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一种检测血小板第3因子样活性新方法的研发。

Development of a new method for detection of platelet factor 3 like activity.

作者信息

Opartkiattikul N, Funahara Y, Hijikata-Okunomiya A, Yamaguchi N, Talalak P

机构信息

Department of Clinical Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:47-51.

PMID:1298993
Abstract

We asked the question, "Can thalassemic erythrocytes play some role in alteration of the hemostatic system?", because clinical examination of thalassemic patients shows symptoms and signs related to alterations in hemostatic and circulatory systems, and thalassemic erythrocytes are different from normal erythrocytes. We obtained one of the answers to the question: The erythrocytes of postsplenectomized patients of beta-thalassemia/HbE disease could stimulate their own platelets to aggregate spontaneously. To know the role of erythrocytes in platelet aggregation, we wanted to examine the effect of thalassemic erythrocytes on the coagulation system by focusing of PF3-like activity of erythrocytes, because PF3-like activity of the ghosts of erythrocytes had been reported. For the study, we tried to develop a technique that was accurate and sensitive enough to detect PF3-like activity of blood. The system we developed was the following: 1) We activated the intrinsic coagulation pathway of commercial standard plasma by ellagic acid. 2) CaCl2, a fixed amount of PF 3 and synthetic thrombin inhibitor MD 805 were added to the reaction mixture. 3) At a fixed time, thrombin activity in the mixture was measured by using S-2238 as a substrate. At full activation of the contact system by ellagic acid, the amount of thrombin formed in a certain time depended on the amount of PF3-like substances such as cephalin, freeze-thawed platelets or ghosts of erythrocytes added to the test system, indicating that PF3-like activity of those substances can be measured by the activity of thrombin generated in a fixed time.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们提出了这样一个问题

“地中海贫血红细胞能否在止血系统改变中发挥某种作用?”,因为对地中海贫血患者的临床检查显示出与止血和循环系统改变相关的症状和体征,而且地中海贫血红细胞与正常红细胞不同。我们得到了这个问题的一个答案:β-地中海贫血/HbE病脾切除术后患者的红细胞能够刺激自身血小板自发聚集。为了了解红细胞在血小板聚集中的作用,我们想通过关注红细胞的PF3样活性来研究地中海贫血红细胞对凝血系统的影响,因为已有报道称红细胞膜空壳具有PF3样活性。为了进行这项研究,我们试图开发一种技术,该技术要足够准确和灵敏,以检测血液中的PF3样活性。我们开发的系统如下:1)我们用鞣花酸激活商业标准血浆的内源性凝血途径。2)向反应混合物中加入氯化钙、固定量的PF3和合成凝血酶抑制剂MD 805。3)在固定时间,以S-2238为底物测量混合物中的凝血酶活性。当鞣花酸使接触系统完全激活时,在一定时间内形成的凝血酶量取决于加入测试系统中的PF3样物质(如脑磷脂、冻融血小板或红细胞膜空壳)的量,这表明这些物质的PF3样活性可以通过固定时间内产生的凝血酶活性来测量。(摘要截短于250字)

相似文献

1
Development of a new method for detection of platelet factor 3 like activity.一种检测血小板第3因子样活性新方法的研发。
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:47-51.
2
Detection of PF3 availability in whole blood from volunteers and beta-thalassemia/HbE patients: a promising method for prediction of thrombotic tendency.检测志愿者及β地中海贫血/HbE患者全血中PF3的可用性:一种预测血栓形成倾向的有前景的方法。
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:52-9.
3
PF3 activity in normal subjects and beta-thalassemia trait.正常受试者和β地中海贫血特征患者的PF3活性。
Southeast Asian J Trop Med Public Health. 1993;24 Suppl 1:216-8.
4
Increase in spontaneous platelet aggregation in beta-thalassemia/hemoglobin E disease: a consequence of splenectomy.β地中海贫血/血红蛋白E病患者自发性血小板聚集增加:脾切除术后的结果
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:36-41.
5
Interaction between endothelial cells and thalassemic red cells in vitro.体外内皮细胞与地中海贫血红细胞之间的相互作用。
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:101-4.
6
Morphological assessment of platelet activation in thalassemia.地中海贫血中血小板活化的形态学评估。
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:60-4.
7
Differentiation of platelets from red cell fragments using laser technology: comparison between splenectomized and nonsplenectomized thalassemic patients.利用激光技术区分血小板与红细胞碎片:脾切除和未脾切除的地中海贫血患者的比较
Southeast Asian J Trop Med Public Health. 1993;24 Suppl 1:250-2.
8
Size distribution curves of blood cells in thalassemias and hemoglobin H diseases.地中海贫血和血红蛋白H病中血细胞的大小分布曲线。
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:79-85.
9
Increased platelet adhesion under flow conditions is induced by both thalassemic platelets and red blood cells.在流动条件下,地中海贫血患者的血小板和红细胞均会导致血小板黏附增加。
Thromb Haemost. 2008 Nov;100(5):864-70.
10
Protein C and protein S deficiency in thalassemic patients.地中海贫血患者的蛋白C和蛋白S缺乏症
Southeast Asian J Trop Med Public Health. 1992;23 Suppl 2:65-73.

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