SAGE Journals Online
Advertisement
Sign In to gain access to subscriptions and/or personal tools.

 

Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Advertisement

Sign In to gain access to subscriptions and/or personal tools.
Journal of Cardiovascular Pharmacology and Therapeutics
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Henning, R. J.
Right arrow Articles by Chiou, S.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Henning, R. J.
Right arrow Articles by Chiou, S.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Cocaine Increases β-Myosin Heavy-Chain Protein Expression in Cardiac Myocytes

Robert J. Henning

University of South Florida College of Medicine, James A. Haley Veterans' Hospital, Tampa, FL

Jose Silva

James A. Haley Veterans' Hospital, Tampa, FL

Vijaya Reddy

James A. Haley Veterans' Hospital, Tampa, FL

Seema Kamat

James A. Haley Veterans' Hospital, Tampa, FL

Michael B. Morgan

University of South Florida College of Medicine, James A. Haley Veterans' Hospital, Tampa, FL

Yong Xiang Li

University of South Florida College of Medicine, James A. Haley Veterans' Hospital, Tampa, FL

Shirley Chiou

James A. Haley Veterans' Hospital, Tampa, FL

Background: As many as 47% of chronic cocaine users develop cardiac ventricular hypertrophy. The presence and degree of cocaine-induced ventricular hypertrophy is not correlated with the use of other substances of abuse such as alcohol or cigarettes. Moreover, this hypertrophy occurs in individuals without sustained increases in arterial blood pressure or heart rate, or increases in the plasma concentration of renin, aldosterone, norepinephrine, or cortisol. Therefore, we investigated whether cocaine, in concentrations commonly found in cocaine users, has any direct effects on the protein content in cardiac ventricular myocytes. We compared the effects of cocaine with norepinephrine, which increases the total protein content, especially β-myosin heavy-chain contractile protein (β-MHC), in cardiac ventricular myocytes.

Methods: Experiments were performed on 30-day-old rat ventricular myocytes suspended in culture media and cultured in flasks. In 12 suspension-culture experiments, cocaine or norepinephrine, in doses of 0 (control) or 10-6 mol/L was added to each culture and the cells were harvested on day 5. In 16 tlask-culture experiments, cocaine or norepinephrine was added to each culture on day 7 in doses of 0 (control-vehicle), 10-7, or 10-6 mol/L and the cells were harvested on day 10. The total protein content and the myosin protein expression of the myocytes in each culture were determined. Juvenile and adult rat cardiac myosin protein is predominately {alpha}-myosin heavy-chain protein ({alpha}-MHC), whereas β-MHC occurs primarily in fetal rat hearts.

Results: In the suspension-culture experiments, cocaine, 10-6 mol/L, increased the cardiomyocyte total protein concentration by 29% ± 2% (P < .001) and the β-MHC expression by 81% ± 10% (P < .01) in comparison with the control myocytes. Cocaine slightly decreased cardiomyocyte {alpha}-MHC. Norepinephrine increased the total protein concentration by 21% ± 3% ( P < .001) and the β-MHC expression by 59% ± 10% (P < .01), but did not increase {alpha}-MHC expression. In the flask-culture experiments, cocaine, 10-6 mol/L, maximally increased the total protein concentration by 28% (P < .001), the protein/cell ratio by 57% ± 10% (P < .01), and the β-MHC expression by 85% ± 8% (P < .01). Cocaine slightly decreased {alpha}-MHC. Norepinephrine, 10-6 mol/L, maximally increased the total protein concentration by 35%, the protein/cell ratio by 63% ± 9% (P < .01), and the expression of β-MHC by 78% ± 11% (P < .01). Norepinephrine did not increase {alpha}-MHC expression. In 18 separate flask-culture experiments, cocaine, 10-6 mol/L, was added to the cardiomyocyte cultures after the addition of phentolamine (n = 9), in concentrations of 10-7 to 10-5 mol/L, or metoprolol (n = 9), in concentrations of 10-7 to 10-5 mol/L. Neither phentolamine nor metoprolol inhibited the cocaine-induced increase in cardiomyocyte total protein content or the expression of β-MHC.

Conclusion: Cocaine, similar to norepinephrine, significantly increases the total protein content and the expression of β-MHC in cardiac ventricular myocytes. In this manner, cocaine may cause cardiac ventricular hypertrophy. This process is not inhibited by {alpha}- or β-adrenergic receptor blockade.

Key Words: cocaine • cardiac myocytes • myosin • β-myosin heavy-chain protein • cardiac hypertrophy • ventricular hypertrophy.

Journal of Cardiovascular Pharmacology and Therapeutics, Vol. 5, No. 4, 313-322 (2000)
DOI: 10.1054/JCPT.2000.19331


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?




Advertisement