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利多卡因对心室肌和浦肯野纤维电生理特性的影响。

Effect of lidocaine on the electrophysiological properties of ventricular muscle and purkinje fibers.

作者信息

Bigger J T, Mandel W J

出版信息

J Clin Invest. 1970 Jan;49(1):63-77. doi: 10.1172/JCI106224.

Abstract

Preparations of right ventricular papillary muscle and false tendon (Purkinje fiber) were obtained from dog hearts, placed in a bath perfused with Tyrode solution, and observed both under control conditions and during exposure to lidocaine in concentrations from 1 x 10(-7) to 5 x 10(-4) mole/liter. Transmembrane voltages were recorded from both ventricular muscle (VM) and Purkinje fibers (PF) of spontaneously beating and electrically driven preparations. Low concentrations (1 x 10(-6) and 1 x 10(-5) mole/liter) attenuated or abolished phase 4 (diastolic) depolarization and spontaneous firing in PF without decreasing their diastolic excitability. Concentrations of 1 x 10(-5) mole/liter produced maximal shortening of both action potential duration (APD) and effective refractory period (ERP) and made the ERP long relative to APD; the latter alteration was more prominent in VM. At concentrations </= 1 x 10(-5) mole/liter, lidocaine either caused a slight increase or no change in peak maximum rate of phase 0 depolarization (V(max)) and membrane responsiveness, the relationship between transmembrane activation voltage (MAV) and V(max) of the resultant action potential; these concentrations had no significant effect on resting potential (RP) in VM, maximal diastolic transmembrane voltage (DTMV(max)) in PF, or action potential amplitude in either fiber type. High (toxic) concentrations (>/= 1 x 10(-4) mole/liter) did not cause further shortening of APD or ERP in either VM or PF but did produce a decrease in peak V(max) of phase 0 and membrane responsiveness. In most cases, these concentrations also caused a decrease in RP or DTMV(max) and action potential amplitude, with progression to bizarre action potential depolarization and inexcitability. These properties of lidocaine are strikingly different from those of quinidine or procaine amide. The mechanisms responsible for lidocaine's in vivo antiarrhythmic action are discussed.

摘要

从狗心脏获取右心室乳头肌和假腱索(浦肯野纤维)标本,置于用台氏液灌注的浴槽中,在对照条件下以及暴露于浓度为1×10⁻⁷至5×10⁻⁴摩尔/升的利多卡因期间进行观察。记录自发搏动和电驱动标本的心室肌(VM)和浦肯野纤维(PF)的跨膜电压。低浓度(1×10⁻⁶和1×10⁻⁵摩尔/升)可减弱或消除PF中的4期(舒张期)去极化和自发放电,而不降低其舒张期兴奋性。1×10⁻⁵摩尔/升的浓度可使动作电位时程(APD)和有效不应期(ERP)最大程度缩短,并使ERP相对于APD延长;后一种改变在VM中更明显。在浓度≤1×10⁻⁵摩尔/升时,利多卡因要么使0期去极化的峰值最大速率(V(max))和膜反应性略有增加,要么无变化,即所产生动作电位的跨膜激活电压(MAV)与V(max)之间的关系;这些浓度对VM中的静息电位(RP)、PF中的最大舒张跨膜电压(DTMV(max))或两种纤维类型的动作电位幅度均无显著影响。高(毒性)浓度(≥1×10⁻⁴摩尔/升)在VM或PF中均不会导致APD或ERP进一步缩短,但会使0期峰值V(max)和膜反应性降低。在大多数情况下,这些浓度还会导致RP或DTMV(max)以及动作电位幅度降低,并逐渐发展为奇异的动作电位去极化和兴奋性丧失。利多卡因的这些特性与奎尼丁或普鲁卡因胺的特性显著不同。文中讨论了利多卡因体内抗心律失常作用的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/322445/5458d6d08b54/jcinvest00217-0074-a.jpg

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