TY - JOUR T1 - The Novel 5-Hydroxytryptamine<sub>1A</sub> Antagonist LY426965: Effects on Nicotine Withdrawal and Interactions with Fluoxetine JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 688 LP - 700 VL - 294 IS - 2 AU - Kurt Rasmussen AU - David O. Calligaro AU - Janet F. Czachura AU - Laura J. Dreshfield-Ahmad AU - David C. Evans AU - Susan K. Hemrick-Luecke AU - Mary Jeanne Kallman AU - William T. Kendrick AU - J. David Leander AU - David L. Nelson AU - Carl D. Overshiner AU - David B. Wainscott AU - Mary C. Wolff AU - David T. Wong AU - Theresa A. Branchek AU - John M. Zgombick AU - Yao-chang Xu Y1 - 2000/08/01 UR - http://jpet.aspetjournals.org/content/294/2/688.abstract N2 - LY426965 [(2S)-(+)-1-cyclohexyl-4-[4-(2-methoxyphenyl)-1-piperazinyl]2-methyl-2-phenyl-1-butanone monohydrochloride] is a novel compound with high affinity for the cloned human 5-hydroxytryptamine (HT)1A receptor (Ki = 4.66 nM) and 20-fold or greater selectivity over other serotonin and nonserotonin receptor subtypes. Both in vitro and in vivo studies indicate that LY426965 is a full antagonist and has no partial agonist properties. LY426965 did not stimulate [35S]guanosine-5′-O-(3-thio) triphosphate (GTPγS) binding to homogenates of cells expressing the cloned human 5-HT1A receptor in vitro but did inhibit 300 nM 5-HT-stimulated [35S]GTPγS binding with aKi value of 3.07 nM. After both p.o. and s.c. administration, LY426965 blocked the lower lip retraction, flat body posture, hypothermia, and increase in rat serum corticosterone induced by the 5-HT1A agonist 8-OH-DPAT (8-hydroxy-2-dipropylaminotetralin). In pigeons, LY426965 dose-dependently blocked the stimulus cue induced by 8-OH-DPAT but had no 8-OH-DPAT-like discriminative properties. LY426965 completely reversed the effects of nicotine withdrawal on the auditory startle reflex in rats. In microdialysis experiments, LY426965 administered together with fluoxetine significantly increased extracellular levels of serotonin above those achievable with fluoxetine alone. In electrophysiological studies, the administration of LY426965 produced a slight elevation of the firing rate of 5-HT neurons in the dorsal raphe nucleus of anesthetized rats and both blocked and reversed the effects of fluoxetine on 5-HT neuronal activity. These preclinical results indicate that LY426965 is a selective, full 5-HT1Aantagonist that may have clinical use as pharmacotherapy for smoking cessation and depression and related disorders. The American Society for Pharmacology and Experimental Therapeutics ER -