ArticlesAbstractPharmacognosy Research,2016,8,2,89-96.DOI:10.4103/0974-8490.172658Published:February 2016Type:Original ArticleAuthors:Oluwatosin Adekunle Adaramoye, Adesola Fausat Azeez, and Olufunke Elizabeth Ola‑Davies Author(s) affiliations:Oluwatosin Adekunle Adaramoye1, Adesola Fausat Azeez1, Olufunke Elizabeth Ola-Davies2 1Department of Biochemistry, Faculty of Basic Medical Sciences, University of Ibadan, Ibadan, NIGERIA. 2Department of Veterinary Physiology, Biochemistry and Pharmacology, Faculty of Veterinary Medicine, University of Ibadan, Ibadan, NIGERIA. Abstract:Background: Cisplatin (Cis) is used in the treatment of solid tumors and is known to elicit serious side effects. Objective: The present study investigated the protective effects of chloroform fraction of Cocos nucifera husk fiber (CFCN) against Cis‑induced organs’ damage and chromosomal defect in rats. Quercetin (QUE), standard antioxidant, served as positive control. Materials and Methods: Thirty male Wistar rats were assigned into six groups and treated with corn oil (control), Cis alone, Cis + CFCN, CFCN alone, Cis + QUE, and QUE alone. QUE and CFCN were given at 50 and 200 mg/kg/day, respectively, by oral gavage for 7 days before the rats were exposed to a single dose of Cis (10 mg/kg, intraperitoneal) at the last 36 h of study. Results: Administration of Cis alone caused a significant (P < 0.05) increase in the levels of serum creatinine and urea by 72% and 70%, respectively, when compared with the control. The activity of serum aspartate aminotransferase was significantly (P < 0.05) increased while alanine aminotransferase and alkaline phosphatase were insignificantly (P > 0.05) affected in Cis‑treated rats. Furthermore, the activities of hepatic and renal catalase, superoxide dismutase, glutathione S‑transferase, glutathione peroxidase, and levels of reduced glutathione were significantly (P < 0.05) decreased in Cis‑treated rats with concomitant elevation of malondialdehyde. Cis exposure increased the frequency of micro nucleated polychromatic erythrocytes (mPCE) by 92%. Pretreatment with CFCN inhibited lipid peroxidation, enhanced the activities of some antioxidative enzymes and reduced the frequency of mPCE. Conclusions: Chloroform fraction of CFCN may protect against organs damage by Cis. Further studies are required to determine the component of the plant responsible for this activity. Keywords:Antioxidant, Cisplatin, Clastogenicity, Cocos nucifera, Lipid peroxidationView:PDF (1.61 MB) PDF Thumbnails Document Outline Search Document Find Toggle Sidebar Previous Next Page: Fullscreen Print Download Current View Zoom Out Zoom In Automatic Zoom Actual Size Fit Page Full Width 50% 75% 100% 125% 150% 200% More Information Less Information Close Click here to download the PDF file. Images Effects of CFCN on the activities of serum AST and ALT in rats treated with cisplatin. *Significantly different from control (P < 0.05). **Significantly different from control (P < 0.05). CFCN = Chloroform fraction of methanal extract of Cocos nucifera husk fiber, QUE = Quercetin, Cis = Cisplatin KeywordsAntioxidantCisplatinClastogenicityCocos nuciferaLipid peroxidation ‹ Oxidative Stress Parameters and Erythrocyte Membrane Adenosine Triphosphatase Activities in Streptozotocin‑induced Diabetic Rats Administered Aqueous Preparation of Kalanchoe Pinnata Leaves up Evaluation of Skin Anti‑aging Potential of Citrus reticulata Blanco Peel ›