Maternal and postweaning diet interaction alters hypothalamic gene expression and modulates response to a high-fat diet in male offspring

被引:90
作者
Page, Kathleen C. [1 ]
Malik, Raleigh E. [1 ]
Ripple, Joshua A. [1 ]
Anday, Endla K. [2 ]
机构
[1] Bucknell Univ, Dept Biol, Lewisburg, PA 17837 USA
[2] Drexel Univ, Coll Med, Philadelphia, PA 19104 USA
关键词
development; hypothalamus; obesity; CATCH-UP GROWTH; LEPTIN RECEPTOR; NEUROPEPTIDE-Y; RAT HYPOTHALAMUS; INDUCED OBESITY; FETAL ORIGINS; INDUCED ANOREXIA; ARCUATE NUCLEUS; INSULIN; 3-KINASE;
D O I
10.1152/ajpregu.90585.2008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Page KC, Malik RE, Ripple JA, Anday EK. Maternal and postweaning diet interaction alters hypothalamic gene expression and modulates response to a high-fat diet in male offspring. Am J Physiol Regul Integr Comp Physiol 297: R1049-R1057, 2009. First published August 5, 2009; doi: 10.1152/ajpregu.90585.2008.-Epidemiological data and results from animal studies indicate that imbalances in maternal nutrition impact the expression of metabolic disorders in the offspring. We tested the hypothesis that consumption of excess saturated fats during pregnancy and lactation contributes to adult metabolic dysfunction and that these disturbances can be further influenced by the postweaning diet. Adult male offspring from chow-fed dams were compared with males from dams fed a diet high in saturated fat (45 kcal/100 kcal) before mating, pregnancy, and lactation. Offspring were weaned to a standard chow diet or high fat diet. Animals were killed at 120 days after a 24-h fast. Body weight, energy intake, fat deposition, serum leptin, and insulin were significantly higher in offspring from control or high-fat dams if fed a high-fat diet from weaning to adulthood. Only fat-fed offspring from fat-fed dams were hyperglycemic. Leptin receptor, proopiomelanocortin, and neuropeptide Y (NPY) were also significantly increased in offspring exposed to excess saturated fat during gestation and into adulthood, whereas NPY1 receptor was downregulated. Signal transducer and activator of transcription 3 mRNA level was significantly higher in offspring from high-fat-fed dams compared with controls; however, no change was detected in cocaine and amphetamine-regulated transcript or suppressor of cytokine signaling 3. An increase in agouti-related protein expression did not reach significance. A significant reduction in phosphatidylinositol 3-kinase regulatory subunit (p85 alpha) coupled to an upregulation of protein kinase B was observed in offspring from high-fat-fed dams transitioned to chow food, whereas p85 alpha expression was significantly increased in high-fat offspring weaned to the high-fat diet. These data support the hypothesis that early life exposure to excess fat is associated with changes in hypothalamic regulation of body weight and energy homeostasis and that postweaning diet influences development of metabolic dysfunction and obesity.
引用
收藏
页码:R1049 / R1057
页数:9
相关论文
共 43 条
[1]   Fetal origins of adult disease:: strength of effects and biological basis [J].
Barker, DJP ;
Eriksson, JG ;
Forsén, T ;
Osmond, C .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2002, 31 (06) :1235-1239
[2]   Trophic action of leptin on hypothalamic neurons that regulate feeding [J].
Bouret, SG ;
Draper, SJ ;
Simerly, RB .
SCIENCE, 2004, 304 (5667) :108-110
[3]   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
[4]   The phosphoinositide 3-kinase pathway [J].
Cantley, LC .
SCIENCE, 2002, 296 (5573) :1655-1657
[5]   Cross-talk between the insulin and leptin signaling systems in rat hypothalamus [J].
Carvalheira, JBC ;
Torsoni, MA ;
Ueno, M ;
Amaral, ME ;
Araújo, EP ;
Velloso, LA ;
Gontijo, JAR ;
Saad, MJA .
OBESITY RESEARCH, 2005, 13 (01) :48-57
[6]   Maternal High-Fat Diet and Fetal Programming: Increased Proliferation of Hypothalamic Peptide-Producing Neurons That Increase Risk for Overeating and Obesity [J].
Chang, Guo-Qing ;
Gaysinskaya, Valeriya ;
Karatayev, Olga ;
Leibowitz, Sarah F. .
JOURNAL OF NEUROSCIENCE, 2008, 28 (46) :12107-12119
[7]   A role for suppressed thermogenesis favoring catch-up fat in the pathophysiology of catch-up growth [J].
Crescenzo, R ;
Samec, S ;
Antic, V ;
Rohner-Jeanrenaud, F ;
Seydoux, J ;
Montani, JP ;
Dulloo, AG .
DIABETES, 2003, 52 (05) :1090-1097
[8]   Two defects contribute to hypothalamic leptin resistance in mice with diet-induced obesity [J].
El-Haschimi, K ;
Pierroz, DD ;
Hileman, SM ;
Bjorbæk, C ;
Flier, JS .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (12) :1827-1832
[9]   Leptin differentially regulates NPY and POMC neurons projecting to the lateral hypothalamic area [J].
Elias, CF ;
Aschkenasi, C ;
Lee, C ;
Kelly, J ;
Ahima, RS ;
Bjorbæk, C ;
Flier, JS ;
Saper, CB ;
Elmquist, JK .
NEURON, 1999, 23 (04) :775-786
[10]   Long-term consequences of maternal high-fat feeding on hypothalamic leptin sensitivity and diet-induced obesity in the offspring [J].
Ferezou-Viala, Jacqueline ;
Roy, Anne-France ;
Serougne, Colette ;
Gripois, Daniel ;
Parquet, Michel ;
Bailleux, Virginie ;
Gertler, Arieh ;
Delplanque, Bernadette ;
Djiane, Jean ;
Riottot, Michel ;
Taouis, Mohammed .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2007, 293 (03) :R1056-R1062