Ethanol extract of Tetrapleura tetraptera fruit peels: Chemical characterization, and antioxidant potentials against free radicals and lipid peroxidation in hepatic tissues

• Published in: Journal of Taibah University for Science Vol. 11; no. 6; pp. 861 - 867
• Main Authors: Erukainure, Ochuko L., Onifade, Olayinka F., Odjobo, Benedict O., Olasehinde, Tosin A., Adesioye, Temiloluwa A., Tugbobo-Amisu, Adesewa O., Adenekan, Sunday O., Okonrokwo, Grace I.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.11.2017; Taylor & Francis; Taylor & Francis Group
• Subjects: Antioxidant; Lipid peroxidation; Phytochemicals; Secondary metabolites; Lipid peroxidation; Secondary metabolites; Phytochemicals; Antioxidant
• ISSN: 1658-3655; 1658-3655
• DOI: 10.1016/j.jtusci.2017.03.007

The chemical and antioxidant properties of the ethanolic extract of Tetrapleura tetraptera fruit peels were investigated. Dried peels of T. tetraptera fruits were extracted with ethanol. The extract was subjected to preliminary phytochemical screening using standard procedures. GC–MS was used in identifying the secondary metabolites. The antioxidant properties of the extract were determined by its ferric reducing activity, 2,2′-diphenyl-1-picrylhydrazyl (DPPH) and nitric oxide (NO) radicals scavenging activities, and the inhibition of lipid peroxidation in hepatic tissues of albino male rats. Preliminary phytochemical screening revealed the presence of flavonoids, phenols, tannins, saponins, terpenoids and phlebotannin. GC–MS analysis revealed the presence of D-fructose, piperazine, octodrine, glycidol, glyceraldehydes, 6-octadecenoic acid and 9,12-octadecenoic acid, with D–fructose being the most predominant compound. The extract exhibited high antioxidant activities both in vitro and ex vivo, as indicated by its ability to scavenge DPPH and nitric oxide as well as inhibition of lipid peroxidation. This is further portrayed by its ferric reducing activity. These results suggest an antioxidant protective effect of the extract against oxidative hepatic damage and can be attributed to a synergetic action of the identified bioactive compounds.