Insulin induced translocation of Na^＋/K^＋-ATPase is decreased in the heart of streptozotocin diabetic rats  

作　　者：Klara ROSTA Eszter TULASSAY Anna ENZSOLY Katalin RONAI Ambrus SZANTHO Tamas PANDICS Andrea FEKETE Peter MANDL Agota VER 

机构地区：[1]Department of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, Budapest, Hungary [2]Department of Anesthesiology and Intensive Therapy, Semmelweis University, Budapest, Hungary [3]University of Coimbra, University Hospital, Coimbra, Portugal [4]National Institute Enviromental Health, Budapest, Hungary [5]Research Group for Pediatrics and Nephrology of the Hungarian Academy of Sciences and of the Semmelweis University, Budapest, Hungary [6]National Institute of Rheumatology and Physiotherapy, Budapest, Hungary

出　　处：《Acta Pharmacologica Sinica》2009年第12期1616-1624,共9页中国药理学报（英文版）

摘　　要：To investigate the effect of acute insulin administration on the subcellular localization of Na^＋/K^＋-ATPase isoforms in cardiac muscle of healthy and streptozotocin-induced diabetic rats. Methods： Membrane fractions were isolated with subcellular fractionation and with cell surface biotinylation technique.Na^＋/K^＋- ATPase subunit isoforms were analysed with ouabain binding assay and Western blotting. Enzyme activity was measured using 3-0- methylfl uorescein-phosphatase activity. Results： In control rat heart muscle α1 isoform of Na^＋/K^＋ ATPase resides mainly in the plasma membrane fraction, while α2 isoform in the intracellular membrane pool. Diabetes decreased the abundance of α1 isoform （25 %, P〈0.05） in plasma membrane and α2 isoform （50%, P〈0.01） in the intracellular membrane fraction. When plasma membrane fractions were isolated by discontinuous sucrose gradients, insulin-stimulated translocation of α2- but not al-subunits was detected, al-Subunit translocation was only detectable by cell surface biotinylation technique. After insulin administration protein level of α2 increased by 3.3-fold, α1 by 1.37-fold and β1 by 1.51-fold （P〈0.02） in the plasma membrane of control, and less than 1.92-fold （P〈0.02）, 1.19-fold （not significant） and 1.34-fold （P〈0.02） in diabetes. The insulin-induced translocation was wortmannin sensitive. Conclusion： This study demonstrate that insulin influences the plasma membrane localization of Na^＋/K^＋-ATPase isoforms in the heart. α2 isoform translocation is the most vulnerable to the reduced insulin response in diabetes, α1 isoform also translocates in response to insulin treatment in healthy rat. Insulin mediates Na^＋/K^＋-ATPase （α1- and α2-subunit translocation to the cardiac muscle plasma membrane via a PI3-kinase-dependent mechanism.To investigate the effect of acute insulin administration on the subcellular localization of Na^＋/K^＋-ATPase isoforms in cardiac muscle of healthy and streptozotocin-induced diabetic rats. Methods： Membrane fractions were isolated with subcellular fractionation and with cell surface biotinylation technique.Na^＋/K^＋- ATPase subunit isoforms were analysed with ouabain binding assay and Western blotting. Enzyme activity was measured using 3-0- methylfl uorescein-phosphatase activity. Results： In control rat heart muscle α1 isoform of Na^＋/K^＋ ATPase resides mainly in the plasma membrane fraction, while α2 isoform in the intracellular membrane pool. Diabetes decreased the abundance of α1 isoform （25 %, P〈0.05） in plasma membrane and α2 isoform （50%, P〈0.01） in the intracellular membrane fraction. When plasma membrane fractions were isolated by discontinuous sucrose gradients, insulin-stimulated translocation of α2- but not al-subunits was detected, al-Subunit translocation was only detectable by cell surface biotinylation technique. After insulin administration protein level of α2 increased by 3.3-fold, α1 by 1.37-fold and β1 by 1.51-fold （P〈0.02） in the plasma membrane of control, and less than 1.92-fold （P〈0.02）, 1.19-fold （not significant） and 1.34-fold （P〈0.02） in diabetes. The insulin-induced translocation was wortmannin sensitive. Conclusion： This study demonstrate that insulin influences the plasma membrane localization of Na^＋/K^＋-ATPase isoforms in the heart. α2 isoform translocation is the most vulnerable to the reduced insulin response in diabetes, α1 isoform also translocates in response to insulin treatment in healthy rat. Insulin mediates Na^＋/K^＋-ATPase （α1- and α2-subunit translocation to the cardiac muscle plasma membrane via a PI3-kinase-dependent mechanism.

关 键 词：rat cardiac muscle streptozotocin-diabetes Na^＋/K^＋-ATPase isoenzyme REDISTRIBUTION 

分 类 号：Q578[生物学—生物化学] T-332[一般工业技术]