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Vol. 293, Issue 2, 599-606, May 2000
Department of Biology, Northwest Nazarene University, Nampa, Idaho
(C.L.K.); Clinical Pharmacology and Gerontology Research Unit,
Department of Veterans Affairs Medical Center, Boise, Idaho (S.C.M.,
R.V.M., S.M.J., R.D.O., R.E.V.); Mountain States Medical Research
Institute, Boise, Idaho (C.L.K., S.C.M., R.V.M., R.D.O., R.E.V.); and
Departments of Medicine and Pharmacology, University of Washington
School of Medicine, Seattle, Washington (S.M.J., R.D.O., R.E.V.)
To characterize age-related changes in
-adrenergic responsiveness
and to test the hypothesis that an increase in the effects of adenosine
contribute to impaired
-adrenergic responsiveness, Fischer 344 rat
right atria (RA), left atria (LA), and left ventricular trabeculae
carnae were exposed to the
-receptor agonist isoproterenol (ISO),
followed by four doses of the selective adenosine A1
receptor agonist cyclopentyladenosine (CPA). Spontaneous contractile
rates of adult RA were inhibited more than senescent RA by CPA.
Contractility (+dF/dt) of adult LA was reduced more than senescent LA
by CPA. Left trabeculae carnae tissue responded weakly to CPA, but
senescent tissue was less responsive than adult tissue. Senescent
atrial A1 receptor density was 56% greater than in adult
tissue, whereas the density in senescent ventricles was 39%
lower than in adult tissue. No significant difference in antagonist
affinities (Kd) of A1 receptor
was observed between adult and senescent atria. In addition, agonist
competition curves indicated a significant increase in senescent atrial
and a decrease in senescent ventricular tissue in the affinity of
agonist for high-affinity A1 receptors with no difference
in dissociation constant (Ki). No
significant age-related differences in atrial or ventricular tissues
occurred in either the antagonist affinity
(Kd) or density
(Bmax) of the
-adrenergic receptors. CPA
was found to inhibit ISO-stimulated adenylate cyclase activity more in
senescent than in adult atrial and ventricular membrane preparations.
We conclude that age-related differences in functional response to ISO
and CPA, A1 receptor density, and ISO-stimulated adenylate
cyclase activity differ in atrial and ventricular myocardium.
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