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剧烈运动通过增加血小板释放促凝微粒而促进剪切诱导的凝血酶生成。

Strenuous exercise promotes shear-induced thrombin generation by increasing the shedding of procoagulant microparticles from platelets.

机构信息

Graduate Institute of Biomedical Sciences, Chang-Gung University, Tao-Yuan, Taiwan.

出版信息

Thromb Haemost. 2010 Aug;104(2):293-301. doi: 10.1160/TH09-09-0633. Epub 2010 Jun 29.

Abstract

Vigorous exercise increases the risk of vascular thrombotic events. Shear stress enhances the shedding of procoagulant microparticles from platelets, and triggers thrombin generation (TG) in blood. This study explicates the manner in which strenuous exercise affects platelet-derived microparticles (PDMP) release and PDMP-mediated TG under various physio-pathological shear flows. Twenty-four sedentary healthy men performed a graded exercise test (up to VO2max) on a bicycle ergometer. At rest, immediately after and 2 hours after exercise, platelet-rich plasma (PRP) was exposed in a cone-and-plate viscometer to imitate static (0 dyne/cm2), physiological low (LS, 10 dyne/cm2) and pathological high (HS, 100 dyne/cm2) shear stresses ex vivo. The PDMP characteristics and dynamic TG were measured by two-colour flow cytometry and calibrated, automatic thrombinography, respectively. The results demonstrated that there is an increased level of total PDMP together with elevated peak height and rate of TG in PRP in response to both LS and HS conditions. Furthermore, HS, but not LS, promoted the binding of FV/Va or FVIII and the exposure of phosphatidylserine (PS) on platelets. Application of HS after strenuous exercise increased the factor (F)V/Va-/FVIII-/tissue factor-rich and PS-exposing PDMP counts, enhanced the PDMP-promoted peak height and rate of TG, as well as increased the ability of FV/Va or FVIII to bind to PDMP or platelets. However, the enhancement of HS-induced procoagulant activity reversed to the pre-exercise status 2 hours following this exercise. Therefore, we conclude that strenuous exercise modestly contributes to the acceleration of shear-induced TG by increasing the release of procoagulant microparticles from platelets.

摘要

剧烈运动增加血管血栓栓塞事件的风险。切应力增强血小板释放促凝微粒,触发血液中凝血酶生成(TG)。本研究阐述了剧烈运动如何影响血小板衍生微粒(PDMP)释放和 PDMP 介导的在各种生理病理切变流下的 TG。24 名久坐健康男性在自行车测力计上进行分级运动测试(直至 VO2max)。在休息、运动后立即和 2 小时后,富含血小板的血浆(PRP)在锥板粘度计中暴露于模拟静态(0 达因/平方厘米)、生理低(LS,10 达因/平方厘米)和病理高(HS,100 达因/平方厘米)的体外切变应力下。通过双色流式细胞术测量 PDMP 特征和动态 TG,并通过自动凝血仪进行校准。结果表明,LS 和 HS 条件下,PRP 中总 PDMP 水平升高,TG 峰值高度和速率升高。此外,HS 而不是 LS 促进了 FV/Va 或 FVIII 的结合以及血小板中磷脂酰丝氨酸(PS)的暴露。剧烈运动后施加 HS 增加了 FV/Va-/FVIII-/组织因子丰富和 PS 暴露的 PDMP 计数,增强了 PDMP 促进的 TG 峰值高度和速率,并增加了 FV/Va 或 FVIII 与 PDMP 或血小板结合的能力。然而,HS 诱导的促凝活性增强在运动后 2 小时恢复到运动前状态。因此,我们得出结论,剧烈运动通过增加血小板释放促凝微粒,适度促进了剪切诱导的 TG 加速。

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