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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...

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Autores principales: Vallöf, Daniel, Kalafateli, Aimilia Lydia, Jerlhag, Elisabet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
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.
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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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