项目名称: 基于内质网钙ATP酶信号研究黄芪皂苷甲改善糖尿病肾病的机制
项目编号: No.81473480
项目类型: 面上项目
立项/批准年度: 2015
项目学科: 医药、卫生
项目作者: 彭文
作者单位: 上海中医药大学
项目金额: 75万元
中文摘要: 内质网(ER)应激与足细胞凋亡在糖尿病肾病中的作用是目前研究的热点,研究发现ER钙ATP酶(SERCA)及其亚型的改变在ER应激过程中起着关键作用。我们前期工作发现糖尿病肾病动物模型SERCA表达异常;黄芪皂苷甲(AS-IV)能明显抑制高糖/棕榈酸引起的足细胞损伤,并上调SERCA的表达。提示AS-IV可能通过影响SERCA及亚型的表达与活性,缓解ER应激,抑制肾小球足细胞凋亡,改善糖尿病肾病发病进程。基于该假说,我们应用钙荧光探针、siRNA、免疫荧光标记等技术研究AS-IV对高糖和棕榈酸引起足细胞SERCA及亚型影响,继而介导ER应激和线粒体功能紊乱导致细胞凋亡的作用;应用western blot、荧光定量PCR技术等观察AS-IV对I、II型糖尿病肾病动物模型肾小球损伤的影响,阐明AS-IV通过调控SERCA信号改善糖尿病肾病的作用机制,为临床治疗提供新的措施和策略。
中文关键词: 糖尿病肾病;黄芪皂苷甲;肌浆网钙ATP酶;内质网应激;线粒体功能
英文摘要: Edoplasmic reticulum (ER) stress and podocyte apoptosis are the research focus on diabetci nephropath recently. Sarcpasmic reiculm Ca2+-ATPase (SERCA) plays a vital role in ER stress. We have demonstrated that Astragaloside IV (AS-IV), which is a major component isolated from Radix Astragali that has a protective effect on kidney, could not only improve renal tubulointerstitial fibrosis, but also inhibit high glucose or free fatty acid induced down-regulation of SERCA, and ER stress induced podocyte apoptosis. Thus, we hypothesized that podocyte apoptosis was mastered by SERCA signaling in diabetic nephropathy, which can be regulated by treatment with AS-IV. On this hypothesis, the present project intends to investigate the effect of AS-IV on high glucose and palmitic acid induced SERCA expression and activity, as well as apoptosis mediated by ER stress and mitochondrial dysfunction by using calcium fluorescent probe, siRNA, immunofluorescence technique. Moreover, the influence of AS-IV on SERCA-ER stress mediated apoptosis, and the downstream signaling molecules such as CHOP, JNK, Caspase-12, and mitochondrial dependent apoptosis pathways will be investigated by means of immunohistochemistry, RT-PCR, Western blot in type I and II diabetic mice models. This project will provide the experimental and theoretical evidences and new treatment strategies for the clinical application of AS-IV in therapy of diabetic nephropathy.
英文关键词: diabetic nephropathy;Astragaloside IV;sarcoplasmic reticulum Ca2+-ATPase;endoplasmic reticulum;mitochondrial function