4.6 Article

Nucleus Accumbens Stimulation Modulates Inhibitory Control by Right Prefrontal Cortex Activation in Obsessive-Compulsive Disorder

期刊

CEREBRAL CORTEX
卷 31, 期 5, 页码 2742-2758

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhaa397

关键词

obsessive-compulsive disorder; deep brain stimulation; nucleus accumbens; prefrontal cortex; response inhibition

资金

  1. European Regional Development Fund (ERDF)
  2. Spanish Ministry of Economy and Competitiveness [PSI2014-58654-JIN, PSI2017-85951-R]
  3. Department of Health of the Andalusia Health Service [PI-0025-2017]
  4. University of Cadiz
  5. tenure-track Ramon y Cajal research fellowship/grant [RYC2015-18467]

向作者/读者索取更多资源

In this study, deep brain stimulation (DBS) of the nucleus accumbens (NAc) was found to significantly improve inhibitory control abilities in OCD patients, leading to increased cortical activation mainly in the right inferior frontal gyrus and medial frontal gyrus. This modulation of neuronal activity in the prefrontal regions may be triggered by reorganizing brain functions and is associated with underlying cortical thinning.
Inhibitory control is considered a compromised cognitive function in obsessive-compulsive (OCD) patients and likely linked to corticostriatal circuitry disturbances. Here, 9 refractory OCD patients treated with deep brain stimulation (DBS) were evaluated to address the dynamic modulations of large-scale cortical network activity involved in inhibitory control after nucleus accumbens (NAc) stimulation and their relationship with cortical thickness. A comparison of DBS On/Off states showed that patients committed fewer errors and exhibited increased intraindividual reaction time variability, resulting in improved goal maintenance abilities and proactive inhibitory control. Visual P3 event-related potentials showed increased amplitudes during Go/NoGo performance. Go and NoGo responses increased cortical activation mainly over the right inferior frontal gyrus and medial frontal gyrus, respectively. Moreover, increased cortical activation in these areas was equally associated with a higher cortical thickness within the prefrontal cortex. These results highlight the critical role of NAc DBS for preferentially modulating the neuronal activity underlying sustained speed responses and inhibitory control in OCD patients and show that it is triggered by reorganizing brain functions to the right prefrontal regions, which may depend on the underlying cortical thinning. Our findings provide updated structural and functional evidence that supports critical dopaminergic-mediated frontal-striatal network interactions in OCD.

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