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HL-60人早幼粒细胞白血病细胞中组胺摄取系统的药理学特性

Pharmacological characterization of the histamine uptake system in HL-60 human promyelocytic leukemia cells.

作者信息

Gespach C, Marrec N, Abita J P

出版信息

Biosci Rep. 1986 Apr;6(4):403-7. doi: 10.1007/BF01116428.

Abstract

Serotonin and histamine H1, H2 receptor agonists or antagonists inhibited [3H]histamine uptake by HL-60 cells, according to the following order of potency: impromidine greater than 4-MH greater than histamine greater than AET greater than PEA and: cimetidine, histamine greater than diphenhydramine, serotonin. It is concluded that histamine uptake by HL-60 cells was specifically controlled by the H2 type histamine receptor and that this active process might be involved in pathophysiological regulations in leukemic and normal granulocytic precursors and in the control of histamine levels in peripheral blood and tissues in man.

摘要

血清素以及组胺H1、H2受体激动剂或拮抗剂可抑制HL-60细胞对[3H]组胺的摄取,其效力顺序如下:英普咪定大于4-甲基组胺大于组胺大于2-氨基乙硫醇大于苯乙胺,以及:西咪替丁、组胺大于苯海拉明、血清素。结论是,HL-60细胞对组胺的摄取受H2型组胺受体特异性控制,这一活跃过程可能参与白血病和正常粒细胞前体的病理生理调节,以及人体外周血和组织中组胺水平的控制。

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