Hull D S, Green K, Hampstead D
Invest Ophthalmol Vis Sci. 1985 Nov;26(11):1465-74.
Hematoporphyrin derivative (HpD) is a systemically administered photosensitizing agent that may be of value in the treatment of solid tumors. When corneal endothelial cells were perfused in the specular microscope with HpD and exposed to a 25-W incandescent light at 5 cm (5.5 mW/cm2) there was anatomic disruption of corneal endothelial cells and swelling of the corneal stroma. Perfusion with 0.2 microliter/ml (1.0 microgram/ml) HpD and 5 min exposure to light resulted in a corneal swelling of 71 +/- 4 microns after 3 hr, whereas perfusion with 0.2 microliter/ml HpD and a 1-min exposure to light resulted in a corneal swelling of 36 +/- 4 microns after 3 hr. Perfusion with 0.2 microliter/ml HpD with no light exposure resulted in a corneal swelling of 22 +/- 4 microns after 3 hr. Inclusion of 100 micrograms/ml catalase in the perfusion solution resulted in a significant 38% reduction of the corneal swelling. The inclusion of either 100 micrograms/ml superoxide dismutase, 15 mM D-mannitol, 5 mM ascorbic acid, 1/4% DMSO, 50 microns EDTA, 50 microns DETAPAC, 10 mM L-histidine, or 1 mM sodium azide did not modify the corneal swelling induced by the photosensitization reaction. Perfusion of corneal endothelial cells with 2 microliters/ml (10 micrograms/ml) HpD and exposure to 25-W incandescent light for 5 min resulted in swelling of mitochondria, the appearance of vacuoles in the cytoplasm, and rapid corneal swelling. The data suggests that corneal endothelial cells can be damaged by hydrogen peroxide generated by the dismutation of superoxide anion produced during the photoreaction. Superoxide anion itself and hydroxyl-free radical do not appear to participate in causing the endothelial cell damage. The role of singlet oxygen remains somewhat unclear. The data suggests that further in vivo studies should be performed to delineate precautions that should be taken to protect the corneal endothelium during photoradiation therapy.
血卟啉衍生物(HpD)是一种经全身给药的光敏剂,可能对实体瘤治疗有价值。当在镜面显微镜下用HpD灌注角膜内皮细胞,并在5厘米处(5.5毫瓦/平方厘米)暴露于25瓦白炽灯下时,角膜内皮细胞出现解剖学破坏,角膜基质肿胀。用0.2微升/毫升(1.0微克/毫升)HpD灌注并光照5分钟,3小时后角膜肿胀71±4微米;而用0.2微升/毫升HpD灌注并光照1分钟,3小时后角膜肿胀36±4微米。用0.2微升/毫升HpD灌注但不光照,3小时后角膜肿胀22±4微米。灌注液中加入100微克/毫升过氧化氢酶可使角膜肿胀显著减少38%。加入100微克/毫升超氧化物歧化酶、15毫摩尔D-甘露醇、5毫摩尔抗坏血酸、1/4%二甲基亚砜、50微米乙二胺四乙酸、50微米二乙撑三胺五乙酸、10毫摩尔L-组氨酸或1毫摩尔叠氮化钠均未改变光敏反应诱导的角膜肿胀。用2微升/毫升(10微克/毫升)HpD灌注角膜内皮细胞并暴露于25瓦白炽灯下5分钟,导致线粒体肿胀、细胞质中出现空泡以及角膜迅速肿胀。数据表明,光反应过程中产生的超氧阴离子歧化生成的过氧化氢可损伤角膜内皮细胞。超氧阴离子本身和羟基自由基似乎不参与导致内皮细胞损伤。单线态氧的作用仍有些不清楚。数据表明,应进行进一步的体内研究,以确定在光辐射治疗期间保护角膜内皮应采取的预防措施。