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黄酮类化合物对肥大细胞组胺分泌抑制作用的动力学

Kinetics of the inhibitory effect of flavonoids on histamine secretion from mast cells.

作者信息

Bronner C, Landry Y

出版信息

Agents Actions. 1985 Apr;16(3-4):147-51. doi: 10.1007/BF01983124.

Abstract

The effect of cromoglycate and of natural flavonoids on histamine release from peritoneal rat mast cells induced by compound 48/80 and ionophore A23187 was studied according to preincubation time of mast cells with drugs and to incubation time of cells with the triggering agent. Preincubation of cells with cromoglycate, dihydroquercetin and amentoflavone, a biflavonoid, decreased the potency of drugs to inhibit the ionophore-induced release; the optimal inhibitions were observed when drugs were added simultaneously with the ionophore A23187. In contrast, a short preincubation (2 min) of cells with quercetin or luteolin decreased their inhibitory effect on the ionophore-induced release, whereas a longer preincubation increased the inhibition. When compound 48/80 was used to trigger histamine secretion, the inhibitory potencies of all the compounds used were decreased according to preincubation time. Dihydroquercetin (taxifolin), previously considered as inactive, showed an interesting cromoglycate-like behaviour.

摘要

根据肥大细胞与药物的预孵育时间以及细胞与触发剂的孵育时间,研究了色甘酸和天然黄酮类化合物对化合物48/80和离子载体A23187诱导的大鼠腹腔肥大细胞组胺释放的影响。肥大细胞与色甘酸、二氢槲皮素和双黄酮穗花杉双黄酮预孵育,会降低药物抑制离子载体诱导释放的效力;当药物与离子载体A23187同时添加时,观察到最佳抑制效果。相反,肥大细胞与槲皮素或木犀草素短时间(2分钟)预孵育会降低它们对离子载体诱导释放的抑制作用,而较长时间的预孵育则会增强抑制作用。当使用化合物48/80触发组胺分泌时,根据预孵育时间,所有所用化合物的抑制效力均降低。先前被认为无活性的二氢槲皮素(花旗松素)表现出有趣的类似色甘酸的行为。

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