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一种用于研究血小板聚集和解聚的体内模型。

An in vivo model for studying platelet aggregation and disaggregation.

作者信息

Page C P, Paul W, Morley J

出版信息

Thromb Haemost. 1982 Jun 28;47(3):210-3.

PMID:7051409
Abstract

A simple minimally invasive technique has been developed for the continuous monitoring of 111-Indium labelled homologous platelets in the thoracic (C1) and abdominal (C2) regions of experimental animals. The effects of the aggregatory agents adenosine diphosphate (ADP), collagen and platelet activating factor (PAF) and the anti-aggregatory agent, prostacyclin (PGI2) have been studied in the guinea-pig. Administration of ADP, collagen or PAF produces an increase in counts in C1, a decrease in counts in C2, and hence an increase in the ratio C1/C2. The rise in C1/C2 is more protracted after collagen administration than after ADP or PAF. PGI2 (50-500 ng/kg) reduces the response to ADP. The present technique is both simple, reproducible and although the present experiments are in the presence of heparin, the technique remains functional in the presence of minimal heparin, thus making it a suitable method for studies of platelet function and the evaluation of anti-aggregatory agents in vivo.

摘要

已开发出一种简单的微创技术,用于连续监测实验动物胸部(C1)和腹部(C2)区域中111-铟标记的同源血小板。在豚鼠中研究了聚集剂二磷酸腺苷(ADP)、胶原蛋白和血小板活化因子(PAF)以及抗聚集剂前列环素(PGI2)的作用。给予ADP、胶原蛋白或PAF会使C1计数增加,C2计数减少,从而使C1/C2比值增加。胶原蛋白给药后C1/C2的升高比ADP或PAF给药后更持久。PGI2(50-500 ng/kg)可降低对ADP的反应。本技术既简单又可重复,尽管目前的实验是在肝素存在的情况下进行的,但该技术在极少肝素存在的情况下仍能发挥作用,因此使其成为体内血小板功能研究和抗聚集剂评估的合适方法。

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