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使用表没食子儿茶素没食子酸酯生物合成的硒纳米颗粒通过抗氧化、抗炎和抗凋亡活性预防戊四氮诱导的小鼠急性癫痫发作。

Biosynthesized Selenium Nanoparticles Using Epigallocatechin Gallate Protect against Pentylenetetrazole-Induced Acute Epileptic Seizures in Mice via Antioxidative, Anti-Inflammatory, and Anti-Apoptotic Activities.

作者信息

Alrashdi Barakat M, Fehaid Alaa, Kassab Rami B, Rizk Sara, Habotta Ola A, Abdel Moneim Ahmed E

机构信息

Biology Department, College of Science, Jouf University, Sakaka 41412, Saudi Arabia.

Department of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Mansoura University, Mansoura 35516, Egypt.

出版信息

Biomedicines. 2023 Jul 11;11(7):1955. doi: 10.3390/biomedicines11071955.

Abstract

Several negative outcomes are associated with current anti-epileptic medications. Epigallocatechin gallate (EGCG) is a plant-derived compound called catechin and has many medicinal activities, such as anti-inflammatory and antioxidant activities. Biosynthesized selenium nanoparticles are also showing their neuroprotective effect. The anti-epileptic effect of EGCG, alone or with SeNPs, is still debated. Here, we aimed to investigate the potential anti-seizure effect of biosynthesized SeNPs using EGCG (EGCG-SeNPs) against epileptic seizures and hippocampal damage, which is enhanced by pentylenetetrazole (PTZ) injection in mice. Mice were grouped as follows: control; PTZ-exposed group (epileptic model); EGCG + PTZ-treated group; sodium selenite (NaSeO) + PTZ-treated group; EGCG-SeNPs + PTZ-treated group; and valproic acid (VPA) + PTZ-treated group. EGCG-SeNPs administration showed anti-epileptic activity by increasing the latency time and reducing the seizure duration following the PTZ injection. Additionally, EGCG-SeNPs counteracted the PTZ-induced changes in oxidants and antioxidants. Moreover, EGCG-SeNPs inhibited the inflammatory response by suppressing the release of pro-inflammatory cytokines and decreasing the immunoreactivity of the glial fibrillary acidic protein and mRNA expression of glutamate receptor subunit zeta-1 (NMDAR; Grin1), showing their inhibitory effect on epilepsy-associated inflammation. Moreover, EGCG-SeNPs reduced PTZ-induced neuronal apoptosis, as indicated by a reduction in the levels of pro-apoptotic proteins and an elevation of the anti-apoptotic protein. Moreover, EGCG-SeNPs administration significantly modulated the PTZ-induced changes in monoamine levels and acetylcholinesterase activity in the hippocampal tissue. The obtained findings suggest the anti-seizure activity of EGCG-SeNPs via their antioxidant, anti-inflammatory, and anti-apoptotic effects, along with their neuromodulatory effect.

摘要

目前的抗癫痫药物存在一些负面结果。表没食子儿茶素没食子酸酯(EGCG)是一种植物来源的化合物,称为儿茶素,具有许多药用活性,如抗炎和抗氧化活性。生物合成的硒纳米颗粒也显示出它们的神经保护作用。EGCG单独或与硒纳米颗粒联合使用的抗癫痫作用仍存在争议。在此,我们旨在研究使用EGCG生物合成的硒纳米颗粒(EGCG-SeNPs)对癫痫发作和海马损伤的潜在抗惊厥作用,戊四氮(PTZ)注射可增强小鼠的癫痫发作和海马损伤。小鼠分为以下几组:对照组;PTZ暴露组(癫痫模型);EGCG + PTZ治疗组;亚硒酸钠(NaSeO)+ PTZ治疗组;EGCG-SeNPs + PTZ治疗组;丙戊酸(VPA)+ PTZ治疗组。给予EGCG-SeNPs后,通过增加PTZ注射后的潜伏期和缩短癫痫发作持续时间显示出抗癫痫活性。此外,EGCG-SeNPs抵消了PTZ诱导的氧化剂和抗氧化剂的变化。此外,EGCG-SeNPs通过抑制促炎细胞因子的释放、降低胶质纤维酸性蛋白的免疫反应性和谷氨酸受体亚基zeta-1(NMDAR;Grin1)的mRNA表达来抑制炎症反应,显示出它们对癫痫相关炎症的抑制作用。此外,EGCG-SeNPs减少了PTZ诱导的神经元凋亡,可以通过促凋亡蛋白水平的降低和抗凋亡蛋白的升高来表明。此外,给予EGCG-SeNPs显著调节了PTZ诱导的海马组织中单胺水平和乙酰胆碱酯酶活性的变化。获得的研究结果表明,EGCG-SeNPs通过其抗氧化、抗炎和抗凋亡作用以及神经调节作用具有抗惊厥活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80c2/10377216/a6fc21917a75/biomedicines-11-01955-g001.jpg

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