Jang E-H, Moon J-S, Ko J H, Ahn C-W, Lee H-H, Shin J-K, Park C-S, Kang J-H
Department of Pharmacology and Medicinal Toxicology Research Center, Inha Research Institute for Medical Sciences, College of Medicine, Inha University, Incheon, South Korea.
Int J Obes (Lond). 2008 Jul;32(7):1161-70. doi: 10.1038/ijo.2008.60. Epub 2008 Apr 15.
To investigate the mechanisms underlying the antiobesity effects of a novel isoflavone-free peptide mixture (BSP) derived from black soybean.
Long-term effects of BSP were evaluated in diet-induced obese (DIO) mice fed a high-fat (HF) diet without or with BSP (2, 5 or 10% of energy) for 13 weeks, or for 8 weeks in combination with exercise. Acute effects of BSP on food intake and body weight in rats and leptin-deficient ob/ob mice were evaluated. Cell culture models or tissue extracts were used to investigate the mechanisms underlying the antiobesity effect.
Total food intake, body weight gain, white adipose tissue (WAT) mass, plasma concentrations of leptin, adiponectin, cholesterol and triglyceride were measured. Janus kinase 2 (JAK2)-dependent signal transducers and activators of the transcription 3 (STAT3) phosphorylation and AMP-activated protein kinase (AMPK) activity were determined using Western-blot in cultured cells or tissue extracts.
DIO mice fed an HF diet with BSP (2, 5 or 10%) for 13 weeks gained less body weight (21.4, 19.8 or 17.1 g, respectively) than the mice fed an HF diet without BSP (22.6 g) concurrent with inhibition of total food intake in a dose-dependent manner. BSP also significantly decreased food intake in rats and leptin-deficient ob/ob mice. The highest dose of BSP (10%) significantly elevated the plasma adiponectin and decreased plasma triglyceride. BSP activated JAK2-dependent STAT3 in a cell model, and elevated the level of hypothalamic phospho-STAT3 in ob/ob mice. BSP also phosphorylated AMPK and acetyl-CoA carboxylase of C2C12 myocytes in a dose-dependent manner. The antiobesity effect was augmented by low-intensity wheel-based exercise. In exercised mice, BSP significantly decreased periepididymal WAT mass and body weight gain.
These results provided evidences that BSP decreased appetite and HF diet-induced body weight gain particularly in combination with exercise, through leptin-like STAT3 phosphorylation and AMPK activation.
研究一种源自黑豆的新型无异黄酮肽混合物(BSP)的抗肥胖作用机制。
在饮食诱导肥胖(DIO)小鼠中评估BSP的长期作用,这些小鼠喂食高脂(HF)饮食,分别添加或不添加BSP(能量的2%、5%或10%)持续13周,或添加BSP并结合运动8周。评估BSP对大鼠和瘦素缺乏的ob/ob小鼠食物摄入量和体重的急性影响。使用细胞培养模型或组织提取物研究抗肥胖作用的机制。
测量总食物摄入量、体重增加、白色脂肪组织(WAT)质量、血浆中瘦素、脂联素、胆固醇和甘油三酯的浓度。使用蛋白质免疫印迹法在培养细胞或组织提取物中测定Janus激酶2(JAK2)依赖性信号转导子和转录激活子3(STAT3)的磷酸化以及AMP激活的蛋白激酶(AMPK)活性。
喂食含BSP(2%、5%或10%)的HF饮食13周的DIO小鼠体重增加量(分别为21.4、19.8或17.1克)低于喂食不含BSP的HF饮食的小鼠(22.6克),同时以剂量依赖方式抑制总食物摄入量。BSP还显著降低了大鼠和瘦素缺乏的ob/ob小鼠的食物摄入量。最高剂量的BSP(10%)显著提高了血浆脂联素水平并降低了血浆甘油三酯水平。BSP在细胞模型中激活了JAK2依赖性STAT3,并提高了ob/ob小鼠下丘脑磷酸化STAT3的水平。BSP还以剂量依赖方式使C2C12肌细胞的AMPK和乙酰辅酶A羧化酶磷酸化。低强度轮转运动增强了抗肥胖作用。在运动的小鼠中,BSP显著降低了附睾周围WAT质量和体重增加量。
这些结果表明,BSP通过类似瘦素的STAT3磷酸化和AMPK激活降低食欲以及HF饮食诱导的体重增加,尤其是与运动相结合时。