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必需氨基酸可改善衰老大鼠比目鱼肌中胰岛素对 AKT/MTOR 信号的激活作用。

Essential amino acids improve insulin activation of AKT/MTOR signaling in soleus muscle of aged rats.

机构信息

Department of Experimental Medicine, University of LAquila, Italy.

出版信息

Int J Immunopathol Pharmacol. 2010 Jan-Mar;23(1):81-9. doi: 10.1177/039463201002300108.

DOI:10.1177/039463201002300108
PMID:20377997
Abstract

Essential amino acids (EAA) improve basal muscle protein synthesis in the elderly. Nevertheless, in settings of prolonged supplementation, putative signal pathways of EAA are currently unknown. The purpose of this study was to test the effects of prolonged supplementation of EAA enriched mixture (12-L-Amin) on Insulin/Insulin-like Growth Factor-1 (IGF1) pathway by measuring total and phosphorylated Akt (Ser473) and its upstream (IRS1 at Ser636) and downstream (mTOR at Ser2448, p70S6K at Thr389) targets in basal conditions and following acute insulin (0.1 U/L) incubation in vitro. To this aim, soleus muscles were dissected from male Wistar rats divided in three groups of 7 each: adults (AD, 10 mo of age), elderly (EL, 22 mo of age) and elderly supplemented (EL-AA, 12-L-Amin 1.5gr/Kg die in drinking water for 3 mo). EL showed reduced basal and post-insulin mTOR and p70S6K activation and reduced post-insulin IRS1 degradation relative to AD. EL-AA showed an increase of post-insulin Akt activation, no change in basal and post-insulin phospho-mTOR, lower reduction of phospho-p70S6K and increased post-insulin IRS1 degradation relative to AD. These results demonstrate that chronic 12-LAmin administration exerts anti-ageing effects on the activation/inactivation of the Insulin/IGF1/mTOR pathway which is identified as putative target of EAA in the elderly.

摘要

必需氨基酸(EAA)可改善老年人的基础肌肉蛋白质合成。然而,在长期补充的情况下,EAA 的潜在信号通路目前尚不清楚。本研究的目的是通过测量基础条件下和体外急性胰岛素(0.1 U/L)孵育后总和磷酸化 Akt(Ser473)及其上游(IRS1 在 Ser636)和下游(mTOR 在 Ser2448,p70S6K 在 Thr389)靶标,测试长期补充富含 EAA 的混合物(12-L-Amin)对胰岛素/胰岛素样生长因子-1(IGF1)通路的影响。为此,从雄性 Wistar 大鼠中分离出比目鱼肌,分为三组,每组 7 只:成年(AD,10 月龄)、老年(EL,22 月龄)和老年补充组(EL-AA,12-L-Amin 1.5gr/Kg 溶于饮用水中,连续 3 个月)。EL 组的基础和胰岛素刺激后的 mTOR 和 p70S6K 激活以及胰岛素刺激后的 IRS1 降解均低于 AD 组。EL-AA 组的胰岛素激活后 Akt 增加,基础和胰岛素刺激后的磷酸化 mTOR 没有变化,磷酸化 p70S6K 的减少减少,胰岛素刺激后的 IRS1 降解增加,与 AD 组相比。这些结果表明,慢性 12-LAmin 给药对胰岛素/IGF1/mTOR 通路的激活/失活产生抗衰老作用,该通路被确定为老年人 EAA 的潜在靶点。

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