首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Medicine >Inhibition of 15-lipoxygenase (15-LOX) reverses hypoxia-induced down-regulation of potassium channels Kv1.5 and Kv2.1Inhibition of 15-lipoxygenase (15-LOX) reverses hypoxia-induced down-regulation of potassium channels Kv1.5 and Kv2.1
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Inhibition of 15-lipoxygenase (15-LOX) reverses hypoxia-induced down-regulation of potassium channels Kv1.5 and Kv2.1Inhibition of 15-lipoxygenase (15-LOX) reverses hypoxia-induced down-regulation of potassium channels Kv1.5 and Kv2.1

机译:抑制15-脂氧合酶(15-LOX)逆转低氧诱导的钾通道Kv1.5和Kv2.1的抑制抑制15-脂氧合酶(15-LOX)逆转低氧诱导的钾通道Kv1.5和Kv2.1的向下调节。 Kv2.1

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摘要

The inhibition of voltage-gated potassium channels (Kv) plays an important role in the cerebral hypoxia-induced cell death. The activity of Kv can be inhibited by 15-hydroxyeicosatetrienoic acid (15-HETE). Therefore, as the key enzyme which catalyzed the formation of 15-HETE, 15-LOX may be involved in Kv inhibition induced by cerebral hypoxia. In our study, Wistar rats cerebral arterial smooth muscle cells (CASMCs) were placed under the condition of hypoxia and control, 15-LOX was proved involved in hypoxia-induced vasoconstriction. Furthermore, 15-LOX gene over expression under normoxic condition, as well as 15-LOX gene knockout or inhibition under hypoxic condition was performed to investigate the expression and activity of Kv1.5 and Kv2.1 in CASMCs. Results showed that both hypoxia and 15-LOX over expression could cause Kv1.5 and Kv2.1 suppression, but no suppression was observed under hypoxic condition when 15-LOX gene was knockout or inhibited, which made 15-LOX a new target for the treatment of cerebral hypoxia. In conclusion, AA/15-LOX/15-HETE induces vasoconstriction by down-regulating Kv channels, and Kv2.1/1.5 channels are the targets. Our study also suggests a therapeutic strategy to improve ischemic vascular occlusion by lowering 15-HETE level and preventing Kv channel down-regulation, which makes 15-LOX as a new target for the treatment of cerebral hypoxia.
机译:电压门控钾通道(Kv)的抑制在脑缺氧诱导的细胞死亡中起重要作用。 Kv的活性可以被15-羟基二十二碳三烯酸(15-HETE)抑制。因此,15-LOX作为催化15-HETE形成的关键酶可能参与了脑缺氧诱导的Kv抑制。在我们的研究中,将Wistar大鼠脑动脉平滑肌细胞(CASMC)置于缺氧和对照条件下,事实证明15-LOX参与了缺氧诱导的血管收缩。此外,进行了15-LOX基因在常氧条件下的过度表达以及15-LOX基因敲低或在低氧条件下的抑制,以研究CASMC中Kv1.5和Kv2.1的表达和活性。结果表明,低氧和15-LOX过表达均可引起Kv1.5和Kv2.1抑制,但是在低氧条件下敲除或抑制15-LOX基因未见抑制作用,这使15-LOX成为新的靶标。治疗脑缺氧。总之,AA / 15-LOX / 15-HETE通过下调Kv通道诱导血管收缩,而Kv2.1 / 1.5通道是目标。我们的研究还提出了通过降低15-HETE水平和防止Kv通道下调来改善缺血性血管闭塞的治疗策略,这使15-LOX成为治疗脑缺氧的新靶标。

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