CAJ | 학술논문

目的探讨体外循环(CPB)时血小板(PL)的构象与功能变化以及血液麻醉对PL的保护作用.方法人工血管材料聚对苯二甲酸乙二醇脂(polyethylene terephthalate,PET)表面处理后接枝牛血清白蛋白(BSA)成为PET-BSA.取PET和PET-BSA试片进行对比实验:(1)通过PL乳酸脱氢酶(LDH)的定量测定,计算材料表面吸附的PL量;(2)通过PL的膜糖蛋白GMP140单克隆抗体免疫学测定,计算材料表面活化的PL量;(3)在材料表面进行PL吸附实验,通过扫描电镜观察PL的形态.(4)选择体外循环心内直视手术30例随机分为抑肽酶组和对照组;检测转流中不同时期血液中FDP、PK、PLG和TXB2的量;记录24 h纵隔和心包引流量;电镜观察PL构象.结果 PET-BSA表面吸附的PL量明显低于对照组(P<0.05),活化PL量仅为对照组的20%.扫描电镜显示白蛋白涂层吸附PL少;对照组PL呈重叠状且有伪足.血液麻醉组较对照组纤维蛋白溶解酶原(PLG)分解少,纤溶系统被抑制,PL结构被保护.结论 CPB时血浆蛋白彼此竞争吸附于血管壁上,然后PL与被吸附的血浆蛋白相互作用,PL与构象变化的纤维蛋白在其γ链C端结合位点上结合;同时PL被激活并暴露其CPⅡb/Ⅲa作用位点;构象变化的PL引发凝血的综合进展.抑肽酶的血液麻醉作用是对纤溶酶和激肽释放酶活化的抑制;保护PL结构中的GPⅡb免受破坏,保护了PL术后的凝血功能.
목적 탐토체외순배(CPB)시혈소판(PL)적구상여공능변화이급혈액마취대PL적보호작용.방법 인공혈관재료취대분이갑산을이순지(polyethylene terephthalate,PET)표면처리후접지우혈청백단백(BSA)성위PET-BSA.취PET화PET-BSA시편진행대비실험:(1)통과PL유산탈경매(LDH)적정량측정,계산재료표면흡부적PL량;(2)통과PL적막당단백GMP140단극륭항체면역학측정,계산재료표면활화적PL량;(3)재재료표면진행PL흡부실험,통과소묘전경관찰PL적형태.(4)선택체외순배심내직시수술30례수궤분위억태매조화대조조;검측전류중불동시기혈액중FDP、PK、PLG화TXB2적량;기록24 h종격화심포인류량;전경관찰PL구상.결과 PET-BSA표면흡부적PL량명현저우대조조(P<0.05),활화PL량부위대조조적20%.소묘전경현시백단백도층흡부PL소;대조조PL정중첩상차유위족.혈액마취조교대조조섬유단백용해매원(PLG)분해소,섬용계통피억제,PL결구피보호.결론 CPB시혈장단백피차경쟁흡부우혈관벽상,연후PL여피흡부적혈장단백상호작용,PL여구상변화적섬유단백재기γ련C단결합위점상결합;동시PL피격활병폭로기CPⅡb/Ⅲa작용위점;구상변화적PL인발응혈적종합진전.억태매적혈액마취작용시대섬용매화격태석방매활화적억제;보호PL결구중적GPⅡb면수파배,보호료PL술후적응혈공능.
Objective To study the construction and function of platelet (PL) and the protection of PL by blood anesthesia during the eardiopulmonary bypass (CPB). Methods Bovine serum albumin (BSA) was immobi-lized on the surface of polyethylene terephthalate(PET) which was used as artificial vascular materials,to obtain the samples of PET-BSA. (1) The quantity of PL adhesion of PET and PET-BSA samples were investigated by lactate de-hydrogenase(LDH) test. (2) The quantity of PL activation was investigated by a-granule membrane protein-140 (GMPI40) test. (3)PL adhesion test was conducted on the surface of the samples and the morphology of the adhered PL was examined by scanning electron microscopy (SEM). (4)30 patients undergoing cardiac surgery under CPB were randomly divided into aprotinin group and control group,quantities of FDP, PK, PLG and thromboxance B2 (TXB2) in the blood were measured in various time, PLs were observed by electron microscopy, and postoperative blood loss from chest and medium were recorded during first 24 hours. Results Compared with the control group,the quantity of PL adhesion on the PET-BSA samples significantly decreased and the quantity of PL activation of the PET-BSA group was only 20% of the control group. The results of SEM showed PL on PET-BSA surface was few,whereas on the PET sur-face overlaped and had pseudopodium. The decomposition of PLG is fewer in blood anaesthesia group,indicated the fi-brinolytie system was inhibited and construction of PL was protected. Conclusion During CPB,plasma proteins com-pete against each other to adhere on the tube of CPB,then PL interact to the adhered proteins,and PL combine with conformation changed fibrin at its C extreme of γ chain. At the same time,PL is activated and its GPⅡb/Ⅲa point is ex-posed. The function of blood anesthesia of aprotinin is to inhibit the activation of PIg; and PK,protect the GPⅡb of PL from being destroyed, and protect the coagulation funeion of PL of postoperation.