Liu F, Kim J, Li Y, Liu X, Li J, Chen X
Edison Biotechnology Institute, Department of Biomedical Sciences, College of Osteopathic Medicine, Athens, OH 45701, USA.
J Nutr. 2001 Sep;131(9):2242-7. doi: 10.1093/jn/131.9.2242.
The effects of extracts isolated from Lagerstroemia speciosa L. (banaba) on glucose transport and adipocyte differentiation in 3T3-L1 cells were studied. Glucose uptake-inducing activity of banaba extract (BE) was investigated in differentiated adipocytes using a radioactive assay, and the ability of BE to induce differentiation in preadipocytes was examined by Northern and Western blot analyses. The hot water BE and the banaba methanol eluent (BME) stimulated glucose uptake in 3T3-L1 adipocytes with an induction time and a dose-dependent response similar to those of insulin. Furthermore, there were no additive or synergistic effects found between BE and insulin on glucose uptake, and the glucose uptake activity of insulin could be reduced to basal levels by adding increasing amounts of BE. Unlike insulin, BE did not induce adipocyte differentiation in the presence of 3-isobutyl-1-methylxanthine (IBMX) and dexamethasone (DEX). BE inhibited the adipocyte differentiation induced by insulin plus IBMX and DEX (IS-IBMX-DEX) of 3T3-L1 preadipocytes in a dose-dependent manner. The differences in the glucose uptake and differentiation inhibitory activities between untreated cells and those treated with BE were significant (P < 0.01). The inhibitory activity was further demonstrated by drastic reductions of peroxisome proliferator-activated receptor gamma2 (PPARgamma2) mRNA and glucose transporter-4 (GLUT4) protein in cells induced from preadipocytes with IS-IBMX-DEX in the presence of BE. The unique combination of a glucose uptake stimulatory activity, the absence of adipocyte differentiation activity and effective inhibition of adipocyte differentiation induced by IS-IBMX-DEX in 3T3-L1 cells suggest that BE may be useful for prevention and treatment of hyperglycemia and obesity in type II diabetics.
研究了从紫薇(banaba)中分离的提取物对3T3-L1细胞葡萄糖转运和脂肪细胞分化的影响。使用放射性测定法研究了banaba提取物(BE)在分化脂肪细胞中的葡萄糖摄取诱导活性,并通过Northern和Western印迹分析检测了BE诱导前脂肪细胞分化的能力。热水BE和banaba甲醇洗脱液(BME)刺激3T3-L1脂肪细胞摄取葡萄糖,其诱导时间和剂量依赖性反应与胰岛素相似。此外,BE和胰岛素对葡萄糖摄取没有相加或协同作用,并且通过添加越来越多的BE可将胰岛素的葡萄糖摄取活性降低至基础水平。与胰岛素不同,在存在3-异丁基-1-甲基黄嘌呤(IBMX)和地塞米松(DEX)的情况下,BE不会诱导脂肪细胞分化。BE以剂量依赖性方式抑制3T3-L1前脂肪细胞中胰岛素加IBMX和DEX(IS-IBMX-DEX)诱导的脂肪细胞分化。未处理细胞与用BE处理的细胞之间的葡萄糖摄取和分化抑制活性差异显著(P <0.01)。在存在BE的情况下,从用IS-IBMX-DEX诱导的前脂肪细胞中诱导的细胞中过氧化物酶体增殖物激活受体γ2(PPARγ2)mRNA和葡萄糖转运蛋白4(GLUT4)蛋白的急剧减少进一步证明了这种抑制活性。3T3-L1细胞中葡萄糖摄取刺激活性、缺乏脂肪细胞分化活性以及有效抑制IS-IBMX-DEX诱导的脂肪细胞分化的独特组合表明,BE可能对预防和治疗II型糖尿病患者的高血糖和肥胖有用。