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幼龄和老龄动物制动性萎缩的恢复能力及可能机制

Capacity for recovery and possible mechanisms in immobilization atrophy of young and old animals.

作者信息

Zarzhevsky N, Menashe O, Carmeli E, Stein H, Reznick A Z

机构信息

Musculo-Skeletal Laboratory, Department of Anatomy and Cell Biology, The Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel.

出版信息

Ann N Y Acad Sci. 2001 Apr;928:212-25. doi: 10.1111/j.1749-6632.2001.tb05651.x.

Abstract

The effect of limb immobilization on muscle wasting and recovery of young and old rats was studied. Limb immobilization caused rapid and pronounced muscle weight loss, which was overcome efficiently in the muscles of young animals. However, muscles of old animals did not recover as well, indicating that muscle turnover (degradation and synthesis of proteins) is slower in old muscles than in young ones. The mechanisms of muscle wasting due to immobilization may involve two stages, the fast phase employing calcium-dependent proteolysis and the slower phase recruiting the lysosomal and ubiquitin-proteosome systems. The slow phase most probably involves the penetration of white cells between the muscle fibers and involves the secretion of cytokines that mediate a cascade of intracellular events, which culminates in muscle protein degradation. Thus, it was shown in our study and in other similar reports that through the influence of TNF-alpha and an increase in oxidative stress, there is marked activation of transcription factor NF-kappaB, which in turn induces many proteins to carry the signals that eventually result in protein breakdown. Because protein turnover was shown to slow down with age, it will be of great interest to study these events in aging muscles and to try to ascertain the specific events that make protein breakdown in aged muscles different from that in young ones.

摘要

研究了肢体固定对年轻和老年大鼠肌肉萎缩及恢复的影响。肢体固定导致肌肉重量迅速且显著下降,年轻动物的肌肉能有效克服这一情况。然而,老年动物的肌肉恢复不佳,这表明老年肌肉中的肌肉更新(蛋白质降解和合成)比年轻肌肉更慢。因固定导致肌肉萎缩的机制可能涉及两个阶段,快速阶段采用钙依赖性蛋白水解,较慢阶段则动用溶酶体和泛素 - 蛋白酶体系统。较慢阶段很可能涉及白细胞穿透肌纤维之间,并涉及细胞因子的分泌,这些细胞因子介导一系列细胞内事件,最终导致肌肉蛋白质降解。因此,我们的研究以及其他类似报告表明,通过肿瘤坏死因子 -α 的影响和氧化应激增加,转录因子 NF-κB 显著激活,进而诱导许多蛋白质传递信号,最终导致蛋白质分解。由于蛋白质更新随年龄增长而减缓,研究衰老肌肉中的这些事件,并试图确定使老年肌肉中蛋白质分解不同于年轻肌肉的具体事件将非常有趣。

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