Hypoxia suppresses Kv 2.1 channel expression through endogenous 15-hydroxyeicosatetraenoic acid in rat pulmonary artery

被引:7
|
作者
Guo, Lei [1 ]
Qiu, Zhaoping [1 ]
Zhang, Lei [1 ]
Chen, Shuo [1 ]
Zhu, Daling [1 ,2 ]
机构
[1] Harbin Med Univ, Dept Biopharmaceut Sci, Coll Pharm, Harbin 150081, Heilongjiang, Peoples R China
[2] Biopharmaceut Key Lab Heilongjiang Prov, Harbin 150081, Peoples R China
来源
JOURNAL OF PHYSIOLOGICAL SCIENCES | 2010年 / 60卷 / 05期
基金
中国国家自然科学基金;
关键词
Kv2.1; 15-HETE; 5-HETE; 12-HETE; Hypoxia; SMOOTH-MUSCLE; K+ CHANNELS; GENE-EXPRESSION; VASOCONSTRICTION; MYOCYTES; OXYGEN; CELLS; INHIBITION; SUBUNIT; 15-HETE;
D O I
10.1007/s12576-010-0105-z
中图分类号
Q4 [生理学];
学科分类号
071003 ;
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.
引用
收藏
页码:373 / 381
页数:9
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