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      Prenatal cortisol exposure impairs adrenal function but not glucose metabolism in adult sheep

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          Abstract

          Adverse environmental conditions before birth are known to programme adult metabolic and endocrine phenotypes in several species. However, whether increments in fetal cortisol concentrations of the magnitude commonly seen in these conditions can cause developmental programming remains unknown. Thus, this study investigated the outcome of physiological increases in fetal cortisol concentrations on glucose–insulin dynamics and pituitary–adrenal function in adult sheep. Compared with saline treatment, intravenous fetal cortisol infusion for 5 days in late gestation did not affect birthweight but increased lamb body weight at 1–2 weeks after birth. Adult glucose dynamics, insulin sensitivity and insulin secretion were unaffected by prenatal cortisol overexposure, assessed by glucose tolerance tests, hyperinsulinaemic–euglycaemic clamps and acute insulin administration. In contrast, prenatal cortisol infusion induced adrenal hypo-responsiveness in adulthood with significantly reduced cortisol responses to insulin-induced hypoglycaemia and exogenous adrenocorticotropic hormone (ACTH) administration relative to saline treatment. The area of adrenal cortex expressed as a percentage of the total cross-sectional area of the adult adrenal gland was also lower after prenatal cortisol than saline infusion. In adulthood, basal circulating ACTH but not cortisol concentrations were significantly higher in the cortisol than saline-treated group. The results show that cortisol overexposure before birth programmes pituitary–adrenal development with consequences for adult stress responses. Physiological variations in cortisol concentrations before birth may, therefore, have an important role in determining adult phenotypical diversity and adaptability to environmental challenges.

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          Most cited references62

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          Effect of in utero and early-life conditions on adult health and disease.

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            Early developmental conditioning of later health and disease: physiology or pathophysiology?

            Extensive experimental animal studies and epidemiological observations have shown that environmental influences during early development affect the risk of later pathophysiological processes associated with chronic, especially noncommunicable, disease (NCD). This field is recognized as the developmental origins of health and disease (DOHaD). We discuss the extent to which DOHaD represents the result of the physiological processes of developmental plasticity, which may have potential adverse consequences in terms of NCD risk later, or whether it is the manifestation of pathophysiological processes acting in early life but only becoming apparent as disease later. We argue that the evidence suggests the former, through the operation of conditioning processes induced across the normal range of developmental environments, and we summarize current knowledge of the physiological processes involved. The adaptive pathway to later risk accords with current concepts in evolutionary developmental biology, especially those concerning parental effects. Outside the normal range, effects on development can result in nonadaptive processes, and we review their underlying mechanisms and consequences. New concepts concerning the underlying epigenetic and other mechanisms involved in both disruptive and nondisruptive pathways to disease are reviewed, including the evidence for transgenerational passage of risk from both maternal and paternal lines. These concepts have wider implications for understanding the causes and possible prevention of NCDs such as type 2 diabetes and cardiovascular disease, for broader social policy and for the increasing attention paid in public health to the lifecourse approach to NCD prevention. Copyright © 2014 the American Physiological Society.
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              The thrifty phenotype hypothesis

                Author and article information

                Journal
                J Endocrinol
                J Endocrinol
                JOE
                The Journal of Endocrinology
                Bioscientifica Ltd (Bristol )
                0022-0795
                1479-6805
                29 January 2024
                18 December 2023
                01 March 2024
                : 260
                : 3
                : e230326
                Affiliations
                [1 ]Department of Physiology , Development and Neuroscience, University of Cambridge, Downing Street, Cambridge, UK
                [2 ]The Ritchie Centre , Hudson Institute of Medical Research, Clayton, Australia
                [3 ]MRC Metabolic Diseases Unit , Mouse Biochemistry Laboratory, Cambridge Biomedical Campus, Cambridge, UK
                [4 ]Endocrine Laboratory , Blood Sciences, Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge, UK
                [5 ]Department of Biological and Medical Sciences , Oxford Brookes University, Oxford, UK
                Author notes
                Correspondence should be addressed to A L Fowden: alf1000@ 123456cam.ac.uk
                Author information
                http://orcid.org/0000-0002-3384-4467
                Article
                JOE-23-0326
                10.1530/JOE-23-0326
                10895281
                38109257
                5fdc8a53-62fe-4fa9-9d67-930a67b41cab
                © the author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 17 October 2023
                : 18 December 2023
                Funding
                Funded by: Biotechnology and Biological Sciences Research Council, doi http://dx.doi.org/10.13039/501100000268;
                Funded by: University of Cambridge, doi http://dx.doi.org/10.13039/501100000735;
                Categories
                Research

                Endocrinology & Diabetes
                cortisol,glucose–insulin dynamics,pituitary–adrenal function,developmental programming

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