Tumeric Ethanol Extract Up-regulated the Lipolysis by Activation of Lipase Related Pathway in HepG2 Cells

D. Oh, Dakyung Kim, Minhee Lee, Jeongmin Lee
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Abstract

In current, we investigated the effect of tumeric ethanol extract (TEE) on underlying mechanisms of lipolysis in HepG2 hepatocytes. The intracellular lipid droplets were stained and quantified. In comparison with the control, lipid accumulation with 72-hours treatment of TEE was significantly decreased by 25.8% at concentration of 100 µg/mL. In consistence with a result, the cellular triglyceride (TG) content was reduced by 22.3% at concentration of 100 µg/mL, respectively. To determine the action mode of reduction in TG content, the glycerol release and level of glucose uptake were measured. At first, incubation of HepG2 hepatocytes with 50 and 100 g/mL of TEE for 4 hours significantly decreased the extracellular uptake of glucose by 7.4% and 10.4%. The free glycerol level released into the cultured media were significantly increased with 50 and 100 µg/mL of TEE treatment by 20.8% and 29.1%, but there was no time-dependent effect. As subsequently measured by quantitative real-time polymerase chain reaction, mRNA level of hormone-sensitive lipase (HSL) and adipose triglyceride lipase (ATGL), but not lipoprotein lipase (LPL), was significantly increased by 25.2% and 31.1% at concentration of 100 µg/mL. The present study suggested that TEE partially inhibited lipogenesis by suppressing glucose uptake and enhanced lipolysis through upregulation of HSL and ATGL mRNA expression, resulting in increased glycerol release.
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姜黄乙醇提取物通过激活脂肪酶相关通路上调HepG2细胞的脂肪分解
目前,我们研究了姜黄乙醇提取物(TEE)对HepG2肝细胞脂肪分解的潜在机制的影响。对细胞内脂滴进行染色和定量。与对照组相比,TEE浓度为100µg/mL,处理72小时后脂质积累显著减少25.8%。结果表明,当浓度为100µg/mL时,细胞甘油三酯(TG)含量分别降低22.3%。为了确定降低TG含量的作用方式,测量了甘油释放量和葡萄糖摄取水平。首先,HepG2肝细胞与50和100 g/mL TEE孵卵4小时后,细胞外葡萄糖摄取显著降低7.4%和10.4%。50µg/mL和100µg/mL TEE处理后,释放到培养基中的游离甘油水平分别显著提高20.8%和29.1%,但不存在时间依赖性。随后通过实时定量聚合酶链反应测定,在100µg/mL浓度下,激素敏感脂肪酶(HSL)和脂肪甘油三酯脂肪酶(ATGL) mRNA水平显著升高25.2%和31.1%,而脂蛋白脂肪酶(LPL) mRNA水平未见显著升高。本研究提示,TEE通过上调HSL和ATGL mRNA表达,抑制葡萄糖摄取和促进脂肪分解,从而增加甘油释放,从而部分抑制脂肪生成。
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