Bryon P A, Lagarde M, Dechavanne M
Pathol Biol (Paris). 1975 Dec;23 suppl:37-43.
A stereological model, which provides quantitative information on the morphology of the platelet release reaction as isolated from platelet aggregation, was developed for the human platelets separated from blood by Mustard's procedure. Three morphologically defined spaces (granules, surface-connected canalicular system S.C.S., cytoplasm) were used to characterize platelet degranulation (with the variation of the volume density of the granules) and contraction (with the variation of the volume density of both granules and S.C.S.). This model was applied to the evaluation of ultrastructural changes associated with the thrombin-induced release reaction. Degranulation and contraction were associated in the platelets which had been allowed to release for 1,5 and 150 sec. Under conditions of the study, prostaglandins E1 (10(-7) M) inhibited both degranulation and contraction (p less than 0,001). Aspirin (10(-4) M) only inhibited contraction (p less than 0.01) and dibutyryl-AMPc (10(-4)) only inhibited granulation (p less than 0,001).
我们为通过芥末法从血液中分离出的人体血小板建立了一个立体学模型,该模型能够提供与血小板聚集相分离的血小板释放反应形态学的定量信息。利用三个形态学定义的空间(颗粒、表面连接小管系统S.C.S.、细胞质)来表征血小板脱颗粒(随着颗粒体积密度的变化)和收缩(随着颗粒和S.C.S.体积密度的变化)。该模型被应用于评估与凝血酶诱导释放反应相关的超微结构变化。在已释放1、5和150秒的血小板中,脱颗粒和收缩相关。在本研究条件下,前列腺素E1(10(-7)M)抑制脱颗粒和收缩(p<0.001)。阿司匹林(10(-4)M)仅抑制收缩(p<0.01),二丁酰-AMPc(10(-4))仅抑制颗粒化(p<0.001)。