Antidiarrhoeal activity of an ethanol extract of the stem bark of Piliostigma reticulatum (Caesalpiniaceae) in rats.

K Dosso, B B N'guessan, A P Bidie, B N Gnangoran, S M��it��, D N'guessan, A P Yapo, E E Ehil��
Author Information
  1. K Dosso: Laboratory of Physiology, Pharmacology and Phytotherapy, UFR SN, University of Abobo- Adjam��, 02 BP 801 Abidjan 02, C��te d'Ivoire.

Abstract

Piliostigma reticulatum (Caesalpiniaceae) is used in Africa as a traditional medicine for the treatment of many diseases, such as malaria, tuberculosis and diarrhoea. We investigated the antidiarrhoeal properties of a crude ethanol extract from the stem bark of Piliostigma reticulatum (EEPR) in Wistar albino rats to substantiate its traditional use and to determine its phytochemical constituents. The antidiarrhoeal activity of the plant extract was evaluated in a castor oil-induced diarrhoea model in rats and compared with loperamide. The effect of the extract on gastrointestinal motility was also determined by the oral administration of charcoal meal and castor oil-induced intestinal fluid accumulation (enteropooling). EEPR showed remarkable dose-dependent antidiarrhoeal activity evidenced by a reduction of defecation frequency and change in consistency. Extracts at 250, 500 and 1000 mg/kg body weight significantly reduced diarrhoeal faeces. EEPR also significantly inhibited gastrointestinal motility and castor oil-induced enteropooling at 500 and 1000 mg/kg, similar to the inhibition obtained in control rats treated by atropine. Phytochemical screening revealed the presence of tannins, flavonoids, polyphenols and reducing sugars in the stem bark of P. reticulatum. No mortality or visible signs of general weakness were observed in the rats following administration of the crude extract in doses up to 6000 mg/kg body weight in an acute toxicity study. Our results show that the stem bark of P. reticulatum possesses antidiarrhoeal activity and strongly suggest that its use in traditional medicine practice could be justified.

Keywords

References

  1. J Pharm Pharmacol. 1993 Dec;45(12):1054-9 [PMID: 7908974]
  2. Prog Clin Biol Res. 1986;213:489-92 [PMID: 2872681]
  3. Life Sci. 1987 Aug 24;41(8):917-25 [PMID: 3039278]
  4. Phytochemistry. 2008 Aug;69(11):2245-50 [PMID: 18582911]
  5. Clin Infect Dis. 2001 Feb 1;32(3):331-51 [PMID: 11170940]
  6. Proc Natl Acad Sci U S A. 2002 Mar 5;99(5):3042-6 [PMID: 11854470]
  7. J Ethnopharmacol. 1989 Sep;26(2):101-9 [PMID: 2601351]
  8. J Pharm Pharm Sci. 2004 Feb 25;7(1):70-5 [PMID: 15144737]
  9. N Engl J Med. 1989 Sep 21;321(12):800-6 [PMID: 2671736]
  10. J Ethnopharmacol. 2005 Mar 21;97(3):549-54 [PMID: 15740894]
  11. Am J Clin Nutr. 1980 Mar;33(3):637-63 [PMID: 6766662]
  12. Arzneimittelforschung. 1974 Oct;24(10):1633-6 [PMID: 4479775]
  13. Phytother Res. 2001 Aug;15(5):431-4 [PMID: 11507737]
  14. Planta Med. 1997 Apr;63(2):146-9 [PMID: 9140229]
  15. Phytother Res. 2000 Aug;14(5):381-3 [PMID: 10925410]
  16. Biochem Pharmacol. 1990 Aug 15;40(4):793-7 [PMID: 2386548]
  17. J Pharm Pharmacol. 1978 Jan;30(1):41-5 [PMID: 22723]
  18. Prostaglandins. 1976 May;11(5):809-28 [PMID: 935512]
  19. J Ethnopharmacol. 2005 Nov 14;102(2):213-6 [PMID: 16054314]
  20. J Vet Pharmacol Ther. 2001 Oct;24(5):349-51 [PMID: 11696085]
  21. Prostaglandins. 1977 Feb;13(2):321-31 [PMID: 847235]
  22. Life Sci. 1997;61(20):2049-55 [PMID: 9366512]
  23. Phytother Res. 2004 Nov;18(11):873-6 [PMID: 15597302]
  24. Drug Metab Rev. 2003 Feb;35(1):35-98 [PMID: 12635815]
  25. Planta Med. 1993 Aug;59(4):333-6 [PMID: 8372151]
  26. Bull Soc Pathol Exot. 2007 Oct;100(4):246-9 [PMID: 17982852]
  27. J Ethnopharmacol. 2008 Feb 28;116(1):125-30 [PMID: 18164567]
  28. Phytother Res. 2005 Jun;19(6):481-5 [PMID: 16114083]
  29. Indian J Exp Biol. 1997 Dec;35(12):1310-4 [PMID: 9567766]
  30. Naunyn Schmiedebergs Arch Pharmacol. 1981 Sep;317(2):178-9 [PMID: 6272133]
  31. Br J Pharmacol. 1994 Dec;113(4):1127-30 [PMID: 7889264]
  32. Phytother Res. 2009 Jul;23(7):965-71 [PMID: 19140171]
  33. Gastroenterology. 1971 Jan;60(1):22-32 [PMID: 5544090]
  34. Life Sci. 1978 Sep 11;23(10):1001-9 [PMID: 713678]
  35. Lancet. 1988 May 28;1(8596):1234-5 [PMID: 2897052]
  36. BMC Complement Altern Med. 2004 Jul 06;4:8 [PMID: 15238156]
  37. Phytother Res. 2001 Mar;15(2):131-4 [PMID: 11268112]
  38. Bull World Health Organ. 1982;60(4):605-13 [PMID: 6982783]

MeSH Term

Animals
Antidiarrheals
Atropine
Castor Oil
Charcoal
Defecation
Diarrhea
Dose-Response Relationship, Drug
Feces
Female
Gastrointestinal Motility
Loperamide
Magnoliopsida
Male
Medicine, African Traditional
Phytotherapy
Plant Bark
Plant Extracts
Plant Stems
Polyphenols
Rats
Rats, Wistar
Tannins

Chemicals

Antidiarrheals
Plant Extracts
Polyphenols
Tannins
Charcoal
Loperamide
Atropine
Castor Oil

Word Cloud

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