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姜黄素通过调节枯否细胞极化激活 PPARγ,从而保护小鼠免受原位肝移植引起的缺血再灌注损伤。

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

机构信息

Department of Gastroenterology, The Fifth People's Hospital of Chengdu, Chengdu, 611130, PR China.

Department of Hepatobiliary Surgery and Chongqing Key Laboratory of Hepatobiliary Surgery, Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, PR China.

出版信息

Int Immunopharmacol. 2018 Sep;62:270-276. doi: 10.1016/j.intimp.2018.07.013. Epub 2018 Jul 23.

Abstract

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.

摘要

姜黄素因其抗炎和抗氧化功能对各种疾病显示出保护作用;然而,其对器官移植的影响尚未完全阐明。为了了解其在肝缺血/再灌注(I/R)损伤中的作用,我们研究了其对原位肝移植(OLT)和枯否细胞(KCs)极化的影响及其潜在机制。我们首先研究了 KCs 的活性氧(ROS)积累和细胞因子谱,姜黄素预处理可下调细胞内 ROS 和促炎细胞因子的 mRNA 水平,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来检测肝损伤。与对照组相比,姜黄素预处理显著减轻了肝损伤,改善了肝功能和整体移植后存活率。Western blot 显示,姜黄素通过激活过氧化物酶体增殖物激活受体γ(PPARγ)抑制核因子κB(NF-κB)信号通路,从而抑制 KCs 的功能,流式细胞术显示姜黄素抑制 KCs 的促炎表型(M1),同时促进其抗炎表型(M2)极化。这些结果表明,姜黄素可能通过抑制 NF-κB 通路的激活并重塑 KCs 的极化来发挥对 OLT 后 I/R 损伤的积极作用。这可能为肝移植后 I/R 损伤提供一种潜在的治疗方法。

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