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Improvement of insulin resistance via increase of GLUT4 and PPARγ in metabolic syndrome‐induced rats treated with omega‐3 fatty acid or l ‐carnitine
Author(s) -
Zayed Eman Adel,
AinShoka Afaf A.,
El Shazly Kamal A.,
Abd El Latif Hekma A.
Publication year - 2018
Publication title -
journal of biochemical and molecular toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.526
H-Index - 58
eISSN - 1099-0461
pISSN - 1095-6670
DOI - 10.1002/jbt.22218
Subject(s) - medicine , carnitine , endocrinology , insulin resistance , glut4 , metformin , metabolic syndrome , adiponectin , fructose , glucose transporter , chemistry , dyslipidemia , peroxisome proliferator activated receptor , omega 3 fatty acid , rosiglitazone , insulin , fatty acid , diabetes mellitus , receptor , docosahexaenoic acid , biochemistry , polyunsaturated fatty acid
Abstract Background Frequent consumption of fructose and saturated fatty acids increase risk of metabolic syndrome (MS). Features of MS include insulin resistance, dyslipidemia, visceral obesity, and hypertension. The aim of this study was to investigate the role of omega‐3 and l ‐carnitine in ameliorating features of MS. Methods MS was induced in rats by high‐fructose high‐fat fed diet for 8 weeks. They were randomly divided into five groups: normal control, MS control group treated with saline, MS groups given omega‐3 (260 mg/kg), l ‐carnitine (200 mg/kg), or metformin (100 mg/kg) daily for 4 weeks. Body weight, relative organ weight, glucose, insulin, adiponectin, and lipid profiles were estimated. Also glucose transporter 4 (GLUT4) content and peroxisome proliferator‐activated receptor‐gamma (PPARγ) protein expressions were determined. Results Omega‐3 and l ‐carnitine caused decrease in both MS‐induced increase in body weight and glucose similar to metformin. They reduced insulin level and resistance with increased adiponectin, and correction of MS‐induced hyperlipidemia. Drugs also increased GLUT4 and PPARγ protein expression compared with MS control group. Conclusion Omega‐3 and l ‐carnitine improve features of MS via increased GLUT4 and PPARγ expression.