Inhalation of 7.5% carbon dioxide increases alerting and orienting attention network function
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The development of experimental models that readily translate between animals and humans is required to better integrate and clarify the biological, behavioural and cognitive mechanisms that underlie normal fear and pathological anxiety. Inhalation of low concentrations of carbon dioxide (CO2) increases anxiety and autonomic arousal in humans, triggers related behaviours in small animals, and increases selective attention to threat in healthy humans. However the effects on broader cognitive (non-emotional) processes that characterize anxiety are not known.
To examine the effect of 7.5 % CO2 inhalation (vs. air) on the efficiency of discrete attention networks implicated in anxiety: alerting (maintaining an alert state), orienting (the selection of information from sensory input) and executive control (resolving cognitive conflict).
Twenty-three healthy human participants completed a computerized Attention Network Test (ANT) during inhalation of 7.5 % CO2 enriched and normal/medical air. Gas was administered blind to participants with inhalation order counterbalanced across participants. Measures of heart rate, blood pressure and subjective mood/anxiety were obtained at baseline and following each inhalation period.
CO2 inhalation increased anxiety, autonomic arousal and the efficiency of alerting and orienting attention network function. Autonomic response to CO2 correlated with increased orienting; and CO2–induced anxiety, autonomic arousal and orienting network function increased with chronic (trait) anxiety.
Evidence that CO2 modulates attention mechanisms involved in the temporal detection and spatial location of salient stimuli converges with evidence that CO2 triggers fear behaviour in animals via direct innervation of a distributed neural network that facilitates environmental hypervigilance.
KeywordsCarbon dioxide Anxiety Cognition Autonomic arousal Attention Network Test Noradrenaline
We would like to thank M Hotton and C Struthers (University of Bristol) for their help with data collection.
Conflict of Interest
DB has acted as a paid consultant to a number of companies with an interest in anxiety disorders (Eli Lilly, GlaxoSmithKline, Grunenthal, Lundbeck, Pfizer, Servier) and has held grants (on behalf of his employer) from Lundbeck and Pfizer. He has accepted paid speaking engagements in industry supported satellite symposia at international and national meetings organized by Lundbeck, Pfizer and Servier. There are no Conflicts of Interest for MG, AA, MRM.
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