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The cellular electropharmacology of mexiletine in papillary muscles of guinea pigs chronically treated with amiodarone.胺碘酮长期治疗豚鼠乳头肌中美西律的细胞电药理学。
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Effects of mexiletine on transmembrane action potentials as affected by external potassium concentration and by rate of stimulation in guinea-pig papillary muscles.美西律对豚鼠乳头肌跨膜动作电位的影响:受细胞外钾离子浓度和刺激频率的影响
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Effects of lisinopril on electromechanical properties and membrane currents in guinea-pig cardiac preparations.赖诺普利对豚鼠心脏标本机电特性和膜电流的影响。
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本文引用的文献

1
Some statistical methods useful in circulation research.一些在循环研究中有用的统计方法。
Circ Res. 1980 Jul;47(1):1-9. doi: 10.1161/01.res.47.1.1.
2
Suppression of resistant ventricular arrhythmias by twice daily dosing with flecainide.通过每日两次服用氟卡尼抑制耐药性室性心律失常。
Am J Cardiol. 1981 Dec;48(6):1133-40. doi: 10.1016/0002-9149(81)90331-3.
3
Slow recovery of the maximal rate of rise (Vmax) of the action potential in sheep cardiac Purkinje fibers.绵羊心脏浦肯野纤维动作电位最大上升速率(Vmax)恢复缓慢。
Pflugers Arch. 1982 Jul;394(1):90-3. doi: 10.1007/BF01108313.
4
Oral flecainide acetate for the treatment of ventricular arrhythmias.口服醋酸氟卡尼治疗室性心律失常。
N Engl J Med. 1981 Aug 27;305(9):473-7. doi: 10.1056/NEJM198108273050901.
5
Structure-activity relations for frequency-dependent sodium channel block in nerve by local anesthetics.局部麻醉药对神经中频率依赖性钠通道阻滞的构效关系。
J Pharmacol Exp Ther. 1980 Apr;213(1):114-9.
6
Kinetics of onset of rate-dependent effects of Class I antiarrhythmic drugs are important in determining their effects on refractoriness in guinea-pig ventricle, and provide a theoretical basis for their subclassification.I类抗心律失常药物速率依赖性效应的起效动力学在确定其对豚鼠心室不应期的影响方面很重要,并为其亚分类提供了理论基础。
Cardiovasc Res. 1983 Jun;17(6):344-52. doi: 10.1093/cvr/17.6.344.
7
Voltage- and time-dependent depression of maximum rate of depolarisation of guinea-pig ventricular action potentials by two new antiarrhythmic drugs, flecainide and lorcainide.两种新型抗心律失常药物氟卡尼和劳卡尼对豚鼠心室动作电位最大去极化速率的电压和时间依赖性抑制作用。
Cardiovasc Res. 1983 May;17(5):251-8. doi: 10.1093/cvr/17.5.251.
8
Sodium current in freshly isolated and in cultured single rat myocardial cells: frequency and voltage-dependent block by mexiletine.新鲜分离的和培养的单个大鼠心肌细胞中的钠电流:美西律的频率和电压依赖性阻滞
J Mol Cell Cardiol. 1983 Jul;15(7):431-44. doi: 10.1016/0022-2828(83)90263-8.
9
Effects of flecainide on electrophysiological properties of accessory pathways in the Wolff-Parkinson-White syndrome.氟卡尼对预激综合征旁路电生理特性的影响。
Eur Heart J. 1983 May;4(5):347-53. doi: 10.1093/oxfordjournals.eurheartj.a061472.
10
Quantifying antiarrhythmic drug blocking during action potentials in guinea-pig papillary muscle.量化豚鼠乳头肌动作电位期间抗心律失常药物的阻滞作用。
J Mol Cell Cardiol. 1983 Nov;15(11):749-57. doi: 10.1016/0022-2828(83)90334-6.

美西律与氟卡尼联合应用对豚鼠心室肌纤维的电生理效应

Electrophysiological effects of the combination of mexiletine and flecainide in guinea-pig ventricular fibres.

作者信息

Delpón E, Valenzuela C, Tamargo J

机构信息

Department of Pharmacology, School of Medicine, Universidad Complutense, Madrid, Spain.

出版信息

Br J Pharmacol. 1991 Jun;103(2):1411-6. doi: 10.1111/j.1476-5381.1991.tb09803.x.

DOI:10.1111/j.1476-5381.1991.tb09803.x
PMID:1909200
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908390/
Abstract
  1. The effects of flecainide alone, mexiletine alone and their combination at the Na+ channel level were studied in guinea-pig papillary muscles. The maximum upstroke velocity (Vmax) was used as an indirect index of the magnitude of the fast inward Na+ current (INa). 2. In muscles driven at 0.02 Hz, neither mexiletine (10(-5) M) nor flecainide (10(-6) M) nor the combination of both drugs modified the action potential characteristics. Mexiletine, but not flecainide, increased the effective refractory period/action potential duration ratio; this enhancement was greater when flecainide was also present. 3. Mexiletine or flecainide alone produced a frequency-dependent Vmax block. Although at 0.5 Hz the blockade induced by the combination of flecainide and mexiletine was similar to that produced by flecainide alone, in muscles driven at 1 and 2 Hz the combination increased the magnitude and the onset rate of the Vmax block. 4. The time constant of recovery of Vmax block was similar in the presence of flecainide or the combination mexiletine plus flecainide (tau re = 16.4 +/- 2.3 s and 16.7 +/- 2.7 s, respectively), but the combination decreased the magnitude of the slow component of reactivation induced by flecainide (93.8 +/- 1.5% versus 68.9 +/- 1.7%). Moreover, the combination of both drugs was more effective in inhibiting the Vmax of early test stimuli than either drug alone. 5. It is concluded that the combination of mexiletine and flecainide is synergistic at driving rates faster than 0.5 Hz without detracting from the characteristics of flecainide.
摘要
  1. 在豚鼠乳头肌中研究了氟卡尼单独使用、美西律单独使用及其联合使用在钠通道水平的作用。最大除极速率(Vmax)被用作快速内向钠电流(INa)大小的间接指标。2. 在以0.02Hz驱动的肌肉中,美西律(10⁻⁵M)、氟卡尼(10⁻⁶M)或两种药物联合使用均未改变动作电位特征。美西律增加了有效不应期/动作电位时程比值,而氟卡尼没有;当同时存在氟卡尼时,这种增强作用更大。3. 美西律或氟卡尼单独使用均产生频率依赖性的Vmax阻滞。虽然在0.5Hz时,氟卡尼与美西律联合使用引起的阻滞与氟卡尼单独使用时相似,但在以1Hz和2Hz驱动的肌肉中,联合使用增加了Vmax阻滞的程度和起始速率。4. 在存在氟卡尼或美西律加氟卡尼联合使用的情况下,Vmax阻滞的恢复时间常数相似(分别为τre = 16.4±2.3s和16.7±2.7s),但联合使用降低了氟卡尼诱导的再激活慢成分的幅度(分别为93.8±1.5%和68.9±1.7%)。此外,两种药物联合使用在抑制早期测试刺激的Vmax方面比单独使用任何一种药物都更有效。5. 得出结论,在驱动频率高于0.5Hz时,美西律和氟卡尼联合使用具有协同作用,且不影响氟卡尼的特性。