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非甾体抗炎药、二丁酰环磷腺苷和磷酸二酯酶抑制剂对正常及必需脂肪酸缺乏大鼠血小板聚集和血小板释放反应的影响。

The effect of non-steroid anti-inflammatory drugs, dibutyryl cyclic 3',5'-adenosine monophosphate and phosphodiesterase inhibitors on platelet aggregation and the platelet release reaction in normal and essential fatty acid deficient rats.

作者信息

Vincent J E, Zijlstra F J, Bonta I L

出版信息

Prostaglandins. 1975 Nov;10(5):899-911. doi: 10.1016/0090-6980(75)90017-9.

Abstract

A comparison was made of the action of three classes of substances with platelet aggregation inhibiting effect in normal and essential fatty acid deficient rats. In the latter group, the effect of indomethacin was considerably reduced, whereas the difference was smaller with aspirin. Dibutyryl cyclic AMP had the same inhibiting effect in both groups. Of the phosphodiesterase inhibitors tested, dipyridamole was inactive, whereas the inhibiting effects of caffeine and papaverine are slightly reduced in the deficient animals. The same differences between the two groups were seen in the magnitude of the release reaction after 14C-serotonin labelling. These data support the idea that the non-steroid anti-inflammatory drugs act by inhibiting the formation of an aggregation-inducing substance from arachidonic acid.

摘要

对三类具有血小板聚集抑制作用的物质在正常大鼠和必需脂肪酸缺乏大鼠中的作用进行了比较。在后一组中,吲哚美辛的作用显著降低,而阿司匹林的差异较小。二丁酰环磷腺苷在两组中具有相同的抑制作用。在所测试的磷酸二酯酶抑制剂中,双嘧达莫无活性,而咖啡因和罂粟碱的抑制作用在缺乏必需脂肪酸的动物中略有降低。在14C-血清素标记后的释放反应程度上,两组之间也观察到了相同的差异。这些数据支持了非甾体抗炎药通过抑制花生四烯酸形成聚集诱导物质而起作用的观点。

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