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首页> 外文期刊>Japanese Journal of Pharmacology >BIOCHEMICAL STUDIES ON MECHANISM OF THE ACTION OF CARDIAC GLYCOSIDES
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BIOCHEMICAL STUDIES ON MECHANISM OF THE ACTION OF CARDIAC GLYCOSIDES

机译:糖苷作用机理的生物化学研究

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References(22) The effect of cardiac glycosides on the metabolism of cardiac muscles has been a leading subject of study from both pharmacological and clinical points of view in association with the clarification of a mechanism of action of cardiac glycosides and of digitalis intoxication. Particularly, the influence of cardiac glycosides on the metabolism of energyrich phosphate compounds, which are regarded as sources of the contractile energy of cardiac muscles, are now studied attentively by many of researchers. Many investigations have been made of the effect of cardiac glycosides on oxidative-phosphorylation in order to inquire into their effect on the production of energy-rich phosphate compounds in cardiac muscles. It was reported that cardiac glycosides produce no effect on oxidativephosphorylation in both heart homogenates ?? Wollenberger (1), Herrmann (2), and Reiter and Barron (3) ?? and mitochondria ?? Langemann (4) and Kimura (5) ?? . Of late, Goldschmidt and Lamprecht (6) have found that k-strophanthin has an uncoupling effect in heart sarcosomes. In the preceding paper the author showed that ouabain and digitoxin only in high concentrations produced a slight uncoupling effect in guinea pig cyclophorases (7).As described above, the general current of opinion in this field is that cardiac glycosides have no effect on oxidative-phosphorylation. Some of workers, however, express the opinion that they have an uncoupling effect. This discrepancy in opinion suggests the necessity of further investigations. In addition to this, most of those workers tended to carry out their experiments with only one of cardiac glycosides and, on the basis of the results obtained, to discuss universally an effect of cardiac glycosides on oxidative-phosphorylation.Therefore, the author attempted to observe an effect of g-strophanthin, desacetyl lanatoside C (cedilanid), digoxin, digitoxin, two kinds of water-soluble cardiac principles extracted from digitalis purpurea at this department, and digitoxigenin on oxidativephosphorylation in pig heart mitochondria, and to draw the general conclusion on the effect of cardiac glycosides on oxidative-phosphorylation in cardiac muscles.
机译:参考文献(22)从药理学和临床角度,结合对强心苷的作用机理和洋地黄中毒的阐明,强心苷对心肌代谢的影响一直是研究的主要课题。尤其是,现在许多研究人员都在集中研究强心苷对高能磷酸盐化合物代谢的影响,高能磷酸盐化合物被认为是心肌收缩能量的来源。为了调查心肌苷对心肌中富含能量的磷酸盐化合物的产生的影响,已经进行了许多关于心肌苷的作用的研究。据报道,强心苷对两种心脏匀浆中的氧化磷酸化都没有作用。 Wollenberger(1),Herrmann(2)和Reiter和Barron(3)?和线粒体??朗格曼(4)和木村(5)?? 。最近,Goldschmidt和Lamprecht(6)发现,k-卵磷脂在心脏肌小体中具有解偶联作用。在先前的论文中,作者表明哇巴因和洋地黄毒蛋白仅在高浓度时对豚鼠环氧化酶产生轻微的解偶联作用(7)。如上所述,该领域的普遍观点是强心苷对氧化-氧化酶没有影响。磷酸化。但是,有些工人表示他们具有解耦作用。这种观点上的差异表明有必要进行进一步调查。除此之外,大多数工人倾向于只使用一种强心苷进行实验,并根据获得的结果广泛讨论强心苷对氧化磷酸化的影响。观察该部门的g-链花黄素,去乙酰基羊毛脂苷C(cedilanid),地高辛,洋地黄毒苷,两种洋地黄提取物的水溶性心脏原理和洋地黄毒苷对猪心脏线粒体氧化磷酸化的影响,并得出一般结论对强心苷对心肌氧化磷酸化的影响。

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