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组胺及组胺类似物对豚鼠淋巴细胞激活的抑制作用。

Inhibition of guinea-pig lymphocyte activation by histamine and histamine analogues.

作者信息

Beets J L, Dale M M

出版信息

Br J Pharmacol. 1979 Jul;66(3):365-72. doi: 10.1111/j.1476-5381.1979.tb10839.x.

Abstract

1 The incorporation of [3H]-thymidine into guinea-pig lymphocytes stimulated by a plant lectin (concanavalin A), soluble antigen (tuberculin (P.P.D.)) and syngeneic hepatoma cells, was partially inhibited (50%) by histamine in vitro. 2 The effect of histamine on both mitogen and antigen dose-response curves suggests a non-competitive, probably physiological antagonism. 3 The inhibitory dose range of histamine lay between 10 nM and 30 microM with an ID50 of approximately 400 nM. 4 The potency order for histamine analogues for the inhibition of lymphocyte activation was histamine greater than or equal to 4-methylhistamine greater than 2-methylhistamine greater than 3-methylhistamine. This is in accord with the mediation of the response through an H2-receptor. 5 H2-receptor antagonists reversed the inhibitory effect of histamine in a dose-related manner, but both metiamide and burimamide, in high concentrations, augmented lymphocyte activation in their own right. This precluded the determination of affinity constants and made it impossible to state with certainty that the inhibition of lymphocyte activation by histamine was mediated by an H2-receptor.

摘要
  1. 在体外,组胺可部分抑制(50%)[3H] - 胸腺嘧啶核苷掺入由植物凝集素(刀豆球蛋白A)、可溶性抗原(结核菌素(PPD))和同基因肝癌细胞刺激的豚鼠淋巴细胞。2. 组胺对有丝分裂原和抗原剂量反应曲线的影响表明存在非竞争性、可能是生理性的拮抗作用。3. 组胺的抑制剂量范围在10 nM至30 μM之间,半数抑制剂量(ID50)约为400 nM。4. 组胺类似物抑制淋巴细胞活化的效力顺序为组胺≥4 - 甲基组胺>2 - 甲基组胺>3 - 甲基组胺。这与通过H2受体介导反应一致。5. H2受体拮抗剂以剂量相关方式逆转组胺的抑制作用,但高浓度的甲硫咪胺和布立马胺自身会增强淋巴细胞活化。这妨碍了亲和力常数的测定,使得无法确定地说明组胺对淋巴细胞活化的抑制是由H2受体介导的。

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