Inhibition of hyaluronan synthesis in rats reduces renal ability to excrete fluid and electrolytes during acute hydration
Abstract Background. Hyaluronan (HA) is the dominant glycosaminoglycan in the renomedullary interstitium. Renomedullary HA has been implicated in tubular fluid handling due to its water-attracting properties and the changes occurring in parallel to acute variations in the body hydration status. Meth...
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description | Abstract
Background. Hyaluronan (HA) is the dominant glycosaminoglycan in the renomedullary interstitium. Renomedullary HA has been implicated in tubular fluid handling due to its water-attracting properties and the changes occurring in parallel to acute variations in the body hydration status.
Methods. HA production was inhibited by 4-methylumbelliferone (4-MU in drinking water for 5 days, 1.45 ± 0.07 g/day/kg body weight) in rats prior to hydration.
Results. Following hypotonic hydration for 135 min in control animals, diuresis and osmotic excretion increased while sodium excretion and glomerular filtration rate (GFR) remained unchanged. The medullary and cortical HA contents were 7.85 ± 1.29 ng/mg protein and 0.08 ± 0.01 ng/mg protein, respectively. Medullary HA content after 4-MU was 38% of that in controls (2.98 ± 0.95 ng/g protein, p < 0.05), while the low cortical levels were unaffected. Baseline urine flow was not different from that in controls. The diuretic response to hydration was, however, only 51% of that in controls (157 ± 36 versus 306 ± 54 µl/g kidney weight/135 min, p < 0.05) and the osmolar excretion only 47% of that in controls (174 ± 47 versus 374 ± 41 µOsm/g kidney weight/135 min, p < 0.05). Sodium excretion, GFR, and arterial blood pressure were similar to that in control rats and unaltered during hydration.
Conclusions. Reduction of renomedullary interstitial HA using 4-MU reduces the ability of the kidney to respond appropriately upon acute hydration. The results strengthen the concept of renomedullary HA as a modulator of tubular fluid handling by changing the physicochemical properties of the interstitial space. |
doi_str_mv | 10.3109/03009734.2013.834013 |
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Background. Hyaluronan (HA) is the dominant glycosaminoglycan in the renomedullary interstitium. Renomedullary HA has been implicated in tubular fluid handling due to its water-attracting properties and the changes occurring in parallel to acute variations in the body hydration status.
Methods. HA production was inhibited by 4-methylumbelliferone (4-MU in drinking water for 5 days, 1.45 ± 0.07 g/day/kg body weight) in rats prior to hydration.
Results. Following hypotonic hydration for 135 min in control animals, diuresis and osmotic excretion increased while sodium excretion and glomerular filtration rate (GFR) remained unchanged. The medullary and cortical HA contents were 7.85 ± 1.29 ng/mg protein and 0.08 ± 0.01 ng/mg protein, respectively. Medullary HA content after 4-MU was 38% of that in controls (2.98 ± 0.95 ng/g protein, p < 0.05), while the low cortical levels were unaffected. Baseline urine flow was not different from that in controls. The diuretic response to hydration was, however, only 51% of that in controls (157 ± 36 versus 306 ± 54 µl/g kidney weight/135 min, p < 0.05) and the osmolar excretion only 47% of that in controls (174 ± 47 versus 374 ± 41 µOsm/g kidney weight/135 min, p < 0.05). Sodium excretion, GFR, and arterial blood pressure were similar to that in control rats and unaltered during hydration.
Conclusions. Reduction of renomedullary interstitial HA using 4-MU reduces the ability of the kidney to respond appropriately upon acute hydration. The results strengthen the concept of renomedullary HA as a modulator of tubular fluid handling by changing the physicochemical properties of the interstitial space.</description><identifier>ISSN: 0300-9734</identifier><identifier>ISSN: 2000-1967</identifier><identifier>EISSN: 2000-1967</identifier><identifier>DOI: 10.3109/03009734.2013.834013</identifier><identifier>PMID: 24102146</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject>Animals ; Blood Pressure ; Catheterization ; Diuresis ; Drinking Water ; Electrolytes - chemistry ; fluid balance ; Glomerular Filtration Rate ; Glycosaminoglycans - chemistry ; hyaluronan ; Hyaluronic Acid - antagonists & inhibitors ; Hydration ; Hymecromone - chemistry ; Indicators and Reagents - chemistry ; interstitium ; kidney ; Kidney - drug effects ; Kidney - metabolism ; Male ; matrix ; MEDICIN ; MEDICINE ; medulla ; Original ; Proteins ; Rats ; Rats, Sprague-Dawley ; Rodents ; Sodium - chemistry ; Water - chemistry</subject><ispartof>Upsala journal of medical sciences, 2013-11, Vol.118 (4), p.217-221</ispartof><rights>Informa Healthcare 2013</rights><rights>Informa Healthcare. 2013. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c612t-1fa9ca77ae0077fac3543a38ea9b9feae9905c87d2ad7c0106c5b74873da1c0c3</citedby><cites>FETCH-LOGICAL-c612t-1fa9ca77ae0077fac3543a38ea9b9feae9905c87d2ad7c0106c5b74873da1c0c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190891/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190891/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,723,776,780,860,881,27479,27901,27902,53766,53768,59116,59117,61191,61192</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24102146$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-100470$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:rkh:diva-1084$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-209756$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Stridh, Sara</creatorcontrib><creatorcontrib>Palm, Fredrik</creatorcontrib><creatorcontrib>Hansell, Peter</creatorcontrib><title>Inhibition of hyaluronan synthesis in rats reduces renal ability to excrete fluid and electrolytes during acute hydration</title><title>Upsala journal of medical sciences</title><addtitle>Ups J Med Sci</addtitle><description>Abstract
Background. Hyaluronan (HA) is the dominant glycosaminoglycan in the renomedullary interstitium. Renomedullary HA has been implicated in tubular fluid handling due to its water-attracting properties and the changes occurring in parallel to acute variations in the body hydration status.
Methods. HA production was inhibited by 4-methylumbelliferone (4-MU in drinking water for 5 days, 1.45 ± 0.07 g/day/kg body weight) in rats prior to hydration.
Results. Following hypotonic hydration for 135 min in control animals, diuresis and osmotic excretion increased while sodium excretion and glomerular filtration rate (GFR) remained unchanged. The medullary and cortical HA contents were 7.85 ± 1.29 ng/mg protein and 0.08 ± 0.01 ng/mg protein, respectively. Medullary HA content after 4-MU was 38% of that in controls (2.98 ± 0.95 ng/g protein, p < 0.05), while the low cortical levels were unaffected. Baseline urine flow was not different from that in controls. The diuretic response to hydration was, however, only 51% of that in controls (157 ± 36 versus 306 ± 54 µl/g kidney weight/135 min, p < 0.05) and the osmolar excretion only 47% of that in controls (174 ± 47 versus 374 ± 41 µOsm/g kidney weight/135 min, p < 0.05). Sodium excretion, GFR, and arterial blood pressure were similar to that in control rats and unaltered during hydration.
Conclusions. Reduction of renomedullary interstitial HA using 4-MU reduces the ability of the kidney to respond appropriately upon acute hydration. The results strengthen the concept of renomedullary HA as a modulator of tubular fluid handling by changing the physicochemical properties of the interstitial space.</description><subject>Animals</subject><subject>Blood Pressure</subject><subject>Catheterization</subject><subject>Diuresis</subject><subject>Drinking Water</subject><subject>Electrolytes - chemistry</subject><subject>fluid balance</subject><subject>Glomerular Filtration Rate</subject><subject>Glycosaminoglycans - chemistry</subject><subject>hyaluronan</subject><subject>Hyaluronic Acid - antagonists & inhibitors</subject><subject>Hydration</subject><subject>Hymecromone - chemistry</subject><subject>Indicators and Reagents - chemistry</subject><subject>interstitium</subject><subject>kidney</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Male</subject><subject>matrix</subject><subject>MEDICIN</subject><subject>MEDICINE</subject><subject>medulla</subject><subject>Original</subject><subject>Proteins</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rodents</subject><subject>Sodium - chemistry</subject><subject>Water - chemistry</subject><issn>0300-9734</issn><issn>2000-1967</issn><issn>2000-1967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><sourceid>D8T</sourceid><recordid>eNqF0stu1DAUBuAIgehQeAOELLFBKhns2BPHm6Kq3CpVYgNsrTOOM3Hx2MUX2rw9jqYtDIt25YW_8zt2_qp6SfCSEizeYYqx4JQtG0zosqOsLI-qRYMxrolo-eNqMZN6NgfVsxgvyk6LOX1aHTSM4IawdlFNZ240a5OMd8gPaJzA5uAdOBQnl0YdTUTGoQApoqD7rPS8OrAI1saaNKHkkb5WQSeNBptNj8D1SFutUvB2SsX3ORi3QaByMePUl7By3PPqyQA26hc362H1_dPHb6df6vOvn89OT85r1ZIm1WQAoYBz0BhzPoCiK0aBdhrEWgwatBB4pTreN9BzhQlu1WrNWcdpD0RhRQ-rt7vceKUv81peBrOFMEkPRn4wP06kDxuZs2zKa67awo8e5uHnKAnuWNH1w9qaXDRmHBd_vPMFb3WvtEsB7N7Y_o4zo9z435IRgTtBSsCbm4Dgf2Udk9yaqLS14LTPURLGShMYaUShr_-jFz6H8uuibIgQDW5bSotiO6WCjzHo4e5jCJZz0eRt0eRcNLkrWhl79e9F7oZum1XA-x0wbvBhC1c-2F4mmKwPQwCnTJzj7z3ieC9h1GDTqCDovxe5N-APaMr5bg</recordid><startdate>20131101</startdate><enddate>20131101</enddate><creator>Stridh, Sara</creator><creator>Palm, Fredrik</creator><creator>Hansell, Peter</creator><general>Informa Healthcare</general><general>Taylor & Francis</general><general>Open Academia</general><scope>0YH</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><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>DG8</scope><scope>D8T</scope><scope>ZZAVC</scope><scope>DF2</scope></search><sort><creationdate>20131101</creationdate><title>Inhibition of hyaluronan synthesis in rats reduces renal ability to excrete fluid and electrolytes during acute hydration</title><author>Stridh, Sara ; Palm, Fredrik ; Hansell, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c612t-1fa9ca77ae0077fac3543a38ea9b9feae9905c87d2ad7c0106c5b74873da1c0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Blood Pressure</topic><topic>Catheterization</topic><topic>Diuresis</topic><topic>Drinking Water</topic><topic>Electrolytes - chemistry</topic><topic>fluid balance</topic><topic>Glomerular Filtration Rate</topic><topic>Glycosaminoglycans - chemistry</topic><topic>hyaluronan</topic><topic>Hyaluronic Acid - antagonists & inhibitors</topic><topic>Hydration</topic><topic>Hymecromone - chemistry</topic><topic>Indicators and Reagents - chemistry</topic><topic>interstitium</topic><topic>kidney</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Male</topic><topic>matrix</topic><topic>MEDICIN</topic><topic>MEDICINE</topic><topic>medulla</topic><topic>Original</topic><topic>Proteins</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rodents</topic><topic>Sodium - chemistry</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stridh, Sara</creatorcontrib><creatorcontrib>Palm, Fredrik</creatorcontrib><creatorcontrib>Hansell, Peter</creatorcontrib><collection>Taylor & Francis Open Access</collection><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Linköpings universitet</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><collection>SWEPUB Uppsala universitet</collection><jtitle>Upsala journal of medical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stridh, Sara</au><au>Palm, Fredrik</au><au>Hansell, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of hyaluronan synthesis in rats reduces renal ability to excrete fluid and electrolytes during acute hydration</atitle><jtitle>Upsala journal of medical sciences</jtitle><addtitle>Ups J Med Sci</addtitle><date>2013-11-01</date><risdate>2013</risdate><volume>118</volume><issue>4</issue><spage>217</spage><epage>221</epage><pages>217-221</pages><issn>0300-9734</issn><issn>2000-1967</issn><eissn>2000-1967</eissn><abstract>Abstract
Background. Hyaluronan (HA) is the dominant glycosaminoglycan in the renomedullary interstitium. Renomedullary HA has been implicated in tubular fluid handling due to its water-attracting properties and the changes occurring in parallel to acute variations in the body hydration status.
Methods. HA production was inhibited by 4-methylumbelliferone (4-MU in drinking water for 5 days, 1.45 ± 0.07 g/day/kg body weight) in rats prior to hydration.
Results. Following hypotonic hydration for 135 min in control animals, diuresis and osmotic excretion increased while sodium excretion and glomerular filtration rate (GFR) remained unchanged. The medullary and cortical HA contents were 7.85 ± 1.29 ng/mg protein and 0.08 ± 0.01 ng/mg protein, respectively. Medullary HA content after 4-MU was 38% of that in controls (2.98 ± 0.95 ng/g protein, p < 0.05), while the low cortical levels were unaffected. Baseline urine flow was not different from that in controls. The diuretic response to hydration was, however, only 51% of that in controls (157 ± 36 versus 306 ± 54 µl/g kidney weight/135 min, p < 0.05) and the osmolar excretion only 47% of that in controls (174 ± 47 versus 374 ± 41 µOsm/g kidney weight/135 min, p < 0.05). Sodium excretion, GFR, and arterial blood pressure were similar to that in control rats and unaltered during hydration.
Conclusions. Reduction of renomedullary interstitial HA using 4-MU reduces the ability of the kidney to respond appropriately upon acute hydration. The results strengthen the concept of renomedullary HA as a modulator of tubular fluid handling by changing the physicochemical properties of the interstitial space.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>24102146</pmid><doi>10.3109/03009734.2013.834013</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Blood Pressure Catheterization Diuresis Drinking Water Electrolytes - chemistry fluid balance Glomerular Filtration Rate Glycosaminoglycans - chemistry hyaluronan Hyaluronic Acid - antagonists & inhibitors Hydration Hymecromone - chemistry Indicators and Reagents - chemistry interstitium kidney Kidney - drug effects Kidney - metabolism Male matrix MEDICIN MEDICINE medulla Original Proteins Rats Rats, Sprague-Dawley Rodents Sodium - chemistry Water - chemistry |
title | Inhibition of hyaluronan synthesis in rats reduces renal ability to excrete fluid and electrolytes during acute hydration |
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