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Abstract
The human brain extracts meaning using an extensive neural system for semantic knowledge. Whether broadly distributed systems depend on or can compensate after losing a highly interconnected hub is controversial. We report intracranial recordings from two patients during a speech prediction task, obtained minutes before and after neurosurgical treatment requiring disconnection of the left anterior temporal lobe (ATL), a candidate semantic knowledge hub. Informed by modern diaschisis and predictive coding frameworks, we tested hypotheses ranging from solely neural network disruption to complete compensation by the indirectly affected language-related and speech-processing sites. Immediately after ATL disconnection, we observed neurophysiological alterations in the recorded frontal and auditory sites, providing direct evidence for the importance of the ATL as a semantic hub. We also obtained evidence for rapid, albeit incomplete, attempts at neural network compensation, with neural impact largely in the forms stipulated by the predictive coding framework, in specificity, and the modern diaschisis framework, more generally. The overall results validate these frameworks and reveal an immediate impact and capability of the human brain to adjust after losing a brain hub.
The human brain is a distributed system composed of highly interconnected hubs. Here, patients undergoing a rare operation reveal the immediate impact and compensatory brain network changes that occur when a key hub is removed.
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1 University of Iowa, Department of Neurosurgery, Iowa City, USA (GRID:grid.214572.7) (ISNI:0000 0004 1936 8294); Newcastle University Medical School, Biosciences Institute, Newcastle upon Tyne, UK (GRID:grid.1006.7) (ISNI:0000 0001 0462 7212); Carnegie Mellon University, Neuroscience Institute, Pittsburgh, USA (GRID:grid.147455.6) (ISNI:0000 0001 2097 0344)
2 University of Wisconsin, Departments of Neuroscience and Psychology, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675)
3 Newcastle University, CNNP Lab, Interdisciplinary Computing and Complex BioSystems Group, School of Computing, Newcastle upon Tyne, UK (GRID:grid.1006.7) (ISNI:0000 0001 0462 7212); Queen Square, UCL Institute of Neurology, London, UK (GRID:grid.436283.8) (ISNI:0000 0004 0612 2631)
4 University of Iowa, Department of Neurosurgery, Iowa City, USA (GRID:grid.214572.7) (ISNI:0000 0004 1936 8294); Newcastle University Medical School, Biosciences Institute, Newcastle upon Tyne, UK (GRID:grid.1006.7) (ISNI:0000 0001 0462 7212)
5 University of Iowa, Department of Psychological and Brain Science, Iowa City, USA (GRID:grid.214572.7) (ISNI:0000 0004 1936 8294)
6 University of Iowa, Department of Neurosurgery, Iowa City, USA (GRID:grid.214572.7) (ISNI:0000 0004 1936 8294)
7 Gonzaga University, Psychology Department, Spokane, USA (GRID:grid.256410.4) (ISNI:0000 0001 0668 7980)
8 Newcastle University Medical School, Biosciences Institute, Newcastle upon Tyne, UK (GRID:grid.1006.7) (ISNI:0000 0001 0462 7212)
9 University of Iowa, Department of Neurosurgery, Iowa City, USA (GRID:grid.214572.7) (ISNI:0000 0004 1936 8294); University of Iowa, Department of Radiology, Iowa City, USA (GRID:grid.214572.7) (ISNI:0000 0004 1936 8294); University of Iowa, Iowa Neuroscience Institute, Iowa City, USA (GRID:grid.214572.7) (ISNI:0000 0004 1936 8294)
10 University of Iowa, Department of Communication Sciences and Disorders, Iowa City, USA (GRID:grid.214572.7) (ISNI:0000 0004 1936 8294)
11 Cambridge University, Department of Clinical Neurosciences, Cambridge, UK (GRID:grid.5335.0) (ISNI:0000 0001 2188 5934); Cambridge University, MRC Cognition and Brain Sciences Unit, Cambridge, UK (GRID:grid.5335.0) (ISNI:0000000121885934)