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Activation of PPARγ by Curcumin protects mice from ischemia/reperfusion injury induced by orthotopic liver transplantation via modulating polarization of Kupffer cells

机译:通过姜黄素通过调节kupffer细胞的偏振来激活来自通过鉴定肝移植诱导的缺血/再灌注损伤的小鼠

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摘要

Curcumin shows protective effects on various diseases due to its anti-inflammatory and anti-oxidative functions; however, its effect on organ transplantation has not been fully elucidated. To understand its role in liver ischemia/reperfusion (I/R) injury, we studied its impact on orthotopic liver transplantation (OLT) and Kupffer cells (KCs) polarization and its underlying mechanisms. We first investigated the reactive oxygen species (ROS) accumulation and cytokines profile of KCs, intracellular ROS and the mRNA level of pro-inflammatory cytokines were downregulated while the mRNA level of anti-inflammatory cytokine was upregulated by the pretreatment of Curcumin; Then the liver injury was detected by histopathological examination and liver function. Pretreatment with Curcumin significantly alleviated liver injury while improving liver function and overall post-transplantation survival compared with the control groups. The Western blotting showed that Curcumin inhibited the function of KCs via down-regulating the nuclear factor κb (NF-κb) signaling pathway by activating peroxisome proliferator-activated receptor γ (PPARγ) and flow cytometry revealed that Curcumin suppressed pro-inflammatory phenotype (M1) of KCs while promoting its anti-inflammatory phenotype (M2) polarization. These results showed that Curcumin may exert positive effects on I/R injury after OLT through activating PPARγ by inhibiting the activation of NF-κb pathway and remodeling the polarization of KCs. This may reveal a potential therapy for I/R injury after liver transplantation.
机译:姜黄素表现出由于其抗炎和抗氧化功能而对各种疾病的保护作用;然而,它对器官移植的影响尚未完全阐明。为了了解其在肝脏缺血/再灌注(I / R)损伤中的作用,我们研究了对原位肝移植(OLT)和Kupffer细胞(KCS)极化的影响及其潜在机制。我们首先研究了KCs的反应性氧物质(ROS)积累和细胞因子谱,促炎细胞因子的细胞内ROS和mRNA水平在姜黄素的预处理上调抗炎细胞因子的mRNA水平;然后通过组织病理学检查和肝功能检测肝损伤。预处理姜黄素显着缓解肝损伤,同时改善肝功能和与对照组相比的整体移植后存活。 Western印迹显示,姜黄素通过激活过氧缺血剂增殖物激活的受体γ(PPARγ)和流式细胞抑制姜黄素抑制促炎促炎表型(M1)来抑制KCs的功能)KCS,同时促进其抗炎表型(M2)极化。这些结果表明,通过抑制NF-κB途径的激活并改造KCS的极化,通过激活PPARγ对抗钙蛋白对I / R损伤产生阳性作用。这可能揭示肝移植后I / R损伤的潜在治疗。

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