Qiang Guifen, Yang Xiuying, Shi Lili, Zhang Hengai, Chen Bainian, Zhao Yan, Zu Mian, Zhou Dan, Guo Jing, Yang Haiguang, Zhang Li, Du Guanhua
Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Cell Physiol Biochem. 2015;36(1):395-408. doi: 10.1159/000430258. Epub 2015 May 7.
BACKGROUND/AIMS: Diabetes mellitus (DM) characterized by hyperglycemia contributes to macrovascular and microvascular complications. Salvianolic acid A (SalA) is a polyphenolic compound isolated from the root of Salvia miltiorrhiza Bunge, which is a traditional Chinese medicine widely used to treat cardiovascular diseases. However, little is known about its antidiabetic effect. Our study aimed to investigate the in vivo and in vitro antidiabetic effect of SalA and the underlying mechanisms.
Alloxan-induced type 1 diabetic mice and high-fat diet (HFD) and low-dose streptozotocin (STZ)-induced type 2 diabetic rats received SalA treatment. Blood glucose, oral glucose tolerance test (OGTT), 24-h food and water intake were monitored. In vitro, glucose consumption and uptake were measured in HepG2 cells and L6 myotubes. Mitochondrial function was detected in hepatic and skeletal muscle mitochondria. AMP-activated protein kinase (AMPK) and Akt were analyzed by western blot.
In both type 1 and type 2 diabetic animals, SalA lowered fasting blood glucose (FBG) and fed blood glucose in dose-dependent manner, as well as reduced 24-h food and water intake. In vitro, SalA caused dose-dependent increase in glucose consumption and enhanced glucose uptake. SalA significantly increased ATP production from 10 min to 12 h in HepG2 cells and L6 myotubes. Interestingly, SalA decreased mitochondrial membrane potential (MMP) in HepG2 cells. Furthermore, SalA improved hepatic and skeletal muscle mitochondrial function, increased ATP production, and concurrently decreased MMP. In particularly, SalA activated AMPK phosphorylation through Ca(2+)/calmodulin-dependent protein kinase kinase β (CaMKKβ)/AMPK signaling pathway, independent of liver kinase 1 (LKB1)/AMPK pathway. However, SalA didn't show any effect on insulin secretagogue and activation of PI3K/Akt signaling pathway.
SalA exhibits the antidiabetic effects in diabetic animal models through improving mitochondrial function, increasing ATP production, and decreasing MMP via CaMKKβ/AMPK signaling pathway.
背景/目的:以高血糖为特征的糖尿病(DM)会导致大血管和微血管并发症。丹酚酸A(SalA)是从丹参根中分离出的一种多酚化合物,丹参是一种广泛用于治疗心血管疾病的传统中药。然而,其抗糖尿病作用鲜为人知。我们的研究旨在探讨SalA在体内和体外的抗糖尿病作用及其潜在机制。
用四氧嘧啶诱导的1型糖尿病小鼠以及高脂饮食(HFD)和低剂量链脲佐菌素(STZ)诱导的2型糖尿病大鼠接受SalA治疗。监测血糖、口服葡萄糖耐量试验(OGTT)、24小时食物和水摄入量。在体外,测量HepG2细胞和L6肌管中的葡萄糖消耗和摄取。检测肝脏和骨骼肌线粒体的功能。通过蛋白质印迹法分析AMP激活的蛋白激酶(AMPK)和Akt。
在1型和2型糖尿病动物中,SalA均以剂量依赖的方式降低空腹血糖(FBG)和进食后血糖,并减少24小时食物和水摄入量。在体外,SalA导致葡萄糖消耗呈剂量依赖性增加,并增强葡萄糖摄取。SalA在10分钟至12小时内显著增加HepG2细胞和L6肌管中的ATP生成。有趣的是,SalA降低了HepG2细胞中的线粒体膜电位(MMP)。此外,SalA改善了肝脏和骨骼肌线粒体功能,增加了ATP生成,同时降低了MMP。特别是,SalA通过钙(2+)/钙调蛋白依赖性蛋白激酶激酶β(CaMKKβ)/AMPK信号通路激活AMPK磷酸化,独立于肝脏激酶1(LKB1)/AMPK通路。然而,SalA对胰岛素促分泌剂和PI3K/Akt信号通路的激活没有任何影响。
SalA通过改善线粒体功能、增加ATP生成并通过CaMKKβ/AMPK信号通路降低MMP,在糖尿病动物模型中表现出抗糖尿病作用。