Forced catch-up growth after fetal protein restriction alters the adipose tissue gene expression program leading to obesity in adult mice

被引:103
作者
Bol, V. V. [1 ]
Delattre, A-I. [2 ]
Reusens, B. [1 ]
Raes, M. [2 ]
Remacle, C. [1 ]
机构
[1] Catholic Univ Louvain, Cell Biol Lab, Inst Life Sci, B-1348 Louvain, Belgium
[2] Fac Univ Notre Dame Paix, Res Unit Cell Biol Namur, B-5000 Namur, Belgium
关键词
fetal programming; adipokines; leptin; DEPENDENT DIABETES-MELLITUS; GESTATIONAL-AGE; METABOLIC SYNDROME; BIRTH-WEIGHT; INSULIN; ENDOCRINE; CHILDHOOD; ORIGINS; LEPTIN; HYPERTENSION;
D O I
10.1152/ajpregu.90497.2008
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Bol VV, Delattre AI, Reusens B, Raes M, Remacle C. Forced catch-up growth after fetal protein restriction alters the adipose tissue gene expression program leading to obesity in adult mice. Am J Physiol Regul Integr Comp Physiol 297: R291-R299, 2009. First published May 20, 2009; doi:10.1152/ajpregu.90497.2008.-A mismatch between fetal and postnatal environment can permanently alter the body structure and physiology and therefore contribute later to obesity and related disorders, as revealed by epidemiological studies. Early programming of adipose tissue might be central in this observation. Moreover, adipose tissue secretes adipokines that provide a molecular link between obesity and its related disorders. Therefore, our aim was to investigate whether a protein restriction during fetal life, followed by catch-up growth could lead to obesity in 9-mo-old male mice and could alter the adipose tissue gene expression profile. Dams were fed a low-protein (LP) or an isocaloric control (C) diet during gestation. Postnatal catch-up growth was induced in LP offspring by feeding dams with control diet and by culling LP litters to four pups instead of eight in the C group. At weaning, male mice were fed by lab chow alone (C) or supplemented with a hypercaloric diet (HC), to induce obesity (C-C, C-HC, LP-C, and LP-HC groups). At 9 mo, LP offspring featured increased relative fat mass, hyperglycemia, hypercholesterolemia, and hyperleptinemia. Using a microarray designed to study the expression of 89 genes involved in adipose tissue differentiation/function, we demonstrated that the expression profile of several genes were dependent upon the maternal diet. Among the diverse genes showing altered expression, we could identify genes encoding several enzymes involved in lipid metabolism. These results indicated that offspring submitted to early mismatched nutrition exhibited alterations in adipose tissue gene expression that probably increases their susceptibility to overweight when challenged after weaning with a HC diet.
引用
收藏
页码:R291 / R299
页数:9
相关论文
共 58 条
[1]
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
[2]
Comparative aspects of lipid metabolism: Impact on contemporary research and use of animal models [J].
Bergen, WG ;
Mersmann, HJ .
JOURNAL OF NUTRITION, 2005, 135 (11) :2499-2502
[3]
Prenatal protein restriction does not affect the proliferation and differentiation of rat preadipocytes [J].
Bieswal, F ;
Hay, SM ;
McKinnon, C ;
Reusens, B ;
Cuignet, M ;
Rees, WD ;
Remacle, C .
JOURNAL OF NUTRITION, 2004, 134 (06) :1493-1499
[4]
The importance of catch-up growth after early malnutrition for the programming of obesity in male rat [J].
Bieswal, Florence ;
Ahn, Marie-Therese ;
Reusens, Brigitte ;
Holvoet, Paul ;
Raes, Martine ;
Rees, William D. ;
Remacle, Claude .
OBESITY, 2006, 14 (08) :1330-1343
[5]
Formation of projection pathways from the arcuate nucleus of the hypothalamus to hypothalamic regions implicated in the neural control of feeding behavior in mice [J].
Bouret, SG ;
Draper, SJ ;
Simerly, RB .
JOURNAL OF NEUROSCIENCE, 2004, 24 (11) :2797-2805
[6]
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]
Low birthweight and adult insulin resistance: the "catch-up growth" hypothesis [J].
Cianfarani, S ;
Germani, D ;
Branca, F .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1999, 81 (01) :F71-F73
[8]
Physiological and nutritional regulation of enzymes of triacylglycerol synthesis [J].
Coleman, RA ;
Lewin, TM ;
Muoio, DM .
ANNUAL REVIEW OF NUTRITION, 2000, 20 :77-103
[9]
Sugars, insulin sensitivity, and the postprandial state [J].
Daly, M .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2003, 78 (04) :865S-872S
[10]
de Longueville F, 2004, COMB CHEM HIGH T SCR, V7, P207