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泼尼松龙-3,20-双胍腙:钠钾ATP酶抑制作用和正性肌力作用。

Prednisolone-3, 20-bisguanylhydrazone: Na+, K+-ATPase inhibition and positive inotropic action.

作者信息

Yamamoto S, Akera T, Brody T M

出版信息

Eur J Pharmacol. 1978 May 15;49(2):121-32. doi: 10.1016/0014-2999(78)90068-7.

Abstract

The relationship between two known actions of prednisolone-3, 20-bisguanylhydrazone (PBGH); Na+, K+-ATPase inhibition and positive inotropic effects, was investigated. In electrically driven left atrial preparations of guinea pig heart, the positive inotropic action of PBGH was not affected by beta-adrenergic or histamine antagonists. Pretreatment of animals with reserpine also failed to influence the positive inotropic action of PBGH. Inotropic concentrations of PBGH inhibited Na+, K+-ATPase and the ATP-dependent binding of (3/)-ouabain to Na+, K+- ATPase preparations in vitro. Additionally, ouabain-sensitive 86Rb uptake, an estimate of sodium pump activity was inhibited when sodium-loaded ventricular slices were obtained from Langendorff preparations at the peak inotropic response to PBGH. Guinea pig heart was highly sensitive to PBGH to the positive inotropic action, the inhibition of Na+, K+ -ATPase and (3H)-ouabain binding, whereas rat, rabbit and dog heart were markedly less sensitive. These findings suggest that the mechanism of the positive inotropic action of PBGH resembles that of ouabain and probably involves Na+, K+ -ATPase inhibition, although the mode of interaction of these steroids with Na+, K+ -ATPase may be different.

摘要

研究了泼尼松龙-3,20-双胍腙(PBGH)的两种已知作用之间的关系;抑制钠钾ATP酶和正性肌力作用。在豚鼠心脏的电驱动左心房标本中,PBGH的正性肌力作用不受β-肾上腺素能拮抗剂或组胺拮抗剂的影响。用利血平预处理动物也未能影响PBGH的正性肌力作用。在体外,PBGH的正性肌力浓度抑制钠钾ATP酶以及(3H)哇巴因与钠钾ATP酶制剂的ATP依赖性结合。此外,当从Langendorff标本中获取钠负荷心室切片,处于对PBGH的正性肌力反应峰值时,哇巴因敏感的86Rb摄取(一种钠泵活性的估计指标)受到抑制。豚鼠心脏对PBGH的正性肌力作用、对钠钾ATP酶的抑制以及(3H)哇巴因结合高度敏感,而大鼠、兔和犬心脏的敏感性则明显较低。这些发现表明,PBGH的正性肌力作用机制类似于哇巴因,可能涉及抑制钠钾ATP酶,尽管这些甾体与钠钾ATP酶的相互作用方式可能不同。

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