Wang Haiyan, Arias Edward B, Cartee Gregory D
Muscle Biology Laboratory, School of Kinesiology, University of Michigan, Ann Arbor, Michigan; College of Physical Education and Health, East China Normal University, Shanghai, China;
Muscle Biology Laboratory, School of Kinesiology, University of Michigan, Ann Arbor, Michigan;
Am J Physiol Regul Integr Comp Physiol. 2016 Mar 1;310(5):R449-58. doi: 10.1152/ajpregu.00449.2015. Epub 2016 Jan 6.
Skeletal muscle insulin resistance is associated with many common age-related diseases, but moderate calorie restriction (CR) can substantially elevate glucose uptake by insulin-stimulated skeletal muscle from both young and old rats. The current study evaluated the isolated epitrochlearis muscle from ∼24.5-mo-old rats that were either fed ad libitum (AL) or subjected to CR (consuming ∼65% of ad libitum, AL, intake beginning at ∼22.5 mo old). Some muscles were also incubated with MK-2206, a potent and selective Akt inhibitor. The most important results were that in isolated muscles, CR vs. AL resulted in 1) greater insulin-stimulated glucose uptake 2) that was accompanied by significantly increased insulin-mediated activation of Akt2, as indicated by greater phosphorylation on both Thr(309) and Ser(474) along with greater Akt2 activity, 3) concomitant with enhanced phosphorylation of several Akt substrates, including an Akt substrate of 160 kDa on Thr(642) and Ser(588), filamin C on Ser(2213) and proline-rich Akt substrate of 40 kDa on Thr(246), but not TBC1D1 on Thr(596); and 4) each of the CR effects was eliminated by MK-2206. These data provide compelling new evidence linking greater Akt2 activation to the CR-induced elevation of insulin-stimulated glucose uptake by muscle from old animals.
骨骼肌胰岛素抵抗与许多常见的年龄相关疾病有关,但适度的热量限制(CR)可显著提高年轻和老年大鼠胰岛素刺激的骨骼肌对葡萄糖的摄取。本研究评估了约24.5月龄大鼠的离体肱三头肌,这些大鼠要么自由进食(AL),要么进行热量限制(从约22.5月龄开始摄入约65%的自由进食量)。一些肌肉还与MK-2206(一种强效且选择性的Akt抑制剂)一起孵育。最重要的结果是,在离体肌肉中,与自由进食相比,热量限制导致:1)胰岛素刺激的葡萄糖摄取增加;2)伴随着Akt2的胰岛素介导的激活显著增加,这表现为Thr(309)和Ser(474)的磷酸化增加以及Akt2活性增强;3)同时几种Akt底物的磷酸化增强,包括160 kDa的Akt底物在Thr(642)和Ser(588)处、细丝蛋白C在Ser(2213)处以及40 kDa的富含脯氨酸的Akt底物在Thr(246)处,但不包括TBC1D1在Thr(596)处;4)MK-2206消除了热量限制的每种效应。这些数据提供了令人信服的新证据,将更大的Akt2激活与热量限制诱导的老年动物肌肉胰岛素刺激的葡萄糖摄取增加联系起来。