首页> 外文期刊>Metabolic brain disease >Nanoformulated ellagic acid ameliorates pentylenetetrazol-induced experimental epileptic seizures by modulating oxidative stress, inflammatory cytokines and apoptosis in the brains of male mice
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Nanoformulated ellagic acid ameliorates pentylenetetrazol-induced experimental epileptic seizures by modulating oxidative stress, inflammatory cytokines and apoptosis in the brains of male mice

机译:纳米配方的鞣花酸通过调节雄性小鼠大脑中的氧化应激、炎性细胞因子和细胞凋亡来改善戊烯四唑诱导的实验性癫痫发作

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摘要

The present study evaluated the neuroprotective and antiepileptic efficacy of ellagic acid (EA) encapsulated in calcium-alginate nanoparticles (Ca2+-ALG NPs) in pentylenetetrazol (PTZ)-induced seizures in male mice. EA was encapsulated in ALG NPs using a nanospray drying method followed by ionotropic crosslinking with Ca2+. Characterization of the developed Ca2+-crosslinked EA-ALG NPs showed spherical, high stability NPs; successful loading of EA within crosslinked ALG NPs; and sustained release of EA. Male Swiss albino mice were divided into ten groups as follows; Group I- (control), Group II (50?mg EA /kg) - (EA), Group III polyethylene glycol (PEG), Group IV EA NPs (50?mg/kg) - (EA NP), Group (50?mg/kg alginate) V void V NPs - (void NPs), Group VI: (37.5 PTZ mg/kg) -(PTZ), Group VII: PTZ and EA – (PTZ-EA). Group VIII: animals received PTZ and PEG concurrently (PTZ-PEG). Group IX; animals received PTZ and void NPs concurrently - (PTZ-void). Group X: animals received PTZ and EA NPs concurrently (PTZ-EA NPs). PTZ was used to induce experimental epilepsy. Ca2+-ALG NPs prevented seizures throughout the experimental period and had a more prominent effect than free EA did. Ca2+-ALG NPs prevented increased glutamate, decreased GABA concentrations and ameliorated increased amyloid-β and homocysteine levels in the serum and brain. Ca2+-EA-ALG NPs were superior to free EA in improving increased IL-6 and TNF-α. Ca2+-ALG NPs ameliorated PTZ-induced oxidative stress, as evidenced by decreased 4HNE levels and enhanced GSH, GR and GPx levels in the brain. These changes were accompanied by amelioration of apoptosis and its regulating proteins, including Cytochrome C, P53, Bax, Bcl2 and caspase-3 and caspase-9, and protected against DNA damage. Histological examination of the hippocampus confirmed that the neuroprotective effect of Ca2+-EA-ALG NPs was superior and more effective than that of free EA.
机译:本研究评估了海藻酸钙纳米颗粒(Ca2+-ALG NPs)包封的鞣花酸(EA)在戊四唑(PTZ)诱导的雄性小鼠癫痫发作中的神经保护和抗癫痫功效。使用纳米喷雾干燥方法将EA封装在ALG NPs中,然后与Ca2+离子交联。对开发的Ca2+交联EA-ALG NPs的表征显示出球形、高稳定性的NPs;在交联的 ALG NP 中成功加载 EA;将雄性瑞士白化小鼠分为以下10组;I组-(对照),II组(50?mg EA/kg)-(EA),III组聚乙二醇(PEG),IV组EA NPs(50?mg/kg)-(EA NP),V组(50?mg/kg海藻酸盐)V空隙V-NPs-(void NPs),VI组:(37.5 PTZ mg/kg)-(PTZ),VII组:PTZ和EA-(PTZ-EA)。第八组:动物同时接受PTZ和PEG(PTZ-PEG)。第九组;动物同时接受 PTZ 和 void NP - (PTZ-void)。X组:动物同时接受PTZ和EA NPs(PTZ-EA NPs)。PTZ用于诱发实验性癫痫。Ca2+-ALG NPs在整个实验期间防止癫痫发作,并且比游离EA具有更突出的效果。Ca2+-ALG NPs可防止血清和脑中谷氨酸的增加,降低GABA浓度,并改善淀粉样蛋白β和同型半胱氨酸水平的增加。Ca2+-EA-ALG NPs在改善IL-6和TNF-α升高方面优于游离EA。Ca2+-ALG NPs 改善了 PTZ 诱导的氧化应激,这表现为大脑中 4HNE 水平降低和 GSH、GR 和 GPx 水平升高。这些变化伴随着细胞凋亡及其调节蛋白(包括细胞色素 C、P53、Bax、Bcl2 和 caspase-3 和 caspase-9)的改善,并防止 DNA 损伤。海马组织学检查证实,Ca2+-EA-ALG NPs的神经保护作用优于游离EA,更有效。

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