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Defensive eye-blink startle responses in a human experimental model of anxiety

Inhalation of low concentrations of carbon dioxide (CO(2)) triggers anxious behaviours in rodents via chemosensors in the amygdala, and increases anxiety, autonomic arousal and hypervigilance in healthy humans. However, it is not known whether CO(2) inhalation modulates defensive behaviours coordina...

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Detalles Bibliográficos
Autores principales: Pinkney, Verity, Wickens, Robin, Bamford, Susan, Baldwin, David S, Garner, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876426/
https://www.ncbi.nlm.nih.gov/pubmed/24899597
http://dx.doi.org/10.1177/0269881114532858
Descripción
Sumario:Inhalation of low concentrations of carbon dioxide (CO(2)) triggers anxious behaviours in rodents via chemosensors in the amygdala, and increases anxiety, autonomic arousal and hypervigilance in healthy humans. However, it is not known whether CO(2) inhalation modulates defensive behaviours coordinated by this network in humans. We examined the effect of 7.5% CO(2) challenge on the defensive eye-blink startle response. A total of 27 healthy volunteers completed an affective startle task during inhalation of 7.5% CO(2) and air. The magnitude and latency of startle eye-blinks were recorded whilst participants viewed aversive and neutral pictures. We found that 7.5% CO(2) increased state anxiety and raised concurrent measures of skin conductance and heart rate (HR). CO(2) challenge did not increase startle magnitude, but slowed the onset of startle eye-blinks. The effect of CO(2) challenge on HR covaried with its effects on both subjective anxiety and startle latency. Our findings are discussed with reference to startle profiles during conditions of interoceptive threat, increased cognitive load and in populations characterised by anxiety, compared with acute fear and panic.