Leptin-like effects of MTII are augmented in MSG-obese rats

被引:17
作者
Kim, YW
Choi, DW
Park, YH
Huh, JY
Won, KC
Choi, KH
Park, SY
Kim, JY
Lee, SK
机构
[1] Yeungnam Univ, Coll Med, Dept Physiol, Namgu 705717, Daegu, South Korea
[2] Yeungnam Univ, Coll Med, Dept Pediat, Namgu 705717, Daegu, South Korea
[3] Yeungnam Univ, Coll Med, Dept Internal Med, Namgu 705717, Daegu, South Korea
关键词
melanocortin receptor; leptin resistance; appetite; thermogenesis;
D O I
10.1016/j.regpep.2004.10.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To evaluate whether MTII, a melanocortin receptor 3/4 agonist, is working in hypophagic and hypothermogenic obese model, we measured food intake, body weight, oxygen consumption, and fat mass following intracerebroventricular (i.c.v.) infusion of MTII in monosodium glutamate (MSG)-induced obese rats. MTII, or artificial cerebrospinal fluid (aCSF), was infused into i.c.v. with an osmotic minipump for 1 week. MSG-obese rats were induced by neonatal injection of MSG. Five-month-old MSG rats were characterized by hypophagia, lower oxygen consumption, hyperleptinemia, and obesity compared to age-matched control rats. The infusion of MTII decreased their food intake, visceral fat, and body weight in MSG-obese rats compared with aCSF-infused rats. The oxygen consumption was increased by MTII treatment in MSG-obese rats compared with aCSF as well as pair fed (PF) rats. Interestingly, these leptin-like effects of MTII were greater in MSG-obese rats than in controls, which might be related to the increased expression of melanocortin receptor 4 (MC4R) in the hypothalamus of MSG-obese rats. Our results suggested that both anorexic and thermogenic mechanisms were activated by MTII in the MSG-obese rats and contributed to the decrease in body weight and fat mass. Moreover, there was a sensitization to MTII caused by upregulation of the melanocortin receptor in the MSG-obese rats. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 70
页数:8
相关论文
共 27 条
[1]   Responsiveness to peripherally administered melanocortins in lean and obese mice [J].
Blüher, S ;
Ziotopoulou, M ;
Bullen, JW ;
Moschos, SJ ;
Ungsunan, L ;
Kokkotou, E ;
Maratos-Flier, E ;
Mantzoros, CS .
DIABETES, 2004, 53 (01) :82-90
[2]   The neuropeptide Y agouti gene-related protein (AGRP) brain circuitry in normal, anorectic, and monosodium glutamate-treated mice [J].
Broberger, C ;
Johansen, J ;
Johansson, C ;
Schalling, M ;
Hökfelt, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :15043-15048
[3]   Central injection in rats of α-melanocyte-stimulating hormone analog:: effects on food intake and brain Fos [J].
Brown, KS ;
Gentry, RM ;
Rowland, NE .
REGULATORY PEPTIDES, 1998, 78 (1-3) :89-94
[4]   The leptin-like effects of 3-d peripheral administration of a melanocortin agonist are more marked in genetically obese zucker (fa/fa) than in lean rats [J].
Cettour-Rose, P ;
Rohner-Jeanrenaud, F .
ENDOCRINOLOGY, 2002, 143 (06) :2277-2283
[5]   Linkage and association studies between the melanocortin receptors 4 and 5 genes and obesity-related phenotypes in the Quebec Family Study [J].
Chagnon, YC ;
Chen, WJ ;
Perusse, L ;
Chagnon, M ;
Nadeau, A ;
Wilkison, WO ;
Bouchard, C .
MOLECULAR MEDICINE, 1997, 3 (10) :663-673
[6]  
CHROMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156
[7]   Attenuation of leptin-mediated effects by monosodium glutamate-induced arcuate nucleus damage [J].
Dawson, R ;
Pelleymounter, MA ;
Millard, WJ ;
Liu, S ;
Eppler, B .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 273 (01) :E202-E206
[8]  
Fan W., 1997, NATURE, V385, P65
[9]   Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency [J].
Farooqi, IS ;
Yeo, GSH ;
Keogh, JM ;
Aminian, S ;
Jebb, SA ;
Butler, G ;
Cheetham, T ;
O'Rahilly, S .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (02) :271-279
[10]   Feeding effects of hypothalamic injection of melanocortin 4 receptor ligands [J].
Giraudo, SQ ;
Billington, CJ ;
Levine, AS .
BRAIN RESEARCH, 1998, 809 (02) :302-306