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醛固酮导致的内皮细胞肿胀

Endothelial cell swelling by aldosterone.

作者信息

Oberleithner H, Schneider S W, Albermann L, Hillebrand U, Ludwig T, Riethmüller C, Shahin V, Schäfer C, Schillers H

机构信息

Institute of Physiology I, Nanolab, University of Münster, Robert-Koch-Str. 27a, D-48149 Münster, Germany.

出版信息

J Membr Biol. 2003 Dec 1;196(3):163-72. doi: 10.1007/s00239-003-0635-6.

Abstract

There is accumulating evidence that mineralocorticoids not only act on kidney but also on the cardiovascular system. We investigated the response of human umbilical venous endothelial cells (HUVECs) to aldosterone at a time scale of 20 minutes in absence and presence of the aldosterone antagonist spironolactone or other transport inhibitors. We applied atomic force microscopy (AFM), which measures cell volume and volume shifts between cytosol and cell nucleus. We observed an immediate cell volume increase (about 10%) approximately 1 min after addition of aldosterone (0.1 micromol/l), approaching a maximum (about 18%) 10 min after aldosterone treatment. Cell volume returned to normal 20 min after hormone exposure. Spironolactone (1 micromol/l) or amiloride (1 micromol/l) prevented the late aldosterone-induced volume changes but not the immediate change observed 1 min after hormone exposure. AFM revealed nuclear swelling 5 min after aldosterone addition, followed by nuclear shrinkage 15 min later. The Na(+)/H(+) exchange blocker cariporide (10 micromol/l) was ineffective. We conclude: (i). Aldosterone induces immediate (1 min) swelling independently of plasma membrane Na(+) channels and intracellular mineralocorticoid receptors followed by late mineralocorticoid receptor- and Na(+)-channel-dependent swelling. (ii). Intracellular macromolecule shifts cause the changes in cell volume. (iii). Both amiloride and spironolactone may be useful for medical applications to prevent aldosterone-induced vasculopathies.

摘要

越来越多的证据表明,盐皮质激素不仅作用于肾脏,还作用于心血管系统。我们研究了在不存在和存在醛固酮拮抗剂螺内酯或其他转运抑制剂的情况下,人脐静脉内皮细胞(HUVECs)在20分钟时间尺度内对醛固酮的反应。我们应用了原子力显微镜(AFM),它可以测量细胞体积以及细胞质和细胞核之间的体积变化。我们观察到,添加醛固酮(0.1微摩尔/升)后约1分钟,细胞体积立即增加(约10%),醛固酮处理10分钟后接近最大值(约18%)。激素暴露20分钟后细胞体积恢复正常。螺内酯(1微摩尔/升)或阿米洛利(1微摩尔/升)可防止醛固酮后期诱导的体积变化,但不能防止激素暴露1分钟后观察到的即时变化。AFM显示添加醛固酮5分钟后细胞核肿胀,随后15分钟后细胞核收缩。Na(+)/H(+)交换阻滞剂卡里波罗德(10微摩尔/升)无效。我们得出以下结论:(i)。醛固酮诱导即时(1分钟)肿胀,与质膜Na(+)通道和细胞内盐皮质激素受体无关,随后是盐皮质激素受体和Na(+)通道依赖性肿胀。(ii)。细胞内大分子移位导致细胞体积变化。(iii)。阿米洛利和螺内酯在预防醛固酮诱导的血管病变的医学应用中可能都有用。

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