Zoccarato F, Ruzzene M, Cavallini L, Doni M G, Francesconi M A, Deana R, Alexandre A
Department of Biological Chemistry, C.N.R. Unit for the Study of Mitochondrial Physiology, University of Padova, Italy.
Biochim Biophys Acta. 1991 Mar 19;1092(1):72-8. doi: 10.1016/0167-4889(91)90178-z.
We studied the action of the alpha 2 adrenergic agonist adrenaline on the platelet responses evoked by the activation of protein kinase C or by the ionophore induced increase of cytosolic Ca2+. Both the phorbol ester and ionomycin-induced aggregation are strongly potentiated by adrenaline which per se does not behave as an activating agonist. The potentiation by adrenaline is observed both when added before and after the aggregating agent; in the latter case the effect increases on increasing the delay of adrenaline addition. Adrenaline also reverses the inhibition by cAMP of the PMA (or ionomycin) induced aggregation. It also has a strong potentiating effect (over 100%) on the phorbol ester induced ATP secretion and a weaker effect on the secretion induced by ionomycin. The effect on secretion is visible only when adrenaline is added prior to the stimulus. The inhibition by cAMP of the PMA or ionomycin induced secretion is also counteracted by adrenaline. In no case adrenaline modifies the pattern of platelet phosphoproteins. Ionomycin induces some platelet aggregation also in the presence of the protein kinase inhibitor staurosporine; also this phosphoprotein independent aggregation is strongly stimulated by adrenaline.
我们研究了α2肾上腺素能激动剂肾上腺素对蛋白激酶C激活或离子载体诱导的胞质Ca2+增加所引发的血小板反应的作用。佛波酯和离子霉素诱导的聚集均被肾上腺素强烈增强,而肾上腺素本身并不表现为激活激动剂。无论在聚集剂添加之前还是之后添加肾上腺素,均能观察到其增强作用;在后一种情况下,随着肾上腺素添加延迟时间的增加,效应增强。肾上腺素还能逆转cAMP对PMA(或离子霉素)诱导聚集的抑制作用。它对佛波酯诱导的ATP分泌也有很强的增强作用(超过100%),而对离子霉素诱导的分泌作用较弱。仅当在刺激之前添加肾上腺素时,对分泌的效应才可见。肾上腺素也能抵消cAMP对PMA或离子霉素诱导分泌的抑制作用。在任何情况下,肾上腺素均不改变血小板磷蛋白的模式。在蛋白激酶抑制剂星形孢菌素存在的情况下,离子霉素也能诱导一些血小板聚集;这种不依赖磷蛋白的聚集也被肾上腺素强烈刺激。