The theory of developmental programming suggests that diseases such as the metabolic syndrome may be 'programmed' by exposure to adverse stimuli during early development. The developmental programming literature encompasses the study of a wide range of suboptimal intrauterine environments in a variety of species and correlates these with diverse phenotypic outcomes in the offspring. At a molecular level, a large number of variables have been measured and suggested as the basis of the programmed phenotype. The range of both dependent and independent variables studied often makes the developmental programming literature complex to interpret and the drawing of definitive conclusions difficult. A common, though under-explored, theme of many developmental programming models is a sex difference in offspring outcomes. This holds true across a range of interventions, including dietary, hypoxic, and surgical models. The molecular and phenotypic outcomes of adverse in utero conditions are often more prominent in male than female offspring, although there is little consideration given to the basis for this observation in most studies. We review the evidence that maternal energy investment in male and female conceptuses may not be equal and may be environment dependent. It is suggested that male and female development could be viewed as separate processes from the time of conception, with differences in both timing and outcomes. Reproduction (2013) 145 R1-R13
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Univ Mississippi, Med Ctr, Dept Pediat, Jackson, MS 39216 USA
Univ Mississippi, Med Ctr, Womens Hlth Res Ctr, Jackson, MS 39216 USAUniv Mississippi, Med Ctr, Dept Pediat, Jackson, MS 39216 USA
Ojeda, N. B.
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Intapad, S.
Alexander, B. T.
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Univ Mississippi, Med Ctr, Womens Hlth Res Ctr, Jackson, MS 39216 USA
Univ Mississippi, Med Ctr, Dept Physiol & Biophys, Jackson, MS 39216 USAUniv Mississippi, Med Ctr, Dept Pediat, Jackson, MS 39216 USA
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Univ Cambridge, Metab Res Labs, Level 4,Box 289, Cambridge CB2 0QQ, England
Addenbrookes Hosp, MRC Metab Dis Unit, Wellcome Trust MRC Inst Metab Sci, Addenbrookes Treatment Ctr, Level 4,Box 289, Cambridge CB2 0QQ, EnglandUniv Cambridge, Metab Res Labs, Level 4,Box 289, Cambridge CB2 0QQ, England
Dearden, Laura
Bouret, Sebastien G.
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Univ Southern Calif, Childrens Hosp Los Angeles, Dev Neurosci Program, Saban Res Inst, Los Angeles, CA 90027 USA
Univ Southern Calif, Childrens Hosp Los Angeles, Diabet & Obes Program, Ctr Endocrinol Diabet & Metab, Los Angeles, CA 90027 USA
Univ Lille 2, Jean Pierre Aubert Res Ctr, INSERM, U1172, F-59045 Lille, FranceUniv Cambridge, Metab Res Labs, Level 4,Box 289, Cambridge CB2 0QQ, England
Bouret, Sebastien G.
Ozanne, Susan E.
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Univ Cambridge, Metab Res Labs, Level 4,Box 289, Cambridge CB2 0QQ, England
Addenbrookes Hosp, MRC Metab Dis Unit, Wellcome Trust MRC Inst Metab Sci, Addenbrookes Treatment Ctr, Level 4,Box 289, Cambridge CB2 0QQ, EnglandUniv Cambridge, Metab Res Labs, Level 4,Box 289, Cambridge CB2 0QQ, England
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Dominican Univ, Dept Psychol, River Forest, IL 60305 USADominican Univ, Dept Psychol, River Forest, IL 60305 USA
Krafnick, Anthony J.
Evans, Tanya M.
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Univ Virginia, Ctr Adv Study Teaching & Learning, Curry Sch Educ & Human Dev, Charlottesville, VA USADominican Univ, Dept Psychol, River Forest, IL 60305 USA