| Literature DB >> 35145580 |
Ismail Bozkurt1, Yasar Ozturk2, Guven Guney3, Burak Arslan4,5, Ozlem Gulbahar4, Yahya Guvenc6, Salim Senturk7, Mesut Emre Yaman8.
Abstract
Traumatic brain injury (TBI) continues to be a significant public healthcare concern. Neuroinflammation that occurs in the secondary phase of TBI leads to cognitive and physical dysfunction. A number of therapeutic modalities have been evaluated in an attempt to find a suitable treatment. The only drug approved for the treatment of idiopathic pulmonary fibrosis, pirfenidone, has been evaluated for its antifibrotic, anti-inflammatory, and anti-oxidant properties for various disorders, but this is the first study to examine its effects in an experimental TBI model. Twenty-four Wistar rats were randomly divided into three groups: control, trauma, and pirfenidone. The two latter groups underwent experimental diffuse cortical injury mimicking TBI. Neurological assessment was performed using the Garcia test, histological analysis was performed to examine neuroprotective and anti-inflammatory effects, and biochemical analyses of neuron-specific enolase (NSE), S-100B, caspase-3, and thiobarbituric acid reactive substances were performed. The pirfenidone group had a better Garcia test score (P=0.001), an increased anti-inflammatory effect (P<0.001), and an enhanced neuroprotective effect (P=0.007) along with decreased NSE, S100B, and TBARS levels compared to the trauma group. However, pirfenidone did not show a beneficial effect on caspase-3 levels. Pirfenidone may help decrease mortality and morbidity rates after TBI through its anti-inflammatory and antioxidant effects. IJCEPEntities:
Keywords: Pirfenidone; anti-inflammatory; anti-oxidant; neuroprotective; traumatic brain injury
Year: 2022 PMID: 35145580 PMCID: PMC8822207
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625