In vitro skeletal muscle models for type 2 diabetes.

IF 2.9 Q2 BIOPHYSICS
Biophysics reviews Pub Date : 2022-09-01 Epub Date: 2022-09-13 DOI:10.1063/5.0096420
Christina Y Sheng, Young Hoon Son, Jeongin Jang, Sung-Jin Park
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引用次数: 0

Abstract

Type 2 diabetes mellitus, a metabolic disorder characterized by abnormally elevated blood sugar, poses a growing social, economic, and medical burden worldwide. The skeletal muscle is the largest metabolic organ responsible for glucose homeostasis in the body, and its inability to properly uptake sugar often precedes type 2 diabetes. Although exercise is known to have preventative and therapeutic effects on type 2 diabetes, the underlying mechanism of these beneficial effects is largely unknown. Animal studies have been conducted to better understand the pathophysiology of type 2 diabetes and the positive effects of exercise on type 2 diabetes. However, the complexity of in vivo systems and the inability of animal models to fully capture human type 2 diabetes genetics and pathophysiology are two major limitations in these animal studies. Fortunately, in vitro models capable of recapitulating human genetics and physiology provide promising avenues to overcome these obstacles. This review summarizes current in vitro type 2 diabetes models with focuses on the skeletal muscle, interorgan crosstalk, and exercise. We discuss diabetes, its pathophysiology, common in vitro type 2 diabetes skeletal muscle models, interorgan crosstalk type 2 diabetes models, exercise benefits on type 2 diabetes, and in vitro type 2 diabetes models with exercise.

2 型糖尿病的体外骨骼肌模型。
2 型糖尿病是一种以血糖异常升高为特征的代谢性疾病,在全球范围内造成了日益沉重的社会、经济和医疗负担。骨骼肌是负责体内葡萄糖平衡的最大代谢器官,骨骼肌无法正常摄取糖分往往是 2 型糖尿病的先兆。尽管运动对 2 型糖尿病有预防和治疗作用,但这些有益作用的基本机制却大多不为人知。为了更好地了解 2 型糖尿病的病理生理学以及运动对 2 型糖尿病的积极影响,已经开展了动物研究。然而,体内系统的复杂性和动物模型无法完全捕捉人类 2 型糖尿病遗传学和病理生理学是这些动物研究的两大局限。幸运的是,能够重现人类遗传学和生理学的体外模型为克服这些障碍提供了有希望的途径。本综述总结了目前的体外 2 型糖尿病模型,重点关注骨骼肌、器官间串联和运动。我们将讨论糖尿病及其病理生理学、常见的体外 2 型糖尿病骨骼肌模型、器官间串联 2 型糖尿病模型、运动对 2 型糖尿病的益处,以及有运动的体外 2 型糖尿病模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.60
自引率
0.00%
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