Department of Biochemistry, Maharshi Dayanand University, Rohtak, Haryana-124001, India.
Curr Med Chem. 2020;27(13):2161-2188. doi: 10.2174/0929867326666181129095309.
Metabolic pathways perturbations lead to skeletal muscular atrophy in the cachexia and sarcopenia due to increased catabolism. Pro-inflammatory cytokines induce the catabolic pathways that impair the muscle integrity and function. Hence, this review primarily concentrates on the effects of pro-inflammatory cytokines in regulation of skeletal muscle metabolism.
This review will discuss the role of pro-inflammatory cytokines in skeletal muscles during muscle wasting conditions. Moreover, the coordination among the pro-inflammatory cytokines and their regulated molecular signaling pathways which increase the protein degradation will be discussed.
During normal conditions, pro-inflammatory cytokines are required to balance anabolism and catabolism and to maintain normal myogenesis process. However, during muscle wasting their enhanced expression leads to marked destructive metabolism in the skeletal muscles. Proinflammatory cytokines primarily exert their effects by increasing the expression of calpains and E3 ligases as well as of Nf-κB, required for protein breakdown and local inflammation. Proinflammatory cytokines also locally suppress the IGF-1and insulin functions, hence increase the FoxO activation and decrease the Akt function, the central point of carbohydrates lipid and protein metabolism.
Current advancements have revealed that the muscle mass loss during skeletal muscular atrophy is multifactorial. Despite great efforts, not even a single FDA approved drug is available in the market. It indicates the well-organized coordination among the pro-inflammatory cytokines that need to be further understood and explored.
代谢途径的紊乱会导致恶病质和肌肉减少症中的骨骼肌萎缩,这是由于分解代谢增加所致。促炎细胞因子会诱导分解代谢途径,损害肌肉的完整性和功能。因此,本篇综述主要集中于促炎细胞因子在调节骨骼肌代谢中的作用。
本综述将讨论促炎细胞因子在肌肉减少症情况下骨骼肌中的作用。此外,还将讨论促炎细胞因子之间的协调及其调节的分子信号通路,这些信号通路会增加蛋白质降解。
在正常情况下,促炎细胞因子需要平衡合成代谢和分解代谢,以维持正常的肌生成过程。然而,在肌肉减少症的情况下,它们的过度表达会导致骨骼肌明显的破坏性代谢。促炎细胞因子主要通过增加钙蛋白酶和 E3 连接酶的表达以及 NF-κB 的表达来发挥作用,这些都是蛋白质分解和局部炎症所必需的。促炎细胞因子还会局部抑制 IGF-1 和胰岛素的功能,从而增加 FoxO 的激活和降低 Akt 的功能,这是碳水化合物、脂质和蛋白质代谢的中心。
目前的研究进展表明,骨骼肌萎缩过程中的肌肉质量损失是多因素的。尽管付出了巨大的努力,但市场上甚至没有一种获得 FDA 批准的药物。这表明促炎细胞因子之间存在着良好的组织协调,需要进一步理解和探索。