Hong Ki Whan, Kim Ki Young, Lee Jeong Hyun, Shin Hwa Kyoung, Kwak Yong Geun, Kim Sun-Ok, Lim Hong, Yoo Sung-Eun
Department of Pharmacology, College of Medicine, Pusan National University, Pusan, Korea.
J Pharmacol Exp Ther. 2002 Apr;301(1):210-6. doi: 10.1124/jpet.301.1.210.
This study shows the preventive effect of KR-31378 [(2S,3S,4R)-N"-cyano-N-(6-amino-3,4-dihydro-3-hydroxy-2-methyl-2-dimethoxymethyl-2H-benzopyran-4-yl)-N'-benzylguanidine] against cerebral infarct via antioxidant and antiapoptotic actions evoked by subjecting rats to 2 h of occlusion of the left middle cerebral artery followed by 24 h of reperfusion. The brain infarct zone in the cortex and striatum of the left hemisphere was consistently identified in the cortex and striatum of the left hemisphere. The infarct area was significantly reduced after three intraperitoneal administrations of 10, 30, or 50 mg/kg KR-31378 at 5 min, 4 h, and 8 h after the completion of 2 h of ischemia. Treatment with KR-31378 (30 or 50 mg/kg) significantly reduced the increase in the number of terminal deoxynucleotidyl transferase dUTP nick-end labeling positive cells as well as strongly suppressed the laddered feature of DNA fragmentation in the lateral cortical tissue corresponding to the penumbra. The findings of samples from penumbral zone, which showed markedly reduced Bcl-2 protein level and increased Bax protein and cytochrome c release, were wholly reversed by treatment with KR-31378. In conclusion, postischemic treatment with KR-31378 provided significant levels of cortical neuroprotection in association with inhibition of apoptotic cell death through the up-regulation of Bcl-2 expression, and the down-regulation of Bax protein and cytochrome c release.
本研究显示了KR-31378[(2S,3S,4R)-N"-氰基-N-(6-氨基-3,4-二氢-3-羟基-2-甲基-2-二甲基氧甲基-2H-苯并吡喃-4-基)-N'-苄基胍]对脑梗死的预防作用,该作用是通过对大鼠进行2小时的左大脑中动脉闭塞并随后再灌注24小时所引发的抗氧化和抗凋亡作用来实现的。在左半球的皮质和纹状体中持续识别出左半球皮质和纹状体中的脑梗死区域。在缺血2小时结束后的5分钟、4小时和8小时,腹腔注射10、30或50mg/kg的KR-31378三次后,梗死面积显著减小。用KR-31378(30或50mg/kg)治疗可显著减少末端脱氧核苷酸转移酶dUTP缺口末端标记阳性细胞数量的增加,并强烈抑制与半暗带相对应的外侧皮质组织中DNA片段化的梯状特征。来自半暗带区域的样本结果显示,Bcl-2蛋白水平显著降低,Bax蛋白增加,细胞色素c释放,而用KR-31378治疗可完全逆转这些结果。总之,缺血后用KR-31378治疗通过上调Bcl-2表达、下调Bax蛋白和细胞色素c释放来抑制凋亡细胞死亡,从而提供了显著水平的皮质神经保护作用。