Section on Integrative Physiology and Metabolism, Joslin Diabetes Center and Department of Medicine, Harvard Medical School, Boston, MA.
Section on Integrative Physiology and Metabolism, Joslin Diabetes Center and Department of Medicine, Harvard Medical School, Boston, MA
Diabetes. 2014 Jul;63(7):2232-43. doi: 10.2337/db14-0568. Epub 2014 Jun 15.
Insulin receptors, as well as IGF-1 receptors and their postreceptor signaling partners, are distributed throughout the brain. Insulin acts on these receptors to modulate peripheral metabolism, including regulation of appetite, reproductive function, body temperature, white fat mass, hepatic glucose output, and response to hypoglycemia. Insulin signaling also modulates neurotransmitter channel activity, brain cholesterol synthesis, and mitochondrial function. Disruption of insulin action in the brain leads to impairment of neuronal function and synaptogenesis. In addition, insulin signaling modulates phosphorylation of tau protein, an early component in the development of Alzheimer disease. Thus, alterations in insulin action in the brain can contribute to metabolic syndrome, and the development of mood disorders and neurodegenerative diseases.
胰岛素受体以及 IGF-1 受体及其受体后信号伙伴在整个大脑中都有分布。胰岛素通过这些受体作用于外周代谢,包括调节食欲、生殖功能、体温、白色脂肪量、肝葡萄糖输出以及对低血糖的反应。胰岛素信号还调节神经递质通道活性、脑胆固醇合成和线粒体功能。大脑中胰岛素作用的破坏会导致神经元功能和突触发生受损。此外,胰岛素信号还调节 tau 蛋白的磷酸化,tau 蛋白是阿尔茨海默病发展的早期成分。因此,大脑中胰岛素作用的改变可能导致代谢综合征以及情绪障碍和神经退行性疾病的发生。