摘要
作者以紫外线(50cm,剂量为298.48mW/cm2,照射面积为120cm2)分别不同体表部位照射3组脑血栓患者1次,其中1组照射前静脉注射氨甲苯酸0.05g,分别观察3组照射前、照射后2h血浆纤维蛋白原含量(PFL)和优球蛋白溶解时间(ELT),以及其中1组紫外线照射后PFL的动态变化,结果表明,2组照射后PFL较照射前减低;照射后ELT比照射前缩短(P均<0.01);照射部位或脑血栓病期的不同,其结果均无显著差异性(P均>0.05);应用氨甲苯酸组照射后PFL不再比照射前降低,照射后ELT不再比照射前缩短(P均>0.05),实验证明,1次强红斑量紫外线局部照射能够激活脑血栓患者纤维蛋白溶解系统活性,且其激活作用不受脑血栓病期以及照射部位的影响;其作用机理推测与紫外线照射促进了组织型纤溶酶原激活物释放有关.本实验对探讨紫外线应用于脑血栓的预防和溶栓、抗凝治疗具有实用意义.
In our experiment,cerebral thrombosis (CT patients in 3 groups were irradiated by ultraviolet(UV)(50 cm, 298. 48 mW/cm2 , irradiated area was 120 cm2 )once on one different body surface position, inone of the 3 groups every patient was administered by 0.05 g p-aminomethylbenzoic acid (p-AA)before irra-diation, in order to observe separately every plasma fibrinogen level (PFL)and euglobin lytic time(ELT) be-fore irradiation and 2 h after irradiation, and PFL in one of the two groups without using P- AA at differenttime after irradiation, the result shows that in the two groups without using P-AA, every PFL or ELT after irradiation is lower or shorter than that before irradiation (all P<0.01), and that UV effect has no relation with its irradiation position or CT period(all P>0. 05); and that reduction of PFL at different time after ir-radiation shows curve; and that PFL or ELT 2 h after irradiation in the group with p- AA is not lower orshorter than that before administration any more(all P>0. 05 ). The result of our experiment indicates thatonce local UV irradiation can enhance the fibrinolytic system activity of CT patients , and that UV effect hasno relation with its irradiation position or CT period,and that its mechanism is related to that UV irradiationcan accelerate the release of tissular plasminogen activator. This experiment may play an important role forinvestigating the anti- coagulation, thrombolytic therapy and prevention to CT with UV.
出处
《第四军医大学学报》
1994年第5期366-368,共3页
Journal of the Fourth Military Medical University
关键词
紫外线
脑血栓
纤维蛋白
溶解系统
ultraviolet
cerebral thrombosis
fibrinolytic system
p- aminomethylbenzoic acid