Prevention of vincristine-induced peripheral neuropathy by protecting the endothelial glycocalyx shedding.

Blood–nerve barrier Endothelial glycocalyx Vincristine-induced peripheral neuropathy

Journal

Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516

Informations de publication

Date de publication:
21 Nov 2023
Historique:
received: 10 11 2023
accepted: 16 11 2023
medline: 29 11 2023
pubmed: 29 11 2023
entrez: 28 11 2023
Statut: aheadofprint

Résumé

Vincristine-induced peripheral neuropathy (VIPN) adversely affects the quality of life and treatment continuity of patients. The endothelial glycocalyx (eGCX) protects nerves from harmful substances released from the capillary vessels, but its role in peripheral neuropathy remains unclear. We investigated the impact of eGCX protection on VIPN. Using a murine model of VIPN, we administered nafamostat mesylate to protect the eGCX shedding, and analyzed the eGCX integrity and manifestation of peripheral neuropathy. Nafamostat treatment suppressed allodynia associated with neuropathy. Additionally, nafamostat administration resulted in the suppression of increased vascular permeability in capillaries of peripheral nerves, further indicating its positive influence on eGCX in VIPN model mice. This study provided the importance of eGCX in VIPN. With the potential for rapid clinical translation through drug repositioning, nafamostat may be a new promising treatment for the prevention of VIPN.

Identifiants

pubmed: 38016339
pii: S0006-291X(23)01380-3
doi: 10.1016/j.bbrc.2023.149286
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

149286

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest All authors declare no conflicts of interest.

Auteurs

Kazufumi Ohmura (K)

Department of Neurosurgery, Gifu University Graduate School of Medicine, Gifu, Japan; Department of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.

Takamasa Kinoshita (T)

Department of Neurosurgery, Ogaki Tokusyukai Hospital, Gifu, Japan.

Hiroyuki Tomita (H)

Department of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan; Center for One Medicine Innovative Translational Research, Gifu University Institute for Advanced Study, Gifu, Japan. Electronic address: tomita.hiroyuki.y6@f.gifu-u.ac.jp.

Hideshi Okada (H)

Center for One Medicine Innovative Translational Research, Gifu University Institute for Advanced Study, Gifu, Japan; Department of Emergency and Disaster Medicine, Gifu University Graduate School of Medicine, Gifu, Japan. Electronic address: okada.hideshi.a4@f.gifu-u.ac.jp.

Masayoshi Shimizu (M)

Department of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.

Kosuke Mori (K)

Department of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.

Toshiaki Taniguchi (T)

Department of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.

Akio Suzuki (A)

Department of Pharmacy, Gifu University Hospital, Gifu, Japan.

Toru Iwama (T)

Department of Neurosurgery, Gifu University Graduate School of Medicine, Gifu, Japan.

Akira Hara (A)

Department of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.

Classifications MeSH