Pasqualini L, Pirro M, Lombardini R, Ciuffetti G, Dragani P, Mannarino E
Internal Medicine, Angiology and Arteriosclerosis Disease Clinic, Department of Clinical and Experimental Medicine, University of Perugia, 06122 Perugia, Italy.
J Clin Pathol. 2002 Dec;55(12):946-50. doi: 10.1136/jcp.55.12.946.
In humans, little is known about the effects of platelet-leucocyte interactions on blood viscosity and microvascular perfusion. This study tested the hypotheses that (1) activation and interactions between platelets and leucocytes may have an impact on microvascular blood viscosity and perfusion in patients with stage II peripheral arterial occlusive disease, and (2) a powerful antiplatelet drug such as Clopidogrel might help to improve microvascular perfusion by reducing platelet-leucocyte activation and blood viscosity.
Plasma concentrations of certain markers of leucocyte and platelet activation, in addition to low and high shear rate blood viscosity, were measured before and after a repeated exercise treadmill test. Functional parameters including maximum walking time, transcutaneous oxygen pressure, and half recovery time were also measured.
Blocking platelet activation only with a single dose of Clopidogrel (300 mg) did not improve microvascular blood viscosity and perfusion after repeated exercise, but a significant improvement in microvascular perfusion during controlled ischaemia and a lack of post exercise increase in low shear rate blood viscosity was achieved when both platelet and leucocyte activation were suppressed by a relatively longer treatment with Clopidogrel (four days).
Clopidogrel, by inhibiting platelet activation and aggregation, might also block the vicious cycle of leucocyte-platelet activation, thus improving the functioning of the microcirculation.
在人类中,关于血小板与白细胞相互作用对血液粘度和微血管灌注的影响知之甚少。本研究检验了以下假设:(1)血小板与白细胞之间的激活和相互作用可能会影响II期外周动脉闭塞性疾病患者的微血管血液粘度和灌注;(2)一种强效抗血小板药物如氯吡格雷可能有助于通过减少血小板 - 白细胞激活和血液粘度来改善微血管灌注。
在重复运动平板试验前后,测量白细胞和血小板激活的某些标志物的血浆浓度,以及低和高剪切率血液粘度。还测量了包括最大步行时间、经皮氧分压和半恢复时间在内的功能参数。
仅用单剂量氯吡格雷(300毫克)阻断血小板激活并不能改善重复运动后的微血管血液粘度和灌注,但当通过相对较长时间(四天)的氯吡格雷治疗抑制血小板和白细胞激活时,在控制性缺血期间微血管灌注有显著改善,且运动后低剪切率血液粘度没有增加。
氯吡格雷通过抑制血小板激活和聚集,可能还会阻断白细胞 - 血小板激活的恶性循环,从而改善微循环功能。