首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Interaction of histamine H1-and H2-receptor antagonists with histamine uptake and metabolism by guinea-pig isolated atrium and mouse neoplastic mast cells cells in vitro.
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Interaction of histamine H1-and H2-receptor antagonists with histamine uptake and metabolism by guinea-pig isolated atrium and mouse neoplastic mast cells cells in vitro.

机译:组胺H1和H2受体拮抗剂与豚鼠离体中庭和小鼠赘生性肥大细胞的组胺摄取和代谢的相互作用。

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摘要

1. Burimamide, metiamide, chlorpheniramine, triprolidine and cocaine, were tested as inhibitors of histamine uptake and metabolism in the guinea-pig atrium and in mouse neoplastic mast cells. 2. Cocaine did not affect the uptake and metabolism of histamine, either in the atrium or in the mast cells. All the antihistamines tested blocked the uptake and metabolism of histamine in both preparations. The order of potency was burimamide greater than chlorpheniramine greater than triprolidine greater than metiamide in the atrium; and burimamide greater than metiamide greater than triprolidine greater than chlorpheniramine, in the mase cells. 3. Comparison of the present results with the antihistamine activity of these blocking agents suggests that no correlation exists between the receptor blocking activity and the ability of these substances to act as inhibitors of histamine uptake and metabolism.
机译:1.在豚鼠心房和小鼠肿瘤性肥大细胞中,检测了Burimamide,metiamide,扑尔敏,三苯吡啶和可卡因作为组胺摄取和新陈代谢的抑制剂。 2.可卡因在中庭或肥大细胞中均不影响组胺的摄取和代谢。所有测试的所有抗组胺药均阻止了这两种制剂中组胺的吸收和代谢。在心房中,效力顺序为:burimamide大于chlorpheniramine大于triprolidine大于metiamide。胃癌细胞中的比阿米特胺大于甲酰胺,比三甲胺大于氯苯那敏。 3.本结果与这些阻断剂的抗组胺活性的比较表明,受体阻断活性与这些物质作为组胺摄取和代谢抑制剂的能力之间不存在相关性。

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