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Provedor de dados: |
56
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País: |
Brazil
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Título: |
Chronic aerobic exercise associated to low-dose L-NAME improves contractility without changing calcium handling in rat cardiomyocytes
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Autores: |
Luchi,T.C.
Coelho,P.M.
Cordeiro,J.P.
Assis,A.L.E.M.
Nogueira,B.V.
Marques,V.B.
dos Santos,L.
Lima-Leopoldo,A.P.
Lunz,W.
Leopoldo,A.S.
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Data: |
2020-01-01
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Ano: |
2020
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Palavras-chave: |
Nitric oxide
Aerobic exercise
Cardiac remodeling
Cardiomyocyte
Calcium
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Resumo: |
Nitric oxide (NO) inhibition by high-dose NG-nitro-L-arginine methyl ester (L-NAME) is associated with several detrimental effects on the cardiovascular system. However, low-dose L-NAME increases NO synthesis, which in turn induces physiological cardiovascular benefits, probably by activating a protective negative feedback mechanism. Aerobic exercise, likewise, improves several cardiovascular functions in healthy hearts, but its effects are not known when chronically associated with low-dose L-NAME. Thus, we tested whether the association between low-dose L-NAME administration and chronic aerobic exercise promotes beneficial effects to the cardiovascular system, evaluating the cardiac remodeling process. Male Wistar rats were randomly assigned to control (C), L-NAME (L), chronic aerobic exercise (Ex), and chronic aerobic exercise associated to L-NAME (ExL). Aerobic training was performed with progressive intensity for 12 weeks; L-NAME (1.5 mg·kg-1·day-1) was administered by orogastric gavage. Low-dose L-NAME alone did not change systolic blood pressure (SBP), but ExL significantly increased SBP at week 8 with normalization after 12 weeks. Furthermore, ExL promoted the elevation of left ventricle (LV) end-diastolic pressure without the presence of cardiac hypertrophy and fibrosis. Time to 50% shortening and relaxation were reduced in ExL, suggesting a cardiomyocyte contractile improvement. In addition, the time to 50% Ca2+ peak was increased without alterations in Ca2+ amplitude and time to 50% Ca2+ decay. In conclusion, the association of chronic aerobic exercise and low-dose L-NAME prevented cardiac pathological remodeling and induced cardiomyocyte contractile function improvement; however, it did not alter myocyte affinity and sensitivity to intracellular Ca2+ handling.
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Tipo: |
Info:eu-repo/semantics/article
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Idioma: |
Inglês
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Identificador: |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2020000300611
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Editor: |
Associação Brasileira de Divulgação Científica
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Relação: |
10.1590/1414-431x20198761
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Formato: |
text/html
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Fonte: |
Brazilian Journal of Medical and Biological Research v.53 n.3 2020
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Direitos: |
info:eu-repo/semantics/openAccess
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