Maurer H M, Haggins J C, Still W J
Am J Hematol. 1976;1(1):89-96. doi: 10.1002/ajh.2830010110.
Phototherapy with blue fluorescent light is widely employed for treatment of neonatal hyperbilirubinemia. Functional, biochemical, and morphologic changes produced by blue fluorescent light in human platelets were identified and characterized. Platelet-rich plasma was exposed for up to 170 min to amounts of light equivalent to that used in phototherapy of neonatal hyperbilirubinemia. Within 110 min of light exposure, platelets were essentially no longer aggregable by ADP and connective tissue suspension and were depleted of ADP, ATP, and glycogen. Electron photomicrographs revealed these platelets to be swollen, depleted of glycogen granules and organelles, and to have ill-defined membranes. Platelet injury could be accelerated by adding a photosensitizing agent, hematoporphyrin, to platelet samples before exposure. In contrast, control platelets kept in the dark for 170 min or nonirradiated platelets resuspended in irradiated plasma maintained their integrity. The results indicate that platelets are damaged in vitro when exposed to amounts of blue light used in phototherapy.
蓝光光疗被广泛用于治疗新生儿高胆红素血症。人们已识别并描述了蓝光在人血小板中引起的功能、生化及形态学变化。将富含血小板的血浆暴露于相当于新生儿高胆红素血症光疗所用剂量的光线下长达170分钟。在光照110分钟内,血小板基本上不再能被二磷酸腺苷(ADP)和结缔组织悬液凝集,且ADP、三磷酸腺苷(ATP)和糖原耗竭。电子显微镜照片显示这些血小板肿胀,糖原颗粒和细胞器缺失,且膜界限不清。在暴露前向血小板样品中加入光敏剂血卟啉可加速血小板损伤。相比之下,在黑暗中保存170分钟的对照血小板或重悬于经照射血浆中的未照射血小板保持其完整性。结果表明,当暴露于光疗所用剂量的蓝光下时,血小板在体外会受到损伤。