![]() |
|
|
Vol. 281, Issue 2, 690-698, 1997
Department of Pharmacology, Faculty of Medicine, University of the
Basque Country, E-48940 Leioa, Vizcaya, Spain
The population of reserve alpha-2 adrenoceptors that
mediate the inhibitory effect of clonidine on the activity of locus
coeruleus neurons has been studied using extracellular recordings in
anesthetized rats. Animals were pretreated with the irreversible
receptor antagonist N-ethoxycarbonyl-2-ethoxy-1-2-dihydroquinoline (EEDQ).
In rats pretreated with EEDQ (1, 2 and 6 mg/kg, i.p., 6 hr before
experiment), there was an increase in firing rate, a reduction in
firing regularity (i.e., increased variation
coefficient) and an increase in burst firing of locus coeruleus
neurons. Partial receptor inactivation with EEDQ (1 and 2 mg/kg, i.p.)
caused a dose-dependent shift to the right of dose-effect curves for
i.v. administered clonidine together with a reduction in its maximal
effect. Higher doses of EEDQ (6 mg/kg, i.p.) completely abolished the
effect induced by clonidine. This blockade was associated with a
progressive decrease in the number of remaining receptors
(noninactivated receptors). The pseudo-constant of dissociation for the
drug-receptor complex was calculated to be approximately 70 µg/kg.
The receptor occupancy-effect relationship was hyperbolic giving a
value of only ~ 4% occupancy at 50% maximal effect. Estimates
of noninactivated receptors and percentage of receptor occupancy at
50% of maximal effect were comparable when locally administered
clonidine was used. After complete receptor inactivation with EEDQ (6 mg/kg), dose-effect curves for clonidine recovered gradually. The
inhibitory effect of clonidine returned faster (half-life = 14 hr)
than the receptor pool (half-life = 37 hr). These results indicate
that locus coeruleus neurons have a large reserve of
2
adrenoceptors that in addition, are rapidly turned over.