Efficacy of oral supplemental hydration for the prevention of contrast-induced nephropathy in rats
Purpose To compare oral rehydration solution (ORS) with saline infusion for preventing contrast-induced nephropathy (CIN) in a rat model. Materials and methods Adult male Sprague–Dawley rats (310–360 g) received intravenous indomethacin (10 mg/kg), N G -nitro- l -arginine methyl ester (10 mg/kg), an...
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Veröffentlicht in: | Japanese journal of radiology 2017-04, Vol.35 (4), p.190-196 |
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creator | Matsunami, Tamaki Hino, Kazuo Dosho, Rie Miyatake, Sho Ebisu, Goro Kuwatsuru, Ryohei |
description | Purpose
To compare oral rehydration solution (ORS) with saline infusion for preventing contrast-induced nephropathy (CIN) in a rat model.
Materials and methods
Adult male Sprague–Dawley rats (310–360 g) received intravenous indomethacin (10 mg/kg),
N
G
-nitro-
l
-arginine methyl ester (10 mg/kg), and iohexol (10 mL/kg) to induce acute contrast-induced renal injury (CIN group); control rats received saline only. For hydration, rats received either continuous infusion (20 mL/kg/h) of saline or three oral doses (20 mL/kg each) of ORS. Acute renal injury was evaluated by assaying urine collected for 24 h beginning 2 h before the contrast injection, evaluating blood taken 22 h after the contrast injection, and examining the kidneys histopathologically.
Results
Hydration with saline prevented only the contrast-induced increase in plasma creatinine, whereas ORS prevented deleterious changes in plasma creatinine, blood urea nitrogen, and creatinine clearance as well as in urinary protein, albumin, and
N
-acetyl-
d
-glucosaminidase concentrations. Histopathologic changes noted in the CIN group were diminished in both saline and ORS groups.
Conclusion
Both intravenous saline administration and oral hydration with ORS decreased the severity of CIN. Hydration with ORS was comparable to intravenous saline infusion in preventing CIN-associated abnormalities. |
doi_str_mv | 10.1007/s11604-017-0620-4 |
format | Article |
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To compare oral rehydration solution (ORS) with saline infusion for preventing contrast-induced nephropathy (CIN) in a rat model.
Materials and methods
Adult male Sprague–Dawley rats (310–360 g) received intravenous indomethacin (10 mg/kg),
N
G
-nitro-
l
-arginine methyl ester (10 mg/kg), and iohexol (10 mL/kg) to induce acute contrast-induced renal injury (CIN group); control rats received saline only. For hydration, rats received either continuous infusion (20 mL/kg/h) of saline or three oral doses (20 mL/kg each) of ORS. Acute renal injury was evaluated by assaying urine collected for 24 h beginning 2 h before the contrast injection, evaluating blood taken 22 h after the contrast injection, and examining the kidneys histopathologically.
Results
Hydration with saline prevented only the contrast-induced increase in plasma creatinine, whereas ORS prevented deleterious changes in plasma creatinine, blood urea nitrogen, and creatinine clearance as well as in urinary protein, albumin, and
N
-acetyl-
d
-glucosaminidase concentrations. Histopathologic changes noted in the CIN group were diminished in both saline and ORS groups.
Conclusion
Both intravenous saline administration and oral hydration with ORS decreased the severity of CIN. Hydration with ORS was comparable to intravenous saline infusion in preventing CIN-associated abnormalities.</description><identifier>ISSN: 1867-1071</identifier><identifier>EISSN: 1867-108X</identifier><identifier>DOI: 10.1007/s11604-017-0620-4</identifier><identifier>PMID: 28205100</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Acute Kidney Injury - chemically induced ; Acute Kidney Injury - prevention & control ; Animals ; Contrast Media - adverse effects ; Disease Models, Animal ; Fluid Therapy - methods ; Imaging ; Indomethacin - pharmacology ; Iohexol - adverse effects ; Male ; Medicine ; Medicine & Public Health ; NG-Nitroarginine Methyl Ester - pharmacology ; Nuclear Medicine ; Original Article ; Radiology ; Radiotherapy ; Random Allocation ; Rats ; Rats, Sprague-Dawley ; Sodium Chloride - administration & dosage</subject><ispartof>Japanese journal of radiology, 2017-04, Vol.35 (4), p.190-196</ispartof><rights>Japan Radiological Society 2017</rights><rights>Japanese Journal of Radiology is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c567t-5ffcc9e29c72d7e37ea62cfdee4b137caa60c7317b949ff04fefeb00ac89644d3</citedby><cites>FETCH-LOGICAL-c567t-5ffcc9e29c72d7e37ea62cfdee4b137caa60c7317b949ff04fefeb00ac89644d3</cites><orcidid>0000-0003-1960-6400</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11604-017-0620-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11604-017-0620-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27928,27929,41492,42561,51323</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28205100$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsunami, Tamaki</creatorcontrib><creatorcontrib>Hino, Kazuo</creatorcontrib><creatorcontrib>Dosho, Rie</creatorcontrib><creatorcontrib>Miyatake, Sho</creatorcontrib><creatorcontrib>Ebisu, Goro</creatorcontrib><creatorcontrib>Kuwatsuru, Ryohei</creatorcontrib><title>Efficacy of oral supplemental hydration for the prevention of contrast-induced nephropathy in rats</title><title>Japanese journal of radiology</title><addtitle>Jpn J Radiol</addtitle><addtitle>Jpn J Radiol</addtitle><description>Purpose
To compare oral rehydration solution (ORS) with saline infusion for preventing contrast-induced nephropathy (CIN) in a rat model.
Materials and methods
Adult male Sprague–Dawley rats (310–360 g) received intravenous indomethacin (10 mg/kg),
N
G
-nitro-
l
-arginine methyl ester (10 mg/kg), and iohexol (10 mL/kg) to induce acute contrast-induced renal injury (CIN group); control rats received saline only. For hydration, rats received either continuous infusion (20 mL/kg/h) of saline or three oral doses (20 mL/kg each) of ORS. Acute renal injury was evaluated by assaying urine collected for 24 h beginning 2 h before the contrast injection, evaluating blood taken 22 h after the contrast injection, and examining the kidneys histopathologically.
Results
Hydration with saline prevented only the contrast-induced increase in plasma creatinine, whereas ORS prevented deleterious changes in plasma creatinine, blood urea nitrogen, and creatinine clearance as well as in urinary protein, albumin, and
N
-acetyl-
d
-glucosaminidase concentrations. Histopathologic changes noted in the CIN group were diminished in both saline and ORS groups.
Conclusion
Both intravenous saline administration and oral hydration with ORS decreased the severity of CIN. Hydration with ORS was comparable to intravenous saline infusion in preventing CIN-associated abnormalities.</description><subject>Acute Kidney Injury - chemically induced</subject><subject>Acute Kidney Injury - prevention & control</subject><subject>Animals</subject><subject>Contrast Media - adverse effects</subject><subject>Disease Models, Animal</subject><subject>Fluid Therapy - methods</subject><subject>Imaging</subject><subject>Indomethacin - pharmacology</subject><subject>Iohexol - adverse effects</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>NG-Nitroarginine Methyl Ester - pharmacology</subject><subject>Nuclear Medicine</subject><subject>Original Article</subject><subject>Radiology</subject><subject>Radiotherapy</subject><subject>Random Allocation</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sodium Chloride - administration & dosage</subject><issn>1867-1071</issn><issn>1867-108X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkctKxDAUhoMo3h_AjQTcuKmetJmkWYp4A8GNgruQpidOpZPUpBXm7c0wKiIIrnI53_-H8BFyxOCMAcjzxJgAXgCTBYgSCr5BdlktZMGgft783ku2Q_ZSegUQvOJ8m-yUdQmzXLFLmivnOmvskgZHQzQ9TdMw9LhAP-bDfNlGM3bBUxciHedIh4jveba6ygkb_BhNGovOt5PFlnoc5jEMZpwvaedpDqcDsuVMn_Dwc90nT9dXj5e3xf3Dzd3lxX1hZ0KOxcw5axWWysqylVhJNKK0rkXkDaukNUaAlRWTjeLKOeAOHTYAxtZKcN5W--R03TvE8DZhGvWiSxb73ngMU9KsVqyWQnH2D1QoEBWoOqMnv9DXMEWfP5KpesaU4kJliq0pG0NKEZ0eYrcwcakZ6JUrvXalsyu9cqV5zhx_Nk_NAtvvxJecDJRrIOWRf8H44-k_Wz8AiIegQA</recordid><startdate>20170401</startdate><enddate>20170401</enddate><creator>Matsunami, Tamaki</creator><creator>Hino, Kazuo</creator><creator>Dosho, Rie</creator><creator>Miyatake, Sho</creator><creator>Ebisu, Goro</creator><creator>Kuwatsuru, Ryohei</creator><general>Springer Japan</general><general>Springer Nature B.V</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>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1960-6400</orcidid></search><sort><creationdate>20170401</creationdate><title>Efficacy of oral supplemental hydration for the prevention of contrast-induced nephropathy in rats</title><author>Matsunami, Tamaki ; Hino, Kazuo ; Dosho, Rie ; Miyatake, Sho ; Ebisu, Goro ; Kuwatsuru, Ryohei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c567t-5ffcc9e29c72d7e37ea62cfdee4b137caa60c7317b949ff04fefeb00ac89644d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acute Kidney Injury - chemically induced</topic><topic>Acute Kidney Injury - prevention & control</topic><topic>Animals</topic><topic>Contrast Media - adverse effects</topic><topic>Disease Models, Animal</topic><topic>Fluid Therapy - methods</topic><topic>Imaging</topic><topic>Indomethacin - pharmacology</topic><topic>Iohexol - adverse effects</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>NG-Nitroarginine Methyl Ester - pharmacology</topic><topic>Nuclear Medicine</topic><topic>Original Article</topic><topic>Radiology</topic><topic>Radiotherapy</topic><topic>Random Allocation</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sodium Chloride - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsunami, Tamaki</creatorcontrib><creatorcontrib>Hino, Kazuo</creatorcontrib><creatorcontrib>Dosho, Rie</creatorcontrib><creatorcontrib>Miyatake, Sho</creatorcontrib><creatorcontrib>Ebisu, Goro</creatorcontrib><creatorcontrib>Kuwatsuru, Ryohei</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>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology 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>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</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>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</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>MEDLINE - Academic</collection><jtitle>Japanese journal of radiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsunami, Tamaki</au><au>Hino, Kazuo</au><au>Dosho, Rie</au><au>Miyatake, Sho</au><au>Ebisu, Goro</au><au>Kuwatsuru, Ryohei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of oral supplemental hydration for the prevention of contrast-induced nephropathy in rats</atitle><jtitle>Japanese journal of radiology</jtitle><stitle>Jpn J Radiol</stitle><addtitle>Jpn J Radiol</addtitle><date>2017-04-01</date><risdate>2017</risdate><volume>35</volume><issue>4</issue><spage>190</spage><epage>196</epage><pages>190-196</pages><issn>1867-1071</issn><eissn>1867-108X</eissn><abstract>Purpose
To compare oral rehydration solution (ORS) with saline infusion for preventing contrast-induced nephropathy (CIN) in a rat model.
Materials and methods
Adult male Sprague–Dawley rats (310–360 g) received intravenous indomethacin (10 mg/kg),
N
G
-nitro-
l
-arginine methyl ester (10 mg/kg), and iohexol (10 mL/kg) to induce acute contrast-induced renal injury (CIN group); control rats received saline only. For hydration, rats received either continuous infusion (20 mL/kg/h) of saline or three oral doses (20 mL/kg each) of ORS. Acute renal injury was evaluated by assaying urine collected for 24 h beginning 2 h before the contrast injection, evaluating blood taken 22 h after the contrast injection, and examining the kidneys histopathologically.
Results
Hydration with saline prevented only the contrast-induced increase in plasma creatinine, whereas ORS prevented deleterious changes in plasma creatinine, blood urea nitrogen, and creatinine clearance as well as in urinary protein, albumin, and
N
-acetyl-
d
-glucosaminidase concentrations. Histopathologic changes noted in the CIN group were diminished in both saline and ORS groups.
Conclusion
Both intravenous saline administration and oral hydration with ORS decreased the severity of CIN. Hydration with ORS was comparable to intravenous saline infusion in preventing CIN-associated abnormalities.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>28205100</pmid><doi>10.1007/s11604-017-0620-4</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-1960-6400</orcidid><oa>free_for_read</oa></addata></record> |
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ispartof | Japanese journal of radiology, 2017-04, Vol.35 (4), p.190-196 |
issn | 1867-1071 1867-108X |
language | eng |
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source | MEDLINE; SpringerNature Journals |
subjects | Acute Kidney Injury - chemically induced Acute Kidney Injury - prevention & control Animals Contrast Media - adverse effects Disease Models, Animal Fluid Therapy - methods Imaging Indomethacin - pharmacology Iohexol - adverse effects Male Medicine Medicine & Public Health NG-Nitroarginine Methyl Ester - pharmacology Nuclear Medicine Original Article Radiology Radiotherapy Random Allocation Rats Rats, Sprague-Dawley Sodium Chloride - administration & dosage |
title | Efficacy of oral supplemental hydration for the prevention of contrast-induced nephropathy in rats |
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