Zhang Tingmin, Zhu Qijin, Shao Yunxia, Wang Kun, Wu Yonggui
Department of Nephrology, the First Affiliated Hospital, Anhui Medical University Hefei.
Biosci Trends. 2017 Jul 24;11(3):308-318. doi: 10.5582/bst.2017.01104. Epub 2017 Jun 18.
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.
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。