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Connectomic imaging reveals Huntington‐related pathological and pharmaceutical effects in a mouse model
Author(s) -
Chang WeiTang,
Puspitasari Fiftarina,
GarciaMiralles Marta,
Yeow Ling Yun,
Tay HuiChien,
Koh Katrianne Bethia,
Tan Liang Juin,
Pouladi Mahmoud A.,
Chuang KaiHsiang
Publication year - 2018
Publication title -
nmr in biomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.278
H-Index - 114
eISSN - 1099-1492
pISSN - 0952-3480
DOI - 10.1002/nbm.4007
Subject(s) - neuroscience , memantine , default mode network , huntington's disease , functional connectivity , resting state fmri , basal ganglia , somatosensory system , psychology , biology , disease , medicine , central nervous system , dementia
Recent studies suggest that neurodegenerative diseases could affect brain structure and function in disease‐specific network patterns; however, how spontaneous activity affects structural covariance network (SC) is not clear. We hypothesized that hyper‐excitability in Huntington disease (HD) disrupts the coordinated structural and functional connectivity, and treatment with memantine helps to reduce excitotoxicity and normalize the connectivity. MRI was conducted to measure somatosensory activation, resting‐state functional‐connectivity (rsFC), SC, amplitude of low frequency fluctuation (ALFF) and ALFF covariance (ALFFC) in the YAC128 mouse model of HD. We found somatosensory activation was unchanged but the subcortical ALFF was increased in HD mice, indicating subcortical but not cortical hyperactivity. The reduced sensorimotor rsFC but spared hippocampal and default mode networks in the HD mice was consistent with the more pronounced impairment in motor function compared with cognitive performance. The disease suppressed SC globally and reduced ALFFC in the basal ganglia network as well as its anti‐correlation with the default mode network. By comparing these connectivity measures, we found that the originally coupled rsFC‐SC relationship was impaired whereas SC‐ALFFC correlation was increased by HD, suggesting disease facilitated covariation of brain volume and activity amplitude but not neural synchrony. The comparison with mono‐synaptic axonal projection supports the hypothesis that rsFC, but not SC or ALFFC, is highly dependent on structural connectivity under healthy conditions. Treatment with memantine had a strong effect on normalizing the SC and reducing ALFF while slightly increasing other connectivity measures and restoring the rsFC‐SC coupling, which is consistent with its effect on alleviating hyper‐excitability and improving the coordinated neural growth. These results indicate that HD affects the cerebral structure–function relationship which could be partially reverted by NMDA antagonism. These connectivity measures provide unique insights into pathological and pharmaceutical effects in brain circuitry, and could be translatable biomarkers for evaluating drug effect and refining its efficacy.