Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA.
J Endocrinol. 2020 Jun;245(3):R23-R48. doi: 10.1530/JOE-20-0044.
Insulin resistance is a common feature of many metabolic disorders. The dramatic rise in the incidence of insulin resistance over the past decade has enhanced focus on its developmental origins. Since various developmental insults ranging from maternal disease, stress, over/undernutrition, and exposure to environmental chemicals can all program the development of insulin resistance, common mechanisms may be involved. This review discusses the possibility that increases in maternal androgens associated with these various insults are key mediators in programming insulin resistance. Additionally, the intermediaries through which androgens misprogram tissue insulin sensitivity, such as changes in inflammatory, oxidative, and lipotoxic states, epigenetic, gut microbiome and insulin, as well as data gaps to be filled are also discussed.
胰岛素抵抗是许多代谢紊乱的共同特征。在过去十年中,胰岛素抵抗的发病率急剧上升,这使得人们更加关注其发育起源。由于从母体疾病、压力、营养过剩/不足到接触环境化学物质等各种发育性损伤都可能导致胰岛素抵抗的发生,因此可能涉及共同的机制。本综述讨论了与这些各种损伤相关的母体雄激素增加是否是导致胰岛素抵抗的关键介质。此外,还讨论了雄激素错误编程组织胰岛素敏感性的中介,如炎症、氧化和脂肪毒性状态、表观遗传、肠道微生物组和胰岛素的变化,以及有待填补的数据空白。