Nishiwaki H, Ogura Y, Miyamoto K, Matsuda N, Honda Y
Department of Ophthalmology, Faculty of Medicine, Kyoto University, Japan.
Arch Ophthalmol. 1996 Jun;114(6):726-30. doi: 10.1001/archopht.1996.01100130718014.
Interferon alfa has been suggested as a possible treatment for choroidal neovascularization. However, retinal complications following interferon therapy have been reported.
To evaluate the effects of interferon alfa on leukocyte dynamics in the rat retinal microcirculation.
Interferon alfa of different doses was intravenously administered in rats. Leukocyte dynamics were observed with acridine orange digital fluorography, which uses a nuclear fluorescent dye of acridine orange and scanning laser ophthalmoscopy. This technique allows visualization of leukocyte movements in the retinal microcirculation in vivo.
After interferon alfa was administered, leukocytes adhered to vascular walls and became trapped in the retinal microcirculation. Leukocyte trapping was dose-dependent.
Interferon alfa increased leukocyte adherence to vascular endothelium and subsequent leukocyte trapping in the retinal capillaries. Interferon alfa may activate leukocytes, and activated leukocytes may be involved in the pathogenesis of microinfarction associated with interferon-induced retinopathy.
有人提出干扰素α可能是脉络膜新生血管的一种治疗方法。然而,已有关于干扰素治疗后视网膜并发症的报道。
评估干扰素α对大鼠视网膜微循环中白细胞动力学的影响。
对大鼠静脉注射不同剂量的干扰素α。采用吖啶橙数字荧光造影术观察白细胞动力学,该技术使用吖啶橙这种核荧光染料以及扫描激光检眼镜。此技术可在体内观察视网膜微循环中白细胞的运动。
给予干扰素α后,白细胞黏附于血管壁并被困在视网膜微循环中。白细胞滞留呈剂量依赖性。
干扰素α增加了白细胞对血管内皮的黏附以及随后在视网膜毛细血管中的白细胞滞留。干扰素α可能激活白细胞,而激活的白细胞可能参与了与干扰素诱导的视网膜病变相关的微梗死的发病机制。