Colwell J A, Sagel J, Crook L, Chambers A, Laimins M
Metabolism. 1977 Mar;26(3):279-85. doi: 10.1016/0026-0495(77)90074-9.
Second-phase platelet aggregation induced by adenosine diphosphate (ADP) and epinephrine was measured in fasting platelet-rich plasma in normals, "prediabetics," and diabetics with or without vascular disease. "Plasma factor" potentiation of ADP-induced second-phase platelet aggregation was also estimated, as were megathrombocyte numbers in the same patient groups. There was an increased sensitivity of second-phase platelet aggregation noted with both aggregating agents in all diabetic groups except for the prediabetics. This activity was paralleled by an increase in plasma factor activity. In vivo evidence of an increased turnover of platelets in frank diabetics was suggested by increased numbers of megathrombocytes. These studies demonstrate that platelets from diabetics are sensitive to aggregating agents and that this sensitivity may be related to plasma factor(s) present in diabetics. In vivo platelet aggregation may be present in diabetics. Longitudinal studies will be necessary to establish the relationship of these findings to the genesis of diabetic vascular disease.
在正常受试者、“糖尿病前期患者”以及患有或未患有血管疾病的糖尿病患者的空腹富血小板血浆中,测量了由二磷酸腺苷(ADP)和肾上腺素诱导的二期血小板聚集。还评估了“血浆因子”对ADP诱导的二期血小板聚集的增强作用,以及同一患者组中的巨血小板数量。除糖尿病前期患者外,所有糖尿病组中使用这两种聚集剂时,二期血小板聚集的敏感性均增加。这种活性与血浆因子活性的增加平行。巨血小板数量增加提示显性糖尿病患者体内血小板更新增加的体内证据。这些研究表明,糖尿病患者的血小板对聚集剂敏感,并且这种敏感性可能与糖尿病患者体内存在的血浆因子有关。糖尿病患者体内可能存在血小板聚集。需要进行纵向研究以确定这些发现与糖尿病血管疾病发生的关系。