Literature DB >> 16554011

Overnourishing pregnant adolescent ewes preserves perirenal fat deposition in their growth-restricted fetuses.

Masatoshi Matsuzaki1, John S Milne, Raymond P Aitken, Jacqueline M Wallace.   

Abstract

Overnourishing the adolescent sheep promotes rapid maternal growth at the expense of the gravid uterus. The growth of the placenta is impaired and results in the premature delivery of low-birthweight lambs. The present study details fetal adipose tissue development in these growth-restricted pregnancies. Singleton pregnancies were established by embryo transfer and, thereafter, adolescent ewes were offered a high (H; n = 12) or moderate (M; n = 14) level of a complete diet until necropsy on Day 131 of gestation. Fetal weight was lower (P < 0.001) in H compared with M groups. High maternal intake preserved brain and perirenal fat weight (P < 0.003), whereas relative weights of the heart, lungs, spleen and liver were unaltered. High nutrient intake resulted in significantly elevated maternal plasma concentrations of insulin, leptin, prolactin and glucose, no significant changes in fetal insulin, leptin or non-esterified fatty acids and attenuated fetal prolactin concentrations. Irrespective of nutritional intake, maternal plasma leptin, prolactin and glucose concentrations were negatively correlated with fetal weight and were positively correlated with fetal perirenal fat proportion (all P < 0.01). The mRNA expression for leptin, prolactin receptor and uncoupling protein (UCP) 1 in fetal perirenal fat was equivalent between groups, but, irrespective of maternal nutrition, UCP1 mRNA levels were negatively correlated with fetal weight (P < 0.01). Thus, overnourishing pregnant adolescent sheep preserves fat deposition in their growth-restricted fetuses, which may have implications for neonatal thermogenesis and for programming of postnatal adiposity.

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Year:  2006        PMID: 16554011     DOI: 10.1071/rd05067

Source DB:  PubMed          Journal:  Reprod Fertil Dev        ISSN: 1031-3613            Impact factor:   2.311


  4 in total

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Authors:  Rita S Strakovsky; Yuan-Xiang Pan
Journal:  Biol Reprod       Date:  2012-03-22       Impact factor: 4.285

2.  Undernutrition and stage of gestation influence fetal adipose tissue gene expression.

Authors:  Jacqueline M Wallace; John S Milne; Raymond P Aitken; Dale A Redmer; Lawrence P Reynolds; Justin S Luther; Graham W Horgan; Clare L Adam
Journal:  J Mol Endocrinol       Date:  2015-04-27       Impact factor: 5.098

3.  Ovine prenatal growth-restriction and sex influence fetal adipose tissue phenotype and impact postnatal lipid metabolism and adiposity in vivo from birth until adulthood.

Authors:  Jacqueline M Wallace; John S Milne; Beth W Aitken; Raymond P Aitken; Clare L Adam
Journal:  PLoS One       Date:  2020-02-14       Impact factor: 3.240

4.  Placental contribution to the origins of sexual dimorphism in health and diseases: sex chromosomes and epigenetics.

Authors:  Anne Gabory; Tessa J Roseboom; Tom Moore; Lorna G Moore; Claudine Junien
Journal:  Biol Sex Differ       Date:  2013-03-21       Impact factor: 5.027

  4 in total

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