Konturek P C, Konturek J W, Cześnikiewicz-Guzik M, Brzozowski T, Sito E, Konturek S J
Department of Physiology, Jagiellonian University Medical College, Cracow, Poland.
J Physiol Pharmacol. 2005 Dec;56 Suppl 6:5-25.
Obesity is one of the most common metabolic diseases and the greatest threats of the health because of possibility of numerous complications. In order to design effective drugs or apply the helpful surgical procedure it is essential to understand physiology of appetite control and pathophysiology of obesity. According to the first law of thermodynamics, the energy input in the form of food, equals energy expenditure through exercise, basal metabolism, thermogenesis and fat biosynthesis. The control of body weight actually concerns the control of adipose tissue with the key role of hypothalamus, possessing several neuronal centers such as that in lateral hypothalamic nuclei considered to be "hunger" center and in ventromedial nuclei serving as the "satiety" center. In addition, paraventricular and arcuate hypothalamic nuclei (ARC) are the sites where multiple hormones, released from the gut and adipose tissue, converge to regulate food intake and energy expenditure. There are two distinct types of neurons in ARC that are important in control of food intake; (1) preopiomelanocortin (POMC) neurons activated by an orexigenic hormones and releasing alpha-melanocyte-stimulating hormone (alpha-MSH) in satiety center and (2) neurons activated by orexigenic peptides such as ghrelin that release the substances including neuropeptide Y (NPY) and Agouti-Related Peptide (AgRP) in hunger center. ARC integrates neural (mostly vagal) and humoral inputs such as enteropeptides including orexigenic (ghrelin and orexins) and an orexigenic peptides (cholecystokinin, polypeptide YY, glucagon-like peptide-1, oxyntomodulin, leptin and others) that exert a physiological role in regulating appetite and satiety. The peripherally (gut, adipose tissue) and centrally expressed modulators of appetitive behavior act through specific receptors in the afferent (mostly vagal) nerves and hypothalamic neurons implicated in adiposity signaling and regulation of food intake.
肥胖是最常见的代谢性疾病之一,因其可能引发众多并发症,对健康构成极大威胁。为了设计有效的药物或应用有益的外科手术,了解食欲控制的生理学和肥胖的病理生理学至关重要。根据热力学第一定律,食物形式的能量输入等于通过运动、基础代谢、产热和脂肪生物合成所消耗的能量。体重控制实际上涉及对脂肪组织的控制,下丘脑起着关键作用,它拥有多个神经中枢,如外侧下丘脑核中的神经中枢被认为是“饥饿”中枢,腹内侧核则作为“饱腹感”中枢。此外,室旁核和弓状下丘脑核(ARC)是肠道和脂肪组织释放的多种激素汇聚以调节食物摄入和能量消耗的部位。ARC中有两种不同类型的神经元对食物摄入控制很重要;(1)前阿黑皮素原(POMC)神经元,被促食欲激素激活,在饱腹感中枢释放α-黑素细胞刺激素(α-MSH);(2)被促食欲肽如胃饥饿素激活的神经元,在饥饿中枢释放包括神经肽Y(NPY)和刺鼠相关肽(AgRP)在内的物质。ARC整合神经(主要是迷走神经)和体液输入,如肠肽,包括促食欲的(胃饥饿素和食欲素)和一种抑食欲肽(胆囊收缩素、多肽YY、胰高血糖素样肽-1、胃动素、瘦素等),它们在调节食欲和饱腹感方面发挥生理作用。外周(肠道、脂肪组织)和中枢表达的食欲行为调节因子通过传入(主要是迷走神经)神经和下丘脑神经元中的特定受体发挥作用,这些神经元参与肥胖信号传导和食物摄入调节。