ATP-sensitive K<sup>+</sup> channels (K<sub>ATP</sub>) are major component of preventing ischemia-reperfusion injury. However, there is little information regarding to the expressional difference of K<sub>ATP</sub>...
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https://www.riss.kr/link?id=A105380380
2011
-
518
SCIE,SCOPUS,KCI등재
학술저널
189-194(6쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
ATP-sensitive K<sup>+</sup> channels (K<sub>ATP</sub>) are major component of preventing ischemia-reperfusion injury. However, there is little information regarding to the expressional difference of K<sub>ATP</sub>...
ATP-sensitive K<sup>+</sup> channels (K<sub>ATP</sub>) are major component of preventing ischemia-reperfusion injury. However, there is little information regarding to the expressional difference of K<sub>ATP</sub> and its function between left and right ventricles. In this study, we measured the lactate dehydrogenase release of rabbit heart slices in vitro and determined the difference of the K<sub>ATP</sub> expression at the both ventricles by measuring the level of K<sub>ATP</sub>-forming Kir6.2 (OcKir6.2) mRNA using in situ hybridization. The hearts were preconditioned with 15 min hypoxia and reoxygenated for 15 min before a hypoxic period of 60 min, followed by reoxygenation for 180 min. With hypoxic preconditioning (100% N<sub>2</sub>) with 15 min, left ventricles (LV) showed higher release of LDH comparing with right ventricles (RV). Adding K<sub>ATP</sub> blocker glibenclamide (10ՌM) prior to a hypoxic period of 60 min, hypoxic preconditioning effect of RV was more abolished than LV. With in situ hybridization, the optical density of OcKir6.2 was higher in RV. Therefore, we suggest that different K<sub>ATP</sub> expression between LV and RV is responsible for the different response to hypoxia and hypoxic preconditioning of rabbit hearts.