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Functional analysis of myocardial performance in murine hearts overexpressing the human beta 2-adrenergic receptor.

Publication ,  Journal Article
Bittner, HB; Chen, EP; Milano, CA; Lefkowitz, RJ; Van Trigt, P
Published in: J Mol Cell Cardiol
March 1997

Transgenic mice overexpressing the human beta 2-adrenergic receptor gene were compared with wild mice type in terms of cardiac function, using a modified work-performing isolated murine heart preparation and on-line computer analysis. A preload-dependent experiment was performed, in which venous return was gradually increased in 5 mmHg increments from 5 mmHg to 25 mmHg. At each preload, aortic flow, left atrial pressure and aortic pressure were measured in all hearts, and from these parameters stroke volume, contractility, and cardiac index (cardiac output divided by body weight in g) were calculated and compared between groups. At increasing preload levels, the heart rates ranged from 322 beats/min (+/-29) to 369 beats/min (+/-39) in control mice and from 469 beats/min (+/-36) to 540 beats/min (+/-39) in transgenic mice. Cardiac index increased from 138 microliters/min/g (+/-13) and 48 microliters/min/g (+/-5) for transgenic and control mice, respectively at 5 mmHg preload to 262 microliters/min/g (+/-51) and 167 microliters/min/g (+/-15), respectively at 20 mmHg preload. The contractility in the transgenic mice were significantly increased at lower preload levels compared to control mice (1420 mmHg/s +/- 204 v 1187 mmHg/s +/- 127). An increase in myocardial adrenergic receptor density (100-200 fold) leads to significantly higher indices of cardiac function in transgenic mice compared to control mice. The increased heart rate leading to a positive inotropic effect in the hearts of transgenic mice is, at least in part, due to the overexpression of adrenergic receptors. These findings suggest a possible alternative method of establishing a positive chronotropic and inotropic state without the use of pharmacological agents.

Duke Scholars

Published In

J Mol Cell Cardiol

DOI

ISSN

0022-2828

Publication Date

March 1997

Volume

29

Issue

3

Start / End Page

961 / 967

Location

England

Related Subject Headings

  • Receptors, Adrenergic, beta-2
  • Myocardium
  • Myocardial Contraction
  • Mice, Transgenic
  • Mice
  • In Vitro Techniques
  • Humans
  • Hemodynamics
  • Heart
  • Gene Expression
 

Citation

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MLA
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Bittner, H. B., Chen, E. P., Milano, C. A., Lefkowitz, R. J., & Van Trigt, P. (1997). Functional analysis of myocardial performance in murine hearts overexpressing the human beta 2-adrenergic receptor. J Mol Cell Cardiol, 29(3), 961–967. https://doi.org/10.1006/jmcc.1996.0339
Bittner, H. B., E. P. Chen, C. A. Milano, R. J. Lefkowitz, and P. Van Trigt. “Functional analysis of myocardial performance in murine hearts overexpressing the human beta 2-adrenergic receptor.J Mol Cell Cardiol 29, no. 3 (March 1997): 961–67. https://doi.org/10.1006/jmcc.1996.0339.
Bittner HB, Chen EP, Milano CA, Lefkowitz RJ, Van Trigt P. Functional analysis of myocardial performance in murine hearts overexpressing the human beta 2-adrenergic receptor. J Mol Cell Cardiol. 1997 Mar;29(3):961–7.
Bittner, H. B., et al. “Functional analysis of myocardial performance in murine hearts overexpressing the human beta 2-adrenergic receptor.J Mol Cell Cardiol, vol. 29, no. 3, Mar. 1997, pp. 961–67. Pubmed, doi:10.1006/jmcc.1996.0339.
Bittner HB, Chen EP, Milano CA, Lefkowitz RJ, Van Trigt P. Functional analysis of myocardial performance in murine hearts overexpressing the human beta 2-adrenergic receptor. J Mol Cell Cardiol. 1997 Mar;29(3):961–967.
Journal cover image

Published In

J Mol Cell Cardiol

DOI

ISSN

0022-2828

Publication Date

March 1997

Volume

29

Issue

3

Start / End Page

961 / 967

Location

England

Related Subject Headings

  • Receptors, Adrenergic, beta-2
  • Myocardium
  • Myocardial Contraction
  • Mice, Transgenic
  • Mice
  • In Vitro Techniques
  • Humans
  • Hemodynamics
  • Heart
  • Gene Expression