Protective Effects of Protocatechuic Acid on Seizure-Induced Neuronal Death

被引:22
|
作者
Lee, Song Hee [1 ]
Choi, Bo Young [1 ]
Kho, A. Ra [1 ]
Jeong, Jeong Hyun [1 ]
Hong, Dae Ki [1 ]
Lee, Sang Hwon [1 ]
Lee, Sang Yup [2 ]
Lee, Min Woo [3 ]
Song, Hong Ki [3 ]
Choi, Hui Chul [3 ]
Suh, Sang Won [1 ]
机构
[1] Hallym Univ, Coll Med, Dept Physiol, Chunchon 24252, South Korea
[2] Western Univ, Fac Med Sci, London, ON N6A 5C1, Canada
[3] Hallym Univ, Coll Med Neurol, Chunchon 24252, South Korea
基金
新加坡国家研究基金会;
关键词
epilepsy; pilocarpine; neuron death; protocatechuic acid; microglia; oxidative stress; PILOCARPINE-INDUCED SEIZURES; OXIDATIVE STRESS; MICROGLIAL ACTIVATION; IN-VIVO; NEURODEGENERATIVE DISORDERS; ALZHEIMERS-DISEASE; EPILEPTIC SEIZURES; GLUTATHIONE LEVELS; NADPH OXIDASE; BRAIN;
D O I
10.3390/ijms19010187
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protocatechuic acid (PCA) is a type of phenolic acid found in green tea and has been shown to have potent antioxidant and anti-inflammatory properties. However, the effect of PCA on pilocarpine seizure-induced neuronal death in the hippocampus has not been evaluated. In the present study, we investigated the potential therapeutic effects of PCA on seizure-induced brain injury. Epileptic seizure was induced by intraperitoneal (i.p.) injection of pilocarpine (25 mg/kg) in adult male rats, and PCA (30 mg/kg) was injected into the intraperitoneal space for three consecutive days after the seizure. Neuronal injury and oxidative stress were evaluated three days after a seizure. To confirm whether PCA increases neuronal survival and reduced oxidative injury in the hippocampus, we performed Fluoro-Jade-B (FJB) staining to detect neuronal death and 4-hydroxynonenal (4HNE) staining to detect oxidative stress after the seizure. In the present study, we found that, compared to the seizure vehicle-treated group, PCA administration reduced neuronal death and oxidative stress in the hippocampus. To verify whether a decrease of neuronal death by PCA treatment was due to reduced glutathione (GSH) concentration, we measured glutathione with N-ethylmaleimide (GS-NEM) levels in hippocampal neurons. A seizure-induced reduction in the hippocampal neuronal GSH concentration was preserved by PCA treatment. We also examined whether microglia activation was affected by the PCA treatment after a seizure, using CD11b staining. Here, we found that seizure-induced microglia activation was significantly reduced by the PCA treatment. Therefore, the present study demonstrates that PCA deserves further investigation as a therapeutic agent for reducing hippocampal neuronal death after epileptic seizures.
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页数:12
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