Ghrelin regulates adiposity in white adipose tissue and UCP1 mRNA expression in brown adipose tissue in mice

被引:88
作者
Tsubone, T [1 ]
Masaki, T [1 ]
Katsuragi, I [1 ]
Tanaka, K [1 ]
Kakuma, T [1 ]
Yoshimatsu, H [1 ]
机构
[1] Oita Med Univ, Sch Med, Dept Internal Med 1, Fac Med, Oita 8795593, Japan
基金
日本学术振兴会;
关键词
ghrelin; adiposity; brown adipose tissue; white adipose tissue;
D O I
10.1016/j.regpep.2005.04.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To examine the involvement of ghrelin in obesity, we investigated the effects of treatment with peripherally administered ghrelin on food intake, adiposity, and expression of uncoupling protein (UCP) mRNA in brown (BAT) and white (WAT) adipose tissue in mice. Acute bolus administration of ghrelin at a dose of 120 nmol/kg increased cumulative food intake over 4 and 24 h as compared to controls (p < 0.05 for each), whereas 12 nmol/kg/day ghrelin showed no remarkable effect (p > 0.1). Chronic repeated treatment with 12 nmol/kg/day ghrelin for 7 days increased body weight and adiposity assessed by the weight of adipose tissue, triglyceride content in WAT (p < 0.05 for each versus control). In addition, the same treatment decreased and increased mRNA expression of BAT UCP I and WAT UCP2, respectively (p < 0.05 for each). In conclusion, ghrelin can regulate body weight, adiposity and UCPs mRNA expression in mice. The present results provide evidence for a. new regulatory loop involving ghrelin and UCP, and add novel insights into the regulatory mechanisms of obesity. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:97 / 103
页数:7
相关论文
共 31 条
[1]   Ghrelin stimulates insulin secretion from the pancreas of normal and diabetic rats [J].
Adeghate, E ;
Ponery, AS .
JOURNAL OF NEUROENDOCRINOLOGY, 2002, 14 (07) :555-560
[2]   Ghrelin can bind to a species of high density lipoprotein associated with paraoxonase [J].
Beaumont, NJ ;
Skinner, VO ;
Tan, TMM ;
Ramesh, BS ;
Byrne, DJ ;
MacColl, GS ;
Keen, JN ;
Bouloux, PM ;
Mikhailidis, DP ;
Bruckdorfer, KR ;
Vanderpump, MP ;
Srai, KS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (11) :8877-8880
[3]   Linkage between markers in the vicinity of the uncoupling protein 2 gene and resting metabolic rate in humans [J].
Bouchard, C ;
Perusse, L ;
Chagnon, YC ;
Warden, C ;
Ricquier, D .
HUMAN MOLECULAR GENETICS, 1997, 6 (11) :1887-1889
[4]   Growth hormone-releasing peptide (GHRP) [J].
Bowers, CY .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1998, 54 (12) :1316-1329
[5]   The role of ghrelin and growth hormone secretagroogues receptor on rat adipogenesis [J].
Choi, KC ;
Roh, SG ;
Hong, YH ;
Shrestha, YB ;
Hishikawa, D ;
Chen, C ;
Kojima, M ;
Kangawa, K ;
Sasaki, SI .
ENDOCRINOLOGY, 2003, 144 (03) :754-759
[6]   The role of the gastric afferent vagal nerve in ghrelin-induced feeding and growth hormone secretion in rats [J].
Date, Y ;
Murakami, N ;
Toshinai, K ;
Matsukura, S ;
Niijima, A ;
Matsuo, H ;
Kangawa, K ;
Nakazato, M .
GASTROENTEROLOGY, 2002, 123 (04) :1120-1128
[7]  
Dickson SL, 2002, J NEUROENDOCRINOL, V14, P83
[8]   Mice lacking mitochondrial uncoupling protein are cold-sensitive but not obese [J].
Enerback, S ;
Jacobsson, A ;
Simpson, EM ;
Guerra, C ;
Yamashita, H ;
Harper, ME ;
Kozak, LP .
NATURE, 1997, 387 (6628) :90-94
[9]   Ghrelin is a growth-hormone-releasing acylated peptide from stomach [J].
Kojima, M ;
Hosoda, H ;
Date, Y ;
Nakazato, M ;
Matsuo, H ;
Kangawa, K .
NATURE, 1999, 402 (6762) :656-660
[10]   Ghrelin: discovery of the natural endogenous ligand for the growth hormone secretagogue receptor [J].
Kojima, M ;
Hosoda, H ;
Matsuo, H ;
Kangawa, K .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2001, 12 (03) :118-122