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Functional evaluation of NK(1) antagonism on cue reactivity in opiate dependence; An fMRI study
BACKGROUND: Opiate addiction is a major health challenge with substantial societal cost. Though harm minimisation strategies have been effective, there is a growing need for new treatments for detoxification and relapse prevention. Preclinical research has found neurokinin 1 (NK(1)) receptors have p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047866/ https://www.ncbi.nlm.nih.gov/pubmed/33548897 http://dx.doi.org/10.1016/j.drugalcdep.2021.108564 |
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author | Fonville, Leon Paterson, Louise Herlinger, Katherine Hayes, Alexandra Hill, Raymond Nutt, David Lingford-Hughes, Anne |
author_facet | Fonville, Leon Paterson, Louise Herlinger, Katherine Hayes, Alexandra Hill, Raymond Nutt, David Lingford-Hughes, Anne |
author_sort | Fonville, Leon |
collection | PubMed |
description | BACKGROUND: Opiate addiction is a major health challenge with substantial societal cost. Though harm minimisation strategies have been effective, there is a growing need for new treatments for detoxification and relapse prevention. Preclinical research has found neurokinin 1 (NK(1)) receptors have prominent effects on opiate reward and reinforcement, and human studies have found NK(1) antagonism led to reductions in craving and withdrawal. However, its effect on brain mechanisms in opiate addiction has not yet been examined. METHODS: This study aims to assess the impact of NK(1) antagonist aprepitant on heroin cue-elicited changes in blood-oxygenation level dependent (BOLD) signal in opiate dependent individuals undergoing detoxification. Participants will attend two scanning sessions and receive a single dose of aprepitant (320 mg) and a placebo in a randomised, cross-over design. During functional magnetic resonance imaging participants will undergo two runs of a cue reactivity task, which consists of passive viewing of drug cues or neutral cues in a block design fashion. We hypothesise that NK(1) antagonism will attenuate the BOLD response to drug cues in the caudate nucleus and amygdala. Regions of interest were selected based on NK(1) receptor density and their role in cue reactivity and craving. |
format | Online Article Text |
id | pubmed-8047866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80478662021-04-21 Functional evaluation of NK(1) antagonism on cue reactivity in opiate dependence; An fMRI study Fonville, Leon Paterson, Louise Herlinger, Katherine Hayes, Alexandra Hill, Raymond Nutt, David Lingford-Hughes, Anne Drug Alcohol Depend Registered Report BACKGROUND: Opiate addiction is a major health challenge with substantial societal cost. Though harm minimisation strategies have been effective, there is a growing need for new treatments for detoxification and relapse prevention. Preclinical research has found neurokinin 1 (NK(1)) receptors have prominent effects on opiate reward and reinforcement, and human studies have found NK(1) antagonism led to reductions in craving and withdrawal. However, its effect on brain mechanisms in opiate addiction has not yet been examined. METHODS: This study aims to assess the impact of NK(1) antagonist aprepitant on heroin cue-elicited changes in blood-oxygenation level dependent (BOLD) signal in opiate dependent individuals undergoing detoxification. Participants will attend two scanning sessions and receive a single dose of aprepitant (320 mg) and a placebo in a randomised, cross-over design. During functional magnetic resonance imaging participants will undergo two runs of a cue reactivity task, which consists of passive viewing of drug cues or neutral cues in a block design fashion. We hypothesise that NK(1) antagonism will attenuate the BOLD response to drug cues in the caudate nucleus and amygdala. Regions of interest were selected based on NK(1) receptor density and their role in cue reactivity and craving. Elsevier 2021-04-01 /pmc/articles/PMC8047866/ /pubmed/33548897 http://dx.doi.org/10.1016/j.drugalcdep.2021.108564 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Registered Report Fonville, Leon Paterson, Louise Herlinger, Katherine Hayes, Alexandra Hill, Raymond Nutt, David Lingford-Hughes, Anne Functional evaluation of NK(1) antagonism on cue reactivity in opiate dependence; An fMRI study |
title | Functional evaluation of NK(1) antagonism on cue reactivity in opiate dependence; An fMRI study |
title_full | Functional evaluation of NK(1) antagonism on cue reactivity in opiate dependence; An fMRI study |
title_fullStr | Functional evaluation of NK(1) antagonism on cue reactivity in opiate dependence; An fMRI study |
title_full_unstemmed | Functional evaluation of NK(1) antagonism on cue reactivity in opiate dependence; An fMRI study |
title_short | Functional evaluation of NK(1) antagonism on cue reactivity in opiate dependence; An fMRI study |
title_sort | functional evaluation of nk(1) antagonism on cue reactivity in opiate dependence; an fmri study |
topic | Registered Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047866/ https://www.ncbi.nlm.nih.gov/pubmed/33548897 http://dx.doi.org/10.1016/j.drugalcdep.2021.108564 |
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