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氨氯吡咪和哇巴因对豚鼠盲肠带中细胞内镁离子调节机制的影响

Mechanisms of intracellular Mg2+ regulation affected by amiloride and ouabain in the guinea-pig taenia caeci.

作者信息

Nakayama S, Nomura H

机构信息

Department of Physiology, School of Medicine, Nagoya University, Japan.

出版信息

J Physiol. 1995 Oct 1;488 ( Pt 1)(Pt 1):1-12. doi: 10.1113/jphysiol.1995.sp020941.

Abstract
  1. The effects of amiloride and ouabain on the regulation of the intracellular, free Mg2+ concentration ([Mg2+]i) were investigated in the taenia isolated from the guinea-pig caecum, using nuclear magnetic resonance (NMR) techniques. 2. [Mg2+]i were mainly estimated from the separation of the alpha- and beta-ATP peaks observed in 31P NMR spectra. In normal (physiological) and nominally Ca(2+)-free solutions, [Mg2+]i was approximately 0.3-0.4 mM. Application of either amiloride or ouabain in Ca(2+)-free solutions significantly increased [Mg2+]i, with only a small change in ATP content. Washout of the drugs reversed the changes in [Mg2+]i. 3. Changes in pHi were estimated from: (1) the chemical shift of phosphoethanolamine, and (2) solving two relational equations of pHi and [Mg2+]i obtained from the beta- and gamma-ATP peaks. Both estimations revealed some intracellular alkalosis during application of these two drugs. After correction for pHi, a significant increase in [Mg2+]i was still obtained 150 min after application of either drug. 4. In the presence of amiloride, simultaneous removal of extracellular Mg2+ and Ca2+ significantly depleted intracellular Mg2+. This result suggests the presence of an amiloride-insensitive (or less sensitive) pathway which passively transports Mg2+ across the plasma membrane. 5. The intracellular Rb+ concentration was monitored as an index of Na(+)-K+ pump activity, using 87Rb NMR. In Ca(2+)-free solutions containing 5 mM Rb+, the intracellular Rb+ concentration was hardly changed by amiloride, but was depleted by additional applications of ouabain. Wash-out of ouabain restored the intracellular Rb+ in the presence of amiloride. 6. These results are consistent with the presence of Na(+)-Mg2+ exchange as an effective Mg(2+)-extruding mechanism in smooth muscle. Although many other factors may cause changes in [Mg2+]i, it seems likely that amiloride directly inhibits the Na(+)-Mg2+ exchanger, whilst ouabain does so indirectly through reduction of the Na+ gradient across the plasma membrane.
摘要
  1. 采用核磁共振(NMR)技术,研究了氨氯吡脒和哇巴因对豚鼠盲肠分离出的条带中细胞内游离镁离子浓度([Mg2+]i)调节的影响。2. [Mg2+]i主要通过31P NMR谱中观察到的α-和β-ATP峰的分离来估算。在正常(生理)溶液和名义上无Ca(2+)的溶液中,[Mg2+]i约为0.3 - 0.4 mM。在无Ca(2+)溶液中应用氨氯吡脒或哇巴因均可显著增加[Mg2+]i,而ATP含量仅有微小变化。洗脱药物可逆转[Mg2+]i的变化。3. pHi的变化通过以下方式估算:(1)磷酸乙醇胺的化学位移,以及(2)求解从β-和γ-ATP峰获得的pHi和[Mg2+]i的两个关系式。两种估算均显示在应用这两种药物期间存在一些细胞内碱中毒。校正pHi后,应用任何一种药物150分钟后仍可显著增加[Mg2+]i。4. 在存在氨氯吡脒的情况下,同时去除细胞外Mg2+和Ca2+可显著耗尽细胞内Mg2+。该结果表明存在一条对氨氯吡脒不敏感(或较不敏感)的途径,该途径可被动地将Mg2+转运穿过质膜。5. 使用87Rb NMR监测细胞内Rb+浓度作为Na(+)-K+泵活性的指标。在含有5 mM Rb+的无Ca(2+)溶液中,氨氯吡脒几乎不改变细胞内Rb+浓度,但额外应用哇巴因会使其耗尽。在存在氨氯吡脒的情况下,洗脱哇巴因可恢复细胞内Rb+。6. 这些结果与Na(+)-Mg2+交换作为平滑肌中一种有效的Mg(2+)排出机制的存在相一致。尽管许多其他因素可能导致[Mg2+]i的变化,但氨氯吡脒似乎直接抑制Na(+)-Mg2+交换体,而哇巴因则通过降低质膜两侧的Na+梯度间接抑制。

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