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Ghrelin inhibits oxLDL-induced inflammation in RAW264.7 mouse macrophages through down-regulation of LOX-1 expression via NF-kappa B signaling pathway

机译:Ghrelin通过下调NF-κB信号通路LOX-1的表达来抑制oxLDL诱导的RAW264.7小鼠巨噬细胞的炎症

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Oxidized low-density lipoprotein (oxLDL) is one of the many causes of the initiation and progression of atherosclerosis, which can subsequently promote the uptake of oxLDL by macrophages and lead to inflammation in the blood vessels. In the present study, we evaluated the protective effects of ghrelin on oxLDL-induced RAW264.7 mouse macrophages. Ghrelin was able to inhibit the release of several pro-inflammatory cytokines including tumor necrosis factor (TNF)-alpha and interleukin (IL)-6. In addition, ghrelin also inhibited the expression of Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) in oxLDL treated macrophages. Furthermore, we demonstrated that ghrelin could inhibit the expression of p-I kappa B alpha, and the inhibitory effects could be blocked by BAY 117082. Taken together, ghrelin possesses anti-inflammatory effects on oxLDL-induced inflammation in macrophages, suggesting that it can prevent or treat atherosclerosis, and deserves to be further studied and developed to be potent drug for treating atherosclerosis.
机译:氧化的低密度脂蛋白(oxLDL)是引发和发展动脉粥样硬化的多种原因之一,其随后可促进巨噬细胞摄取oxLDL并导致血管发炎。在本研究中,我们评估了生长激素释放肽对oxLDL诱导的RAW264.7小鼠巨噬细胞的保护作用。 Ghrelin能够抑制多种促炎细胞因子的释放,包括肿瘤坏死因子(TNF)-α和白介素(IL)-6。此外,生长素释放肽还抑制oxLDL处理的巨噬细胞中凝集素样氧化型低密度脂蛋白受体1(LOX-1)的表达。此外,我们证明ghrelin可以抑制pI kappa B alpha的表达,并且抑制作用可以被BAY 117082阻断。总的来说,ghrelin对oxLDL诱导的巨噬细胞炎症具有抗炎作用,表明它可以预防或抑制巨噬细胞的炎症。治疗动脉粥样硬化,值得进一步研究和发展成为治疗动脉粥样硬化的有效药物。

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