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The effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia

Maintaining a good ventricular systolic function is important in the long-term therapy of dogs with supraventricular tachyarrhythmia (SVTA). The objective of this study was to evaluate the inhibitory effect of telmisartan on myocardial injury and the resulting ventricular systolic dysfunction in a c...

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Autores principales: KAWAGUCHI, Takae, HASHIMOTO, Rina, YASUKAWA, Youko, YAMADA, Shusaku, YOSHIMURA, Aritada, HIRAO, Daiki, OHMORI, Takahiro, FUKUSHIMA, Ryuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541858/
https://www.ncbi.nlm.nih.gov/pubmed/30956271
http://dx.doi.org/10.1292/jvms.18-0772
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author KAWAGUCHI, Takae
HASHIMOTO, Rina
YASUKAWA, Youko
YAMADA, Shusaku
YOSHIMURA, Aritada
HIRAO, Daiki
OHMORI, Takahiro
FUKUSHIMA, Ryuji
author_facet KAWAGUCHI, Takae
HASHIMOTO, Rina
YASUKAWA, Youko
YAMADA, Shusaku
YOSHIMURA, Aritada
HIRAO, Daiki
OHMORI, Takahiro
FUKUSHIMA, Ryuji
author_sort KAWAGUCHI, Takae
collection PubMed
description Maintaining a good ventricular systolic function is important in the long-term therapy of dogs with supraventricular tachyarrhythmia (SVTA). The objective of this study was to evaluate the inhibitory effect of telmisartan on myocardial injury and the resulting ventricular systolic dysfunction in a canine model of SVTA. A total of 14 dogs were randomly assigned to a Telmisartan (oral telmisartan, 1.0 mg/kg daily, n=7) or a Control (no drug administration, n=7) group; the duration of rapid atrial pacing (RAP) was 3 weeks for both groups. The cardiac troponin I (cTnI) concentration in the Control group was significantly increased after 3 weeks compared to that before RAP initiation (baseline), but no significant difference was observed in the Telmisartan group. Moreover, the cTnI concentration at 3 weeks was significantly lower in the Telmisartan group than in the Control group. The left ventricular fractional shortening was significantly decreased at 3 weeks compared to that at baseline in both groups. However, fractional shortening at 3 weeks was significantly higher in the Telmisartan group than in the Control group. The cardiac output values in the Control group were significantly decreased at 3 weeks compared with those at baseline, but no significant difference was observed in the Telmisartan group. This study demonstrates that telmisartan inhibits the reduction in ventricular systolic function and prevents myocardial injury in a canine model of SVTA. Therefore, telmisartan is suggested as a novel treatment for canine SVTA.
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spelling pubmed-65418582019-06-11 The effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia KAWAGUCHI, Takae HASHIMOTO, Rina YASUKAWA, Youko YAMADA, Shusaku YOSHIMURA, Aritada HIRAO, Daiki OHMORI, Takahiro FUKUSHIMA, Ryuji J Vet Med Sci Internal Medicine Maintaining a good ventricular systolic function is important in the long-term therapy of dogs with supraventricular tachyarrhythmia (SVTA). The objective of this study was to evaluate the inhibitory effect of telmisartan on myocardial injury and the resulting ventricular systolic dysfunction in a canine model of SVTA. A total of 14 dogs were randomly assigned to a Telmisartan (oral telmisartan, 1.0 mg/kg daily, n=7) or a Control (no drug administration, n=7) group; the duration of rapid atrial pacing (RAP) was 3 weeks for both groups. The cardiac troponin I (cTnI) concentration in the Control group was significantly increased after 3 weeks compared to that before RAP initiation (baseline), but no significant difference was observed in the Telmisartan group. Moreover, the cTnI concentration at 3 weeks was significantly lower in the Telmisartan group than in the Control group. The left ventricular fractional shortening was significantly decreased at 3 weeks compared to that at baseline in both groups. However, fractional shortening at 3 weeks was significantly higher in the Telmisartan group than in the Control group. The cardiac output values in the Control group were significantly decreased at 3 weeks compared with those at baseline, but no significant difference was observed in the Telmisartan group. This study demonstrates that telmisartan inhibits the reduction in ventricular systolic function and prevents myocardial injury in a canine model of SVTA. Therefore, telmisartan is suggested as a novel treatment for canine SVTA. The Japanese Society of Veterinary Science 2019-04-08 2019-05 /pmc/articles/PMC6541858/ /pubmed/30956271 http://dx.doi.org/10.1292/jvms.18-0772 Text en ©2019 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Internal Medicine
KAWAGUCHI, Takae
HASHIMOTO, Rina
YASUKAWA, Youko
YAMADA, Shusaku
YOSHIMURA, Aritada
HIRAO, Daiki
OHMORI, Takahiro
FUKUSHIMA, Ryuji
The effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia
title The effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia
title_full The effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia
title_fullStr The effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia
title_full_unstemmed The effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia
title_short The effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia
title_sort effect of telmisartan on the ventricular systolic function in dogs with experimental supraventricular tachyarrhythmia
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541858/
https://www.ncbi.nlm.nih.gov/pubmed/30956271
http://dx.doi.org/10.1292/jvms.18-0772
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