Dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancy

Objective: Maternal and environmental factors control the epigenetic fetal programming of the embryo, thereby defining the susceptibility for metabolic or endocrine disorders in the offspring. Pharmacological interventions required as a consequence of gestational problems, e.g. hypertension, can pot...

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Main Authors: Rebecca Oelkrug, Beate Herrmann, Cathleen Geissler, Lisbeth Harder, Christiane Koch, Hendrik Lehnert, Henrik Oster, Henriette Kirchner, Jens Mittag
Format: Article
Language:English
Published: Elsevier 2017-10-01
Series:Molecular Metabolism
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2212877817303678
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spelling doaj-1ac8db61e2f54cfbbe627e268a31c5142020-11-24T21:36:02ZengElsevierMolecular Metabolism2212-87782017-10-016101126113610.1016/j.molmet.2017.06.016Dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancyRebecca Oelkrug0Beate Herrmann1Cathleen Geissler2Lisbeth Harder3Christiane Koch4Hendrik Lehnert5Henrik Oster6Henriette Kirchner7Jens Mittag8Department of Molecular Endocrinology/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyDepartment of Molecular Endocrinology/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyDepartment of Epigenetics & Metabolism/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyDepartment of Molecular Endocrinology/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyDepartment of Chronophysiology/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyDepartment of Experimental Neuroendocrinology/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyDepartment of Chronophysiology/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyDepartment of Epigenetics & Metabolism/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyDepartment of Molecular Endocrinology/CBBM, University of Lübeck, Ratzeburger Allee 160, 23562 Lübeck, GermanyObjective: Maternal and environmental factors control the epigenetic fetal programming of the embryo, thereby defining the susceptibility for metabolic or endocrine disorders in the offspring. Pharmacological interventions required as a consequence of gestational problems, e.g. hypertension, can potentially interfere with correct fetal programming. As epigenetic alterations are usually only revealed later in life and not detected in studies focusing on early perinatal outcomes, little is known about the long-term epigenetic effects of gestational drug treatments. We sought to test the consequences of maternal α1-adrenergic antagonism during pregnancy, which can occur e.g. during hypertension treatment, for the endocrine and metabolic phenotype of the offspring. Methods: We treated C57BL/6NCrl female mice with the α1-adrenergic antagonist prazosin during pregnancy and analyzed the male and female offspring for endocrine and metabolic abnormalities. Results: Our data revealed that maternal α1-adrenergic blockade caused dwarfism, elevated body temperature, and insulin resistance in male offspring, accompanied by reduced IGF-1 serum concentrations as the result of reduced hepatic growth hormone receptor (Ghr) expression. We subsequently identified increased CpG DNA methylation at the transcriptional start site of the alternative Ghr promotor caused by the maternal treatment, which showed a strong inverse correlation to hepatic Ghr expression. Conclusions: Our results demonstrate that maternal α1-adrenergic blockade can constitute an epigenetic cause for dwarfism and insulin resistance. The findings are of immediate clinical relevance as combined α/β-adrenergic blockers are first-line treatment of maternal hypertension.http://www.sciencedirect.com/science/article/pii/S2212877817303678Brown fatPregnancyThermogenesisFeverInsulin resistanceIGF-1
collection DOAJ
language English
format Article
sources DOAJ
author Rebecca Oelkrug
Beate Herrmann
Cathleen Geissler
Lisbeth Harder
Christiane Koch
Hendrik Lehnert
Henrik Oster
Henriette Kirchner
Jens Mittag
spellingShingle Rebecca Oelkrug
Beate Herrmann
Cathleen Geissler
Lisbeth Harder
Christiane Koch
Hendrik Lehnert
Henrik Oster
Henriette Kirchner
Jens Mittag
Dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancy
Molecular Metabolism
Brown fat
Pregnancy
Thermogenesis
Fever
Insulin resistance
IGF-1
author_facet Rebecca Oelkrug
Beate Herrmann
Cathleen Geissler
Lisbeth Harder
Christiane Koch
Hendrik Lehnert
Henrik Oster
Henriette Kirchner
Jens Mittag
author_sort Rebecca Oelkrug
title Dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancy
title_short Dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancy
title_full Dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancy
title_fullStr Dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancy
title_full_unstemmed Dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancy
title_sort dwarfism and insulin resistance in male offspring caused by α1-adrenergic antagonism during pregnancy
publisher Elsevier
series Molecular Metabolism
issn 2212-8778
publishDate 2017-10-01
description Objective: Maternal and environmental factors control the epigenetic fetal programming of the embryo, thereby defining the susceptibility for metabolic or endocrine disorders in the offspring. Pharmacological interventions required as a consequence of gestational problems, e.g. hypertension, can potentially interfere with correct fetal programming. As epigenetic alterations are usually only revealed later in life and not detected in studies focusing on early perinatal outcomes, little is known about the long-term epigenetic effects of gestational drug treatments. We sought to test the consequences of maternal α1-adrenergic antagonism during pregnancy, which can occur e.g. during hypertension treatment, for the endocrine and metabolic phenotype of the offspring. Methods: We treated C57BL/6NCrl female mice with the α1-adrenergic antagonist prazosin during pregnancy and analyzed the male and female offspring for endocrine and metabolic abnormalities. Results: Our data revealed that maternal α1-adrenergic blockade caused dwarfism, elevated body temperature, and insulin resistance in male offspring, accompanied by reduced IGF-1 serum concentrations as the result of reduced hepatic growth hormone receptor (Ghr) expression. We subsequently identified increased CpG DNA methylation at the transcriptional start site of the alternative Ghr promotor caused by the maternal treatment, which showed a strong inverse correlation to hepatic Ghr expression. Conclusions: Our results demonstrate that maternal α1-adrenergic blockade can constitute an epigenetic cause for dwarfism and insulin resistance. The findings are of immediate clinical relevance as combined α/β-adrenergic blockers are first-line treatment of maternal hypertension.
topic Brown fat
Pregnancy
Thermogenesis
Fever
Insulin resistance
IGF-1
url http://www.sciencedirect.com/science/article/pii/S2212877817303678
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