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原儿茶酸对癫痫诱导的神经元死亡的保护作用。

Protective Effects of Protocatechuic Acid on Seizure-Induced Neuronal Death.

机构信息

Department of Physiology, College of Medicine, Hallym University, Chuncheon 24252, Korea.

Faculty of Medical Sciences, Western University, London, ON N6A 5C1, Canada.

出版信息

Int J Mol Sci. 2018 Jan 8;19(1):187. doi: 10.3390/ijms19010187.

Abstract

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 -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.

摘要

原儿茶酸(PCA)是一种存在于绿茶中的酚酸,已被证明具有强大的抗氧化和抗炎特性。然而,PCA 对匹罗卡品诱发的海马神经元死亡的影响尚未得到评估。在本研究中,我们研究了 PCA 对癫痫发作引起的脑损伤的潜在治疗作用。通过腹腔内(i.p.)注射匹罗卡品(25mg/kg)在成年雄性大鼠中诱导癫痫发作,并且在癫痫发作后连续 3 天腹腔内注射 PCA(30mg/kg)。在癫痫发作后 3 天评估神经元损伤和氧化应激。为了确认 PCA 是否增加海马神经元的存活并减轻氧化损伤,我们进行了 Fluoro-Jade-B(FJB)染色以检测神经元死亡和 4-羟壬烯醛(4HNE)染色以检测氧化应激。在本研究中,我们发现与癫痫发作载体处理组相比,PCA 给药可减少海马中的神经元死亡和氧化应激。为了验证 PCA 处理减少神经元死亡是否归因于还原型谷胱甘肽(GSH)浓度的降低,我们测量了海马神经元中的 -乙基maleimide(GS-NEM)水平的谷胱甘肽(GSH)浓度。PCA 处理可保留癫痫发作引起的海马神经元 GSH 浓度降低。我们还检查了 PCA 处理后癫痫发作后是否影响微胶质细胞的激活,使用 CD11b 染色。在这里,我们发现 PCA 处理可显著降低癫痫发作引起的小胶质细胞激活。因此,本研究表明 PCA 作为减少癫痫发作后海马神经元死亡的治疗剂值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d090/5796136/f4bad89c9f1d/ijms-19-00187-g001.jpg

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