The Mouse Model of Internal Capsule Demyelination: A Novel Tool for Investigating Motor Functional Changes Caused by Demyelination and for Evaluating Drugs That Promote Remyelination.

asymmetric motor deficit demyelination internal capsule lysophosphatidylcholine remyelination

Journal

Acta histochemica et cytochemica
ISSN: 0044-5991
Titre abrégé: Acta Histochem Cytochem
Pays: Japan
ID NLM: 0147110

Informations de publication

Date de publication:
29 Feb 2024
Historique:
received: 11 01 2024
accepted: 23 01 2024
medline: 11 3 2024
pubmed: 11 3 2024
entrez: 11 3 2024
Statut: ppublish

Résumé

Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system, characterized by remyelination failure and axonal dysfunction. Remyelination by oligodendrocytes is critical for improvement of neurological deficits associated with demyelination. Rodent models of demyelination are frequently used to develop and evaluate therapies for MS. However, a suitable mouse model for assessing remyelination-associated recovery of motor functions is currently unavailable. In this review, we describe the development of the mouse model of internal capsule (IC) demyelination by focal injection of lysolecithin into brain and its application in the evaluation of drugs for demyelinating diseases. This mouse model exhibits motor deficits and subsequent functional recovery accompanying IC remyelination. Notably, this model shows enhancement of functional recovery as well as tissue regeneration when treated with clemastine, a drug that promotes remyelination. The IC demyelination mouse model should contribute to the development of novel drugs that promote remyelination and ameliorate neurological deficits in demyelinating diseases.

Identifiants

pubmed: 38463203
doi: 10.1267/ahc.24-00005
pmc: PMC10918433
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1-5

Informations de copyright

2024 The Japan Society of Histochemistry and Cytochemistry.

Déclaration de conflit d'intérêts

VThere are no conflicts of interest.

Auteurs

Reiji Yamazaki (R)

Department of Anatomy, Division of Histology and Cell Biology, School of Medicine, Jichi Medical University, Shimotsuke, Japan.

Nobuhiko Ohno (N)

Department of Anatomy, Division of Histology and Cell Biology, School of Medicine, Jichi Medical University, Shimotsuke, Japan.
Division of Ultrastructural Research, National Institute for Physiological Sciences, Okazaki, Japan.

Classifications MeSH