Inci Sahin-Erdemli , Russell M. Medford , Emel Songu-Mize
{"title":"高血压大鼠组织中Na+,K+- atp酶α-亚基亚型的调控","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":"{\"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}","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}
Regulation of Na+,K+-ATPase α-subunit isoforms in rat tissues during hypertension
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.