We have evaluated the physiological and behavioral effects of the CNS-selective
nicotinic agonist (E)-N-methyl-4-(3-pyridinyl) -3-butene-1-amine (RJR-2403) using a number of different methods, including 1) reversal of pharmacologically induced
amnesia in a step-through passive avoidance paradigm, 2) radial arm maze performance in rats with chemically induced brain lesions, 3) changes in HR and blood pressure in rats and 4) changes in body temperature, Y-maze activity, acoustic startle response and respiration in mice. Our results indicate that
RJR-2403 is equal to or better than
nicotine on measures of CNS function and cognitive enhancement. Specifically,
RJR-2403 significantly improved passive avoidance retention after
scopolamine-induced
amnesia and enhanced both working and reference memory in rats with
ibotenic acid lesions of the forebrain
cholinergic projection system in an 8-arm radial maze paradigm. By comparison,
RJR-2403 was 15 to 30-fold less potent than
nicotine in decreasing body temperature, respiration, Y-maze rears and crosses and acoustic startle response.
RJR-2403 also demonstrated greatly reduced cardiovascular effects.
RJR-2403 was approximately 10-fold less potent than
nicotine in increasing HR and 20-fold less potent in increasing blood pressure. These results are consistent with in vitro data indicating this compound's high selectivity for CNS nicotinic
ACh receptor subtypes relative to peripheral ganglionic and muscle-type nicotinic
ACh receptors. Therefore,
RJR-2403 may be a valuable tool for understanding the central and peripheral pharmacology of nicotinic
cholinergic systems as well as a potential lead compound for the development of nicotinic
therapeutics to treat neurological diseases where
cholinergic neurotransmission has been compromised.