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内毒素介导的人血小板聚集抑制作用。

Endotoxin-mediated inhibition of human platelet aggregation.

作者信息

Saba H I, Saba S R, Morelli G, Hartmann R C

出版信息

Thromb Res. 1984 Apr 1;34(1):19-33. doi: 10.1016/0049-3848(84)90103-8.

Abstract

A variety of endotoxins, when added to human platelet-rich plasma (PRP) or to suspensions of washed platelets (WP), demonstrated an inhibitory effect on platelet aggregation induced by various aggregating agents. Endotoxin blocked the release of 14C serotonin from platelets but had no influence on cyclic AMP production. Endotoxin did not interfere with thromboxane generation by platelets. However, endotoxin-treated platelets failed to respond to added thromboxane. The inhibitory effect of endotoxin on platelet aggregation was more pronounced in the presence of ionophore A23187 as compared to other aggregating agents and was effectively reversed by calcium but not by magnesium, another divalent cation. Furthermore, endotoxin failed to inhibit the ristocetin-induced agglutination of formaldehyde-fixed platelets; a non-calcium dependent phenomenon. These findings appear to suggest that endotoxin-mediated inhibitory activity of platelet aggregation is related to the interference in the role of calcium. The antiaggregatory activity of endotoxin appears to be due to a direct and rapid action on platelets and not due to a non-specific binding, as the effect was not abolished by washing the endotoxin-incubated platelets. Endotoxin-mediated alteration of platelet function may contribute to bleeding diathesis in septecemic and endotoxemic patients.

摘要

多种内毒素在添加到人富含血小板血浆(PRP)或洗涤血小板(WP)悬液中时,对各种聚集剂诱导的血小板聚集表现出抑制作用。内毒素阻断了血小板中14C血清素的释放,但对环磷酸腺苷(cAMP)的产生没有影响。内毒素不干扰血小板生成血栓素。然而,经内毒素处理的血小板对添加的血栓素无反应。与其他聚集剂相比,在离子载体A23187存在的情况下,内毒素对血小板聚集的抑制作用更明显,并且能被钙有效逆转,但不能被另一种二价阳离子镁逆转。此外,内毒素不能抑制瑞斯托菌素诱导的甲醛固定血小板的凝集,这是一种不依赖钙的现象。这些发现似乎表明,内毒素介导的血小板聚集抑制活性与对钙作用的干扰有关。内毒素的抗聚集活性似乎是由于对血小板的直接快速作用,而不是由于非特异性结合,因为洗涤经内毒素孵育的血小板后,这种作用并未消除。内毒素介导的血小板功能改变可能导致败血症和内毒素血症患者的出血倾向。

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