Suppr超能文献

多形核白细胞作为钙和镁依赖性细胞活化的模型。钙通道阻滞剂的作用。

Polymorphonuclear leucocytes as a model of Ca++ and Mg++-dependent cellular activation. Effect of calcium entry blockers.

作者信息

Di Perri T, Laghi Pasini F, Pasqui A L, Ceccatelli L, Orrico A, Capecchi P L

出版信息

Int J Tissue React. 1985;7(4):291-301.

PMID:3934096
Abstract

Flunarizine inhibited FMLP- and A23187-induced aggregation, enzyme release and O2- generation from human PMN as a function of its concentration. A23187-dependent PMN aggregation was also studied in media devoid of Ca++ or Mg++. Flunarizine (2.4 X 10(-5)M) significantly affected not only Ca++-supported but also Mg++-sustained PMN aggregation. The inhibiting effect of the drug was reversed by increasing the level of Ca++ (1.2 mM) or Mg++ (2 mM). Nifedipine, another Ca++-entry blocker, was shown to inhibit enzyme release and O2- generation induced by FMLP and A23187 as a function of its concentration, but only slightly affected PMN aggregation at very high concentration (10(-4)M). A role for flunarizine as a specific Mg++-entry blocker is suggested.

摘要

氟桂利嗪抑制了FMLP和A23187诱导的人中性粒细胞的聚集、酶释放及超氧阴离子生成,且呈浓度依赖性。还在无钙离子或镁离子的培养基中研究了A23187依赖性中性粒细胞聚集。氟桂利嗪(2.4×10⁻⁵M)不仅显著影响钙离子支持的中性粒细胞聚集,也显著影响镁离子维持的中性粒细胞聚集。增加钙离子(1.2 mM)或镁离子(2 mM)水平可逆转该药物的抑制作用。硝苯地平,另一种钙离子内流阻滞剂,也呈浓度依赖性地抑制FMLP和A23187诱导的酶释放及超氧阴离子生成,但仅在非常高的浓度(10⁻⁴M)时对中性粒细胞聚集有轻微影响。提示氟桂利嗪具有特异性镁离子内流阻滞剂的作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验