Leptin prevents posthibernation weight gain but does not reduce energy expenditure in Arctic ground squirrels

被引:38
作者
Boyer, BB [1 ]
Ormseth, OA
Buck, L
Nicolson, M
Pelleymounter, MA
Barnes, BM
机构
[1] Univ Alaska, Inst Arctic Biol, Fairbanks, AK 99775 USA
[2] Amgen Inc, Dept Immunol & Neurobiol, Thousand Oaks, CA 91320 USA
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY | 1997年 / 118卷 / 03期
关键词
obesity; leptin; food intake; hyperphagia; energy expenditure; seasonal; nonshivering thermogenesis; uncoupling protein; Spermophilus;
D O I
10.1016/S0742-8413(97)00172-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mammals, leptin reduces energy intake and may increase energy expenditure as a means to maintain body weight and/or adiposity at an appropriate level. Hibernating mammals seasonally alter body mass, food intake, and body composition and, therefore, represent an attractive model for investigating the physiological regulation of changing body mass and adiposity. Previous experiments in our laboratory demonstrated that administration of mouse recombinant leptin reduces food intake and body weight in arctic ground squirrels during prehibernation fattening. In addition, leptin appeared to reduce metabolic efficiency (weight gain per unit of energy intake). This result suggests that reduced food intake alone may not account for the observed weight loss. Here, we describe the effect of a 3-week constant infusion of leptin given to posthibernation arctic ground squirrels on food consumption and energy expenditure. Mouse recombinant leptin (1 mg/ml) was administered through subcutaneously implanted mini-osmotic pumps (10 mu l/hr flow rate). Resting metabolic rate was monitored before and during the 3-week leptin administration period by indirect calorimetry. Body temperature and Locomotory activity were monitored continuously by abdominal radiotransmitters. At the end of the leptin administration period, thermogenic capacity was evaluated by measuring brown fat uncoupling protein-1 mRNA and protein levels. Leptin administration resulted in reduced food intake and prevented posthibernation weight gain, but it did not alter any of the measured parameters of energy expenditure. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:405 / 412
页数:8
相关论文
共 41 条
[1]   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
[2]  
[Anonymous], 1961, FIRE LIFE
[3]   Obese gene expression alters the ability of 30A5 preadipocytes to respond to lipogenic hormones [J].
Bai, YL ;
Zhang, SY ;
Kim, KS ;
Lee, JK ;
Kim, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (24) :13939-13942
[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]   Leptin-induced decrease in food intake is not associated with changes in gastric emptying in lean mice [J].
Barrachina, MD ;
Martinez, V ;
Wei, JY ;
Tache, Y .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1997, 272 (03) :R1007-R1011
[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 MITOCHONDRIAL UNCOUPLING PROTEIN GENE IN BROWN FAT - CORRELATION BETWEEN DNASE-I HYPERSENSITIVITY AND EXPRESSION IN TRANSGENIC MICE [J].
BOYER, BB ;
KOZAK, LP .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (08) :4147-4156
[8]  
Boyer Bert B., 1996, P237
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   A 27-MER OLIGONUCLEOTIDE PROBE FOR THE DETECTION AND MEASUREMENT OF THE MESSENGER-RNA FOR UNCOUPLING PROTEIN IN BROWN ADIPOSE-TISSUE OF DIFFERENT SPECIES [J].
BRANDER, F ;
KEITH, JS ;
TRAYHURN, P .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1993, 104 (01) :125-131