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首页> 外文期刊>Biochemical and Biophysical Research Communications >Linoleic acid and stearic acid elicit opposite effects on AgRP expression and secretion via TLR4-dependent signaling pathways in immortalized hypothalamic N38 cells
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Linoleic acid and stearic acid elicit opposite effects on AgRP expression and secretion via TLR4-dependent signaling pathways in immortalized hypothalamic N38 cells

机译:亚油酸和硬脂酸通过永生化的下丘脑N38细胞中的TLR4依赖性信号通路对AgRP表达和分泌产生相反的影响

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The regulation of food intake is a promising way to combat obesity. It has been implicated that various fatty acids exert different effects on food intake and body weight. However, the underlying mechanism remains poorly understood. The aim of the present study was to investigate the effects of linoleic acid (LA) and stearic acid (SA) on agouti-related protein (AgRP) expression and secretion in immortalized mouse hypothalamic N38 cells and to explore the likely underlying mechanisms. Our results demonstrated that LA inhibited, while SA stimulated AgRP expression and secretion of N38 cells in a dose dependent manner. In addition, LA suppressed the protein expression of toll-like receptor 4 (TLR4), phosphorylation levels of JNK and IKK alpha/beta, suggesting the inhibition of TLR4-dependent inflammation pathway. However, the above mentioned inhibitory effects of LA were eliminated by TLR4 agonist lipopolysaccharide (LPS). In contrast, SA promoted TLR4 protein expression and activated TLR4-dependent inflammation pathway, with elevated ratio of p-JNK/JNK. While TLR4 siRNA reversed the stimulatory effects of SA on AgRP expression and TLR4-dependent inflammation. Moreover, we found that TLR4 was also involved in LA-enhanced and SA-impaired leptin/insulin signal pathways in N38 cells. In conclusion, our findings indicated that LA elicited inhibitory while SA exerted stimulatory effects on AgRP expression and secretion via TLR4-dependent inflammation and leptin/insulin pathways in N38 cells. These data provided a better understanding of the mechanism underlying fatty acids-regulated food intake and suggested the potential role of long-chain unsaturated fatty acids such as LA in reducing food intake and treating obesity. (C) 2016 Elsevier Inc. All rights reserved.
机译:调节食物摄入量是对抗肥胖的一种有前途的方法。已经暗示各种脂肪酸对食物摄入和体重产生不同的影响。但是,基本机制仍然知之甚少。本研究的目的是研究亚油酸(LA)和硬脂酸(SA)对永生化小鼠下丘脑N38细胞中鼠尾草相关蛋白(AgRP)表达和分泌的影响,并探讨可能的潜在机制。我们的结果表明,LA可以抑制LA,而SA可以以剂量依赖的方式刺激AgRP的表达和N38细胞的分泌。此外,LA抑制了Toll样受体4(TLR4)的蛋白表达,JNK和IKK alpha / beta的磷酸化水平,表明抑制了TLR4依赖性炎症途径。但是,TLR4激动剂脂多糖(LPS)消除了LA的上述抑制作用。相比之下,SA促进TLR4蛋白表达并激活TLR4依赖性炎症途径,同时增加p-JNK / JNK的比例。 TLR4 siRNA逆转了SA对AgRP表达和TLR4依赖性炎症的刺激作用。此外,我们发现TLR4还参与N38细胞中LA增强和SA受损的瘦素/胰岛素信号通路。总之,我们的研究结果表明,LA引起抑制作用,而SA通过N38细胞中TLR4依赖性炎症和瘦素/胰岛素途径对AgRP表达和分泌产生刺激作用。这些数据更好地了解了脂肪酸调节食物摄入的潜在机制,并暗示了长链不饱和脂肪酸(例如LA)在减少食物摄入和治疗肥胖中的潜在作用。 (C)2016 Elsevier Inc.保留所有权利。

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