Nigrostriatal tract defects in mice with aromatic l-amino acid decarboxylase deficiency.

Aromatic l-amino acid decarboxylase deficiency Dopamine deficiency Nigrostriatal tract Striatum Substantia nigra

Journal

Neurobiology of disease
ISSN: 1095-953X
Titre abrégé: Neurobiol Dis
Pays: United States
ID NLM: 9500169

Informations de publication

Date de publication:
19 Oct 2024
Historique:
received: 21 07 2024
revised: 08 10 2024
accepted: 16 10 2024
medline: 22 10 2024
pubmed: 22 10 2024
entrez: 21 10 2024
Statut: aheadofprint

Résumé

The development of the nigrostriatal dopaminergic (DA) pathway in the brain involves many transcriptional and chemotactic molecules, and a deficiency of these molecules can cause nigrostriatal tract defects. However, the role of the end product, dopamine, in nigrostriatal pathway development has not been described. In the present study, we analyzed a mouse model of congenital dopamine and serotonin deficiency, namely, the aromatic l-amino acid decarboxylase (AADC) deficiency (Ddc

Identifiants

pubmed: 39433135
pii: S0969-9961(24)00307-3
doi: 10.1016/j.nbd.2024.106707
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106707

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no financial interests or personal relationships that may be considered potential competing interests.

Auteurs

Ni-Chung Lee (NC)

Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.

Pei-Chun Hsu (PC)

Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.

Yu-Han Liu (YH)

Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.

Hao-Chun Wang (HC)

Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.

Tsu-I Chen (TI)

Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.

Yin-Hsiu Chien (YH)

Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.

Wuh-Liang Hwu (WL)

Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan; Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan; Center for Precision Medicine, China Medical University Hospital, Taichung, Taiwan. Electronic address: hwuwlntu@ntu.edu.tw.

Classifications MeSH