Jorkasky D, Cox M, Feldman G M
Am J Physiol. 1985 Apr;248(4 Pt 1):G424-31. doi: 10.1152/ajpgi.1985.248.4.G424.
We studied rat distal colon during in vitro incubation with aldosterone and dexamethasone. Both hormones caused short-circuit current (Isc) to increase with a latency period of approximately 3 h. At the 7th h of incubation, control colons had a Isc of 72 +/- 8 microA . cm-2 while tissues incubated with 10(-5) M aldosterone and 10(-8) M dexamethasone, the respective maximal stimulatory concentrations, had similarly increased Isc, 211 +/- 21 and 185 +/- 18 microA . cm-2, respectively. The increase in Isc induced by steroids reflected increased net sodium transport: control, 3.4 +/- 0.8; aldosterone, 6.7 +/- 0.7 (P less than 0.05); and dexamethasone, 7.5 +/- 1.0 mueq . h-1 . cm-2 (P less than 0.025). Spironolactone inhibited the response to both steroids, but the molar ratio of antagonist to agonist was less for aldosterone (approximately 5,000:1) than for dexamethasone (approximately 50,000:1). Amiloride inhibited a greater fraction of aldosterone-induced Isc (0.70 +/- 0.07) than that of dexamethasone (0.37 +/- 0.07; P less than 0.025). The latter value was similar to the effect of amiloride on control tissues (0.35 +/- 0.04). These data provide evidence that the cellular mechanisms by which aldosterone and dexamethasone induce Na+ transport are different.
我们在体外培养条件下,用醛固酮和地塞米松处理大鼠远端结肠进行研究。两种激素均使短路电流(Isc)增加,潜伏期约为3小时。在培养的第7小时,对照结肠的Isc为72±8微安·厘米⁻²,而用10⁻⁵M醛固酮和10⁻⁸M地塞米松(各自的最大刺激浓度)处理的组织,Isc同样增加,分别为211±21和185±18微安·厘米⁻²。类固醇诱导的Isc增加反映了钠净转运的增加:对照为3.4±0.8;醛固酮为6.7±0.7(P<0.05);地塞米松为7.5±1.0微当量·小时⁻¹·厘米⁻²(P<0.025)。螺内酯抑制了对两种类固醇的反应,但醛固酮的拮抗剂与激动剂的摩尔比(约5000∶1)低于地塞米松(约50000∶1)。氨氯地平抑制醛固酮诱导的Isc的比例(0.70±0.07)大于抑制地塞米松诱导的Isc的比例(0.37±0.07;P<0.025)。后一数值与氨氯地平对对照组织的作用(0.35±0.04)相似。这些数据提供了证据,表明醛固酮和地塞米松诱导Na⁺转运的细胞机制不同。