Pomytkin Igor, Pinelis Vsevolod
Department of Advanced Cell Technologies, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
National Medical Research Center for Children's Health, 119296 Moscow, Russia.
Life (Basel). 2021 Mar 22;11(3):262. doi: 10.3390/life11030262.
Current hypotheses implicate insulin resistance of the brain as a pathogenic factor in the development of Alzheimer's disease and other dementias, Parkinson's disease, type 2 diabetes, obesity, major depression, and traumatic brain injury. A variety of genetic, developmental, and metabolic abnormalities that lead to disturbances in the insulin receptor signal transduction may underlie insulin resistance. Insulin receptor substrate proteins are generally considered to be the node in the insulin signaling system that is critically involved in the development of insulin insensitivity during metabolic stress, hyperinsulinemia, and inflammation. Emerging evidence suggests that lower activation of the insulin receptor (IR) is another common, while less discussed, mechanism of insulin resistance in the brain. This review aims to discuss causes behind the diminished activation of IR in neurons, with a focus on the functional relationship between mitochondria and IR during early insulin signaling and the related roles of oxidative stress, mitochondrial hypometabolism, and glutamate excitotoxicity in the development of IR insensitivity to insulin.
目前的假说认为,大脑的胰岛素抵抗是阿尔茨海默病和其他痴呆症、帕金森病、2型糖尿病、肥胖症、重度抑郁症和创伤性脑损伤发生发展的致病因素。多种导致胰岛素受体信号转导紊乱的遗传、发育和代谢异常可能是胰岛素抵抗的基础。胰岛素受体底物蛋白通常被认为是胰岛素信号系统中的节点,在代谢应激、高胰岛素血症和炎症期间,该节点与胰岛素不敏感的发生密切相关。新出现的证据表明,胰岛素受体(IR)激活降低是大脑中胰岛素抵抗的另一种常见但较少被讨论的机制。本综述旨在探讨神经元中IR激活降低的原因,重点关注早期胰岛素信号传导过程中线粒体与IR之间的功能关系,以及氧化应激、线粒体代谢减退和谷氨酸兴奋性毒性在IR对胰岛素不敏感发生发展中的相关作用。