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在存在麦胚凝集素的情况下,N-乙酰葡糖胺和血小板抑制剂对血小板与聚集剂协同相互作用的影响。

Effects of N-acetylglucosamine and platelet inhibitors on the synergistic interaction of platelets and aggregating agents in the presence of wheat germ agglutinin.

作者信息

Tandon N N, Ordinas A, Jamieson G A

出版信息

Biochim Biophys Acta. 1982 Nov 24;719(2):388-95. doi: 10.1016/0304-4165(82)90114-3.

Abstract

Low concentrations of wheat germ agglutinin (4 micrograms/ml) have been shown to act synergistically to induce platelet aggregation with epinephrine, collagen, arachidonate and ionophore A23187. Aggregation ceased on the addition of the haptenic sugar N-acetylglucosamine at any time following the onset of aggregation with these agonists and a small degree of disaggregation was observed during the reversible first wave with the biphasic aggregating agents epinephrine and ADP. Cyclooxygenase inhibitors such as indomethacin and aspirin blocked the second wave of aggregation with the biphasic aggregating agents epinephrine and ADP but a synergistic response continued to be shown with the first wave in the presence of these inhibitors. Release of [14C]serotonin and the mobilization of [3H]arachidonate by epinephrine and collagen were markedly stimulated in the presence of wheat germ agglutinin but there was no increase of either radiolabel in the case of ADP. Platelet shape change, but not aggregation, occurred with low levels of wheat germ agglutinin and the synergistic response with ADP, collagen or ionophore A23187 occurred without further shape change. Wheat germ agglutinin did not affect the basal or stimulated levels of cyclic AMP. The membrane fluidity of platelets was not affected by the lectin or by thrombin as shown by the lack of change in fluorescence polarization with diphenylhexatriene. It is suggested that the binding of wheat germ agglutinin to the platelet surface induces platelet activation by mechanisms similar to those of other agonists and that it may affect the distribution of membrane-bound Ca2+ by a reversible perturbation of the platelet membrane.

摘要

低浓度的麦胚凝集素(4微克/毫升)已被证明可与肾上腺素、胶原蛋白、花生四烯酸和离子载体A23187协同作用诱导血小板聚集。在用这些激动剂诱导聚集开始后的任何时间,加入半抗原糖N-乙酰葡糖胺后聚集即停止,并且在用双相聚集剂肾上腺素和ADP进行的可逆第一波聚集过程中观察到了一定程度的解聚。环氧化酶抑制剂如吲哚美辛和阿司匹林可阻断双相聚集剂肾上腺素和ADP诱导的第二波聚集,但在这些抑制剂存在的情况下,第一波仍继续表现出协同反应。在麦胚凝集素存在的情况下,肾上腺素和胶原蛋白对[14C]5-羟色胺的释放及[3H]花生四烯酸的动员有明显刺激作用,但ADP的情况下两种放射性标记均未增加。低水平的麦胚凝集素可引起血小板形状改变但不引起聚集,并且与ADP、胶原蛋白或离子载体A23187的协同反应在无进一步形状改变的情况下发生。麦胚凝集素不影响环磷酸腺苷的基础水平或刺激水平。如用二苯基己三烯检测荧光偏振未发生变化所示,凝集素或凝血酶均不影响血小板的膜流动性。提示麦胚凝集素与血小板表面的结合通过与其他激动剂类似的机制诱导血小板活化,并且它可能通过对血小板膜的可逆性扰动影响膜结合Ca2+的分布。

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