Depression of excitability by sphingosine 1-phosphate in rat ventricular myocytes

被引:24
作者
MacDonell, KL
Severson, DL
Giles, WR
机构
[1] Univ Calgary, Hlth Sci Ctr, Dept Physiol & Biophys, Calgary, AB T2N 4N1, Canada
[2] Heritage Med Res Ctr, Dept Pharmacol & Therapeut, Calgary, AB, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1998年 / 275卷 / 06期
关键词
sphingolipids; action potential; sodium current; threshold;
D O I
10.1152/ajpheart.1998.275.6.H2291
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sphingosine 1-phosphate (S-1-P) is a bioactive sphingolipid that is released from activated platelets. Extracellular S-1-P augments an inwardly rectifying potassium conductance in cultured atrial preparations, but the electrophysiological effects of this compound in the ventricle are unknown. The electrophysiological effects of S-1-P were examined in single myocytes from rat ventricular muscle. Action potential waveforms and underlying ionic currents in the presence and absence of 3 mu M S-1-P (1-6 min) were recorded. S-1-P increased the minimum stimulus current needed to elicit an action potential by similar to 100 pA. Pertussis toxin or preexposure to S-1-P did not alter this effect. The action potential waveform was unchanged by S-1-P. The inward sodium current (I-Na) was examined in a range of membrane potentials just negative to the potential for firing an action potential. S-1-P reversibly inhibited peak I-Na by similar to 50 pA, whereas the inward rectifier potassium current was not significantly changed. The results of this study suggest that S-1-P inhibits rat ventricular excitability by reducing I-Na.
引用
收藏
页码:H2291 / H2299
页数:9
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