Cargando…
Achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis
Bisoprolol is a drug that acts via the mechanism of specifically and selectively inhibiting the β(1)-adrenoreceptor in cardiac myocytes, and provides a pure reduction of heart rate without changing other cardiac parameters. It has long been clinically used to treat cerebrovascular and cardiovascular...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038470/ https://www.ncbi.nlm.nih.gov/pubmed/27698689 http://dx.doi.org/10.3892/etm.2016.3570 |
_version_ | 1782455898046726144 |
---|---|
author | Xiang, Shizhao Zhang, Ning Yang, Zheng Bian, Zhouyan Yuan, Yuan Tang, Qizhu |
author_facet | Xiang, Shizhao Zhang, Ning Yang, Zheng Bian, Zhouyan Yuan, Yuan Tang, Qizhu |
author_sort | Xiang, Shizhao |
collection | PubMed |
description | Bisoprolol is a drug that acts via the mechanism of specifically and selectively inhibiting the β(1)-adrenoreceptor in cardiac myocytes, and provides a pure reduction of heart rate without changing other cardiac parameters. It has long been clinically used to treat cerebrovascular and cardiovascular illnesses. However, there is little information available on whether the role of bisoprolol in the attenuation of ventricular remodeling is dependent upon the achievement of a target dose, and whether it must be used as a preferred option. The aim of the present study was to clarify the underlying benefits of bisoprolol in the attenuation of pressure overload-induced cardiac hypertrophy and fibrosis at different doses. C57BL/6J male mice, aged 6–8 weeks, were treated with saline or one of three different doses of bisoprolol (Biso: 2.5, 5 or 10 mg/kg/day) for 8 weeks from day 1 after aortic banding (AB). A number of mice underwent sham surgery and were treated with saline or bisoprolol. The mice were randomly assigned into the sham (n=24) and AB (n=62) groups. The results revealed that bisoprolol had a protective role against the cardiac hypertrophy, fibrosis and dysfunction caused by AB. This was determined on the basis of heart/body and lung/body weight ratios and heart weight/tibia length ratios, as well as echocardiographic and hemodynamic parameters, histological analysis, and the gene expression levels of hypertrophic and fibrotic markers. The present study revealed that administration of bisoprolol for a long time period may enhance its role in the prevention of cardiac hypertrophy and fibrosis induced by AB, whereas no statistically significant difference was observed between the middle- and high-doses. These observations indicated that the function of bisoprolol in protecting against cardiac hypertrophy, fibrosis and dysfunction is time-dependent. Furthermore, it is proposed that a middle dose of bisoprolol may be a better option for patients with cardiovascular illnesses, particularly those undertaking coronary artery bypass graft and cardiac pacemaker surgeries. These promising results require further clinical investigation. |
format | Online Article Text |
id | pubmed-5038470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-50384702016-10-03 Achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis Xiang, Shizhao Zhang, Ning Yang, Zheng Bian, Zhouyan Yuan, Yuan Tang, Qizhu Exp Ther Med Articles Bisoprolol is a drug that acts via the mechanism of specifically and selectively inhibiting the β(1)-adrenoreceptor in cardiac myocytes, and provides a pure reduction of heart rate without changing other cardiac parameters. It has long been clinically used to treat cerebrovascular and cardiovascular illnesses. However, there is little information available on whether the role of bisoprolol in the attenuation of ventricular remodeling is dependent upon the achievement of a target dose, and whether it must be used as a preferred option. The aim of the present study was to clarify the underlying benefits of bisoprolol in the attenuation of pressure overload-induced cardiac hypertrophy and fibrosis at different doses. C57BL/6J male mice, aged 6–8 weeks, were treated with saline or one of three different doses of bisoprolol (Biso: 2.5, 5 or 10 mg/kg/day) for 8 weeks from day 1 after aortic banding (AB). A number of mice underwent sham surgery and were treated with saline or bisoprolol. The mice were randomly assigned into the sham (n=24) and AB (n=62) groups. The results revealed that bisoprolol had a protective role against the cardiac hypertrophy, fibrosis and dysfunction caused by AB. This was determined on the basis of heart/body and lung/body weight ratios and heart weight/tibia length ratios, as well as echocardiographic and hemodynamic parameters, histological analysis, and the gene expression levels of hypertrophic and fibrotic markers. The present study revealed that administration of bisoprolol for a long time period may enhance its role in the prevention of cardiac hypertrophy and fibrosis induced by AB, whereas no statistically significant difference was observed between the middle- and high-doses. These observations indicated that the function of bisoprolol in protecting against cardiac hypertrophy, fibrosis and dysfunction is time-dependent. Furthermore, it is proposed that a middle dose of bisoprolol may be a better option for patients with cardiovascular illnesses, particularly those undertaking coronary artery bypass graft and cardiac pacemaker surgeries. These promising results require further clinical investigation. D.A. Spandidos 2016-10 2016-08-04 /pmc/articles/PMC5038470/ /pubmed/27698689 http://dx.doi.org/10.3892/etm.2016.3570 Text en Copyright: © Xiang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Xiang, Shizhao Zhang, Ning Yang, Zheng Bian, Zhouyan Yuan, Yuan Tang, Qizhu Achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis |
title | Achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis |
title_full | Achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis |
title_fullStr | Achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis |
title_full_unstemmed | Achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis |
title_short | Achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis |
title_sort | achievement of a target dose of bisoprolol may not be a preferred option for attenuating pressure overload-induced cardiac hypertrophy and fibrosis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038470/ https://www.ncbi.nlm.nih.gov/pubmed/27698689 http://dx.doi.org/10.3892/etm.2016.3570 |
work_keys_str_mv | AT xiangshizhao achievementofatargetdoseofbisoprololmaynotbeapreferredoptionforattenuatingpressureoverloadinducedcardiachypertrophyandfibrosis AT zhangning achievementofatargetdoseofbisoprololmaynotbeapreferredoptionforattenuatingpressureoverloadinducedcardiachypertrophyandfibrosis AT yangzheng achievementofatargetdoseofbisoprololmaynotbeapreferredoptionforattenuatingpressureoverloadinducedcardiachypertrophyandfibrosis AT bianzhouyan achievementofatargetdoseofbisoprololmaynotbeapreferredoptionforattenuatingpressureoverloadinducedcardiachypertrophyandfibrosis AT yuanyuan achievementofatargetdoseofbisoprololmaynotbeapreferredoptionforattenuatingpressureoverloadinducedcardiachypertrophyandfibrosis AT tangqizhu achievementofatargetdoseofbisoprololmaynotbeapreferredoptionforattenuatingpressureoverloadinducedcardiachypertrophyandfibrosis |