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强心甾体的研究。III. 不同强心苷在不同细胞外钾浓度下对收缩性和节律性的影响特征

Studies on cardioactive steroids. III. Characterization of different cardiac glycosides by their effects on contractility and rhythmicity at different extracellular potassium concentrations.

作者信息

Haustein K O, Graumann G, Stephan B

出版信息

Acta Biol Med Ger. 1975;34(6):1065-73.

PMID:1199622
Abstract

In the present paper, the naturally occurring glycosides digitoxin, gitoxin, 16-acetyl-gitoxin, digoxin, cymarol, ouabain, and proscillaridin, and the semi-synthetic 16-epi-gitoxin and 16-acetyl-16-epi-gitoxin are investigated as to their inotropic action and their effects on rhythmicity at isolated spontaneously beating atria of the guinea-pig heart in dependence on the variation of the potassium concentration of the nutritive fluid ([K+]0: 1.34, 2.68, and 5.36 mM resp.). The major results are as follows. 1. Effects of raising [K+]0 from 1.34 to 2.68 mM: The range of the inotropically effective concentrations as well as the size of the maximum inotropic action are more or less strongly improved with all glycosides. The glycoside concentrations required to get inotropic maximum had to be increased to a high degree with proscillaridin and digoxin. The mean arrhythmia percentage occurring at the inotropic maximum is either decreased (gitoxin, 16-epi-gitoxin, digoxin, proscillaridin), unchanged (digitoxin, 16-acetyl-16-epi-gitoxin) or even increased (16-acetyl-gitoxin, cymarol, ouabain). The inotropic value is improved to a high extent with gitoxin only. 2. Effect of raising [K+]0 from 2.68 to 5.36 mM: The range of the inotropically effective concentrations is extended (digitoxin and cymarol) or diminished (proscillaridin), but remains essentially unchanged with most glycosides. The size of the maximum inotropic effect is increased with digoxin, ouabain and 16-epi-gitoxin, but decreased significantly with digitoxin and proscillaridin. The glycoside concentrations required to produce the inotropic maximum are essentially unchanged with the exception of 16-epi-gitoxin, 16-acetyl-gitoxin and ouabain. The mean arrhythmia percentage at the maximum inotropic effect is dramatically reduced with digoxin, cymarol and proscillaridin. The inotropic value is improved with all glycosides except digitoxin. 3. Evaluation of the various glycosides: When judged on the basis of the range of inotropically effective concentrations, the maximum inotropic effect, the mean arrhythmia percentage at the inotropic maximum and the inotropic value, the best first three glycosides include 16-epi-gitoxin and digoxin. 16-Epi-gitoxin and its 16-acetate show that most favourable relationship between the effect on contractility and rhythmicity. The cause of the differential actions of the structurally-different glycosides on contractility and rhythmicity is hypothesized to be due to divergences in structure and/or conformation of the receptor areas of (Na+ + K+)-ATPase of contractile and excitable cells.

摘要

在本论文中,对天然存在的糖苷地高辛、吉托辛、16-乙酰基吉托辛、洋地黄毒苷、 cymarol、哇巴因和海葱苷A,以及半合成的16-表吉托辛和16-乙酰基-16-表吉托辛,就它们对豚鼠心脏离体自发跳动心房的变力作用及其对节律性的影响进行了研究,该研究依赖于营养液中钾浓度的变化([K+]0分别为1.34、2.68和5.36 mM)。主要结果如下。1. 将[K+]0从1.34 mM提高到2.68 mM的影响:所有糖苷的变力有效浓度范围以及最大变力作用的大小或多或少都有显著改善。使用海葱苷A和地高辛时,达到变力最大值所需的糖苷浓度必须大幅增加。在变力最大值时出现的平均心律失常百分比要么降低(吉托辛、16-表吉托辛、地高辛、海葱苷A),不变(洋地黄毒苷、16-乙酰基-16-表吉托辛),甚至增加(16-乙酰基吉托辛、cymarol、哇巴因)。仅吉托辛的变力值有很大程度的提高。2. 将[K+]0从2.68 mM提高到5.36 mM的影响:变力有效浓度范围扩大(洋地黄毒苷和cymarol)或缩小(海葱苷A),但大多数糖苷基本保持不变。最大变力效应的大小在使用地高辛、哇巴因和16-表吉托辛时增加,但在使用洋地黄毒苷和海葱苷A时显著降低。产生变力最大值所需的糖苷浓度除16-表吉托辛、16-乙酰基吉托辛和哇巴因外基本不变。在最大变力效应时的平均心律失常百分比在使用地高辛、cymarol和海葱苷A时显著降低。除洋地黄毒苷外,所有糖苷的变力值均有所提高。3. 对各种糖苷的评估:根据变力有效浓度范围、最大变力效应、变力最大值时的平均心律失常百分比和变力值来判断,最好的三种糖苷包括16-表吉托辛和地高辛。16-表吉托辛及其16-乙酸酯在对收缩性和节律性的影响之间显示出最有利的关系。推测结构不同的糖苷对收缩性和节律性产生不同作用的原因是由于收缩性和兴奋性细胞的(Na+ + K+)-ATP酶受体区域的结构和/或构象存在差异。

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