{"title":"Visual and vestibular reweighting after cyber- and space-sickness.","authors":"Tess Bonnard, Emilie Doat, Jean-René Cazalets, Dominique Guehl, Etienne Guillaud","doi":"10.1113/EP092966","DOIUrl":null,"url":null,"abstract":"<p><p>Sensory conflicts are widely recognized as the primary drivers of motion sickness (MS), though the underlying integrative processes remain poorly understood. This study investigated sensory reweighting following exposure to two different sensory conflict paradigms. Visual and vestibular reflexes were assessed before and after sensory conflict. In the first paradigm, participants were exposed to a visuo-vestibular conflict using visually induced illusory motion (vection) in two environments in immersive virtual reality. In the second paradigm, vestibular conflict was induced by gravitational changes in parabolic flight. Semi-circular canal integration was measured via the vestibulo-ocular reflex (VOR) suppression task, while visual weight was assessed through optokinetic nystagmus (OKN). Our findings revealed that, following virtual reality exposure, VOR response decreased by 12%, indicating a reduced reliance on vestibular inputs. Conversely, after parabolic flight, OKN performance was diminished by 13%, indicating a diminished weight of visual inputs. These findings suggest that the sensory modality failing to detect the motion was considered less reliable and therefore assigned a reduced contribution during the integration process, regardless of its actual accuracy. Additionally, visual sensitivity was associated with increased susceptibility to cybersickness, whereas vestibular sensitivity seemed to correlate MS severity in parabolic flight. Altogether, our data suggest that the sensitivity of the most stimulated sensory modality during a sensory conflict may predict an individual's susceptibility to MS.</p>","PeriodicalId":12092,"journal":{"name":"Experimental Physiology","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental Physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1113/EP092966","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Sensory conflicts are widely recognized as the primary drivers of motion sickness (MS), though the underlying integrative processes remain poorly understood. This study investigated sensory reweighting following exposure to two different sensory conflict paradigms. Visual and vestibular reflexes were assessed before and after sensory conflict. In the first paradigm, participants were exposed to a visuo-vestibular conflict using visually induced illusory motion (vection) in two environments in immersive virtual reality. In the second paradigm, vestibular conflict was induced by gravitational changes in parabolic flight. Semi-circular canal integration was measured via the vestibulo-ocular reflex (VOR) suppression task, while visual weight was assessed through optokinetic nystagmus (OKN). Our findings revealed that, following virtual reality exposure, VOR response decreased by 12%, indicating a reduced reliance on vestibular inputs. Conversely, after parabolic flight, OKN performance was diminished by 13%, indicating a diminished weight of visual inputs. These findings suggest that the sensory modality failing to detect the motion was considered less reliable and therefore assigned a reduced contribution during the integration process, regardless of its actual accuracy. Additionally, visual sensitivity was associated with increased susceptibility to cybersickness, whereas vestibular sensitivity seemed to correlate MS severity in parabolic flight. Altogether, our data suggest that the sensitivity of the most stimulated sensory modality during a sensory conflict may predict an individual's susceptibility to MS.
期刊介绍:
Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged.
Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.