Literature DB >> 27439860

Constituents and functional implications of the rat default mode network.

Li-Ming Hsu1, Xia Liang2, Hong Gu2, Julia K Brynildsen2, Jennifer A Stark2, Jessica A Ash3, Ching-Po Lin4, Hanbing Lu2, Peter R Rapp3, Elliot A Stein2, Yihong Yang5.   

Abstract

The default mode network (DMN) has been suggested to support a variety of self-referential functions in humans and has been fractionated into subsystems based on distinct responses to cognitive tasks and functional connectivity architecture. Such subsystems are thought to reflect functional hierarchy and segregation within the network. Because preclinical models can inform translational studies of neuropsychiatric disorders, partitioning of the DMN in nonhuman species, which has previously not been reported, may inform both physiology and pathophysiology of the human DMN. In this study, we sought to identify constituents of the rat DMN using resting-state functional MRI (rs-fMRI) and diffusion tensor imaging. After identifying DMN using a group-level independent-component analysis on the rs-fMRI data, modularity analyses fractionated the DMN into an anterior and a posterior subsystem, which were further segregated into five modules. Diffusion tensor imaging tractography demonstrates a close relationship between fiber density and the functional connectivity between DMN regions, and provides anatomical evidence to support the detected DMN subsystems. Finally, distinct modulation was seen within and between these DMN subcomponents using a neurocognitive aging model. Taken together, these results suggest that, like the human DMN, the rat DMN can be partitioned into several subcomponents that may support distinct functions. These data encourage further investigation into the neurobiological mechanisms of DMN processing in preclinical models of both normal and disease states.

Entities:  

Keywords:  aging; default mode network; functional connectivity; modularity; rat brain

Mesh:

Year:  2016        PMID: 27439860      PMCID: PMC4978262          DOI: 10.1073/pnas.1601485113

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


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