Division of Diabetes, Department of Medicine, University of Texas Health Science Center at San Antonio, Texas 78229, USA.
J Clin Endocrinol Metab. 2010 Jan;95(1):422-9. doi: 10.1210/jc.2009-1387. Epub 2009 Oct 28.
Mitochondrial dysfunction has been proposed as an underlying mechanism in the pathogenesis of insulin resistance and type 2 diabetes mellitus.
To determine whether mitochondrial dysfunction plays a role in the free fatty acid (FFA)-induced impairment in insulin action in skeletal muscle of healthy subjects.
Eleven lean normal glucose tolerant individuals received 8 h lipid and saline infusion on separate days with a euglycemic insulin clamp during the last 2 h. Vastus lateralis muscle biopsies were performed at baseline and after 6 h lipid or saline infusion. Inner mitochondrial membrane potential (Psi(m)) and mitochondrial mass were determined ex vivo by confocal microscopy.
Compared with saline infusion, lipid infusion reduced whole-body glucose uptake by 22% (P < 0.05). Psi(m) decreased by 33% (P < 0.005) after lipid infusion and the decrement in Psi(m) correlated with change in plasma FFA after lipid infusion (r = 0.753; P < 0.005). Mitochondrial content and morphology did not change after lipid infusion. No significant changes in genes expression, citrate synthase activity, and total ATP content were observed after either lipid or saline infusion.
Short-term physiological increase in plasma FFA concentration in lean normal glucose tolerant subjects induces insulin resistance and impairs mitochondrial membrane potential but has no significant effects on mitochondrial content, gene expression, ATP content, or citrate synthase activity.
线粒体功能障碍被认为是胰岛素抵抗和 2 型糖尿病发病机制中的一个潜在机制。
确定线粒体功能障碍是否在健康受试者的游离脂肪酸(FFA)引起的胰岛素作用受损中起作用。
11 名瘦型正常糖耐量个体在不同天接受 8 小时的脂肪和盐水输注,并在最后 2 小时进行葡萄糖钳夹期间进行。在基线和脂肪或盐水输注后 6 小时进行股外侧肌活检。通过共聚焦显微镜测定内膜电位(Psi(m))和线粒体质量。
与盐水输注相比,脂肪输注使全身葡萄糖摄取减少 22%(P < 0.05)。脂肪输注后 Psi(m)降低了 33%(P < 0.005),并且 Psi(m)的降低与脂肪输注后的血浆 FFA 变化相关(r = 0.753;P < 0.005)。脂肪输注后线粒体含量和形态没有变化。在脂肪或盐水输注后,基因表达、柠檬酸合酶活性和总 ATP 含量均无明显变化。
在瘦型正常糖耐量个体中,短期生理血浆 FFA 浓度升高可引起胰岛素抵抗和损害线粒体膜电位,但对线粒体含量、基因表达、ATP 含量或柠檬酸合酶活性无显著影响。