Effect of volume expansion with hypertonic- and isotonic saline and isotonic glucose on sodium and water transport in the principal cells in the kidney
The renal distal nephron plays an important role in the maintenance of sodium balance, extra cellular volume and blood pressure. The degree of water transport, via aquaporin2 water channels (AQP2), and sodium transport, via epithelial sodium channels (ENaC) in renal collecting duct principal cells a...
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description | The renal distal nephron plays an important role in the maintenance of sodium balance, extra cellular volume and blood pressure. The degree of water transport, via aquaporin2 water channels (AQP2), and sodium transport, via epithelial sodium channels (ENaC) in renal collecting duct principal cells are reflected by the level of urinary excretion of AQP2 (u-AQP2) and the γ-fraction of ENaC (u-ENaCγ). The effects of an acute intravenous volume load with isotonic saline, hypertonic saline and glucose on u-AQP2, u-ENaCγ and underlying mechanisms have never been studied in a randomized, placebo-controlled trial in healthy humans.
We studied the effects of 0.9% saline (23 ml/kg), 3% saline (7 ml/kg) and 5% glucose (23 ml/kg) on u-AQP2 and u-ENaCγ, fractional sodium excretion (FENa), free water clearance (CH2O), and plasma concentrations of vasopressin (AVP), renin (PRC), angiotensin II (ANG II) and aldosterone (Aldo) in a randomized, crossover study of 23 healthy subjects, who consumed a standardized diet, regarding calories, sodium and fluid for 4 days before each examination day.
After isotonic saline infusion, u-AQP2 increased (27%). CH2O and u-ENaCγ were unchanged, whereas FENa increased (123%). After hypertonic saline infusion, there was an increase in u-AQP2 (25%), u-ENaCγ (19%) and FENa (96%), whereas CH2O decreased (-153%). After isotonic glucose infusion, there was a decrease in u-AQP2 (-16%), ENaCγ (-10%) and FENa (-44%) whereas CH2O increased (164%). AVP remained unchanged after isotonic saline and glucose, but increased after hypertonic saline (139%). PRC, AngII and p-Aldo decreased after isotonic and hypertonic saline infusion, but not after glucose infusion.
Volume expansion with 3% and 0.9% saline increased u-AQP2, while isotonic glucose decreased u-AQP2. Infusion of hypertonic saline increased u-ENaCγ, whereas u-ENaCγ was not significantly changed after isotonic saline and tended to decrease after glucose. Thus, the transport of water and sodium is changed both via the aquaporin 2 water channels and the epithelial sodium channels during all three types of volume expansion to regulate and maintain water- and sodium homeostasis in the body.
Clinical Trial no: NCT01414088. |
doi_str_mv | 10.1186/1471-2369-14-202 |
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We studied the effects of 0.9% saline (23 ml/kg), 3% saline (7 ml/kg) and 5% glucose (23 ml/kg) on u-AQP2 and u-ENaCγ, fractional sodium excretion (FENa), free water clearance (CH2O), and plasma concentrations of vasopressin (AVP), renin (PRC), angiotensin II (ANG II) and aldosterone (Aldo) in a randomized, crossover study of 23 healthy subjects, who consumed a standardized diet, regarding calories, sodium and fluid for 4 days before each examination day.
After isotonic saline infusion, u-AQP2 increased (27%). CH2O and u-ENaCγ were unchanged, whereas FENa increased (123%). After hypertonic saline infusion, there was an increase in u-AQP2 (25%), u-ENaCγ (19%) and FENa (96%), whereas CH2O decreased (-153%). After isotonic glucose infusion, there was a decrease in u-AQP2 (-16%), ENaCγ (-10%) and FENa (-44%) whereas CH2O increased (164%). AVP remained unchanged after isotonic saline and glucose, but increased after hypertonic saline (139%). PRC, AngII and p-Aldo decreased after isotonic and hypertonic saline infusion, but not after glucose infusion.
Volume expansion with 3% and 0.9% saline increased u-AQP2, while isotonic glucose decreased u-AQP2. Infusion of hypertonic saline increased u-ENaCγ, whereas u-ENaCγ was not significantly changed after isotonic saline and tended to decrease after glucose. Thus, the transport of water and sodium is changed both via the aquaporin 2 water channels and the epithelial sodium channels during all three types of volume expansion to regulate and maintain water- and sodium homeostasis in the body.
Clinical Trial no: NCT01414088.</description><identifier>ISSN: 1471-2369</identifier><identifier>EISSN: 1471-2369</identifier><identifier>DOI: 10.1186/1471-2369-14-202</identifier><identifier>PMID: 24067081</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Angiotensin ; Aquaporin 2 - urine ; Aquaporins ; Blood Volume - drug effects ; Body Water - metabolism ; Cross-Over Studies ; Design ; Diet ; Epithelial Sodium Channels - urine ; Expansion ; Female ; Glucose ; Glucose Solution, Hypertonic - pharmacology ; Homeostasis ; Humans ; Isotonic Solutions - pharmacology ; Kidney - cytology ; Kidney - drug effects ; Kidney - metabolism ; Kidney Tubules - drug effects ; Kidney Tubules - metabolism ; Kidneys ; Male ; Medical research ; Nephrology ; Nephrons - drug effects ; Nephrons - metabolism ; Nutrition research ; Physiological aspects ; Plasma ; Potassium ; Rodents ; Saline Solution, Hypertonic - pharmacology ; Sodium ; Sodium - metabolism</subject><ispartof>BMC nephrology, 2013-09, Vol.14 (1), p.202-202, Article 202</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>2013 Jensen et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2013 Jensen et al.; licensee BioMed Central Ltd. 2013 Jensen et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c491t-6fa91d2e05f52231d7f093f4b708f4cbd2085de88f61642da5905577162deb113</citedby><cites>FETCH-LOGICAL-c491t-6fa91d2e05f52231d7f093f4b708f4cbd2085de88f61642da5905577162deb113</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/PMC3849534/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3849534/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24067081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jensen, Janni M</creatorcontrib><creatorcontrib>Mose, Frank H</creatorcontrib><creatorcontrib>Bech, Jesper N</creatorcontrib><creatorcontrib>Nielsen, Soren</creatorcontrib><creatorcontrib>Pedersen, Erling B</creatorcontrib><title>Effect of volume expansion with hypertonic- and isotonic saline and isotonic glucose on sodium and water transport in the principal cells in the kidney</title><title>BMC nephrology</title><addtitle>BMC Nephrol</addtitle><description>The renal distal nephron plays an important role in the maintenance of sodium balance, extra cellular volume and blood pressure. The degree of water transport, via aquaporin2 water channels (AQP2), and sodium transport, via epithelial sodium channels (ENaC) in renal collecting duct principal cells are reflected by the level of urinary excretion of AQP2 (u-AQP2) and the γ-fraction of ENaC (u-ENaCγ). The effects of an acute intravenous volume load with isotonic saline, hypertonic saline and glucose on u-AQP2, u-ENaCγ and underlying mechanisms have never been studied in a randomized, placebo-controlled trial in healthy humans.
We studied the effects of 0.9% saline (23 ml/kg), 3% saline (7 ml/kg) and 5% glucose (23 ml/kg) on u-AQP2 and u-ENaCγ, fractional sodium excretion (FENa), free water clearance (CH2O), and plasma concentrations of vasopressin (AVP), renin (PRC), angiotensin II (ANG II) and aldosterone (Aldo) in a randomized, crossover study of 23 healthy subjects, who consumed a standardized diet, regarding calories, sodium and fluid for 4 days before each examination day.
After isotonic saline infusion, u-AQP2 increased (27%). CH2O and u-ENaCγ were unchanged, whereas FENa increased (123%). After hypertonic saline infusion, there was an increase in u-AQP2 (25%), u-ENaCγ (19%) and FENa (96%), whereas CH2O decreased (-153%). After isotonic glucose infusion, there was a decrease in u-AQP2 (-16%), ENaCγ (-10%) and FENa (-44%) whereas CH2O increased (164%). AVP remained unchanged after isotonic saline and glucose, but increased after hypertonic saline (139%). PRC, AngII and p-Aldo decreased after isotonic and hypertonic saline infusion, but not after glucose infusion.
Volume expansion with 3% and 0.9% saline increased u-AQP2, while isotonic glucose decreased u-AQP2. Infusion of hypertonic saline increased u-ENaCγ, whereas u-ENaCγ was not significantly changed after isotonic saline and tended to decrease after glucose. Thus, the transport of water and sodium is changed both via the aquaporin 2 water channels and the epithelial sodium channels during all three types of volume expansion to regulate and maintain water- and sodium homeostasis in the body.
Clinical Trial no: NCT01414088.</description><subject>Analysis</subject><subject>Angiotensin</subject><subject>Aquaporin 2 - urine</subject><subject>Aquaporins</subject><subject>Blood Volume - drug effects</subject><subject>Body Water - metabolism</subject><subject>Cross-Over Studies</subject><subject>Design</subject><subject>Diet</subject><subject>Epithelial Sodium Channels - urine</subject><subject>Expansion</subject><subject>Female</subject><subject>Glucose</subject><subject>Glucose Solution, Hypertonic - pharmacology</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Isotonic Solutions - pharmacology</subject><subject>Kidney - cytology</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Kidney Tubules - drug effects</subject><subject>Kidney Tubules - metabolism</subject><subject>Kidneys</subject><subject>Male</subject><subject>Medical research</subject><subject>Nephrology</subject><subject>Nephrons - drug effects</subject><subject>Nephrons - metabolism</subject><subject>Nutrition research</subject><subject>Physiological aspects</subject><subject>Plasma</subject><subject>Potassium</subject><subject>Rodents</subject><subject>Saline Solution, Hypertonic - pharmacology</subject><subject>Sodium</subject><subject>Sodium - metabolism</subject><issn>1471-2369</issn><issn>1471-2369</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptUk1v1DAQjRCIfsCdE7LEhUuKx3E-fEGqqlKQKnGBs-W1x7suiR3spO3-Ev4uTj9Wuwj54PHMe29mrFcU74CeAXTNJ-AtlKxqRAm8ZJS9KI53qZd78VFxktINpdB2nL4ujhinTUs7OC7-XFqLeiLBktvQzwMSvB-VTy54cuemDdlsR4xT8E6XRHlDXAoPL5JU7zwe5tb9rENCkskpGDcPD-U7NWEkU8yyY4gTcZ5MGyRjdF67UfVEY9-n5_QvZzxu3xSvrOoTvn26T4ufXy5_XHwtr79ffbs4vy41FzCVjVUCDENa25qxCkxrqagsX-XtLNcrw2hXG-w620DDmVG1oHXdttAwgyuA6rT4_Kg7zqsBjUaf5-xlnm1QcSuDcvKw4t1GrsOtrDou6opngY9PAjH8njFNcnBpWUh5DHOSwGsBNWUty9AP_0Bvwhx9Xi-jqq4Tjaj2UGvVo3TehtxXL6LyPDdsaCtgQZ39B5WPwcHp4NG6nD8g0EeCjiGliHa3I1C5mEkubpGLW3Iks5ky5f3-3-wIz-6p_gLx08XL</recordid><startdate>20130926</startdate><enddate>20130926</enddate><creator>Jensen, Janni M</creator><creator>Mose, Frank H</creator><creator>Bech, Jesper N</creator><creator>Nielsen, Soren</creator><creator>Pedersen, Erling B</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130926</creationdate><title>Effect of volume expansion with hypertonic- and isotonic saline and isotonic glucose on sodium and water transport in the principal cells in the kidney</title><author>Jensen, Janni M ; Mose, Frank H ; Bech, Jesper N ; Nielsen, Soren ; Pedersen, Erling B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c491t-6fa91d2e05f52231d7f093f4b708f4cbd2085de88f61642da5905577162deb113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analysis</topic><topic>Angiotensin</topic><topic>Aquaporin 2 - urine</topic><topic>Aquaporins</topic><topic>Blood Volume - drug effects</topic><topic>Body Water - metabolism</topic><topic>Cross-Over Studies</topic><topic>Design</topic><topic>Diet</topic><topic>Epithelial Sodium Channels - urine</topic><topic>Expansion</topic><topic>Female</topic><topic>Glucose</topic><topic>Glucose Solution, Hypertonic - pharmacology</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Isotonic Solutions - pharmacology</topic><topic>Kidney - cytology</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Kidney Tubules - drug effects</topic><topic>Kidney Tubules - metabolism</topic><topic>Kidneys</topic><topic>Male</topic><topic>Medical research</topic><topic>Nephrology</topic><topic>Nephrons - drug effects</topic><topic>Nephrons - metabolism</topic><topic>Nutrition research</topic><topic>Physiological aspects</topic><topic>Plasma</topic><topic>Potassium</topic><topic>Rodents</topic><topic>Saline Solution, Hypertonic - pharmacology</topic><topic>Sodium</topic><topic>Sodium - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jensen, Janni M</creatorcontrib><creatorcontrib>Mose, Frank H</creatorcontrib><creatorcontrib>Bech, Jesper N</creatorcontrib><creatorcontrib>Nielsen, Soren</creatorcontrib><creatorcontrib>Pedersen, Erling B</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>Calcium & Calcified Tissue Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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>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 Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jensen, Janni M</au><au>Mose, Frank H</au><au>Bech, Jesper N</au><au>Nielsen, Soren</au><au>Pedersen, Erling B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of volume expansion with hypertonic- and isotonic saline and isotonic glucose on sodium and water transport in the principal cells in the kidney</atitle><jtitle>BMC nephrology</jtitle><addtitle>BMC Nephrol</addtitle><date>2013-09-26</date><risdate>2013</risdate><volume>14</volume><issue>1</issue><spage>202</spage><epage>202</epage><pages>202-202</pages><artnum>202</artnum><issn>1471-2369</issn><eissn>1471-2369</eissn><abstract>The renal distal nephron plays an important role in the maintenance of sodium balance, extra cellular volume and blood pressure. The degree of water transport, via aquaporin2 water channels (AQP2), and sodium transport, via epithelial sodium channels (ENaC) in renal collecting duct principal cells are reflected by the level of urinary excretion of AQP2 (u-AQP2) and the γ-fraction of ENaC (u-ENaCγ). The effects of an acute intravenous volume load with isotonic saline, hypertonic saline and glucose on u-AQP2, u-ENaCγ and underlying mechanisms have never been studied in a randomized, placebo-controlled trial in healthy humans.
We studied the effects of 0.9% saline (23 ml/kg), 3% saline (7 ml/kg) and 5% glucose (23 ml/kg) on u-AQP2 and u-ENaCγ, fractional sodium excretion (FENa), free water clearance (CH2O), and plasma concentrations of vasopressin (AVP), renin (PRC), angiotensin II (ANG II) and aldosterone (Aldo) in a randomized, crossover study of 23 healthy subjects, who consumed a standardized diet, regarding calories, sodium and fluid for 4 days before each examination day.
After isotonic saline infusion, u-AQP2 increased (27%). CH2O and u-ENaCγ were unchanged, whereas FENa increased (123%). After hypertonic saline infusion, there was an increase in u-AQP2 (25%), u-ENaCγ (19%) and FENa (96%), whereas CH2O decreased (-153%). After isotonic glucose infusion, there was a decrease in u-AQP2 (-16%), ENaCγ (-10%) and FENa (-44%) whereas CH2O increased (164%). AVP remained unchanged after isotonic saline and glucose, but increased after hypertonic saline (139%). PRC, AngII and p-Aldo decreased after isotonic and hypertonic saline infusion, but not after glucose infusion.
Volume expansion with 3% and 0.9% saline increased u-AQP2, while isotonic glucose decreased u-AQP2. Infusion of hypertonic saline increased u-ENaCγ, whereas u-ENaCγ was not significantly changed after isotonic saline and tended to decrease after glucose. Thus, the transport of water and sodium is changed both via the aquaporin 2 water channels and the epithelial sodium channels during all three types of volume expansion to regulate and maintain water- and sodium homeostasis in the body.
Clinical Trial no: NCT01414088.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24067081</pmid><doi>10.1186/1471-2369-14-202</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Angiotensin Aquaporin 2 - urine Aquaporins Blood Volume - drug effects Body Water - metabolism Cross-Over Studies Design Diet Epithelial Sodium Channels - urine Expansion Female Glucose Glucose Solution, Hypertonic - pharmacology Homeostasis Humans Isotonic Solutions - pharmacology Kidney - cytology Kidney - drug effects Kidney - metabolism Kidney Tubules - drug effects Kidney Tubules - metabolism Kidneys Male Medical research Nephrology Nephrons - drug effects Nephrons - metabolism Nutrition research Physiological aspects Plasma Potassium Rodents Saline Solution, Hypertonic - pharmacology Sodium Sodium - metabolism |
title | Effect of volume expansion with hypertonic- and isotonic saline and isotonic glucose on sodium and water transport in the principal cells in the kidney |
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