首页   按字顺浏览 期刊浏览 卷期浏览 Mechanisms for IMPULSE INITIATION IN HUMAN ATRIAL FIBERS
Mechanisms for IMPULSE INITIATION IN HUMAN ATRIAL FIBERS

 

作者: Luc MARY-RABINE,   ALLAN HORDOF,   PETER DANILO,   JAMES MALM,   MICHAEL ROSEN,  

 

期刊: Circulation Research  (OVID Available online 1980)
卷期: Volume 47, issue 2  

页码: 267-277

 

ISSN:0009-7330

 

年代: 1980

 

出版商: OVID

 

数据来源: OVID

 

摘要:

We used standard microelectrode techniques to study Tyrode's-superfused human atrial fibers obtained at cardiac surgery. Two types of sustained rhythmic activity occurred. One resulted from slow phase 4 depolarization and had a spontaneous rate = 20-26 beats/min. Epinephrine increased and the slow channel blockers, AHR-2666 (AHR) and verapamil decreased both phase 4 slope and spontaneous rate. Acetylcholine (ACh) and lidocaine decreased the slope of phase 4, but the slowing of rate was less than that induced by AHR and verapamil. Tetrodotoxin (TTX) also decreased the slope of phase 4 and spontaneous rate, to an extent that was intermediate between the actions of AHR-verapamil and ACh-lidocaine. A second type of sustained rhythmic activity was triggered by delayed afterdepolarizations (DAD). DAD amplitude increased as stimulus cycle length decreased and, at critical cycle lengths, DAD initiated trains of spontaneous action potentials at rates > 70 beats/min. Spontaneously occurring DAD were suppressed by AHR and were transiently diminished by ACh. This effect of ACh was accompanied by hyperpolarization of the fibers. DAD also were induced by epineph-rine. These DAD were unaffected by TTX, lidocaine, or ACh and were suppressed by AHR and verapamil. In summary, the slow inward current contributes to the sustained rhythmic activity that occurs with automaticity or DAD in human atrium. A TTX-sensitive current also contributes to automaticity. DAD that occur spontaneously are largely insensitive to the effects of agents that increase K conductance (although ACh has a transient effect) and those that are induced in the presence of epinephrine do not respond to agents which increase K conductance (ACh, lidocaine) or TTX.Circ Res 47: 267-277, 1980

 

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