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巴西绿蜂胶及其主要成分对氧葡萄糖剥夺应激的神经保护作用及基因表达分析。

Neuroprotective effects of Brazilian green propolis and its main constituents against oxygen-glucose deprivation stress, with a gene-expression analysis.

机构信息

Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University, Gifu, Japan.

出版信息

Phytother Res. 2009 Oct;23(10):1431-8. doi: 10.1002/ptr.2797.

Abstract

Our purpose was to investigate the neuroprotective effects (and the underlying mechanism) exerted by water extract of Brazilian green propolis (WEP) and its main constituents against the neuronal damage induced by oxygen-glucose deprivation (OGD)/reoxygenation in retinal ganglion cells (RGC-5, a rat ganglion cell-line transformed using E1A virus). Cell damage was induced by OGD 4 h plus reoxygenation 18 h exposure. In RGC-5, and also in PC12 (rat pheochromocytoma, neuronal cells), WEP and some of its main constituents attenuated the cell damage. At the end of the period of OGD/reoxygenation, RNA was extracted and DNA microarray analysis was performed to examine the gene-expression profile in RGC-5. Expression of casein kinase 2 (CK2) was down-regulated and that of Bcl-2-related ovarian killer protein (Bok) was up-regulated following OGD stress, results that were confirmed by quantitative reverse transcriptase-PCR (qRT-PCR). These effects were normalized by WEP. Our findings indicate that WEP has neuroprotective effects against OGD/reoxygenation-induced cell damage and that certain constituents of WEP (caffeoylquinic acid derivatives, artepillin C, and p-coumaric acid) may be partly responsible for its neuroprotective effects. Furthermore, the protective mechanism may involve normalization of the expressions of antioxidant- and apoptosis-related genes (such as CK2 and Bok, respectively).

摘要

我们的目的是研究巴西绿蜂胶(WEP)及其主要成分对氧葡萄糖剥夺(OGD)/再氧合诱导的视网膜神经节细胞(RGC-5,一种使用 E1A 病毒转化的大鼠神经节细胞系)神经元损伤的神经保护作用(及其潜在机制)。通过 4 小时 OGD 加 18 小时再氧合暴露诱导细胞损伤。在 RGC-5 中,以及在 PC12(大鼠嗜铬细胞瘤,神经元细胞)中,WEP 和其一些主要成分减轻了细胞损伤。在 OGD/再氧合结束时,提取 RNA 并进行 DNA 微阵列分析,以检查 RGC-5 中的基因表达谱。OGD 应激后,酪蛋白激酶 2(CK2)的表达下调,Bcl-2 相关卵巢杀伤蛋白(Bok)的表达上调,定量逆转录 PCR(qRT-PCR)的结果也证实了这一点。WEP 使这些作用正常化。我们的研究结果表明,WEP 对 OGD/再氧合诱导的细胞损伤具有神经保护作用,WEP 的某些成分(咖啡酰奎宁酸衍生物、artepillin C 和对香豆酸)可能部分负责其神经保护作用。此外,保护机制可能涉及抗氧化剂和凋亡相关基因(如 CK2 和 Bok)表达的正常化。

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