Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability

Ventricular hypertrophy is one of the major myocardial responses to pressure overload (PO). Most studies on early myocardial response focus on the days or even weeks after induction of hypertrophic stimuli. Since mechanotransduction pathways are immediately activated in hearts undergoing increased w...

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Main Authors: Ana Carolina Deckmann, Thaís Holz Theizen, Francisco Javier Medrano, Kleber Gomes Franchini, Gonçalo Amarante Guimarães Pereira
Format: Article
Language:English
Published: Sociedade Brasileira de Genética 2010-01-01
Series:Genetics and Molecular Biology
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100004
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spelling doaj-c10bc304d7804604b6091599f889877a2020-11-25T00:39:58ZengSociedade Brasileira de GenéticaGenetics and Molecular Biology1415-47571678-46852010-01-013311216Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availabilityAna Carolina DeckmannThaís Holz TheizenFrancisco Javier MedranoKleber Gomes FranchiniGonçalo Amarante Guimarães PereiraVentricular hypertrophy is one of the major myocardial responses to pressure overload (PO). Most studies on early myocardial response focus on the days or even weeks after induction of hypertrophic stimuli. Since mechanotransduction pathways are immediately activated in hearts undergoing increased work load, it is reasonable to infer that the myocardial gene program may be regulated in the first few hours. In the present study, we monitored the expression of some genes previously described in the context of myocardial hypertrophic growth by using the Northern blot technique, to estimate the mRNA content of selected genes in rat myocardium for the periods 1, 3, 6, 12 and 48 h after PO stimuli. Results revealed an immediate switch in the expression of genes encoding alpha and beta isoforms of myosin heavy chain, and up-regulation of the cardiac isoform of alpha actin. We also detected transitory gene regulation as the increase in mitochondrial cytochrome c oxidase 1 gene expression, parallel to down-regulation of genes encoding sarco(endo)plasmic reticulum Ca+2 ATPase and sodium-calcium exchanger. Taken together, these results indicate that initial myocardial responses to increased work load include alterations in the contractile properties of sarcomeres and transitory adjustment of mitochondrial bioenergetics and calcium availability.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100004pressure overloadmyocardial hypertrophygene expressionSERCA2
collection DOAJ
language English
format Article
sources DOAJ
author Ana Carolina Deckmann
Thaís Holz Theizen
Francisco Javier Medrano
Kleber Gomes Franchini
Gonçalo Amarante Guimarães Pereira
spellingShingle Ana Carolina Deckmann
Thaís Holz Theizen
Francisco Javier Medrano
Kleber Gomes Franchini
Gonçalo Amarante Guimarães Pereira
Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability
Genetics and Molecular Biology
pressure overload
myocardial hypertrophy
gene expression
SERCA2
author_facet Ana Carolina Deckmann
Thaís Holz Theizen
Francisco Javier Medrano
Kleber Gomes Franchini
Gonçalo Amarante Guimarães Pereira
author_sort Ana Carolina Deckmann
title Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability
title_short Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability
title_full Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability
title_fullStr Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability
title_full_unstemmed Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability
title_sort immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability
publisher Sociedade Brasileira de Genética
series Genetics and Molecular Biology
issn 1415-4757
1678-4685
publishDate 2010-01-01
description Ventricular hypertrophy is one of the major myocardial responses to pressure overload (PO). Most studies on early myocardial response focus on the days or even weeks after induction of hypertrophic stimuli. Since mechanotransduction pathways are immediately activated in hearts undergoing increased work load, it is reasonable to infer that the myocardial gene program may be regulated in the first few hours. In the present study, we monitored the expression of some genes previously described in the context of myocardial hypertrophic growth by using the Northern blot technique, to estimate the mRNA content of selected genes in rat myocardium for the periods 1, 3, 6, 12 and 48 h after PO stimuli. Results revealed an immediate switch in the expression of genes encoding alpha and beta isoforms of myosin heavy chain, and up-regulation of the cardiac isoform of alpha actin. We also detected transitory gene regulation as the increase in mitochondrial cytochrome c oxidase 1 gene expression, parallel to down-regulation of genes encoding sarco(endo)plasmic reticulum Ca+2 ATPase and sodium-calcium exchanger. Taken together, these results indicate that initial myocardial responses to increased work load include alterations in the contractile properties of sarcomeres and transitory adjustment of mitochondrial bioenergetics and calcium availability.
topic pressure overload
myocardial hypertrophy
gene expression
SERCA2
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000100004
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