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
Department of Biochemistry, Medical School, Chonbuk National University, Jeonju, Republic of Korea.
J Med Food. 2009 Apr;12(2):304-9. doi: 10.1089/jmf.2008.1010.
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.
我们研究了土贝母提取物(RDTEs)对血脂、体重和脂肪生成酶的影响。给小鼠喂食标准饲料、60%高脂饲料或含RDTE的高脂饲料。与喂食高脂饲料的小鼠相比,喂食含RDTE高脂饲料的小鼠体重和附睾脂肪组织重量增加较少,肝脂肪变性发生率降低。RDTE诱导的肥胖减轻导致血浆肿瘤坏死因子-α、瘦素和葡萄糖水平降低,脂联素水平升高。与高脂组相比,给予RDTE还导致甘油三酯、总血浆胆固醇和低密度脂蛋白胆固醇显著降低。为了确定RDTE诱导其抗肥胖作用的机制,我们研究了在喂食高脂饲料的小鼠中诱导的固醇调节元件结合蛋白(SREBP)转录系统。发现RDTE可抑制喂食高脂饲料小鼠脂肪和肝脏组织中SREBP-1以及脂肪酸合酶的表达。这些发现表明,RDTE对喂食高脂饲料小鼠的抗肥胖作用可能是由于抑制了SREBP-1依赖性脂肪生成途径。