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Vol. 296, Issue 1, 15-21, January 2001
Department of Pharmacology and Physiology, University of Rochester
Medical Center, Rochester, New York
When nicotine is administered s.c. to rats, tyrosine hydroxylase (TH)
enzyme activity and TH gene transcription rate are activated, and TH
mRNA and TH protein are induced in adrenal medulla. In this report we
test whether nicotine elicits these responses via trans-synaptic
mechanisms initiated by the actions of the drug in the brain. Our
results demonstrate that intraventricular (i.v.t.) administration of
nicotine produces a dose-dependent activation of adrenal TH, which is
blocked by i.v.t. administration of hexamethonium, but not by i.p.
administration of this nicotinic acetylcholine receptor antagonist. We
also show that surgical transection of the splanchnic nerve blocks the
activation of adrenal TH by i.v.t.-administered nicotine. Repeated
i.v.t. administration of nicotine over a 3-h period (injections spaced
30 min apart) leads to a sustained activation of adrenal TH, suggesting
that this central response to nicotine does not readily desensitize.
Intraventricular administration of nicotine also stimulates the TH gene
transcription rate in rat adrenal medulla. When administered repeatedly
i.v.t. or s.c. over 3 h, nicotine induces adrenal TH mRNA. This
induction is dependent on innervation of the adrenal medulla, even when
the drug is injected s.c. Our results demonstrate that the central effects of nicotine are sufficient to activate TH and induce TH gene
expression in rat adrenal medulla. Furthermore, our results suggest
that this centrally mediated response to nicotine is essential for the
induction of adrenal TH mRNA.
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