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Histamine Release Induced by Human Leukocyte Lysates REABSORPTION OF PREVIOUSLY RELEASED HISTAMINE AFTER EXPOSURE TO CYCLIC AMP-ACTIVE AGENTS

机译:人白细胞溶解产物诱导的组胺释放暴露于循环活性剂后先前释放的组胺的吸收

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摘要

The role of cyclic AMP in histamine release induced by human leukocyte lysates was investigated. Leukocytes were incubated with leukocyte lysates prepared by ultrasonic disruption, and histamine was determined fluorimetrically. Several cyclic AMP-active agents had a marked inhibitory effect on histamine release. Theophylline and isoproterenol produced 50% inhibition at concentrations of less than 10-5 M. Prostaglandin E1 and dibutyryl cyclic AMP inhibited release by 50% at 7 × 10-8 M and 6 × 10-5 M concentrations, respectively. Histamine, which has recently been shown to increase leukocyte cyclic AMP, had a pronounced inhibitory effect on lysate-induced histamine release, producing 50% inhibition at a concentration of only 2.5 × 10-12 M.
机译:研究了环AMP在人白细胞溶解产物诱导的组胺释放中的作用。将白细胞与通过超声破坏制备的白细胞裂解物一起温育,并通过荧光法测定组胺。几种环状AMP活性剂对组胺释放具有明显的抑制作用。茶碱和异丙肾上腺素在小于10-5 M的浓度下产生50%的抑制作用。前列腺素E1和二丁酰环AMP在7×10-8 M和6×10-5 M的浓度下分别抑制50%的释放。组胺,最近已显示可增加白细胞环状AMP,对溶胞产物诱导的组胺释放具有明显的抑制作用,在浓度仅为2.5×10-12 M时产生50%的抑制作用。

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