Clauss W, Dürr J, Skadhauge E, Hörnicke H
Pflugers Arch. 1985 Feb;403(2):186-92. doi: 10.1007/BF00584098.
The effects of pre-treatment in vivo with aldosterone and dexamethasone were investigated on rabbit distal colon. Apical Na-permeability and net sodium transport were measured in vitro. In this epithelium, Na-transport is entirely electrogenic. It can therefore be measured electrically as the fraction of short circuit current which is blockable by amiloride. The epithelia were studied in an Ussing chamber and the electrical values recorded by a computerized digital voltage clamp. Transepithelial parameters, and the transapical membrane parameters (in preparations depolarized from the serosal side) were investigated after treatment with the two hormones. Under transepithelial conditions, aldosterone and dexamethasone stimulated the short circuit current (Isc) from control (17.4 microA/cm2) to a similar degree (86.6 and 93.8 microA/cm2). However, whereas aldosterone did not alter the transepithelial resistance (RT) significantly, dexamethasone reduced RT from 357 to 167 omega X cm2. The stimulation of the potential difference (VT) under control condition (6.6 mV) was therefore significantly different between aldosterone (28.7 mV) and dexamethasone (16 mV). Mucosal amiloride (0.1 mM) inhibited Isc and VT completely under all conditions. Steady state current-voltage relations were obtained by voltage clamping the tissues in "staircase" increments before and after mucosal treatment with amiloride. As measured by the difference between these two states, Na-currents were calculated both for the transepithelial and the transapical condition. Intracellular Na-activity and apical Na-permeability were then calculated by the Nernst and Goldman-Hodgkin-Katz equations. These values were found to be increased after treatment with both hormones. Dexamethasone was a more potent stimulator of both values.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了醛固酮和地塞米松在体内对兔远端结肠进行预处理的效果。体外测量顶端钠通透性和净钠转运。在这种上皮组织中,钠转运完全是电生性的。因此,可以将其作为可被氨氯吡脒阻断的短路电流的一部分进行电测量。在尤斯灌流小室中研究上皮组织,并通过计算机数字电压钳记录电值。在用这两种激素处理后,研究了跨上皮参数和顶端膜参数(在从浆膜侧去极化的制剂中)。在跨上皮条件下,醛固酮和地塞米松将短路电流(Isc)从对照值(17.4微安/平方厘米)刺激到相似程度(86.6和93.8微安/平方厘米)。然而,醛固酮并未显著改变跨上皮电阻(RT),而地塞米松将RT从357降低至167欧姆×平方厘米。因此,在对照条件下(6.6毫伏),醛固酮(28.7毫伏)和地塞米松(16毫伏)对电位差(VT)的刺激存在显著差异。黏膜氨氯吡脒(0.1毫摩尔)在所有条件下均完全抑制Isc和VT。在用氨氯吡脒进行黏膜处理前后,通过以“阶梯”增量对组织进行电压钳制来获得稳态电流-电压关系。根据这两种状态之间的差异进行测量,计算了跨上皮和顶端条件下的钠电流。然后通过能斯特方程和戈德曼-霍奇金- Katz方程计算细胞内钠活性和顶端钠通透性。发现用这两种激素处理后这些值均升高。地塞米松对这两个值的刺激作用更强。(摘要截取自250字)