Mdzinarishvili Alexander, Geldenhuys Werner J, Abbruscato Thomas J, Bickel Ulrich, Klein Jochen, Van der Schyf Cornelis J
Department of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University HSC, Amarillo, 79106-1712, USA.
Neurosci Lett. 2005;383(1-2):49-53. doi: 10.1016/j.neulet.2005.03.042. Epub 2005 Apr 13.
NGP1-01, a member of the pentacycloundecylamine cage compound family, was recently shown to exhibit both NMDA receptor channel blocking and L-type calcium channel antagonism activity. In the present study, focal ischemia was induced in mice by permanent middle cerebral artery occlusion (MCAO) to test for potential neuroprotective properties of the compound. In female CD-1 mice injected 30 min before MCAO, NGP1-01 (20 mg/kg) reduced infarct area by 42.6% (P < 0.05) compared to vehicle-treated controls as visualized by 2,3,5-triphenyltetrazolium chloride (TTC) staining. Concomitantly, NGP1-01 reduced brain swelling by 78.3% (P < 0.001), compared to vehicle (DMSO) treated controls. These data identify NGP1-01 and related compounds as potential lead structures to develop neuroprotective compounds based on a dual mechanism of action.
NGP1-01是五环十一胺笼状化合物家族的成员,最近被证明具有NMDA受体通道阻断和L型钙通道拮抗活性。在本研究中,通过永久性大脑中动脉闭塞(MCAO)诱导小鼠局灶性缺血,以测试该化合物的潜在神经保护特性。在MCAO前30分钟注射的雌性CD-1小鼠中,与用2,3,5-三苯基氯化四氮唑(TTC)染色显示的溶媒处理对照组相比,NGP1-01(20mg/kg)使梗死面积减少了42.6%(P<0.05)。同时,与溶媒(二甲基亚砜)处理对照组相比,NGP1-01使脑肿胀减少了78.3%(P<0.001)。这些数据确定NGP1-01及相关化合物是基于双重作用机制开发神经保护化合物的潜在先导结构。