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The novel triple reuptake inhibitor JZAD-IV-22 exhibits an antidepressant pharmacological profile without locomotor stimulant or sensitization properties.
Caldarone, Barbara J; Paterson, Neil E; Zhou, Jia; Brunner, Daniela; Kozikowski, Alan P; Westphal, Koen G C; Korte-Bouws, Gerdien A H; Prins, Jolanda; Korte, S Mechiel; Olivier, Berend; Ghavami, Afshin.
Affiliation
  • Caldarone BJ; PsychoGenics, Inc, 765 Old Saw Mill River Rd, Tarrytown, New York 10591, USA. barbara.caldarone@psychogenics.com
J Pharmacol Exp Ther ; 335(3): 762-70, 2010 Dec.
Article in En | MEDLINE | ID: mdl-20864506
ABSTRACT
Triple reuptake inhibitors (TRIs) that block the dopamine transporter (DAT), norepinephrine transporter, and serotonin transporter are being developed as a new class of antidepressant that may have better efficacy and fewer side effects compared with traditional antidepressants. We describe a novel TRI, 2-[4-(4-chlorophenyl)-1-methylpiperidin-3-ylmethylsulfanyl]-1-(3-methylpiperidin-1-yl)-ethanone (JZAD-IV-22), that inhibits all three monoamine transporters with approximately equal potency in vitro. (+/-)-1-(3,4-dichlorophenyl)-3-azabicyclo-[3.1.0]hexane hydrochloride (DOV 216,303), a TRI shown to be an effective antidepressant in a clinical trial, shows reuptake inhibition similar to that of JZAD-IV-22 in vitro. Furthermore, both JZAD-IV-22 and DOV 216,303 increase levels of dopamine, norepinephrine, and serotonin in the mouse prefrontal cortex when administered by peripheral injection. JZAD-IV-22 and DOV 216,303 exhibited antidepressant-like efficacy in the mouse forced-swim and tail-suspension tests at doses that increased neurotransmitter levels. Because development of DAT inhibitors could be hindered by abuse liability, both JZAD-IV-22 and DOV 216,303 were compared in two assays that are markers of abuse potential. Both JZAD-IV-22 and DOV 216,303 partially substituted for cocaine in a drug discrimination assay in rats, and high doses of DOV 216,303 produced locomotor sensitization in mice. JZAD-IV-22 showed no evidence of sensitization at any dose tested. These results demonstrate that JZAD-IV-22 is a TRI with antidepressant-like activity similar to that of DOV 216,303. The striking feature that distinguishes the two TRIs is that locomotor sensitization, a common underlying feature of drugs of abuse, is seen with DOV 216,303 but is completely lacking in JZAD-IV-22. These findings may have implications for the potential for abuse liability in humans.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperidines / Neurotransmitter Uptake Inhibitors / Locomotion / Antidepressive Agents Language: En Journal: J Pharmacol Exp Ther Year: 2010 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Piperidines / Neurotransmitter Uptake Inhibitors / Locomotion / Antidepressive Agents Language: En Journal: J Pharmacol Exp Ther Year: 2010 Document type: Article Affiliation country: United States