Department of Biology and Biochemistry, Center for Nuclear Receptors and Cell Signaling, University of Houston, Houston, TX, 77004, USA.
Cell Mol Life Sci. 2014 Oct;71(19):3799-809. doi: 10.1007/s00018-014-1650-z. Epub 2014 Jun 4.
Obesity and metabolic disorders, such as type 2 diabetes and hypertension, have attracted considerable attention as life-threatening diseases not only in developed countries but also worldwide. Additionally, the rate of obesity in young people all over the world is rapidly increasing. Accumulated evidence suggests that the central nervous system may participate in the development of and/or protection from obesity. For example, in the brain, the hypothalamic melanocortin system senses and integrates central and peripheral metabolic signals and controls the degree of energy expenditure and feeding behavior, in concert with metabolic status, to regulate whole-body energy homeostasis. Currently, researchers are studying the mechanisms by which peripheral metabolic molecules control feeding behavior and energy balance through the central melanocortin system. Accordingly, recent studies have revealed that some inflammatory molecules and transcription factors participate in feeding behavior and energy balance by controlling the central melanocortin pathway, and have thus become new candidates as therapeutic targets to fight metabolic diseases such as obesity and diabetes.
肥胖症和代谢紊乱,如 2 型糖尿病和高血压,不仅在发达国家,而且在全球范围内,都已成为危及生命的疾病,引起了相当大的关注。此外,全世界年轻人的肥胖率正在迅速上升。越来越多的证据表明,中枢神经系统可能参与肥胖症的发生和/或保护。例如,在大脑中,下丘脑黑素皮质素系统感知和整合中枢和外周代谢信号,并根据代谢状态控制能量消耗和摄食行为的程度,以调节全身能量平衡。目前,研究人员正在研究外周代谢分子通过中枢黑素皮质素系统控制摄食行为和能量平衡的机制。因此,最近的研究表明,一些炎症分子和转录因子通过控制中枢黑素皮质素途径参与摄食行为和能量平衡,因此成为治疗肥胖症和糖尿病等代谢疾病的新候选治疗靶点。