Suppr超能文献

天然全血与二磷酸腺苷(ADP)短暂接触会促进血小板α颗粒内容物的释放,但不会促进致密体内容物的释放,并且会增加血小板在玻璃珠柱上的滞留。

A brief contact of native whole blood with adenosine diphosphate (ADP) promotes the release of the contents of platelet alpha granules but not dense bodies and increases platelet retention to glass bead columns.

作者信息

Pengo V, Boschello M, Baca M, Marzari A, Banzato A, Ferrari G, Shivazappa L, Dalla Volta S

机构信息

Department of Cardiology, Padua University, Italy.

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1990;117(3):359-64.

PMID:1703103
Abstract

We have previously demonstrated that a brief contact of native whole blood with ADP, promotes a dose dependent release of the contents of platelet alpha granules. In the present study we have shown that in our system there is not a parallel release of the contents of platelet dense bodies as measured by the release of serotonin (5 HT). This early and partial platelet activation determines an increase in platelet retention in glass bead columns. After exactly 15 seconds of activation of native whole blood from 6 healthy volunteers with ADP, in fact, there was a significant fall in the platelet count following the flow of native whole blood across glass beads. A significant decrease (from x = 182,000 +/- 13,700 to x = 120,000 +/- 8,00/microliters p less than 0.001) was present when the blood was stimulated with 0.4 microM ADP final concentration. These results suggest that early, partial platelet activation by ADP could facilitate their possible adhesion to a suitable surface exposed along the vascular tree.

摘要

我们之前已经证明,天然全血与ADP短暂接触会促进血小板α颗粒内容物的剂量依赖性释放。在本研究中,我们发现,在我们的系统中,通过血清素(5-HT)释放所测量的血小板致密体内容物并没有平行释放。这种早期和部分血小板活化决定了玻璃珠柱中血小板滞留的增加。事实上,在用ADP激活6名健康志愿者的天然全血15秒后,当天然全血流经玻璃珠时,血小板计数显著下降。当用终浓度为0.4 microM的ADP刺激血液时,出现了显著下降(从x = 182,000 +/- 13,700降至x = 120,000 +/- 8,00/微升,p小于0.001)。这些结果表明,ADP引起的早期、部分血小板活化可能促进它们与沿血管树暴露的合适表面的可能粘附。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验