Detecting the spike protein of COVID-19 deteriorates insulin resistance of skeletal muscle in Chinese diabetes patients: analysis of blood glucose metabolism.

IF 3.2 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Tianqi Zhang, Hui Peng, Changjv Chen, Hongbing Zheng, Dawei Yang, Ying Liu
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Abstract

Blood glucose metabolism is a key process for maintaining normal physiological functions of the human body. The maintenance of its homeostasis relies on complex hormone regulation and the synergistic effect of tissues and organs. However, when insulin resistance occurs in skeletal muscles, insulin signalling is impaired, and glucose uptake decreases, leading to elevated blood sugar levels. This study investigates the SARS-CoV-2 spike protein's effect on insulin resistance in type 2 diabetes (T2DM) skeletal muscle in a specific demographic. In the cell experiment, we used human C2C12 skeletal muscle cells and co-cultured them with the spike protein to observe the effects of the spike protein on the proliferation, apoptosis, and glucose uptake. The research results show that the spike protein may reduce the expression and transport of GLUT4 by inhibiting the PI3K/AKT/mTOR signalling pathway, thereby decreasing glucose uptake, intensifying insulin resistance in skeletal muscle, and affecting blood glucose metabolism.

检测新型冠状病毒刺突蛋白可恶化中国糖尿病患者骨骼肌胰岛素抵抗:血糖代谢分析
血糖代谢是维持人体正常生理机能的关键过程。其稳态的维持依赖于复杂的激素调节和组织器官的协同作用。然而,当骨骼肌发生胰岛素抵抗时,胰岛素信号受损,葡萄糖摄取减少,导致血糖水平升高。本研究探讨了特定人群中SARS-CoV-2刺突蛋白对2型糖尿病(T2DM)骨骼肌胰岛素抵抗的影响。在细胞实验中,我们使用人C2C12骨骼肌细胞与刺突蛋白共培养,观察刺突蛋白对细胞增殖、凋亡和葡萄糖摄取的影响。研究结果表明,刺突蛋白可能通过抑制PI3K/AKT/mTOR信号通路,降低GLUT4的表达和转运,从而降低葡萄糖摄取,增强骨骼肌胰岛素抵抗,影响血糖代谢。
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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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