dc.contributor.author | Divani, AA | |
dc.contributor.author | Phan, J-A | |
dc.contributor.author | Salazar, P | |
dc.contributor.author | Santacruz, KS | |
dc.contributor.author | Bachour, O | |
dc.contributor.author | Mahmoudi, J | |
dc.contributor.author | Zhu, X-H | |
dc.contributor.author | Pomper, MG | |
dc.date.accessioned | 2018-08-26T08:38:27Z | |
dc.date.available | 2018-08-26T08:38:27Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52930 | |
dc.description.abstract | We present a longitudinal study of cerebral metabolism using [18F]fluorodeoxyglucose (FDG) positron emission tomography (PET) in a rat model of shockwave-induced traumatic brain injury (SW-TBI). Anesthetized rats received 5 or 10 SW pulses to the right anterior lateral or dorsal frontal regions using SW lithotripsy. Animals were scanned for FDG uptake at baseline, 3 h post-injury, and 3 days post-injury, using a small animal PET/computed tomography (CT) scanner. FDG uptake at all time-points was quantified as the ratio of brain activity relative to peripheral activity in the left ventricle (LV) in the heart (Abrain/ALV) for the entire brain, each hemisphere, and four cortices (motor, cingulate, somatosensory, and retrosplenial). The mixed-designed models analysis of variance (ANOVA) for the hemispheric and global FDG uptake ratio showed a significant effect of the time-of-scan (p = 0.038) and measured region (p = 6.12e-09). We also observed a significant effect of the time-of-scan (p = 0.046) and measured region (p = 2.28e-09) for the FDG uptake ratio in four cortical regions. None of the measurements (global or local) showed a significant effect for the number of SW pulses (5 or 10) or SW location (lateral or dorsal frontal regions). Our data suggest that SW-TBI causes hypermetabolism on the impact side of the rat brain at 3 h post-injury compared with the baseline measurements. However, the increase in FDG uptake by day 3 post-injury was not significant. Further studies on post-TBI metabolic changes are needed to understand better the pathophysiology of the injury. é Copyright 2018, Mary Ann Liebert, Inc. 2018. | |
dc.language.iso | English | |
dc.relation.ispartof | Journal of Neurotrauma | |
dc.subject | amyloid precursor protein | |
dc.subject | buprenorphine | |
dc.subject | fluorodeoxyglucose f 18 | |
dc.subject | glial fibrillary acidic protein | |
dc.subject | ketoprofen | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | animal tissue | |
dc.subject | Article | |
dc.subject | brain function | |
dc.subject | brain metabolism | |
dc.subject | cingulate gyrus | |
dc.subject | controlled study | |
dc.subject | electroencephalogram | |
dc.subject | experimental traumatic brain injury | |
dc.subject | glucose transport | |
dc.subject | heart left ventricle | |
dc.subject | hemisphere | |
dc.subject | histopathology | |
dc.subject | hypermetabolism | |
dc.subject | lithotripsy | |
dc.subject | longitudinal study | |
dc.subject | male | |
dc.subject | motor cortex | |
dc.subject | nonhuman | |
dc.subject | positron emission tomography | |
dc.subject | rat | |
dc.subject | retrosplenial cortex | |
dc.subject | shock wave | |
dc.subject | somatosensory cortex | |
dc.subject | Wistar rat | |
dc.title | Changes in [18F]Fluorodeoxyglucose Activities in a Shockwave-Induced Traumatic Brain Injury Model Using Lithotripsy | |
dc.type | Article | |
dc.citation.volume | 35 | |
dc.citation.issue | 1 | |
dc.citation.spage | 187 | |
dc.citation.epage | 194 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.1089/neu.2017.5208 | |