Role of AQP1 in endotoxemia-induced acute kidney injury
1 Department of Medicine, University of Colorado Health Sciences Center, Denver, Colorado; and 2 Department of Pathology, Dubrava University Hospital, Zagreb, Croatia Submitted 22 January 2008 ; accepted in final form 14 April 2008 The effect of endotoxemia (lipopolysaccharide, 2.5 mg/kg ip) was inv...
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Veröffentlicht in: | American journal of physiology. Renal physiology 2008-06, Vol.294 (6), p.F1473-F1480 |
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creator | Wang, Weidong Li, Chunling Summer, Sandra N Falk, Sandor Wang, Wei Ljubanovic, Danica Schrier, Robert W |
description | 1 Department of Medicine, University of Colorado Health Sciences Center, Denver, Colorado; and 2 Department of Pathology, Dubrava University Hospital, Zagreb, Croatia
Submitted 22 January 2008
; accepted in final form 14 April 2008
The effect of endotoxemia (lipopolysaccharide, 2.5 mg/kg ip) was investigated in aquaporin (AQP) 1 knockout (KO) compared with wild-type (WT) mice. At baseline, KO mice exhibited higher water intake (WI) and urine output (UO). After endotoxemia, WI and UO remained higher in the KO than WT mice, and urine osmolality was lower. The higher serum osmolality in AQP1-KO mice during endotoxemia was associated with higher AQP2 (133 ± 8 vs. 100 ± 3%, P < 0.01), AQP3 (140 ± 8 vs. 100 ± 4%, P < 0.001) and Na + -K + -2Cl – cotransporter type 2 (NKCC2; 152 ± 14 vs. 100 ± 15%, P < 0.05) expression than that in WT mice. These responses during endotoxemia in the AQP1-KO mice compared with WT were associated with lower glomerular filtration rate (GFR) (69 ± 8 vs. 96 ± 8 ml/min, P < 0.05) and renal blood flow (0.77 ± 0.1 vs. 1.01 ± 0.1 ml/min, P < 0.01). Urinary sodium excretion and fractional sodium excretion were higher in KO compared with WT mice in endotoxemia and were accompanied by more severe tubular injury. With water repletion and comparable serum osmolalities, GFR was still lower in KO (57 ± 13 vs. 120 ± 6 ml/min, P < 0.01) compared with WT during endotoxemia. The abundance of AQP2 and AQP3 protein in KO mice was not different from WT mice; however, NKCC2, Na + /H + exchanger type 3, and fractional sodium excretion remained higher in KO compared with WT. Thus the polyuria in AQP1-KO mice does not protect against endotoxemia-induced acute kidney injury but rather absence of AQP1 predisposed to enhanced endotoximic renal injury.
lipopolysaccharide; sepsis; glomerular filtration rate; polyuria; aquaporin-1
Address for reprint requests and other correspondence: R. W. Schrier, Division of Renal Diseases and Hypertension, Univ. of Colorado Health Sciences Center, 4200 East 9 th Ave., Box B173, Denver, CO 80262 (e-mail: Robert.Schrier{at}UCHSC.EDU ) |
doi_str_mv | 10.1152/ajprenal.00036.2008 |
format | Article |
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Submitted 22 January 2008
; accepted in final form 14 April 2008
The effect of endotoxemia (lipopolysaccharide, 2.5 mg/kg ip) was investigated in aquaporin (AQP) 1 knockout (KO) compared with wild-type (WT) mice. At baseline, KO mice exhibited higher water intake (WI) and urine output (UO). After endotoxemia, WI and UO remained higher in the KO than WT mice, and urine osmolality was lower. The higher serum osmolality in AQP1-KO mice during endotoxemia was associated with higher AQP2 (133 ± 8 vs. 100 ± 3%, P < 0.01), AQP3 (140 ± 8 vs. 100 ± 4%, P < 0.001) and Na + -K + -2Cl – cotransporter type 2 (NKCC2; 152 ± 14 vs. 100 ± 15%, P < 0.05) expression than that in WT mice. These responses during endotoxemia in the AQP1-KO mice compared with WT were associated with lower glomerular filtration rate (GFR) (69 ± 8 vs. 96 ± 8 ml/min, P < 0.05) and renal blood flow (0.77 ± 0.1 vs. 1.01 ± 0.1 ml/min, P < 0.01). Urinary sodium excretion and fractional sodium excretion were higher in KO compared with WT mice in endotoxemia and were accompanied by more severe tubular injury. With water repletion and comparable serum osmolalities, GFR was still lower in KO (57 ± 13 vs. 120 ± 6 ml/min, P < 0.01) compared with WT during endotoxemia. The abundance of AQP2 and AQP3 protein in KO mice was not different from WT mice; however, NKCC2, Na + /H + exchanger type 3, and fractional sodium excretion remained higher in KO compared with WT. Thus the polyuria in AQP1-KO mice does not protect against endotoxemia-induced acute kidney injury but rather absence of AQP1 predisposed to enhanced endotoximic renal injury.
lipopolysaccharide; sepsis; glomerular filtration rate; polyuria; aquaporin-1
Address for reprint requests and other correspondence: R. W. Schrier, Division of Renal Diseases and Hypertension, Univ. of Colorado Health Sciences Center, 4200 East 9 th Ave., Box B173, Denver, CO 80262 (e-mail: Robert.Schrier{at}UCHSC.EDU )]]></description><identifier>ISSN: 0363-6127</identifier><identifier>ISSN: 1931-857X</identifier><identifier>EISSN: 2161-1157</identifier><identifier>EISSN: 1522-1466</identifier><identifier>DOI: 10.1152/ajprenal.00036.2008</identifier><identifier>PMID: 18434389</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Acute Disease ; Animals ; Aquaporin 1 - genetics ; Aquaporin 1 - metabolism ; Blood ; Blood Pressure ; Drinking - physiology ; Endotoxemia - metabolism ; Endotoxemia - pathology ; Endotoxemia - physiopathology ; Glomerular Filtration Rate ; Infections ; Kidney - pathology ; Kidney - physiology ; Kidney diseases ; Kidney Diseases - metabolism ; Kidney Diseases - pathology ; Kidney Diseases - physiopathology ; Lipopolysaccharides - pharmacology ; Male ; Mice ; Mice, Knockout ; Polyuria - metabolism ; Polyuria - pathology ; Polyuria - physiopathology ; Renal Circulation ; Rodents ; Toxins ; Urine ; Water - metabolism</subject><ispartof>American journal of physiology. Renal physiology, 2008-06, Vol.294 (6), p.F1473-F1480</ispartof><rights>Copyright American Physiological Society Jun 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-de229a83d35e8f3efdb9c20e841d0181a180252fb58efe234098d36735f1620d3</citedby><cites>FETCH-LOGICAL-c422t-de229a83d35e8f3efdb9c20e841d0181a180252fb58efe234098d36735f1620d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,3026,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18434389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Weidong</creatorcontrib><creatorcontrib>Li, Chunling</creatorcontrib><creatorcontrib>Summer, Sandra N</creatorcontrib><creatorcontrib>Falk, Sandor</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><creatorcontrib>Ljubanovic, Danica</creatorcontrib><creatorcontrib>Schrier, Robert W</creatorcontrib><title>Role of AQP1 in endotoxemia-induced acute kidney injury</title><title>American journal of physiology. Renal physiology</title><addtitle>Am J Physiol Renal Physiol</addtitle><description><![CDATA[1 Department of Medicine, University of Colorado Health Sciences Center, Denver, Colorado; and 2 Department of Pathology, Dubrava University Hospital, Zagreb, Croatia
Submitted 22 January 2008
; accepted in final form 14 April 2008
The effect of endotoxemia (lipopolysaccharide, 2.5 mg/kg ip) was investigated in aquaporin (AQP) 1 knockout (KO) compared with wild-type (WT) mice. At baseline, KO mice exhibited higher water intake (WI) and urine output (UO). After endotoxemia, WI and UO remained higher in the KO than WT mice, and urine osmolality was lower. The higher serum osmolality in AQP1-KO mice during endotoxemia was associated with higher AQP2 (133 ± 8 vs. 100 ± 3%, P < 0.01), AQP3 (140 ± 8 vs. 100 ± 4%, P < 0.001) and Na + -K + -2Cl – cotransporter type 2 (NKCC2; 152 ± 14 vs. 100 ± 15%, P < 0.05) expression than that in WT mice. These responses during endotoxemia in the AQP1-KO mice compared with WT were associated with lower glomerular filtration rate (GFR) (69 ± 8 vs. 96 ± 8 ml/min, P < 0.05) and renal blood flow (0.77 ± 0.1 vs. 1.01 ± 0.1 ml/min, P < 0.01). Urinary sodium excretion and fractional sodium excretion were higher in KO compared with WT mice in endotoxemia and were accompanied by more severe tubular injury. With water repletion and comparable serum osmolalities, GFR was still lower in KO (57 ± 13 vs. 120 ± 6 ml/min, P < 0.01) compared with WT during endotoxemia. The abundance of AQP2 and AQP3 protein in KO mice was not different from WT mice; however, NKCC2, Na + /H + exchanger type 3, and fractional sodium excretion remained higher in KO compared with WT. Thus the polyuria in AQP1-KO mice does not protect against endotoxemia-induced acute kidney injury but rather absence of AQP1 predisposed to enhanced endotoximic renal injury.
lipopolysaccharide; sepsis; glomerular filtration rate; polyuria; aquaporin-1
Address for reprint requests and other correspondence: R. W. Schrier, Division of Renal Diseases and Hypertension, Univ. of Colorado Health Sciences Center, 4200 East 9 th Ave., Box B173, Denver, CO 80262 (e-mail: Robert.Schrier{at}UCHSC.EDU )]]></description><subject>Acute Disease</subject><subject>Animals</subject><subject>Aquaporin 1 - genetics</subject><subject>Aquaporin 1 - metabolism</subject><subject>Blood</subject><subject>Blood Pressure</subject><subject>Drinking - physiology</subject><subject>Endotoxemia - metabolism</subject><subject>Endotoxemia - pathology</subject><subject>Endotoxemia - physiopathology</subject><subject>Glomerular Filtration Rate</subject><subject>Infections</subject><subject>Kidney - pathology</subject><subject>Kidney - physiology</subject><subject>Kidney diseases</subject><subject>Kidney Diseases - metabolism</subject><subject>Kidney Diseases - pathology</subject><subject>Kidney Diseases - physiopathology</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Polyuria - metabolism</subject><subject>Polyuria - pathology</subject><subject>Polyuria - physiopathology</subject><subject>Renal Circulation</subject><subject>Rodents</subject><subject>Toxins</subject><subject>Urine</subject><subject>Water - metabolism</subject><issn>0363-6127</issn><issn>1931-857X</issn><issn>2161-1157</issn><issn>1522-1466</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kFFrFDEURoNY7Lb6CwQZfPBttjc3M5kMPpXiWqHQKvU5ZCc33VlnJ2MyQzv_3rS7VhF8CiTnfITD2FsOS85LPDPbIVBvuiUACLlEAPWCLZBLnqf36iVbpGuRS47VMTuJcQuAKJV8xY65KkQhVL1g1TffUeZddv71hmdtn1Fv_egfaNeavO3t1JDNTDONlP1obU9zYrZTmF-zI2e6SG8O5yn7vvp0e3GZX11__nJxfpU3BeKYW0KsjRJWlKScIGfXdYNAquAWuOKGK8AS3bpU5AhFAbWyQlaidFwiWHHKPux3h-B_ThRHvWtjQ11nevJT1BWXhUh4At__A279FFKeqFEAhwoQEiT2UBN8jIGcHkK7M2HWHPRjVP07qn6Kqh-jJuvdYXpa78j-cQ4VE_BxD2zau819G0gPmzm2vvN3s15NXXdLD-PzNNaFlnrFi0rowbpkn_3ffv7PX5b4BRUEmK4</recordid><startdate>20080601</startdate><enddate>20080601</enddate><creator>Wang, Weidong</creator><creator>Li, Chunling</creator><creator>Summer, Sandra N</creator><creator>Falk, Sandor</creator><creator>Wang, Wei</creator><creator>Ljubanovic, Danica</creator><creator>Schrier, Robert W</creator><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080601</creationdate><title>Role of AQP1 in endotoxemia-induced acute kidney injury</title><author>Wang, Weidong ; Li, Chunling ; Summer, Sandra N ; Falk, Sandor ; Wang, Wei ; Ljubanovic, Danica ; Schrier, Robert W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-de229a83d35e8f3efdb9c20e841d0181a180252fb58efe234098d36735f1620d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acute Disease</topic><topic>Animals</topic><topic>Aquaporin 1 - genetics</topic><topic>Aquaporin 1 - metabolism</topic><topic>Blood</topic><topic>Blood Pressure</topic><topic>Drinking - physiology</topic><topic>Endotoxemia - metabolism</topic><topic>Endotoxemia - pathology</topic><topic>Endotoxemia - physiopathology</topic><topic>Glomerular Filtration Rate</topic><topic>Infections</topic><topic>Kidney - pathology</topic><topic>Kidney - physiology</topic><topic>Kidney diseases</topic><topic>Kidney Diseases - metabolism</topic><topic>Kidney Diseases - pathology</topic><topic>Kidney Diseases - physiopathology</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Polyuria - metabolism</topic><topic>Polyuria - pathology</topic><topic>Polyuria - physiopathology</topic><topic>Renal Circulation</topic><topic>Rodents</topic><topic>Toxins</topic><topic>Urine</topic><topic>Water - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Weidong</creatorcontrib><creatorcontrib>Li, Chunling</creatorcontrib><creatorcontrib>Summer, Sandra N</creatorcontrib><creatorcontrib>Falk, Sandor</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><creatorcontrib>Ljubanovic, Danica</creatorcontrib><creatorcontrib>Schrier, Robert W</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. Renal physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Weidong</au><au>Li, Chunling</au><au>Summer, Sandra N</au><au>Falk, Sandor</au><au>Wang, Wei</au><au>Ljubanovic, Danica</au><au>Schrier, Robert W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of AQP1 in endotoxemia-induced acute kidney injury</atitle><jtitle>American journal of physiology. Renal physiology</jtitle><addtitle>Am J Physiol Renal Physiol</addtitle><date>2008-06-01</date><risdate>2008</risdate><volume>294</volume><issue>6</issue><spage>F1473</spage><epage>F1480</epage><pages>F1473-F1480</pages><issn>0363-6127</issn><issn>1931-857X</issn><eissn>2161-1157</eissn><eissn>1522-1466</eissn><abstract><![CDATA[1 Department of Medicine, University of Colorado Health Sciences Center, Denver, Colorado; and 2 Department of Pathology, Dubrava University Hospital, Zagreb, Croatia
Submitted 22 January 2008
; accepted in final form 14 April 2008
The effect of endotoxemia (lipopolysaccharide, 2.5 mg/kg ip) was investigated in aquaporin (AQP) 1 knockout (KO) compared with wild-type (WT) mice. At baseline, KO mice exhibited higher water intake (WI) and urine output (UO). After endotoxemia, WI and UO remained higher in the KO than WT mice, and urine osmolality was lower. The higher serum osmolality in AQP1-KO mice during endotoxemia was associated with higher AQP2 (133 ± 8 vs. 100 ± 3%, P < 0.01), AQP3 (140 ± 8 vs. 100 ± 4%, P < 0.001) and Na + -K + -2Cl – cotransporter type 2 (NKCC2; 152 ± 14 vs. 100 ± 15%, P < 0.05) expression than that in WT mice. These responses during endotoxemia in the AQP1-KO mice compared with WT were associated with lower glomerular filtration rate (GFR) (69 ± 8 vs. 96 ± 8 ml/min, P < 0.05) and renal blood flow (0.77 ± 0.1 vs. 1.01 ± 0.1 ml/min, P < 0.01). Urinary sodium excretion and fractional sodium excretion were higher in KO compared with WT mice in endotoxemia and were accompanied by more severe tubular injury. With water repletion and comparable serum osmolalities, GFR was still lower in KO (57 ± 13 vs. 120 ± 6 ml/min, P < 0.01) compared with WT during endotoxemia. The abundance of AQP2 and AQP3 protein in KO mice was not different from WT mice; however, NKCC2, Na + /H + exchanger type 3, and fractional sodium excretion remained higher in KO compared with WT. Thus the polyuria in AQP1-KO mice does not protect against endotoxemia-induced acute kidney injury but rather absence of AQP1 predisposed to enhanced endotoximic renal injury.
lipopolysaccharide; sepsis; glomerular filtration rate; polyuria; aquaporin-1
Address for reprint requests and other correspondence: R. W. Schrier, Division of Renal Diseases and Hypertension, Univ. of Colorado Health Sciences Center, 4200 East 9 th Ave., Box B173, Denver, CO 80262 (e-mail: Robert.Schrier{at}UCHSC.EDU )]]></abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>18434389</pmid><doi>10.1152/ajprenal.00036.2008</doi></addata></record> |
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source | MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Acute Disease Animals Aquaporin 1 - genetics Aquaporin 1 - metabolism Blood Blood Pressure Drinking - physiology Endotoxemia - metabolism Endotoxemia - pathology Endotoxemia - physiopathology Glomerular Filtration Rate Infections Kidney - pathology Kidney - physiology Kidney diseases Kidney Diseases - metabolism Kidney Diseases - pathology Kidney Diseases - physiopathology Lipopolysaccharides - pharmacology Male Mice Mice, Knockout Polyuria - metabolism Polyuria - pathology Polyuria - physiopathology Renal Circulation Rodents Toxins Urine Water - metabolism |
title | Role of AQP1 in endotoxemia-induced acute kidney injury |
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