KKHA-761, a potent D3 receptor antagonist with high 5-HT1A receptor affinity, exhibits antipsychotic properties in animal models of schizophrenia

Pharmacol Biochem Behav. 2005 Oct;82(2):361-72. doi: 10.1016/j.pbb.2005.09.006. Epub 2005 Oct 10.

Abstract

KKHA-761, 1-{4-[3-(3,4-dimethoxy-phenyl)-isoxazol-5-yl]-butyl}-4-(2-methoxy-phenyl)-piperazine, has a high affinity (Ki=3.85 nM) for human dopamine D3 receptor with about 70-fold selectivity over the human dopamine D(2L) receptor (Ki=270 nM). KKHA-761 also showed high affinity for cloned human 5-HT1A receptor (Ki=6.4 nM). KKHA-761 exhibited D3 and 5-HT1A receptor antagonist activities in vitro, reversing dopamine- or 5-HT-mediated stimulation of [35S]GTPrS binding. The in vivo pharmacological profile of KKHA-761 was compared with both typical and atypical antipsychotics including clozapine and haloperidol. Apomorphine-induced dopaminergic behavior, cage climbing, in mice was potently blocked by a single administration (i.p.) of KKHA-761 (ID50=4.06 mg/kg) or clozapine (ID50=4.0 mg/kg). Cocaine- or MK-801-induced hyperactivity in animals was markedly inhibited by KKHA-761 or clozapine. In addition, KKHA-761 significantly reversed the disruption of prepulse inhibition (PPI) produced by apomorphine in mice, indicating the antidopaminergic or antipsychotic activity of KKHA-761 in mice. However, KKHA-761 was inactive in the forced swimming behavioral despair model in mice, suggesting lack of antidepressant properties. KKHA-761 attenuated the hypothermia induced by a selective dopamine D3 agonist, 7-OH-DPAT, in mice, whereas clozapine enhanced it. Moderate doses of both KKHA-761 and clozapine did not increase serum prolactin levels in rats. Lower doses of, however, haloperidol significantly increased prolactin secretion. KKHA-761 did not induce cataleptic response up to 20 mg/kg, but significant catalepsy was shown at lower doses of clozapine and haloperidol. Furthermore, KKHA-761 showed a low incidence of rotarod ataxia (TD50=34.4 mg/kg, i.p.) in mice. The present results, therefore, suggest that KKHA-761 is a potent antipsychotic agent with combined dopamine D3 and serotonin 5-HT1A receptors modulation activity, which may further enhance its therapeutic potential for anxiety, psychotic depression, and other related disorders.

MeSH terms

  • Animals
  • Antipsychotic Agents*
  • Body Temperature / drug effects
  • Catalepsy / chemically induced
  • Catalepsy / psychology
  • Cell Line
  • Dopamine Uptake Inhibitors / pharmacology
  • Guanosine 5'-O-(3-Thiotriphosphate) / metabolism
  • Humans
  • Ion Channels / drug effects
  • Ion Channels / metabolism
  • Isoxazoles / pharmacokinetics
  • Isoxazoles / pharmacology*
  • Male
  • Mice
  • Mice, Inbred ICR
  • Piperazines / pharmacokinetics
  • Piperazines / pharmacology*
  • Postural Balance / drug effects
  • Prolactin / metabolism
  • Radioligand Assay
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Serotonin, 5-HT1A / drug effects
  • Receptor, Serotonin, 5-HT1A / metabolism*
  • Receptors, Dopamine D1 / metabolism
  • Receptors, Dopamine D3 / antagonists & inhibitors*
  • Receptors, Dopamine D4 / drug effects
  • Receptors, Dopamine D4 / metabolism
  • Reflex, Startle / drug effects
  • Schizophrenia / drug therapy*
  • Schizophrenic Psychology
  • Serotonin Receptor Agonists / pharmacology
  • Spiperone / metabolism
  • Swimming / psychology

Substances

  • Antipsychotic Agents
  • Dopamine Uptake Inhibitors
  • Ion Channels
  • Isoxazoles
  • KKHA-761
  • Piperazines
  • Receptors, Dopamine D1
  • Receptors, Dopamine D3
  • Serotonin Receptor Agonists
  • Receptor, Serotonin, 5-HT1A
  • Receptors, Dopamine D4
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • Spiperone
  • Prolactin