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

1998 ◽  
Vol 275 (6) ◽  
pp. H2291-H2299 ◽  
Author(s):  
Karen L. MacDonell ◽  
David L. Severson ◽  
Wayne R. Giles

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 μM S-1- P (1–6 min) were recorded. S-1- P increased the minimum stimulus current needed to elicit an action potential by ∼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 ∼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.

1999 ◽  
Vol 277 (2) ◽  
pp. H826-H833 ◽  
Author(s):  
Seiko Tanabe ◽  
Toshio Hata ◽  
Masayasu Hiraoka

To explore a possible ionic basis for the prolonged Q-T interval in women compared with that in men, we investigated the electrophysiological effects of estrogen in isolated guinea pig ventricular myocytes. Action potentials and membrane currents were recorded using the whole cell configuration of the patch-clamp technique. Application of 17β-estradiol (10–30 μM) significantly prolonged the action potential duration (APD) at 20% (APD20) and 90% repolarization (APD90) at stimulation rates of 0.1–2.0 Hz. In the presence of 30 μM 17β-estradiol, APD20 and APD90 at 0.1 Hz were prolonged by 46.2 ± 17.1 and 63.4 ± 11.7% of the control ( n = 5), respectively. In the presence of 30 μM 17β-estradiol the peak inward Ca2+ current ( I CaL) was decreased to 80.1 ± 2.5% of the control ( n = 4) without a shift in its voltage dependence. Application of 30 μM 17β-estradiol decreased the rapidly activating component of the delayed outward K+ current ( I Kr) to 63.4 ± 8% and the slowly activating component ( I Ks) to 65.8 ± 8.7% with respect to the control; the inward rectifier K+ current was barely affected. The results suggest that 17β-estradiol prolonged APD mainly by inhibiting the I Kcomponents I Krand I Ks.


1988 ◽  
Vol 254 (6) ◽  
pp. H1157-H1166 ◽  
Author(s):  
J. A. Wasserstrom ◽  
J. J. Salata

We studied the effects of tetrodotoxin (TTX) and lidocaine on transmembrane action potentials and ionic currents in dog isolated ventricular myocytes. TTX (0.1-1 x 10(-5) M) and lidocaine (0.5-2 x 10(-5) M) decreased action potential duration, but only TTX decreased the maximum rate of depolarization (Vmax). Both TTX (1-2 x 10(-5) M) and lidocaine (2-5 x 10(-5) M) blocked a slowly inactivating toward current in the plateau voltage range. The voltage- and time-dependent characteristics of this current are virtually identical to those described in Purkinje fibers for the slowly inactivating inward Na+ current. In addition, TTX abolished the outward shift in net current at plateau potentials caused by lidocaine alone. Lidocaine had no detectable effect on the slow inward Ca2+ current and the inward K+ current rectifier, Ia. Our results indicate that 1) there is a slowly inactivating inward Na+ current in ventricular cells similar in time, voltage, and TTX sensitivity to that described in Purkinje fibers; 2) both TTX and lidocaine shorten ventricular action potentials by reducing this slowly inactivating Na+ current; 3) lidocaine has no additional actions on other ionic currents that contribute to its ability to abbreviate ventricular action potentials; and 4) although both agents shorten the action potential by the same mechanism, only TTX reduces Vmax. This last point suggests that TTX produces tonic block of Na+ current, whereas lidocaine may produce state-dependent Na+ channel block, namely, blockade of Na+ current only after Na+ channels have already been opened (inactivated-state block).


Extracellular application of potassium channel blocking agents is known to increase the amplitude and duration of the compound action potential in non-myelinated and demyelinated axons, but not in mature mammalian myelinated fibres. In the present study we used intra-axonal and whole nerve recording techniques to study the effects of the potassium channel blocking agent 4-aminopyridine (4-AP) on regenerating rat nerve fibres. Our results indicate that early regenerating (premyelinated) axons show considerable broadening of the action potential after 4-AP application and late regenerating (myelinated) axons give rise to burst activity following a single stimulus after 4-AP application. 4-AP did not affect spike waveform or firing properties of normal mature sciatic nerve fibres. These results demonstrate the importance of potassium conductance in stabilizing firing properties of myelinated regenerating axons.


1968 ◽  
Vol 21 (1) ◽  
pp. 37 ◽  
Author(s):  
L Munk ◽  
E PGeorge

A mathematical model for the action potential in Purkinje fibres is developed. It is based on voltage-clamp results which show that inactivation of sodium current in these muscles is much slower than in squid axon and that the latent rise in potassium conductance is not present. Both the sodium and the potassium conductances are represented as a sum of slow and fast components. This is incorporated in the suitably adjusted Hodgkin-Huxley model for the squid axon. It is shown that such a model can account satisfactorily for the shape of the action potentials in Purkinje fibres.


1993 ◽  
Vol 61 ◽  
pp. 269
Author(s):  
Kaichiro Kamiya ◽  
Jianhua Cheng ◽  
Ryoko Suzuki ◽  
Hirokazu Iwata ◽  
Itsuo Kodama ◽  
...  

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