Skip Navigation

Cardiovascular Research 2003 60(3):598-607; doi:10.1016/j.cardiores.2003.09.020
© 2003 by European Society of Cardiology
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Ross, S. A
Right arrow Articles by Perez, D. M
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ross, S. A
Right arrow Articles by Perez, D. M
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Copyright © 2003, European Society of Cardiology

The {alpha}1B-adrenergic receptor decreases the inotropic response in the mouse Langendorff heart model

Sean A Rossa,1, Boyd R Rorabaugha, Dan Chalothornb, June Yuna, Pedro J Gonzalez-Cabreraa, Dan F McCunea, Michael T Piascikb and Dianne M Perez*,a

aThe Department of Molecular Cardiology NB50, The Lerner Research Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA
bThe Department of Pharmacology and the Vascular Biology Research Group, The University of Kentucky College of Medicine, Lexington, KY 40536, USA

*Corresponding author. Tel.: +1-216-444-2058; fax: +1-216-444-9263. Email address: perezd{at}ccf.org

Objective: {alpha}1-Adrenergic receptors (ARs) are known mediators of a positive inotropy in the heart, which may play even more important roles in heart disease. Due to a lack of sufficiently selective ligands, the contribution of each of the three {alpha}1-AR subtypes ({alpha}1A, {alpha}1B and {alpha}1D) to cardiac function is not clearly defined. In this study, we used a systemically expressing mouse model that overexpresses the {alpha}1B-AR to define the role of this subtype in cardiac function. Methods: We used the mouse Langendorff heart model to assess changes in contractility under basal and phenylephrine-induced conditions. Results: We find that a 50% increase of the {alpha}1B-AR in the heart does not change basal cardiac parameters compared to age-matched normals (heart rate, ±dP/dT and coronary flow). However, the inotropic response to phenylephrine is blunted. The same results were obtained in isolated adult myocytes. The difference in inotropy could be blocked by the selective {alpha}1A-AR antagonist, 5-methylurapidil, which correlated with decreases in {alpha}1A-AR density, suggesting that the {alpha}1B-AR had caused a compensatory downregulation of the {alpha}1A-AR. Conclusions: These results suggest that the {alpha}1B-AR does not have a major role in the positive inotropic response in the mouse myocardium but may negatively modulate the response of the {alpha}1A-AR.

KEYWORDS Adrenergic receptor; Heart; Myocyte; Inotropy


1 Present Address: GlaxoSmithKline, Research Triangle Park, NC.

Time for primary review 48 days


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
CirculationHome page
D. Jane-wit, C. Z. Altuntas, J. M. Johnson, S. Yong, P. J. Wickley, P. Clark, Q. Wang, Z. B. Popovic, M. S. Penn, D. S. Damron, et al.
{beta}1-Adrenergic Receptor Autoantibodies Mediate Dilated Cardiomyopathy by Agonistically Inducing Cardiomyocyte Apoptosis
Circulation, July 24, 2007; 116(4): 399 - 410.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
D. Urboniene, F. A.L. Dias, J. R. Pena, L. A. Walker, R. J. Solaro, and B. M. Wolska
Expression of Slow Skeletal Troponin I in Adult Mouse Heart Helps to Maintain the Left Ventricular Systolic Function During Respiratory Hypercapnia
Circ. Res., July 8, 2005; 97(1): 70 - 77.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
G. A. MacGowan, J. Rager, S. G. Shroff, and M. A. Mathier
In vivo {alpha}-adrenergic responses and troponin I phosphorylation: anesthesia interactions
J Appl Physiol, April 1, 2005; 98(4): 1163 - 1170.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
B. R. Rorabaugh, S. A. Ross, R. J. Gaivin, R. S. Papay, D. F. McCune, P. C. Simpson, and D. M. Perez
{alpha}1A- but not {alpha}1B-adrenergic receptors precondition the ischemic heart by a staurosporine-sensitive, chelerythrine-insensitive mechanism
Cardiovasc Res, February 1, 2005; 65(2): 436 - 445.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.