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螺内酯和诺勃酮对大鼠洋地黄类化合物毒性的影响。

Effect of spironolactone and norbolethone on the toxicity of digitalis compounds in the rat.

作者信息

Selye H, Mécs I, Tamura T

出版信息

Br J Pharmacol. 1969 Oct;37(2):485-8. doi: 10.1111/j.1476-5381.1969.tb10585.x.

Abstract
  1. In the rat, both spironolactone (an antimineralocorticoid) and norbolethone (an anabolic steroid) inhibit the characteristic neuromuscular disturbances and the mortality produced by digitoxin, gitalin, proscillaridin, digoxin and digitalin. The corresponding effects of strophanthin K, ouabain and digitoxigenin could not be prevented.2. It may be concluded that, in our experimental conditions, both spironolactone and norbolethone counteract the toxicity of some, but not all, digitalis compounds tested and that both the protective steroids affect the toxicity of the same digitalis derivatives.3. This antidigitalis effect is not merely a secondary consequence of either antimineralocorticoid or anabolic potency because spironolactone lacks anabolic and norbolethone lacks antimineralocorticoid properties. Indeed, it appears that the ability to antagonize the toxicity of digitalis compounds represents a pharmacological property independent of all known steroid hormone actions, since spironolactone is virtually devoid of these.
摘要
  1. 在大鼠中,螺内酯(一种抗盐皮质激素)和诺勃酮(一种合成代谢类固醇)均可抑制洋地黄毒苷、吉他林、海葱苷、地高辛和洋地黄制剂所引起的特征性神经肌肉紊乱及死亡。毒毛花苷K、哇巴因和洋地黄毒苷元的相应作用则无法被阻止。

  2. 可以得出结论,在我们的实验条件下,螺内酯和诺勃酮均可抵消部分(而非全部)受试洋地黄化合物的毒性,且这两种具有保护作用的类固醇对相同洋地黄衍生物的毒性均有影响。

  3. 这种抗洋地黄作用并非仅仅是抗盐皮质激素或合成代谢效力的次要结果,因为螺内酯缺乏合成代谢特性,而诺勃酮缺乏抗盐皮质激素特性。实际上,似乎拮抗洋地黄化合物毒性的能力代表了一种独立于所有已知类固醇激素作用的药理特性,因为螺内酯几乎不具备这些特性。

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