicinal plant knowledge and use increased with age when the community suffered an important erosion of ethnomedicinal plant knowledge.

The indigenous medicinal plant knowledge and use was independent of the educational level of traditional healers. This suggests that traditional healers could inherit the knowledge and use of ethnomedicine from parents as long as they belong to a knowledgeable family member irrespective of their educational status. This finding is in agreement with the work of [24] who reported that the proportion of healers who transferred their knowledge and those who did not was similar irrespective of their educational level. Results also revealed that many of the traditional healers reported to transfer their knowledge and use of ethnomedicinal plants orally to their favorite family member. Such transfer of indigenous knowledge is liable to erosion as it could vanish when knowledgeable elders die before the knowledge is transferred or during resettlements of individuals or communities [25, 26].

The agreement among the traditional healers on the use of ethnomedicinal plant species was high for tumor, rabies, insect bite, rheumatism and Rissaa. This may indicate that the incidence of such diseases was relatively high in the study area. But consensus among the traditional healers was not observed for the majority of the diseases reported, which might be due to individual differences in the indigenous knowledge or the diverse backgrounds of healers [27].

High fidelity level was recoded on the use of G. superba, R. communis, C. arereh, J. schimperiana and C. uncinulata by traditional healers to treat tumor, rabies, insect bite, rheumatism and Rissaa, respectively. Low fidelity level for some of the species used against the aforementioned ailments shows that the species were used by the healers to treat many diseases.

The two species frequently used by traditional healers to treat tumor were G. superba and P. zeylanica. P. zeylanica was indicated to have antioxidant [28], antiviral [29], antiplasmodial [30], antibacterial [31, 32] and stimulatory [33] properties. Even though these activities of P. zeylanica were not related to the traditional use in treating tumor, they may have therapeutic potential to treat rheumatism.

Anti-inflammatory activity from the methanolic extract of the roots of R. communis was reported by [34] while [35] reported a hepatoprotective effect of N-demethyl ricinine isolated from the leaves of this species. Anticonceptive effect [36, 37] and antidote properties against scorpion venom [38] were also reported for this species. Moreover, [39] found the lectins from R. communis to inhibit HIV-1 reverse transcriptase. The latter antiviral activity of R. communis could validate its traditional use in the study area to treat rabies.

The species with the second highest fidelity level next to J. schimperiana used by healers to treat rheumatism was C. macrostachyus. Purgative and inflammatory activities were reported from seeds of this species [40]. M. foetida, which was found to have antiplasmodial activity [41] and C. anisata, which was screened to have antimicrobial [42, 43] and hypoglycaemic [44] activities, were also used by traditional healers to manage rheumatism.

High diversity of ethnomedicinal plant species was reported by traditional healers. The diversity of ethnomedicinal plant species decreased with increasing altitude. A study conducted by [45] in New Zealand also showed that altitude had by far the strongest effect on species richness.

Leaves were the most reported plant parts in the preparation of remedies. The preference of leaves to other plant parts could be due to ease of preparation, preparation of medicinal teas [46] and the presence of more bioactive ingredients in leaves developed in response to phytophagous organisms since they are the most vulnerable parts of a plant [47]. The use of more than one medicinal plant species was reported by healers to treat health problems, which could be attributed to the additive or synergistic effects of the mixtures [48].

Preservation of remedies was not reported by healers of the study area since the remedies were used mainly in their fresh forms. This might also be attributed to the availability of ethnomedicinal plant species in the area as most of them were woody species. In North Peru, [49] reported that some remedies were prepared using dried plant material when fresh material was not available, and when the plant material had to be transported from other regions.

Traditional healers reported that they prescribed different doses of remedies for different age groups. Preferably, more amounts of remedies were given for adults than children to treat the same disease. Though such prescription differences were practiced, still the amount prescribed by healers for both children and adults might not confirm with the standard prescriptions in modern medical literature [50].

Though the majority of healers reported that the remedies used to treat ailments had no adverse effects on patients, few healers noted the presence of some side effects in some remedies prepared from certain species of ethnomedicinal plants. A similar study conducted by [24] also showed that most of the remedies reported by healers had no serious adverse effects except vomiting and temporary inflammations. However, the low recognition of adverse effects by traditional healers for the majority of remedy preparations coupled with the absence of antidotes for those remedies, even with reported adverse effects, might sometimes worsen the health problem of patients.

Most of the ethnomedicinal plant species used by healers to treat human ailments were reported to be rare and the abundance of ethnomedicinal plant species differed significantly with respect to the plant part used, plant condition used, marketability and multiple use of the species. This might be due to impact of such factors on anthropogenic pressure and the survival of ethnomedicinal plant species.

The findings of the current study showed that ethnomedicinal plants were under serious threat mainly due to deforestation and drought. Another study conducted by [51] at Bale Mountains National Park, Southeastern Ethiopia, also showed that deforestation for various purposes and agricultural expansion and intensification were the principal threats to medicinal plant species. A study by [52] also indicated that over-exploitation and deforestation were the main causes for the depletion of medicinal plants in northwest Yunnan, China. Although the medicinal plant species were under threat, traditional healers do not practice any conservation measures to ensure the sustainability of such plant resources. Therefore, interventions are required to mitigate the underlying threats of ethnomedicinal plant resources and ensure their conservation and sustainable utilization.

Declarations

Acknowledgements

We thank the Research and Publications Office of Jimma University for provision of financial support. We are also grateful to Jimma University Regional Herbarium and The National Herbarium, Addis Ababa University, for letting to utilize the available facilities. Traditional healers of the study area are deeply recognized and acknowledged for sharing their ethnomedicinal knowledge, and we thank the language translators and field assistants Ms. Amberu Hussien, Ms. Almaz and Mr. Nuru Haji Hassen. We are grateful to Mr. Ermias Lulekal and Mr. Melaku Wondafrash for their assistance in identification of specimens. The Administration Offices of Kersa, Omo Nada and Tiro Afeta Districts are also thanked for giving us permission to reach the traditional healers. Endaweke Assegid (GIS specialist) constructed map of the study area. Three anonymous reviewers are acknowledged for shaping the paper in its present form through their constructive comments.

Authors’ Affiliations

(1)
Department of Biology, Jimma University
(2)
FSC Africa

References

  1. Abebe D: The role of medicinal plants in healthcare coverage of Ethiopia, the possible benefits of integration. Conservation and sustainable use of medicinal plants in Ethiopia, Proceedings of the National workshop, 28 April – 01 May 1998. Edited by: Zewdu M. 2001, Addis Ababa. Demissie A: Institute of Biodiversity Conservation and Research, 6-21.Google Scholar
  2. Srivastava R: Studying the information needs of medicinal plant stakeholders in Europe. 2000, UK: TRAFFIC-InternationalGoogle Scholar
  3. Marshal NT: Searching for a cure: Conservation of medicinal wildlife resources in East and Southern Africa. 1998, Cambridge, UK: TRAFFIC-InternationalGoogle Scholar
  4. Hamilton AC: Medicinal plants, conservation and livelihoods. Biodiversity and Conservation. 2004, 13: 1477-1517. 10.1023/B:BIOC.0000021333.23413.42.View ArticleGoogle Scholar
  5. Abebe D, Ayehu A: Medicinal plants and enigmatic health practices of Northern Ethiopia. 1993, Addis Ababa: B.S.P.E.Google Scholar
  6. Addis G, Abebe D, Urga K: A survey of traditional medicinal plants in Shirka District, Arsi Zone, Ethiopia. Ethiopian Pharmaceutical Journal. 2001, 19: 30-47.Google Scholar
  7. CSA: National statistics: Tables B.3 and B.4. 2005, Ethiopia: Central Statistical AgencyGoogle Scholar
  8. Appiah KA, Gates HL: Africana: The Encyclopedia of the African and African American experience. 1999, New York: Basic Ciritasd BooksGoogle Scholar
  9. Burckhardt G: Participation and practice: Some experiences of project work in Ethiopia. Adult Education and Development. Edited by: Hinzen H. 2000, Wilhelmstrasse: Obere Institute for International Cooperation of the German Adult Education, 301-314.Google Scholar
  10. Muudee HM: Hamid Muudees Oromo Dictionary. 1995, Atlanta: Sagalee Oromoo Publishing, I:Google Scholar
  11. Hussen JW: A cultural representation of women in the Oromo society. African Study Monographs. 2004, 25: 103-147.Google Scholar
  12. Martin GJ: Ethnobotany: a methods manual. 1995, London, UK: Chapman and HallView ArticleGoogle Scholar
  13. Hedberg I, Edwards S, eds: Flora of Ethiopia and Eritrea. Pittosporaceae to Araliaceae. 1989, The National Herbarium, Addis Ababa, Ethiopia, and Department of Systematic Botany, Uppsala, Sweden, 3:Google Scholar
  14. Hedberg I, Edwards S, eds: Flora of Ethiopia and Eritrea. Poaceae. 1995, The National Herbarium, Addis Ababa, Ethiopia, and Department of Systematic Botany, Uppsala, Sweden, 7:Google Scholar
  15. Friis I: Forests and forest trees of Northeast Tropical Africa. 1992, Kew Bulletin Additional Series XV, London, Kew Botanical Gardens: HMSOGoogle Scholar
  16. Edwards S, Tadesse M, Hedberg I, eds: Flora of Ethiopia and Eritrea. Canellaceae to Euphorbiaceae. 1995, The National Herbarium, Addis Ababa, Ethiopia, and Department of Systematic Botany, Uppsala, Sweden, 2 (part 2):Google Scholar
  17. Edwards S, Demissew S, Hedberg I, eds: Flora of Ethiopia and Eritrea. Hydrocharitaceae to Arecaceae. 1997, The National Herbarium, Addis Ababa, Ethiopia, and Department of Systematic Botany, Uppsala, Sweden, 6:Google Scholar
  18. Edwards S, Tadesse M, Demissew S, Hedberg I, eds: Flora of Ethiopia and Eritrea. Magnoliaceae to Flacourtiaceae. 2000, The National Herbarium, Addis Ababa, Ethiopia, and Department of Systematic Botany, Uppsala, Sweden, 2 (part 1):Google Scholar
  19. Hedberg I, Edwards S, Nemomissa S, eds: Flora of Ethiopia and Eritrea. Apiaceae to Dipsacaceae. 2003, The National Herbarium, Addis Ababa, Ethiopia, and Department of Systematic Botany, Uppsala, Sweden, 4 (part 1):Google Scholar
  20. Hedberg I, Friis I, Edwards S, eds: Flora of Ethiopia and Eritrea. Asteraceae. 2004, The National Herbarium, Addis Ababa, Ethiopia, and Department of Systematic Botany, Uppsala, Sweden, 4 (part 2):Google Scholar
  21. Trotter R, Logan M: Informant consensus: new approach for identifying potentially effective medicinal plants. Indigenous Medicine and Diet: Behavioural Approaches. Edited by: Etkin NL. 1986, New York: Redgrave Publishers, 91-112.Google Scholar
  22. Friedman J, Zohara Y, Amotz D, Palewitch D: A preliminary classification of the healing potential of medicinal plants, based on a rational analysis of an ethnopharmacological field survey among Bedouins in the Negev Desert, Israel. Journal of Ethnopharmacology. 1986, 16: 275-278. 10.1016/0378-8741(86)90094-2.View ArticlePubMedGoogle Scholar
  23. Estomba D, Ladio A, Lozada M: Medicinal wild plant knowledge and gathering patterns in Mapuche community from North-western Patagonia. J Ethnopharmacol. 2006, 103 (1): 109-119. 10.1016/j.jep.2005.07.015.View ArticlePubMedGoogle Scholar
  24. Yineger H, Yewhalaw D: Traditional medicinal plant knowledge and use by local healers in Sekoru District, Jimma Zone, southwestern Ethiopia. Journal of Ethnobiology and Ethnomedicine. 2007, 3: 24-10.1186/1746-4269-3-24.PubMed CentralView ArticlePubMedGoogle Scholar
  25. Addis G, Abebe D, Genebo T, Urga K: Perceptions and practices of modern and traditional health practitioners about traditional medicine in Shirka District, Arsi Zone, Ethiopia. The Ethiopian Journal of Health Development. 2002, 16: 19-29.View ArticleGoogle Scholar
  26. Yineger H, Kelbessa E, Bekele T, Lulekal E: Ethnoveterinary medicinal plants at Bale Mountains National Park, Ethiopia. J Ethnopharmacol. 2007, 112 (1): 55-70. 10.1016/j.jep.2007.02.001.View ArticlePubMedGoogle Scholar
  27. Almeida CFC, Amorim ELC, Albuquerque UP, Maia MBS: Medicinal plants popularly used in the Xingó region – a semi-arid location in Northeastern Brazil. Journal of Ethnobiology and Ethnomedicine. 2006, 2: 15-10.1186/1746-4269-2-15.PubMed CentralView ArticleGoogle Scholar
  28. Natarajan KS, Narasimhan M, Shanmugasundaram KR, Shanmugasundaram ERB: Antioxidant activity of a salt-spice-herbal mixture against free radical induction. J Ethnopharmacol. 2006, 105 (1-2): 76-83. 10.1016/j.jep.2005.09.043.View ArticlePubMedGoogle Scholar
  29. Gebre-Mariam T, Neubert R, Schmidt PC, Wutzler P, Schmidtke M: Antiviral activities of some Ethiopian medicinal plants used for the treatment of dermatological disorders. JJ Ethnopharmacol. 2006, 104 (1-2): 182-187. 10.1016/j.jep.2005.08.071.View ArticleGoogle Scholar
  30. Simonsen HT, Nordskjold JB, Smitt UW, Nyman U, Palpu P, Joshi P, Varughese G: In vitro screening of Indian medicinal plants for antiplasmodial activity. J Ethnopharmacol. 2001, 74 (2): 195-204. 10.1016/S0378-8741(00)00369-X.View ArticlePubMedGoogle Scholar
  31. Ahmad I, Mehmood Z, Mohammad F: Screening of some Indian medicinal plants for their antimicrobial properties. J Ethnopharmacol. 1998, 62 (2): 183-193. 10.1016/S0378-8741(98)00055-5.View ArticlePubMedGoogle Scholar
  32. Aqil F, Ahmad I, Owais M: Evaluation of anti-methicillin-resistant Staphylococcus aureus (MRSA) activity and synergy of some bioactive plant extracts. Biotechnol J. 2006, 1 (10): 1093-1102. 10.1002/biot.200600130.View ArticlePubMedGoogle Scholar
  33. Bopaiah CP, Pradhan N: Central nervous system stimulatory action from the root extract of Plumbago zeylanica in rats. Phytother Res. 2001, 15 (2): 153-156. 10.1002/ptr.702.View ArticlePubMedGoogle Scholar
  34. Ilavarasan R, Mallika M, Venkataraman S: Anti-inflammatory and free radical scavenging activity of Ricinus communis root extract. J Ethnopharmacol. 2006, 103 (3): 478-480. 10.1016/j.jep.2005.07.029.View ArticlePubMedGoogle Scholar
  35. Shukla B, Visen PKS, Patnaik GK, Kapoor NK, Dhawan BN: Hepatoprotective effect of an active constituent isolated from the leaves of Ricinus communis Linn. Drug Development Research. 1992, 26: 183-193. 10.1002/ddr.430260207.View ArticleGoogle Scholar
  36. Okwuasaba FK, Osunkwo UA, Ekwenchi MM, Ekpenyong KI, Onwukeme KE, Olayinka AO, Uguru MO, Das SC: Anticonceptive and estrogenic effects of a seed extract of Ricinus communis var. minor. J Ethnopharmacol. 1991, 34 (2-3): 141-145. 10.1016/0378-8741(91)90031-8.View ArticlePubMedGoogle Scholar
  37. Das SC, Isichei CO, Okwuasaba FK, Uguru VE, Onoruvwe O, Olayinka AO, Ekwere EO, Dafur SJ, Parry O: Chemical, pathological and toxicological studies of the effects of RICOM-1013-J of Ricinus communis var Minor on women volunteers and rodents. Phytother Res. 2000, 14 (1): 15-19. 10.1002/(SICI)1099-1573(200002)14:1<15::AID-PTR205>3.0.CO;2-P.View ArticlePubMedGoogle Scholar
  38. Uawonggul N, Chaveerach A, Thammasirirak S, Arkaravichien T, Chuachan C, Daduang S: Screening of plants acting against Heterometrus laoticus scorpion venom activity on fibroblast cell lysis. J Ethnopharmacol. 2006, 103 (2): 201-207. 10.1016/j.jep.2005.08.003.View ArticlePubMedGoogle Scholar
  39. Wang HX, Ng TB: Examination of lectins, polysaccharopeptide, polysaccharide, alkaloid, coumarin and trypsin inhibitors for inhibitory activity against Human Immunodeficiency Virus Reverse Transcriptase and Glycohydrolases. Planta Med. 2001, 67 (7): 669-672. 10.1055/s-2001-17359.View ArticlePubMedGoogle Scholar
  40. Mazzanti G, Bolle P, Martinoli L, Piccinelli D, Grgurina I, Animati F, Mugnè Y: Croton macrostachys, a plant used in traditional medicine: purgative and inflammatory activity. J Ethnopharmacol. 1987, 19 (2): 213-219. 10.1016/0378-8741(87)90043-2.View ArticlePubMedGoogle Scholar
  41. Waako PJ, Gumede B, Smith P, Folb PI: The in vitro and in vivo antimalarial activity of Cardiospermum halicacabum L. and Momordica foetida Schumach. Et Thonn. Journal of Ethnopharmacology. 2005, 99: 137-143. 10.1016/j.jep.2005.02.017.View ArticlePubMedGoogle Scholar
  42. Gundidza M, Chinyanganya F, Chagonda L, De Pooter HL, Mavi S: Phytoconstituents and antimicrobial activity of the leaf essential oil of Clausena anisata (Willd.) J.D. Hook ex. Benth. Flavour and Fragrance Journal. 1994, 9: 299-303. 10.1002/ffj.2730090604.View ArticleGoogle Scholar
  43. Hamza OJM, Bout-van den Beukel van den CJP, Matee MIN, Moshi MJ, Mikx FHM, Selemani HO, Mbwambo ZH, Ven Van der AJAM, Verweij PE: Antifungal activity of some Tanzanian plants used traditionally for the treatment of fungal infections. J Ethnopharmacol. 2006, 108 (1): 124-132. 10.1016/j.jep.2006.04.026.View ArticlePubMedGoogle Scholar
  44. Ojewole JAO: Hypoglycaemic effect of Clausena anisata (Willd) Hook methanolic root extract in rats. J Ethnopharmacol. 2002, 81 (2): 231-237. 10.1016/S0378-8741(02)00085-5.View ArticlePubMedGoogle Scholar
  45. Ohlemüller R, Wilson JB: Vascular plant species richness along latitudinal and altitudinal gradients: a contribution from New Zealand temperate rainforests. Ecology Letters. 2000, 3: 262-266. 10.1046/j.1461-0248.2000.00151.x.View ArticleGoogle Scholar
  46. Gazzaneo LRS, Lucena RFP, Albuquerque UP: Knowledge and use of medicinal plants by local specialists in an region of Atlantic Forest in the state of Pernambuco (Northeastern Brazil). Journal of Ethnobiology and Ethnomedicine. 2005, 1: 9-10.1186/1746-4269-1-9.PubMed CentralView ArticlePubMedGoogle Scholar
  47. Bhattarai S, Chaudhary RP, Taylor RSL: Ethnomedicinal plants used by the people of Manang district, central Nepal. Journal of Ethnobiology and Ethnomedicine. 2006, 2: 41-10.1186/1746-4269-2-41.PubMed CentralView ArticlePubMedGoogle Scholar
  48. Igoli JO, Tor-Anyiin TA, Usman SS, Oluma HOA, Igoli NP: Folk medicines of the lower Benue valley of Nigeria. Recent Progress in Medicinal Plants. Edited by: Singh VK, Govil JN, Hashmi S, Singh G. 2002, USA: Sci. Tech. Pub., 327-338. [Govil JN and Singh VK (Series Editors) Ethnomedicine and Pharmacognosy, vol 7.]Google Scholar
  49. Bussmann R, Sharon D: Traditional medicinal plant use in Northern Peru: tracking two thousand years of healing culture. Journal of Ethnobiology and Ethnomedicine. 2006, 2: 47-10.1186/1746-4269-2-47.PubMed CentralView ArticlePubMedGoogle Scholar
  50. Seifu T, Asres K, Gebre-Mariam T: Ethnobotanical and ethnopharmaceutical studies on medicinal plants of Chifra District, Afar Region, Northeastern Ethiopia. Ethiopian Pharmaceutical Journal. 2006, 24: 41-58.View ArticleGoogle Scholar
  51. Yineger H: A study on the ethnobotany of medicinal plants and floristic composition of the dry Afromontane forest at Bale Mountains National Park, Ethiopia. M.Sc. Thesis. 2005, Addis Ababa UniversityGoogle Scholar
  52. Ji H, Shengji P, Chunlin L: An ethnobotanical study of medicinal plants used by the lisu people in Nujiang, northwest Yunnan, China. Economic Botany. 2005, 58: 253-264. 10.1663/0013-0001(2004)58[S253:AESOMP]2.0.CO;2.View ArticleGoogle Scholar

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