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Study on the effect of vitamin D on obesity and fatty liver induced by monosodium glutamate in male albino rats

Background One of the most common hepatic disorders is nonalcoholic fatty-liver disease. The best model used for nonalcoholic fatty-liver disease is the monosodium glutamate (MSG)-induced obesity. MSG is a common flavor enhancer used in different food products. Vitamin-D deficiency increased risks o...

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Bibliographic Details
Published in:Tanta Medical Journal 2022-04, Vol.50 (2), p.125-131
Main Authors: Shakour, Salma, Barhoma, Ramez, Tahoon, Nahid M, ELshrbiny, Romysaa
Format: Article
Language:English
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Summary:Background One of the most common hepatic disorders is nonalcoholic fatty-liver disease. The best model used for nonalcoholic fatty-liver disease is the monosodium glutamate (MSG)-induced obesity. MSG is a common flavor enhancer used in different food products. Vitamin-D deficiency increased risks of obesity and nonalcoholic fatty-liver disease. However, much is still unknown about the link between vitamin D and nonalcoholic fatty-liver disease in obesity. Aim The aim was to investigate the effect of vitamin D on MSG-induced obesity and nonalcoholic fatty-liver disease in rats. Materials and methods Forty adult male albino rats were divided into four equal groups: control group, vitamin-D-treated group, MSG-treated group, MSG, and vitamin-D-treated group, at the end of the experimental period, blood samples were taken. Also, livers were dissected for histopathology. Results Vitamin D+MSG significantly decreased the body weight, serum levels of glucose, insulin and homeostasis model assessment-estimated insulin resistance, triglycerides, tumor necrosis factor-alpha, aspartate aminotransferase, alanine aminotransferase, and the liver malondialdehyde, while increased the liver glutathione levels and improved the liver histological findings compared with MSG group. Conclusion Vitamin D has a hepatoprotective effect on the MSG-induced obesity and nonalcoholic fatty-liver disease.
ISSN:1110-1415
2314-8624
DOI:10.4103/tmj.tmj_75_21