Models of fetal growth restriction

被引:46
作者
Schröder, HJ [1 ]
机构
[1] Univ Hamburg, Hosp Eppendorf, Abt Expt Med, Klin & Poliklin Frauenheilkunde & Geburtshilfe, D-20246 Hamburg, Germany
关键词
substrate supply; control mechanisms; gene mutants; fetal growth;
D O I
10.1016/S0301-2115(03)00170-2
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The growth of the fetus is determined by substrate supply mostly for mass accretion and energy gain, and by control systems. Experiments with whole animal models will face the following problems: (1) The fetus. like a three compartmental "Russian doll", is at the end of a long supply chain. There are interactions (e.g. hormones) and partitioning of substrates between the compartments. (2) The fetal organism is growing and differentiating at the same time and not in a steady-state. Experimental results thus depend on gestational age. (3) About 75% of animal experiments on fetal growth restriction have been performed in rats and mice. The possible experimental methods and the results depend on the species which include sheep, pigs, rabbits, guinea pigs, horses and non-human primates. Many experiments have clearly shown that restriction of substrate supply will usually impair fetal growth. Less is known about growth control mechanisms but recent studies in gene mutant mice have opened a new approach to study the effects of systemic and local controlling factors. It appears that insulin-like growth factors and their binding proteins may play an important role for fetal growth. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:S29 / S39
页数:11
相关论文
共 63 条
[1]   HEAT STRESS AND DEVELOPMENT OF CONCEPTUS IN DOMESTIC SHEEP [J].
ALEXANDER, G ;
WILLIAMS, D .
JOURNAL OF AGRICULTURAL SCIENCE, 1971, 76 (FEB) :53-+
[2]  
ALEXANDER G, 1987, J DEV PHYSIOL, V9, P1
[3]  
ALEXANDER G, 1964, J REPROD FERTIL, V7, P307, DOI 10.1530/jrf.0.0070307
[4]  
BAKER J, 1993, CELL, V75, P73, DOI 10.1016/0092-8674(93)90680-O
[5]   FETAL AND INFANT ORIGINS OF CARDIOVASCULAR-DISEASE [J].
BARKER, DJP ;
FALL, CHD .
ARCHIVES OF DISEASE IN CHILDHOOD, 1993, 68 (06) :797-799
[6]   A DIRECT PHYSICAL ASSOCIATION BETWEEN ETS AND AP-1 TRANSCRIPTION FACTORS IN NORMAL HUMAN T-CELLS [J].
BASSUK, AG ;
LEIDEN, JM .
IMMUNITY, 1995, 3 (02) :223-237
[7]  
Bocking A. D., 2001, FETAL GROWTH DEV
[8]  
CARTER AM, 1991, PLACENTA : BASIC RESEARCH FOR CLINICAL APPLICATION, P23
[9]   CURRENT TOPIC - RESTRICTION OF PLACENTAL AND FETAL GROWTH IN THE GUINEA-PIG [J].
CARTER, AM .
PLACENTA, 1993, 14 (02) :125-135
[10]  
CARTER AM, 1994, HDB LAB ANIMAL SCI, V2, P77