Neuroprotective effect of newly synthesized 4-aminopyridine derivatives on cuprizone-induced demyelination in mice-a behavioral and immunohistochemical study.


Journal

Amino acids
ISSN: 1438-2199
Titre abrégé: Amino Acids
Pays: Austria
ID NLM: 9200312

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 29 12 2020
accepted: 30 06 2021
pubmed: 10 7 2021
medline: 31 12 2021
entrez: 9 7 2021
Statut: ppublish

Résumé

The aim of this study was to assess the effect of newly synthesized derivatives of 4-aminopyridine (4-AP) on cuprizone-induced model of brain demyelination in mice. 4-AP is already approved for the treatment of walking difficulties in patients with multiple sclerosis. The model of demyelination was carried out by the administration of cuprizone to the drinking water of the experimental mice. Besides cuprizone, 4-AP derivatives and 4-AP were administered to the groups in order to assess their protective effect on the demyelination. We used immunohistochemistry for visualization of changes in corpus callosum. Memory storage processes were also assessed with the passive avoidance test on the last two days of the experiment. The experimental mice treated with compounds 4b and 4c increased significantly their latency time on the second day in comparison to the control group which indicated an improved memory process. The number of mature oligodendrocytes in the groups treated with compounds 4b, 4c and 4-AP is closer to those in the control group. The results of our studies showed that the newly synthesized compounds 4b and 4c reverse the effect of cuprizone. These groups also showed increased latency time in the passive avoidance test in comparison to the control group.

Identifiants

pubmed: 34240251
doi: 10.1007/s00726-021-03035-2
pii: 10.1007/s00726-021-03035-2
doi:

Substances chimiques

Neuroprotective Agents 0
Cuprizone 5N16U7E0AO
4-Aminopyridine BH3B64OKL9

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1279-1286

Subventions

Organisme : Medical University of Sofia, Bulgaria
ID : Project №82/23.04.2019

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.

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Auteurs

Ivanka Kostadinova (I)

Department of Pharmacology, Pharmacotherapy and Toxicology, Faculty of Pharmacy, Medical University of Sofia, 2 Dunav Str., 1000, Sofia, Bulgaria. i.kostadinova@pharmfac.mu-sofia.bg.

Boycho Landzhov (B)

Department of Anatomy, Histology and Embryology, Faculty of Medicine, Medical University of Sofia, 2 Zdrave Str., 1431, Sofia, Bulgaria.

Lyubomir Marinov (L)

Department of Pharmacology, Pharmacotherapy and Toxicology, Faculty of Pharmacy, Medical University of Sofia, 2 Dunav Str., 1000, Sofia, Bulgaria.

Lyubomir Vezenkov (L)

Department of Organic Chemistry, University of Chemical Technology and Metallurgy, 8 St. Kliment Ohridski Blvd., 1756, Sofia, Bulgaria.

Nikolai Danchev (N)

Department of Pharmacology, Pharmacotherapy and Toxicology, Faculty of Pharmacy, Medical University of Sofia, 2 Dunav Str., 1000, Sofia, Bulgaria.

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