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Comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice

AIM: Indoleamine 2,3‐dioxygenase 1 (IDO1) metabolizes the essential amino acid tryptophan into kynurenine derivatives, which are involved in neural activity via the kynurenine pathway (KP). IDO1 is an initial rate‐limiting enzyme in the KP and is activated by stress and/or inflammation. The perturba...

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Autores principales: Hirata, Nao, Hattori, Satoko, Shoji, Hirotaka, Funakoshi, Hiroshi, Miyakawa, Tsuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292290/
https://www.ncbi.nlm.nih.gov/pubmed/30175526
http://dx.doi.org/10.1002/npr2.12019
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author Hirata, Nao
Hattori, Satoko
Shoji, Hirotaka
Funakoshi, Hiroshi
Miyakawa, Tsuyoshi
author_facet Hirata, Nao
Hattori, Satoko
Shoji, Hirotaka
Funakoshi, Hiroshi
Miyakawa, Tsuyoshi
author_sort Hirata, Nao
collection PubMed
description AIM: Indoleamine 2,3‐dioxygenase 1 (IDO1) metabolizes the essential amino acid tryptophan into kynurenine derivatives, which are involved in neural activity via the kynurenine pathway (KP). IDO1 is an initial rate‐limiting enzyme in the KP and is activated by stress and/or inflammation. The perturbation of IDO1 activity, which causes KP imbalance, is associated with psychiatric and neurological disorders. It has been reported that wild‐type (WT) mice under inflammatory conditions show increased anxiety‐like behavior and decreased novel object recognition, whereas Ido1 knockout (KO) mice do not display these behaviors. However, the behavioral phenotypes of Ido1 KO mice have not yet been fully examined under non‐inflammatory conditions. METHODS: We subjected Ido1 KO mice to a comprehensive behavioral test battery under normal conditions. RESULTS: Ido1 KO mice and WT mice showed similar locomotor activity, anxiety‐like behavior, social behavior, depression‐like behavior, and fear memory. In the T‐maze test, Ido1 KO mice exhibited weak but nominally significant impairment in the working memory task of the T‐maze, but this result failed to reach study‐wide significance. CONCLUSIONS: Ido1 KO mice did not show any clear behavioral abnormalities under normal conditions. Further studies may be necessary to investigate their behavioral phenotype under inflammatory conditions due to their known roles in inflammation.
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spelling pubmed-72922902020-12-08 Comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice Hirata, Nao Hattori, Satoko Shoji, Hirotaka Funakoshi, Hiroshi Miyakawa, Tsuyoshi Neuropsychopharmacol Rep Original Articles AIM: Indoleamine 2,3‐dioxygenase 1 (IDO1) metabolizes the essential amino acid tryptophan into kynurenine derivatives, which are involved in neural activity via the kynurenine pathway (KP). IDO1 is an initial rate‐limiting enzyme in the KP and is activated by stress and/or inflammation. The perturbation of IDO1 activity, which causes KP imbalance, is associated with psychiatric and neurological disorders. It has been reported that wild‐type (WT) mice under inflammatory conditions show increased anxiety‐like behavior and decreased novel object recognition, whereas Ido1 knockout (KO) mice do not display these behaviors. However, the behavioral phenotypes of Ido1 KO mice have not yet been fully examined under non‐inflammatory conditions. METHODS: We subjected Ido1 KO mice to a comprehensive behavioral test battery under normal conditions. RESULTS: Ido1 KO mice and WT mice showed similar locomotor activity, anxiety‐like behavior, social behavior, depression‐like behavior, and fear memory. In the T‐maze test, Ido1 KO mice exhibited weak but nominally significant impairment in the working memory task of the T‐maze, but this result failed to reach study‐wide significance. CONCLUSIONS: Ido1 KO mice did not show any clear behavioral abnormalities under normal conditions. Further studies may be necessary to investigate their behavioral phenotype under inflammatory conditions due to their known roles in inflammation. John Wiley and Sons Inc. 2018-08-11 /pmc/articles/PMC7292290/ /pubmed/30175526 http://dx.doi.org/10.1002/npr2.12019 Text en © 2018 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Hirata, Nao
Hattori, Satoko
Shoji, Hirotaka
Funakoshi, Hiroshi
Miyakawa, Tsuyoshi
Comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice
title Comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice
title_full Comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice
title_fullStr Comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice
title_full_unstemmed Comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice
title_short Comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice
title_sort comprehensive behavioral analysis of indoleamine 2,3‐dioxygenase knockout mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292290/
https://www.ncbi.nlm.nih.gov/pubmed/30175526
http://dx.doi.org/10.1002/npr2.12019
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