Leptin prevents the fall in plasma osteocalcin during starvation in male mice

被引:37
作者
Goldstone, AP
Howard, JK
Lord, GM
Ghatei, MA
Gardiner, JV
Wang, ZL
Wang, RM
Girgis, SI
Bailey, CJ
Bloom, SR
机构
[1] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Sch Med, Endocrine Unit, London W12 0NN, England
[2] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Sch Med, Dept Immunol, London W12 0NN, England
[3] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Sch Med, Dept Metab Med, London W12 0NN, England
[4] Aston Univ, Dept Pharmaceut & Biol Sci, Birmingham B4 7ET, W Midlands, England
基金
英国医学研究理事会;
关键词
leptin; obesity; osteoporosis; osteoblast; osteocalcin; starvation; fasting; bone; anorexia nervosa; testosterone;
D O I
10.1016/S0006-291X(02)00697-6
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
Plasma osteocalcin, a marker of osteoblastic activity, is reduced in starvation, malnutrition, and anorexia nervosa, resulting in low bone turnover osteoporosis. Contradictory findings about the role of leptin as a link between nutritional status and bone physiology have been reported. We demonstrate that leptin-deficient ob/ob and leptin-resistant db/db male mice have increased plasma osteocalcin, and that in male ob/ob mice osteocalcin is not decreased by starvation, unlike control mice. Intraperitoneal leptin administration increased plasma osteocalcin in male ob/ob mice, and prevented its fall during 24 h fasting and 5 days of food restriction in normal male mice. This effect may be mediated via actions on the hypothalamic-pituitary-testicular or -growth hormone axes, or a direct action on osteoblasts. These studies support the hypothesis that the fall in leptin during starvation and weight loss is responsible for the associated reduction in osteoblast activity, and suggest a role for leptin in regulating bone turnover. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:475 / 481
页数:7
相关论文
共 53 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]   Serum leptin level is a predictor of bone mineral density in postmenopausal women [J].
Blain, H ;
Vuillemin, A ;
Guillemin, F ;
Durant, R ;
Hanesse, B ;
De Talance, N ;
Doucet, B ;
Jeandel, C .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (03) :1030-1035
[3]   Leptin reduces ovariectomy-induced bone loss in rats [J].
Burguera, B ;
Hofbauer, LC ;
Thomas, T ;
Gori, F ;
Evans, GL ;
Khosla, S ;
Riggs, BL ;
Turner, RT .
ENDOCRINOLOGY, 2001, 142 (08) :3546-3553
[4]   Molecular basis and clinical application of biological markers of bone turnover [J].
Calvo, MS ;
Eyre, DR ;
Gundberg, CM .
ENDOCRINE REVIEWS, 1996, 17 (04) :333-368
[5]   Regulation of in vivo growth hormone secretion by leptin. [J].
Carro, E ;
Senaris, R ;
Considine, RV ;
Casanueva, FF ;
Dieguez, C .
ENDOCRINOLOGY, 1997, 138 (05) :2203-2206
[6]   Low circulating leptin levels in protein-energy malnourished chronically ill elderly patients [J].
Cederholm, T ;
Arner, P ;
Palmblad, J .
JOURNAL OF INTERNAL MEDICINE, 1997, 242 (05) :377-382
[7]   Splice variants of the OB receptor gene are differentially expressed in brain and peripheral tissues of mice [J].
Chen, SC ;
Kochan, JP ;
Campfield, LA ;
Burn, P ;
Smeyne, RJ .
JOURNAL OF RECEPTOR AND SIGNAL TRANSDUCTION RESEARCH, 1999, 19 (1-4) :245-266
[8]   Insulin increases histomorphometric indices of bone formation in vivo [J].
Cornish, J ;
Callon, KE ;
Reid, IR .
CALCIFIED TISSUE INTERNATIONAL, 1996, 59 (06) :492-495
[9]   CLINICAL ASPECTS OF GROWTH-HORMONE DEFICIENCY IN ADULTS [J].
DEBOER, H ;
BLOK, GJ ;
VANDERVEEN, EA .
ENDOCRINE REVIEWS, 1995, 16 (01) :63-86
[10]   Leptin inhibits bone formation through a hypothalamic relay: A central control of bone mass [J].
Ducy, P ;
Amling, M ;
Takeda, S ;
Priemel, M ;
Schilling, AF ;
Beil, FT ;
Shen, JH ;
Vinson, C ;
Rueger, JM ;
Karsenty, G .
CELL, 2000, 100 (02) :197-207