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通过亚缺氧性氧含量下降上调心脏保护蛋白SUR2A

Upregulation of cardioprotective SUR2A by sub-hypoxic drop in oxygen.

作者信息

Mohammed Abdul Khaja Shameem, Jovanović Sofija, Sukhodub Andriy, Du Qingyou, Jovanović Aleksandar

机构信息

Medical Research Institute, Division of Cardiovascular & Diabetic Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, DD1 9SY Scotland, UK.

Medical Research Institute, Division of Cardiovascular & Diabetic Medicine, Ninewells Hospital & Medical School, University of Dundee, Dundee, DD1 9SY Scotland, UK.

出版信息

Biochim Biophys Acta. 2014 Nov;1843(11):2424-31. doi: 10.1016/j.bbamcr.2014.07.007. Epub 2014 Jul 23.

Abstract

The effects of hypoxia on gene expression have been vigorously studied, but possible effects of small changes in oxygen tension have never been addressed. SUR2A is an atypical ABC protein serving as a regulatory subunit of sarcolemmal ATP-sensitive K(+) (KATP) channels. Up-regulation of SUR2A is associated with cardioprotection and improved physical endurance. Here, we have found that a 24h-long exposure to slightly decreased ambient fractional concentration of oxygen (20% oxygen), which is an equivalent to oxygen tension at 350m above sea level, significantly increased levels of SUR2A in the heart despite that this drop of oxygen did not affect levels of O2, CO2 and hematocrit in the blood or myocardial levels of ATP, lactate and NAD/NADH/NAD(+). Hearts from mice exposed to 20% oxygen were significantly more resistant to ischaemia-reperfusion when compared to control ones. Decrease in fractional oxygen concentration of just 0.9% was associated with phosphorylation of ERK1/2, but not Akt, which was essential for up-regulation of SUR2A. These findings indicate that a small drop in oxygen tension up-regulates SUR2A in the heart by activating ERK signaling pathway. This is the first report to suggest that a minimal change in oxygen tension could have a profound signaling effect.

摘要

缺氧对基因表达的影响已得到深入研究,但氧张力微小变化可能产生的影响却从未被探讨过。SUR2A是一种非典型ABC蛋白,作为肌膜ATP敏感性钾(KATP)通道的调节亚基。SUR2A的上调与心脏保护和耐力提高有关。在此,我们发现,在相当于海拔350米处的氧张力的环境氧分数浓度略有降低(20%氧气)的条件下暴露24小时,尽管这种氧含量下降并未影响血液中的O2、CO2和血细胞比容水平或心肌中的ATP、乳酸和NAD/NADH/NAD(+)水平,但心脏中SUR2A的水平却显著增加。与对照小鼠相比,暴露于20%氧气环境下的小鼠心脏对缺血再灌注的耐受性明显更强。氧分数浓度仅降低0.9%就与ERK1/2的磷酸化有关,但与Akt无关,而ERK1/2的磷酸化是SUR2A上调所必需的。这些发现表明,氧张力的微小下降通过激活ERK信号通路来上调心脏中的SUR2A。这是第一份表明氧张力的微小变化可能产生深远信号效应的报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e01f/4331663/edcdd695e57c/gr1.jpg

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