HORMONAL-CONTROL OF GROWTH IN THE GENETICALLY-OBESE ZUCKER RAT .1. LINEAR GROWTH, PLASMA INSULIN-LIKE GROWTH FACTOR-I (IGP-I) AND IGF-BINDING PROTEINS

被引:26
作者
NGUYENYAMAMOTO, L
DEAL, CL
FINKELSTEIN, JA
VANVLIET, G
机构
[1] UNIV MONTREAL, DEPT PEDIAT, MONTREAL H3T 1C5, PQ, CANADA
[2] NE OHIO UNIV, COLL MED, DEPT ANAT, ROOTSTOWN, OH 44272 USA
[3] ST JUSTINE HOSP, RES CTR, REPROD & DEV BIOL UNIT, MONTREAL H3T 1C5, PQ, CANADA
关键词
D O I
10.1210/en.134.3.1382
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The genetically obese Zucker rat is a widely used model of early-onset obesity. Like obese children, these obese rats are hyperinsulinemic and have low GH secretion. However, data on linear growth and insulin-like growth factor-I (IGF-I) levels in this model are scanty and contradictory. In the present study, we investigated linear growth and its hormonal control in Zucker rats (male and female) from 4-20 weeks of age. In the obese animals, compared to their lean littermates, the naso-anal length was normal or slightly greater, whereas the tails and femurs were shorter. The plasma concentration of IGF-I increased between 4-20 weeks of age, and IGF-I levels were normal or slightly higher in the obese animals. The serum level of IGF-binding protein-3 (IGFBP-3) measured by Western ligand blotting was not significantly different in lean vs, obese rats. To assess the IGF-I response to GH, bovine GH was administered (250 mu g/100 g BW, ip, daily for 3 days) to 16- to 20-week-old female Zucker rats; plasma IGF-I concentrations increased more in the obese (percent increase over baseline, 347 +/- 44% vs. 194 +/- 31%; P < 0.01). These results show that despite low GH secretion, genetically obese Zucker rats have 1) normal linear (nasoanal) growth, 2) normal or increased circulating levels of IGF-I and IGFBP-3, and 3) increased plasma IGF-I responses to exogenous GH. These results suggest that the GH-independent growth in this model could result from direct effects of hyperinsulinism on circulating IGF-I and IGFBP-3 levels and/or indirect effects through increased GH receptor function.
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页码:1382 / 1388
页数:7
相关论文
共 50 条
[31]   TIME COURSE AND MECHANISM OF GROWTH-HORMONES NEGATIVE FEEDBACK EFFECT ON ITS OWN SPONTANEOUS RELEASE [J].
LANZI, R ;
TANNENBAUM, GS .
ENDOCRINOLOGY, 1992, 130 (02) :780-788
[32]   DEVELOPMENTAL AND SEX-RELATED CHANGES OF THE GROWTH-HORMONE AXIS IN LEAN AND OBESE ZUCKER RATS [J].
LEIDY, JW ;
ROMANO, TM ;
MILLARD, WJ .
NEUROENDOCRINOLOGY, 1993, 57 (02) :213-223
[33]  
LEWITT MS, 1993, 75TH ANN M END SOC L, P55
[34]   TOTAL SYNTHESIS OF INSULIN-LIKE GROWTH FACTOR-I (SOMATOMEDIN-C) [J].
LI, CH ;
YAMASHIRO, D ;
GOSPODAROWICZ, D ;
KAPLAN, SL ;
VANVLIET, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (08) :2216-2220
[35]   SKELETAL UNLOADING IN RAT DECREASES PROLIFERATION OF RAT BONE AND MARROW-DERIVED OSTEOBLASTIC CELLS [J].
MACHWATE, M ;
ZERATH, E ;
HOLY, X ;
HOTT, M ;
MODROWSKI, D ;
MALOUVIER, A ;
MARIE, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (05) :E790-E799
[36]   LOW SERUM SOMATOMEDIN-C IN INSULIN-DEPENDENT DIABETES - EVIDENCE FOR A POSTRECEPTOR MECHANISM [J].
MAES, M ;
UNDERWOOD, LE ;
KETELSLEGERS, JM .
ENDOCRINOLOGY, 1986, 118 (01) :377-382
[37]  
MARTIN JL, 1992, GROWTH REGULAT, V2, P88
[38]  
MARTIN RJ, 1989, INT J OBESITY, V13, P327
[39]   INTEGRATED CONCENTRATIONS OF GROWTH-HORMONE, INSULIN, C-PEPTIDE AND PROLACTIN IN HUMAN OBESITY [J].
MEISTAS, MT ;
FOSTER, GV ;
MARGOLIS, S ;
KOWARSKI, AA .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1982, 31 (12) :1224-1228
[40]  
MILLARD WJ, 1991, GROWTH DEVELOP AGING, V55, P91