##plugins.themes.bootstrap3.article.main##

The acute and chronic toxicity evaluation of Ethanol leaf extract of Merremia tridentata (Linn) Halier F. (MTELE) was carried out on albino wistar rats. Phytochemical screening and acute toxicity profile of the extract were determined using standard methods. The animals were assigned into groups and administered varying doses of MTELE (100, 200, 400 mg/kg body weight and 0.2 ml of distilled water) for a period of hundred days (fourteen weeks). The body weight, relative organ weight, haematology, serum biochemical indices and histopathological studies of the liver, kidney, spleen, heart, and lungs were appropriately carried out to determine propensity of possible toxicity. Phytochemical screening revealed the presence of alkaloids, tannins, cardiac glycosides, saponins, steroids, triterpenes, flavonoids while anthraquinone and cyanogenic glycosides were absent. The median lethal dose LD50 was estimated as 2200 mg/kg body weight. There was significant (p<0.05) reduction in the percentage change in body weight of rats administered 200 and 400 mg/kg/day dose of the extract for 100days when compared to the control group. Moreover, there was a significant (p<0.05) reduction in the relative weight of the spleen of rats and significant (p<0.05) increase in the relative weight of the liver, kidney, heart and lungs of rats administered 400 mg/kg/day dose. All serum biochemical parameters studied showed significant (p<0.05) increase in group administered 400 mg/kg body weight dose while alkaline phosphatase, aspartate amino transferase, creatine kinase, lactate dehydrogesase and potassium ion showed significant increase (p<0.05) in the group administered 200 mg/kg/day. There is no significant change in hematological parameters like RBC, hemoglobin, hematocrit, platelets, monocytes, basophils, MCV, MCH, MCHC, in the extract treated animals except the lymphocyte that showed a significant (p<0.05) reduction only in the group treated with 400 mg/kg body weight dose. Administration of MTELE at 200 mg/kg body weight did not occasioned any histo-architectural change in the liver and spleen but caused varying degree of remarkable histological derangement in the other tissues. Furthermore, there were remarkable pathologies in the liver, kidney, spleen, heart and lungs ranging from vascular congestion, haemorrhage, fibrosis, to renal and myocardial damage in the group treated with 400 mg/kg/day dose for hundred days. However, 100 mg/kg body weight dose showed no significant difference (p>0.05) in all the parameters evaluated indicating safety at this dosage. Ethanol leaf extract of Merremia tridentata (Linn) Halier F. (MTELE) may not be safe at chronic administration even at dosage as low as 200 mg/kg body weight. The plant should be cautiously employed to avoid unwarranted complication on long term administration.

References

  1. M.O. Soladoye and O.O Oyesiku, “Taxonomy of Nigerian Medicinal Plants” in A Textbook of Medicinal Plants from Nigeria, T. Odubgemi, Ed., Akoka-Yaba Lagos: Lagos University Press, 2008, ch 11, pp 93-149.
     Google Scholar
  2. C.P. Khare, Indian Medicinal Plants: An Illustrated Dictionary. Springer, New Delhi, 2007, pp. 410–411.
     Google Scholar
  3. Sowndhararajan, K and Nyuk, L.C. (2014). Antioxidant and Anti-ulcer Effects of Ethyl Acetate Fraction of Merremia Tridentata (L.) Hallier F. Root Agriculture and Agricultural Science Procedia, 2, pp. 406-414.
     Google Scholar
  4. K, Arunachalam, T, Parimelazhagan and S. Manian, Analgesic and anti-inflammatory effects of Merremia tridentata (l.) hallier f. Int J Pharm Pharm Sci 2011; 3: pp75-79.
     Google Scholar
  5. K., Arunachalam, and T. Parimelazhagan, Antidiabetic activity of aqueous root extract of Merremia tridentata (L.) Hall. f. in streptozotocin–induced–diabetic rats. Asian Pacific Journal of tropical medicine, 2012. 5(3), pp 175-179.
     Google Scholar
  6. B.C. Hatapakki, V. Hukkeri, D.N Patil, and M.J. Chavan. Wound Healing Activity of Merremia Tridentata. Indian Drugs 2004, 41, 532.
     Google Scholar
  7. M., Kamalutheen, S., Gopalakrishnan,and T.S., Ismail,. Anti-Inflammatory and Anti-Arthritic Activities of Merremia Tridentata (L.) Hall. f. E. Journal of Chemistry, 2009: 6, pp 943–948.
     Google Scholar
  8. A., Aschfalk, H., Steingass, W., Muller and E. Drochner, Merremia tridentata as a Supplementary Feed to the Grass Panicum Maximum forYoung West African Dwarf Sheep. Tropical Animal Health and Production, 2002, 34, pp 45–50.
     Google Scholar
  9. D. Lorke, A new approach to practical acute toxicity testing. Archives of Toxicology, 1983, 54: pp 275 – 287.
     Google Scholar
  10. P. Kalaiselvi, M., Uma, M., Suresh, K. Thulasiraman, and E. Lakshmidevi, Chronic toxicity studies of aqueous leaf extract of Indian traditional medicinal plant Ocimum tenuiflorum (Linn.) in rats European Journal of Experimental Biology, 2013, 3(5): pp 240-247.
     Google Scholar
  11. Evenson M.E. (1999). “Spectrophotometric Technique”. In: Tietz Textbook of Clinical Chemistry, 3rd ed, CA Burtis, ER Ashwood, Eds. Philadelphia:WB Saunders Co., pp. 75-93.
     Google Scholar
  12. J. Ochei and A. Kolhatkar, “Histopathological Techniques and Cytology”. In: Textbook of Medical Laboratory Technology- Theory and Practice, 3rd ed. 2008, Tata McGraw-Hill Publishing Company Limited, New Delhi: pp.418 – 426.
     Google Scholar
  13. C.A. Pieme, V.N. Penlap, B. Nkegoum, C.L. Taziebou, E.M. Tekwe, F.X. Etoa and J. Ngongang, Evaluation of acute and subacute toxicities of aqueous ethanol extract of leaves of Senna alata (L.) Roxb (Ceasalpiniaceae). Afriican Journal of Biotechnology, 2006, 5(3): pp. 283-289.
     Google Scholar
  14. K.C. Patrick-Iwuanyanwu, M.O. Wegwu and J.K. Okiyi Hepatoprotective effects of African locust bean (Parkia clappertoniana) and negro pepper (Xylopia aethiopica) in CCl4 -induced liver damage in Wistar albino rats. International Journal of Pharmaceutics 6, 2010, pp.744-749.
     Google Scholar
  15. S. Kumar, P.Singh, G. Mishra, S. Srivastar, KK. Jha, RL. Khosa, Phytopharmacological review of Alternanthera brasiliana (Amaranthaceae). Asian Journal of Plants Science Research,2011.1(1): pp.41- 47.
     Google Scholar
  16. C.U. Osifo, U. Akpamu, C.I. Idehen, W.A. Adisa, and K.E. Azeke, The effect of chronic ingestion of crude garcinia kola on the histology of the liver, European Journal of. Experimental Biology, 2012. 2 (2): pp.404-409.
     Google Scholar
  17. S.O. Ogbonnia, S, G.O. Mbaka, F.E. Nkemehule, J.E. Emordi, N.C. Okpagu and D.A. Ota, Acute and subchronic evaluation of aqueous extracts of Newbouldia laevis (Bignoniaceae) and Nauclea latifolia (Rubiaceae) roots used singly or in combination in Nigerian traditional medicines. British Journal of Pharmacology and Toxicology., 2014. 5(1): pp. 55-62.
     Google Scholar
  18. W.J. Brock, H.J. Trochimowicz, R.J. Millischer, C. Farr, T. Kawano and G.M. Rusch, Acute and subchronic toxicity of 1,1-dichloro-1- fluoroethane (HCFC-141b). Food and Chemical Toxicology, 1995. 33, pp. 483–490.
     Google Scholar
  19. A.J. Fridous, S. N. L. M. Islam and A.B.M. Faruque, Antimicrobial activity of the leaves of Adhatoda vasica, Calotropis gigantea, Nerium odorum and Ocimum sanctum. Bangladesh. Journal of Botany. 1990. 19: 227-229.
     Google Scholar
  20. G.V. Pierangeli and L.R Windell, Antimicrobial activity and cytotoxicity of Chromolaena odorata (L. f). King and Robinson and Uncaria perrottetii (A. Rich) Merr. extracts. Journal Medicinal Plants Research, 2009. 3(7): pp.511-518.
     Google Scholar
  21. M. Raza, O.A. Al-Shabanah, T.M. El-hadiyah and A.A. Al-Majed Effect of Prolonged Vigabatrin Treatment on Hematological and Biochemical Parameters in Plasma, Liver and Kidney of Swiss Albino Mice. Scientia Pharmaceutica, 2002, 70, pp. 135-145.
     Google Scholar
  22. S.K. Thanabhorn, S. Jenjoy, K. Thamaree, K. Ingkaninan and A. Panthong, Acute and subacute toxicity study of the ethanol extract from Lonicera japonica Thunb. Journal of. Ethnopharmacol., 2006. 107: pp. 370-373.
     Google Scholar
  23. R. Nirogi, V.K. Goyal, S. Jana, S.K. Pandey, and A. Gothi, What suits best for organ weight analysis: review of relationship between organ weight and body / brain weight for rodent toxicity studies International Journal of Pharmaceutical Science and Research, 2014, Vol. 5(4): 1525-1532.
     Google Scholar
  24. S.A Bailey, R.H. Zidell and R.W. Perry, Relationships between organ weight and body/brain weight in the rat: What is the best analytical endpoint? Toxicol. Pathol. 2004. 32, 448–466.
     Google Scholar
  25. H. Rhiouani, J. El-Hilalya, Z.H. Israili and B. Lyoussia, Acute and Sub-chronic toxicity of an aqueous extract of the leavesof Herniara glabra in rodents. Journal of Ethnopharmacology, 2008, 118, 378-386.
     Google Scholar
  26. R.K Koshy, B.R Kapoor and M. Azmathulla, 2010. Pharmacology online, 3, pp. 229-242.
     Google Scholar
  27. D.W. Martin P.A. Mayes and Y.M. Rodwell, In:Harper’s Review of Biochemistry. 18th edn, Lange Medical, CA, 1981, pp:61.
     Google Scholar
  28. R. Horton, L.A. Moran, R. Ochs, J.D. Rawn and K.G.Scrimgeour, Principles of Biochemistry. 2nd Edn., 1996, Prentice Hall.
     Google Scholar
  29. K.M. Wasan, S. Najafi, J. Wong, and M. Kwong Assessing plasma lipid levels, body weight and hepatic and renal toxicity following chronic oral administration of a water soluble phytostanol compound. Journal of Pharmaceutical Science., 2001.4(3): 228-234.
     Google Scholar
  30. M.A. Crook, Clinical Chemistry and Metabolic Medicine. 7th Edn., Hodder Arnold, London, 2006. pp: 426.
     Google Scholar
  31. J. Ochei and A. Kolhatkar, Textbook of Medical Laboratory Technology- Theory and Practice, 3rd ed. 2008, Tata McGraw-Hill Publishing Company Limited, New Delhi: pp.180–182.
     Google Scholar