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色甘酸酯和一些黄酮类化合物对核苷二磷酸激酶以及对通透化肥大细胞胞吐作用的抑制

Inhibition by cromoglycate and some flavonoids of nucleoside diphosphate kinase and of exocytosis from permeabilized mast cells.

作者信息

Martin M W, O'Sullivan A J, Gomperts B D

机构信息

Department of Physiology, University College London.

出版信息

Br J Pharmacol. 1995 Jul;115(6):1080-6. doi: 10.1111/j.1476-5381.1995.tb15921.x.

Abstract
  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.
摘要
  1. 据报道,抗过敏化合物色甘酸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. 我们测试了色甘酸以及一组十种结构相关的植物源黄酮类化合物抑制NDPK反应和透化肥大细胞胞吐过程的能力。选择透化条件(使用基于谷氨酸钠的等渗介质)以确保NDPK活性是诱导Ca(2+)诱导的胞吐作用的重要组成部分,其中ATP是生成GTP所必需的。为了进行比较,我们还测量了GTP-γ-S诱导的胞吐作用的抑制;这在没有ATP的情况下进行,并且绕过了对NDPK活性的需求。3. 我们发现色甘酸不能区分Ca2+和GTP-γ-S诱导的胞吐作用,并且是NDPK活性的弱抑制剂。抑制所有这些功能需要毫摩尔范围内的浓度。相比之下,许多黄酮类化合物在微摩尔范围内的浓度下是有效的。4. 虽然我们无法辨别它们抑制这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抑制Ca(2+)诱导的但不抑制GTP-γ-S诱导的胞吐作用。因此,这些化合物对肥大细胞刺激-反应途径后期阶段的抑制可能是由于对NDPK的抑制以及随之而来的无法生成GTP。

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Inhibition of histamine secretion from mast cells.抑制肥大细胞分泌组胺。
Nature. 1981 Jan 15;289(5794):186-7. doi: 10.1038/289186a0.
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Effect of quercetin on membrane-linked activities.槲皮素对膜相关活性的影响。
Biochem Pharmacol. 1969 Jun;18(6):1495-500. doi: 10.1016/0006-2952(69)90264-0.

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