Chronic nicotine and mecamylamine treatment increase brain nicotinic receptor binding without changing α4 or β2 mRNA levels

James R. Pauly, Michael J. Marks, Scott F. Robinson, Jennifer L. Van De Kamp, Allan C. Collins

Research output: Contribution to journalArticlepeer-review

128 Scopus citations

Abstract

It has recently been shown using regionally dissected tissue that both chronic mecamylamine treatment and chronic nicotine treatment increase the number of [3H]-nicotine binding sites in mouse brain, and that additive increases in the number of binding sites is observed after cotreatment with the two drugs. The studies reported here extend these findings by using quantitative autoradiographic methods to analyze the brains of chronically treated mice at a finer anatomical level of resolution. DBA/2 mice were chronically infused (i.v.) with saline, 4.0 mg/kg/hr nicotine, 4.0 mg/kg/hr mecamylamine or both drugs for 7 days. The brains of these mice were subsequently analyzed to determine the effects of chronic drug treatment on [3H]-nicotine binding and on the levels of mRNA encoding the nicotinic receptor subunits, α4 and β2. [3H]-Nicotine binding was in creased in 37 of 46 brain regions after chronic nicotine treatment (average increase = 66.5%), in 41 of 46 regions after chronic mecamylamine treatment (average increase = 56.5%), and in 45 of 46 brain regions after chronic treatment with both drugs (average increase = 107.1%). The changes in [3H]-nicotine binding produced by the two drugs across brain regions were highly (r = 0.98) and significantly correlated. These results are consistent with the proposal that the same receptors are affected by agonist or antagonist treatment. Chronic treatment had no significant effect on the levels of α4 or β2 mRNA as measured by in situ hybridization. Therefore, the increases in [3H]-nicotine binding do not arise from changes in the steady-state levels of either α4 or β2 mRNA which are believed to encode the subunits of this nicotinic receptor subtype.

Original languageEnglish
Pages (from-to)361-369
Number of pages9
JournalJournal of Pharmacology and Experimental Therapeutics
Volume278
Issue number1
StatePublished - Jul 1996

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

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