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Prepulse inhibition in fawn-hooded rats: increased sensitivity to 5-HT1A receptor stimulation.
Eur Neuropsychopharmacol. 2004 Oct; 14(5):373-9.EN

Abstract

Prepulse inhibition of startle is a model of sensorimotor gating, which is disrupted in alcoholism, as well as mental illnesses such as schizophrenia. The fawn-hooded (FH) rat strain has been used as an animal model of alcoholism. FH rats showed significantly lower startle amplitude than Wistar-Kyoto (WKY) rats and Sprague-Dawley (SD) rats. Increasing doses of the 5-HT(1A) receptor agonist 8-OH-DPAT caused disruption of PPI, with the effect being significantly greater in FH rats compared to WKY rats. In all strains, treatment with 0.5 mg/kg of 8-OH-DPAT significantly reduced PPI. In contrast, 0.1 mg/kg of 8-OH-DPAT caused disruption only in the FH strain. Treatment with amphetamine, apomorphine and MK-801 also significantly reduced PPI, however, there was no difference between the strains. This study shows increased sensitivity of FH rats to the disruption of PPI caused by 5-HT(1A) receptor stimulation, suggesting a link between 5-HT(1A) receptors, sensorimotor gating and aspects of the FH rat phenotype.

Authors+Show Affiliations

Behavioural Neuroscience Laboratory, Mental Health Research Institute, Parkville, Victoria 3052, Australia.No affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Journal Article

Language

eng

PubMed ID

15336298

Citation

Martin, Sally, et al. "Prepulse Inhibition in Fawn-hooded Rats: Increased Sensitivity to 5-HT1A Receptor Stimulation." European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology, vol. 14, no. 5, 2004, pp. 373-9.
Martin S, Lawrence AJ, van den Buuse M. Prepulse inhibition in fawn-hooded rats: increased sensitivity to 5-HT1A receptor stimulation. Eur Neuropsychopharmacol. 2004;14(5):373-9.
Martin, S., Lawrence, A. J., & van den Buuse, M. (2004). Prepulse inhibition in fawn-hooded rats: increased sensitivity to 5-HT1A receptor stimulation. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology, 14(5), 373-9.
Martin S, Lawrence AJ, van den Buuse M. Prepulse Inhibition in Fawn-hooded Rats: Increased Sensitivity to 5-HT1A Receptor Stimulation. Eur Neuropsychopharmacol. 2004;14(5):373-9. PubMed PMID: 15336298.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Prepulse inhibition in fawn-hooded rats: increased sensitivity to 5-HT1A receptor stimulation. AU - Martin,Sally, AU - Lawrence,Andrew J, AU - van den Buuse,Maarten, PY - 2003/06/17/received PY - 2003/09/30/revised PY - 2003/10/28/accepted PY - 2004/9/1/pubmed PY - 2004/12/16/medline PY - 2004/9/1/entrez SP - 373 EP - 9 JF - European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology JO - Eur Neuropsychopharmacol VL - 14 IS - 5 N2 - Prepulse inhibition of startle is a model of sensorimotor gating, which is disrupted in alcoholism, as well as mental illnesses such as schizophrenia. The fawn-hooded (FH) rat strain has been used as an animal model of alcoholism. FH rats showed significantly lower startle amplitude than Wistar-Kyoto (WKY) rats and Sprague-Dawley (SD) rats. Increasing doses of the 5-HT(1A) receptor agonist 8-OH-DPAT caused disruption of PPI, with the effect being significantly greater in FH rats compared to WKY rats. In all strains, treatment with 0.5 mg/kg of 8-OH-DPAT significantly reduced PPI. In contrast, 0.1 mg/kg of 8-OH-DPAT caused disruption only in the FH strain. Treatment with amphetamine, apomorphine and MK-801 also significantly reduced PPI, however, there was no difference between the strains. This study shows increased sensitivity of FH rats to the disruption of PPI caused by 5-HT(1A) receptor stimulation, suggesting a link between 5-HT(1A) receptors, sensorimotor gating and aspects of the FH rat phenotype. SN - 0924-977X UR - https://www.unboundmedicine.com/medline/citation/15336298/Prepulse_inhibition_in_fawn_hooded_rats:_increased_sensitivity_to_5_HT1A_receptor_stimulation_ DB - PRIME DP - Unbound Medicine ER -