Matsubara A, Tomida K, Matsuda Y, Tamai K, Tashita A, Jomori T, Tsujikawa A, Ogura Y
Department of Ophthalmology, Nagoya City University Medical School, Nagoya, Japan.
Exp Eye Res. 2000 Sep;71(3):283-93. doi: 10.1006/exer.2000.0880.
A newly developed selSep;71(3)28 to block P- and L-selectins in vitro. We examined its inhibition of leukocyte-endothelial interactions in vivo against retinal ischemia-reperfusion injury and protective effects on ischemia-induced retinal damage. Retinal ischemia was induced by temporary ligation of the optic sheath for 60 min in anesthetized pigmented rats. SKK-60060 was administered 5 min before reperfusion and 4, 12, 24 and 48 hr thereafter, and leukocyte dynamics in the retinal microcirculation were evaluated using acridine orange digital fluorography. After 7 days of reperfusion, ischemia-induced retinal damage was also assessed histologically.SKK-60060 treatment suppressed leukocyte rolling during the reperfusion period; their numbers in the SKK-60060-treated rats were reduced by 67.0% (P < 0. 01) and 53.2% (P < 0.01) at 12 and 24 hr, respectively. The subsequent leukocyte accumulation was also inhibited in SKK-60060-treated rats; accumulated leukocytes in the SKK-60060-treated rats were reduced by 72.8% (P < 0.01) and 53.4% (P < 0.01) at 12 and 24 hr, respectively. Retinal venous vasodilation in SKK-60060-treated rats were significantly suppressed at each time point (P < 0.05). Histological examination demonstrated protective effects of SKK-60060 on ischemia-induced retinal damage, which were more substantial in the inner retina (P < 0.01).SKK-60060 significantly inhibits the leukocyte rolling along the major retinal veins and their accumulation during the reperfusion period. These results suggest therapeutic potential of SKK-60060 for ischemia-reperfusion injury.
一种新开发的selSep;71(3)28可在体外阻断P-选择素和L-选择素。我们研究了其在体内对视网膜缺血再灌注损伤时白细胞与内皮细胞相互作用的抑制作用以及对缺血诱导的视网膜损伤的保护作用。通过在麻醉的有色大鼠中暂时结扎视神经鞘60分钟诱导视网膜缺血。在再灌注前5分钟给予SKK-60060,此后4、12、24和48小时给药,使用吖啶橙数字荧光造影评估视网膜微循环中的白细胞动态。再灌注7天后,还通过组织学评估缺血诱导的视网膜损伤。SKK-60060治疗可抑制再灌注期间的白细胞滚动;在SKK-60060治疗的大鼠中,12小时和24小时时白细胞数量分别减少了67.0%(P<0.01)和53.2%(P<0.01)。SKK-60060治疗的大鼠随后的白细胞聚集也受到抑制;在SKK-60060治疗的大鼠中,12小时和24小时时聚集的白细胞分别减少了72.8%(P<0.01)和53.4%(P<0.01)。SKK-60060治疗的大鼠在每个时间点的视网膜静脉血管舒张均受到显著抑制(P<0.05)。组织学检查显示SKK-60060对缺血诱导的视网膜损伤具有保护作用,在内层视网膜中更为显著(P<0.01)。SKK-60060可显著抑制再灌注期间白细胞沿视网膜主要静脉的滚动及其聚集。这些结果表明SKK-60060对缺血再灌注损伤具有治疗潜力。