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芍药苷预防2型糖尿病肾病中TLR2/4介导的炎症反应。

Paeoniflorin prevents TLR2/4-mediated inflammation in type 2 diabetic nephropathy.

作者信息

Zhang Tingmin, Zhu Qijin, Shao Yunxia, Wang Kun, Wu Yonggui

机构信息

Department of Nephrology, the First Affiliated Hospital, Anhui Medical University Hefei.

出版信息

Biosci Trends. 2017 Jul 24;11(3):308-318. doi: 10.5582/bst.2017.01104. Epub 2017 Jun 18.

DOI:10.5582/bst.2017.01104
PMID:28626209
Abstract

Paeoniflorin is an effective Chinese traditional medicine with anti-inflammatory and immune-regulatory effects. The aim of this study was to investigate the underlying renoprotective mechanism of Paeoniflorin. In vivo, db/db mice were intraperitoneally injected with Paeoniflorin at a dose of 15, 30, or 60 mg/kg respectively. The immunostaining of TLR2, TLR4, CD68, NF-kB p65 and the mRNA level of inflammatory factors, together with the protein expression of TLR2/4 signaling were evaluated. Our data demonstrated that Paeoniflorin could decrease the urinary albumin excretion rate and inhibit macrophage infiltration and activation through blockage of the TLR2/4 signaling pathway compared with the db/db group in vivo. In vitro, RAW264.7 cells were categorized into control, bovin serum albumin (BSA)-stimulated, advanced glycation end products (AGEs)-stimulated, Paeoniflorin intervention and oxidized phospholipid (OxPAPC)-inhibited groups. The cell viability, the optimal stimulated time and concentration were measured as well as the TLR2/4 signaling activation determined by RT-PCR, Western blot and ELISA. Our data demonstrated that Paeoniflorin reduced the AGEs-induced TLR2/4 activation and inflammatory responses, which was consistent with the TLR2/4 inhibitor group. These findings indicate that Paeoniflorin prevents macrophage activation via inhibition of TLR2/4 signaling expression in type 2 diabetic nephropathy.

摘要

芍药苷是一种具有抗炎和免疫调节作用的有效中药。本研究旨在探讨芍药苷潜在的肾脏保护机制。在体内实验中,分别以15、30或60mg/kg的剂量给db/db小鼠腹腔注射芍药苷。评估了TLR2、TLR4、CD68、NF-κB p65的免疫染色以及炎症因子的mRNA水平,同时检测了TLR2/4信号通路的蛋白表达。我们的数据表明,与体内db/db组相比,芍药苷可通过阻断TLR2/4信号通路降低尿白蛋白排泄率,并抑制巨噬细胞浸润和活化。在体外实验中,将RAW264.7细胞分为对照组、牛血清白蛋白(BSA)刺激组、晚期糖基化终产物(AGEs)刺激组、芍药苷干预组和氧化磷脂(OxPAPC)抑制组。检测了细胞活力、最佳刺激时间和浓度,并通过RT-PCR、Western印迹和ELISA测定TLR2/4信号通路的激活情况。我们的数据表明,芍药苷可降低AGEs诱导的TLR2/4激活和炎症反应,这与TLR2/4抑制剂组一致。这些发现表明,在2型糖尿病肾病中,芍药苷通过抑制TLR2/4信号表达来防止巨噬细胞活化。

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