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Administration of Protocatechuic Acid Reduces Traumatic Brain Injury-Induced Neuronal Death.
- Source :
-
International Journal of Molecular Sciences . Dec2017, Vol. 18 Issue 12, p2510. 13p. - Publication Year :
- 2017
-
Abstract
- Protocatechuic acid (PCA) was first purified from green tea and has shown numerous biological activities, including anti-apoptotic, anti-inflammatory, and anti-atherosclerotic effects. The effect of PCA on traumatic brain injury (TBI)-induced neuronal death has not previously been evaluated. TBI is defined as damage to the brain resulting from external mechanical force, such as rapid acceleration or deceleration, impact, blast waves, or penetration by a projectile. TBI causes neuronal death in the hippocampus and cerebral cortex. The present study aimed to evaluate the therapeutic potential of PCA on TBI-induced neuronal death. Here, TBI was induced by a controlled cortical impact model using rats. PCA (30 mg/kg) was injected into the intraperitoneal (ip) space immediately after TBI. Neuronal death was evaluated with Fluoro Jade-B (FJB) staining at 24 h after TBI. Oxidative injury was detected by 4-hydroxy-2-nonenal (4HNE), glutathione (GSH) concentration was analyzed by glutathione adduct with N-ethylmaleimide (GS-NEM) staining at 24 h after TBI, and microglial activation in the hippocampus was detected by CD11b immunohistochemistry at one week after TBI. We found that the proportion of degenerating neurons, oxidative injury, GSH depletion, and microglia activation in the hippocampus and cortex were all reduced by PCA treatment following TBI. Therefore, our study suggests that PCA may have therapeutic potential in preventing TBI-induced neuronal death. [ABSTRACT FROM AUTHOR]
- Subjects :
- *BRAIN injuries
*BRAIN damage
*GLUTATHIONE
*IMMUNOHISTOCHEMISTRY
*LABORATORY rats
Subjects
Details
- Language :
- English
- ISSN :
- 16616596
- Volume :
- 18
- Issue :
- 12
- Database :
- Academic Search Index
- Journal :
- International Journal of Molecular Sciences
- Publication Type :
- Academic Journal
- Accession number :
- 126966197
- Full Text :
- https://doi.org/10.3390/ijms18122510