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Paternal low protein diet programs preimplantation embryo gene expression, fetal growth and skeletal development in mice.
Watkins, Adam J; Sirovica, Slobodan; Stokes, Ben; Isaacs, Mark; Addison, Owen; Martin, Richard A.
Afiliação
  • Watkins AJ; Aston Research Centre for Healthy Ageing, School of Life and Health Sciences, Aston University, Birmingham B4 7ET, United Kingdom. Electronic address: a.watkins1@aston.ac.uk.
  • Sirovica S; Aston Institute of Materials Research, School of Engineering and Applies Science and Aston Research Centre for Healthy Ageing, Aston University, Birmingham, B4 7ET, United Kingdom.
  • Stokes B; School of Life and Health Sciences, Aston University, Birmingham B4 7ET, United Kingdom.
  • Isaacs M; European Bioenergy Research Institute, Aston University, Birmingham B4 7ET, United Kingdom.
  • Addison O; Biomaterials Unit, University of Birmingham School of Dentistry, College of Medical and Dental Sciences, Edgbaston, Birmingham B15 2TT, United Kingdom.
  • Martin RA; Aston Institute of Materials Research, School of Engineering and Applies Science and Aston Research Centre for Healthy Ageing, Aston University, Birmingham, B4 7ET, United Kingdom.
Biochim Biophys Acta Mol Basis Dis ; 1863(6): 1371-1381, 2017 06.
Article em En | MEDLINE | ID: mdl-28189722
ABSTRACT
Defining the mechanisms underlying the programming of early life growth is fundamental for improving adult health and wellbeing. While the association between maternal diet, offspring growth and adult disease risk is well-established, the effect of father's diet on offspring development is largely unknown. Therefore, we fed male mice an imbalanced low protein diet (LPD) to determine the impact on post-fertilisation development and fetal growth. We observed that in preimplantation embryos derived from LPD fed males, expression of multiple genes within the central metabolic AMPK pathway was reduced. In late gestation, paternal LPD programmed increased fetal weight, however, placental weight was reduced, resulting in an elevated fetalplacental weight ratio. Analysis of gene expression patterns revealed increased levels of transporters for calcium, amino acids and glucose within LPD placentas. Furthermore, placental expression of the epigenetic regulators Dnmt1 and Dnmt3L were increased also, coinciding with altered patterns of maternal and paternal imprinted genes. More strikingly, we observed fetal skeletal development was perturbed in response to paternal LPD. Here, while offspring of LPD fed males possessed larger skeletons, their bones comprised lower volumes of high mineral density in combination with reduced maturity of bone apatite. These data offer new insight in the underlying programming mechanisms linking poor paternal diet at the time of conception with the development and growth of his offspring.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complicações na Gravidez / Efeitos Tardios da Exposição Pré-Natal / Deficiência de Proteína / Blastocisto / Proteínas Alimentares / Regulação da Expressão Gênica no Desenvolvimento / Epigênese Genética / Desenvolvimento Musculoesquelético / Desenvolvimento Fetal Limite: Animals / Pregnancy Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complicações na Gravidez / Efeitos Tardios da Exposição Pré-Natal / Deficiência de Proteína / Blastocisto / Proteínas Alimentares / Regulação da Expressão Gênica no Desenvolvimento / Epigênese Genética / Desenvolvimento Musculoesquelético / Desenvolvimento Fetal Limite: Animals / Pregnancy Idioma: En Ano de publicação: 2017 Tipo de documento: Article