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首页> 外文期刊>Japanese Journal of Pharmacology >STUDIES ON THE MECHANISMS OF THE INHIBITORY EFFECT OF N-5' ON HISTAMINE RELEASE FROM RAT PERITONEAL EXUDATE CELLS
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STUDIES ON THE MECHANISMS OF THE INHIBITORY EFFECT OF N-5' ON HISTAMINE RELEASE FROM RAT PERITONEAL EXUDATE CELLS

机译:N-5'对大鼠腹膜渗出液中组胺释放的抑制作用机理研究

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References(21) Cited-By(13) To investigate the mechanisms for the inhibition of IgE-mediated histamine release from rat peritoneal exudate cells (PEC) by N-5', we studied the relation between the inhibitory effect of N-5' on histamine release and the intracellular levels of adenine nucleotides such as ATP and cAMP. Evident histamine release was induced by the addition of specific antigen to rat PEC sensitized with IgE antiserum in vitro, and the release showed a maximum 30 sec after the antigen challenge. In the same time course as the histamine release, the intracellular levels of ATP and cAMP decreased. N-5' significantly inhibited the histamine release and a decrease in ATP level as a result of the antigen-antibody reaction. A decrease in cAMP level showed a tendency to be sup pressed by N-5'. Antigen-induced 14CO2 production for 6-14C-glucose in the sensitized PEC was 3 times that seen in the case without antigen. N-5' dramatically suppressed the accerelation in the production of 14CO2. Differing from the action of papaverine, the inhibitory effect of N-5' on the IgE-mediated histamine release from rat PEC was identical both in the presence or in the absence of glucose. N-5' scarcely affected the ATP level in the non-sensitized PEC in the glucose-free medium. On the other hand, N-5' inhibited the activity of Na+, K+-ATPase, one of the ATP-consuming enzymes, in a dose dependent fashion. From these results, it is presumed that the suppression of ATP utilization through the inhibition of Na+, K+-ATPase activity is involved in the inhibition of histamine release by N-5'. The relation between the inhibitory effect of N-5' on histamine release and both nucleotides was also discussed.
机译:参考文献(21)By-By(13)为了研究N-5'抑制IgE介导的组胺从大鼠腹膜渗出细胞(PEC)释放的机制,我们研究了N-5'抑制作用之间的关系。组胺释放和腺嘌呤核苷酸(如ATP和cAMP)的细胞内水平。通过向体外用IgE抗血清敏化的大鼠PEC添加特异性抗原诱导明显的组胺释放,并且在抗原激发后30 s内释放最多。在与组胺释放相同的时间过程中,ATP和cAMP的细胞内水平下降。由于抗原-抗体反应,N-5'显着抑制了组胺的释放和ATP水平的降低。 cAMP水平的降低表明被N-5'抑制的趋势。致敏的PEC中抗原诱导的14-14C-葡萄糖的14CO2产生是没有抗原的情况下的3倍。 N-5'大大抑制了14CO2生产中的加速作用。与罂粟碱的作用不同,在有或没有葡萄糖的情况下,N-5'对大鼠PEC中IgE介导的组胺释放的抑制作用是相同的。在不含葡萄糖的培养基中,N-5'几乎不会影响非致敏PEC中的ATP水平。另一方面,N-5'以剂量依赖的方式抑制Na +,K + -ATPase(一种消耗ATP的酶)的活性。根据这些结果,推测通过抑制Na +,K + -ATP酶活性来抑制ATP利用与N-5'释放组胺有关。还讨论了N-5'对组胺释放的抑制作用与两个核苷酸之间的关系。

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