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ω-3多不饱和脂肪酸对大鼠A7r5血管平滑肌细胞中受体介导的非选择性阳离子电流的抑制作用。

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

作者信息

Asano M, Nakajima T, Iwasawa K, Hazama H, Omata M, Soma M, Yamashita K, Okuda Y

机构信息

Second Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.

出版信息

Br J Pharmacol. 1997 Apr;120(7):1367-75. doi: 10.1038/sj.bjp.0701047.

DOI:10.1038/sj.bjp.0701047
PMID:9105714
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1564604/
Abstract
  1. The effects of omega-3 polyunsaturated fatty acids on receptor-mediated non-selective cation current (Icat) 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 microM) 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 (Icat). 4. La3+ and Cd2+ (1 mM) completely abolished these agonist-induced Icat, but nifedipine (10 microM) failed to inhibit it significantly. 5. omega-3 polyunsaturated fatty acids (3-100 microM), EPA, DHA and docosapentaenoic acids (DPA), inhibited the agonist-induced Icat 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 microM. 6. Arachidonic and linoleic acids (10, 30 microM) showed a smaller inhibitory effect compared to omega-3 fatty acids. Also, oleic and stearic acids (30 microM) did not show a significant inhibitory effect on Icat. 7. A similar inhibitory action of EPA was observed when Icat 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.
摘要
  1. 研究了ω-3多不饱和脂肪酸对胎鼠主动脉平滑肌细胞(A7r5细胞)中受体介导的非选择性阳离子电流(Icat)和钾离子电流的影响。采用了全细胞膜片钳技术。2. 在含钾溶液中,二十碳五烯酸(EPA)和二十二碳六烯酸(DHA,30微摩尔)在-40毫伏的钳制电位下产生外向电流。这种反应在膜片钳微管溶液中被四乙铵(20毫摩尔)或铯离子抑制,并且EPA诱导电流的反转电位以接近能斯特方式跟随钾离子平衡电位。3. 在含铯离子的微管溶液条件下,血管加压素和内皮素-1(100纳摩尔)在-60毫伏的钳制电位下均诱导出持久的内向电流。这些激动剂诱导电流的反转电位约为+0毫伏,并且在细胞外或细胞内氯离子浓度替换时没有显著改变,表明诱导电流是阳离子选择性电流(Icat)。4. 镧离子和镉离子(1毫摩尔)完全消除了这些激动剂诱导的Icat,但硝苯地平(10微摩尔)未能显著抑制它。5. ω-3多不饱和脂肪酸(3 - 100微摩尔)、EPA、DHA和二十二碳五烯酸(DPA)以浓度依赖方式抑制激动剂诱导的Icat。抑制作用的效力为EPA>DHA>DPA,EPA的半数最大抑制浓度(IC50)约为7微摩尔。6. 花生四烯酸和亚油酸(10、30微摩尔)与ω-3脂肪酸相比显示出较小的抑制作用。此外,油酸和硬脂酸(30微摩尔)对Icat没有显著抑制作用。7. 当在没有激动剂的情况下通过细胞内应用GTPγS激活Icat时,观察到EPA有类似的抑制作用,表明ω-3脂肪酸的作用位点不在受体上。8. 这些结果表明,ω-3多不饱和脂肪酸可以激活钾离子电流,并且还能有效抑制大鼠A7r5血管平滑肌细胞中受体介导的非选择性阳离子电流。因此,数据表明ω-3脂肪酸可能在血管张力调节中起重要作用。

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