The arcuate nucleus as a conduit for diverse signals relevant to energy homeostasis

被引:435
作者
Cone, RD [1 ]
Cowley, MA [1 ]
Butler, AA [1 ]
Fan, W [1 ]
Marks, DL [1 ]
Low, MJ [1 ]
机构
[1] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97201 USA
关键词
leptin; POMC; neuropeptide Y; AgRP; MC3-R; MSH; regulation;
D O I
10.1038/sj.ijo.0801913
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Arcuate nucleus neurons are known to be responsive to a wide array of hormones and nutrients, including leptin, insulin, gonadal steroids and glucose. In addition to potential transport mechanisms, peripheral substances may access these neurons via arcuate cell bodies in and projections to the median eminence, a region considered to be a circumventricular organ. The arcuate is a potent site of leptin action, probably mediating a component of leptin's effects via arcuate neuropeptide Y/agouti-related peptide (NPY/AgRP) and pro-opiomelanocortin (POMC) neurons, and implicating this structure in the long-term control of energy stores. However, ghrelin, the endogenous ligand of the growth hormone secretagogue receptor, may also stimulate feeding and weight gain, in part through action on receptors in arcuate NPY neurons. Since ghrelin is secreted by the stomach upon content depletion, with a half-life of no more than an hour, the arcuate nucleus may also be important in sensing and responding to acute changes in nutrients. We have developed a system for recording from arcuate POMC neurons using a mouse containing a transgene in which the POMC promoter is driving expression of the green fluorescent protein (GFP). In these mice, 99% of the beta-endorphin positive neurons express GFP, making whole cell patch clamp recordings from the sparsely distributed POMC neurons facile. All of the POMC neurons appear to be activated by leptin, via two different mechanisms, while approximately 30-50% of the neurons appear to be inhibited by a gamma-melanocyte stimulating hormone (MSH) specific agonist. The latter result suggests that the melanocortin-3 receptor (MC3-R) may act as an autoinhibitory receptor on some POMC neurons. This hypothalamic slice preparation also confirms the responsiveness of arcuate POMC neurons to a wide variety of nutrients and hormones. Thus the arcuate melanocortin system is best described as a conduit of many diverse signals involved in energy homeostasis, with leptin acting tonically to regulate the responsiveness of the circuit to a wide variety of hormones and nutrients.
引用
收藏
页码:S63 / S67
页数:5
相关论文
共 17 条
[1]   ANDROGEN REGULATION OF PROOPIOMELANOCORTIN GENE-EXPRESSION AND PEPTIDE CONTENT IN THE BASAL HYPOTHALAMUS [J].
BLUM, M ;
ROBERTS, JL ;
WARDLAW, SL .
ENDOCRINOLOGY, 1989, 124 (05) :2283-2288
[2]   Independent and additive effects of central POMC and leptin pathways on murine obesity [J].
Boston, BA ;
Blaydon, KM ;
Varnerin, J ;
Cone, RD .
SCIENCE, 1997, 278 (5343) :1641-1644
[3]   Melanocortin-4 receptor is required for acute homeostatic responses to increased dietary fat [J].
Butler, AA ;
Marks, DL ;
Fan, W ;
Kuhn, CM ;
Bartolome, M ;
Cone, RD .
NATURE NEUROSCIENCE, 2001, 4 (06) :605-611
[4]   Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus [J].
Cowley, MA ;
Smart, JL ;
Rubinstein, M ;
Cordán, MG ;
Diano, S ;
Horvath, TL ;
Cone, RD ;
Low, MJ .
NATURE, 2001, 411 (6836) :480-484
[5]   Leptin activates neurons in ventrobasal hypothalamus and brainstem [J].
Elmquist, JK ;
Ahima, RS ;
MaratosFlier, E ;
Flier, JS ;
Safer, CB .
ENDOCRINOLOGY, 1997, 138 (02) :839-842
[6]   Attenuation of the obesity syndrome of ob/ob mice by the loss of neuropeptide Y [J].
Erickson, JC ;
Hollopeter, G ;
Palmiter, RD .
SCIENCE, 1996, 274 (5293) :1704-1707
[7]   Role of melanocortinergic neurons in feeding and the agouti obesity syndrome [J].
Fan, W ;
Boston, BA ;
Kesterson, RA ;
Hruby, VJ ;
Cone, RD .
NATURE, 1997, 385 (6612) :165-168
[8]   Expression of leptin receptor mRNA in the hypothalamic arcuate nucleus - Relationship with NPY neurones [J].
Hakansson, ML ;
Hulting, AL ;
Meister, B .
NEUROREPORT, 1996, 7 (18) :3087-3092
[9]   Localization of leptin receptor mRNA expression in mouse brain [J].
Huang, XF ;
Koutcherov, I ;
Lin, S ;
Wang, HQ ;
Storlien, L .
NEUROREPORT, 1996, 7 (15-17) :2635-2638
[10]   Targeted disruption of the melanocortin-4 receptor results in obesity in mice [J].
Huszar, D ;
Lynch, CA ;
FairchildHuntress, V ;
Dunmore, JH ;
Fang, Q ;
Berkemeier, LR ;
Gu, W ;
Kesterson, RA ;
Boston, BA ;
Cone, RD ;
Smith, FJ ;
Campfield, LA ;
Burn, P ;
Lee, F .
CELL, 1997, 88 (01) :131-141