Tubular effects of acetaminophen in the isolated perfused rat kidney
The effects of different acetaminophen (APAP) concentrations (1, 5 or 10 mM) on renal function were investigated in the isolated perfused rat kidney (IPK). APAP was added to the perfusion media as a single dose after a equilibration time and control periods. Changes in fractional excretion of sodium...
Gespeichert in:
Veröffentlicht in: | Archives of toxicology 1995-02, Vol.69 (4), p.248-252 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 252 |
---|---|
container_issue | 4 |
container_start_page | 248 |
container_title | Archives of toxicology |
container_volume | 69 |
creator | TRUMPER, L MONASTEROLO, L. A OCHOA, E ELIAS, M. M |
description | The effects of different acetaminophen (APAP) concentrations (1, 5 or 10 mM) on renal function were investigated in the isolated perfused rat kidney (IPK). APAP was added to the perfusion media as a single dose after a equilibration time and control periods. Changes in fractional excretion of sodium (FENa), water (FEH2O), glucose (FEglu) and in glomerular filtration rate (GFR) were measured. The lower concentration used only modified the FEH2O. APAP 10 mM induced an increment in FEH2O (72% higher than control preparation), FENa (79% higher than control preparation) and an elevation in glucose excretion (55% higher than control preparation), associated with a decrease in GFR (23% lower than control preparation). The influence of PGE2 on the effects of APAP was also investigated. PGE2 prevented the APAP-induced decrease in GFR and in glucose reabsorption, but did not change the pattern of sodium and water handling. The effects of another vasodilator, verapamil, on APAP-induced renal effects were also tested. Verapamil prevented the glomerular but not the tubular effects of APAP. Urinary APAP excretion data showed a similar availability of APAP to the tubular cells in all the groups. Our data suggest that APAP exerts a direct action in the IPK, affecting hemodynamic and tubular functions, and that the latter are not a consequence of hemodynamic alterations. |
doi_str_mv | 10.1007/s002040050166 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1007_s002040050166</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>7755485</sourcerecordid><originalsourceid>FETCH-LOGICAL-c383t-d015ce45be5fa6ccdfdc789d8dd4d3ebbf657331dc7ed67b1bcce06521b2b51e3</originalsourceid><addsrcrecordid>eNpVkE1Lw0AQhhdRaq0ePQp78BqdyWZ306PUTyh4qeewH7M0miZhNzn03xtpKXial3kfBuZh7BbhAQH0YwLIoQCQgEqdsTkWIs9Ai_KczUEUkEmt8JJdpfQNgHm5FDM201rKopRz9rwZ7diYyCkEckPiXeDG0WB2ddv1W2p53fJhS7xOXWMG8rynGMY0hWgG_lP7lvbX7CKYJtHNcS7Y1-vLZvWerT_fPlZP68yJUgyZB5SOCmlJBqOc88E7XS596X3hBVkblNRC4LQlr7RF6xyBkjna3EoksWDZ4a6LXUqRQtXHemfivkKo_mRU_2RM_N2B70e7I3-ij99P_f2xN8mZJkTTujqdsEkeFgrFL9GwZ6s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Tubular effects of acetaminophen in the isolated perfused rat kidney</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>TRUMPER, L ; MONASTEROLO, L. A ; OCHOA, E ; ELIAS, M. M</creator><creatorcontrib>TRUMPER, L ; MONASTEROLO, L. A ; OCHOA, E ; ELIAS, M. M</creatorcontrib><description>The effects of different acetaminophen (APAP) concentrations (1, 5 or 10 mM) on renal function were investigated in the isolated perfused rat kidney (IPK). APAP was added to the perfusion media as a single dose after a equilibration time and control periods. Changes in fractional excretion of sodium (FENa), water (FEH2O), glucose (FEglu) and in glomerular filtration rate (GFR) were measured. The lower concentration used only modified the FEH2O. APAP 10 mM induced an increment in FEH2O (72% higher than control preparation), FENa (79% higher than control preparation) and an elevation in glucose excretion (55% higher than control preparation), associated with a decrease in GFR (23% lower than control preparation). The influence of PGE2 on the effects of APAP was also investigated. PGE2 prevented the APAP-induced decrease in GFR and in glucose reabsorption, but did not change the pattern of sodium and water handling. The effects of another vasodilator, verapamil, on APAP-induced renal effects were also tested. Verapamil prevented the glomerular but not the tubular effects of APAP. Urinary APAP excretion data showed a similar availability of APAP to the tubular cells in all the groups. Our data suggest that APAP exerts a direct action in the IPK, affecting hemodynamic and tubular functions, and that the latter are not a consequence of hemodynamic alterations.</description><identifier>ISSN: 0340-5761</identifier><identifier>EISSN: 1432-0738</identifier><identifier>DOI: 10.1007/s002040050166</identifier><identifier>PMID: 7755485</identifier><identifier>CODEN: ARTODN</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Acetaminophen - toxicity ; Analysis of Variance ; Animals ; Biological and medical sciences ; Dinoprostone - pharmacology ; Drug Interactions ; Drug toxicity and drugs side effects treatment ; In Vitro Techniques ; Kidney Tubules - drug effects ; Male ; Medical sciences ; Perfusion ; Pharmacology. Drug treatments ; Rats ; Rats, Wistar ; Toxicity: urogenital system ; Verapamil - pharmacology</subject><ispartof>Archives of toxicology, 1995-02, Vol.69 (4), p.248-252</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-d015ce45be5fa6ccdfdc789d8dd4d3ebbf657331dc7ed67b1bcce06521b2b51e3</citedby><cites>FETCH-LOGICAL-c383t-d015ce45be5fa6ccdfdc789d8dd4d3ebbf657331dc7ed67b1bcce06521b2b51e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3401461$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7755485$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TRUMPER, L</creatorcontrib><creatorcontrib>MONASTEROLO, L. A</creatorcontrib><creatorcontrib>OCHOA, E</creatorcontrib><creatorcontrib>ELIAS, M. M</creatorcontrib><title>Tubular effects of acetaminophen in the isolated perfused rat kidney</title><title>Archives of toxicology</title><addtitle>Arch Toxicol</addtitle><description>The effects of different acetaminophen (APAP) concentrations (1, 5 or 10 mM) on renal function were investigated in the isolated perfused rat kidney (IPK). APAP was added to the perfusion media as a single dose after a equilibration time and control periods. Changes in fractional excretion of sodium (FENa), water (FEH2O), glucose (FEglu) and in glomerular filtration rate (GFR) were measured. The lower concentration used only modified the FEH2O. APAP 10 mM induced an increment in FEH2O (72% higher than control preparation), FENa (79% higher than control preparation) and an elevation in glucose excretion (55% higher than control preparation), associated with a decrease in GFR (23% lower than control preparation). The influence of PGE2 on the effects of APAP was also investigated. PGE2 prevented the APAP-induced decrease in GFR and in glucose reabsorption, but did not change the pattern of sodium and water handling. The effects of another vasodilator, verapamil, on APAP-induced renal effects were also tested. Verapamil prevented the glomerular but not the tubular effects of APAP. Urinary APAP excretion data showed a similar availability of APAP to the tubular cells in all the groups. Our data suggest that APAP exerts a direct action in the IPK, affecting hemodynamic and tubular functions, and that the latter are not a consequence of hemodynamic alterations.</description><subject>Acetaminophen - toxicity</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Dinoprostone - pharmacology</subject><subject>Drug Interactions</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>In Vitro Techniques</subject><subject>Kidney Tubules - drug effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Perfusion</subject><subject>Pharmacology. Drug treatments</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Toxicity: urogenital system</subject><subject>Verapamil - pharmacology</subject><issn>0340-5761</issn><issn>1432-0738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE1Lw0AQhhdRaq0ePQp78BqdyWZ306PUTyh4qeewH7M0miZhNzn03xtpKXial3kfBuZh7BbhAQH0YwLIoQCQgEqdsTkWIs9Ai_KczUEUkEmt8JJdpfQNgHm5FDM201rKopRz9rwZ7diYyCkEckPiXeDG0WB2ddv1W2p53fJhS7xOXWMG8rynGMY0hWgG_lP7lvbX7CKYJtHNcS7Y1-vLZvWerT_fPlZP68yJUgyZB5SOCmlJBqOc88E7XS596X3hBVkblNRC4LQlr7RF6xyBkjna3EoksWDZ4a6LXUqRQtXHemfivkKo_mRU_2RM_N2B70e7I3-ij99P_f2xN8mZJkTTujqdsEkeFgrFL9GwZ6s</recordid><startdate>19950201</startdate><enddate>19950201</enddate><creator>TRUMPER, L</creator><creator>MONASTEROLO, L. A</creator><creator>OCHOA, E</creator><creator>ELIAS, M. M</creator><general>Springer</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19950201</creationdate><title>Tubular effects of acetaminophen in the isolated perfused rat kidney</title><author>TRUMPER, L ; MONASTEROLO, L. A ; OCHOA, E ; ELIAS, M. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-d015ce45be5fa6ccdfdc789d8dd4d3ebbf657331dc7ed67b1bcce06521b2b51e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Acetaminophen - toxicity</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Dinoprostone - pharmacology</topic><topic>Drug Interactions</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>In Vitro Techniques</topic><topic>Kidney Tubules - drug effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Perfusion</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Toxicity: urogenital system</topic><topic>Verapamil - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TRUMPER, L</creatorcontrib><creatorcontrib>MONASTEROLO, L. A</creatorcontrib><creatorcontrib>OCHOA, E</creatorcontrib><creatorcontrib>ELIAS, M. M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Archives of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TRUMPER, L</au><au>MONASTEROLO, L. A</au><au>OCHOA, E</au><au>ELIAS, M. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tubular effects of acetaminophen in the isolated perfused rat kidney</atitle><jtitle>Archives of toxicology</jtitle><addtitle>Arch Toxicol</addtitle><date>1995-02-01</date><risdate>1995</risdate><volume>69</volume><issue>4</issue><spage>248</spage><epage>252</epage><pages>248-252</pages><issn>0340-5761</issn><eissn>1432-0738</eissn><coden>ARTODN</coden><abstract>The effects of different acetaminophen (APAP) concentrations (1, 5 or 10 mM) on renal function were investigated in the isolated perfused rat kidney (IPK). APAP was added to the perfusion media as a single dose after a equilibration time and control periods. Changes in fractional excretion of sodium (FENa), water (FEH2O), glucose (FEglu) and in glomerular filtration rate (GFR) were measured. The lower concentration used only modified the FEH2O. APAP 10 mM induced an increment in FEH2O (72% higher than control preparation), FENa (79% higher than control preparation) and an elevation in glucose excretion (55% higher than control preparation), associated with a decrease in GFR (23% lower than control preparation). The influence of PGE2 on the effects of APAP was also investigated. PGE2 prevented the APAP-induced decrease in GFR and in glucose reabsorption, but did not change the pattern of sodium and water handling. The effects of another vasodilator, verapamil, on APAP-induced renal effects were also tested. Verapamil prevented the glomerular but not the tubular effects of APAP. Urinary APAP excretion data showed a similar availability of APAP to the tubular cells in all the groups. Our data suggest that APAP exerts a direct action in the IPK, affecting hemodynamic and tubular functions, and that the latter are not a consequence of hemodynamic alterations.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>7755485</pmid><doi>10.1007/s002040050166</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0340-5761 |
ispartof | Archives of toxicology, 1995-02, Vol.69 (4), p.248-252 |
issn | 0340-5761 1432-0738 |
language | eng |
recordid | cdi_crossref_primary_10_1007_s002040050166 |
source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Acetaminophen - toxicity Analysis of Variance Animals Biological and medical sciences Dinoprostone - pharmacology Drug Interactions Drug toxicity and drugs side effects treatment In Vitro Techniques Kidney Tubules - drug effects Male Medical sciences Perfusion Pharmacology. Drug treatments Rats Rats, Wistar Toxicity: urogenital system Verapamil - pharmacology |
title | Tubular effects of acetaminophen in the isolated perfused rat kidney |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T15%3A17%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tubular%20effects%20of%20acetaminophen%20in%20the%20isolated%20perfused%20rat%20kidney&rft.jtitle=Archives%20of%20toxicology&rft.au=TRUMPER,%20L&rft.date=1995-02-01&rft.volume=69&rft.issue=4&rft.spage=248&rft.epage=252&rft.pages=248-252&rft.issn=0340-5761&rft.eissn=1432-0738&rft.coden=ARTODN&rft_id=info:doi/10.1007/s002040050166&rft_dat=%3Cpubmed_cross%3E7755485%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/7755485&rfr_iscdi=true |