Medical Journals

Pleiotropic Effects of the Beta-adrenoceptor Blocker Carvedilol on Calcium Regulation During Oxidative Stress-induced Apoptosis in Cardiomyocytes.

Authors:
  • Wang Ruijuan
  • Miura Toshiro
  • Harada Nozomu
  • Kametani Ryosuke
  • Shibuya Masaki
  • Fukagawa Yasuhiro
  • Kawamura Shuji
  • Ikeda Yasuhiro
  • Hara Masayuki
  • Matsuzaki Masunori

From: Division of Cardiology, Department of Medicine and Clinical Science, Yamaguchi University Graduate School of Medicine, 1-1-1 Minami-Kogushi, Ube, Yamaguchi 755-8505 Japan.

The Journal of pharmacology and experimental therapeutics

  • Publish Date: Jul 2006
  • ISSN: 0022-3565
  • Volume: 318
  • Issue: 1
  • Pages: 45-52
  • Medium: Print
  • Language: English
  • Citation (JAMA): Wang Ruijuan, Miura Toshiro, Harada Nozomu, et al. Pleiotropic Effects of the Beta-adrenoceptor Blocker Carvedilol on Calcium Regulation During Oxidative Stress-induced Apoptosis in Cardiomyocytes.. J. Pharmacol. Exp. Ther. Jul 2006;318:45-52

Abstract

Carvedilol is a nonselective beta-adrenoceptor blocker with multiple pleiotropic actions. A recent clinical study suggested that carvedilol may be superior to other beta-adrenoceptor blockers in the treatment of heart failure. Despite numerous investigations, the underlying mechanisms of carvedilol on improving heart failure are yet to be fully established. The purpose of this study is to clarify the pleiotropic effect of carvedilol on cytosolic and mitochondrial calcium regulation during oxidative stress-induced apoptosis in cardiomyocytes. Carvedilol (10 microM), but not metoprolol (10 microM), reduced H2O2 (100 microM)-induced apoptosis in neonatal rat cardiomyocytes. During the process, changes in cytosolic calcium concentration ([Ca2+]i) and mitochondrial calcium concentration ([Ca2+]m) and mitochondrial membrane potential (DeltaPsim) were measured by fluorescent probes [Fluo-3/acetoxymethyl ester (AM), Rhod-2/AM, and tetramethylrhodamine ethyl ester, respectively] and imaged by laser confocal microscopy. The results showed that H2O2 caused [Ca2]m overload first, followed by [Ca2+]i overload, leading to DeltaPsim dissipation and the induction of apoptosis. Carvedilol (10 microM) significantly delayed these processes and reduced apoptosis. These effects were not observed with other beta-adrenoceptor blockers (metoprolol, atenolol, and propranolol) or with a combination of the alpha (phentolamine)- and the beta-adrenoceptor blocker. The antioxidant N-acetyl-L-cysteine (NAC, 5 mM) and the combination of NAC and propranolol (10 microM) showed an effect similar to that of carvedilol. Therefore, the effect of carvedilol on H2O2-induced changes in [Ca2+]m, [Ca2+]i, and DeltaPsi(m) is independent of alpha- and beta-adrenoceptors but is probably dependent on the antioxidant effect.

Mesh Headings (Keywords): Adrenergic beta-Antagonists, Animals, Apoptosis, Calcium, Carbazoles, Cells, Cultured, Dose-Response Relationship, Drug, Myocytes, Cardiac, Oxidative Stress, Propanolamines, Rats, Rats, Wistar


Check for Full Text / PubMed Unique Identifier (PMID): 16611853


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.