Magnetic resonance imaging of white matter response to diesel exhaust particles

Author:

Chakhoyan Ararat1,Shkirkova Kristina1,Sizdahkhani Saman1,Huuskonen Mikko T.1,Lamorie-Foote Krista1,Diaz Arnold2,Chen Selena1,Liu Qinghai1,D’Agostino Carla2,Zhang Hongqiao2,Mack Wendy J.3,Sioutas Constantinos4,Finch Caleb E.2,Zlokovic Berislav1,Mack William J.1

Affiliation:

1. Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California

2. Leonard Davis School of Gerontology, University of Southern California

3. Department of Population and Public Health Sciences, Keck School of Medicine

4. Viterbi School of Engineering, University of Southern California

Abstract

Abstract Air pollution is associated with risks of dementia and accelerated cognitive decline. Rodent air pollution models have shown white matter vulnerability. This study uses diffusion tensor imaging (DTI) to quantify changes to white matter microstructure and tractography in multiple myelinated regions after exposure to diesel exhaust particulate (DEP). Adult C57BL/6 male mice were exposed to re-aerosolized DEP (NIST SRM 2975) at a concentration of 100 ug/m3 for 200 hours. Ex-vivo MRI analysis and fractional anisotropy (FA)-aided white matter tractography were conducted to study the effect of DEP exposure on the brain white matter tracts. Immunohistochemistry was used to assess myelin and axonal structure. DEP exposure for 8 weeks altered myelin composition in multiple regions. Diffusion tensor imaging (DTI) showed decreased FA in the corpus callosum (30%), external capsule (15%), internal capsule (15%), and cingulum (31%). Separate immunohistochemistry analyses confirmed prior findings. Myelin basic protein (MBP) was decreased (corpus callosum: 28%, external capsule: 29%), and degraded MPB increased (corpus callosum: 32%, external capsule: 53%) in the DEP group. White matter is highly susceptible to chronic DEP exposure. This study demonstrates the utility of DTI as a neuroanatomical tool in the context of air pollution and white matter myelin vulnerability.

Publisher

Research Square Platform LLC

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