节俭的生长素:肌肉衰老的秘密

Yuxiang Sun
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引用次数: 1

摘要

骨骼肌减少症是一种使人衰弱的肌肉萎缩疾病,是老年人身体虚弱和残疾的主要原因。胃饥饿素(又名酰化胃饥饿素,AG)是一种循环肽激素,在Ser3上具有独特的辛烷酰化。AG通过其受体生长激素促分泌受体(GHS-R)诱导生长激素(GH)分泌,增加食物摄入量,促进肥胖和胰岛素抵抗。与AG不同的是,unacylated ghrelin (UAG)是由同一个ghrelin基因产生的肽,其氨基酸序列与AG相同,但没有辛酸化修饰,因此UAG不会激活GHS-R。有趣的是,AG和UAG均可促进肌肉C2C12细胞的分化和融合,调节肌管中的代谢和线粒体信号通路,并减轻禁食或去神经支配诱导的肌肉萎缩。此外,也有研究表明,饥饿素基因缺乏增加了衰老小鼠对禁食引起的肌肉损失的易感性,AG和UAG对衰老小鼠的肌肉萎缩有有效的保护作用。因为UAG不与GHS-R结合,所以它不会像AG那样产生GHS-R释放增加和肥胖增加的副作用。综上所述,UAG对衰老过程中的肌肉萎缩具有显著的抗萎缩作用,有潜力成为肌肉减少症等肌肉萎缩疾病的独特而优越的治疗候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thrifty Hormone Ghrelin: The Secret of Aging Muscularly
Sarcopenia is a debilitating muscle-wasting disease that is the major cause of frailty and disability in aging. Ghrelin (aka acylated ghrelin, AG) is a circulating peptide hormone with an unique octanoylation on Ser3. AG induces growth hormone (GH) secretion, increases food intake, and promotes adiposity and insulin resistance via its receptor, Growth Hormone Secretagogue Receptor (GHS-R). Unlike AG, unacylated ghrelin (UAG) is a peptide generated from the same ghrelin gene with amino acid sequence identical to AG but without the octanoylation modification, so UAG does not activate GHS-R. Intriguingly, both AG and UAG have been shown to promote differentiation and fusion of muscle C2C12 cells, regulate metabolic and mitochondrial signaling pathways in myotubes, and attenuate fasting- or denervation-induced muscle atrophy. Furthermore, it has also been shown that ghrelin gene deficiency increases vulnerability to fasting-induced muscle loss in aging mice, and AG and UAG effectively protects against muscle atrophy of aging mice. Because UAG doesn’t bind to GHS-R, it doesn’t have the undesired side-effects of elevated GH-release and increased obesity as AG. In summary, UAG has an impressive anti-atrophic effect in muscle protecting against muscle atrophy in aging, it has potential to be a unique and superior therapeutic candidate for muscle-wasting diseases such as sarcopenia.
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