Modulation of cardiac A1-adenosine receptors in rats following treatment with agents affecting heart rate

N. Balas, M. Arad, B. Rabinowitz, A. Shainberg*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Effects of chronic treatment affecting heart rate on A1 adenosine receptor levels and their functions were studied. Treatment of rats with isoproterenol for 10 days accelerated heart rate and increased the level of adenosine receptors, in both the atria and ventricles. Negative dromotropic response of isolated heart to adenosine was enhanced in isoproterenol-treated rats. Similar results were obtained following treatment with atropine sulfate, or swimming training but not after treatment with thyroxine. On the other hand, treatment with amiodarone, which normally causes a decrease in heart rate, also increased the level of adenosine receptors in both atria and ventricles. The sensitivity of the isolated heart to the negative dromotropic and chronotropic effects of adenosine was not enhanced in the amiodarone treated rats. Similar results were obtained following treatment with propranolol, while treatment with PTU (6-n-propyl-2-thiouracil) increased adenosine sensitivity in the isolated heart. It was concluded that the levels of A1 adenosine receptors in the heart correspond to heart rate, and to cardiac efficiency. While an increase in heart rate was followed by up-regulation of A1 adenosine receptors, a decrease in heart rate caused a moderate elevation of these receptors.

Original languageEnglish
Pages (from-to)107-116
Number of pages10
JournalMolecular and Cellular Biochemistry
Volume231
Issue number1-2
DOIs
StatePublished - 2002

Funding

FundersFunder number
Research Authority of Bar-Ilan University
Ministry of Health, State of Israel

    Keywords

    • 8-cyclopentyl 1,3-dipropylxanthine
    • Adenosine
    • Heart rate
    • Ligand binding

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