The effect of external divalent cations on spontaneous non‐selective cation channel currents in rabbit portal vein myocytes

1 The effects of external divalent cations on spontaneous single non‐selective cation channel currents were studied in outside‐out patches from rabbit portal vein smooth muscle cells in K+‐free conditions. 2 In an external medium containing 1.5 mm Ca2+ (Ca2+o) the majority of spontaneous channel currents had a unitary conductance of 23 pS, reversal potential (Vr) of +10 mV and a low open probability (Po) at negative patch potentials. Some channels opened to a lower conductance state of about 13 pS suggesting that the cation channels have two conductance states. Open time and burst duration distributions could both be described by two exponentials with time constants of about of 1 ms and 7 ms for open times and 3 ms and 16 ms for burst durations. 3 In 0 Ca2+o the majority of spontaneous cation channels had a unitary conductance of 13 pS and Vr was shifted to +4 mV. Moreover the longer open time and longer burst duration time constants were both reduced to approximately half the values in 1.5 mm Ca2+o. 4 Compared to 0 Ca2+o the single channel currents in 3 μm and 100 μm Ca2+o had a 5‐ to 6‐fold increase in Po which was accompanied by increases in both open times and burst durations. In 3 μm and 100 μm Ca2+o the unitary conductance of the single channel currents was between 22 and 26 pS. 5 At positive membrane potentials the single channel currents had an increased Po compared to negative potentials which was associated with increased open times and burst durations but these values were similar in 3 μm, 100 μm and 1.5 mm Ca2+o. 6 In 1.5 mm Sr2+o and 1.5 mm Ba2+o channels opened to the higher conductance state of about 22–25 pS and had a 3‐ to 7‐fold greater Po than in 0 Ca2+o. 7 In conclusion, external divalent cations have marked effects on the unitary conductance and kinetic behaviour of non‐selective cation channels in rabbit portal vein smooth muscle cells.

[1]  RyujiInoue,et al.  The Transient Receptor Potential Protein Homologue TRP6 Is the Essential Component of Vascular α1-Adrenoceptor–Activated Ca2+-Permeable Cation Channel , 2001 .

[2]  A. Aromolaran,et al.  Agents that increase tyrosine phosphorylation activate a non‐selective cation current in single rabbit portal vein smooth muscle cells , 2001, The Journal of physiology.

[3]  R. Keynes The ionic channels in excitable membranes. , 1975, Ciba Foundation symposium.

[4]  A. Aromolaran,et al.  Comparison of the effects of divalent cations on the noradrenaline‐evoked cation current in rabbit portal vein smooth muscle cells , 1999, The Journal of physiology.

[5]  Alan G. Hawkes,et al.  The Principles of the Stochastic Interpretation of Ion-Channel Mechanisms , 1983 .

[6]  W. Large,et al.  Comparison of spontaneous and noradrenaline‐evoked non‐selective cation channels in rabbit portal vein myocytes , 2001, The Journal of physiology.

[7]  R. Helliwell,et al.  Dual effect of external Ca2+ on noradrenaline‐activated cation current in rabbit portal vein smooth muscle cells. , 1996, The Journal of physiology.

[8]  K L Magleby,et al.  Burst kinetics of single calcium‐activated potassium channels in cultured rat muscle. , 1983, The Journal of physiology.

[9]  R. Helliwell,et al.  Facilitatory effect of Ca2+ on the noradrenaline‐evoked cation current in rabbit portal vein smooth muscle cells , 1998, The Journal of physiology.

[10]  Y. Hara,et al.  The Transient Receptor Potential Protein Homologue TRP6 Is the Essential Component of Vascular &agr;1-Adrenoceptor–Activated Ca2+-Permeable Cation Channel , 2001, Circulation research.

[11]  W. Large,et al.  Membrane ionic mechanisms activated by noradrenaline in cells isolated from the rabbit portal vein. , 1988, The Journal of physiology.

[12]  W. Large,et al.  Noradrenaline‐evoked cation conductance recorded with the nystatin whole‐cell method in rabbit portal vein cells. , 1991, The Journal of physiology.