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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Cleistocalyx nervosum var. paniala berry fruit protects neurotoxicity against endoplasmic reticulum stress-induced apoptosis
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Cleistocalyx nervosum var. paniala berry fruit protects neurotoxicity against endoplasmic reticulum stress-induced apoptosis

机译:CleiStocalyx术语var。 Paniala Berry Fruit保护神经毒性对内质网胁迫诱导的细胞凋亡

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Oxidative and endoplasmic reticulum (ER) stresses cause neuronal damage leading to neurodegenerative disorders. Cleistocalyx nervosum var. paniala (CNP) berry fruit has been shown to possess powerful antioxidant properties. Here, we investigated the neuroprotective effect of CNP extract against glutamate-mediated oxidative/ER stress-induced cell death in mouse hippocampal neuronal HT22 cells. CNP extract was clarified for its radical scavenging activities, total phenolic and anthocyanin contents. The key anthocyanin cyanidin-3-glucoside was used as a marker to standardize the extract used in the study. We found that pretreated cells with CNP extract (0.05-1 mu g/ml) prevented neuronal cell death in response to 5 mM glutamate evaluated by cell viability Nur, LDH and apoptosisinecrosis Annexin V/ propidium iodide co-staining assays. For mechanistic approach, glutamate-induced cell death through reactive oxygen species (ROS)-mediated ER stress pathways, indicating the increase of ROS and ER stress signature molecules including calpain, caspases-12 and C/EBP homologous proteins (CHOP). CNP extract inhibited ROS production. Moreover, the extract also suppressed the specific-ER stress apoptotic proteins level in glutamate-induced cells by upregulating the gene expression of cellular antioxidant enzymes (SODS, CAT, GPx and GSTs). Taken together, our results provide information about and the molecular mechanism of CNP extract as a promising neuroprotectant and antioxidant. (C) 2017 Elsevier Ltd. All rights reserved.
机译:氧化和内质网(ER)应力导致神经元损伤导致神经变性障碍。 CleiStocalyx术语var。 PANIALA(CNP)浆果果实已被证明具有强大的抗氧化特性。在这里,我们研究了CNP提取物对小鼠海马神经元HT22细胞中谷氨酸介导的氧化氧化/ ER应激诱导的细胞死亡的神经保护作用。澄清了CNP提取物,用于其自由基清除活性,总酚类和花青素含量。键花青素Cyanidin-3-葡糖苷用作标记物,以标准化研究中使用的提取物。我们发现,具有CNP提取物(0.05-1μg/ ml)的预处理细胞阻止了神经元细胞死亡,响应于通过细胞活力NUR,LDH和凋亡症坏死inexin v /碘化丙啶共染料测定评估的5mm谷氨酸。对于机械方法,通过反应性氧(ROS)介导的ER应激途径的谷氨酸诱导的细胞死亡,表明ROS和ER应激签名分子的增加,包括CALPAIN,CASPASES-12和C / EBP同源蛋白(CHOP)。 CNP提取物抑制ROS生产。此外,提取物还通过上调细胞抗氧化酶(SODS,CAT,GPX和GSTS)的基因表达,抑制谷氨酸诱导的细胞中的特异性反应凋亡蛋白水平。我们的结果一起参加,提供了CNP提取物作为有前途的神经保护剂和抗氧化剂的信息和分子机制。 (c)2017 Elsevier Ltd.保留所有权利。

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