Inhibitory effect of n-3 fish oil fatty acids on cardiac Na+/Ca2+ exchange currents in HEK293t cells

被引:63
作者
Xiao, YF
Ke, QH
Chen, Y
Morgan, JP
Leaf, A [1 ]
机构
[1] Harvard Univ, Sch Med, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Charles A Dana Res Inst, Boston, MA 02215 USA
[3] Harvard Univ, Beth Israel Deaconess Med Ctr, Thorndike Lab, Div Cardiovasc, Boston, MA 02215 USA
关键词
Na+/Ca2+ exchanger; eicosapentaenoic acid; docosahexaenoic acid; arrhythmia; human embryonic kidney cells;
D O I
10.1016/j.bbrc.2004.06.114
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Abnormal activity of the cardiac Na+/Ca2+ exchanger (NCX1) can affect intracellular Ca2+ homeostasis and cause arrhythmias. The n-3 polyunsaturated fatty acids (PUFAs), however, may prevent arrhythmias. To test the effect of PUFAs on the cardiac NCX1 current (I-NCX1), the canine NCX1 cDNA was expressed in human embryonic kidney (HEK293t) cells. The average density Of I-NCX1 I was 10.9 +/- 2.6 pA/pF (n=44) in NCX1-transfected cells and eicosapentaenoic acid (EPA, C20:5n-3) significantly inhibited I-NCX1. The suppression of I-NCX1 by EPA was concentration-dependent with an IC50 of 0.82 +/- 0.27 muM. EPA had a similar effect on outward or inward I-NCX1. Docosahexaenoic acid (DHA, C22:6n-3) and arachidonic acid (AA, C20:4n-6) also significantly inhibited I-NCX1, whereas the saturated fatty acid, stearic acid (SA, C 18:0), did not. Our data demonstrate that the n-3 PUFAs significantly suppress cardiac I-NCX1, which is probably one of their protective effects against lethal arrhythmias. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:116 / 123
页数:8
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