Covington Brittney A, Chen Wenbiao
Department of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232, USA.
Biomedicines. 2024 Feb 20;12(3):473. doi: 10.3390/biomedicines12030473.
Type 2 diabetes (T2D) has become a worldwide epidemic, primarily driven by obesity from overnutrition and sedentariness. Recent results reveal there is heterogeneity in both pathology and treatment responses in T2D patients. Therefore, a variety of T2D animal models are necessary to obtain a mechanistic understanding of distinct disease processes. T2D results from insufficient insulin, either due to beta cell loss or inborn deficiency. Although decreases in beta cell mass can occur through loss of identity or cell death, in this review, we will highlight the T2D animal models that display beta cell death, including the Zucker Diabetic Fatty Rat, sand rat, db/db mouse, and a novel diabetic zebrafish model, the Zebrafish Muscle Insulin-Resistant (zMIR) fish. Procuring a mechanistic understanding of different T2D progression trajectories under a variety of contexts is paramount for developing and testing more individualized treatments.
2型糖尿病(T2D)已成为一种全球性流行病,主要由营养过剩和久坐不动导致的肥胖引起。最近的研究结果表明,T2D患者在病理和治疗反应方面存在异质性。因此,需要多种T2D动物模型来深入了解不同的疾病进程机制。T2D是由胰岛素不足引起的,这可能是由于β细胞丢失或先天性缺陷所致。虽然β细胞数量的减少可能是由于细胞身份丧失或细胞死亡,但在本综述中,我们将重点介绍表现出β细胞死亡的T2D动物模型,包括Zucker糖尿病脂肪大鼠、沙鼠、db/db小鼠,以及一种新型糖尿病斑马鱼模型——斑马鱼肌肉胰岛素抵抗(zMIR)鱼。在各种情况下深入了解不同的T2D进展轨迹机制对于开发和测试更个性化的治疗方法至关重要。