Yang Zhi, Yin Ji-Ye, Gong Zhi-Cheng, Huang Qiong, Chen Hao, Zhang Wei, Zhou Hong-Hao, Liu Zhao-Qian
Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University Xiangya School of Medicine, Changsha, Hunan 410078, PR China.
Clin Chim Acta. 2009 Oct;408(1-2):98-104. doi: 10.1016/j.cca.2009.07.021. Epub 2009 Aug 11.
The aims of this study were to investigate the effects of clozapine on adipocyte differentiation and its regulation for fat-cell derived factors.
3T3-L1 preadipocytes were induced into differentiated adipocytes by the addition of 5 microg/ml of insulin, 1 micromol/l dexamethasone, 10 mmol/l IBMX, 1% DMSO, and 10% FBS in DMEM medium. The semi-quantitative RT-PCR was performed to determine the mRNA levels of PPAR gamma, C/EBP alpha, ADD1/SREBP(1C), LPL, and DGAT1. The expression levels of LPL and DGAT1 proteins in the adipocytes treated with clozapine or rosiglitazone were determined by Western blot analysis. The triglyceride concentration was determined by use of GPO-POD assay Kit.
Clozapine enhanced the expression level of ADD1/SREBP(1C) mRNA and triglyceride concentration in the differentiated adipocytes. Clozapine significantly suppressed the expression levels of LPL mRNA and LPL protein with a dose-dependent and time-dependent manner, respectively.
These data suggest that clozapine might play an important role in inducing adipocyte differentiation and the regulation of fat-cell derived factors.
本研究旨在探讨氯氮平对脂肪细胞分化的影响及其对脂肪细胞衍生因子的调控作用。
在DMEM培养基中添加5μg/ml胰岛素、1μmol/l地塞米松、10mmol/l异丁基甲基黄嘌呤、1%二甲基亚砜和10%胎牛血清,将3T3-L1前脂肪细胞诱导分化为脂肪细胞。采用半定量RT-PCR法检测过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT/增强子结合蛋白α(C/EBPα)、脂肪分化相关蛋白1/固醇调节元件结合蛋白1C(ADD1/SREBP(1C))、脂蛋白脂肪酶(LPL)和二酰甘油酰基转移酶1(DGAT1)的mRNA水平。通过蛋白质免疫印迹分析检测氯氮平或罗格列酮处理的脂肪细胞中LPL和DGAT1蛋白的表达水平。使用甘油磷酸氧化酶-过氧化物酶法试剂盒测定甘油三酯浓度。
氯氮平可提高分化脂肪细胞中ADD1/SREBP(1C) mRNA的表达水平和甘油三酯浓度。氯氮平分别以剂量依赖性和时间依赖性方式显著抑制LPL mRNA和LPL蛋白的表达水平。
这些数据表明,氯氮平可能在诱导脂肪细胞分化和调控脂肪细胞衍生因子方面发挥重要作用。