TY - JOUR
T1 - Visually induced nausea causes characteristic changes in cerebral, autonomic and endocrine function in humans
AU - Farmer, Adam D
AU - Ban, Vin F
AU - Coen, Steven J
AU - Sanger, Gareth J
AU - Barker, Gareth J
AU - Gresty, Michael A
AU - Giampietro, Vincent P
AU - Williams, Steven C
AU - Webb, Dominic-Luc
AU - Hellström, Per M
AU - Andrews, Paul Lr
AU - Aziz, Qasim
PY - 2015/3/1
Y1 - 2015/3/1
N2 - An integrated understanding of the physiological mechanisms involved in the genesis of nausea remains lacking. We aimed to describe the psychophysiological changes accompanying visually induced motion sickness, using a motion video, hypothesizing that differences would be evident between subjects who developed nausea in comparison to those that did not. A motion, or a control, stimulus was presented to 98 healthy subjects in a randomized crossover design. Validated questionnaires and visual analogue scales (VAS) were used for the assessment of anxiety and nausea. Autonomic and electrogastrographic activity were measured at baseline and continuously thereafter. Plasma vasopressin and ghrelin were measured in response to the motion video. Subjects were stratified into quartiles based on VAS nausea scores, with the upper and lower quartiles considered to be nausea sensitive and resistant respectively. 28 subjects were exposed to the motion video during functional neuroimaging. During the motion video, nausea sensitive subjects had lower normogastria:tachygastria ratio and cardiac vagal tone but higher cardiac sympathetic index in comparison to the control video. Furthermore, nausea sensitive subjects had decreased plasma ghrelin and demonstrated increased activity the left anterior cingulate cortex. Nausea VAS scores positively correlated with plasma vasopressin, left inferior frontal and middle occipital gyri activity and negatively correlated with plasma ghrelin and brain activity in the right cerebellar tonsil, declive, culmen, lingual gyrus and cuneus. This study demonstrates that the subjective sensation of nausea is associated with objective changes in autonomic, endocrine and brain networks, and thus identifies potential objective biomarkers and targets for therapeutic interventions.
AB - An integrated understanding of the physiological mechanisms involved in the genesis of nausea remains lacking. We aimed to describe the psychophysiological changes accompanying visually induced motion sickness, using a motion video, hypothesizing that differences would be evident between subjects who developed nausea in comparison to those that did not. A motion, or a control, stimulus was presented to 98 healthy subjects in a randomized crossover design. Validated questionnaires and visual analogue scales (VAS) were used for the assessment of anxiety and nausea. Autonomic and electrogastrographic activity were measured at baseline and continuously thereafter. Plasma vasopressin and ghrelin were measured in response to the motion video. Subjects were stratified into quartiles based on VAS nausea scores, with the upper and lower quartiles considered to be nausea sensitive and resistant respectively. 28 subjects were exposed to the motion video during functional neuroimaging. During the motion video, nausea sensitive subjects had lower normogastria:tachygastria ratio and cardiac vagal tone but higher cardiac sympathetic index in comparison to the control video. Furthermore, nausea sensitive subjects had decreased plasma ghrelin and demonstrated increased activity the left anterior cingulate cortex. Nausea VAS scores positively correlated with plasma vasopressin, left inferior frontal and middle occipital gyri activity and negatively correlated with plasma ghrelin and brain activity in the right cerebellar tonsil, declive, culmen, lingual gyrus and cuneus. This study demonstrates that the subjective sensation of nausea is associated with objective changes in autonomic, endocrine and brain networks, and thus identifies potential objective biomarkers and targets for therapeutic interventions.
UR - http://www.scopus.com/inward/record.url?scp=84923387202&partnerID=8YFLogxK
U2 - 10.1113/jphysiol.2014.284240
DO - 10.1113/jphysiol.2014.284240
M3 - Article
C2 - 25557265
SN - 0022-3751
VL - 593
SP - 1183
EP - 1196
JO - The Journal of Physiology
JF - The Journal of Physiology
IS - 5
ER -