Off-campus WSU users: To download campus access dissertations, please use the following link to log into our proxy server with your WSU access ID and password, then click the "Off-campus Download" button below.
Non-WSU users: Please talk to your librarian about requesting this dissertation through interlibrary loan.
Access Type
WSU Access
Date of Award
January 2022
Degree Type
Dissertation
Degree Name
Ph.D.
Department
Biomedical Engineering
First Advisor
Juri G. Gelovani
Abstract
The fundamental role of epigenetic regulatory mechanisms involved in neuroplasticity and adaptive responses to traumatic brain injury (TBI) is gaining increased recognition. TBI-induced neurodegeneration is associated with several changes in the expression and activity of various epigenetic-regulatory enzymes, including histone deacetylases (HDACs). In this study, PET/CT with 6-([18F]trifluoroacetamido)-1-hexanoicanilide ([18F]TFAHA) to image the spatial and temporal dynamics of HDACs class IIa expression-activity in the brain of rats subjected to a weight drop model of diffuse, non-penetrating brain injury (termed mild TBI; mTBI), that was validated by histopathological and immunohistochemical analyses of brain tissue sections for the localization and magnitude of expression of heat shock protein-70 kDa (HSP70), amyloid precursor protein (APP), cannabinoid receptor-2 (CB2), and ionized calcium binding adapter protein-1 (IBA1), and histone deacetylases 4 and 5 (HDAC4 and HDAC5). As compared to baseline, the expression-activities of HDAC4 and of HDAC5 were downregulated in the hippocampus, nucleus accumbens, periaqueductal gray, and substantia nigra at 1-3 days post mTBI, and remained low at 7-8 days post mTBI. Reduced levels of HDAC4 and HDAC5 expression observed in neurons of these brain structures post mTBI were associated with the reduced nuclear and neuropil levels of HDAC4 and HDAC5 with predominant shift to cytoplasmic localization of these enzymes. These results support the rationale for the development of therapeutic strategies aimed to upregulate the expression-activity of HDACs class IIa post-TBI. PET/CT(MRI) with [18F]TFAHA can facilitate the development and clinical translation of novel therapeutic approaches to upregulate the expression and activity of HDACs class IIa enzymes in the brain after TBI.
Recommended Citation
Kamal, Swatabdi Rohana, "Monitoring Hdac Class Iia Activity In The Rat Brain After Traumatic Brain Injury (tbi) Using Noninvasive Pet Imaging With [18f]tfaha" (2022). Wayne State University Dissertations. 3494.
https://digitalcommons.wayne.edu/oa_dissertations/3494