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地马普明对酵母聚糖刺激的人粒细胞β-葡萄糖醛酸酶释放的抑制作用。

Dimaprit inhibition of zymosan-stimulated beta-glucuronidase release from human granulocytes.

作者信息

Busse W W, Cooper W, Anderson C

出版信息

Agents Actions. 1980 Apr;10(1 Pt 2):15-8. doi: 10.1007/BF02024173.

Abstract

Histamine inhibits the in vitro release of granulocytic lysosomal beta-glucuronidase when incubated with complement activated zymosan particles and this is an H2-receptor response. The highly specific histamine H2-receptor agonist, dimaprit, also inhibits this secretory enzyme release but is less potent (-log molar ED50 6.71 with histamine vs. -log ED50 5.97 with dimaprit, p less than 0.05). No change in beta-glucuronidase release was found with the H1-agonst, 2-(2 pyridyl)-ethylamine. The antagonist activity of metiamide was similar with the two agonists (KB = 2.9 x 10(-8) M with histamine and KB = 3.6 x 10(-8) M with dimaprit). Diphenhydramine did not change the granulocyte response to either histamine or dimaprit.

摘要

组胺与补体激活的酵母聚糖颗粒一起孵育时,可抑制粒细胞溶酶体β-葡萄糖醛酸酶的体外释放,这是一种H2受体反应。高度特异性的组胺H2受体激动剂二甲双胍也能抑制这种分泌酶的释放,但效力较弱(组胺的-log摩尔ED50为6.71,二甲双胍的-log ED50为5.97,p<0.05)。H1激动剂2-(2-吡啶基)-乙胺对β-葡萄糖醛酸酶的释放没有影响。甲硫咪胺对两种激动剂的拮抗活性相似(组胺的KB = 2.9 x 10(-8) M,二甲双胍的KB = 3.6 x 10(-8) M)。苯海拉明对粒细胞对组胺或二甲双胍的反应没有影响。

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