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首页> 外文期刊>The Journal of Physiological Sciences >Hypoxia suppresses Kv 2.1 channel expression through endogenous 15-hydroxyeicosatetraenoic acid in rat pulmonary artery
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Hypoxia suppresses Kv 2.1 channel expression through endogenous 15-hydroxyeicosatetraenoic acid in rat pulmonary artery

机译:缺氧通过大鼠肺动脉内源性15-羟基二十碳四烯酸抑制Kv 2.1通道表达

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摘要

We have previously reported that hypoxia activates lung 15-lipoxygenase (15-LOX), which catalyzes arachidonic acid to produce 15-HETE, leading to constriction of neonatal rabbit pulmonary arteries. Hypoxia suppresses Kv2.1 channel expression. Although the Kv channel inhibition by hypoxia is likely to be mediated through 15-HETE, direct evidence is still lacking. To explore whether 15-LOX/15-HETE pathway contributes to the hypoxia-induced down-regulation of Kv2.1 channel, we performed studies using 15-LOX blockers, semi-quantitative PCR and western blot analysis. We found that Kv2.1 channel expression at the mRNA and protein levels was greatly up-regulated in pulmonary arterial smooth muscle cells (PASMCs) and pulmonary artery (PA) after blockade of endogenous 15-HETE under hypoxic condition. 15-HETE further decreased Kv2.1 channel expression in comparison with 12-HETE and 5-HETE in cultured PASMCs and PA under normoxic conditions. These data indicate that hypoxia suppresses Kv2.1 channel expression through endogenous 15-HETE in PA.
机译:先前我们曾报道过,低氧激活肺15-脂氧合酶(15-LOX),该酶催化花生四烯酸产生15-HETE,从而导致新生兔肺动脉收缩。缺氧抑制Kv2.1通道表达。尽管低氧对Kv通道的抑制作用可能是通过15-HETE介导的,但仍然缺乏直接的证据。为了探讨15-LOX / 15-HETE通路是否有助于缺氧诱导的Kv2.1通道下调,我们使用15-LOX阻断剂,半定量PCR和Western blot分析进行了研究。我们发现在缺氧条件下内源性15-HETE阻断后,肺动脉平滑肌细胞(PASMCs)和肺动脉(PA)中mRNA和蛋白水平的Kv2.1通道表达大大上调。在常氧条件下,培养的PASMC和PA中15-HETE与12-HETE和5-HETE相比进一步降低了Kv2.1通道表达。这些数据表明低氧通过PA中的内源性15-HETE抑制Kv2.1通道表达。

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