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乳清肽通过强烈调节肌细胞分化来缓解肌肉萎缩。

Whey Peptide Alleviates Muscle Atrophy by Strongly Regulating Myocyte Differentiation in Mice.

机构信息

Department of Herbology, Daegu Haany University, Deagu 42158, Republic of Korea.

Research Center for Herbal Convergence on Liver Disease, Daegu Haany University, 1, Hanuidae-ro, Gyeongsan-si 38610, Republic of Korea.

出版信息

Medicina (Kaunas). 2024 Mar 5;60(3):433. doi: 10.3390/medicina60030433.

Abstract

: Muscle atrophy occurs when protein degradation exceeds protein synthesis, resulting in imbalanced protein homeostasis, compromised muscle contraction, and a reduction in muscle mass. The incidence of muscle atrophy is increasingly recognized as a significant worldwide public health problem. The aim of the current study was to evaluate the effect of whey peptide (WP) on muscle atrophy induced by dexamethasone (DEX) in mice. C57BL/6 mice were divided into six groups, each consisting of nine individuals. WPs were orally administered to C57BL/6 mice for 6 weeks. DEX was administered for 5-6 weeks to induce muscle atrophy (intraperitoneal injection, i.p.). : Microcomputer tomography (CT) analysis confirmed that WP significantly increased calf muscle volume and surface area in mice with DEX-induced muscle atrophy, as evidenced by tissue staining. Furthermore, it increased the area of muscle fibers and facilitated greater collagen deposition. Moreover, WP significantly decreased the levels of serum biomarkers associated with muscle damage, kidney function, and inflammatory cytokines. WP increased p-mTOR and p-p70S6K levels through the IGF-1/PI3K/Akt pathway, while concurrently decreasing protein catabolism via the FOXO pathway. Furthermore, the expression of proteins associated with myocyte differentiation increased noticeably. : These results confirm that WP reduces muscle atrophy by regulating muscle protein homeostasis. Additionally, it is believed that it helps to relieve muscle atrophy by regulating the expression of myocyte differentiation factors. Therefore, we propose that WP plays a significant role in preventing and treating muscle wasting by functioning as a supplement to counteract muscle atrophy.

摘要

肌肉萎缩是指蛋白质降解超过合成,导致蛋白质平衡失调、肌肉收缩受损以及肌肉质量减少。肌肉萎缩的发生率日益被认为是一个全球性的重大公共健康问题。本研究旨在评估乳清肽(WP)对皮质酮(DEX)诱导的小鼠肌肉萎缩的影响。C57BL/6 小鼠分为六组,每组 9 只。WP 通过口服给予 C57BL/6 小鼠 6 周。DEX 用于诱导肌肉萎缩(腹腔注射,i.p.)5-6 周。

微计算机断层扫描(CT)分析证实,WP 显著增加了 DEX 诱导的肌肉萎缩小鼠的小腿肌肉体积和表面积,组织染色结果也表明了这一点。此外,它增加了肌肉纤维的面积并促进了更多的胶原蛋白沉积。此外,WP 显著降低了与肌肉损伤、肾功能和炎症细胞因子相关的血清生物标志物水平。WP 通过 IGF-1/PI3K/Akt 通路增加了 p-mTOR 和 p-p70S6K 的水平,同时通过 FOXO 通路减少了蛋白质分解代谢。此外,与肌细胞分化相关的蛋白质表达明显增加。

这些结果证实 WP 通过调节肌肉蛋白质平衡来减少肌肉萎缩。此外,据信它通过调节肌细胞分化因子的表达来帮助缓解肌肉萎缩。因此,我们提出 WP 通过作为对抗肌肉萎缩的补充剂来发挥重要作用,以预防和治疗肌肉消耗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a869/10971974/2e6275d013f1/medicina-60-00433-g001.jpg

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