The effects of meclizine on motion sickness revisited.

neuroscience < neuropharmacology ophthalmology therapeutics < clinical pharmacology

Journal

British journal of clinical pharmacology
ISSN: 1365-2125
Titre abrégé: Br J Clin Pharmacol
Pays: England
ID NLM: 7503323

Informations de publication

Date de publication:
08 2020
Historique:
received: 14 05 2019
revised: 21 01 2020
accepted: 22 01 2020
pubmed: 23 2 2020
medline: 3 7 2021
entrez: 21 2 2020
Statut: ppublish

Résumé

Antihistamines make up the first line of treatments against motion-sickness. Still, their efficacy and specific mechanism have come into question. The aim of this study was to investigate the effect of meclizine on motion-sensitivity. This study was carried out as a triple-blinded randomized trial involving 12 healthy subjects who were exposed to (i) vestibular (VES), (ii) visual (VIS) and (iii) visual-vestibular (VIS+VES) stimulations in the roll plane. Subjects were divided into 2 groups by stratified randomization, receiving either meclizine or a placebo. Stimulations were carried out before, and after, drug administration, presented at 2 intensity levels of 14 and 28°/s Susceptibility had no effect on intervention outcome. Despite large variations, repeated ANOVAS showed that meclizine led to a relative increase in torsional velocity compared to placebo during vestibular stimulation for both intensities: 2.36 (7.65) from -0.01 (4.17) during low intensities, and 2.61 (6.67) from -3.49 (4.76) during high. The visual-vestibular stimuli yielded a decrease during low acceleration, -0.40 (3.87) from 3.75 (5.62), but increased during high, 3.88 (6.51) from -3.88 (8.55). Meclizine had an inhibitory effect on eye movement reflexes for low accelerations during VIS+VES trials. This indicates that meclizine may not primarily work through sensory-specific mechanisms, but rather on a more central level. Practically, meclizine shows promise in targeting motion-sickness evoked by everyday activities, but its use may be counterproductive in high-acceleration environments.

Identifiants

pubmed: 32077140
doi: 10.1111/bcp.14257
pmc: PMC7373708
doi:

Substances chimiques

Meclizine 3L5TQ84570

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1510-1518

Informations de copyright

© 2020 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

Références

Exp Brain Res. 2014 Aug;232(8):2493-510
pubmed: 24961738
Clin Pharmacol Ther. 1994 Jun;55(6):670-80
pubmed: 8004883
Nucleic Acids Res. 2018 Jan 4;46(D1):D1091-D1106
pubmed: 29149325
Front Physiol. 2017 Jun 14;8:412
pubmed: 28659825
Aviat Space Environ Med. 2014 Jun;85(6):638-44
pubmed: 24919385
Acta Otolaryngol. 1970 Jul;70(1):6-9
pubmed: 5311676
Ann Allergy Asthma Immunol. 1995 May;74(5):419-26
pubmed: 7749974
Aviat Space Environ Med. 2000 Oct;71(10):1003-12
pubmed: 11051307
Invest Ophthalmol Vis Sci. 2019 Mar 1;60(4):1021-1027
pubmed: 30897617
Cereb Cortex. 2010 Aug;20(8):1964-73
pubmed: 20034998
Acta Otolaryngol. 1979;88(1-2):110-6
pubmed: 474109
Audiol Neurootol. 2012;17(4):235-42
pubmed: 22517315
Exp Brain Res. 1983;50(1):9-33
pubmed: 6357831
Exp Brain Res. 2006 Nov;175(3):567-74
pubmed: 16791595
Exp Brain Res. 1985;59(1):185-96
pubmed: 4018196
J Neuroeng Rehabil. 2014 Jun 10;11:99
pubmed: 24912769
Aerosp Med. 1968 May;39(5):453-5
pubmed: 5648730
Br J Pharmacol. 2019 Dec;176 Suppl 1:S297-S396
pubmed: 31710714
J Vestib Res. 1994 May-Jun;4(3):215-20
pubmed: 7921339
Exp Brain Res. 1977 Apr 21;27(5):523-38
pubmed: 404173
PLoS One. 2020 Jan 3;15(1):e0227370
pubmed: 31900468
J R Soc Med. 1978 Nov;71(11):819-29
pubmed: 731645
Acta Otolaryngol. 1987 Mar-Apr;103(3-4):280-90
pubmed: 3577761
Auton Neurosci. 2006 Oct 30;129(1-2):67-76
pubmed: 16931173
Br J Math Stat Psychol. 2013 May;66(2):224-44
pubmed: 22624658
Arch Neurol. 1972 Aug;27(2):129-35
pubmed: 4339240
ORL J Otorhinolaryngol Relat Spec. 1977;39(6):309-20
pubmed: 307721
Ann N Y Acad Sci. 2005 Apr;1039:554-7
pubmed: 15827021
Acta Otolaryngol Suppl. 2001;545:84-7
pubmed: 11677750
J Neurophysiol. 1950 Nov;13(6):395-407
pubmed: 14784863
Q J Exp Physiol Cogn Med Sci. 1968 Jul;53(3):312-26
pubmed: 5188316
Br J Clin Pharmacol. 2020 Aug;86(8):1510-1518
pubmed: 32077140
Physiol Rev. 1970 Jan;50(1):1-39
pubmed: 4904269
Brain Res Bull. 1998 Nov 15;47(5):507-16
pubmed: 10052582

Auteurs

Tobias Wibble (T)

Department of Clinical Neuroscience, Division of Ophthalmology and Vision, Marianne Bernadotte Centre, Karolinska Institutet, Stockholm, Sweden.
St Erik Eye Hospital, Stockholm, Sweden.

Johanna Engström (J)

Department of Clinical Neuroscience, Division of Ophthalmology and Vision, Marianne Bernadotte Centre, Karolinska Institutet, Stockholm, Sweden.

Luca Verrecchia (L)

Department of Clinical Neuroscience, Division of Ophthalmology and Vision, Marianne Bernadotte Centre, Karolinska Institutet, Stockholm, Sweden.
The Hearing and Balance Clinic, The Karolinska University Hospital, Stockholm, Sweden.

Tony Pansell (T)

Department of Clinical Neuroscience, Division of Ophthalmology and Vision, Marianne Bernadotte Centre, Karolinska Institutet, Stockholm, Sweden.
St Erik Eye Hospital, Stockholm, Sweden.

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Classifications MeSH