Melanin-concentrating hormone: a functional melanocortin antagonist in the hypothalamus

被引:194
作者
Ludwig, DS
Mountjoy, KG
Tatro, JB
Gillette, JA
Frederich, RC
Flier, JS
Maratos-Flier, E
机构
[1] Joslin Diabet Ctr, Elliott P Joslin Res Lab, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Dept Med, Div Endocrinol & Metab, Boston, MA 02115 USA
[3] Childrens Hosp, Dept Med, Div Endocrinol, Boston, MA 02115 USA
[4] Tufts Univ, Sch Med, New England Med Ctr,Tupper Res Inst, Dept Med,Div Endocrinol Metab & Mol Med, Boston, MA 02111 USA
[5] Univ Auckland, Res Ctr Dev Med, Auckland 1, New Zealand
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1998年 / 274卷 / 04期
关键词
obesity; eating;
D O I
10.1152/ajpendo.1998.274.4.E627
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Melanin-concentrating hormone (MCH) and alpha-melanocyte-stimulating hormone (alpha-MSH) demonstrate opposite actions on skin coloration in teleost fish. Both peptides are present in the mammalian brain, although their specific physiological roles remain largely unknown. In this study, we examined the interactions between MCH and alpha-MSH after intracerebroventricular administration in rats. MCH increased food intake in a dose-dependent manner and lowered plasma glucocorticoid levels through a mechanism involving ACTH. In contrast, alpha-MSH decreased food intake and increased glucocorticoid levels. MCH, at a twofold molar excess, antagonized both actions of alpha-MSH. alpha-MSH, at a threefold molar excess, blocked the orexigenic properties of MCH. MCH did not block alpha-MSH binding or the ability of alpha-MSH to induce cAMP in cells expressing either the MC3 or MC4 receptor, the principal brain alpha-MSH receptor subtypes. These data suggest that MCH and alpha-MSH exert opposing and antagonistic influences on feeding behavior and the stress response and may function in a coordinate manner to regulate metabolism through a novel mechanism mediated in part by an MCH receptor.
引用
收藏
页码:E627 / E633
页数:7
相关论文
共 44 条
[1]  
ADAN RA, 1996, MOL PHARMACOL, V46, P1182
[2]   Role of leptin in the neuroendocrine response to fasting [J].
Ahima, RS ;
Prabakaran, D ;
Mantzoros, C ;
Qu, DQ ;
Lowell, B ;
MaratosFlier, E ;
Flier, JS .
NATURE, 1996, 382 (6588) :250-252
[3]  
ALVARO JD, 1996, MOL PHARMACOL, V50, P683
[4]   THE ROLE OF MELANIN-CONCENTRATING HORMONE IN COLOR-CHANGE [J].
BAKER, BI .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1993, 680 :279-289
[5]   SALMONID MELANIN-CONCENTRATING HORMONE INHIBITS CORTICOTROPIN RELEASE [J].
BAKER, BI ;
BIRD, DJ ;
BUCKINGHAM, JC .
JOURNAL OF ENDOCRINOLOGY, 1985, 106 (02) :R5-R8
[6]   THE MELANIN-CONCENTRATING HORMONE SYSTEM OF THE RAT-BRAIN - AN IMMUNIZATION AND HYBRIDIZATION HISTOCHEMICAL CHARACTERIZATION [J].
BITTENCOURT, JC ;
PRESSE, F ;
ARIAS, C ;
PETO, C ;
VAUGHAN, J ;
NAHON, JL ;
VALE, W ;
SAWCHENKO, PE .
JOURNAL OF COMPARATIVE NEUROLOGY, 1992, 319 (02) :218-245
[7]   MOLECULAR CHARACTERIZATION OF THE MOUSE AGOUTI LOCUS [J].
BULTMAN, SJ ;
MICHAUD, EJ ;
WOYCHIK, RP .
CELL, 1992, 71 (07) :1195-1204
[8]   Evidence that the diabetes gene encodes the leptin receptor: Identification of a mutation in the leptin receptor gene in db/db mice [J].
Chen, H ;
Charlat, O ;
Tartaglia, LA ;
Woolf, EA ;
Weng, X ;
Ellis, SJ ;
Lakey, ND ;
Culpepper, J ;
Moore, KJ ;
Breitbart, RE ;
Duyk, GM ;
Tepper, RI ;
Morgenstern, JP .
CELL, 1996, 84 (03) :491-495
[9]   Phenotypes of mouse diabetes and rat fatty due to mutations in the OB (leptin) receptor [J].
Chua, SC ;
Chung, WK ;
WuPeng, XS ;
Zhang, YY ;
Liu, SM ;
Tartaglia, L ;
Leibel, RL .
SCIENCE, 1996, 271 (5251) :994-996
[10]   NEUROPEPTIDE-Y AND HUMAN PANCREATIC-POLYPEPTIDE STIMULATE FEEDING-BEHAVIOR IN RATS [J].
CLARK, JT ;
KALRA, PS ;
CROWLEY, WR ;
KALRA, SP .
ENDOCRINOLOGY, 1984, 115 (01) :427-429