Cardiovascular Diseases Research Center, Birjand University of Medical Sciences, Birjand, Iran.
Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran.
J Cell Physiol. 2019 Aug;234(8):12516-12529. doi: 10.1002/jcp.28112. Epub 2019 Jan 22.
As many individuals worlwide are exposed to arsenic, it is necessary to unravel the role of arsenic in the risk of obesity and diabetes. Therefore, the present study reviewed the effects of arsenic exposure on the risk and potential etiologic mechanisms of obesity and diabetes. It has been suggested that inflammation, oxidative stress, and apoptosis contribute to the pathogenesis of arsenic-induced diabetes and obesity. Though arsenic is known to cause diabetes through different mechanisms, the role of adipose tissue in diabetes is still unclear. This review exhibited the effects of arsenic on the metabolism and signaling pathways within adipose tissue (such as sirtuin 3 [SIRT3]- forkhead box O3 [FOXO3a], mitogen-activated protein kinase [MAPK], phosphoinositide-dependant kinase-1 [PDK-1], unfolded protein response, and C/EBP homologous protein [CHOP10]). Different types of adipokines involved in arsenic-induced diabetes are yet to be elucidated. Arsenic exerts negative effects on the white adipose tissue by decreasing adipogenesis and enhancing lipolysis. Some epidemiological studies have shown that arsenic can promote obesity. Nevertheless, few studies have indicated that arsenic may induce lipodystrophy. Arsenic multifactorial effects include accelerating birth and postnatal weight gains, elevated body fat content, glucose intolerance, insulin resistance, and increased serum lipid profile. Arsenic also elevated cord blood and placental, as well as postnatal serum leptin levels. The data from human studies indicate an association between inorganic arsenic exposure and the risk of diabetes and obesity. However, the currently available evidence is insufficient to conclude that low-moderate dose arsenic is associated with diabetes or obesity development. Therefore, more investigations are needed to determine biological mechanisms linking arsenic exposure to obesity and diabetes.
由于全世界有许多人接触到砷,因此有必要阐明砷在肥胖和糖尿病风险中的作用。因此,本研究综述了砷暴露对肥胖和糖尿病风险及潜在病因机制的影响。据认为,炎症、氧化应激和细胞凋亡有助于砷诱导的糖尿病和肥胖的发病机制。虽然砷已知通过不同的机制导致糖尿病,但脂肪组织在糖尿病中的作用仍不清楚。本综述展示了砷对脂肪组织代谢和信号通路的影响(如 SIRT3-FOXO3a、MAPK、PDK-1、未折叠蛋白反应和 CHOP10)。涉及砷诱导糖尿病的不同类型的脂肪因子仍有待阐明。砷通过减少脂肪生成和增强脂肪分解对白色脂肪组织产生负面影响。一些流行病学研究表明,砷可以促进肥胖。然而,很少有研究表明砷可能会引起脂肪营养不良。砷的多因素作用包括加速出生和产后体重增加、增加体脂肪含量、葡萄糖耐量受损、胰岛素抵抗以及血清脂质谱升高。砷还会升高脐带血和胎盘以及产后血清瘦素水平。来自人类研究的数据表明,无机砷暴露与糖尿病和肥胖风险之间存在关联。然而,目前的证据还不足以得出低剂量到中等剂量砷与糖尿病或肥胖发展相关的结论。因此,需要进行更多的研究来确定将砷暴露与肥胖和糖尿病联系起来的生物学机制。