Literature DB >> 16899555

Effect of periconceptional undernutrition and gender on hypothalamic-pituitary-adrenal axis function in young adult sheep.

D S Gardner1, B W M Van Bon, J Dandrea, P J Goddard, S F May, V Wilson, T Stephenson, M E Symonds.   

Abstract

Glucocorticoids are proposed to act as intermediary factors that transcribe the developmental programming sequelae of maternal nutrient restriction (NR). Periconceptional under-nutrition of sheep markedly activates fetal hypothalamic-pituitary-adrenal (HPA) axis activity leading to preterm birth, while transient undernutrition during late gestation in sheep programs adult HPA axis function. To date, no study has examined resting or stimulated HPA axis function in young adult offspring following a periconceptional nutritional challenge. In the present study, 20 ewes were either periconceptionally undernourished (50% metabolisable energy requirements from days 1 to 30 gestation; NR, n = 8) or fed to control levels (100% requirement; controls, n = 12) to term (147 days gestation). Ewes were blood sampled remotely at 2 and 30 days using automated blood sampling equipment. Thereafter, offspring (controls, n = 6/6 males/females; NR, n = 4/4 males/females) were reared to 1 year of age and on separate days received either an i.v. corticotrophin-releasing hormone (CRH; 0.5 microg/kg) and vasopressin (AVP; 0.1 microg/kg) challenge or a synthetic ACTH i.v. bolus (Synacthen; 1.25 microg/kg), and blood samples were taken (manually and remotely) at appropriate intervals for measurement of plasma ACTH and cortisol accordingly. Resting plasma cortisol, assessed remotely, was similar in ewes during undernutrition (control 18.3 +/- 1.4 vs NR 23.4 +/- 1.9 nmol/l) and in offspring at 4 months of age (control male 17.6 +/- 2.9; control female 17.2 +/- 0.4, NR male 16.5 +/- 3.1, NR female 21.7 +/- 4.0 nmol/l). At 12 months of age, however, resting plasma cortisol was significantly increased in NR females (control male 28.0 +/- 1.5, control female 32.9 +/- 9, NR male 32 +/- 7, NR female 53 +/- 10 nmol/l, F 5.7, P = 0.02) despite no difference in plasma ACTH concentration. There was an interaction between nutritional group and gender for both the pituitary and adrenal responses to CRH and AVP, i.e. for controls, females exhibited increased plasma ACTH or cortisol relative to males but for NR this trend was either not present or reversed. The adrenocortical response to synthetic ACTH was gender-dependent only, being greater in female offspring. Combined CRH and AVP provoked a transient hypertension and marked bradycardia in all animals, irrespective of dietary group or gender and could be effectively reproduced by an AVP bolus alone. In conclusion, the present study has shown that periconceptional undernutrition of sheep has only a minor influence on HPA axis function in their young adult offspring when considered alongside the effect of gender per se.

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Year:  2006        PMID: 16899555     DOI: 10.1677/joe.1.06751

Source DB:  PubMed          Journal:  J Endocrinol        ISSN: 0022-0795            Impact factor:   4.286


  12 in total

1.  The impact of maternal overnutrition and obesity on hypothalamic-pituitary-adrenal axis response of offspring to stress.

Authors:  N M Long; P W Nathanielsz; S P Ford
Journal:  Domest Anim Endocrinol       Date:  2012-01-11       Impact factor: 2.290

2.  Maternal undernutrition programs offspring adrenal expression of steroidogenic enzymes.

Authors:  Naseem M Khorram; Thomas R Magee; Chen Wang; Mina Desai; Michael Ross; Omid Khorram
Journal:  Reprod Sci       Date:  2011-05-12       Impact factor: 3.060

Review 3.  The long-term effects of prenatal development on growth and metabolism.

Authors:  Keith M Godfrey; Hazel M Inskip; Mark A Hanson
Journal:  Semin Reprod Med       Date:  2011-07-18       Impact factor: 1.303

4.  Sex- and age-specific effects of nutrition in early gestation and early postnatal life on hypothalamo-pituitary-adrenal axis and sympathoadrenal function in adult sheep.

Authors:  Kirsten R Poore; Julian P Boullin; Jane K Cleal; James P Newman; David E Noakes; Mark A Hanson; Lucy R Green
Journal:  J Physiol       Date:  2010-04-26       Impact factor: 5.182

Review 5.  Blastocyst environment and its influence on offspring cardiovascular health: the heart of the matter.

Authors:  Adam J Watkins; Tom P Fleming
Journal:  J Anat       Date:  2009-02-09       Impact factor: 2.610

6.  Maternal dietary restriction during the periconceptional period in normal-weight or obese ewes results in adrenocortical hypertrophy, an up-regulation of the JAK/STAT and down-regulation of the IGF1R signaling pathways in the adrenal of the postnatal lamb.

Authors:  Song Zhang; Janna L Morrison; Amreet Gill; Leewen Rattanatray; Severence M MacLaughlin; David Kleemann; Simon K Walker; I Caroline McMillen
Journal:  Endocrinology       Date:  2013-10-09       Impact factor: 4.736

Review 7.  The periconceptional environment and cardiovascular disease: does in vitro embryo culture and transfer influence cardiovascular development and health?

Authors:  Monalisa Padhee; Song Zhang; Shervi Lie; Kimberley C Wang; Kimberley J Botting; I Caroline McMillen; Severence M MacLaughlin; Janna L Morrison
Journal:  Nutrients       Date:  2015-02-18       Impact factor: 5.717

8.  Maternal parity and its effect on adipose tissue deposition and endocrine sensitivity in the postnatal sheep.

Authors:  M A Hyatt; D H Keisler; H Budge; M E Symonds
Journal:  J Endocrinol       Date:  2009-11-24       Impact factor: 4.286

9.  Maternal nutrient restriction between early and midgestation and its impact upon appetite regulation after juvenile obesity.

Authors:  S P Sébert; M A Hyatt; L L Y Chan; N Patel; R C Bell; D Keisler; T Stephenson; H Budge; M E Symonds; D S Gardner
Journal:  Endocrinology       Date:  2008-09-25       Impact factor: 4.736

Review 10.  Periconception weight loss: common sense for mothers, but what about for babies?

Authors:  Kristine Matusiak; Helen L Barrett; Leonie K Callaway; Marloes Dekker Nitert
Journal:  J Obes       Date:  2014-04-02
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