Journal
NEUROPSYCHOPHARMACOLOGY
Volume 23, Issue 2, Pages 138-150Publisher
NATURE PUBLISHING GROUP
DOI: 10.1016/S0893-133X(99)00158-X
Keywords
clonidine; lofexidine; cocaine self-administration; relapse; stress; microdialysis
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The alpha-2 adrenergic receptor agonists, cloindine, lofexidine and guanabenz, blocked stress- but not cocaine-induced reinstatement of cocaine seeking at doses that suppressed footshock-induced release of noradrenaline in prefrontal cortex and amygdala. Rats were trained to self-administer cocaine (0.5 mg/kg/infusion, i.v; 10-12 days) and, after a drug-free period (7-13 days), were returned to the self-administration chambers for daily extinction and reinstatement test sessions. Both intermittent footshock (15 min, 0.6 IIIA) and cocaine priming (20 mg/kg, i.p.) reinstated extinguished drug seeking. Pretreatment with either clonidine (20, or 40 mu g/kg, i.p.) or lofexidine (50, 100, 150, or 200 mu g/kg, i.p.) attenuated footshock- but not cocaine-induced reinstatement of cocaine seeking. Guanabenz (640 mu g/kg, ip) an alpha-2 agonist with low affinity for imidazoline type-1 receptors, also attenuated footshock- but but not cocaine-induced reinstatement of cocaine seeking. The results point to an important role for NE systems in the effects of footshock on relapse to cocaine seeking. (C) 2000 American College of Neuropsychopharmacology. Published by Elsevier Science Inc. All rights reserved.
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