首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Inhibition by cromoglycate and some flavonoids of nucleoside diphosphate kinase and of exocytosis from permeabilized mast cells.
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Inhibition by cromoglycate and some flavonoids of nucleoside diphosphate kinase and of exocytosis from permeabilized mast cells.

机译:Cromoglycate和核黄素二磷酸激酶的某些类黄酮和透化肥大细胞的胞吐作用的抑制作用。

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摘要

1. The anti-allergic compound, cromoglycate, is reported to possess affinity for, and to suppress the autophosphorylation of a 72kDa protein having the sequence of nucleoside diphosphate kinase (NDPK). 2. We have tested the ability of cromoglycate, and a panel of ten structurally related flavonoids of plant origin, to inhibit the NDPK reaction and the exocytotic process of permeabilized mast cells. The conditions of permeabilization (use of an isotonic medium based on sodium glutamate) were selected to ensure that NDPK activity would be an essential component in the induction of Ca(2+)-induced exocytosis in which ATP is required for generation of GTP. For comparison, we also measured the inhibition of exocytosis induced by GTP-gamma-S; this proceeds in the absence of ATP and bypasses the need for NDPK activity. 3. We found that cromoglycate does not discriminate between Ca2+ and GTP-gamma-S-induced exocytosis and is a poor inhibitor of NDPK activity. Concentrations in the millimolar range are required for inhibition of all these functions. By comparison, many of the flavonoids are effective at concentrations in the micromolar range. 4. While we were unable to discern any systematic relationships between their ability to inhibit the three functions, two compounds, quercetin and genistein, inhibit Ca(2+)-induced, but not GTP-gamma-S-induced exocytosis. Inhibition of the late stages of the stimulus-response pathway in mast cells by these compounds is therefore likely to be due to inhibition of NDPK and the consequent failure to generate GTP.
机译:1.据报道,抗过敏化合物Cromoglycate对具有核苷二磷酸激酶(NDPK)序列的72kDa蛋白具有亲和力,并能抑制其自身磷酸化。 2.我们已经测试了Cromoglycate和一组十种植物来源的结构相关类黄酮抑制NDPK反应和透化肥大细胞的胞吐过程的能力。选择通透性的条件(使用基于谷氨酸钠的等渗介质)以确保NDPK活性将是诱导Ca(2+)诱导的胞吐作用(其中需要ATP来生成GTP)的重要组成部分。为了进行比较,我们还测量了由GTP-γ-S诱导的胞吐作用的抑制。在没有ATP的情况下会继续进行,从而绕过NDPK活性的需求。 3.我们发现,色甘酸糖不能区分Ca2 +和GTP-γ-S诱导的胞吐作用,并且是NDPK活性的抑制剂。抑制所有这些功能需要浓度在毫摩尔范围内。相比之下,许多类黄酮在微摩尔浓度范围内均有效。 4.虽然我们无法辨别它们抑制三种功能的能力之间的任何系统关系,但两种化合物槲皮素和染料木黄酮却抑制Ca(2+)诱导的,但不能抑制GTP-γ-S诱导的胞吐作用。因此,这些化合物抑制肥大细胞中的刺激-反应途径的后期很可能是由于NDPK的抑制和因此产生GTP的失败。

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