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Variations in potassium concentration modify the inhibitory effect of lorcainide on myocardial Na(+)-K(+)-ATPase activity.钾离子浓度的变化会改变劳卡尼对心肌钠钾ATP酶活性的抑制作用。
Br J Pharmacol. 1991 Dec;104(4):793-6. doi: 10.1111/j.1476-5381.1991.tb12508.x.
2
Influence of lorcainide on microsomal Na+, K(+)-ATPase in guinea-pig isolated heart preparations.劳卡尼对豚鼠离体心脏制剂微粒体Na⁺、K⁺ -ATP酶的影响。
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Effects of temperature, Na and K concentration and quinidine on transmembrane flux of K42 and incidence of atrial fibrillation.温度、钠和钾浓度以及奎尼丁对K42跨膜通量和心房颤动发生率的影响。
Circ Res. 1958 Jul;6(4):516-21. doi: 10.1161/01.res.6.4.516.
2
Digitalis glycosides: mechanisms and manifestations of toxicity. Part II.洋地黄苷:毒性机制与表现。第二部分。
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Digitalis-sensitive Na+, K+-ATPase: lack of a direct catecholamine-mediated stimulation in bovine myocardial tissue.洋地黄敏感的钠钾ATP酶:牛心肌组织中缺乏儿茶酚胺介导的直接刺激作用
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Effects of chronic depletion of potassium and magnesium upon the action of acetylstrophanthidin on the heart.钾和镁长期缺乏对乙酰毒毛旋花子苷作用于心脏的影响。
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Correlation of antiarrhythmic effects of diphenylhydantoin with digoxin-induced changes in myocardial contractility, sodium-potassium adenosine triphosphatase activity, and potassium efflux.苯妥英钠抗心律失常作用与地高辛诱导的心肌收缩性、钠钾三磷酸腺苷酶活性及钾外流变化的相关性。
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Serum potassium concentration as a risk factor of ventricular arrhythmias early in acute myocardial infarction.血清钾浓度作为急性心肌梗死早期室性心律失常的危险因素。
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9
Pharmacologic causes of arrhythmogenic actions of antiarrhythmic drugs.抗心律失常药物致心律失常作用的药理学原因。
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10
Arrhythmogenic interaction between low potassium and ouabain in isolated guinea-pig ventricular myocytes.低钾与哇巴因在豚鼠离体心室肌细胞中的致心律失常相互作用。
J Physiol. 1988 Jun;400:113-34. doi: 10.1113/jphysiol.1988.sp017114.

钾离子浓度的变化会改变劳卡尼对心肌钠钾ATP酶活性的抑制作用。

Variations in potassium concentration modify the inhibitory effect of lorcainide on myocardial Na(+)-K(+)-ATPase activity.

作者信息

Almotrefi A A, Dzimiri N

机构信息

Department of Pharmacology, King Saud University, Riyadh, Saudi Arabia.

出版信息

Br J Pharmacol. 1991 Dec;104(4):793-6. doi: 10.1111/j.1476-5381.1991.tb12508.x.

DOI:10.1111/j.1476-5381.1991.tb12508.x
PMID:1667285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908833/
Abstract
  1. The inhibitory action of lorcainide on the myocardial Na(+)-K(+)-ATPase (EC 3.6.1.3) activity was studied in guinea-pig heart preparations at medium K+ concentrations of 2.5, 5.0 and 10 mM. 2. Lorcainide exhibited characteristically similar concentration-dependent inhibitory effects at all three K+ concentrations tested. However, the inhibitory potencies were significantly increased at decreased K+ concentrations. 3. The IC50 values were 10.4 +/- 3.2 microM at 2.5 mM, 28.3 +/- 7.9 microM at 5.0 mM and 40.7 +/- 9.2 microM at 10.0 mM K+ respectively. Thus, reduction in the K+ concentration from the 'standard' 5.0 to 2.5 mM enhanced the inhibitory potency of lorcainide, the effective concentrations being shifted towards much lower ranges, while increasing it to 10 mM on the other hand produced opposite but less marked effects. 4. These results show that the inhibition of myocardial Na(+)-K(+)-ATPase activity by lorcainide depends on the K+ concentration of the incubation medium. These effects are probably related to the mechanism by which lorcainide interferes with the electrogenic Na+/K+ pump activity of the enzyme, and hence may contribute to some of its cardiac actions.
摘要
  1. 在豚鼠心脏标本中,于2.5、5.0和10 mM的中等钾离子浓度下研究了劳卡尼对心肌钠钾ATP酶(EC 3.6.1.3)活性的抑制作用。2. 在所有三个测试的钾离子浓度下,劳卡尼均表现出典型的相似浓度依赖性抑制作用。然而,在降低的钾离子浓度下,抑制效力显著增加。3. 在2.5 mM钾离子浓度下,IC50值分别为10.4±3.2 microM;在5.0 mM时为28.3±7.9 microM;在10.0 mM钾离子浓度下为40.7±9.2 microM。因此,将钾离子浓度从“标准”的5.0 mM降低至2.5 mM增强了劳卡尼的抑制效力,有效浓度向低得多的范围偏移,而另一方面将其增加至10 mM则产生相反但不太明显的效果。4. 这些结果表明,劳卡尼对心肌钠钾ATP酶活性的抑制作用取决于孵育介质中的钾离子浓度。这些作用可能与劳卡尼干扰该酶的生电钠/钾泵活性的机制有关,因此可能促成其一些心脏作用。