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Nicorandil Prevents Gα(q)-Induced Progressive Heart Failure and Ventricular Arrhythmias in Transgenic Mice
BACKGROUND: Beneficial effects of nicorandil on the treatment of hypertensive heart failure (HF) and ischemic heart disease have been suggested. However, whether nicorandil has inhibitory effects on HF and ventricular arrhythmias caused by the activation of G protein alpha q (Gα(q)) -coupled recepto...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527603/ https://www.ncbi.nlm.nih.gov/pubmed/23285142 http://dx.doi.org/10.1371/journal.pone.0052667 |
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author | Hirose, Masamichi Takeishi, Yasuchika Nakada, Tsutomu Shimojo, Hisashi Kashihara, Toshihide Nishio, Ayako Suzuki, Satoshi Mende, Ulrike Matsumoto, Kiyoshi Matsushita, Naoko Taira, Eiichi Sato, Fumika Yamada, Mitsuhiko |
author_facet | Hirose, Masamichi Takeishi, Yasuchika Nakada, Tsutomu Shimojo, Hisashi Kashihara, Toshihide Nishio, Ayako Suzuki, Satoshi Mende, Ulrike Matsumoto, Kiyoshi Matsushita, Naoko Taira, Eiichi Sato, Fumika Yamada, Mitsuhiko |
author_sort | Hirose, Masamichi |
collection | PubMed |
description | BACKGROUND: Beneficial effects of nicorandil on the treatment of hypertensive heart failure (HF) and ischemic heart disease have been suggested. However, whether nicorandil has inhibitory effects on HF and ventricular arrhythmias caused by the activation of G protein alpha q (Gα(q)) -coupled receptor (GPCR) signaling still remains unknown. We investigated these inhibitory effects of nicorandil in transgenic mice with transient cardiac expression of activated Gα(q) (Gα(q)-TG). METHODOLOGY/PRINCIPAL FINDINGS: Nicorandil (6 mg/kg/day) or vehicle was chronically administered to Gα(q)-TG from 8 to 32 weeks of age, and all experiments were performed in mice at the age of 32 weeks. Chronic nicorandil administration prevented the severe reduction of left ventricular fractional shortening and inhibited ventricular interstitial fibrosis in Gα(q)-TG. SUR-2B and SERCA2 gene expression was decreased in vehicle-treated Gα(q)-TG but not in nicorandil-treated Gα(q)-TG. eNOS gene expression was also increased in nicorandil-treated Gα(q)-TG compared with vehicle-treated Gα(q)-TG. Electrocardiogram demonstrated that premature ventricular contraction (PVC) was frequently (more than 20 beats/min) observed in 7 of 10 vehicle-treated Gα(q)-TG but in none of 10 nicorandil-treated Gα(q)-TG. The QT interval was significantly shorter in nicorandil-treated Gα(q)-TG than vehicle-treated Gα(q)-TG. Acute nicorandil administration shortened ventricular monophasic action potential duration and reduced the number of PVCs in Langendorff-perfused Gα(q)-TG mouse hearts. Moreover, HMR1098, a blocker of cardiac sarcolemmal K(ATP) channels, significantly attenuated the shortening of MAP duration induced by nicorandil in the Gα(q)-TG heart. CONCLUSIONS/SIGNIFICANCE: These findings suggest that nicorandil can prevent the development of HF and ventricular arrhythmia caused by the activation of GPCR signaling through the shortening of the QT interval, action potential duration, the normalization of SERCA2 gene expression. Nicorandil may also improve the impaired coronary circulation during HF. |
format | Online Article Text |
id | pubmed-3527603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35276032013-01-02 Nicorandil Prevents Gα(q)-Induced Progressive Heart Failure and Ventricular Arrhythmias in Transgenic Mice Hirose, Masamichi Takeishi, Yasuchika Nakada, Tsutomu Shimojo, Hisashi Kashihara, Toshihide Nishio, Ayako Suzuki, Satoshi Mende, Ulrike Matsumoto, Kiyoshi Matsushita, Naoko Taira, Eiichi Sato, Fumika Yamada, Mitsuhiko PLoS One Research Article BACKGROUND: Beneficial effects of nicorandil on the treatment of hypertensive heart failure (HF) and ischemic heart disease have been suggested. However, whether nicorandil has inhibitory effects on HF and ventricular arrhythmias caused by the activation of G protein alpha q (Gα(q)) -coupled receptor (GPCR) signaling still remains unknown. We investigated these inhibitory effects of nicorandil in transgenic mice with transient cardiac expression of activated Gα(q) (Gα(q)-TG). METHODOLOGY/PRINCIPAL FINDINGS: Nicorandil (6 mg/kg/day) or vehicle was chronically administered to Gα(q)-TG from 8 to 32 weeks of age, and all experiments were performed in mice at the age of 32 weeks. Chronic nicorandil administration prevented the severe reduction of left ventricular fractional shortening and inhibited ventricular interstitial fibrosis in Gα(q)-TG. SUR-2B and SERCA2 gene expression was decreased in vehicle-treated Gα(q)-TG but not in nicorandil-treated Gα(q)-TG. eNOS gene expression was also increased in nicorandil-treated Gα(q)-TG compared with vehicle-treated Gα(q)-TG. Electrocardiogram demonstrated that premature ventricular contraction (PVC) was frequently (more than 20 beats/min) observed in 7 of 10 vehicle-treated Gα(q)-TG but in none of 10 nicorandil-treated Gα(q)-TG. The QT interval was significantly shorter in nicorandil-treated Gα(q)-TG than vehicle-treated Gα(q)-TG. Acute nicorandil administration shortened ventricular monophasic action potential duration and reduced the number of PVCs in Langendorff-perfused Gα(q)-TG mouse hearts. Moreover, HMR1098, a blocker of cardiac sarcolemmal K(ATP) channels, significantly attenuated the shortening of MAP duration induced by nicorandil in the Gα(q)-TG heart. CONCLUSIONS/SIGNIFICANCE: These findings suggest that nicorandil can prevent the development of HF and ventricular arrhythmia caused by the activation of GPCR signaling through the shortening of the QT interval, action potential duration, the normalization of SERCA2 gene expression. Nicorandil may also improve the impaired coronary circulation during HF. Public Library of Science 2012-12-20 /pmc/articles/PMC3527603/ /pubmed/23285142 http://dx.doi.org/10.1371/journal.pone.0052667 Text en © 2012 Hirose et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hirose, Masamichi Takeishi, Yasuchika Nakada, Tsutomu Shimojo, Hisashi Kashihara, Toshihide Nishio, Ayako Suzuki, Satoshi Mende, Ulrike Matsumoto, Kiyoshi Matsushita, Naoko Taira, Eiichi Sato, Fumika Yamada, Mitsuhiko Nicorandil Prevents Gα(q)-Induced Progressive Heart Failure and Ventricular Arrhythmias in Transgenic Mice |
title | Nicorandil Prevents Gα(q)-Induced Progressive Heart Failure and Ventricular Arrhythmias in Transgenic Mice |
title_full | Nicorandil Prevents Gα(q)-Induced Progressive Heart Failure and Ventricular Arrhythmias in Transgenic Mice |
title_fullStr | Nicorandil Prevents Gα(q)-Induced Progressive Heart Failure and Ventricular Arrhythmias in Transgenic Mice |
title_full_unstemmed | Nicorandil Prevents Gα(q)-Induced Progressive Heart Failure and Ventricular Arrhythmias in Transgenic Mice |
title_short | Nicorandil Prevents Gα(q)-Induced Progressive Heart Failure and Ventricular Arrhythmias in Transgenic Mice |
title_sort | nicorandil prevents gα(q)-induced progressive heart failure and ventricular arrhythmias in transgenic mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527603/ https://www.ncbi.nlm.nih.gov/pubmed/23285142 http://dx.doi.org/10.1371/journal.pone.0052667 |
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