Takayasu Yuko, Nakaki Junko, Kawasaki Toshiyuki, Koda Ken, Ago Yukio, Baba Akemichi, Matsuda Toshio
Laboratory of Medicinal Pharmacology, Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka, Japan.
J Pharmacol Sci. 2007 Apr;103(4):434-7. doi: 10.1254/jphs.sc0070014. Epub 2007 Apr 4.
Edaravone, a radical scavenger, prevents ischemia/reperfusion injury in the brain, but the detailed mechanism is not known. This study examines the effect of edaravone on mitochondrial permeability transition pore (PTP) in rat brain. Edaravone at 10 - 100 microM inhibited Ca(2+)- and H(2)O(2)-induced swelling of mitochondria isolated from rat brain. Addition of Ca(2+) generated reactive oxygen species (ROS) in isolated mitochondria. Edaravone (10 - 100 microM) inhibited Ca(2+)-induced generation of ROS. These results suggest that edaravone inhibits opening of mitochondrial PTP in the brain, and they imply that inhibition of mitochondrial PTP may account for the neuroprotective effect of edaravone.
依达拉奉是一种自由基清除剂,可预防脑缺血/再灌注损伤,但其具体机制尚不清楚。本研究探讨了依达拉奉对大鼠脑线粒体通透性转换孔(PTP)的影响。10 - 100微摩尔的依达拉奉可抑制从大鼠脑分离的线粒体因钙离子和过氧化氢诱导的肿胀。在分离的线粒体中添加钙离子会产生活性氧(ROS)。依达拉奉(10 - 100微摩尔)可抑制钙离子诱导的ROS生成。这些结果表明依达拉奉可抑制脑线粒体PTP的开放,提示抑制线粒体PTP可能是依达拉奉神经保护作用的机制。