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

Pflügers Archiv - Tập 438 - Trang 642-648 - 1999
J. Guo1, K.L. MacDonell1, W.R. Giles1
1Department of Physiology and Biophysics, University of Calgary, 3330 Hospital Drive NW, Calgary, Alberta T2N 4N1, Canada.

Tóm tắt

The effects of sphingosine 1-phosphate (S-1-P) on pacemaker activity and underlying membrane currents were studied in isolated rabbit sino-atrial (SA) node cells. S-1-P (0.1 µM) 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 µM) activated a pertussis toxin-sensitive, inwardly-rectifying, time-independent K+ current (I K,ACh) that had a reversal potential of –88 mV (K+ equilibrium potential –86 mV). S-1-P (1 µM) had no measurable effect on the L-type Ca2+ current (I Ca,L) or the hyperpolarization-activated inward current (I f) under basal conditions. In the presence of the β-adrenergic agonist, isoproterenol (ISO, 0.1 µM), S-1-P (1 µM) reversed the ISO-induced increase in pacing rate, hyperpolarized the MDP and decreased the ISO-induced enhancement of both I Ca,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,L and I f.