Perinatal exposure to low-dose 2,2′,4,4′-tetrabromodiphenyl ether affects growth in rat offspring: What is the role of IGF-1?

被引:68
作者
Suvorov, Alexander [1 ]
Battista, Marie-Claude [2 ]
Takser, Larissa [1 ]
机构
[1] Univ Sherbrooke, Dept Obstet Gynecol, Fac Med & Sci Sante, Sherbrooke, PQ J1H 5N4, Canada
[2] Univ Sherbrooke, Serv Endocrinol, Fac Med & Sci Sante, Sherbrooke, PQ J1H 5N4, Canada
关键词
Low-dose; PBDE; Rat; IGF-1; Endocrine disruptor; Fetal programming; POLYBROMINATED DIPHENYL ETHERS; BROMINATED FLAME RETARDANTS; CLINICAL-RESEARCH CENTER; FACTOR-I; POLYCHLORINATED-BIPHENYLS; POSTMENOPAUSAL WOMEN; HORMONE ACTION; SEX STEROIDS; HYPOGONADOTROPIC HYPOGONADISM; TRANSDERMAL ESTROGEN;
D O I
10.1016/j.tox.2009.03.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Polybrominated diphenyl ethers (PBDEs) area group of environmental contaminants increasing in North America. Few data are available on their growth effects at low doses exposure. Objectives: Our goal in the present study was to evaluate whether low doses of 2,2',4,4'-tetrabromodiphenyl ether (BDE-47), which is the most abundant PBDE found in human samples, affects growth and insulin-like growth factor I (IGF-1). Methods: Dams were exposed either to the vehicle or low doses of BDE-47 (0.002 and 0.2 mg/kg body weight) every fifth day from gestation day 15 to postnatal day (PND) 20 by intravenous injections. Developmental landmarks, body length and body weight of pups were assessed during the first months of life. A glucose tolerance test was performed on PND 40 and 75. Plasma IGF-1 was analysed in trunk blood on PND 27. Results: Exposure to BDE-47 increased plasma IGF-1 and glucose uptake in male but not in female pups. Developmental landmarks were not influenced by BDE-47 while body weight and body length was increased in both exposed male and female offspring during the first months of development. Conclusion: These results demonstrate alteration of growth in rat offspring induced by BDE-47 at levels found in human population. The possible involvement of the growth hormone-IGF axis is discussed. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:126 / 131
页数:6
相关论文
共 50 条
[1]  
ACKLAND F M, 1987, Pediatrician, V14, P226
[2]   GROWTH-HORMONE SECRETORY RATES IN CHILDREN AS ESTIMATED BY DECONVOLUTION ANALYSIS OF 24-H PLASMA-CONCENTRATION PROFILES [J].
ALBERTSSONWIKLAND, K ;
ROSBERG, S ;
LIBRE, E ;
LUNDBERG, LO ;
GROTH, T .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (06) :E809-E814
[3]   INTRAUTERINE PROGRAMMING OF ADULT DISEASE [J].
BARKER, DJP .
MOLECULAR MEDICINE TODAY, 1995, 1 (09) :418-423
[4]   Effects of oral versus transdermal estrogen on the growth hormone/insulin-like growth factor I axis in younger and older postmenopausal women: A clinical research center study [J].
Bellantoni, MF ;
Vittone, J ;
Campfield, AT ;
Bass, KM ;
Harman, SM ;
Blackman, MR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (08) :2848-2853
[5]   Brominated flame retardants: Cause for concern? [J].
Birnbaum, LS ;
Staskal, DF .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2004, 112 (01) :9-17
[6]   Regulation of somatic growth and the somatotropic axis by gonadal steroids: Primary effect on insulin-like growth factor I gene expression and secretion [J].
Borski, RJ ;
Tsai, W ;
DeMottFriberg, R ;
Barkan, AL .
ENDOCRINOLOGY, 1996, 137 (08) :3253-3259
[7]   TERATOGENIC EVALUATION OF A POLYBROMODIPHENYL OXIDE MIXTURE IN NEW-ZEALAND WHITE-RABBITS FOLLOWING ORAL-EXPOSURE [J].
BRESLIN, WJ ;
KIRK, HD ;
ZIMMER, MA .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1989, 12 (01) :151-157
[8]   Gene expression and estrogen sensitivity in rat uterus after developmental exposure to the polybrominated dinheylether PBDE 99 and PCB [J].
Ceecatelli, R ;
Faass, O ;
Schlumpf, M ;
Lichtensteiger, W .
TOXICOLOGY, 2006, 220 (2-3) :104-116
[9]   The regulation of GH secretion by sex steroids [J].
Chowen, JA ;
Frago, LM ;
Argente, J .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2004, 151 :U95-U100
[10]   Brominated flame retardants as possible endocrine disrupters [J].
Darnerud, P. O. .
INTERNATIONAL JOURNAL OF ANDROLOGY, 2008, 31 (02) :152-160