Effects of Dietary Salt Load and Salt Depletion on the Course of Hypertension and Angiotensin II Levels in Male and Female Heterozygous Ren-2 Transgenic Rats
Background: In the present study we evaluated plasma and kidney angiotensin II (ANG II) levels in female and male Ren-2 transgenic rats (TGR) in comparison to age-matched female and male normotensive Hannover Sprague-Dawley rats. Methods: The rats were maintained on a normal sodium (NS) diet (0.6% N...
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Veröffentlicht in: | Kidney & blood pressure research 2007-01, Vol.30 (1), p.45-55 |
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creator | Husková, Zuzana Kramer, Herbert J. Vaňourková, Zdenka Thumová, Monika Malý, Jan Opočenský, Martin Škaroupková, Petra Kolský, Alexander Vernerová, Zdena Červenka, Luděk |
description | Background: In the present study we evaluated plasma and kidney angiotensin II (ANG II) levels in female and male Ren-2 transgenic rats (TGR) in comparison to age-matched female and male normotensive Hannover Sprague-Dawley rats. Methods: The rats were maintained on a normal sodium (NS) diet (0.6% NaCl) or fed a high sodium (HS) diet (2% NaCl) for 4 days or were sodium depleted by administration of 40 mg furosemide per liter drinking water overnight followed by 3 days of low sodium diet (0.01% NaCl) (LS + F). ANG II levels were determined by radioimmunoassay. Results: Female TGR at the age of 38 days were already hypertensive and had developed cardiac hypertrophy, whereas male TGR at this age still exhibited a normotensive phenotype. HS diet increased the blood pressure (BP) but did not alter the ANG II levels in TGR at any age. LS + F decreased the BP without significant change in ANG II concentrations in TGR. Female TGR responded to salt loading and salt depletion by more pronounced changes in BP than male TGR. Conclusions: Female TGR develop hypertension more rapidly and the salt-sensitive component of hypertension is more pronounced in female than in male TGR. |
doi_str_mv | 10.1159/000099028 |
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Methods: The rats were maintained on a normal sodium (NS) diet (0.6% NaCl) or fed a high sodium (HS) diet (2% NaCl) for 4 days or were sodium depleted by administration of 40 mg furosemide per liter drinking water overnight followed by 3 days of low sodium diet (0.01% NaCl) (LS + F). ANG II levels were determined by radioimmunoassay. Results: Female TGR at the age of 38 days were already hypertensive and had developed cardiac hypertrophy, whereas male TGR at this age still exhibited a normotensive phenotype. HS diet increased the blood pressure (BP) but did not alter the ANG II levels in TGR at any age. LS + F decreased the BP without significant change in ANG II concentrations in TGR. Female TGR responded to salt loading and salt depletion by more pronounced changes in BP than male TGR. Conclusions: Female TGR develop hypertension more rapidly and the salt-sensitive component of hypertension is more pronounced in female than in male TGR.</description><identifier>ISSN: 1420-4096</identifier><identifier>EISSN: 1423-0143</identifier><identifier>DOI: 10.1159/000099028</identifier><identifier>PMID: 17259738</identifier><identifier>CODEN: RPBIEL</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Angiotensin II - blood ; Angiotensin II - metabolism ; Angiotensin II - pharmacology ; Animals ; Animals, Genetically Modified ; Blood Pressure ; Cardiomegaly - blood ; Cardiomegaly - diet therapy ; Female ; Heterozygote ; Hypertension, Renal - blood ; Hypertension, Renal - diet therapy ; Kidney - blood supply ; Kidney - physiopathology ; Male ; Original Paper ; Rats ; Rats, Sprague-Dawley ; Renin - genetics ; Renin - metabolism ; Renin-Angiotensin System - physiology ; Sex Characteristics ; Sodium Chloride, Dietary - therapeutic use</subject><ispartof>Kidney & blood pressure research, 2007-01, Vol.30 (1), p.45-55</ispartof><rights>2007 S. Karger AG, Basel</rights><rights>Copyright 2007 S. Karger AG, Basel.</rights><rights>Copyright (c) 2007 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c361t-b2760b8d33aff01839f10bdfb92e86526e0347e41d2fae065634ea863c5e94b93</citedby><cites>FETCH-LOGICAL-c361t-b2760b8d33aff01839f10bdfb92e86526e0347e41d2fae065634ea863c5e94b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,2423,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17259738$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Husková, Zuzana</creatorcontrib><creatorcontrib>Kramer, Herbert J.</creatorcontrib><creatorcontrib>Vaňourková, Zdenka</creatorcontrib><creatorcontrib>Thumová, Monika</creatorcontrib><creatorcontrib>Malý, Jan</creatorcontrib><creatorcontrib>Opočenský, Martin</creatorcontrib><creatorcontrib>Škaroupková, Petra</creatorcontrib><creatorcontrib>Kolský, Alexander</creatorcontrib><creatorcontrib>Vernerová, Zdena</creatorcontrib><creatorcontrib>Červenka, Luděk</creatorcontrib><title>Effects of Dietary Salt Load and Salt Depletion on the Course of Hypertension and Angiotensin II Levels in Male and Female Heterozygous Ren-2 Transgenic Rats</title><title>Kidney & blood pressure research</title><addtitle>Kidney Blood Press Res</addtitle><description>Background: In the present study we evaluated plasma and kidney angiotensin II (ANG II) levels in female and male Ren-2 transgenic rats (TGR) in comparison to age-matched female and male normotensive Hannover Sprague-Dawley rats. Methods: The rats were maintained on a normal sodium (NS) diet (0.6% NaCl) or fed a high sodium (HS) diet (2% NaCl) for 4 days or were sodium depleted by administration of 40 mg furosemide per liter drinking water overnight followed by 3 days of low sodium diet (0.01% NaCl) (LS + F). ANG II levels were determined by radioimmunoassay. Results: Female TGR at the age of 38 days were already hypertensive and had developed cardiac hypertrophy, whereas male TGR at this age still exhibited a normotensive phenotype. HS diet increased the blood pressure (BP) but did not alter the ANG II levels in TGR at any age. LS + F decreased the BP without significant change in ANG II concentrations in TGR. Female TGR responded to salt loading and salt depletion by more pronounced changes in BP than male TGR. Conclusions: Female TGR develop hypertension more rapidly and the salt-sensitive component of hypertension is more pronounced in female than in male TGR.</description><subject>Angiotensin II - blood</subject><subject>Angiotensin II - metabolism</subject><subject>Angiotensin II - pharmacology</subject><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Blood Pressure</subject><subject>Cardiomegaly - blood</subject><subject>Cardiomegaly - diet therapy</subject><subject>Female</subject><subject>Heterozygote</subject><subject>Hypertension, Renal - blood</subject><subject>Hypertension, Renal - diet therapy</subject><subject>Kidney - blood supply</subject><subject>Kidney - physiopathology</subject><subject>Male</subject><subject>Original Paper</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Renin - genetics</subject><subject>Renin - metabolism</subject><subject>Renin-Angiotensin System - physiology</subject><subject>Sex Characteristics</subject><subject>Sodium Chloride, Dietary - therapeutic use</subject><issn>1420-4096</issn><issn>1423-0143</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkU1r4zAQhkXp0q_dQ8-FInoo9OCtPmzZOob0I4EshW73bGR7lLp1pFRSCul_6X-tHIcW9lIh0Iz0vMNoXoSOKflNaSYvSVxSElbsoAOaMp4QmvLdTUySlEixjw69f4pURgjbQ_s0Z5nMeXGA3q-1hjp4bDW-aiEot8Z_VRfwzKoGK9MM2RUsOwitNTju8Ah4bFfOQ6-arJfgAhjfv_aCkZm3dnNh8HSKZ_AKnccx-aM62BA3sOjDCQRw9m09tyuP78EkDD84ZfwcTFvjexX8T_RDq87Dr-15hP7dXD-MJ8ns7nY6Hs2SmgsakorlglRFw7nSmtCCS01J1ehKMihExgQQnuaQ0oZpBURkgqegCsHrDGRaSX6Ezoe6S2dfVuBDuWh9DV2nDMTmSiH7AbPiW5ARyRllWQTP_gOf4sRM_ETJWEoZz7O-2sUA1c5670CXS9cuogUlJWXvbPnpbGRPtwVX1QKaL3JrZQROBuBZuTm4T2CQfwDAZaXQ</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Husková, Zuzana</creator><creator>Kramer, Herbert J.</creator><creator>Vaňourková, Zdenka</creator><creator>Thumová, Monika</creator><creator>Malý, Jan</creator><creator>Opočenský, Martin</creator><creator>Škaroupková, Petra</creator><creator>Kolský, Alexander</creator><creator>Vernerová, Zdena</creator><creator>Červenka, Luděk</creator><general>S. 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blood</topic><topic>Angiotensin II - metabolism</topic><topic>Angiotensin II - pharmacology</topic><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>Blood Pressure</topic><topic>Cardiomegaly - blood</topic><topic>Cardiomegaly - diet therapy</topic><topic>Female</topic><topic>Heterozygote</topic><topic>Hypertension, Renal - blood</topic><topic>Hypertension, Renal - diet therapy</topic><topic>Kidney - blood supply</topic><topic>Kidney - physiopathology</topic><topic>Male</topic><topic>Original Paper</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Renin - genetics</topic><topic>Renin - metabolism</topic><topic>Renin-Angiotensin System - physiology</topic><topic>Sex Characteristics</topic><topic>Sodium Chloride, Dietary - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Husková, Zuzana</creatorcontrib><creatorcontrib>Kramer, Herbert J.</creatorcontrib><creatorcontrib>Vaňourková, Zdenka</creatorcontrib><creatorcontrib>Thumová, Monika</creatorcontrib><creatorcontrib>Malý, Jan</creatorcontrib><creatorcontrib>Opočenský, Martin</creatorcontrib><creatorcontrib>Škaroupková, Petra</creatorcontrib><creatorcontrib>Kolský, Alexander</creatorcontrib><creatorcontrib>Vernerová, Zdena</creatorcontrib><creatorcontrib>Červenka, Luděk</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>SIRS Editorial</collection><collection>Biotechnology Research Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Kidney & blood pressure research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Husková, Zuzana</au><au>Kramer, Herbert J.</au><au>Vaňourková, Zdenka</au><au>Thumová, Monika</au><au>Malý, Jan</au><au>Opočenský, Martin</au><au>Škaroupková, Petra</au><au>Kolský, Alexander</au><au>Vernerová, Zdena</au><au>Červenka, Luděk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Dietary Salt Load and Salt Depletion on the Course of Hypertension and Angiotensin II Levels in Male and Female Heterozygous Ren-2 Transgenic Rats</atitle><jtitle>Kidney & blood pressure research</jtitle><addtitle>Kidney Blood Press Res</addtitle><date>2007-01-01</date><risdate>2007</risdate><volume>30</volume><issue>1</issue><spage>45</spage><epage>55</epage><pages>45-55</pages><issn>1420-4096</issn><eissn>1423-0143</eissn><coden>RPBIEL</coden><abstract>Background: In the present study we evaluated plasma and kidney angiotensin II (ANG II) levels in female and male Ren-2 transgenic rats (TGR) in comparison to age-matched female and male normotensive Hannover Sprague-Dawley rats. Methods: The rats were maintained on a normal sodium (NS) diet (0.6% NaCl) or fed a high sodium (HS) diet (2% NaCl) for 4 days or were sodium depleted by administration of 40 mg furosemide per liter drinking water overnight followed by 3 days of low sodium diet (0.01% NaCl) (LS + F). ANG II levels were determined by radioimmunoassay. Results: Female TGR at the age of 38 days were already hypertensive and had developed cardiac hypertrophy, whereas male TGR at this age still exhibited a normotensive phenotype. HS diet increased the blood pressure (BP) but did not alter the ANG II levels in TGR at any age. LS + F decreased the BP without significant change in ANG II concentrations in TGR. Female TGR responded to salt loading and salt depletion by more pronounced changes in BP than male TGR. Conclusions: Female TGR develop hypertension more rapidly and the salt-sensitive component of hypertension is more pronounced in female than in male TGR.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>17259738</pmid><doi>10.1159/000099028</doi><tpages>11</tpages></addata></record> |
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subjects | Angiotensin II - blood Angiotensin II - metabolism Angiotensin II - pharmacology Animals Animals, Genetically Modified Blood Pressure Cardiomegaly - blood Cardiomegaly - diet therapy Female Heterozygote Hypertension, Renal - blood Hypertension, Renal - diet therapy Kidney - blood supply Kidney - physiopathology Male Original Paper Rats Rats, Sprague-Dawley Renin - genetics Renin - metabolism Renin-Angiotensin System - physiology Sex Characteristics Sodium Chloride, Dietary - therapeutic use |
title | Effects of Dietary Salt Load and Salt Depletion on the Course of Hypertension and Angiotensin II Levels in Male and Female Heterozygous Ren-2 Transgenic Rats |
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