Zhang Xiao-Hong, Matsuda Naoyuki, Jesmin Subrina, Sakuraya Fumika, Gando Satoshi, Kemmotsu Osamu, Hattori Yuichi
Department of Anesthesiology and Critical Care Medicine, Hokkaido University School of Medicine, Sapporo 060-8638, Japan.
Eur J Pharmacol. 2003 Aug 22;476(1-2):131-7. doi: 10.1016/s0014-2999(03)02151-4.
We investigated the therapeutic effect of edaravone, a free radical scavenger, on alterations in endothelium-dependent relaxation and endothelial nitric oxide synthase (eNOS) expression in the rabbit ear central artery at 2 weeks after exposure to a dose of 45 Gy radiation with a cobalt60 unit. For treatment with edaravone, edaravone was given daily to the animals from the day before irradiation at an intrapenetreal dose of 10 mg/kg twice a day. The endothelium-dependent relaxant response to acetylcholine was markedly impaired in irradiated vessels. Edaravone treatment improved the response to the level observed in nonirradiated control vessels. Using immunohistochemical and Western blot techniques, we showed that protein expression of eNOS in irradiated vessels was reduced to about 50% of control and that edaravone treatment returned it nearly to intact levels. Gene expression of eNOS, analyzed by reverse transcription-competitive polymerase chain reaction, was found to be reduced from the control level by 47% following irradiation. The reduced level of eNOS mRNA in irradiated vessels was almost completely normalized by edaravone treatment. These results suggest that edaravone has a protective effect on the reduced expression of eNOS and its associated endothelial cell dysfunction in the vessels following irradiation. We thus assume that oxygen-free radicals may be closely related to the irradiation-induced derangement of the eNOS gene regulation.
我们研究了自由基清除剂依达拉奉对家兔耳中央动脉内皮依赖性舒张及内皮型一氧化氮合酶(eNOS)表达变化的治疗作用,该动脉在接受钴60装置45 Gy剂量辐射2周后出现上述变化。对于依达拉奉治疗,从照射前一天开始每天给动物腹腔注射依达拉奉,剂量为10 mg/kg,每日两次。辐射后的血管对乙酰胆碱的内皮依赖性舒张反应明显受损。依达拉奉治疗使该反应恢复至未辐射对照血管所观察到的水平。通过免疫组织化学和蛋白质印迹技术,我们发现辐射后血管中eNOS的蛋白表达降至对照的约50%,而依达拉奉治疗使其几乎恢复至完整水平。通过逆转录竞争聚合酶链反应分析发现,辐射后eNOS的基因表达较对照水平降低了47%。依达拉奉治疗几乎完全使辐射后血管中降低的eNOS mRNA水平恢复正常。这些结果表明,依达拉奉对辐射后血管中eNOS表达降低及其相关的内皮细胞功能障碍具有保护作用。因此我们推测,氧自由基可能与辐射诱导的eNOS基因调控紊乱密切相关。