Cargando…

Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice

Novelty-seeking behaviors and impulsivity are personality traits associated with several psychiatric illnesses including attention deficits hyperactivity disorders. The underlying neural mechanisms remain poorly understood. We produced and characterized a line of knockout mice for zdhhc15, which enc...

Descripción completa

Detalles Bibliográficos
Autores principales: Mejias, Rebeca, Rodriguez-Gotor, Juan J., Niwa, Minae, Krasnova, Irina N., Adamczyk, Abby, Han, Mei, Thomas, Gareth M., Xi, Zheng-Xiong, Huganir, Richard L., Pletnikov, Mikhail V., Sawa, Akira, Cadet, Jean-Lud, Wang, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813841/
https://www.ncbi.nlm.nih.gov/pubmed/33462194
http://dx.doi.org/10.1038/s41398-020-01194-6
_version_ 1783637940482605056
author Mejias, Rebeca
Rodriguez-Gotor, Juan J.
Niwa, Minae
Krasnova, Irina N.
Adamczyk, Abby
Han, Mei
Thomas, Gareth M.
Xi, Zheng-Xiong
Huganir, Richard L.
Pletnikov, Mikhail V.
Sawa, Akira
Cadet, Jean-Lud
Wang, Tao
author_facet Mejias, Rebeca
Rodriguez-Gotor, Juan J.
Niwa, Minae
Krasnova, Irina N.
Adamczyk, Abby
Han, Mei
Thomas, Gareth M.
Xi, Zheng-Xiong
Huganir, Richard L.
Pletnikov, Mikhail V.
Sawa, Akira
Cadet, Jean-Lud
Wang, Tao
author_sort Mejias, Rebeca
collection PubMed
description Novelty-seeking behaviors and impulsivity are personality traits associated with several psychiatric illnesses including attention deficits hyperactivity disorders. The underlying neural mechanisms remain poorly understood. We produced and characterized a line of knockout mice for zdhhc15, which encodes a neural palmitoyltransferase. Genetic defects of zdhhc15 were implicated in intellectual disability and behavioral anomalies in humans. Zdhhc15-KO mice showed normal spatial learning and working memory but exhibited a significant increase in novelty-induced locomotion in open field. Striatal dopamine content was reduced but extracellular dopamine levels were increased during the habituation phase to a novel environment. Administration of amphetamine and methylphenidate resulted in a significant increase in locomotion and extracellular dopamine levels in the ventral striatum of mutant mice compared to controls. Number and projections of dopaminergic neurons in the nigrostriatal and mesolimbic pathways were normal. No significant change in the basal palmitoylation of known ZDHHC15 substrates including DAT was detected in striatum of zdhhc15 KO mice using an acyl-biotin exchange assay. These results support that a transient, reversible, and novelty-induced elevation of extracellular dopamine in ventral striatum contributes to novelty-seeking behaviors in rodents and implicate ZDHHC15-mediated palmitoylation as a novel regulatory mechanism of dopamine in the striatum.
format Online
Article
Text
id pubmed-7813841
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-78138412021-01-25 Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice Mejias, Rebeca Rodriguez-Gotor, Juan J. Niwa, Minae Krasnova, Irina N. Adamczyk, Abby Han, Mei Thomas, Gareth M. Xi, Zheng-Xiong Huganir, Richard L. Pletnikov, Mikhail V. Sawa, Akira Cadet, Jean-Lud Wang, Tao Transl Psychiatry Article Novelty-seeking behaviors and impulsivity are personality traits associated with several psychiatric illnesses including attention deficits hyperactivity disorders. The underlying neural mechanisms remain poorly understood. We produced and characterized a line of knockout mice for zdhhc15, which encodes a neural palmitoyltransferase. Genetic defects of zdhhc15 were implicated in intellectual disability and behavioral anomalies in humans. Zdhhc15-KO mice showed normal spatial learning and working memory but exhibited a significant increase in novelty-induced locomotion in open field. Striatal dopamine content was reduced but extracellular dopamine levels were increased during the habituation phase to a novel environment. Administration of amphetamine and methylphenidate resulted in a significant increase in locomotion and extracellular dopamine levels in the ventral striatum of mutant mice compared to controls. Number and projections of dopaminergic neurons in the nigrostriatal and mesolimbic pathways were normal. No significant change in the basal palmitoylation of known ZDHHC15 substrates including DAT was detected in striatum of zdhhc15 KO mice using an acyl-biotin exchange assay. These results support that a transient, reversible, and novelty-induced elevation of extracellular dopamine in ventral striatum contributes to novelty-seeking behaviors in rodents and implicate ZDHHC15-mediated palmitoylation as a novel regulatory mechanism of dopamine in the striatum. Nature Publishing Group UK 2021-01-18 /pmc/articles/PMC7813841/ /pubmed/33462194 http://dx.doi.org/10.1038/s41398-020-01194-6 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mejias, Rebeca
Rodriguez-Gotor, Juan J.
Niwa, Minae
Krasnova, Irina N.
Adamczyk, Abby
Han, Mei
Thomas, Gareth M.
Xi, Zheng-Xiong
Huganir, Richard L.
Pletnikov, Mikhail V.
Sawa, Akira
Cadet, Jean-Lud
Wang, Tao
Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice
title Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice
title_full Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice
title_fullStr Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice
title_full_unstemmed Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice
title_short Increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of Zdhhc15-deficient mice
title_sort increased novelty-induced locomotion, sensitivity to amphetamine, and extracellular dopamine in striatum of zdhhc15-deficient mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813841/
https://www.ncbi.nlm.nih.gov/pubmed/33462194
http://dx.doi.org/10.1038/s41398-020-01194-6
work_keys_str_mv AT mejiasrebeca increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT rodriguezgotorjuanj increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT niwaminae increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT krasnovairinan increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT adamczykabby increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT hanmei increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT thomasgarethm increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT xizhengxiong increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT huganirrichardl increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT pletnikovmikhailv increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT sawaakira increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT cadetjeanlud increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice
AT wangtao increasednoveltyinducedlocomotionsensitivitytoamphetamineandextracellulardopamineinstriatumofzdhhc15deficientmice