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Effect of maternal dietary energy types on placenta nutrient transporter gene expressions and intrauterine fetal growth in rats.

AbstractOBJECTIVE:
The objectives of this study were to investigate the effects of maternal dietary energy types on the mRNA expressions of the placental nutrient transporter and intrauterine fetal growth and to examine whether altered intrauterine fetal growth could be associated with different gene expressions relating to fetal energy metabolism and DNA methylation.
METHODS:
Seventy-two 3-mo-old rats were allocated to one of four groups: low fat/low fiber (L-L), low fat/high fiber, high fat/low fiber (H-L), or high fat/high fiber. Rats were fed the treatment diets 4 wk before mating and continued in pregnancy until sample collections were obtained on days 13.5 and 17.5 of pregnancy.
RESULTS:
The fetal weight in the L-L group was significantly lower than that in the H-L group (P < 0.05). The placental nutrient transporter mRNA expressions of glucose transporter-3 (Slc2a3) and cationic amino acid transporter-1 (Slc7a1) in the L-L group with a decreased fetal weight were downregulated compared with that in the H-L group with an increased fetal weight. However, placental Slc2a1 and the system A amino acid transporter gene Slc38a4 mRNA expressions were adaptively upregulated by the L-L diet with a decreased fetal weight (P < 0.05). For the placental imprinted gene Igf-2 and H19 expressions, lower Igf-2 and higher H19 expressions were associated with the decreased fetal growth in the L-L group compared with the H-L group with an increased fetal weight. Different fetal growth was associated with different DNA methyltransferase-1 and methyltransferase-3a expressions (P > 0.05) and energy metabolism-related genes.
CONCLUSION:
Collectively, these results demonstrated that intrauterine fetal growth could be affected by different energy intake types through placenta nutrient transporter gene expressions, and different fetal growths were associated with altered fetal genes related to DNA methylation and energy metabolism.
AuthorsYan Lin, Yong Zhuo, Zheng-feng Fang, Lian-qiang Che, De Wu
JournalNutrition (Burbank, Los Angeles County, Calif.) (Nutrition) Vol. 28 Issue 10 Pg. 1037-43 (Oct 2012) ISSN: 1873-1244 [Electronic] United States
PMID22607972 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Elsevier Inc. All rights reserved.
Chemical References
  • Amino Acid Transport Systems
  • Dietary Fats
  • Dietary Fiber
  • Glucose Transporter Type 1
  • Glucose Transporter Type 3
  • H19 long non-coding RNA
  • RNA, Long Noncoding
  • RNA, Messenger
  • Insulin-Like Growth Factor II
Topics
  • Amino Acid Transport Systems (genetics, metabolism)
  • Animals
  • Biological Transport (drug effects, genetics)
  • DNA Methylation
  • Diet, Fat-Restricted (adverse effects)
  • Diet, High-Fat
  • Dietary Fats (pharmacology)
  • Dietary Fiber (pharmacology)
  • Energy Metabolism (genetics)
  • Female
  • Fetal Growth Retardation (etiology, genetics, metabolism)
  • Fetal Weight (drug effects, genetics)
  • Gene Expression (drug effects)
  • Gene Expression Regulation, Developmental (drug effects)
  • Glucose Transporter Type 1 (genetics, metabolism)
  • Glucose Transporter Type 3 (genetics, metabolism)
  • Insulin-Like Growth Factor II (genetics, metabolism)
  • Placenta (metabolism)
  • Pregnancy
  • Prenatal Nutritional Physiological Phenomena (genetics)
  • RNA, Long Noncoding (genetics, metabolism)
  • RNA, Messenger (metabolism)
  • Rats, Sprague-Dawley

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