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细胞内钠活性在局部麻醉药对绵羊浦肯野纤维抗心律失常作用中的角色。

The role of intracellular sodium activity in the anti-arrhythmic action of local anaesthetics in sheep Purkinje fibres.

作者信息

Eisner D A, Lederer W J, Sheu S S

出版信息

J Physiol. 1983 Jul;340:239-57. doi: 10.1113/jphysiol.1983.sp014761.

Abstract

The effects of lidocaine have been examined on the arrhythmogenic transient inward current (ITI) in voltage-clamped sheep cardiac Purkinje fibres. Tension and intracellular Na activity (aiNa) were measured simultaneously. The addition of lidocaine (200-300 microM) produced an immediate decrease of inward holding current and a gradual fall of aiNa. The relative magnitudes of the changes of current and aiNa were shown to be consistent with the outward shift of current representing principally a reduction of inward Na current. The Na pump was inhibited by reducing the external Rb concentration in a K-free solution. This produced an after-contraction and transient inward current (ITI) along with a rise of aiNa. The subsequent addition of lidocaine decreased the magnitude of ITI and the after-contraction while decreasing aiNa. Tetrodotoxin (TTX) had qualitatively similar effects to lidocaine on inward holding current, aiNa, ITI and the after-contraction. When aiNa was changed by (i) lidocaine, (ii) TTX or (iii) small changes of external Rb concentration, a hysteresis was seen in the relationship between aiNa and ITI or after-contraction. The hysteresis was similar to that previously found between aiNa and contraction (Eisner, Lederer & Vaughan-Jones, 1981). Despite this hysteresis, neither lidocaine nor TTX affected the relationship between magnitudes of ITI and the after-contraction. It is suggested that the fall of aiNa is a major factor in the reduction of ITI by lidocaine. These results are discussed in relation to the anti-arrhythmic actions of lidocaine.

摘要

研究了利多卡因对电压钳制的绵羊心脏浦肯野纤维中致心律失常的瞬时内向电流(ITI)的影响。同时测量了张力和细胞内钠活性(aiNa)。加入利多卡因(200 - 300微摩尔)后,内向钳制电流立即降低,aiNa逐渐下降。电流和aiNa变化的相对幅度表明,电流向外移动主要代表内向钠电流的减少。在无钾溶液中降低外部铷浓度可抑制钠泵。这会产生后收缩和瞬时内向电流(ITI),同时aiNa升高。随后加入利多卡因可降低ITI的幅度和后收缩,同时降低aiNa。河豚毒素(TTX)对内向钳制电流、aiNa、ITI和后收缩的影响在性质上与利多卡因相似。当aiNa因(i)利多卡因、(ii)TTX或(iii)外部铷浓度的微小变化而改变时,在aiNa与ITI或后收缩之间的关系中观察到滞后现象。这种滞后现象与先前在aiNa与收缩之间发现的滞后现象相似(艾斯纳、莱德勒和沃恩 - 琼斯,1981年)。尽管存在这种滞后现象,但利多卡因和TTX均未影响ITI幅度与后收缩之间的关系。提示aiNa的下降是利多卡因降低ITI的主要因素。结合利多卡因的抗心律失常作用对这些结果进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6913/1199208/2fb23a0b8323/jphysiol00656-0252-a.jpg

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