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.
Citations in the library
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