Inhibitory effects of omega-3 polyunsaturated fatty acids on receptor-mediated non-selective cation currents in rat A7r5 vascular smooth muscle cells

被引:20
作者
Asano, M
Nakajima, T
Iwasawa, K
Hazama, H
Omata, M
Soma, M
Yamashita, K
Okuda, Y
机构
[1] UNIV TOKYO,FAC MED,DEPT INTERNAL MED 2,BUNKYO KU,TOKYO 113,JAPAN
[2] UNIV TSUKUBA,INST CLIN MED,DEPT INTERNAL MED,TSUKUBA,IBARAKI 305,JAPAN
[3] MOCHIDA PHARMACEUT CO LTD,SHINJUKU KU,TOKYO 160,JAPAN
关键词
vascular smooth muscle cells; A7r5; cells; omega-3 polyunsaturated fatty acids; eicosapentaenoic acid; docosahexaenoic acid; arachidonic acid; non-selective cation current; vasopressin; endothelin-1; K+ currents;
D O I
10.1038/sj.bjp.0701047
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The effects of omega-3 polyunsaturated fatty acids on receptor-mediated non-selective cation current (I-cat) and K+ current were investigated in aortic smooth muscle cells from foetal rat aorta (A7r5 cells). The whole-cell voltage clamp technique was employed. 2 With a K+-containing solution, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA, 30 mu M) produced an outward current at a holding potential of -40 mV. This response was inhibited by tetraethylammonium (20 mM) or Cs+ in the patch pipette solution, and the reversal potential of the EPA-induced current followed the K+ equilibrium potential in a near Nernstian manner. 3 Under conditions with a Cs+-containing pipette solution, both vasopressin and endothelin-1 (100 nM) induced a long-lasting inward current at a holding potential of -60 mV. The reversal potential of these agonist-induced currents was about +0 mV, and was not significantly altered by the replacement of the extracellular or intracellular Cl- concentration, suggesting that the induced current was a cation-selective current (I-cat). 4 La3+ and Cd2+ (1 mM) completely abolished these agonist-induced I-cat but nifedipine (10 mu M) failed to inhibit it significantly. 5 omega-3 polyunsaturated fatty acids (3-100 mu M), EPA, DHA and docosapentaenoic acids (DPA), inhibited the agonist-induced I-cat in a concentration-dependent manner. The potency of the inhibitory effect was EPA > DHA > DPA, and the half maximal inhibitory concentration (IC50) of EPA was about 7 mu M. 6 Arachidonic and linoleic acids (10, 30 mu M) showed a smaller inhibitory effect compared to omega-3 fatty acids. Also, oleic and stearic acids (30 mu M) did not show a significant inhibitory effect on I-cat. 7 A similar inhibitory action of EPA was observed when I-cat was activated by intracellularly applied GTP gamma S in the absence of agonists, suggesting that the site of action of omega-3 fatty acids is not located on the receptor. 8 These results demonstrate that omega-3 polyunsaturated fatty acids can activate a K+ current and also effectively inhibit receptor-mediated non-selective cation currents in rat A7r5 vascular smooth muscle cells. Thus, the data suggest that omega-3 fatty acids may play an important role in the regulation of vascular tone.
引用
收藏
页码:1367 / 1375
页数:9
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