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Vol. 280, Issue 1, 332-345, 1997
Departments of
Anesthesiology (D.E.W., J.P.K., W.G., S.M.),
Pharmacology (S.M.),
Biomathematical Sciences (I.S.),
Physiology and
Biophysics (I.S.) and
Medicine (E.N.S.), Mount Sinai School of Medicine
of the City University of New York, New York, New York
Activation of beta-2 adrenoceptors (BAR) in smooth
muscle preparations is associated with a rapid, reversible and
incomplete receptor desensitization, resulting in a steady-state
relaxation response to BAR agonists. Based on results from cell culture
studies, we hypothesize that, in the isolated guinea pig trachea, this steady state is a result of a concurrent resensitization of
desensitizing BAR. In tracheal segments maintained at mechanical tone
(4-6 g), isoproterenol (ISO) and the partial BAR agonist salbutamol
(SALB) elicited a monotonic, rapid (1-3 min) and reproducible
relaxation response that could be maintained for up to 45 min and was
completely reversed by propranolol. Similarly, tissues preconstricted
with 0.1 µM carbachol (CARB) responded with a sustained relaxation response to ISO. In contrast, in tissues preconstricted with 0.3 to 10 µM CARB or with 75 mM KCl, the relaxation elicited by ISO was
followed by a slow (20-30 min) and partial restoration of muscle tone
("fade"). The relaxation and fade were observed when CARB-constricted tissues were relaxed with SALB (0.2 or 10 µM) or 10 µM salmeterol. No response to SALB was observed when tissues were
preconstricted with KCl. The fade met criteria for its classification as a homologous desensitization of the relaxation response at the BAR
level. In desensitized washed tissues, a complete recovery of the
original relaxation response could be detected within 60 min of drug
removal. A propranolol- and ICI 118-551-sensitive steady state was
achieved 30 to 35 min after the addition of BAR agonists to the
isolated tissues. A three-compartment phenomenological kinetic model
accurately described the observed data, defining one steady-state and
three rate constants, describing relaxation (k1), desensitization
(k2) and resensitization
(k3). The values of
k2 and k3 for the
response to SALB and to salmeterol were significantly larger than those
observed for ISO. In the presence of KCl, the values of
k2 and k3 for the
response to ISO were indistinguishable from those measured in the
presence of CARB. Given the parameters defined by our model, we propose
that desensitization and resensitization of BAR in the isolated guinea
pig trachea are distinct concurrent processes whose net result actively
maintains a sustained partial relaxation response to ISO, SALB or
salmeterol. The component of resensitization in the presence of agonist
may account for the clinical efficacy of inhaled BAR agonists.
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