Literature DB >> 35622533

Metabolic signatures of pregnancy-induced cardiac growth.

Kyle L Fulghum1, Juliette B Smith1, Julia Chariker2, Lauren F Garrett1, Kenneth R Brittian1, Pawel K Lorkiewicz1, Lindsey A McNally1, Shizuka Uchida3, Steven P Jones1, Bradford G Hill1, Helen E Collins1.   

Abstract

The goal of this study was to develop an atlas of the metabolic, transcriptional, and proteomic changes that occur with pregnancy in the maternal heart. Timed pregnancy studies in FVB/NJ mice revealed a significant increase in heart size by day 8 of pregnancy (midpregnancy; MP), which was sustained throughout the rest of the term compared with nonpregnant control mice. Cardiac hypertrophy and myocyte cross-sectional area were highest 7 days after birth (postbirth; PB) and were associated with significant increases in end-diastolic and end-systolic left ventricular volumes and higher cardiac output. Metabolomics analyses revealed that by day 16 of pregnancy (late pregnancy; LP) metabolites associated with nitric oxide production as well as acylcholines, sphingomyelins, and fatty acid species were elevated, which coincided with a lower activation state of phosphofructokinase and higher levels of pyruvate dehydrogenase kinase 4 (Pdk4) and β-hydroxybutyrate dehydrogenase 1 (Bdh1). In the postpartum period, urea cycle metabolites, polyamines, and phospholipid levels were markedly elevated in the maternal heart. Cardiac transcriptomics in LP revealed significant increases in not only Pdk4 and Bdh1 but also genes that regulate glutamate and ketone body oxidation, which were preceded in MP by higher expression of transcripts controlling cell proliferation and angiogenesis. Proteomics analysis of the maternal heart in LP and PB revealed significant reductions in several contractile filament and mitochondrial subunit complex proteins. Collectively, these findings describe the coordinated molecular changes that occur in the maternal heart during and after pregnancy.NEW & NOTEWORTHY Little is known of the underlying molecular and cellular mechanisms that contribute to pregnancy-induced cardiac growth. Several lines of evidence suggest that changes in cardiac metabolism may contribute. Here, we provide a comprehensive metabolic atlas of the metabolomic, proteomic, and transcriptomic changes occurring in the maternal heart. We show that pregnancy-induced cardiac growth is associated with changes in glycerophospholipid, nucleotide, and amino acid metabolism, with reductions in cardiac glucose catabolism. Collectively, these results suggest that substantial metabolic changes occur in the maternal heart during and after pregnancy.

Entities:  

Keywords:  hypertrophy; metabolomics; pregnancy; proteomics; transcriptomics

Mesh:

Year:  2022        PMID: 35622533      PMCID: PMC9236881          DOI: 10.1152/ajpheart.00105.2022

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   5.125


  90 in total

1.  Activation of the neuregulin/ErbB system during physiological ventricular remodeling in pregnancy.

Authors:  Katrien Lemmens; Kris Doggen; Gilles W De Keulenaer
Journal:  Am J Physiol Heart Circ Physiol       Date:  2010-12-24       Impact factor: 4.733

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Review 4.  Pregnancy as a cardiac stress model.

Authors:  Eunhee Chung; Leslie A Leinwand
Journal:  Cardiovasc Res       Date:  2014-01-20       Impact factor: 10.787

5.  Plasma homoarginine concentrations in ewe's pregnancy and association with the number of fetuses.

Authors:  Salvatore Sotgia; Fiammetta Berlinguer; Christian Porcu; Valeria Pasciu; Giovanni Molle; Maria Dattena; Marilia Gallus; Stefania Bassu; Arduino A Mangoni; Ciriaco Carru; Angelo Zinellu
Journal:  Res Vet Sci       Date:  2021-11-19       Impact factor: 2.534

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Authors:  José G Soñanez-Organis; José A Godoy-Lugo; Magally L E Hernández-Palomares; Daniel Rodríguez-Martínez; Jesús A Rosas-Rodríguez; Guadalupe González-Ochoa; Adolfo Virgen-Ortiz; Rudy M Ortiz
Journal:  Gene       Date:  2016-06-14       Impact factor: 3.688

8.  Homoarginine Supplementation Prevents Left Ventricular Dilatation and Preserves Systolic Function in a Model of Coronary Artery Disease.

Authors:  Roman N Rodionov; Hoshimjon Begmatov; Natalia Jarzebska; Ketul Patel; Matthew T Mills; Zulaikha Ghani; Doreen Khakshour; Pankti Tamboli; Mitul N Patel; Mirette Abdalla; Maryann Assaf; Stefan R Bornstein; Jose Luis Millan; Stefanie M Bode-Böger; Jens Martens-Lobenhoffer; Norbert Weiss; Olga V Savinova
Journal:  J Am Heart Assoc       Date:  2019-07-15       Impact factor: 5.501

9.  The failing heart utilizes 3-hydroxybutyrate as a metabolic stress defense.

Authors:  Julie L Horton; Michael T Davidson; Clara Kurishima; Rick B Vega; Jeffery C Powers; Timothy R Matsuura; Christopher Petucci; E Douglas Lewandowski; Peter A Crawford; Deborah M Muoio; Fabio A Recchia; Daniel P Kelly
Journal:  JCI Insight       Date:  2019-02-21

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Authors:  Eunhee Chung; Joseph Heimiller; Leslie A Leinwand
Journal:  PLoS One       Date:  2012-07-31       Impact factor: 3.240

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