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卵孢醇相关化合物(4-酰基异香豆素)对化合物48/80介导的大鼠离体肥大细胞组胺释放的抑制作用。

Inhibition of compound 48/80-mediated histamine release from isolated rat mast cells by oosponol-related compounds (4-acyl-isocoumarins).

作者信息

Kimura M, Waki I, Kokubo M

出版信息

Jpn J Pharmacol. 1978 Oct;28(5):693-7. doi: 10.1254/jjp.28.693.

Abstract

Oosponol (4-hydroxymethylketone-8-hydroxyisocoumarin) is a metabolic product isolated from Oospora astringens which originated from house dust in a room of an asthmatic patient. The compound and the structurally related isocoumarins were studied to determine the inhibition of histamine release induced by compound 48/80 from isolated rat peritoneal mast cells. The released histamine was assayed by fluorometry. The compounds tested were not observed to release histamine. Some of 4-acyl-isocoumarins inhibited the histamine release at doses less than 10 micrometers, whereas the 3-acyl- and the 4-alkyl-compounds were not effective at doses over 100 microns. The pretreatment of mast cell with the compound for 15 min before the application of compound 48/80 was more effective than the simultaneous administration. The mode of inhibitory action of KIT-302, 4-(4'-carboxy-benzoyl)-isocoumarin, was non-competitive antagonism to compound 48/80 on the mast cells.

摘要

卵孢醇(4 - 羟甲基酮 - 8 - 羟基异香豆素)是从一名哮喘患者房间的室内灰尘中分离出的收敛卵孢霉中得到的一种代谢产物。对该化合物及结构相关的异香豆素进行了研究,以确定其对化合物48/80诱导的大鼠离体腹膜肥大细胞组胺释放的抑制作用。释放的组胺通过荧光测定法进行检测。未观察到所测试的化合物释放组胺。一些4 - 酰基 - 异香豆素在剂量小于10微米时抑制组胺释放,而3 - 酰基 - 和4 - 烷基 - 化合物在剂量超过100微米时无效。在应用化合物48/80之前,用该化合物对肥大细胞预处理15分钟比同时给药更有效。KIT - 302,即4 -(4'-羧基 - 苯甲酰基) - 异香豆素的抑制作用模式是对肥大细胞上的化合物48/80产生非竞争性拮抗作用。

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