Journal of medicinal food · 2009
Antiobesity activity of aqueous extracts of Rhizoma Dioscoreae Tokoronis on high-fat diet-induced obesity in mice.
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Song Mi-Young, Lv Na, Kim Eun-Kyung, Kwon Keun Sang, Yoo Young-Bum, Kim Jin-Hang, Lee Si-Woo, Song Je-Ho, Lee Jung-Han, Lee Su-Kyung, Shin Byung-Cheul, Ryu Do-Gon, Park Byung-Hyun, Kwon Kang-Beom
Аннотация
We examined the effects of Rhizoma Dioscoreae Tokoronis extracts (RDTEs) on plasma lipids, body weight, and lipogenic enzymes. Mice were administered a standard chow diet, a 60% high-fat diet, or a high-fat diet with RDTE. Mice that were fed a high-fat diet containing RDTE were found to have lower increases in body and epididymal adipose tissue weights and a lessened occurrence of hepatic steatosis than mice that were fed a high-fat diet. The decreased adiposity that was induced by RDTE accounted for lower plasma levels of tumor necrosis factor-alpha, leptin, and glucose and a higher level of adiponectin. RDTE administration also resulted in a significant decrease in triglyceride, total plasma cholesterol, and low-density lipoprotein-cholesterol when compared to the high-fat group. To identify the mechanism by which RDTE induced its antiobesity effect, we investigated the sterol response element binding protein (SREBP) transcription system, which was induced in mice that were fed the high-fat diet. RDTE was found to suppress the expression of SREBP-1 as well as that of fatty acid synthase in adipose and liver tissues in mice provided the high-fat diet. These findings suggest that the antiobesity action of RDTE in mice that are fed a high-fat diet may occur in response to suppression of the SREBP-1-dependent lipogenic pathway.
Предметные рубрики MeSH
AdiponectinAdipose TissueAnimalsAnti-Obesity AgentsBlood GlucoseBody WeightCholesterolDietary FatsDioscoreaEpididymisFatty Acid SynthasesFatty LiverGene ExpressionLeptinMaleMiceMice, Inbred C57BLObesityOrgan SizePhytotherapyPlant ExtractsRNA, MessengerRhizomeSterol Regulatory Element Binding Protein 1TriglyceridesTumor Necrosis Factor-alpha