Modulation of the atrial specific Kv1.5 channel by the n-3 polyunsaturated fatty acid, α-linolenic acid

被引:33
作者
Guizy, Miriam [1 ]
David, Miren [1 ]
Arias, Cristina [1 ]
Zhang, Lian [2 ]
Cofan, Montserrat [3 ,4 ]
Ruiz-Gutierrez, Valentina [5 ]
Ros, Emilio [3 ,4 ]
Lillo, M. Pilar [6 ]
Martens, Jeffrey R. [2 ]
Valenzuela, Carmen [1 ]
机构
[1] Univ Complutense, Sch Med, Inst Pharmacol & Toxicol, CSIC UCM, E-28040 Madrid, Spain
[2] Univ Michigan, Sch Med, Dept Pharmacol, Ann Arbor, MI 48109 USA
[3] IDIBAPS, Inst Invest Biomed August Pi & Sunyer, Unitat Lipids, Servei Endocrinol & Nutricio,Hosp Clin, Barcelona 08036, Spain
[4] Inst Salud Carlos III, Ciber CB06 03 Fisiopatol Obesidad & Nutric, Madrid, Spain
[5] CSIC, Inst Grasa, Seville 41012, Spain
[6] CSIC, Inst Quim Fis Rocasolano, E-28006 Madrid, Spain
关键词
PUFA; Kv1.5; alpha-linolenic acid; DHA; EPA; arrhythmias; channels; protein expression; membrane fluidity; membraneorder; fluorescence anisotropy;
D O I
10.1016/j.yjmcc.2007.11.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epidemiological, clinical and experimental studies suggest that the cardioprotective effect of fish intake is mainly due to the antiarrhythmic properties of marine n-3 polyunsaturated fatty acids (PUFA), which modulate ion currents. Emerging evidences point to similar effects of a-linolenic acid (ALA), a vegetable n-3 PUFA, but much less is known about its effects on the specific cardiac ion channels. Using electrophysiology, protein biochemistry and fluorescence anisotropy measurements, we tested the effects of ALA on the atrial specific Kv1.5 channel. In stably transfected Ltk(-) cells, ALA blocked Kv1.5 channels in a time- and voltage-dependent manner with an IC50 value of 3.7 +/- 0.3 mu M. ALA at 2.5 mu M inhibited the Kv1.5 current, shifted the midpoint of the activation curve by - 8.8 +/- 4.3 mV (p < 0.05), accelerated the activation kinetics of Kv1.5 due to a negative shift in its voltage dependency and slowed its deactivation process. Marine n-3 PUFA eicosapentaenoic and docosahexaenoic (EPA and DHA) acids, but not ALA, reduced the steady-state levels of Kv 1.5 protein. DHA, but not ALA, increased the cell membrane order parameter. These results demonstrate that ALA directly blocks atria-specific Kv 1.5 channels without modifying their expression or the bilayer order. Together, these effects suggest that the antiarrhythmic potential of diets enriched with plant-derived n-3 PUFA result, in part, from direct effects on cardiac ion channels. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:323 / 335
页数:13
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