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阿魏酸调节局灶性脑缺血中一氧化氮合酶的表达。

Ferulic acid modulates nitric oxide synthase expression in focal cerebral ischemia.

作者信息

Koh Phil-Ok

机构信息

Department of Anatomy, College of Veterinary Medicine, Research Institute of Life Science, Gyeongsang National University, Jinju, Korea.

出版信息

Lab Anim Res. 2012 Dec;28(4):273-8. doi: 10.5625/lar.2012.28.4.273. Epub 2012 Dec 26.

DOI:10.5625/lar.2012.28.4.273
PMID:23326288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3542386/
Abstract

Nitric oxide (NO) is generated by three different NO synthase (NOS) isoforms, endothelial NOS (eNOS), inducible NOS (iNOS), and neuronal NOS (nNOS). It is known that eNOS produces NO, which exerts a protective effect, while iNOS produces NO with neurotoxic effects. Ferulic acid preserves neuronal cells against from cerebral ischemia and glutamate-induced excitotoxicity. This study confirmed the neuroprotective effect of ferulic acid and investigated the levels of three NOS isoforms in focal cerebral ischemia with or without ferulic acid. Rats were immediately treated with ferulic acid (100 mg/kg, i.v.) after middle cerebral artery occlusion (MCAO). Brains tissues were collected at 24 h after the onset of occlusion. The expressions of these three isoforms in cerebral ischemia with ferulic acid were analyzed using Western blot technique. Ferulic acid treatment significantly decreases the number of TUNEL-positive cells in the cerebral cortex against MCAO injury. The levels of eNOS decreased in MCAO-operated animals, while ferulic acid treatment attenuated the MCAO-induced decrease of eNOS. However, iNOS and nNOS expression levels increased during MCAO, and ferulic acid prevented injury-induced increase of these isoforms. Thus, these findings suggest that the up- and down modulation of three isoforms by ferulic acid is associated with a neuroprotective mechanism.

摘要

一氧化氮(NO)由三种不同的一氧化氮合酶(NOS)同工型产生,即内皮型一氧化氮合酶(eNOS)、诱导型一氧化氮合酶(iNOS)和神经元型一氧化氮合酶(nNOS)。已知eNOS产生具有保护作用的NO,而iNOS产生具有神经毒性作用的NO。阿魏酸可保护神经元细胞免受脑缺血和谷氨酸诱导的兴奋毒性作用。本研究证实了阿魏酸的神经保护作用,并研究了在有或没有阿魏酸的局灶性脑缺血中三种NOS同工型的水平。大鼠在大脑中动脉闭塞(MCAO)后立即接受阿魏酸(100mg/kg,静脉注射)治疗。在闭塞开始后24小时收集脑组织。使用蛋白质印迹技术分析阿魏酸处理的脑缺血中这三种同工型的表达。阿魏酸治疗可显著减少大脑皮质中TUNEL阳性细胞的数量,以对抗MCAO损伤。在MCAO手术的动物中,eNOS水平降低,而阿魏酸治疗可减轻MCAO诱导的eNOS降低。然而,在MCAO期间,iNOS和nNOS表达水平升高,而阿魏酸可防止损伤诱导的这些同工型增加。因此,这些发现表明阿魏酸对三种同工型的上调和下调与神经保护机制有关。

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