Overexpression of tyrosine hydroxylase in dopaminergic neurons increased sensitivity to methamphetamine.


Journal

Neurochemistry international
ISSN: 1872-9754
Titre abrégé: Neurochem Int
Pays: England
ID NLM: 8006959

Informations de publication

Date de publication:
03 2023
Historique:
received: 14 09 2022
revised: 20 01 2023
accepted: 24 01 2023
pubmed: 29 1 2023
medline: 15 3 2023
entrez: 28 1 2023
Statut: ppublish

Résumé

Drug abuse is one of the great social problems in the world and a major healthcare challenge. It is supposed that sensitivity and reactivity to abuse drugs may vary from person to person, while its molecular basis is largely unknown. Dopaminergic neurons are deeply involved in addiction, and tyrosine hydroxylase (TH) catalyzes the first and rate-limiting step of the biosynthesis of dopamine (DA). We investigated the effects of increased TH expression on the metabolism of DA and reactivity to methamphetamine (METH), a drug of abuse, in mice. Wild-type TH (WT-TH) or the S40E mutant of TH (S40E-TH), which is an active form of TH mimicking phosphorylated TH at the 40th serine, was expressed in midbrain dopaminergic neurons using an adeno-associated virus (AAV) vector. The biochemical analysis showed that the turnover rates of DA in the nerve terminals were increased by the expression of WT-TH and S40E-TH, while there were few changes in the DA contents. Next, we administered METH to TH-overexpressing mice. We found that the S40E-TH-expressing mice responded to lower doses of METH than the control mice and WT-TH mice. The stereotyped behaviors appeared first in S40E-TH mice and then in WT-TH and control mice in this order. These data showed that the TH activity and expression level differentially affect DA metabolism in the nerve terminals from that in the cell bodies and that the TH activity and expression level are one of the determining factors for sensitivity and reactivity to METH. We suggest that TH may be a drug target for ameliorating sensitivity to drugs of abuse.

Identifiants

pubmed: 36709046
pii: S0197-0186(23)00019-0
doi: 10.1016/j.neuint.2023.105491
pii:
doi:

Substances chimiques

Methamphetamine 44RAL3456C
Tyrosine 3-Monooxygenase EC 1.14.16.2
Dopamine VTD58H1Z2X

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

105491

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest S.M. owns equity in a gene therapy company (Gene Therapy Research Institution, Co., Ltd.) that commercializes the use of AAV vectors for gene therapy applications. To the extent that the work in this manuscript increases the value of these commercial holdings, there is a conflict of interest. The other authors of this manuscript have no conflicts of interest.

Auteurs

Yuka Nago-Iwashita (Y)

School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.

Yuki Moriya (Y)

Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Satoshi Hara (S)

School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.

Ryohei Ogawa (R)

School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.

Rina Aida (R)

School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.

Katsuya Miyajima (K)

School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.

Takenobu Shimura (T)

School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.

Shin-Ichi Muramatsu (SI)

Division of Neurological Gene Therapy, Jichi Medical University, Shimotsuke, Tochigi, Japan; Center for Gene & Cell Therapy, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

Soichiro Ide (S)

Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Kazutaka Ikeda (K)

Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Hiroshi Ichinose (H)

School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan. Electronic address: hichinos@bio.titech.ac.jp.

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Classifications MeSH