Double activity imaging reveals distinct cellular targets of haloperidol, clozapine and dopamine D(3) receptor selective RGH-1756

Neuropharmacology. 2001 Mar;40(3):383-93. doi: 10.1016/s0028-3908(00)00163-5.

Abstract

Acute administration of typical (haloperidol) and atypical (clozapine) antipsychotics results in distinct and overlapping regions of immediate-early gene expression in the rat brain. RGH-1756 is a recently developed atypical antipsychotic with high affinity to dopamine D(3) receptors that results in a unique pattern of c-Fos induction. A single injection of either antipsychotic results in c-fos mRNA expression that peaks around 30 min after drug administration, while the maximum of c-Fos protein induction is seen 2 h after challenge. The transient and distinct temporal inducibility of c-fos mRNA and c-Fos protein was exploited to reveal and compare cellular targets of different antipsychotic drugs by concomitant localization of c-fos mRNA and c-Fos immunoreactivity in brain sections of rats that were timely challenged with two different antipsychotics. Double activity imaging revealed that haloperidol, clozapine and RGH-1756 share cellular targets in the nucleus accumbens, where 40% of all labeled neurons displayed both c-fos mRNA and c-Fos protein. Haloperidol activates cells in the caudate putamen, while clozapine-responsive, single labeled neurons were dominant in the prefrontal cortex and major island of Calleja. RGH-1756 targets haloperidol-sensitive cells in the caudate putamen, but cells that are activated by clozapine and RGH-1756 in the major island of Calleja are different.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antipsychotic Agents / administration & dosage
  • Brain / anatomy & histology
  • Brain / drug effects
  • Brain / metabolism*
  • Cell Count / statistics & numerical data
  • Clozapine / administration & dosage*
  • Clozapine / pharmacokinetics
  • Densitometry
  • Genes, Immediate-Early / drug effects
  • Haloperidol / administration & dosage*
  • Haloperidol / pharmacokinetics
  • Immunohistochemistry
  • In Situ Hybridization
  • Injections, Intraperitoneal
  • Male
  • Neurons / cytology
  • Neurons / metabolism
  • Piperazines / administration & dosage*
  • Piperazines / pharmacokinetics
  • Proto-Oncogene Proteins c-fos / analysis
  • Proto-Oncogene Proteins c-fos / biosynthesis
  • Proto-Oncogene Proteins c-fos / genetics
  • RNA, Messenger / analysis
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Wistar
  • Receptors, Dopamine D2 / metabolism*
  • Receptors, Dopamine D3
  • Thiazoles / administration & dosage*
  • Thiazoles / pharmacokinetics
  • Tissue Distribution

Substances

  • 1-(2-methoxy-phenyl)-4-(4-(4-(6-imidazol(2,1-b) thiazolyl)-phenoxy)-butyl-4-(14)C)-piperazine dimethane
  • Antipsychotic Agents
  • Drd3 protein, rat
  • Piperazines
  • Proto-Oncogene Proteins c-fos
  • RNA, Messenger
  • Receptors, Dopamine D2
  • Receptors, Dopamine D3
  • Thiazoles
  • Clozapine
  • Haloperidol