Hatton C J, Peers C
Institute for Cardiovascular Research, University of Leeds, Leeds LS2 9JT, UK.
Brain Res. 1998 Mar 23;787(2):315-20. doi: 10.1016/s0006-8993(97)01486-8.
Whole-cell patch-clamp recordings were used to investigate the effects of arachidonic acid (AA) on K+ and Ca2+ channels in isolated rat type I carotid body cells. AA (2-20 microM) produced a concentration-dependent inhibition of both K+ currents and Ca2+ channel currents. The effects of AA on K+ currents were unaffected by indomethacin (5 microM), phenidone (5 microM) or 1-aminobenzotriazole (3 mM), suggesting that AA did not exert its effects via cyclo-oxygenase, lipoxygenase or cytochrome P-450 (cP-450) metabolism. Our results suggest that AA directly and non-selectively inhibits ionic currents in rat type I carotid body cells.
采用全细胞膜片钳记录技术,研究花生四烯酸(AA)对分离的大鼠I型颈动脉体细胞中钾离子(K+)通道和钙离子(Ca2+)通道的影响。AA(2 - 20微摩尔)对K+电流和Ca2+通道电流均产生浓度依赖性抑制作用。AA对K+电流的影响不受吲哚美辛(5微摩尔)、非那吡啶(5微摩尔)或1 - 氨基苯并三唑(3毫摩尔)的影响,这表明AA并非通过环氧化酶、脂氧化酶或细胞色素P - 450(cP - 450)代谢发挥其作用。我们的结果表明,AA直接且非选择性地抑制大鼠I型颈动脉体细胞中的离子电流。