Sun Min, Li Yan, Bu Wenjie, Zhao Jindong, Zhu Jianliang, Gu Lingling, Zhang Pingping, Fang Zhaohui
Anhui Province Key Laboratory of R&D of Chinese Medicine, School of Life Science, Anhui University, Hefei, Anhui 230601, China.
Department of Endocrinology, The First Affiliated Hospital of Anhui University of TCM, Hefei, Anhui 230031, China.
Evid Based Complement Alternat Med. 2017;2017:2942830. doi: 10.1155/2017/2942830. Epub 2017 May 29.
The antidiabetic properties and anti-inflammatory effects of Danzhi Jiangtang Capsules (DJC) have been demonstrated in clinical and laboratory experiments. In this study, we explored whether DJC can ameliorate advanced glycation end products- (AGEs-) mediated cell injury and the precise mechanisms of DJC in treating diabetic nephropathy (DN). Western blot analysis was employed to assess the expressions of iNOS, COX2, and SOCS and the phosphorylation of JAK2, STAT1, and STAT3 in glomerular mesangial cells (GMCs) after treatment with DJC. TNF-, IL-6, and MCP-1 were determined using double-antibody sandwich ELISA. ROS and NADPH oxidase activity were measured by DCFH-DA assay and lucigenin-enhanced chemiluminescence, respectively. DJC significantly reversed the AGEs-induced expression of COX2 and iNOS. Moreover, DJC inhibited the AGEs-induced JAK2-STAT1/STAT3 activation, resulting in the inhibition of inflammatory cytokines such as IL-6, MCP-1, and TNF- in a concentration-dependent manner. The ability of DJC to suppress STAT activation was also verified by the observation that DJC significantly increased the SOCS3 protein level. DJC reversed the AGEs-induced accumulation of ROS and NADPH oxidase activity, thus confirming that DJC possesses antioxidant activity. The results suggest that the anti-inflammatory effects of DJC in GMCs may be due to its ability to suppress the JAK2-STAT1/STAT3 cascades and reduce ROS production.
丹蛭降糖胶囊(DJC)的抗糖尿病特性和抗炎作用已在临床和实验室实验中得到证实。在本研究中,我们探讨了DJC是否能改善晚期糖基化终产物(AGEs)介导的细胞损伤以及DJC治疗糖尿病肾病(DN)的精确机制。采用蛋白质印迹分析评估DJC处理后肾小球系膜细胞(GMCs)中诱导型一氧化氮合酶(iNOS)、环氧化酶2(COX2)和细胞因子信号转导抑制因子(SOCS)的表达以及Janus激酶2(JAK2)、信号转导和转录激活因子1(STAT1)和信号转导和转录激活因子3(STAT3)的磷酸化。使用双抗体夹心酶联免疫吸附测定法(ELISA)测定肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和单核细胞趋化蛋白-1(MCP-1)。分别通过2′,7′-二氯二氢荧光素二乙酸酯(DCFH-DA)测定法和光泽精增强化学发光法测量活性氧(ROS)和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶活性。DJC显著逆转了AGEs诱导的COX2和iNOS表达。此外,DJC抑制AGEs诱导的JAK2-STAT1/STAT3激活,从而以浓度依赖性方式抑制IL-6、MCP-1和TNF-α等炎性细胞因子。DJC显著增加SOCS3蛋白水平的观察结果也证实了DJC抑制STAT激活的能力。DJC逆转了AGEs诱导的ROS积累和NADPH氧化酶活性,从而证实DJC具有抗氧化活性。结果表明,DJC在GMCs中的抗炎作用可能归因于其抑制JAK2-STAT1/STAT3级联反应和减少ROS产生的能力。