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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of physiology. Renal physiology 2008-06, Vol.294 (6), p.F1473-F1480
Hauptverfasser: Wang, Weidong, Li, Chunling, Summer, Sandra N, Falk, Sandor, Wang, Wei, Ljubanovic, Danica, Schrier, Robert W
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page F1480
container_issue 6
container_start_page F1473
container_title American journal of physiology. Renal physiology
container_volume 294
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
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1152_ajprenal_00036_2008</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71643735</sourcerecordid><originalsourceid>FETCH-LOGICAL-c422t-de229a83d35e8f3efdb9c20e841d0181a180252fb58efe234098d36735f1620d3</originalsourceid><addsrcrecordid>eNp1kFFrFDEURoNY7Lb6CwQZfPBttjc3M5kMPpXiWqHQKvU5ZCc33VlnJ2MyQzv_3rS7VhF8CiTnfITD2FsOS85LPDPbIVBvuiUACLlEAPWCLZBLnqf36iVbpGuRS47VMTuJcQuAKJV8xY65KkQhVL1g1TffUeZddv71hmdtn1Fv_egfaNeavO3t1JDNTDONlP1obU9zYrZTmF-zI2e6SG8O5yn7vvp0e3GZX11__nJxfpU3BeKYW0KsjRJWlKScIGfXdYNAquAWuOKGK8AS3bpU5AhFAbWyQlaidFwiWHHKPux3h-B_ThRHvWtjQ11nevJT1BWXhUh4At__A279FFKeqFEAhwoQEiT2UBN8jIGcHkK7M2HWHPRjVP07qn6Kqh-jJuvdYXpa78j-cQ4VE_BxD2zau819G0gPmzm2vvN3s15NXXdLD-PzNNaFlnrFi0rowbpkn_3ffv7PX5b4BRUEmK4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>230107020</pqid></control><display><type>article</type><title>Role of AQP1 in endotoxemia-induced acute kidney injury</title><source>MEDLINE</source><source>American Physiological Society</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Wang, Weidong ; Li, Chunling ; Summer, Sandra N ; Falk, Sandor ; Wang, Wei ; Ljubanovic, Danica ; Schrier, Robert W</creator><creatorcontrib>Wang, Weidong ; Li, Chunling ; Summer, Sandra N ; Falk, Sandor ; Wang, Wei ; Ljubanovic, Danica ; Schrier, Robert W</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 0363-6127
ispartof American journal of physiology. Renal physiology, 2008-06, Vol.294 (6), p.F1473-F1480
issn 0363-6127
1931-857X
2161-1157
1522-1466
language eng
recordid cdi_crossref_primary_10_1152_ajprenal_00036_2008
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T04%3A52%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Role%20of%20AQP1%20in%20endotoxemia-induced%20acute%20kidney%20injury&rft.jtitle=American%20journal%20of%20physiology.%20Renal%20physiology&rft.au=Wang,%20Weidong&rft.date=2008-06-01&rft.volume=294&rft.issue=6&rft.spage=F1473&rft.epage=F1480&rft.pages=F1473-F1480&rft.issn=0363-6127&rft.eissn=2161-1157&rft_id=info:doi/10.1152/ajprenal.00036.2008&rft_dat=%3Cproquest_cross%3E71643735%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=230107020&rft_id=info:pmid/18434389&rfr_iscdi=true