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Brain region‐specific neuromedin U signalling regulates alcohol‐related behaviours and food intake in rodents
Albeit neuromedin U (NMU) attenuates alcohol‐mediated behaviours, its mechanisms of action are poorly defined. Providing that the behavioural effects of alcohol are processed within the nucleus accumbens (NAc) shell, anterior ventral tegmental area (aVTA), and laterodorsal tegmental area (LDTg), we...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187236/ https://www.ncbi.nlm.nih.gov/pubmed/31069918 http://dx.doi.org/10.1111/adb.12764 |
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author | Vallöf, Daniel Kalafateli, Aimilia Lydia Jerlhag, Elisabet |
author_facet | Vallöf, Daniel Kalafateli, Aimilia Lydia Jerlhag, Elisabet |
author_sort | Vallöf, Daniel |
collection | PubMed |
description | Albeit neuromedin U (NMU) attenuates alcohol‐mediated behaviours, its mechanisms of action are poorly defined. Providing that the behavioural effects of alcohol are processed within the nucleus accumbens (NAc) shell, anterior ventral tegmental area (aVTA), and laterodorsal tegmental area (LDTg), we assessed the involvement of NMU signalling in the aforementioned areas on alcohol‐mediated behaviours in rodents. We further examined the expression of NMU and NMU receptor 2 (NMUR2) in NAc and the dorsal striatum of high compared with low alcohol‐consuming rats, as this area is of importance in the maintenance of alcohol use disorder (AUD). Finally, we investigated the involvement of NAc shell, aVTA and LDTg in the consumption of chow and palatable peanut butter, to expand the link between NMU and reward‐related behaviours. We demonstrated here, that NMU into the NAc shell, but not aVTA or LDTg, blocked the ability of acute alcohol to cause locomotor stimulation and to induce memory retrieval of alcohol reward, as well as reduced peanut butter in mice. In addition, NMU into NAc shell decreased alcohol intake in rats. On a molecular level, we found increased NMU and decreased NMUR2 expression in the dorsal striatum in high compared with low alcohol‐consuming rats. Both aVTA and LDTg, rather than NAc shell, were identified as novel sites of action for NMU's anorexigenic properties in mice based on NMU's ability to selectively reduce chow intake when injected to these areas. Collectively, these data indicate that NMU signalling in different brain areas selectively modulates different behaviours. |
format | Online Article Text |
id | pubmed-7187236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71872362020-04-28 Brain region‐specific neuromedin U signalling regulates alcohol‐related behaviours and food intake in rodents Vallöf, Daniel Kalafateli, Aimilia Lydia Jerlhag, Elisabet Addict Biol Preclinical Studies Albeit neuromedin U (NMU) attenuates alcohol‐mediated behaviours, its mechanisms of action are poorly defined. Providing that the behavioural effects of alcohol are processed within the nucleus accumbens (NAc) shell, anterior ventral tegmental area (aVTA), and laterodorsal tegmental area (LDTg), we assessed the involvement of NMU signalling in the aforementioned areas on alcohol‐mediated behaviours in rodents. We further examined the expression of NMU and NMU receptor 2 (NMUR2) in NAc and the dorsal striatum of high compared with low alcohol‐consuming rats, as this area is of importance in the maintenance of alcohol use disorder (AUD). Finally, we investigated the involvement of NAc shell, aVTA and LDTg in the consumption of chow and palatable peanut butter, to expand the link between NMU and reward‐related behaviours. We demonstrated here, that NMU into the NAc shell, but not aVTA or LDTg, blocked the ability of acute alcohol to cause locomotor stimulation and to induce memory retrieval of alcohol reward, as well as reduced peanut butter in mice. In addition, NMU into NAc shell decreased alcohol intake in rats. On a molecular level, we found increased NMU and decreased NMUR2 expression in the dorsal striatum in high compared with low alcohol‐consuming rats. Both aVTA and LDTg, rather than NAc shell, were identified as novel sites of action for NMU's anorexigenic properties in mice based on NMU's ability to selectively reduce chow intake when injected to these areas. Collectively, these data indicate that NMU signalling in different brain areas selectively modulates different behaviours. John Wiley and Sons Inc. 2019-05-08 2020-05 /pmc/articles/PMC7187236/ /pubmed/31069918 http://dx.doi.org/10.1111/adb.12764 Text en © 2019 The Authors Addiction Biology published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Preclinical Studies Vallöf, Daniel Kalafateli, Aimilia Lydia Jerlhag, Elisabet Brain region‐specific neuromedin U signalling regulates alcohol‐related behaviours and food intake in rodents |
title | Brain region‐specific neuromedin U signalling regulates alcohol‐related behaviours and food intake in rodents |
title_full | Brain region‐specific neuromedin U signalling regulates alcohol‐related behaviours and food intake in rodents |
title_fullStr | Brain region‐specific neuromedin U signalling regulates alcohol‐related behaviours and food intake in rodents |
title_full_unstemmed | Brain region‐specific neuromedin U signalling regulates alcohol‐related behaviours and food intake in rodents |
title_short | Brain region‐specific neuromedin U signalling regulates alcohol‐related behaviours and food intake in rodents |
title_sort | brain region‐specific neuromedin u signalling regulates alcohol‐related behaviours and food intake in rodents |
topic | Preclinical Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187236/ https://www.ncbi.nlm.nih.gov/pubmed/31069918 http://dx.doi.org/10.1111/adb.12764 |
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