Cargando…
Deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function
Deep brain stimulation (DBS) is a circuit-oriented treatment for mental disorders. Unfortunately, even well-conducted psychiatric DBS clinical trials have yielded inconsistent symptom relief, in part because DBS’ mechanism(s) of action are unclear. One clue to those mechanisms may lie in the efficac...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449385/ https://www.ncbi.nlm.nih.gov/pubmed/30948727 http://dx.doi.org/10.1038/s41467-019-09557-4 |
_version_ | 1783408833948811264 |
---|---|
author | Widge, A. S. Zorowitz, S. Basu, I. Paulk, A. C. Cash, S. S. Eskandar, E. N. Deckersbach, T. Miller, E. K. Dougherty, D. D. |
author_facet | Widge, A. S. Zorowitz, S. Basu, I. Paulk, A. C. Cash, S. S. Eskandar, E. N. Deckersbach, T. Miller, E. K. Dougherty, D. D. |
author_sort | Widge, A. S. |
collection | PubMed |
description | Deep brain stimulation (DBS) is a circuit-oriented treatment for mental disorders. Unfortunately, even well-conducted psychiatric DBS clinical trials have yielded inconsistent symptom relief, in part because DBS’ mechanism(s) of action are unclear. One clue to those mechanisms may lie in the efficacy of ventral internal capsule/ventral striatum (VCVS) DBS in both major depression (MDD) and obsessive-compulsive disorder (OCD). MDD and OCD both involve deficits in cognitive control. Cognitive control depends on prefrontal cortex (PFC) regions that project into the VCVS. Here, we show that VCVS DBS’ effect is explained in part by enhancement of PFC-driven cognitive control. DBS improves human subjects’ performance on a cognitive control task and increases theta (5–8Hz) oscillations in both medial and lateral PFC. The theta increase predicts subjects’ clinical outcomes. Our results suggest a possible mechanistic approach to DBS therapy, based on tuning stimulation to optimize these neurophysiologic phenomena. |
format | Online Article Text |
id | pubmed-6449385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64493852019-04-08 Deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function Widge, A. S. Zorowitz, S. Basu, I. Paulk, A. C. Cash, S. S. Eskandar, E. N. Deckersbach, T. Miller, E. K. Dougherty, D. D. Nat Commun Article Deep brain stimulation (DBS) is a circuit-oriented treatment for mental disorders. Unfortunately, even well-conducted psychiatric DBS clinical trials have yielded inconsistent symptom relief, in part because DBS’ mechanism(s) of action are unclear. One clue to those mechanisms may lie in the efficacy of ventral internal capsule/ventral striatum (VCVS) DBS in both major depression (MDD) and obsessive-compulsive disorder (OCD). MDD and OCD both involve deficits in cognitive control. Cognitive control depends on prefrontal cortex (PFC) regions that project into the VCVS. Here, we show that VCVS DBS’ effect is explained in part by enhancement of PFC-driven cognitive control. DBS improves human subjects’ performance on a cognitive control task and increases theta (5–8Hz) oscillations in both medial and lateral PFC. The theta increase predicts subjects’ clinical outcomes. Our results suggest a possible mechanistic approach to DBS therapy, based on tuning stimulation to optimize these neurophysiologic phenomena. Nature Publishing Group UK 2019-04-04 /pmc/articles/PMC6449385/ /pubmed/30948727 http://dx.doi.org/10.1038/s41467-019-09557-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Widge, A. S. Zorowitz, S. Basu, I. Paulk, A. C. Cash, S. S. Eskandar, E. N. Deckersbach, T. Miller, E. K. Dougherty, D. D. Deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function |
title | Deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function |
title_full | Deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function |
title_fullStr | Deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function |
title_full_unstemmed | Deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function |
title_short | Deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function |
title_sort | deep brain stimulation of the internal capsule enhances human cognitive control and prefrontal cortex function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449385/ https://www.ncbi.nlm.nih.gov/pubmed/30948727 http://dx.doi.org/10.1038/s41467-019-09557-4 |
work_keys_str_mv | AT widgeas deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction AT zorowitzs deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction AT basui deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction AT paulkac deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction AT cashss deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction AT eskandaren deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction AT deckersbacht deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction AT millerek deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction AT doughertydd deepbrainstimulationoftheinternalcapsuleenhanceshumancognitivecontrolandprefrontalcortexfunction |