Inci Sahin-Erdemli , Russell M. Medford , Emel Songu-Mize
{"title":"Regulation of Na+,K+-ATPase α-subunit isoforms in rat tissues during hypertension","authors":"Inci Sahin-Erdemli , Russell M. Medford , Emel Songu-Mize","doi":"10.1016/0926-6917(95)90009-8","DOIUrl":null,"url":null,"abstract":"<div><p>We investigated the regulation of the protein expression of the α isozymes of Na<sup>+</sup>,K<sup>+</sup>-ATPase in reference to the enzyme activity in the heart, brain skeletal muscle of rats during deoxycorticosterone acetate (DOCA)-salt hypertension. Treatment of rats with DOCA and salt for 28 days produced a significant increase in systolic blood pressure compared to the control groups which remained normotensive. Rats treated with DOCA expressed greater amounts of the immunoreactive α-1 isoform than untreated controls in whole heart membranes. However, the DOCA-induced increase in the α-1 isoform did not occur during DOCA-salt hypertension. There was a parallel change in the enzyme activity of the Na<sup>+</sup>,K<sup>+</sup>-ATPase and the protein expression of the α-1 isoform as a result of these treatments. We have also demonstrated that the hearts of DOCA-salt hypertensive rats expressed less of the α-2 isoform compared to the controls. We could not detect any alteration in the α-1 and α-2 isoforms of the skeletal muscle and α-1, α-2 and α-3 isoforms of the whole brain Na<sup>+</sup>,K<sup>+</sup>-ATPase during salt or DOCA treatments alone or DOCA-salt hypertension. Furthermore, the Na<sup>+</sup>,K<sup>+</sup>-ATPase activity was unaltered in these tissues during these treatments. In conclusion, cardiac Na<sup>+</sup>,K<sup>+</sup>-ATPase α-subunit protein expression appears to be regulated during DOCA-salt hypertension. In the skeletal muscle and brain, tissues not subjected directly to increased pressure, this regulation of the Na<sup>+</sup>,K<sup>+</sup>-ATPase was not apparent.</p></div>","PeriodicalId":100501,"journal":{"name":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","volume":"292 2","pages":"Pages 163-171"},"PeriodicalIF":0.0000,"publicationDate":"1995-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6917(95)90009-8","citationCount":"26","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926691795900098","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 26
Abstract
We investigated the regulation of the protein expression of the α isozymes of Na+,K+-ATPase in reference to the enzyme activity in the heart, brain skeletal muscle of rats during deoxycorticosterone acetate (DOCA)-salt hypertension. Treatment of rats with DOCA and salt for 28 days produced a significant increase in systolic blood pressure compared to the control groups which remained normotensive. Rats treated with DOCA expressed greater amounts of the immunoreactive α-1 isoform than untreated controls in whole heart membranes. However, the DOCA-induced increase in the α-1 isoform did not occur during DOCA-salt hypertension. There was a parallel change in the enzyme activity of the Na+,K+-ATPase and the protein expression of the α-1 isoform as a result of these treatments. We have also demonstrated that the hearts of DOCA-salt hypertensive rats expressed less of the α-2 isoform compared to the controls. We could not detect any alteration in the α-1 and α-2 isoforms of the skeletal muscle and α-1, α-2 and α-3 isoforms of the whole brain Na+,K+-ATPase during salt or DOCA treatments alone or DOCA-salt hypertension. Furthermore, the Na+,K+-ATPase activity was unaltered in these tissues during these treatments. In conclusion, cardiac Na+,K+-ATPase α-subunit protein expression appears to be regulated during DOCA-salt hypertension. In the skeletal muscle and brain, tissues not subjected directly to increased pressure, this regulation of the Na+,K+-ATPase was not apparent.