Sandoval Darleen, Cota Daniela, Seeley Randy J
Department of Psychiatry, Genome Research Institute, University of Cincinnati, Cincinnati, OH 45237, USA.
Annu Rev Physiol. 2008;70:513-35. doi: 10.1146/annurev.physiol.70.120806.095256.
The incidences of both obesity and type 2 diabetes mellitus are rising at epidemic proportions. Despite this, the balance between caloric intake and expenditure is tremendously accurate under most circumstances. Growing evidence suggests that nutrient and hormonal signals converge and directly act on brain centers, leading to changes in fuel metabolism and, thus, stable body weight over time. Growing evidence also suggests that these same signals act on the central nervous system (CNS) to regulate glucose metabolism independently. We propose that this is not coincidental and that the CNS responds to peripheral signals to orchestrate changes in both energy and glucose homeostasis. In this way the CNS ensures that the nutrient demands of peripheral tissues (and likely of the brain itself) are being met. Consequently, dysfunction of the ability of the CNS to integrate fuel-sensing signals may underlie the etiology of metabolic diseases such as obesity and diabetes.
肥胖症和2型糖尿病的发病率正以流行的比例上升。尽管如此,在大多数情况下,热量摄入与消耗之间的平衡极其精确。越来越多的证据表明,营养和激素信号汇聚并直接作用于脑中枢,导致燃料代谢发生变化,从而随着时间推移使体重保持稳定。越来越多的证据还表明,这些相同的信号作用于中枢神经系统(CNS)以独立调节葡萄糖代谢。我们认为这并非巧合,并且中枢神经系统对外周信号作出反应以协调能量和葡萄糖稳态的变化。通过这种方式,中枢神经系统确保外周组织(可能还有大脑自身)的营养需求得到满足。因此,中枢神经系统整合燃料感知信号的能力出现功能障碍可能是肥胖症和糖尿病等代谢疾病病因的基础。