Acute and sub-acute toxicity profiles of methanol leaf extract of Psydrax subcordata on swiss albino mice
Contenu principal de l'article
Résumé
Background: Psydrax subcordata (DC) Bridson (Rubiaceae) shows a vast range of pharmacological activities as evident in its folkloric use with little information on its toxicity. The toxic effect of methanol extract of P. subcordata on the kidney biomarkers, structure and haematological parameters were determined using male Swiss albino mice.
Methods: Two groups of mice consisting of three mice each were administered with a single oral dose of 2000mg/kg and 5000mg/kg to determine acute toxicity. Forty mice (n = 10/group) were treated orally with distilled water, 250mg/kg b.w of extract, 500mg/kg b.w of extract and 1000mg/kg b.w of extract for 28 days. Lethality/mortality, haematological, biochemical and histological parameters were determined.
Results: The result of the acute study reveals that the LD50 is more than 5000mg/kg as no death was recorded in the animals. The biochemical parameters reduce with increase in dose same as the haematological parameters, except for the WBC which increases as the dose increases. The monocyte and eosinophils levels remain unchanged. The histopathological analysis of the kidney reveals vascular congestion with increase in dose.
Conclusion: P. subcordata extract causes increasing renal and liver histological deterioration as the doses increases, though no mortality was recorded. Thus, higher doses of the extract are not safe especially when administered for prolonged duration orally.
Téléchargements
Renseignements sur l'article
Cette œuvre est sous licence Creative Commons Attribution - Pas d'Utilisation Commerciale - Pas de Modification 4.0 International.
Références
Atanasov AG, Waltenberger B, Pferschy-Wenzig EM (2015). Discovery and resupply of pharmacologically active plant-derived natural products: A review. Biotechnol Adv. 33(8), 1582–1614.
George P (2011). Concerns regarding the Safety and Toxicity of Medicinal Plants. Journal of Applied Pharmaceutical Science 1(6), 40-44.
Klaasen CS (2008). Pricinciple of toxicology and treatment of poisoning. In: Parker B.K., Blumenthal, B., Buxton, L. (edition) Goodman & Gilman’s; Manual of pharmacology & therapeutics. McGraw Hill. 1115-1119.
Burkill HM (1985). The Useful Plants of West Tropical and Africa. Royal Botanic Gardens: vols. 1-3. 2 edn., 99-102.
Agyare C, Asase A, Lechtenberg M, Niehues M, Deters A, Hensel A (2009). An ethnopharmacological survey and in vitro confirmation of ethnopharmacological use of medicinal plants used for wound healing in Bosomtwi-Atwima-Kwanwoma area, Ghana. Journal of Ethnopharmacology 125(3), 393-403.
Asare GA, Addo P, Bugyei K, Gyan B, Adjei S, Otu-Nyarko LS, Wiredu EK, Nyarko A. Acute toxicity studies of aqueous leaf extract of Phyllanthus niruri. Interdisciplinary toxicology. 2011 Dec;4(4):206.
Lorke D. A new approach to practical acute toxicity testing. Archives of toxicology. 1983 Dec;54(4):275-87.
Nascimento DK, Souza IA, Oliveira AF, Barbosa MO, Santana MA, PEREIRA DF, Lira EC, Vieira JR. Phytochemical screening and acute toxicity of aqueous extract of leaves of Conocarpus erectus Linnaeus in swiss albino mice. Anais da Academia Brasileira de Ciências. 2016 Aug 4; 88:1431-7.
Organisation for economic co-operation and development (OECD) (2001). Guildelines for testing of chemicals 423.Acute oral toxicity-acute toxic class method. #423, Paris, France.
Daanaa S, Abotsi WKM, Boakye-Gyasi E, Woode E (2018). Anticonvulsant effect of the hydroethanolic leaf extract of Psydrax subcordata (DC.)Bridson in murine models. J Ethnopharmacol. 213, 384-394.
Anokwah D, Mensah AY, Amponsah IK, Mireku EA, Mintah DN (2016). Anti-inflammatory, antioxidant and antimicrobial activities of the stem bark of Psydrax subcordata. Der Pharmacia Lettre 8(20), 21-28.
Kotenev BM, Sausen KN, Galushkin AN, Danilova LA (1971). Photometric hemoglobin concentration determination. Biomedical Engineering, 5(3), 144-146.
Babson AL, Greeley SJ, Coleman CM, Phillips GE (1966). Phenolphthalein monophosphate as a substrate for serum alkaline phosphatase. Clinical chemistry, 12(8), 482-490.
Tolman KG, Rej R (1999). Liver function. In: Burtis, C.A., Ashwood, E.R., editions. Tietz textbook of clinical chemistry.3rd edition. Philadelphia: W.B. Saunders, 1125-1177.
Briskin DP (2000). Medicinal plants and phytomedicines.link in plant biochemistry and physiology to human health. Journal of plant physiology 124, 507-514
Teschke R, Wolff A, Frenzel C, Schulze J. herbal hepatotoxicity–an update on traditional Chinese medicine preparations. Alimentary pharmacology & therapeutics. 2014 Jul;40(1):32-50.
Ogbonnia SO, Mbaka GO, Adekunle A, Anyika EO, Gbolade OE, Nwakakwa N (2010). Effect of polyherbal formulation okudiabet on Adoxin-induced diabetic rats. Agricultural Biological. Journal Nigeria.AM. 1(2), 139-145.
Joubouhi C, Mabou FD, Tebou PLF, Ngnokam D, Harakat D, Voutquenne-Nazabadioko L (2015). Five new iridoïd dimers from the fruits of Canthium subcordatum DC (syn. Psydrax subcordata DC). Phytochemistry Letters 13, 348-354.
Oyawaluja BO, Williams JA, Coker HAB (2019). Investigation of antimicrobial and antioxidant activity of the methanolic extract of the leaves of Voacanga africana stapf. (Apocynanceae) and Psydrax subcordata (DC.)Bridson (Rubiaceae). The Nigerian Journal of Pharmacy 53(1), 23-33.
Zhou J, Wu Z, Oyawaluja BO, Coker HAB, Odukoya OA, Yao G, Che CT (2019). Protein Tyrosine Phosphatase 1B Inhibitory Iridoids from Psydrax subcordata. Journal of natural products 82(10), 2916-2924.
Schnell MA, Hardy C, Hawley M, Propert KJ, Wilson JM (2002). Effect of blood collection technique in mice on clinical pathology parameters. Human gene therapy, 13(1), pp.155-161.
Wennecke G (2004). Hematocrit-A review of different analytical methods. Radiometer Medical ApS.
Kokholm G (1991). Simultaneous measurements of blood pH, pCO2, pO2 and concentrations of hemoglobin and its derivatives – a multicenter study. Radiometer publication AS107.
González FHD, Carvalho V, Möller VA, Duarte FR (2001). Blood biochemical profile of dogs and cats in the city of Porto Alegre, Rio Grande do Sul, Brazil. Archives of the Faculty of Veterinary.UFRGS 29 (1), 1-6.
Traynor J, Mactier R, Geddes C, Fox JG (2006). How to measure renal function in clinical practice. BMJ. 333, 733-737.
González FH (2009). Diagnostic and monitoring tools for metabolic diseases. Brazilian Animal Science .1, 1-22
Hoffmann A, Nimtz M, Conradt H (1997). Molecular characterization of ß-trace protein in human serum and urine: a potential diagnostic marker for renal diseases. Glycobiology 7, 499–506.
Pagana KD, Pagana TJ, Pike-MacDonald SA (2018). Mosby's Canadian Manual of Diagnostic and Laboratory Tests-E-Book. Elsevier Health Sciences.