Inhibitory Effects of Bojungchiseub-tang on Adipocyte Differentiation and Adipogenesis in 3T3-L1 Preadipocytes

S. J. Lee
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引用次数: 2

Abstract

Bojungchiseub-tang (BJCST) has been used in symptoms and signs of edema, dampness-phlegm, kidney failure, and so on. BJCST is also expected to have strong anti-obesity activities. However, little is known about the mechanisms of its inhibitory effects on adipocyte differentiation and adipogenesis. In the present study, we examined the effects and mechanism of BJCST on transcription factors and adipogenic genes of 3T3-L1 preadipocytes to understand its inhibitory effects on adipocyte differentiation and adipogenesis. Our results showed that BJCST significantly inhibited differentiation and adipogenesis of 3T3-L1 preadipocytes in a dose-dependent manner. To elucidate the mechanism of the effects of BJCST on lowering lipid content in 3T3-L1 adipocytes, we examined whether BJCST modulate the expressions of transcription factors to induce adipogenesis and adipogenic genes related to regulate accumulation of lipids. As a result, the expression of steroid regulatory element-binding protein (SREBP)1, cytidine-cytidine-adenosine-adenosine-thymidine (CCAAT)/enhancer binding proteins α (C/EBPα), C/EBPβ, C/EBPδ, and peroxisome proliferator-activated receptor γ (PPARγ) genes, which induce the adipose differentiation, liver X receptor (LXR)α and fatty acid synthase (FAS) genes, which induce lipogenesis and adipose-specific aP2, Adipsin, lipoprotein lipase (LPL), CD36, TGF-β, leptin and adiponectin genes, which compose fat formation were decreased. BJCST also reduced the expression of acyl CoA oxidase (ACO) and uncoupling protein (UCP) genes related to lipid oxidation. In conclusion, BJCST could regulate transcript factor related to induction of adipose differentiation and inhibited the accumulation of lipids and expression of adipogenic genes. 
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保正祛脂汤对3T3-L1前脂肪细胞分化和脂肪形成的抑制作用
保正祛痰汤已被用于水肿、湿痰、肾衰竭等症状和体征。BJCST还有望具有很强的抗肥胖活性。然而,其抑制脂肪细胞分化和脂肪形成的机制尚不清楚。本研究通过研究BJCST对3T3-L1前脂肪细胞转录因子和成脂基因的影响及其机制,了解BJCST对脂肪细胞分化和成脂的抑制作用。我们的研究结果表明,BJCST以剂量依赖性的方式显著抑制3T3-L1前脂肪细胞的分化和脂肪形成。为了阐明BJCST降低3T3-L1脂肪细胞脂质含量的作用机制,我们研究了BJCST是否通过调节转录因子的表达诱导脂肪形成,以及调节脂质积累相关的成脂基因的表达。因此,诱导脂肪分化的类固醇调节元件结合蛋白(SREBP)1、胞苷-胞苷-腺苷-腺苷-腺苷-胸腺嘧啶(CCAAT)/增强子结合蛋白α (C/EBPα)、C/EBPβ、C/EBPδ、过氧化物酶体增殖物活化受体γ (PPARγ)基因、诱导脂肪生成的肝脏X受体(LXR)α和脂肪酸合成酶(FAS)基因以及脂肪特异性aP2、Adipsin、脂蛋白脂肪酶(LPL)、CD36、TGF-β、瘦素和脂联素基因的表达,它们组成的脂肪形成减少。BJCST还降低了与脂质氧化相关的酰基辅酶a氧化酶(ACO)和解偶联蛋白(UCP)基因的表达。综上所述,BJCST可以调节脂肪分化诱导相关转录因子,抑制脂质积累和成脂基因的表达。
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