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药理制剂对人角质形成细胞体外有丝分裂的影响。III. 组胺及其甲基化类似物的抑制作用。

Effect of pharmacologic agents on human keratinocyte mitosis in vitro. III. Inhibition by histamine and methylated analogs.

作者信息

Harper R A, Flaxman B A

出版信息

J Invest Dermatol. 1975 Oct;65(4):400-3. doi: 10.1111/1523-1747.ep12607650.

Abstract

Keratinocytes from normal human skin were propagated in vitro. Histamine at 2 times 10(-6) M inhibited mitosis 68%. The side-chain methylated analogs, n-methylhistamine and n,n-dimethylhistamine, produced an inhibitory response of 53 and 60%, respectively, at 1 times 10(-6) M. The side-chain acetylated analog, n-acetylhistamine, did not elicit an inhibitory response in concentrations as high as 1 times 10(-4) M. The ring-methylated analogs, 1-methylhistamine and 4-methylhistamine, produced some degree of mitotic inhibition at 1 times 10(-4) M. When the H1-blocking agent, pyrilamine, or the H2-blocking agent, metiamide, was added in conjunction with histamine, the histamine-induced mitotic inhibition was abolished. These data indicate that human keratinocytes may possess receptors for histamine which could play a role in the regulation of human keratinocyte proliferation in vivo.

摘要

取自正常人类皮肤的角质形成细胞在体外进行增殖培养。2×10⁻⁶ M的组胺可抑制68%的有丝分裂。侧链甲基化类似物N-甲基组胺和N,N-二甲基组胺在1×10⁻⁶ M时分别产生53%和60%的抑制反应。侧链乙酰化类似物N-乙酰组胺在高达1×10⁻⁴ M的浓度下未引发抑制反应。环甲基化类似物1-甲基组胺和4-甲基组胺在1×10⁻⁴ M时产生一定程度的有丝分裂抑制。当H1阻滞剂吡苄明或H2阻滞剂甲硫米特与组胺联合添加时,组胺诱导的有丝分裂抑制作用被消除。这些数据表明人类角质形成细胞可能拥有组胺受体,这可能在体内人类角质形成细胞增殖的调节中发挥作用。

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