Show simple item record

dc.contributor.authorEnogieru, A.B.
dc.contributor.authorOmoruyi, S.I.
dc.contributor.authorEkpo, Okobi
dc.date.accessioned2019-10-07T10:00:07Z
dc.date.available2019-10-07T10:00:07Z
dc.date.issued2018
dc.identifier.citationEnogieru, A.B, Omoruyi, S.I. & Ekpo, O. (2018). Antioxidant and apoptosis-inhibition potential of Carpobrotus edulis in a model of parkinson’s disease. Journal of African Association of Physiological Sciences, 6(1), 126-135.en_US
dc.identifier.issn2449-108X
dc.identifier.urihttps://www.ajol.info/index.php/jaaps/article/view/182001
dc.identifier.urihttp://hdl.handle.net/10566/4987
dc.description.abstractBackground: Parkinson’s disease (PD) is a neurological disorder resulting from the progressive loss of dopaminergic neurons. There is currently no known cure for PD, thus the search for complementary and alternative medicines capable of halting the degeneration of dopaminergic neurons is plausible. Carpobrotus edulis (CE) is an indigenous plant used in South African traditional medicine used for the treatment of a number of disease conditions including tuberculosis, diabetes mellitus and constipation. It has been suggested that CE contains bioactive compounds which are responsible for its acclaimed medicinal potential. No studies have been reported on the potential benefit of CE to the nervous system. This study was therefore done to evaluate the protective effects of CE against 1-methyl-4-phenylpyridinium (MPP+)-induced toxicity in the dopaminergic SH-SY5Y cell line, as well as its underlying mechanism. Methods: In this study, SH-SY5Y cells were treated with varying concentrations of CE and MPP+ respectively to determine the optimal concentrations of MPP+ and CE for further experiments. Thereafter, SH-SY5Y cells were pre-treated with 30 μM of CE before exposure to 2 mM of MPP+ to induce cellular damage. Cell viability was evaluated using the MTT assay, intracellular reactive oxygen species (ROS) production was determined using flow cytometry and the Hoechst nuclear staining was used to visualize apoptosis. Caspases 3/7 and 9 activity was assessed using commercially available kits. Results: MPP+ treatment induced marked cell viability, increased the number of condensed nuclei and apoptotic cells, increased ROS production, initiated caspase 9 and activated caspase 3/7 in SH-SY5Y cells. The observed effects of MPP+-induced toxicity were attenuated by the pre-treatment of SH-SY5Y cells with 30 μM of CE. Conclusion: The protective effects of CE against MPP+-induced toxicity in SH-SY5Y cells may be attributed to its antioxidant and anti-apoptotic properties.en_US
dc.language.isoenen_US
dc.publisherAfrican Association of Physiological Sciencesen_US
dc.subjectParkinson’s diseaseen_US
dc.subjectCarpobrotus edulisen_US
dc.subjectSH-SY5Y cellsen_US
dc.subjectReactive oxygen speciesen_US
dc.subjectApoptosisen_US
dc.titleAntioxidant and apoptosis-inhibition potential of Carpobrotus edulis in a model of parkinson’s diseaseen_US
dc.typeArticleen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record