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去氨加压素:该药物对血管壁有直接作用吗?

DDAVP: does the drug have a direct effect on the vessel wall?

作者信息

Barnhart M I, Chen S, Lusher J M

出版信息

Thromb Res. 1983 Jul 15;31(2):239-53. doi: 10.1016/0049-3848(83)90326-2.

Abstract

Evidence is presented that 1-deamino-8-d-arginine vasopressin (DDAVP), a vasopressin analog, has a direct effect on isolated vessel segments. The most significant finding is increased platelet adhesion and spreading at injury sites. An isologous human umbilical vein perfusion model was used to compare effects of DDAVP with those of epinephrine or zero drug controls. Scanning electron microscopy, in conjunction with morphometry, permitted quantification of platelet adhesion to subendothelium exposed by minimal injury in the model. In addition, umbilical vein effluents were tested for levels of factor VIII moieties (F VIII:C, F VIII:Rag, F VIII:RCof) and the prostanoids, 6 keto PGF1 alpha (stable metabolite of prostacyclin) and TXB2 (stable metabolite of thromboxane A2. Only F VIII:C from DDAVP treated segments was significantly (p less than 0.01) changed from controls.

摘要

有证据表明,血管加压素类似物1-去氨基-8-D-精氨酸血管加压素(DDAVP)对离体血管段有直接作用。最显著的发现是损伤部位血小板黏附和铺展增加。采用同种异体人脐静脉灌注模型比较DDAVP与肾上腺素或零药物对照的效果。扫描电子显微镜结合形态计量学,能够对模型中因轻微损伤而暴露的内皮下层的血小板黏附进行定量分析。此外,检测脐静脉流出物中因子VIII部分(F VIII:C、F VIII:Rag、F VIII:RCof)以及前列腺素、6-酮-前列腺素F1α(前列环素的稳定代谢产物)和TXB2(血栓素A2的稳定代谢产物)的水平。只有DDAVP处理段的F VIII:C与对照相比有显著变化(p小于0.01)。

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