| Literature DB >> 31077843 |
Samuel Cd Cartmell1, Qiyuan Tian2, Brandon J Thio3, Christoph Leuze4, Li Ye5, Nolan R Williams6, Grant Yang2, Gabriel Ben-Dor6, Karl Deisseroth7, Warren M Grill3, Jennifer A McNab4, Casey H Halpern8.
Abstract
Dysregulation of the nucleus accumbens (NAc) is implicated in numerous neuropsychiatric disorders. Treatments targeting this area directly (e.g. deep brain stimulation) demonstrate variable efficacy, perhaps owing to non-specific targeting of a functionally heterogeneous nucleus. Here we provide support for this notion, first observing disparate behavioral effects in response to direct simulation of different locations within the NAc in a human patient. These observations motivate a segmentation of the NAc into subregions, which we produce from a diffusion-tractography based analysis of 245 young, unrelated healthy subjects. We further explore the mechanism of these stimulation-induced behavioral responses by identifying the most probable subset of axons activated using a patient-specific computational model. We validate our diffusion-based segmentation using evidence from several modalities, including MRI-based measures of function and microstructure, human post-mortem immunohistochemical staining, and cross-species comparison of cortical-NAc projections that are known to be conserved. Finally, we visualize the passage of individual axon bundles through one NAc subregion in a post-mortem human sample using CLARITY 3D histology corroborated by 7T tractography. Collectively, these findings extensively characterize human NAc subregions and provide insight into their structural and functional distinctions with implications for stereotactic treatments targeting this region.Entities:
Keywords: Accumbens; CLARITY; Computational modeling; Core; DBS; Shell; Tractography
Mesh:
Year: 2019 PMID: 31077843 PMCID: PMC7341972 DOI: 10.1016/j.neuroimage.2019.05.019
Source DB: PubMed Journal: Neuroimage ISSN: 1053-8119 Impact factor: 6.556