University of Rochester Medical Center, Department of Medicine - Hematology/Oncology, Rochester, NY 14642, USA.
Thromb Res. 2012 Jun;129(6):760-4. doi: 10.1016/j.thromres.2011.12.019. Epub 2012 Jan 4.
Thiazolidinediones (TZDs) are agonists of PPARγ and exert beneficial metabolic effects in patients with diabetes. They may also affect platelet function.
To characterize potential platelet inhibitory effect of pioglitazone alone and in the presence of aspirin.
20 normal and 20 diabetic subjects were enrolled in a prospective study. On day 1, a blood sample was obtained at baseline and a second one after ingestion of 30mg of pioglitazone. PRP was prepared and platelet aggregation and release were evaluated using ADP, collagen and arachidonic acid as agonists. Subjects returned at 6-9days later after ingesting a single 81mg dose of aspirin and a third blood sample was obtained. The subjects then again ingested 30mg of pioglitazone and a fourth and final blood sample was obtained. Platelet aggregation and release were measured. PRP was incubated with thrombin to activate platelets, and the serum was separated and assayed for thromboxane B2, TGFβ and CD40L RESULTS: Pioglitazone alone did not affect aggregation with arachidonic acid. However, following ingestion of both aspirin and pioglitazone aggregation was significantly decreased compared to aspirin alone (P<0.0001). Pioglitazone also potentiated aspirin-induced inhibition of ATP release using either arachidonic acid or collagen. Following pioglitazone alone, TXB(2) release was 32,719±3,585pg/ml which was significantly reduced compared to baseline (42,075±4,479, P=0.0004). Pioglitazone also potentiated the inhibition of TXB(2) release by aspirin.
Pioglitazone inhibits platelet function and potentiates the inhibitory effects of aspirin.
噻唑烷二酮类(TZDs)是过氧化物酶体增殖物激活受体γ(PPARγ)的激动剂,对糖尿病患者具有有益的代谢作用。它们也可能影响血小板功能。
描述吡格列酮单独应用及与阿司匹林合用对血小板的潜在抑制作用。
20 名正常人和 20 名糖尿病患者参与了这项前瞻性研究。第 1 天,在基础状态时和服用 30mg 吡格列酮后分别采集一份血样。用 ADP、胶原和花生四烯酸作为激动剂,制备富含血小板的血浆(PRP),并评估血小板聚集和释放。6-9 天后,患者服用单剂量 81mg 阿司匹林后再次采集血样。然后再次服用 30mg 吡格列酮,采集最后一份血样。测量血小板聚集和释放。用凝血酶激活血小板,分离 PRP 上清液,检测血栓烷 B2、TGFβ 和 CD40L。
吡格列酮单独应用不影响花生四烯酸诱导的聚集。然而,与单独服用阿司匹林相比,服用阿司匹林和吡格列酮后聚集明显减少(P<0.0001)。吡格列酮还增强了阿司匹林诱导的用花生四烯酸或胶原诱导的 ATP 释放抑制。单独服用吡格列酮后,TXB2 释放量为 32719±3585pg/ml,与基线(42075±4479,P=0.0004)相比显著减少。吡格列酮还增强了阿司匹林对 TXB2 释放的抑制作用。
吡格列酮抑制血小板功能,并增强阿司匹林的抑制作用。