Synergism between inositol phosphates and diacylglycerol on native TRPC6-like channels in rabbit portal vein myocytes

被引:69
作者
Albert, AP [1 ]
Large, WA [1 ]
机构
[1] St George Hosp, Sch Med, Dept Basic Med Sci Pharmacol & Clin Pharmacol, London SW17 0RE, England
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2003年 / 552卷 / 03期
关键词
D O I
10.1113/jphysiol.2003.052977
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In rabbit portal vein myocytes noradrenaline activates a non-selective cation current (hat) which involves a transient receptor potential protein (TRPC6). Previously we have shown that the diaylglycerol (DAG) analogue 1-oleoyl-2-acetyl-sn-glycerol (OAG) stimulates I-cat via a protein kinase C (PKC)-independent mechanism, and in the present study we have investigated the interaction between inositol phosphates (InsPs) and OAG on I-cat. With whole-cell recording of hat from freshly isolated rabbit portal vein myocytes the amplitude and rate of activation of noradrenaline-evoked I-cat were much greater than those of OAG-induced hat. Inclusion of inositol 1,4,5-trisphosphate (Ins(1,4,5)P-3) in the pipette solution did not evoke I-cat but greatly potentiated the amplitude and rate of activation of OAG-induced hat. With isolated outside-out patches Ins(1,4,5)P-3 markedly increased the rate of activation and the open probability of OAG-evoked channel activity, with no change in unitary conductance, channel mean open times or burst durations. The effects of Ins(1,4,5)P-3 were mimicked by Ins(2,4,5)P-3, 3-F-Ins(1,4,5)P-3 and Ins(1,4)P-2 but not by Ins(1,3,4,5)P-4 and the potentiating effects of InsPs were not inhibited by heparin. Therefore it is concluded that both DAG and InsPs are necessary for full activation of I-cat by noradrenaline and the effect of InsPs is via a heparin-insensitive mechanism and represents a novel action of InsPs.
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收藏
页码:789 / 795
页数:7
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