Please use this identifier to cite or link to this item: https://etd.cput.ac.za/handle/20.500.11838/1510
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dc.contributor.advisorAboua, Yapo Guillaumeen_US
dc.contributor.advisorBrooks, Nicole L.en_US
dc.contributor.authorMosito, Rosemary Boitumeloen_US
dc.date.accessioned2015-09-04T11:23:18Z-
dc.date.accessioned2016-02-22T04:59:29Z-
dc.date.available2015-09-04T11:23:18Z-
dc.date.available2016-02-22T04:59:29Z-
dc.date.issued2015-
dc.identifier.urihttp://hdl.handle.net/20.500.11838/1510-
dc.descriptionThesis (MTech (Biomedical Technology))--Cape Peninsula University of Technology, 2015en_US
dc.description.abstractOxidative stress (OS) plays a major role in the pathogenesis of different conditions including male infertility. OS is caused by high amounts of reactive oxygen species (ROS) that exceed the antioxidant ability of a system. The sperm membrane is rich in polyunsaturated fatty acids and is prone to damage by ROS. Sperm damage decreases motility, concentration and viability. Testicular oxidative stress impairs Leydig cell function and leads to decreased hormonal control as the cells secrete testosterone. Studies have shown the role of antioxidants in the fight against OS. Recently more studies have been focused on the use of natural antioxidants derived from fruits, vegetables, nuts and oils for this purpose. The effects of Buriti oil supplementation have been investigated in the diet and it had been shown that it is rich in carotenoids and vitamin E. This study explored the antioxidant effects of Buriti oil on testicular tissue, epidymal tissue and hormonal function in male Wistar rats. Experiments were conducted for 6 weeks and male adult Wistar rats (10 weeks) were divided into two groups (n=30) for each group. The control group received standard rat chow and water while the experimental group received Buriti oil, rat chow and water daily. Both groups were exposed to natural physiological OS. The plasma, testicular and epididymal tissue samples of both groups were analysed for various parameters. Testicular weight and epididymal weight of rats fed with Buriti oil were significantly increased compared to the control group. Testicular and epididymal MDA levels were decreased in rats fed with Buriti oil compared to the control group. Superoxide dismutase (SOD), catalase (CAT) and glutathione (GSH) activities were increased in both epididymal and testicular tissue of the Buriti oil fed group than the control group. Data were expressed in mean ± SEM. In conclusion, our findings suggest that Buriti oil supplementation could prevent OS damage in the male reproductive system.en_US
dc.language.isoenen_US
dc.publisherCape Peninsula University of Technologyen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/-
dc.subjectOxidative stressen_US
dc.subjectAntioxidantsen_US
dc.subjectBuriti oilen_US
dc.subjectTesticular tissueen_US
dc.subjectEpididymal tissueen_US
dc.subjectTestosteroneen_US
dc.subjectEstradiolen_US
dc.subjectSuperoxide dismutaseen_US
dc.subjectCatalaseen_US
dc.subjectGlutathione peroxidaseen_US
dc.titleThe effects of dietary Buriti oil (Mauritia flexuosa) supplementation on rat reproductive functionen_US
dc.typeThesisen_US
Appears in Collections:Biomedical Technology - Masters Degrees
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