乳酸脱氢酶
二甲双胍
内科学
内分泌学
促炎细胞因子
胰岛素抵抗
胰岛素
炎症
医学
血糖性
糖尿病
化学
酶
生物化学
作者
Muchao Wu,Weiran Ye,Yijia Zheng,Shanshan Zhang
出处
期刊:Pharmacology
[S. Karger AG]
日期:2017-01-01
卷期号:100 (5-6): 218-228
被引量:7
摘要
Metformin (MET) is the first-line drug for treating type 2 diabetes mellitus (T2DM). However, MET increases blood lactate levels in patients with T2DM. Lactate possesses proinflammatory properties and causes insulin resistance (IR). Oxamate (OXA), a lactate dehydrogenase inhibitor, can decrease tissue lactate production and blood lactate levels. This study was conducted to examine the effects of the combination of OXA and MET on inflammation, and IR in diabetic<i> db/db</i> mice. Supplementation of OXA to MET led to lowered tissue lactate production and serum lactate levels compared to MET alone, accompanied with further decreased tissue and blood levels of pro-inflammatory cytokines, along with better insulin sensitivity, beta-cell mass, and glycemic control in diabetic <i>db/db</i> mice. These results show that OXA enhances the anti-inflammatory and insulin-sensitizing effects of MET through the inhibition of tissue lactate production in <i>db/db</i> mice.
科研通智能强力驱动
Strongly Powered by AbleSci AI