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Stereoselective and region-specific induction of immediate early gene expression in rat parietal cortex by blockade of neurokinin 1 receptors

Department of Pharmacology, University of Oxford, Oxford, UK.

Simone B. Sartori

Department of Pharmacology and Toxicology, Institute of Pharmacy, University of Innsbruck, Innsbruck, Austria.

Anna Halton

University Department of Pharmacology, Oxford, UK.

Qi Pei

University Department of Pharmacology, Oxford, UK.

Catherine Rochat

I.d.R. Servier, 125 chemin de Ronde, 78290 Croissy/Seine, France.

Nicolas Singewald

Department of Pharmacology and Toxicology, Institute of Pharmacy, University of Innsbruck, Innsbruck, Austria.

Trevor Sharp

University Department of Pharmacology, Oxford, UK.

Mark Millan

I.d.R. Servier, 125 chemin de Ronde, 78290 Croissy/Seine, France.

Antagonists at neurokinin 1 (NK1) receptors are attracting attention as potential treatments for depressive states in light of their actions in behavioural models predictive of antidepressant properties, their modulation of corticolimbic monoaminergic transmission, and their influence upon neural plasticity. Here, we evaluated the influence of NK1 receptor blockade upon two immediate early genes, Arc and c-fos, implicated in mechanisms of synaptic plasticity. Administration of the selective NK1 receptor antagonist, GR205,171 (40, but not 1, 5 or 10mg/kg i.p.), elicited a pronounced elevation in mRNA encoding Arc in both outer and inner layers of the parietal cortex of rat brain. This action was region-specific inasmuch as Arc expression did not change in other cortical territories examined including frontal cortex, nor in CA1, CA3 and the dentate gyrus of the hippocampus. In comparison to GR205,171, its less active isomer GR226,206 (1–40mg/kg) did not significantly modify Arc gene expression in parietal cortex or other cortical areas. GR205,171 (40mg/kg) also increased the abundance of c-fosmRNA in outer and inner parietal cortex and caused a corresponding increase in c-fosimmunoreactivity in this region. GR226,206 (40mg/kg i.p.) had no effect on either c-fos mRNA or protein in parietal cortex. In conclusion, administration of GR205,171 elicits a stereospecific increase in Arcand c-fos expression in rat parietal cortex but not in other cortical regions. These data suggest that the parietal cortex plays a role in the central actions of NK1 receptor antagonists.

Key Words: NK1 receptor • rat • c-fos • Arc • in situ hybridization • immunocytochemistry

This version was published on July 1, 2006

Journal of Psychopharmacology, Vol. 20, No. 4, 570-576 (2006)
DOI: 10.1177/0269881105059327


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