Effects of sphingosine 1-phosphate on pacemaker activity in rabbit sino-atrial node cells

被引:69
作者
Guo, J [1 ]
MacDonell, KL [1 ]
Giles, WR [1 ]
机构
[1] Univ Calgary, Dept Physiol & Biophys, Calgary, AB T2N 4N1, Canada
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1999年 / 438卷 / 05期
关键词
sino-atrial node; action potential; sphingosine; 1-phosphate; potassium current; hyperpolarization-activated current; calcium current;
D O I
10.1007/s004240051088
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The effects of sphingosine 1-phosphate (S-1-P) on pacemaker activity and underlying membrane rents were studied in isolated rabbit sino-atrial (SA) node cells. S-1-P (0.1 mu M) reversibly increased the cycle length of spontaneous pacemaker activity from 560 to 1434 ms, and hyperpolarized the maximal diastolic potential (MDP) from -67 to -70 mV. In voltage-clamp experiments, S-1-P (1 mu M) activated a pertussis toxin-sensitive, inwardly-rectifying, time-independent K+ current (I-K,I-ACh) that had a reversal potential of -88 mV (K+ equilibrium potential -86 mV). S-1-P (1 mu M) had no measurable effect on the L-type Ca2+ current (I-Ca,I-L) or the hyperpolarization-activated inward current (I-f) under basal conditions. In the presence of the beta-adrenergic agonist, isoproterenol (ISO, 0.1 mu M), S-1-P (1 mu M) reversed the ISO-induced increase in pacing rate, hyperpolarized the MDP and decreased the ISO-induced enhancement of both I-Ca,I-L (from 171 to 118% of control) and I-f (from 211 to 135% of control). These results demonstrate that under basal conditions S-1-P can significantly slow spontaneous pacing in rabbit SA node cells mainly due to activation of a background, inwardly-rectifying K+ current. In the presence of ISO, S-1-P also slows the spontaneous pacing rate due to activation of the same K+ current, as well as inhibition of I-Ca,I-L and I-f.
引用
收藏
页码:642 / 648
页数:7
相关论文
共 27 条
[11]   MUSCARINIC ACTIVATION OF IONIC CURRENTS MEASURED BY A NEW WHOLE-CELL RECORDING METHOD [J].
HORN, R ;
MARTY, A .
JOURNAL OF GENERAL PHYSIOLOGY, 1988, 92 (02) :145-159
[12]   Characterization of sphingosine 1-phosphate-induced actions and its signaling pathways in rat hepatocytes [J].
Im, DS ;
Fujioka, T ;
Katada, T ;
Kondo, Y ;
Ui, M ;
Okajima, F .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 272 (05) :G1091-G1099
[13]   CARDIAC PACEMAKING IN THE SINOATRIAL NODE [J].
IRISAWA, H ;
BROWN, HF ;
GILES, W .
PHYSIOLOGICAL REVIEWS, 1993, 73 (01) :197-227
[14]   G-PROTEIN CONTROL OF CARDIAC POTASSIUM CHANNELS [J].
KURACHI, Y .
TRENDS IN CARDIOVASCULAR MEDICINE, 1994, 4 (02) :64-69
[15]   Sphingosine-1-phosphate as a ligand for the G protein coupled receptor EDG-1 [J].
Lee, MJ ;
Van Brocklyn, JR ;
Thangada, S ;
Liu, CH ;
Hand, AR ;
Menzeleev, R ;
Spiegel, S ;
Hla, T .
SCIENCE, 1998, 279 (5356) :1552-1555
[16]  
LEVY MN, 1989, PHYSL PATHOPHYSIOLOG
[17]   Depression of excitability by sphingosine 1-phosphate in rat ventricular myocytes [J].
MacDonell, KL ;
Severson, DL ;
Giles, WR .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1998, 275 (06) :H2291-H2299
[18]  
Noh SJ, 1998, J CELL PHYSIOL, V176, P412, DOI 10.1002/(SICI)1097-4652(199808)176:2<412::AID-JCP20>3.0.CO
[19]  
2-3
[20]   Involvement of pertussis toxin-sensitive GTP-binding proteins in sphingosine 1-phosphate-induced activation of phospholipase C-Ca2+ system in HL60 leukemia cells [J].
Okajima, F ;
Tomura, H ;
Sho, K ;
Nochi, H ;
Tamoto, K ;
Kondo, Y .
FEBS LETTERS, 1996, 379 (03) :260-264