Meclizine seasickness medication and its effect on central nervous system oxygen toxicity in a murine model
- PMID: 39675737
- PMCID: PMC12018700
- DOI: 10.28920/dhm54.4.296-300
Meclizine seasickness medication and its effect on central nervous system oxygen toxicity in a murine model
Abstract
Introduction: Diving utilising closed circuit pure oxygen rebreather systems has become popular in professional settings. One of the hazards the oxygen diver faces is central nervous system oxygen toxicity (CNS-OT), causing potentially fatal convulsions. At the same time, divers frequently travel by boat, often suffering seasickness. The over-the-counter medication meclizine is an anticholinergic and antihistaminergic agent that has gained popularity in the treatment of seasickness. Reports have shown the inhibitory effect that acetylcholine has on glutamate, a main component in the mechanism leading to CNS-OT seizure. The goal of the present study was to test the effect of meclizine on the latency to CNS-OT seizures under hyperbaric oxygen conditions.
Methods: Twenty male mice were exposed twice to 608 kPa (6 atmospheres) absolute pressure while breathing oxygen after administration of control solution (carboxymethyl cellulose solvent) or drug solution (meclizine) in a randomised crossover design. Latency to tonic-clonic seizures was visually measured.
Results: Mean latency to seizure did not significantly differ between the control group (414 s, standard deviation [SD] 113 s) and meclizine group (434 s, SD 174 s).
Conclusions: Based on results from this animal model, meclizine may be an appropriate option for divers suffering from seasickness, who plan on diving using pure oxygen rebreather systems.
Keywords: Cholinergic antagonists; Closed circuit rebreathers; Diving; Histamine antagonists; Seizures.
Copyright: This article is the copyright of the authors who grant Diving and Hyperbaric Medicine a non-exclusive licence to publish the article in electronic and other forms.
Conflict of interest statement
No conflicts of interest were declared.
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References
-
- Banham NDG. Oxygen toxicity seizures: 20 years’ experience from a single hyperbaric unit. Diving Hyperb Med. 2011; 41: 202–10. [cited 2024 Jun 1]. Available from: https://dhmjournal.com/images/IndividArticles/41Dec/Banham_dhm.41.4.202-... - PubMed
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