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EMD386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli

Activation of 5-hydroxytyptamine(6) (5-HT(6)) receptors stimulates attentional switching and 5-HT(6) receptor antagonists are putative drugs for psychosis. Latent inhibition (LI) provides a pre-clinical model of attentional switching and ‘antipsychotic-like’ action and is known to be modulated by 5-...

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Autores principales: Cassaday, Helen Joan, Thur, Karen Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947809/
https://www.ncbi.nlm.nih.gov/pubmed/31621457
http://dx.doi.org/10.1177/0269881119882855
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author Cassaday, Helen Joan
Thur, Karen Elizabeth
author_facet Cassaday, Helen Joan
Thur, Karen Elizabeth
author_sort Cassaday, Helen Joan
collection PubMed
description Activation of 5-hydroxytyptamine(6) (5-HT(6)) receptors stimulates attentional switching and 5-HT(6) receptor antagonists are putative drugs for psychosis. Latent inhibition (LI) provides a pre-clinical model of attentional switching and ‘antipsychotic-like’ action and is known to be modulated by 5-hydroxytyptamine. In the present study, LI was shown in a fear conditioning procedure that measured suppression of drinking after conditioning with footshock. In two experiments (each n = 48) it was shown that pre-exposure to both light- and noise-conditioned stimuli reduced conditioned suppression relative to the corresponding non-pre-exposed control. However, counter to prediction, LI was intact after treatment with the 5-HT(6) agonist EMD386088 (5 mg/kg).
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spelling pubmed-69478092020-02-07 EMD386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli Cassaday, Helen Joan Thur, Karen Elizabeth J Psychopharmacol Original Papers Activation of 5-hydroxytyptamine(6) (5-HT(6)) receptors stimulates attentional switching and 5-HT(6) receptor antagonists are putative drugs for psychosis. Latent inhibition (LI) provides a pre-clinical model of attentional switching and ‘antipsychotic-like’ action and is known to be modulated by 5-hydroxytyptamine. In the present study, LI was shown in a fear conditioning procedure that measured suppression of drinking after conditioning with footshock. In two experiments (each n = 48) it was shown that pre-exposure to both light- and noise-conditioned stimuli reduced conditioned suppression relative to the corresponding non-pre-exposed control. However, counter to prediction, LI was intact after treatment with the 5-HT(6) agonist EMD386088 (5 mg/kg). SAGE Publications 2019-10-17 2020-01 /pmc/articles/PMC6947809/ /pubmed/31621457 http://dx.doi.org/10.1177/0269881119882855 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Papers
Cassaday, Helen Joan
Thur, Karen Elizabeth
EMD386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli
title EMD386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli
title_full EMD386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli
title_fullStr EMD386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli
title_full_unstemmed EMD386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli
title_short EMD386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli
title_sort emd386088 (5 mg/kg) has no effect on latent inhibition shown to both light and noise stimuli
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947809/
https://www.ncbi.nlm.nih.gov/pubmed/31621457
http://dx.doi.org/10.1177/0269881119882855
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