Diamant Michaela
Department of Endocrinology, VU University Medical Center, PO BOX 7057, 1007 MB Amsterdam, The Netherlands.
Ideggyogy Sz. 2007 Mar 30;60(3-4):97-108.
The unparalleled global rates of obesity and type 2 diabetes, together with the associated cardiovascular morbidity and mortality, are referred to as the "diabesity pandemic". Changes in lifestyle occurring worldwide, including the increased consumption of high-caloric foods and reduced exercise, are regarded as the main causal factors. Central obesity and insulin resistance have emerged as important linking components. Understanding the aetiology of the cluster of pathologies that leads to the increased risk is instrumental in the development of preventive and therapeutic strategies. Historically, skeletal muscle, adipose tissue and liver were regarded as key insulin target organs involved in insulin-mediated regulation of peripheral carbohydrate, lipid and protein metabolism. The consequences of impaired insulin action in these organs were deemed to explain the functional and structural abnormalities associated with insulin resistance. The discovery of insulin receptors in the central nervous system, the detection of insulin in the cerebrospinal fluid after peripheral insulin administration and the well-documented effects of intracerebroventricularly injected insulin on energy homeostasis, have identified the brain as an important target for insulin action. In addition to its critical role as a peripheral signal integrating the complex network of hypothalamic neuropeptides and neurotransmitters that influence parameters of energy balance, central nervous insulin signalling is also implicated in the regulation of peripheral glucose metabolism. This review summarizes the evidence of insulin action in the brain as part of the multifaceted circuit involved in the central regulation of energy and glucose homeostasis, and discuss the role of impaired central nervous insulin signalling as a pathogenic factor in the obesity and type 2 diabetes epidemic.
全球肥胖症和2型糖尿病发病率空前之高,加之相关的心血管疾病发病率和死亡率,被称为“糖尿病肥胖症大流行”。全球范围内生活方式的改变,包括高热量食物消费增加和运动量减少,被视为主要致病因素。中心性肥胖和胰岛素抵抗已成为重要的关联因素。了解导致风险增加的一系列病理状况的病因,有助于制定预防和治疗策略。从历史上看,骨骼肌、脂肪组织和肝脏被视为胰岛素的关键靶器官,参与胰岛素介导的外周碳水化合物、脂质和蛋白质代谢调节。这些器官中胰岛素作用受损的后果被认为可以解释与胰岛素抵抗相关的功能和结构异常。中枢神经系统中胰岛素受体的发现、外周注射胰岛素后脑脊液中胰岛素的检测以及脑室内注射胰岛素对能量稳态的充分记录的影响,已确定大脑是胰岛素作用的重要靶器官。除了作为整合影响能量平衡参数的下丘脑神经肽和神经递质复杂网络的外周信号发挥关键作用外,中枢神经胰岛素信号传导还参与外周葡萄糖代谢的调节。本综述总结了胰岛素在大脑中作为参与能量和葡萄糖稳态中枢调节的多方面回路一部分的作用证据,并讨论了中枢神经胰岛素信号传导受损作为肥胖症和2型糖尿病流行致病因素的作用。