Beck B
Université Henri Poincaré, Neurocal, Nancy, France.
Philos Trans R Soc Lond B Biol Sci. 2006 Jul 29;361(1471):1159-85. doi: 10.1098/rstb.2006.1855.
Neuropeptide Y (NPY) is one the most potent orexigenic peptides found in the brain. It stimulates food intake with a preferential effect on carbohydrate intake. It decreases latency to eat, increases motivation to eat and delays satiety by augmenting meal size. The effects on feeding are mediated through at least two receptors, the Y1 and Y5 receptors. The NPY system for feeding regulation is mostly located in the hypothalamus. It is formed of the arcuate nucleus (ARC), where the peptide is synthesized, and the paraventricular (PVN), dorsomedial (DMN) and ventromedial (VMN) nuclei and perifornical area where it is active. This activity is modulated by the hindbrain and limbic structures. It is dependent on energy availability, e.g. upregulation with food deprivation or restriction, and return to baseline with refeeding. It is also sensitive to diet composition with variable effects of carbohydrates and fats. Leptin signalling and glucose sensing which are directly linked to diet type are the most important factors involved in its regulation. Absence of leptin signalling in obesity models due to gene mutation either at the receptor level, as in the Zucker rat, the Koletsky rat or the db/db mouse, or at the peptide level, as in ob/ob mouse, is associated with increased mRNA abundance, peptide content and/or release in the ARC or PVN. Other genetic obesity models, such as the Otsuka-Long-Evans-Tokushima Fatty rat, the agouti mouse or the tubby mouse, are characterized by a diminution in NPY expression in the ARC nucleus and by a significant increase in the DMN. Further studies are necessary to determine the exact role of NPY in these latter models. Long-term exposure to high-fat or high-energy palatable diets leads to the development of adiposity and is associated with a decrease in hypothalamic NPY content or expression, consistent with the existence of a counter-regulatory mechanism to diminish energy intake and limit obesity development. On the other hand, an overactive NPY system (increased mRNA expression in the ARC associated with an upregulation of the receptors) is characteristic of rats or rodent strains sensitive to dietary-induced obesity. Finally, NPY appears to play an important role in body weight and feeding regulation, and while it does not constitute the only target for drug treatment of obesity, it may nevertheless provide a useful target in conjunction with others.
神经肽Y(NPY)是在大脑中发现的最有效的促食欲肽之一。它刺激食物摄入,对碳水化合物摄入有优先作用。它缩短进食潜伏期,增加进食动机,并通过增加进食量来延迟饱腹感。对进食的影响至少通过两种受体介导,即Y1和Y5受体。用于调节进食的NPY系统主要位于下丘脑。它由合成该肽的弓状核(ARC)以及该肽发挥作用的室旁核(PVN)、背内侧核(DMN)、腹内侧核(VMN)和穹窿周区组成。这种活动受后脑和边缘结构的调节。它取决于能量供应情况,例如禁食或限制饮食时会上调,重新进食后恢复到基线水平。它对饮食组成也很敏感,碳水化合物和脂肪有不同的影响。与饮食类型直接相关的瘦素信号传导和葡萄糖感知是参与其调节的最重要因素。在肥胖模型中,由于基因突变导致瘦素信号缺失,无论是在受体水平,如在 Zucker 大鼠、Koletsky 大鼠或 db/db 小鼠中,还是在肽水平,如在 ob/ob 小鼠中,都与ARC或PVN中mRNA丰度、肽含量和/或释放增加有关。其他遗传性肥胖模型,如大冢-朗-伊文斯-德岛肥胖大鼠、刺豚鼠或胖鼠,其特征是ARC核中NPY表达减少,DMN中显著增加。需要进一步研究以确定NPY在这些后一种模型中的确切作用。长期暴露于高脂肪或高能量美味饮食会导致肥胖,并与下丘脑NPY含量或表达降低有关,这与存在减少能量摄入和限制肥胖发展的反调节机制一致。另一方面,NPY系统过度活跃(ARC中mRNA表达增加并伴有受体上调)是对饮食诱导肥胖敏感的大鼠或啮齿动物品系的特征。最后,NPY似乎在体重和进食调节中起重要作用,虽然它不是肥胖药物治疗的唯一靶点,但与其他靶点结合可能会提供一个有用的靶点。