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脂质对培养的小鼠皮质集合管细胞中ENaC活性的影响。

Effects of lipids on ENaC activity in cultured mouse cortical collecting duct cells.

作者信息

Wang Su, Meng Fei, Xu Jingyuan, Gu Yuchun

机构信息

Department of Physiology, University of Birmingham, Edgbaston, B15 2TT, UK.

出版信息

J Membr Biol. 2009 Jan;227(2):77-85. doi: 10.1007/s00232-008-9145-1. Epub 2009 Jan 3.

Abstract

Direct effects on epithelial Na+ channels (ENaC) activity by lipids, e.g., arachidonic acid (AA), eicosatetraynoic acid (ETYA), linoleic acid (LA), stearic acid (SA), hydroxyeicosatetraenoic acid (HETE), 11,12-epoxyeicosatrienoic acid (EET), (PGF2), and (PGE2), in cultured mouse cortical collecting duct (M1) cells were clarified by using single-channel recordings in this study. In a cell-attached recording, a bath application of 10 microM AA significantly reduced the ENaC open probability (NPo), whereas 10 microM ETYA or 5 microM LA only induced a slight inhibition. The inside-out recording as a standard protocol was thereafter performed to examine effects of these lipids on ENaC activity. Within 10 min after the formation of the inside-out configuration, the NPo of ENaC in cultured mouse cortical collecting duct (M1) cells remained relatively constant. Application of ETYA or LA or SA exhibited a similar inhibition on the channel NPo when applied to the extracellular side, suggesting that fatty acids could exert a nonspecific inhibition on ENaC activity. 11,12-EET, a metabolite of AA via the cytochrome P450 epoxygenase pathway, significantly inhibited the ENaC NPo, whereas 20-HETE, a metabolite of AA via the hydroxylase pathway, only caused a small inhibition of the ENaC NPo, to a similar degree as that seen with ETYA and LA. However, both PGE2 and PGF2alpha significantly enhanced the ENaC NPo. These results suggest that fatty acids exert a nonspecific effect on ENaC activity due to the interaction between the channel proximity and the lipid. The opposite effects of 11,12-EET and prostaglandin (PG) implicate different mechanisms in regulation of ENaC activity by activation of epoxygenase and cyclooxygenase.

摘要

本研究通过单通道记录明确了脂质(如花生四烯酸(AA)、二十碳四炔酸(ETYA)、亚油酸(LA)、硬脂酸(SA)、羟基花生四烯酸(HETE)、11,12-环氧二十碳三烯酸(EET)、前列腺素F2(PGF2)和前列腺素E2(PGE2))对培养的小鼠皮质集合管(M1)细胞上皮钠通道(ENaC)活性的直接影响。在细胞贴附式记录中,向浴槽中加入10微摩尔的AA可显著降低ENaC的开放概率(NPo),而10微摩尔的ETYA或5微摩尔的LA仅引起轻微抑制。此后,采用标准的内面向外式记录方法来研究这些脂质对ENaC活性的影响。在形成内面向外式构型后的10分钟内,培养的小鼠皮质集合管(M1)细胞中ENaC的NPo保持相对稳定。当将ETYA、LA或SA应用于细胞外侧时,对通道NPo表现出类似的抑制作用,这表明脂肪酸可能对ENaC活性产生非特异性抑制。11,12-EET是AA经细胞色素P450环氧化酶途径的代谢产物,可显著抑制ENaC的NPo,而20-HETE是AA经羟化酶途径的代谢产物,仅对ENaC的NPo产生较小的抑制作用,其程度与ETYA和LA相似。然而,PGE2和PGF2α均显著提高了ENaC的NPo。这些结果表明,由于通道附近与脂质之间的相互作用,脂肪酸对ENaC活性产生非特异性影响。11,12-EET与前列腺素(PG)的相反作用暗示了通过环氧化酶和环氧合酶激活对ENaC活性进行调节的不同机制。

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