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天麻及其活性成分对羟基苄醇通过抗氧化相关基因表达减轻局灶性缺血性脑损伤。

Gastrodia elata blume and an active component, p-hydroxybenzyl alcohol reduce focal ischemic brain injury through antioxidant related gene expressions.

作者信息

Yu Seong Jin, Kim Ju Ran, Lee Chae Kwan, Han Jeong Eun, Lee Jae Hyun, Kim Hye-Sook, Hong Jeong Hwa, Kang Sung Goo

机构信息

School of Biotechnology and Biomedical Science, Institute of Basic Science, Inje University, Gimhae, Korea.

出版信息

Biol Pharm Bull. 2005 Jun;28(6):1016-20. doi: 10.1248/bpb.28.1016.

Abstract

Ischaemic stroke is a leading cause of death and long-lasting disability. Gastrodia elata blume (GEB) is a Chinese herb that is widely used to treat convulsive disorders, such as epilepsy, and p-hydroxybenzyl alcohol (HBA) is the active ingredient in GEB. The present study was conducted to evaluate the effects of GEB and HBA on the brain damage and transcriptional levels of Protein disulfide isomerase (PDI) and 1-Cys peroxiredoxin (1-Cys Prx) genes known to play a role in antioxidant systems after transient focal ischemia in the rat brain. Focal ischemia was induced in rats by middle cerebral artery occlusion (MCAO). All animals underwent ischemia for 1 h, followed by 24 h of reperfusion. Coronal brain slices were stained with 2,3,5-triphenyltetrazolium chloride or total RNA was extracted for the analysis of gene expression. Histopathologic analysis revealed a significant (p<0.05) decrease in infarct size in the ipsilateral brain with GEB extracts or HBA. Moreover, the levels of PDI and 1-Cys Prx transcription were significantly increased in the GEB extract- or HBA-treated group compared with the untreated group (p<0.05). This study therefore indicated that GEB and HBA provide neuroprotection by preventing brain damage through the increased expression of genes encoding antioxidant proteins after transient focal cerebral ischemia and may be effective as neuroprotective agents at the cellular and molecular levels in the brain.

摘要

缺血性中风是导致死亡和长期残疾的主要原因。天麻是一种广泛用于治疗惊厥性疾病(如癫痫)的中药材,对羟基苄醇(HBA)是天麻中的活性成分。本研究旨在评估天麻及其活性成分对羟基苄醇(HBA)对大鼠脑局灶性短暂缺血后已知在抗氧化系统中起作用的蛋白质二硫键异构酶(PDI)和1-半胱氨酸过氧化物酶(1-Cys Prx)基因的脑损伤及转录水平的影响。通过大脑中动脉闭塞(MCAO)诱导大鼠局灶性缺血。所有动物缺血1小时,随后再灌注24小时。冠状脑切片用2,3,5-氯化三苯基四氮唑染色或提取总RNA用于基因表达分析。组织病理学分析显示,使用天麻提取物或对羟基苄醇(HBA)后,同侧脑梗死体积显著减小(p<0.05)。此外,与未治疗组相比,天麻提取物或对羟基苄醇(HBA)治疗组的PDI和1-Cys Prx转录水平显著升高(p<0.05)。因此,本研究表明,天麻及其活性成分对羟基苄醇(HBA)通过在脑局灶性短暂缺血后增加编码抗氧化蛋白的基因表达来预防脑损伤,从而提供神经保护作用,并且在脑的细胞和分子水平上可能作为神经保护剂有效。

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