Baron D N, Green R J
Br J Clin Pharmacol. 1986 Jan;21(1):27-34. doi: 10.1111/j.1365-2125.1986.tb02819.x.
We have studied the in vitro short-term effects of aldosterone (1.0-1000 nmol l-1), cortisol (0.5-5.0 mumol l-1), fludrocortisone (1.0-10 nmol l-1) and carbenoxolone (0.5-3 mmol l-1) on 86rubidium influx (a model for potassium), 22sodium efflux, and [3H]-ouabain binding capacity in intact human leucocytes. No effect of aldosterone (at concentrations present in Conn's syndrome) or fludrocortisone could be demonstrated on cation fluxes or [3H]-ouabain binding compared to controls. No significant effect of cortisol, at concentrations either physiological or present in Cushing's syndrome, could be demonstrated on cation fluxes or [3H]-ouabain binding compared to controls. Carbenoxolone significantly increased 86Rb influx and 22Na efflux at concentrations known to cause hypokalaemia in man. The effect was not blocked by propranolol. No effect could be demonstrated for [3H]-ouabain binding.
我们研究了醛固酮(1.0 - 1000纳摩尔/升)、皮质醇(0.5 - 5.0微摩尔/升)、氟氢可的松(1.0 - 10纳摩尔/升)和生胃酮(0.5 - 3毫摩尔/升)对完整人白细胞中86铷内流(钾的一种模型)、22钠外流以及[3H] - 哇巴因结合能力的体外短期影响。与对照组相比,未发现醛固酮(在原发性醛固酮增多症中的浓度)或氟氢可的松对阳离子通量或[3H] - 哇巴因结合有影响。与对照组相比,无论是生理浓度还是库欣综合征中的浓度,皮质醇对阳离子通量或[3H] - 哇巴因结合均无显著影响。生胃酮在已知可导致人体低钾血症的浓度下,显著增加了86Rb内流和22Na外流。该作用未被普萘洛尔阻断。对于[3H] - 哇巴因结合未发现有影响。