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首页> 外文期刊>BMC Complementary and Alternative Medicine >KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats
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KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats

机译:KBH-1是一种草药成分,可改善高脂饮食诱导的肥胖大鼠的肝脂肪变性和瘦素抵抗性

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Background KBH-1 is an herbal mixture of Saururus chinensis, Curcuma longa and Polygala tenuifolia . Each herb has been reported to have various pharmaceutical activities; however, the synergistic effect of this herbal composition on obesity has not yet been determined. We investigated the alleviation effect of KBH-1 and its possible molecular mechanism in obesity-induced hepatic steatosis and leptin resistance in the hypothalamus. Methods We used HepG2 cells, primary neuronal cells and a high-fat diet (HFD)-induced obesity rat model to determine the effect of KBH-1 in vitro and in vivo on hepatic steatosis and leptin resistance accompanied by obesity. To identify the alleviation effect on lipid accumulation, HepG2 cells stimulated by FFA were stained with Oil Red O; in addition, immunoblotting and qPCR were performed to determine the effect of KBH-1 on the activation of proteins and nuclear enzymes in HepG2 cells and the steatotic liver of HFD-induced obesity rats. To examine the effect of KBH-1 on the leptin resistance of the hypothalamus and its possible molecular mechanism, we examined the effect of KBH-1 on the activation of the leptin resistance-related protein in primary cultured cortical neuron cells and the hypothalamus of an HFD-induced obesity rat model. In addition, we used HPLC analysis to identify the standard compound of KBH-1. Results KBH-1 not only suppressed the lipid deposition in HepG2 cells exposed to free fatty acids (FFA) but also significantly down-regulated major factors in lipogenesis and up-regulated major factors in lipolysis. Similarly, in a HFD-induced obesity model, KBH-1 improved hepatic steatosis by alleviating the effects on lipogenic genes and kinases. In addition, KBH-1 significantly improved the leptin-mediated signals impaired by obesity or FFA in the obesity model and primary cultured cortical neuron cells. In addition, KBH-1 was analyzed to include six standard compounds using HPLC analysis, among these compounds, onji-saponin B and curcumin were potently suppressed the level of triglycerides. Conclusions KBH-1 exhibits alleviating effects by improving hepatic steatosis and leptin resistance by up-regulating the activation of AMPK and suppressing the expression of PPARγ. These findings show the potential of KBH-1 as a functional food supplement or preventive agent in the treatment of obesity.
机译:背景知识KBH-1是五味龙,姜黄和远志的草药混合物。据报道每种草药具有多种药物活性。然而,尚未确定该草药组合物对肥胖症的协同作用。我们研究了KBH-1的减轻作用及其可能的分子机制,在肥胖引起的下丘脑肝脂肪变性和瘦素抵抗方面。方法我们使用HepG2细胞,原代神经元细胞和高脂饮食(HFD)诱导的肥胖大鼠模型,确定KBH-1在体内和体外对伴随肥胖的肝脂肪变性和瘦素抵抗的影响。为了鉴定对脂质蓄积的减轻作用,用油红O对FFA刺激的HepG2细胞进行染色。此外,通过免疫印迹和qPCR来确定KBH-1对HFD诱发的肥胖大鼠HepG2细胞和脂肪肝中蛋白质和核酶活化的影响。为了检查KBH-1对下丘脑瘦素抵抗的影响及其可能的分子机制,我们研究了KBH-1对原代培养的皮层神经元细胞和下丘脑的下丘脑激活瘦素抵抗相关蛋白的作用。 HFD诱发的肥胖大鼠模型。此外,我们使用HPLC分析来鉴定KBH-1的标准化合物。结果KBH-1不仅抑制了暴露于游离脂肪酸(FFA)的HepG2细胞中的脂质沉积,而且还显着下调了脂肪生成的主要因子,并上调了脂解的主要因子。同样,在HFD诱导的肥胖症模型中,KBH-1通过减轻对脂肪生成基因和激酶的影响来改善肝脂肪变性。此外,KBH-1在肥胖模型和原代培养的皮质神经元细胞中显着改善了由肥胖或FFA损害的瘦素介导的信号。另外,通过HPLC分析,KBH-1被分析为包括六个标准化合物,在这些化合物中,onji-皂苷B和姜黄素被有效地抑制了甘油三酸酯的水平。结论KBH-1通过上调AMPK的活化和抑制PPARγ的表达来改善肝脏脂肪变性和瘦素抵抗性,从而起到缓解作用。这些发现表明,KBH-1在治疗肥胖症中作为功能性食品补充剂或预防剂的潜力。

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