Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome

Detalhes bibliográficos
Autor(a) principal: Campanha,Fábio V. G.
Data de Publicação: 2016
Outros Autores: Perone,Denise, Campos,Dijon H. S. de, Luvizotto,Renata de A. M., De Síbio,Maria T., Oliveira,Miriane de, Olimpio,Regiane M. C., Moretto,Fernanda C. F., Padovani,Carlos R., Mazeto,Gláucia M. F. S., Cicogna,Antonio C., Nogueira,Célia R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Arquivos de Endocrinologia e Metabolismo (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972016000600582
Resumo: ABSTRACT Objective The current study was aimed at analyzing sarcoplasmic reticulum Ca2+ ATPase (Serca2) and ryanodine receptor type 2 (Ryr2) gene expression in rats subjected to surgery that induced HF and were subsequently treated with T4 using physiological doses. Materials and methods HF was induced in 18 male Wistar rats by clipping the ascending thoracic aorta to generate aortic stenosis (HFS group), while the control group (9-sham) underwent thoracotomy. After 21 weeks, the HFS group was subdivided into two subgroups. One group (9 Wistar rats) with HF received 1.0 µg of T4/100 g of body weight for five consecutive days (HFS/T4); the other group (9 Wistar rats) received isotonic saline solution (HFS/S). The animals were sacrificed after this treatment and examined for signs of HF. Samples from the left ventricles of these animals were analyzed by RT-qPCR for the expression of Serca2 and Ryr2 genes. Results Rats with HF developed euthyroid sick syndrome (ESS) and treatment with T4 restored the T3 values to the Sham level and increased Serca2 and Ryr2 gene expression, thereby demonstrating a possible benefit of T4 treatment for heart function in ESS associated with HF. Conclusion The T4 treatment can potentially normalize the levels of T3 as well elevated Serca2 and Ryr2 gene expression in the myocardium in heart failure rats with euthyroid sick syndrome.
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spelling Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndromeReverse triiodothyronineheart failuretherapeutic usecalcium channelstriiodothyronineABSTRACT Objective The current study was aimed at analyzing sarcoplasmic reticulum Ca2+ ATPase (Serca2) and ryanodine receptor type 2 (Ryr2) gene expression in rats subjected to surgery that induced HF and were subsequently treated with T4 using physiological doses. Materials and methods HF was induced in 18 male Wistar rats by clipping the ascending thoracic aorta to generate aortic stenosis (HFS group), while the control group (9-sham) underwent thoracotomy. After 21 weeks, the HFS group was subdivided into two subgroups. One group (9 Wistar rats) with HF received 1.0 µg of T4/100 g of body weight for five consecutive days (HFS/T4); the other group (9 Wistar rats) received isotonic saline solution (HFS/S). The animals were sacrificed after this treatment and examined for signs of HF. Samples from the left ventricles of these animals were analyzed by RT-qPCR for the expression of Serca2 and Ryr2 genes. Results Rats with HF developed euthyroid sick syndrome (ESS) and treatment with T4 restored the T3 values to the Sham level and increased Serca2 and Ryr2 gene expression, thereby demonstrating a possible benefit of T4 treatment for heart function in ESS associated with HF. Conclusion The T4 treatment can potentially normalize the levels of T3 as well elevated Serca2 and Ryr2 gene expression in the myocardium in heart failure rats with euthyroid sick syndrome.Sociedade Brasileira de Endocrinologia e Metabologia2016-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972016000600582Archives of Endocrinology and Metabolism v.60 n.6 2016reponame:Arquivos de Endocrinologia e Metabolismo (Online)instname:Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)instacron:SBEM10.1590/2359-3997000000208info:eu-repo/semantics/openAccessCampanha,Fábio V. G.Perone,DeniseCampos,Dijon H. S. deLuvizotto,Renata de A. M.De Síbio,Maria T.Oliveira,Miriane deOlimpio,Regiane M. C.Moretto,Fernanda C. F.Padovani,Carlos R.Mazeto,Gláucia M. F. S.Cicogna,Antonio C.Nogueira,Célia R.eng2016-12-08T00:00:00Zoai:scielo:S2359-39972016000600582Revistahttps://www.aem-sbem.com/https://old.scielo.br/oai/scielo-oai.php||aem.editorial.office@endocrino.org.br2359-42922359-3997opendoar:2016-12-08T00:00Arquivos de Endocrinologia e Metabolismo (Online) - Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)false
dc.title.none.fl_str_mv Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome
title Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome
spellingShingle Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome
Campanha,Fábio V. G.
Reverse triiodothyronine
heart failure
therapeutic use
calcium channels
triiodothyronine
title_short Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome
title_full Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome
title_fullStr Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome
title_full_unstemmed Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome
title_sort Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome
author Campanha,Fábio V. G.
author_facet Campanha,Fábio V. G.
Perone,Denise
Campos,Dijon H. S. de
Luvizotto,Renata de A. M.
De Síbio,Maria T.
Oliveira,Miriane de
Olimpio,Regiane M. C.
Moretto,Fernanda C. F.
Padovani,Carlos R.
Mazeto,Gláucia M. F. S.
Cicogna,Antonio C.
Nogueira,Célia R.
author_role author
author2 Perone,Denise
Campos,Dijon H. S. de
Luvizotto,Renata de A. M.
De Síbio,Maria T.
Oliveira,Miriane de
Olimpio,Regiane M. C.
Moretto,Fernanda C. F.
Padovani,Carlos R.
Mazeto,Gláucia M. F. S.
Cicogna,Antonio C.
Nogueira,Célia R.
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Campanha,Fábio V. G.
Perone,Denise
Campos,Dijon H. S. de
Luvizotto,Renata de A. M.
De Síbio,Maria T.
Oliveira,Miriane de
Olimpio,Regiane M. C.
Moretto,Fernanda C. F.
Padovani,Carlos R.
Mazeto,Gláucia M. F. S.
Cicogna,Antonio C.
Nogueira,Célia R.
dc.subject.por.fl_str_mv Reverse triiodothyronine
heart failure
therapeutic use
calcium channels
triiodothyronine
topic Reverse triiodothyronine
heart failure
therapeutic use
calcium channels
triiodothyronine
description ABSTRACT Objective The current study was aimed at analyzing sarcoplasmic reticulum Ca2+ ATPase (Serca2) and ryanodine receptor type 2 (Ryr2) gene expression in rats subjected to surgery that induced HF and were subsequently treated with T4 using physiological doses. Materials and methods HF was induced in 18 male Wistar rats by clipping the ascending thoracic aorta to generate aortic stenosis (HFS group), while the control group (9-sham) underwent thoracotomy. After 21 weeks, the HFS group was subdivided into two subgroups. One group (9 Wistar rats) with HF received 1.0 µg of T4/100 g of body weight for five consecutive days (HFS/T4); the other group (9 Wistar rats) received isotonic saline solution (HFS/S). The animals were sacrificed after this treatment and examined for signs of HF. Samples from the left ventricles of these animals were analyzed by RT-qPCR for the expression of Serca2 and Ryr2 genes. Results Rats with HF developed euthyroid sick syndrome (ESS) and treatment with T4 restored the T3 values to the Sham level and increased Serca2 and Ryr2 gene expression, thereby demonstrating a possible benefit of T4 treatment for heart function in ESS associated with HF. Conclusion The T4 treatment can potentially normalize the levels of T3 as well elevated Serca2 and Ryr2 gene expression in the myocardium in heart failure rats with euthyroid sick syndrome.
publishDate 2016
dc.date.none.fl_str_mv 2016-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972016000600582
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972016000600582
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/2359-3997000000208
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Endocrinologia e Metabologia
publisher.none.fl_str_mv Sociedade Brasileira de Endocrinologia e Metabologia
dc.source.none.fl_str_mv Archives of Endocrinology and Metabolism v.60 n.6 2016
reponame:Arquivos de Endocrinologia e Metabolismo (Online)
instname:Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
instname_str Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
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reponame_str Arquivos de Endocrinologia e Metabolismo (Online)
collection Arquivos de Endocrinologia e Metabolismo (Online)
repository.name.fl_str_mv Arquivos de Endocrinologia e Metabolismo (Online) - Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
repository.mail.fl_str_mv ||aem.editorial.office@endocrino.org.br
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