Naesh O, Haedersdal C, Hindberg I, Trap-Jensen J
Department of Anesthesiology and Intensive Care, Sahlgrenska Sjukhuset, Gothenburg, Sweden.
Clin Physiol. 1993 May;13(3):299-307. doi: 10.1111/j.1475-097x.1993.tb00330.x.
Platelets are known to become activated in vivo by different stressful stimuli such as surgery and dynamic exercise. Mental stress has been shown to increase platelet aggregability. Platelet activation is thought to be of major importance in atherogenesis and cardiac fatalities. In order to clarify further stress-induced platelet activation with special reference to the period after the stress, we studied eight young, healthy volunteers during and for 1 h after a mental stress test (Stroops Colour Word Conflict Test). Using highly standardized techniques, we have measured platelet aggregability ex vivo and the platelet release products beta-thromboglobulin, platelet factor 4 and serotonin in plasma. As markers of the stress response we measured cyclic-AMP in plasma, heart rate, cardiac output and blood pressure. The stress test induced a significant cardiovascular response with increases in heart rate, blood pressure, and cardiac output and as a measure of adrenergic activity an increase in cyclic AMP in plasma during the test. Platelet aggregability was unaffected during the test but decreased following the stress. During the first hour following the test and release products beta-thromboglobulin and serotonin increased significantly in plasma. We conclude that platelets are activated during mental stress and that this activation involves a post-stress release of vasoactive compounds from platelets.
众所周知,血小板在体内会因手术和动态运动等不同应激刺激而被激活。精神压力已被证明会增加血小板聚集性。血小板激活被认为在动脉粥样硬化形成和心脏死亡中起主要作用。为了进一步阐明应激诱导的血小板激活,特别是应激后的时期,我们对8名年轻健康志愿者在精神压力测试(斯特鲁普颜色词冲突测试)期间及之后1小时进行了研究。我们使用高度标准化的技术,在体外测量了血小板聚集性,并测量了血浆中血小板释放产物β-血小板球蛋白、血小板因子4和血清素。作为应激反应的标志物,我们测量了血浆中的环磷酸腺苷、心率、心输出量和血压。压力测试引起了显著的心血管反应,心率、血压和心输出量增加,作为肾上腺素能活性的指标,测试期间血浆中环磷酸腺苷增加。测试期间血小板聚集性未受影响,但应激后降低。在测试后的第一小时内,血浆中释放产物β-血小板球蛋白和血清素显著增加。我们得出结论,血小板在精神压力期间被激活,并且这种激活涉及应激后血小板释放血管活性化合物。