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输注去氨加压素(DDAVP)后的尿毒症血浆可改善正常血小板与血管内皮下层的相互作用。

Uremic plasma after infusion of desmopressin (DDAVP) improves the interaction of normal platelets with vessel subendothelium.

作者信息

Escolar G, Cases A, Monteagudo J, Garrido M, Lopez J, Ordinas A, Revert L, Castillo R

机构信息

Servicio de Hemoterapia y Hemostasia, Hospital Clinico y Provincial, Facultad de Medicina, Barcelona, Spain.

出版信息

J Lab Clin Med. 1989 Jul;114(1):36-42.

PMID:2738447
Abstract

Effects of 1-deamino-8-D-arginine vasopressin (DDAVP; 0.4 microgram/kg iv) were studied in 11 patients with uremia. Bleeding time, platelet retention on glass beads, factor VIII activities, plasma catecholamine levels, and studies on platelet interaction with the subendothelium were performed before, 1 hour after, and 6 hours after DDAVP infusion. Perfusates consisting of normal washed platelets, uremic platelet-poor plasma (u-PPP) and washed red blood cells were perfused through the Baumgartner perfusion system at a shear rate of 800 sec-1. One hour after DDAVP infusion, a shortening in the bleeding time and an increase in platelet retention on glass beads were noticed in these patients (p less than 0.01). Simultaneously, plasma levels of noradrenaline, factor VIII coagulant (FVIII:C), and von Willebrand factor (vWF) activities were statistically increased. Platelet deposition and platelet aggregate formation on subendothelium were consistently increased (p less than 0.05) in perfusions carried out with blood reconstituted with u-PPP obtained 1 hour after DDAVP. The "in vitro" addition of 1 U/ml vWF or 1 U/ml vWF plus 1 U/ml factor VIII to the pretreatment u-PPP had no significant influence on the parameters that quantify platelet-subendothelium interaction. However, after the addition of 10 ng/ml noradrenaline to a similar system containing basal u-PPP, a clear improvement (p less than 0.05) in platelet deposition was noticed. Our results confirm the hemostatic effectiveness of DDAVP in patients with uremia and reveal an increased platelet interaction with subendothelium mediated by a factor present in uremic plasma after DDAVP administration.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对11例尿毒症患者研究了1-去氨基-8-D-精氨酸加压素(DDAVP;0.4微克/千克静脉注射)的作用。在DDAVP输注前、输注后1小时和6小时进行了出血时间、血小板在玻璃珠上的滞留、因子VIII活性、血浆儿茶酚胺水平以及血小板与内皮下层相互作用的研究。由正常洗涤血小板、尿毒症少血小板血浆(u-PPP)和洗涤红细胞组成的灌注液以800秒-1的剪切速率通过鲍姆加特纳灌注系统进行灌注。DDAVP输注1小时后,这些患者的出血时间缩短,血小板在玻璃珠上的滞留增加(p<0.01)。同时,去甲肾上腺素、因子VIII凝血活性(FVIII:C)和血管性血友病因子(vWF)活性的血浆水平在统计学上有所增加。在用DDAVP输注1小时后获得的u-PPP重构的血液进行的灌注中,内皮下层的血小板沉积和血小板聚集体形成持续增加(p<0.05)。在预处理的u-PPP中“体外”添加1 U/ml vWF或1 U/ml vWF加1 U/ml因子VIII对量化血小板-内皮下层相互作用的参数没有显著影响。然而,在向含有基础u-PPP的类似系统中添加10 ng/ml去甲肾上腺素后,血小板沉积有明显改善(p<0.05)。我们的结果证实了DDAVP对尿毒症患者的止血有效性,并揭示了DDAVP给药后尿毒症血浆中存在的一种因子介导的血小板与内皮下层相互作用增加。(摘要截短于250字)

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