Role of ARC NPY neurons in energy homeostasis

被引:18
作者
King, PJ [1 ]
Williams, G [1 ]
机构
[1] Univ Liverpool, Diabet & Endocrinol Res Unit, Dept Med, Clin Dept, Liverpool L69 3GA, Merseyside, England
关键词
D O I
10.1358/dnp.1998.11.7.659946
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Neuropeptide Y (NPY) is one of the most abundant and widely distributed neurotransmitters in the mammalian brain and appears to be an important regulatory peptide in both the central and peripheral nervous systems. The arcuate nucleus (ARC) is the major site of expression for NPY within neurons in the hypothalamus. The most noticeable effect of NPY is the stimulation of feeding. To date, six NPY receptor subtypes have been cloned and pharmacologically characterized, and there is evidence for further NPY receptor subtypes. The recent isolation and cloning of a rat NPY receptor with the required pharmacology for the feeding response, called the Y-5 receptor, has led to the suggestion that this is the "feeding" receptor. There is, however, still controversy as to whether the Y-5 receptor represents the true "feeding" receptor, since selective Y-1 receptor antagonists are capable of antagonizing NPY-induced hyperphagia, It also is possible that another, as yet unidentified, NPY receptor subtype(s) may mediate the effects of NPY on energy balance. The potency and behavioral specificity of NPY on feeding and its ability to induce obesity, together with the evidence that ARC-NPY neurons operate homeostatically to counteract energy deficits, all suggest that the ARC-PVN projection is important in regulating energy balance. The next few years will tell us whether or not these important physiological lessons will be successfully translated into a safe and effective form of therapy for human obesity. (C) 1998 Pious Science. Ail rights reserved.
引用
收藏
页码:402 / 410
页数:9
相关论文
共 68 条
[1]   HYPOTHALAMIC NEUROPEPTIDE-Y, ITS GENE-EXPRESSION AND RECEPTOR ACTIVITY - RELATION TO CIRCULATING CORTICOSTERONE IN ADRENALECTOMIZED RATS [J].
AKABAYASHI, A ;
WATANABE, Y ;
WAHLESTEDT, C ;
MCEWEN, BS ;
PAEZ, X ;
LEIBOWITZ, SF .
BRAIN RESEARCH, 1994, 665 (02) :201-212
[2]   NEUROPEPTIDE-Y - ROLE IN LIGHT DARK CYCLE ENTRAINMENT OF HAMSTER CIRCADIAN-RHYTHMS [J].
ALBERS, HE ;
FERRIS, CF .
NEUROSCIENCE LETTERS, 1984, 50 (1-3) :163-168
[3]   AN ARCUATO-PARAVENTRICULAR AND ARCUATO-DORSOMEDIAL HYPOTHALAMIC NEUROPEPTIDE Y-CONTAINING SYSTEM WHICH LACKS NORADRENALINE IN THE RAT [J].
BAI, FL ;
YAMANO, M ;
SHIOTANI, Y ;
EMSON, PC ;
SMITH, AD ;
POWELL, JF ;
TOHYAMA, M .
BRAIN RESEARCH, 1985, 331 (01) :172-175
[4]   Leptin enters the brain by a saturable system independent of insulin [J].
Banks, WA ;
Kastin, AJ ;
Huang, WT ;
Jaspan, JB ;
Maness, LM .
PEPTIDES, 1996, 17 (02) :305-311
[5]   CLONING AND FUNCTIONAL EXPRESSION OF A HUMAN Y4 SUBTYPE RECEPTOR FOR PANCREATIC-POLYPEPTIDE, NEUROPEPTIDE-Y, AND PEPTIDE YY [J].
BARD, JA ;
WALKER, MW ;
BRANCHEK, TA ;
WEINSHANK, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26762-26765
[6]   NEUROPEPTIDE-Y IN HYPOTHALAMIC PARAVENTRICULAR NUCLEUS - A CENTER COORDINATING ENERGY-METABOLISM [J].
BILLINGTON, CJ ;
BRIGGS, JE ;
HARKER, S ;
GRACE, M ;
LEVINE, AS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (06) :R1765-R1770
[7]   The central regulation of energy homoeostasis: Roles of neuropeptide Y and other brain peptides [J].
Bing, C ;
Wang, Q ;
Pickavance, L ;
Williams, G .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1996, 24 (02) :559-565
[8]   PORTAL ADIPOSE-TISSUE AS A GENERATOR OF RISK-FACTORS FOR CARDIOVASCULAR-DISEASE AND DIABETES [J].
BJORNTORP, P .
ARTERIOSCLEROSIS, 1990, 10 (04) :493-496
[9]   Subtypes Y1 and Y2 of the neuropeptide Y receptor are respectively expressed in pro-opiomelanocortin- and neuropeptide-Y-containing neurons of the rat hypothalamic arcuate nucleus [J].
Broberger, C ;
Landry, M ;
Wong, H ;
Walsh, JN ;
Hokfelt, T .
NEUROENDOCRINOLOGY, 1997, 66 (06) :393-408
[10]   Immunohistochemical localization of leptin and uncoupling protein in white and brown adipose tissue [J].
Cinti, S ;
Frederich, RC ;
Zingaretti, MC ;
DeMatteis, R ;
Flier, JS ;
Lowell, BB .
ENDOCRINOLOGY, 1997, 138 (02) :797-804