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Low concentration dimethyl sulfoxide (DMSO) modulates epileptiform synchronization in the 4-aminopyridine in vitro model.
- Source :
-
Journal of neuroscience methods [J Neurosci Methods] 2024 Nov; Vol. 411, pp. 110255. Date of Electronic Publication: 2024 Aug 17. - Publication Year :
- 2024
-
Abstract
- Dimethyl sulfoxide (DMSO) is commonly used to dissolve water-insoluble drugs due to its dipolar and aprotic properties. It also serves as a vehicle in many pharmacological studies. However, it has been reported that DMSO can induce seizures in human patients, lower seizure threshold in vivo, and modulate ion receptors activities in vitro. Therefore, we investigated here the effect of 0.03 % and 0.06 % DMSO, which are 10-50 times lower than what usually employed in previous studies, in the 4-aminopyridine (4AP) model of epileptiform synchronization in male mouse brain slices. We found that 0.03 % and 0.06 % DMSO increase 4AP-induced ictal discharge rate, while 0.06 % DMSO decreases ictal discharge duration. Our results suggest that the effects of DMSO on neuronal excitability deserve further analysis and that investigators need to be aware of its confounding effect as a solvent, even at very low concentrations.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Male
Mice
Epilepsy physiopathology
Epilepsy chemically induced
Epilepsy drug therapy
Potassium Channel Blockers pharmacology
Disease Models, Animal
Dose-Response Relationship, Drug
Action Potentials drug effects
Action Potentials physiology
4-Aminopyridine pharmacology
Dimethyl Sulfoxide pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-678X
- Volume :
- 411
- Database :
- MEDLINE
- Journal :
- Journal of neuroscience methods
- Publication Type :
- Academic Journal
- Accession number :
- 39159871
- Full Text :
- https://doi.org/10.1016/j.jneumeth.2024.110255