Cardiometabolic consequences of maternal hyperandrogenemia in male offspring.


Journal

Physiological reports
ISSN: 2051-817X
Titre abrégé: Physiol Rep
Pays: United States
ID NLM: 101607800

Informations de publication

Date de publication:
07 2021
Historique:
revised: 16 05 2021
received: 26 04 2021
accepted: 30 05 2021
entrez: 21 7 2021
pubmed: 22 7 2021
medline: 25 2 2022
Statut: ppublish

Résumé

Polycystic ovary syndrome (PCOS) in women is characterized by hyperandrogenemia, obesity, and oligo- or anovulation. In addition, women with PCOS are often obese, with insulin resistance, hyperlipidemia, and elevated blood pressure. The cardiometabolic consequences for the male offspring of maternal hyperandrogenemia are unclear. The present studies tested the hypothesis that male offspring of a rat model of PCOS would develop cardiometabolic disease as adults. Female Sprague-Dawley rats (hyperandrogenemic females (HAF)) were implanted with dihydrotestosterone or placebo pellets (controls) at 4 weeks of age, and were mated at 10-12 weeks and allowed to lactate their offspring after birth. Body weights in male HAF offspring were lower at birth than in controls until postnatal day 4, but body weights remained similar between male control and HAF offspring from 2 to 8 weeks of age. However, at 16 weeks of age, body weight was lower in HAF male offspring, but there were no differences in fat mass or lean mass factored for body weight in HAF males, compared to controls. Plasma total cholesterol and HDL and proteinuria were higher and nitrate/nitrite excretion was lower in male HAF offspring than in controls. Baseline blood pressure was similar between HAF male offspring and controls, but HAF offspring had an exaggerated pressor response to angiotensin II infusion. These data suggest that adult sons of PCOS mothers may be at increased risk of cardiometabolic disease.

Identifiants

pubmed: 34288567
doi: 10.14814/phy2.14941
pmc: PMC8290632
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14941

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM104357
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20 GM121334
Pays : United States
Organisme : NHLBI NIH HHS
ID : P01 HL051971
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL066072
Pays : United States

Informations de copyright

© 2021 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society.

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Auteurs

Yvonne Zuchowski (Y)

Department of Cell and Molecular Biology, University of Mississippi Medical Center, Jackson, MS, USA.

Carolina Dalmasso (C)

Department of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, KY, USA.

Noha M Shawky (NM)

Department of Cell and Molecular Biology, University of Mississippi Medical Center, Jackson, MS, USA.
Mississippi Center of Excellence in Perinatal Research, University of Mississippi Medical Center, Jackson, MS, USA.

Jane F Reckelhoff (JF)

Department of Cell and Molecular Biology, University of Mississippi Medical Center, Jackson, MS, USA.
Mississippi Center of Excellence in Perinatal Research, University of Mississippi Medical Center, Jackson, MS, USA.

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Classifications MeSH