Frojmovic M M, Milton J G, Duchastel A
J Lab Clin Med. 1983 Jun;101(6):964-76.
Platelet aggregation measured from the decrease in the number of nonaggregated platelets (PA) is compared with that measured from the increase in %T (TA) after ADP addition to a stirred platelet suspension. A number of properties distinguish PA from TA. Half-maximal extent of PA, measured at 3 or 10 sec after ADP addition is attained at significantly lower ADP concentrations ([ADP]) than for TA (velocity and extent), and in particular at [ADP] equal to or less than that required for shape change. PA appears minimally refractory to ADP under conditions causing maximal refractoriness of TA. Examination of the effect of three inhibitors of platelet aggregation acting on extracellular ionized calcium (EDTA) and on platelet adenylate cyclase (PGE1) and phosphodiesterase (anagrelide; BL-4162A) indicates that PA is generally less sensitive to these inhibitors than TA but, of greater significance, that PA and TA reveal aggregation processes with differing ADP sensitivities. It is suggested that these differences reflect different processes determining the strength of interplatelet interactions. Conventional aggregometry is insensitive for measuring the low ADP-dependent aggregation process.
将搅拌的血小板悬液中加入ADP后,通过未聚集血小板数量减少来测量的血小板聚集(PA)与通过%T增加来测量的血小板聚集(TA)进行比较。PA和TA在多个特性上存在差异。PA的半最大聚集程度在加入ADP后3秒或10秒测量,达到该程度所需的ADP浓度([ADP])显著低于TA(速度和程度),特别是在[ADP]等于或低于引起形状改变所需浓度时。在导致TA最大不应性的条件下,PA对ADP的不应性最小。对三种作用于细胞外游离钙(EDTA)、血小板腺苷酸环化酶(PGE1)和磷酸二酯酶(阿那格雷;BL - 4162A)的血小板聚集抑制剂的作用研究表明,PA通常比TA对这些抑制剂的敏感性更低,但更重要的是,PA和TA显示出对ADP敏感性不同的聚集过程。提示这些差异反映了决定血小板间相互作用强度的不同过程。传统的血小板聚集测定法对测量低ADP依赖性聚集过程不敏感。