Analysis of Plasma-Derived Exosomal MicroRNAs as Potential Biomarkers for Canine Idiopathic Epilepsy.
diagnosis
dog
exosome
idiopathic epilepsy
microRNAs
Journal
Animals : an open access journal from MDPI
ISSN: 2076-2615
Titre abrégé: Animals (Basel)
Pays: Switzerland
ID NLM: 101635614
Informations de publication
Date de publication:
13 Jan 2024
13 Jan 2024
Historique:
received:
05
12
2023
revised:
04
01
2024
accepted:
10
01
2024
medline:
23
1
2024
pubmed:
23
1
2024
entrez:
23
1
2024
Statut:
epublish
Résumé
Epilepsy is one of the most prevalent complex neurological diseases in both the canine and human species, with the idiopathic form as its most common diagnosis. MicroRNAs (miRNAs) are small, noncoding RNA molecules that play a role in gene regulation processes and appear to be a promising biological target for convulsion control. These molecules have been reported as constituents of the internal content of exosomes, which are small extracellular vesicles released by cells. In this study, exosome samples were isolated from the plasma of 23 dogs, including 9 dogs with epilepsy responsive to treatment, 6 dogs with drug-resistant epilepsy, and 8 control dogs. Plasma exosomes were then characterized by electron transmission microscopy, nanoparticle tracking analysis, and dot blotting. Afterwards, the microRNA-enriched RNA content of exosomes was isolated, and miRNA quantification was performed by quantitative real-time PCR. Seven circulating miRNAs that have been previously described in the literature as potential diagnostic or prognostic biomarkers for epilepsy were evaluated. We observed significant differences in miR-16 (
Identifiants
pubmed: 38254420
pii: ani14020252
doi: 10.3390/ani14020252
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Gobierno de Aragón
ID : LMP134_21
Organisme : Instituto de Salud Carlos III
ID : PI21/00372
Organisme : Fondo Europeo de Desarrollo Regional
ID : PI21/00372
Organisme : Biomedical Research Networking Center on Neurodegenerative Diseases
ID : CB18/05/0037
Organisme : Gobierno de Aragón
ID : A19_23R