| Literature DB >> 33421075 |
Susan C Schwerin1, Mitali Chatterjee, Elizabeth B Hutchinson2, Francis T Djankpa1,3,4, Regina C Armstrong1,3, Joseph T McCabe1,3, Daniel P Perl3,5, Sharon L Juliano1,3.
Abstract
Blast exposures are a hallmark of contemporary military conflicts. We need improved preclinical models of blast traumatic brain injury for translation of pharmaceutical and therapeutic protocols. Compared with rodents, the ferret brain is larger, has substantial sulci, gyri, a higher white to gray matter ratio, and the hippocampus in a ventral position; these attributes facilitate comparison with the human brain. In this study, ferrets received compressed air shock waves and subsequent evaluation of glia and forms of tau following survival of up to 12 weeks. Immunohistochemistry and Western blot demonstrated altered distributions of astrogliosis and tau expression after blast exposure. Many aspects of the astrogliosis corresponded to human pathology: increased subpial reactivity, gliosis at gray-white matter interfaces, and extensive outlining of blood vessels. MRI analysis showed numerous hypointensities occurring in the 12-week survival animals, appearing to correspond to luminal expansions of blood vessels. Changes in forms of tau, including phosphorylated tau, and the isoforms 3R and 4R were noted using immunohistochemistry and Western blot in specific regions of the cerebral cortex. Of particular interest were the 3R and 4R isoforms, which modified their ratio after blast. Our data strongly support the ferret as an animal model with highly translational features to study blast injury. 2021 American Association of Neuropathologists, Inc. This work is written by US Government employees and is in the public domain in the US.Entities:
Keywords: Aquaporin; Astrocyte; Blood vessels; Phosphorylated tau; Pia; Tau isoforms
Year: 2021 PMID: 33421075 DOI: 10.1093/jnen/nlaa157
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.685