Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme · 2016
α-Amyrin attenuates high fructose diet-induced metabolic syndrome in rats.
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Prabhakar Pankaj, Reeta K H, Maulik Subir Kumar, Dinda Amit Kumar, Gupta Yogendra Kumar
Аннотация
This study investigated the effect of α-amyrin (a pentacyclic triterpene) on high-fructose diet (HFD)-induced metabolic syndrome in rats. Male Wistar rats were randomly distributed into different groups. The control group was fed normal rat chow diet. The HFD group was fed HFD (60%; w/w) for 42 days. Pioglitazone (10 mg/kg, orally, once daily) was used as a standard drug. α-Amyrin was administered in 3 doses (50, 100, and 200 mg/kg, orally, once daily along with HFD). Plasma glucose, total cholesterol, triglycerides, and high-density lipoprotein cholesterol (HDL-C) were estimated. Changes in blood pressure, oral glucose tolerance, and insulin tolerance were measured. Hepatic oxidative stress as well as messenger RNA (mRNA) and protein levels of peroxisome proliferator-activated receptor alpha (PPAR-α) were analyzed. A significant increase in systolic blood pressure, plasma glucose, total cholesterol, and plasma triglycerides and a significant decrease in HDL-C were observed in HFD rats as compared with control rats. Glucose tolerance and insulin tolerance were also significantly impaired with HFD. α-Amyrin prevented these changes in a dose-dependent manner. Hepatic oxidative stress as well as micro- and macrovesicular fatty changes in hepatocytes caused by HFD were also attenuated by α-amyrin. α-Amyrin preserved the hepatic mRNA and protein levels of PPAR-α, which was reduced in HFD group. This study thus demonstrates that α-amyrin attenuates HFD-induced metabolic syndrome in rats.
Предметные рубрики MeSH
Administration, OralAnimalsAntihypertensive AgentsAntioxidantsDiet, Carbohydrate LoadingDose-Response Relationship, DrugFructoseGene Expression RegulationHyperglycemiaHyperlipidemiasHypertensionHypoglycemic AgentsHypolipidemic AgentsInsulin ResistanceLiverMaleMetabolic SyndromeOleanolic AcidOxidative StressPPAR alphaRandom AllocationRats, Wistar