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Reduced multimodal integration of memory features following continuous theta burst stimulation of angular gyrus

Published version
Peer-reviewed

Type

Article

Change log

Authors

Yazar, Y 
Bergström, ZM 
Simons, JS 

Abstract

Background

Lesions of the angular gyrus (AnG) region of human parietal cortex do not cause amnesia, but appear to be associated with reduction in the ability to consciously experience the reliving of previous events.

Objectives/Hypothesis

We used continuous theta burst stimulation to test the hypothesis that the cognitive mechanism implicated in this memory deficit might be the integration of retrieved sensory event features into a coherent multimodal memory representation.

Methods

Healthy volunteers received stimulation to AnG or a vertex control site after studying stimuli that each comprised a visual object embedded in a scene, with the name of the object presented auditorily. Participants were then asked to make memory judgments about the studied stimuli that involved recollection of single event features (visual or auditory), or required integration of event features within the same modality, or across modalities.

Results

Participants' ability to retrieve context features from across multiple modalities was significantly reduced after AnG stimulation compared to stimulation of the vertex. This effect was observed only for the integration of cross-modal context features but not for integration of features within the same modality, and could not be accounted for by task difficulty as performance was matched across integration conditions following vertex stimulation.

Conclusion

These results support the hypothesis that AnG is necessary for the multimodal integration of distributed cortical episodic features into a unified conscious representation that enables the experience of remembering.

Description

Keywords

parietal lobe, memory, recollection, source monitoring, brain stimulation

Journal Title

Brain Stimulation

Conference Name

Journal ISSN

1935-861X
1876-4754

Volume Title

10

Publisher

Elsevier
Sponsorship
Medical Research Council (G0001354)
Medical Research Council (G1000183)
This work was supported by a James S. McDonnell Foundation Scholar Award to JSS. YY was supported by a scholarship from the German National Academic Foundation. The work was completed within the University of Cambridge Behavioural and Clinical Neuroscience Institute, funded by a joint award from the UK Medical Research Council and the Wellcome Trust.