Functional Magnetic Resonance Imaging of Electrical and Optogenetic Deep Brain Stimulation at the Rat Nucleus Accumbens

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作者
Daniel L. Albaugh
Andrew Salzwedel
Nathalie Van Den Berge
Wei Gao
Garret D. Stuber
Yen-Yu Ian Shih
机构
[1] University of North Carolina,Department of Neurology
[2] Biomedical Research Imaging Center,Department of Radiology
[3] University of North Carolina,Department of Biomedical Sciences and Imaging
[4] Curriculum in Neurobiology,Department of Psychiatry
[5] University of North Carolina,Department of Biomedical Engineering
[6] University of North Carolina,undefined
[7] Biomedical Imaging Research Institute,undefined
[8] Cedars-Sinai Medical Center,undefined
[9] Medical Image and Signal Processing Group,undefined
[10] Ghent University,undefined
[11] University of North Carolina,undefined
[12] University of North Carolina,undefined
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摘要
Deep brain stimulation of the nucleus accumbens (NAc-DBS) is an emerging therapy for diverse, refractory neuropsychiatric diseases. Although DBS therapy is broadly hypothesized to work through large-scale neural modulation, little is known regarding the neural circuits and networks affected by NAc-DBS. Using a healthy, sedated rat model of NAc-DBS, we employed both evoked- and functional connectivity (fc) MRI to examine the functional circuit and network changes achieved by electrical NAc stimulation. Optogenetic-fMRI experiments were also undertaken to evaluate the circuit modulation profile achieved by selective stimulation of NAc neurons. NAc-DBS directly modulated neural activity within prefrontal cortex and a large number of subcortical limbic areas (e.g., amygdala, lateral hypothalamus) and influenced functional connectivity among sensorimotor, executive and limbic networks. The pattern and extent of circuit modulation measured by evoked-fMRI was relatively insensitive to DBS frequency. Optogenetic stimulation of NAc cell bodies induced a positive fMRI signal in the NAc, but no other detectable downstream responses, indicating that therapeutic NAc-DBS might exert its effect through antidromic stimulation. Our study provides a comprehensive mapping of circuit and network-level neuromodulation by NAc-DBS, which should facilitate our developing understanding of its therapeutic mechanisms of action.
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