Cox M, Guzzo J, Shook A, Huber G, Singer I
Biochim Biophys Acta. 1979 Mar 23;552(1):162-8. doi: 10.1016/0005-2736(79)90254-2.
The effect of oxytetracycline and demethylchlortetracycline on aldosterone- and insulin-mediated Na+ transport (short-circuit current) were examined in toad urinary bladders mounted in modified Ussing chambers. Oxytetracycline had little or no effect on either basal or aldosterone-mediated Na+ transport. In contrast, demethylchlortetracycline markedly inhibited both basal and aldosterone-mediated Na+ transport. Furthermore, demethylchlortetracycline inhibited the aldosterone response significantly out of proportion to its effects on basal Na+ transport. Neither of the drugs had an effect on insulin-mediated Na+ transport. Consequently, the natriuresis observed in certain patients treated with demethylchlortetracyline may be related to drug-induced renal resistance to the effects of aldosterone.
在安装于改良尤斯灌流小室中的蟾蜍膀胱上,研究了土霉素和去甲金霉素对醛固酮和胰岛素介导的Na⁺转运(短路电流)的影响。土霉素对基础或醛固酮介导的Na⁺转运几乎没有影响或无影响。相比之下,去甲金霉素显著抑制基础和醛固酮介导的Na⁺转运。此外,去甲金霉素对醛固酮反应的抑制作用与其对基础Na⁺转运的影响相比明显不成比例。两种药物对胰岛素介导的Na⁺转运均无影响。因此,在用去甲金霉素治疗的某些患者中观察到的利钠作用可能与药物诱导的肾脏对醛固酮作用的抵抗有关。