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首页> 外文期刊>Japanese Journal of Pharmacology >THE RELATION OF ENDOGENOUS CATECHOLAMINE TO THE ACTION OF STROPHANTHIN-G ON ATRIAL CONTRACTIONS OF RABBITS AND GUINEA-PIGS
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THE RELATION OF ENDOGENOUS CATECHOLAMINE TO THE ACTION OF STROPHANTHIN-G ON ATRIAL CONTRACTIONS OF RABBITS AND GUINEA-PIGS

机译:内源性儿茶酚胺与链霉菌素-G对家兔和豚鼠心房收缩的作用

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References(18) Cited-By(1) It is generally accepted that the remarkable effect of digitalis on heart falure is caused by its specific action on the contractile mechanism of the heart muscle. The mode of pharmacological action of digitalis glycosides have been studied by many investigators, and it has been claimed that digitalis might have some influence on the energy production mechanism of the heart. The metabolic pathway of heart muscle contraction is not positively influenced by digitalis glycosides, though they do bring about an increase in contractile force [Wollenberger (1), Bing et al. (2, 3)]. Szent-Györgyi (4) reported that actomyosin is influenced by ATP and inorganic ions but not by digitalis. However, it has been reported that ATP-ase activity in the muscle cell membrane of rat hearts is promoted by digitalis in therapeutic dosage [Repke (5)]. On the other hand, Hadju and Szent-Györgyi (6) reported that the decrease in K-ion concentrations in the heart muscle induces an increase in contraction, and digitalis augments an efflux of the K-ions in the heart muscle. On contrary, Klaus et al. (7) reported that the influx of 42K-ions into the heart muscle cells was increased by digitalis in therapeutic doses. The cardiac action of digitalis has been explained by some investigators as that of an autonomic drug due to the result that digitalis increases adrenaline action [Donielpolu (8), Fujita (9)]. Our experiment were carried out to discover the relation of digitalis action to endogenous catecholamine mobilization in the atria from the standpoint that the catecholamines in heart muscle are mostly in a bound form and the contractile function of heart is controlled by the released catecholamine available.
机译:参考文献(18)Cited-By(1)人们普遍认为,洋地黄对心衰的显着影响是由于其对心肌收缩机制的特定作用所致。许多研究者已经研究了洋地黄苷的药理作用模式,并声称洋地黄可能对心脏的能量产生机制有一定影响。尽管洋地黄苷确实会增加收缩力,但心肌收缩的代谢途径并未受到积极影响[Wollenberger(1),Bing等。 (2,3)]。 Szent-Györgyi(4)报告说,肌动球蛋白受ATP和无机离子的影响,但不受洋地黄的影响。然而,据报道,洋地黄以治疗剂量促进大鼠心脏肌肉细胞膜中的ATP酶活性[Repke(5)]。另一方面,Hadju和Szent-Györgyi(6)报告说,心肌中K离子浓度的降低会引起收缩的增加,而洋地黄则会增加心肌中K离子的流出。相反,克劳斯等。 (7)报道,洋地黄以治疗剂量增加了42K离子向心肌细胞的流入。由于洋地黄增加肾上腺素的作用,一些研究者将洋地黄的心脏作用解释为一种自主神经药物[Donielpolu(8),Fujita(9)]。从心脏中的儿茶酚胺大部分处于束缚状态并且心脏的收缩功能受到释放的儿茶酚胺的控制的观点出发,我们进行了实验以发现洋地黄作用与心房内源性儿茶酚胺的动员之间的关系。

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