Katsumata Toshiya, Muramatsu Hiromi, Nakamura Hidenori, Nishiyama Yutaka, Aoki Yasuaki, Katayama Yasuo
The Second Department of Internal Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-ku, Tokyo, Japan.
Brain Res. 2003 Apr 18;969(1-2):168-74. doi: 10.1016/s0006-8993(03)02296-0.
NS-7 is a novel, voltage-dependent Na(+) and Ca(2+) channel blocker. This study evaluated the in vivo neuroprotective effect of NS-7 in a rat transient focal ischemic model when administered during occlusion. Left middle cerebral artery occlusion was induced in adult male Sprague-Dawley rats for 120 min using an intraluminal thread method. The rats received a single intravenous injection of NS-7 or saline (control group) just after the onset of ischemia, and at 30, 60 and 120 min after ischemia. Their brains were removed after 48 h reperfusion, sectioned, and stained with hematoxylin and eosin. Animals were evaluated by neurological examination at 120 min ischemia and 48 h reperfusion. Infarcted cortex and striatum were measured quantitatively and infarction volumes were calculated. Cortical infarction volumes were 128+/-74 (NS-7) and 214+/-64 mm(3) (control) immediately after the ischemia group, 155+/-48 (NS-7) and 225+/-12 mm(3) (control) after the 30 min group, 160+/-54 (NS-7) and 225+/-48 mm(3) (control) after the 60 min group, and 176+/-43 (NS-7) and 223+/-38 mm(3) (control) after the 120 min group. Cortices in NS-7-treated groups were significantly less infarcted than in control groups at all treatment times. There was no significant difference in the striatal infarction volume between the treatment and control groups. Neurological examination showed that hemiparesis and abnormal posture of the NS-7 groups were significantly more improved at 48 h reperfusion than those of the control groups without posture examination in the 120 min group. These observations suggest that NS-7 may be a new potential therapeutic agent for the acute phase of cerebral infarction.
NS-7是一种新型的、电压依赖性钠(Na⁺)和钙(Ca²⁺)通道阻滞剂。本研究评估了在闭塞期间给予NS-7对大鼠短暂性局灶性缺血模型的体内神经保护作用。采用腔内丝线法对成年雄性Sprague-Dawley大鼠进行左侧大脑中动脉闭塞120分钟。大鼠在缺血发作后以及缺血后30、60和120分钟接受单次静脉注射NS-7或生理盐水(对照组)。再灌注48小时后取出它们的大脑,切片并用苏木精和伊红染色。在缺血120分钟和再灌注48小时时通过神经学检查对动物进行评估。定量测量梗死皮层和纹状体并计算梗死体积。缺血组即刻,皮质梗死体积在NS-7组为128±74,对照组为214±64立方毫米;30分钟组后,NS-7组为155±48,对照组为225±12立方毫米;60分钟组后,NS-7组为160±54,对照组为225±48立方毫米;120分钟组后,NS-7组为176±43,对照组为223±38立方毫米。在所有治疗时间,NS-7治疗组的皮层梗死面积均显著小于对照组。治疗组和对照组之间的纹状体梗死体积无显著差异。神经学检查显示,在120分钟组中,NS-7组在再灌注48小时时的偏瘫和异常姿势较对照组在未进行姿势检查时显著改善。这些观察结果表明,NS-7可能是脑梗死急性期一种新的潜在治疗药物。