Sesamum indicum diet prevents hyperlipidemia in experimental rats

[Display omitted] •Sesamum indicum administration reverses the dyslipidemia in hyperlipidemic rats.•Hypolipidemic potency of Sesamum indicum is due to inhibition of HMG-CoA reductase activity.•Our findings lend credence to the use of Sesamum indicum as a therapeutic remedy in traditional medicine fo...

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Published in:Food chemistry. Molecular sciences Vol. 4; p. 100092
Main Authors: Adeyanju, Muinat M., Saheed, Idris A., Oyelekan, Oluwaseun I., Dele-Osibanjo, Taiwo A., Adelegan, Ayodeji A., Raimi, Adekunle J., Olalekan, Samuel O., Alabi, Olugbenga S., Alli, Khadijat M.
Format: Journal Article
Language:English
Published: England Elsevier Ltd 30-07-2022
Elsevier
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Summary:[Display omitted] •Sesamum indicum administration reverses the dyslipidemia in hyperlipidemic rats.•Hypolipidemic potency of Sesamum indicum is due to inhibition of HMG-CoA reductase activity.•Our findings lend credence to the use of Sesamum indicum as a therapeutic remedy in traditional medicine for hyperlipidemia and associated morbidities. Cardiovascular diseases and metabolic complications caused by hyperlipidemia are the leading cause of death globally. In this study, the hypolipidemic potency of Sesamum indicum (SI) seeds was investigated. Of the thirty-five (35) male rats used in the study, five (5) were randomly selected for baseline measurements and thirty (30) were fed high fat diet (HFD) for four (4) weeks before random assignment into three (3) groups. The experimental group was treated with 50% SI seed, the positive control group was given a hypolipidemic drug, atorvastatin (5 mg/kg/day) while the untreated group served as the negative control. With SI administration, the dyslipidemia induced by the HFD consumption in the plasma and the investigated body organs was reversed to a comparable degree with that of atorvastatin treatment. Taken together, this study demonstrates the hypolipidemic potency of SI in ameliorating hyperlipidemia and its associated complications, facilitated by the inhibition of HMG-CoA reductase activity.
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ISSN:2666-5662
2666-5662
DOI:10.1016/j.fochms.2022.100092