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Article: Evaluating proxies for motion sickness in rodent

TitleEvaluating proxies for motion sickness in rodent
Authors
KeywordsConditioned taste aversion
Emesis
Motion sickness
Nausea
Pica
Rodent models
Issue Date1-Dec-2023
PublisherElsevier
Citation
IBRO Neuroscience Reports, 2023, v. 15, p. 107-115 How to Cite?
AbstractMotions sickness (MS) occurs when the brain receives conflicting sensory signals from vestibular, visual and proprioceptive systems about a person's ongoing position and/or motion in relation to space. MS is typified by symptoms such as nausea and emesis and implicates complex physiological aspects of sensations and sensorimotor reflexes. Use of animal models has been integral to unraveling the physiological causality of MS. The commonly used rodents (rat and mouse), albeit lacking vomiting reflex, reliably display phenotypic behaviors of pica (eating of non-nutritive substance) and conditioned taste aversion (CTAver) or avoidance (CTAvoi) which utilize neural substrates with pathways that cause gastrointestinal malaise akin to nausea/emesis. As such, rodent pica and CTAver/CTAvoi have been widely used as proxies for nausea/emesis in studies dealing with neural mechanisms of nausea/emesis and MS, as well as for evaluating therapeutics. This review presents the rationale and experimental evidence that support the use of pica and CTAver/CTAvoi as indices for nausea and emesis. Key experimental steps and cautions required when using rodent MS models are also discussed. Finally, future directions are suggested for studying MS with rodent pica and CTAver/CTAvoi models.
Persistent Identifierhttp://hdl.handle.net/10722/366385
ISSN
2023 Impact Factor: 2.0
2023 SCImago Journal Rankings: 0.549

 

DC FieldValueLanguage
dc.contributor.authorZhang, Fu Xing-
dc.contributor.authorXie, Xiao Hang-
dc.contributor.authorGuo, Zi Xin-
dc.contributor.authorWang, Hao Dong-
dc.contributor.authorLi, Hui-
dc.contributor.authorWu, Kenneth Lap Kei-
dc.contributor.authorChan, Ying Shing-
dc.contributor.authorLi, Yun Qing-
dc.date.accessioned2025-11-25T04:19:07Z-
dc.date.available2025-11-25T04:19:07Z-
dc.date.issued2023-12-01-
dc.identifier.citationIBRO Neuroscience Reports, 2023, v. 15, p. 107-115-
dc.identifier.issn2667-2421-
dc.identifier.urihttp://hdl.handle.net/10722/366385-
dc.description.abstractMotions sickness (MS) occurs when the brain receives conflicting sensory signals from vestibular, visual and proprioceptive systems about a person's ongoing position and/or motion in relation to space. MS is typified by symptoms such as nausea and emesis and implicates complex physiological aspects of sensations and sensorimotor reflexes. Use of animal models has been integral to unraveling the physiological causality of MS. The commonly used rodents (rat and mouse), albeit lacking vomiting reflex, reliably display phenotypic behaviors of pica (eating of non-nutritive substance) and conditioned taste aversion (CTAver) or avoidance (CTAvoi) which utilize neural substrates with pathways that cause gastrointestinal malaise akin to nausea/emesis. As such, rodent pica and CTAver/CTAvoi have been widely used as proxies for nausea/emesis in studies dealing with neural mechanisms of nausea/emesis and MS, as well as for evaluating therapeutics. This review presents the rationale and experimental evidence that support the use of pica and CTAver/CTAvoi as indices for nausea and emesis. Key experimental steps and cautions required when using rodent MS models are also discussed. Finally, future directions are suggested for studying MS with rodent pica and CTAver/CTAvoi models.-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofIBRO Neuroscience Reports-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectConditioned taste aversion-
dc.subjectEmesis-
dc.subjectMotion sickness-
dc.subjectNausea-
dc.subjectPica-
dc.subjectRodent models-
dc.titleEvaluating proxies for motion sickness in rodent-
dc.typeArticle-
dc.identifier.doi10.1016/j.ibneur.2023.06.006-
dc.identifier.scopuseid_2-s2.0-85165624862-
dc.identifier.volume15-
dc.identifier.spage107-
dc.identifier.epage115-
dc.identifier.eissn2667-2421-
dc.identifier.issnl2667-2421-

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