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急性运动后,胰岛素刺激的大鼠骨骼肌中 160 kDa 的 Akt 底物去磷酸化速率降低。

Akt substrate of 160 kDa dephosphorylation rate is reduced in insulin-stimulated rat skeletal muscle after acute exercise.

机构信息

School of Kinesiology, University of Michigan, Ann Arbor, MI, USA.

出版信息

Physiol Res. 2018 Mar 16;67(1):143-147. doi: 10.33549/physiolres.933591. Epub 2017 Nov 10.

Abstract

Because greater Akt substrate of 160 kDa (AS160) phosphorylation has been reported in insulin-stimulated skeletal muscles without improved Akt activation several hours post-exercise, we hypothesized that prior exercise would result in attenuated AS160 dephosphorylation in insulin-stimulated rat skeletal muscle. Epitrochlearis muscles were isolated from rats that were sedentary (SED) or exercised 3 h earlier (3 h post-exercise; 3hPEX). Paired muscles were incubated with [(3)H]-2-deoxyglucose (2-DG) without insulin or with insulin. Lysates from other insulin-stimulated muscles from SED or 3hPEX rats were evaluated using AS160(Thr642) and AS160(Ser588) dephosphorylation assays. Prior exercise led to greater 2-DG uptake concomitant with greater AS160(Thr642) phosphorylation and a non-significant trend (P=0.087) for greater AS160(Ser588). Prior exercise also reduced AS160(Thr642) and AS160(Ser588) dephosphorylation rates. These results support the idea that attenuated AS160 dephosphorylation may favor greater AS160 phosphorylation post-exercise.

摘要

由于在运动后数小时内,胰岛素刺激的骨骼肌中已经报道了 Akt 底物 160 kDa(AS160)的磷酸化增加,而 Akt 激活没有改善,我们假设先前的运动将导致胰岛素刺激的大鼠骨骼肌中 AS160 的去磷酸化减弱。从久坐(SED)或 3 小时前运动(3 hPEX)的大鼠中分离出外上髁肌。将配对的肌肉用[(3)H]-2-脱氧葡萄糖(2-DG)孵育,没有胰岛素或有胰岛素。使用 AS160(Thr642)和 AS160(Ser588)去磷酸化测定法评估来自 SED 或 3hPEX 大鼠的其他胰岛素刺激肌肉的裂解物。先前的运动导致 2-DG 摄取增加,同时 AS160(Thr642)磷酸化增加,并且 AS160(Ser588)有增加的非显著趋势(P=0.087)。先前的运动还降低了 AS160(Thr642)和 AS160(Ser588)的去磷酸化速率。这些结果支持这样的观点,即减弱的 AS160 去磷酸化可能有利于运动后 AS160 的磷酸化增加。

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