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1Department of Pharmacology and Experimental Therapeutics; 2Maryland Psychiatric Research Center, University of Maryland School of Medicine; 3Department of Biological Sciences, University of Maryland Baltimore County, Baltimore, Maryland; and 4Department of Pharmacology and Toxicology, Rutgers University, Piscataway, New Jersey
Submitted 20 October 2006; accepted in final form 5 December 2006
Prepulse inhibition (PPI), a measure of sensorimotor gating impaired in patients with schizophrenia, is more sensitive to disruption by apomorphine in prepubertal August Copenhagen Irish (ACI) than Sprague-Dawley (SD) rats. In brain regions including the hippocampus, PPI is modulated by
7* nicotinic receptors (nAChRs) and kynurenic acid (KYNA), a kynurenine metabolite that blocks
7 nAChRs. Here, KYNA levels and nAChR activities were measured in the hippocampi of 10- to 23-day-old ACI and SD rats of both sexes. Hippocampal KYNA levels were not different between ACI and SD rats. In hippocampal slices from both rat strains, choline (10 mM) evoked
7* nAChR-mediated type IA currents in CA1 stratum radiatum (SR) interneurons. In the presence of
7 nAChR antagonists, acetylcholine (ACh, 1 mM) evoked
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2* nAChR-mediated type II currents. ACh also triggered excitatory postsynaptic currents (EPSCs) that resulted from
3
4* nAChR activation in glutamatergic neurons/axons synapsing onto the interneurons. The magnitude of the nicotinic responses did not differ significantly between male and female rats. Only the magnitude of
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4* nAChR responses and the frequency of spontaneous EPSCs recorded from CA1 SR interneurons differed between the rat strains, being significantly larger in ACI than SD rats. These results indicate that the
3
4* nAChR activity in glutamatergic neurons/axons and the number of glutamatergic terminals synapsing onto CA1 SR interneurons are larger in prepubertal ACI than SD rats. The differential sensitivity of these rats to PPI disruption by apomorphine may result from strain-specific levels of glutamatergic activity and its strain-specific modulation by
3
4* nAChRs in the hippocampus.
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