Nicotine-induced changes in cerebrocortical neuroactive steroids and plasma corticosterone concentrations in the rat

Nicotine, one of the most widely used psychotropic substances, is able to induce both anxiolytic and anxiogenic effects. The effect of this drug on the brain and plasma concentrations of neuroactive steroids was examined in the rat. Anxiolytic doses of nicotine (0.03–0.3 mg/kg) had no significant ef...

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Published inPharmacology, biochemistry and behavior Vol. 74; no. 3; pp. 683 - 690
Main Authors Porcu, Patrizia, Sogliano, Cristiana, Cinus, Monica, Purdy, Robert H, Biggio, Giovanni, Concas, Alessandra
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.02.2003
Elsevier Science
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Summary:Nicotine, one of the most widely used psychotropic substances, is able to induce both anxiolytic and anxiogenic effects. The effect of this drug on the brain and plasma concentrations of neuroactive steroids was examined in the rat. Anxiolytic doses of nicotine (0.03–0.3 mg/kg) had no significant effect, whereas administration of anxiogenic doses (0.5 to 2 mg/kg) produced a dose- and time-dependent increase in the cerebrocortical concentrations of pregnenolone, progesterone, and allopregnanolone, with the greatest observed effects (+180%, +223%, and +124%, respectively) apparent at the dose of 2 mg/kg. In contrast, nicotine (1–2 mg/kg) decrease by 31% and 38%, respectively, the concentration of 3α,21-dihydroxy-5α-pregnan-20-one (allotetrahydrodeoxycorticosterone, or THDOC) in the cerebral cortex. Nicotine also increased the plasma concentrations of pregnenolone and progesterone, whereas failed to affect significantly those of allopregnanolone or THDOC. Nicotine induced a dose- and time-dependent increase in the plasma concentration of corticosterone, indicating that this drug activates the hypothalamic–pituitary–adrenal (HPA) axis. These results suggest that the changes in emotional behavior elicited by nicotine, similar to those induced by stressful stimuli or other anxiogenic drugs, are associated with an increase in neuroactive steroids content of the brain.
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ISSN:0091-3057
1873-5177
DOI:10.1016/S0091-3057(02)01065-1