...
首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Neomycin inhibits catecholamine secretion by blocking nicotinic acetylcholine receptors in bovine adrenal chromaffin cells.
【24h】

Neomycin inhibits catecholamine secretion by blocking nicotinic acetylcholine receptors in bovine adrenal chromaffin cells.

机译:新霉素通过阻断牛肾上腺嗜铬细胞中的烟碱乙酰胆碱受体来抑制儿茶酚胺的分泌。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

We investigated the effects of neomycin on nicotinic acetylcholine receptor-induced responses in bovine adrenal chromaffin cells. Neomycin inhibited the nicotinic agonist dimethylphenylpiperazinium iodide (DMPP)-induced norepinephrine secretion in a concentration-dependent manner. Neomycin had also an inhibitory effect on the DMPP-induced increase in cytosolic Ca++ concentration ([Ca++]i). This effect was further confirmed by inhibition of the DMPP-induced fluorescence quenching of fura-2 upon Mn++ entry. Under the same conditions, however, neomycin did not change the bradykinin-induced [Ca++]i increase, which follows the downstream signal of phospholipase C phospholipase C activation in this cell. The inhibitory effect of neomycin on the DMPP-induced [Ca++]i increase was apparent when the neomycin treatment was performed simultaneously with DMPP, suggesting a direct action on the nicotinic receptor. The direct inhibitory action of neomycin on the nicotinic receptor was also evident when neomycin inhibited the DMPP-induced cytosolic Ca++ increase, which is not affected by nifedipine nor omega-conotoxin MVIIC, and the cytosolic Na+ increase, which is not affected by tetrodotoxin. In addition, we observed that neomycin inhibited the binding of nicotine to the acetylcholine receptor in a noncompetitive manner. The data suggest that neomycin inhibits the nicotinic acetylcholine receptor directly, which results in blockage of the nicotinic receptor-mediated signaling without involvement of phospholipase C.
机译:我们调查了新霉素对牛肾上腺嗜铬细胞烟碱型乙酰胆碱受体诱导的反应的影响。新霉素以浓度依赖的方式抑制烟碱型激动剂二甲基二甲基碘化哌嗪(DMPP)诱导的去甲肾上腺素分泌。新霉素还对DMPP诱导的胞质Ca ++浓度([Ca ++] i)升高具有抑制作用。 Mn ++进入后,通过抑制DMPP诱导的fura-2荧光猝灭进一步证实了该效果。然而,在相同条件下,新霉素并没有改变缓激肽诱导的[Ca ++] i的增加,这是在该细胞中跟随磷脂酶C磷脂酶C激活的下游信号而发生的。当新霉素与DMPP同时进行时,新霉素对DMPP诱导的[Ca ++] i增加的抑制作用是显而易见的,表明对烟碱受体具有直接作用。当新霉素抑制DMPP诱导的胞质Ca ++的增加而不受硝苯地平或ω-芋螺毒素MVIIC的影响时,新霉素对烟碱受体的直接抑制作用也很明显;而胞质Na +的增加却不受河豚毒素的影响。此外,我们观察到新霉素以非竞争性方式抑制尼古丁与乙酰胆碱受体的结合。数据表明,新霉素直接抑制烟碱型乙酰胆碱受体,从而导致烟碱样受体介导的信号传导受阻,而没有磷脂酶C参与。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号