Nicotine self-administration and locomotor activity are not modified by the 5-HT3 antagonists ICS 205–930 and MDL 72222

Author:

Corrigall William A.,Coen Kathleen M.

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Biological Psychiatry,Clinical Biochemistry,Pharmacology,Toxicology,Biochemistry

Reference29 articles.

1. Chronic BRL 43694, a selective 5-HT3 receptor antagonist, fails to alter the number of spontaneously active midbrain dopamine neurons;Ashby;Eur. J. Pharmacol.,1990

2. Behavioural studies on WAY100289, a novel 5-HT3 receptor antagonist, in two animal models of anxiety;Bill;Eur. J. Pharmacol.,1992

3. 5-HT3 receptor antagonists block morphine- and nicotine- but not amphetamine-induced;Carboni;Psychopharmacology (Berlin),1989

4. Activation of 5-HT3 receptor by 1-phenylbiguanide increases dopamine release in the rat nucleus accumbens;Chen;Brain Res.,1991

5. Evidence that mesolimbic dopaminergic activation underlies the locomotor stimulant action of nicotine in rats;Clarke;J. Pharmacol. Exp. Ther.,1988

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