Fetal growth restriction and consequences for the offspring in animal models

被引:124
作者
Holemans, K [1 ]
Aerts, L [1 ]
Van Assche, FA [1 ]
机构
[1] Katholieke Univ Leuven, Dept Obstet & Gynaecol, Louvain, Belgium
关键词
D O I
10.1016/S1071-5576(03)00134-5
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: In the present review we discuss rat models in which intra-uterine growth restriction is obtained through pharmacological (streptozotocin), dietary (global food restriction, low protein diet), or surgical (uterine artery ligation) manipulation of the maternal animal. METHODS: A MEDLINE search was performed on rat models of intrauterine growth restriction (IUGR), ie, streptozotocin, food restriction, low protein diet, or uterine artery ligation and pregnancy and fetal programming, long-term effects or adult offspring. RESULTS: We address the impact of the different maternal conditions for the fetal and neonatal development. The rat models we concentrate on were all associated with fetal hypoinsulinemia and intrauterine growth restriction. Both fetus and neonate adapt to the altered perinatal environment. Some of these adaptations may predispose the offspring to the development of insulin resistance, cardiovascular disease, obesity, and even overt diabetes in later he. CONCLUSION: The adaptations of the fetal metabolism to the altered intrauterine environment have consequences for the offspring, persisting into adulthood and into the next generation.
引用
收藏
页码:392 / 399
页数:8
相关论文
共 104 条
[1]  
Aerts L, 1979, J Dev Physiol, V1, P219
[2]   RAT FETAL ENDOCRINE PANCREAS IN EXPERIMENTAL DIABETES [J].
AERTS, L ;
VANASSCHE, FA .
JOURNAL OF ENDOCRINOLOGY, 1977, 73 (02) :339-&
[3]   Ultrastructural evaluation of B-cell recruitment in virgin and pregnant offspring of diabetic mothers [J].
Aerts, L ;
Van Assche, FA .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1998, 41 (01) :9-14
[4]   The endocrine pancreas in virgin and pregnant offspring of diabetic pregnant rats [J].
Aerts, L ;
Vercruysse, L ;
VanAssche, FA .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1997, 38 (01) :9-19
[5]   MATERNAL DIABETES DURING PREGNANCY - CONSEQUENCES FOR THE OFFSPRING [J].
AERTS, L ;
HOLEMANS, K ;
VANASSCHE, FA .
DIABETES-METABOLISM REVIEWS, 1990, 6 (03) :147-167
[6]  
AERTS L, 1989, BIOL NEONATE, V56, P31, DOI 10.1159/000242984
[7]   Decreased β-cell proliferation impairs the adaptation to pregnancy in rats malnourished during perinatal life [J].
Avril, I ;
Blondeau, B ;
Duchene, B ;
Czernichow, P ;
Bréant, B .
JOURNAL OF ENDOCRINOLOGY, 2002, 174 (02) :215-223
[8]  
Barker D J, 1997, Rev Reprod, V2, P105, DOI 10.1530/ror.0.0020105
[9]   TYPE 2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS, HYPERTENSION AND HYPERLIPEMIA (SYNDROME-X) - RELATION TO REDUCED FETAL GROWTH [J].
BARKER, DJP ;
HALES, CN ;
FALL, CHD ;
OSMOND, C ;
PHIPPS, K ;
CLARK, PMS .
DIABETOLOGIA, 1993, 36 (01) :62-67
[10]   FETAL ORIGINS OF CORONARY HEART-DISEASE [J].
BARKER, DJP .
BRITISH MEDICAL JOURNAL, 1995, 311 (6998) :171-174