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Neural Sources and Underlying Mechanisms of Neural Responses to Heartbeats, and their Role in Bodily Self-consciousness: An Intracranial EEG Study.

Hyeong-Dong Park, Fosco Bernasconi, Roy Salomon, Catherine Tallon-Baudry, Laurent Spinelli, Margitta Seeck, Karl Schaller, Olaf Blanke

Cerebral Cortex July 1, 2018 DOI: 10.1093/cercor/bhx136 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Intracranial electroencephalography (EEG) experiments Peer reviewed
Population Patients with epilepsy undergoing intracranial EEG recording
Topics Philosophy of mind
Keywords Neurons Humans Epilepsy Electroencephalography Brain mapping Consciousness Imagination Evoked potentials Blood pressure Heart rate User-computer interface Female Young adult Interoception Electrocorticography
Key findings HEPs shortly after heartbeat onset showed significant single-trial phase concentration at 10% of recording sites, mainly in the insula and operculum, and also in the amygdala and fronto-temporal cortex, without accompanying increases in spectral power. The authors argue this pattern indicates phase resetting rather than an additive evoked-potential mechanism, and that insula HEP modulations reflected an experimentally induced altered sense of self-identification.

Abstract

Recent research has shown that heartbeat-evoked potentials (HEPs), brain activity in response to heartbeats, are a useful neural measure for investigating the functional role of brain-body interactions in cognitive processes including self-consciousness. In 2 experiments, using intracranial electroencephalography (EEG), we investigated (1) the neural sources of HEPs, (2) the underlying mechanisms for HEP generation, and (3) the functional role of HEPs in bodily self-consciousness. In Experiment-1, we found that shortly after the heartbeat onset, phase distributions across single trials were significantly concentrated in 10% of the recording sites, mainly in the insula and the operculum, but also in other regions including the amygdala and fronto-temporal cortex. Such phase concentration was not accompanied by increased spectral power, and did not correlate with spectral power changes, suggesting that a phase resetting, rather than an additive "evoked potential" mechanism, underlies HEP generation. In Experiment-2, we further aimed to anatomically refine previous scalp EEG data that linked HEPs with bodily self-consciousness. We found that HEP modulations in the insula reflected an experimentally induced altered sense of self-identification. Collectively, these results provide novel and solid electrophysiological evidence on the neural sources and underlying mechanisms of HEPs, and their functional role in self-consciousness.

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