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African Journal of Traditional, Complementary and Alternative Medicines
African Ethnomedicines Network
ISSN: 0189-6016
Vol. 3, Num. 1, 2006, pp. 95-100
African Journal. Traditional, Complementary and Alternative Medicines Vol. 3, Num. 1, 2006, pp.95-100

EFFECT OF EREMOMASTAX SPECIOSA ON EXPERIMANTAL DIARRHOEA.

Julius E. *Oben1, Sheila, E. Assi1, Gabriel, A. Agbor2 and David F. Musoro1

1Department of Biochemistry, Faculty of Science, University of Yaounde I, Cameroon
2
Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plant Studies, P.O. Box 6163, Yaounde, Cameroon. *E-mail: juliusoben@hotmail.com

 Code Number: tc06011

Abstract 

This study investigated the anti diarrhoeal activity of the aqueous extract of dried ground leaves of Eremomastax speciosa (Hochst.) Acanthaceae.  Diarrhea was induced in mice by the administration of 0.2 ml of castor oil, with the control group receiving water. The administration by oral garvage of 400 or 800 mg/kg body weight of Eremomastax speciosa extract reduced castor oil induced diarrheoa by reducing the number of wet stools by 42.50 and 48.35% respectively.  This was as a result of the ability of the extract to stimulate the reabsorption of water from the intestinal lumen as well as significantly reducing the intestinal transit time and intestinal motility.  This antidiarrhoeal property could be as a result of the tannins and flavonoids, which were found to be present in Eremomastax speciosa.

Key words: Eremomastax speciosa, antidiarrhoeal activity, castor oil, phytochemicals. 

Introduction 

Traditional medical practitioners play important roles in health care delivery in Cameroon. However, their claims are sometimes unsubstantiated with scientific facts. Eremomastax speciosa (Hochst.) has been used by traditional doctors for many years as a haematopoietic and antidiarrhoeal herb. The stem and the leaves are used in the treatment of dysentery and anemia, while the aerial parts are used in the treatment of irregular menstruation and spurious labour pains.  The leaves are also used to treat fracture, hemorrhoids and urinary tract infection (Adjanohoun, et al., 1996). Eremomastax speciosa is a tropical stout erect multi-branched herb, which grows as a weed in secondary forests (Heine, 1966).  It is however cultivated by many Cameroonians as a result of its numerous medicinal properties. Tan et al., (1996) reported the anti-ulcerogenic activity of Eremomastax speciosa. The present study was designed to study the antidiarrhoeal property of leaves of Eremomastax speciosa in mice. 

Materials and Methods

Plant material 

Fresh leaves ofEremomastax speciosa were collected in Bonamoussadi-Yaounde, Cameroon.  Botanic identification was performed at the Cameroon National Herbarium, Yaounde, Cameroon, and assigned voucher No. HNC/136984. The sample was air-dried in the laboratory (26 -28°C) and then ground to a powder.

Preparation of plant material 

The powdered sample was soaked in boiling water for 30 minutes.  The mixture was then allowed to cool and filtered using a glass funnel plugged with sieve cloth. The residue was further extracted twice with boiling water. The resulting filtrate was then concentrated using a rotary evaporator, and further dried in an oven at 40°C.  The resulting material was then stored in a refrigerator at 4°C until when required.

Animals 

 Male mice (25-30g) obtained from the Animal Unit, Faculty of Medicine and Biomedical Science, University of Yaounde 1 were used for this study.  Their use was in conformity with regulations concerning the use of animals for experimentation in the University of Yaounde 1.

Chemicals 

 Morphine (reference antidiarrhoeal drug), Castor oil (laxative agent), Charcoal Meal (10% activated charcoal in 5% Gum Acacia) were of pharmacological grade. All other reagents were of analytical grade and obtained from BDH.

Phytochemical screening 

The freshly prepared extract of Eremomastax speciosa was quantitatively tested for the presence of chemical constituents. These were identified by characteristic colour changes using standard procedures (Trease and Evans, 1983).

Experimentally induced diarrhea

The method proposed by Galvez et al., (1993) was modified to suit experimental needs. Adult white mice fasted for 18 hours were divided into 5 groups (Group I – Group V) of 6 animals each. The groups received the following treatment by oral garvage: Group I: Distilled water (0.2 ml), Group II: Morphine (25 mg/kg body weight), Group III: Eremomastax speciosa extract 400 mg/kg body weight, Group IV: Eremomastax speciosa extract 800 mg/kg body weight and Group V: Distilled water (0.2 ml). (In Groups III and IV, the extract was dissolved in 0.2 ml of distilled water).  Thirty minutes after the treatments, castor oil (0.2 ml) was administered by garvage to groups II, III, IV and V.

Following the administration of castor oil, the animals were placed in separate wired cages for observation.  The total number of faeces and the number of wet faeces passed was recorded over a period of 4 hours after the administration of castor oil.  The percentage diarrhoea inhibition was calculated as a function of the castor oil control i.e. % Inhibition = (control – test) x 100%/control.

Upper gastrointestinal transit

The method proposed by Aye-Than et al., (1989) was used in groups of eight mice each, using a ‘charcoal meal’ as a marker diet. The mice were given increasing doses of the extract re-dissolved in 0.2 ml of distilled water by garvage.  The intestinal transit was calculated as a percentage of the distance travelled by the charcoal meal compared to the length of the small intestine.

Statistical treatment of the results 

 The results were expressed as means ± standard deviation (SD).  Significance of the differences compared to the control groups was determined using the Student’s t-test. 

Results and Discussion

Castor oil brings about changes in electrolyte and water transport and increases peristaltic activity (Luderer et al., 1980; Capasso et al., 1986).  These changes are associated with prostaglandins that contribute to the patho-physiological functions in the gastro intestinal tract  (Bennet and Sanger, 1982).  Release of prostaglandins is also a major cause of arachidonic acid-induced diarrhoea (Luderer et al., 1980). This is characterized by an increase in the secretion of water and electrolytes, an increase in intestinal transit time and an increase in wet faeces. 

The aqueous extract of Eremomastax speciosa leaves showed significant antidiarrhoeal activity (P<0.01) against castor oil induced diarrhoea in mice. It reduced the number of wet faeces produced by castor oil administration from 20.50 ± 3.69 to 12.00±1.40 (42.50%) and 10.50 ± 1.84 (48.75%) when experimental animals were respectively administered 400 and 800 mg/kg plant extract (Table 2).  The plant extract thus stimulates the reabsorption of water from the intestinal lumen, resulting to the normalisation of the deranged water transport across the mucosal cells which are seen in the type of faeces produced.

Administration of castor oil to experimental animals stimulated small intestinal transit of 90.30 ± 7.82. Administration of Eremomastax speciosa demonstrated a significant (P < 0.01) dose related reduction of this intestinal transit (Table 3) with 800 mg/kg being more effective than the lower dose of extract. This activity is probably due to the ability of the extract to inhibit intestinal motility.

Administration of the Eremomastax speciosa extract and morphine, 30 minutes before (preventive) or 15 minutes after (curative) castor oil administration, significantly (P < 0.01) decreased the intestinal transit time (Table 4). The reduction of the intestinal transit following administration of the Eremomastax speciosa extract before and after the onset of castor oil-induced gut movement demonstrated the ability of the extract to protect the gut from the adverse effect of diarrhoea and the ability to suppress established gut motility respectively. Morphine (25 mg/kg) was more effective as an antidiarrheal agent than the plant extract even when experimental animals were administered an 800 mg/kg dose of the plant extract.  Morphine is a prototypical antidiarrhoeal drug, which acts on the gastrointestinal tract, and mediates both central and local effects (Galligan and Burks, 1983; Megens, 1990).  It stimulates the net absorption of water and electrolytes in the small and large intestine in several species of animals, including man (Couper, 1987). Similar results were obtained in our study in which morphine (25 mg/kg) stimulated the reduction of the intestinal transit time and brought about a complete (100%) inhibition of the onset of diarrhoeal faeces (Tables 2, 3, 4). Phytochemical screening of the crude extract of Eremomastax speciosa revealed the presence of tannins and flavonoids (Table 1), which have been shown to possess antidiarrhoeal activity (Galvez et al., 1991, 1993). Thus, tannins and flavonoids may be responsible for the antidiarrheal activity of Eremomastax speciosa by stimulating the normalization of the deranged water transport across the mucosal cells and the reduction of the intestinal transit, which have more useful therapeutic effects than any action on intestinal motility and propulsion.

References 

  1. Adjanohoun, J.E., Aboubakar, N., Dramane, K., Ebot, M.E., Ekpere, J.A. and Enow-Orock, E.G. (1996).  Traditional Medicine and Pharmacopoeia.  Contribution to Ethnobotanical Floristic studies in Cameroon, CNPMS Porto-Novo Benin, pg 22
  2. Aye-Than, H.J., Kukarni, Wut-hmone and Tha, S.J. (1989).  Antidiarrhoeal efficacy of some Burmese indigenous drug formulations in experimental diarrhoeal test models.  J. Crude Drug Res. 27 (4): 195-200.
  3. Bennet, A. and Sanger, G. J. (1982).  Acidic lipids: prostaglandins. In: Mediators and Drugs in Gastrointestinal Motility. Vol. II G. Bertaccini (ed.), Springer-Verlag, Berlin. Pp 219-238.
  4. Capasso, F., Mascolo, N., Autone, G. and Romano, V. (1986).  Laxatives and the production of autacoids by rat colon.  J. Pharm. Pharmacol. 38: 627-629.
  5. Couper, I. M. (1987).  Opoid action on the intestine: the importance of the intestinal mucosa.  Life Sciences 41: 917. 
  6. Galligan, J.J. and Burks, T.F. (1983).  Centrally mediated inhibition of small intestinal transit and motility by morphine in the rat.  J. Pharmacol. Exp. Ther. 226, 356
  7. Galvez, J., Crespo, M.E., Jimnenez, J., Suarez, A. and Zarzuelo, A. (1993).  Antidiarrhoeic activity of quercitrin in mice and rats.  J. Pharm. Pharmacol. 45: 157-159.
  8. Galvez, J. Zarzuelo, A., Crespo, M. E., Utrilla, M. P. Jiménez J; Spiessens, C. and de Witte P. (1991). Antidiarrhoeic activity of Scleroarya birrea Back Extract and its Active Tannin Constituent in rats. Phytother. Res. 5: 276-278.
  9. Heine, H. (1966). Acantheceae dans Flore du Gabon, Museum National d’histoire Naturelle, Paris, 13: 29-32
  10. Luderer, J. R. Dermers, L. M., Nomides, C. T. and Hayes, A. H. (1980).  Mechanism of action of castor oil: a biochemical link to the prostaglandins. In Advances in Prostaglandin and Thrombosane Research, Vol. 8, ed. by B. Samuelsson, P. W. Ramwell and R. Paoletti, Raven Press, New York pp 1633-1635.
  11. Megens, A. A. H. P., Canters, L.L.J., Awouters, I.H.L and Niemegeers, C. J. E (1990). Normalisation of small intestinal propulsion with loperamide like antidiarrhoeals in rats. European Journal of Pharmacology 17: 357-364).
  12. Tan, P. V., Nditafon, N. G., Yewah, M. P., Dimo, T. and Ayafor, F.J. (1996). Eremomastax speciosa: Effect of leaf aqueous extract on ulcer formation and gastric secretion in rats. J. of Ethnopharmacology 54:139-142
  13. Trease, G.E. and Evans, W. C. (1983). Pharcognosy, 12th Ed. Baillieere Tindal, London.           
© Copyright 2006 -African. Journal. Traditional, Complementary and Alternative Medicines

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