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稳定的血栓素A2类似物使人类血小板胞质游离钙浓度升高。

Elevation of cytoplasmic free calcium concentration by stable thromboxane A2 analogue in human platelets.

作者信息

Kawahara Y, Yamanishi J, Furuta Y, Kaibuchi K, Takai Y, Fukuzaki H

出版信息

Biochem Biophys Res Commun. 1983 Dec 28;117(3):663-9. doi: 10.1016/0006-291x(83)91648-0.

Abstract

9, 11-Epithio-11, 12-methano-thromboxane A2 (STA2), a stable analogue of thromboxane A2, caused a rapid rise in cytoplasmic free Ca2+ concentration ([Ca2+]i) in human platelets as measured with the fluorescent Ca2+ indicator quin2. Concomitantly, this compound induced phosphorylation of myosin light chain which is catalyzed by Ca2+, calmodulin-dependent protein kinase. These reactions were fast enough to trigger serotonin release. 13-Azaprostanoic acid, a receptor level antagonist of thromboxane A2 inhibited STA2-induced elevation of [Ca2+]i, phosphorylation of myosin light chain and serotonin release. These results provide evidence that STA2 interacts with a thromboxane A2 receptor which leads to elevation of [Ca2+]i.

摘要

9,11-环氧-11,12-甲撑血栓素A2(STA2)是血栓素A2的一种稳定类似物,用荧光钙指示剂喹啉2测量发现,它可使人类血小板胞质游离钙浓度([Ca2+]i)迅速升高。同时,该化合物诱导肌球蛋白轻链磷酸化,此过程由钙、钙调蛋白依赖性蛋白激酶催化。这些反应速度足够快,足以引发5-羟色胺释放。13-氮杂前列腺酸是血栓素A2的受体水平拮抗剂,它可抑制STA2诱导的[Ca2+]i升高、肌球蛋白轻链磷酸化及5-羟色胺释放。这些结果证明,STA2与血栓素A2受体相互作用,从而导致[Ca2+]i升高。

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