Loading…

Urine concentrating defect in prostaglandin EP^sub 1^-deficient mice

We investigated the role of the prostaglandin E... (PGE...) EP... receptor in modulating urine concentration as it is expressed along the renal collecting duct where arginine-vasopressin (AVP) exerts its anti-diuretic activity, and in the paraventricular and supraoptic nuclei of the hypothalamus whe...

Full description

Saved in:
Bibliographic Details
Published in:American journal of physiology. Renal physiology 2007-02, Vol.292 (2), p.F868
Main Authors: Kennedy, Chris R J, Xiong, Huaqi, Rahal, Sherine, Vanderluit, Jacqueline
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page
container_issue 2
container_start_page F868
container_title American journal of physiology. Renal physiology
container_volume 292
creator Kennedy, Chris R J
Xiong, Huaqi
Rahal, Sherine
Vanderluit, Jacqueline
description We investigated the role of the prostaglandin E... (PGE...) EP... receptor in modulating urine concentration as it is expressed along the renal collecting duct where arginine-vasopressin (AVP) exerts its anti-diuretic activity, and in the paraventricular and supraoptic nuclei of the hypothalamus where AVP is synthesized. The urine osmolality of EP...-null mice (EP...) failed to match levels achieved by wild-type (WT) counterparts upon water deprivation (WD) for 24 h. This difference was reflected by higher plasma osmolality in WD EP... mice. Along the collecting duct, the induction and subapical to plasma membrane translocation of the aquaporin-2 water channel in WD EP... mice appeared equivalent to that of WD WT mice as determined by quantitative RT-PCR and immunohistochemistry. However, medullary interstitial osmolalities dropped significantly in EP... mice following WD. Furthermore, urinary AVP levels of WD EP... mice were significantly lower than those of WD WT mice. This deficit could be traced back to a blunted induction of hypothalamic AVP mRNA expression in WD EP... mice as determined by quantitative RT-PCR. Administration of the AVP mimetic [deamino-Cys...,D-Arg...]-vasopressin restored a significant proportion of the urine concentrating ability of WD EP... mice. When mice were water loaded to suppress endogenous AVP production, urine osmolalities increased equally for WT and EP... mice. These data suggest that PGE... modulates urine concentration by acting at EP... receptors, not in the collecting duct, but within the hypothalamus to promote AVP synthesis in response to acute WD. (ProQuest Information and Learning: ... denotes formulae/symbols omitted.)
format article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_230098818</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1214286491</sourcerecordid><originalsourceid>FETCH-proquest_journals_2300988183</originalsourceid><addsrcrecordid>eNqNi8sOgjAURBujifj4h8Z9k94iWNaKcelCE1eQWgopwYu25f_twg9wNTOZc2YkgUwIBvs8n8depMBkdngsycr7nnMOICAhp7uzaKgeURsMTgWLHW1Ma3SgFunbjT6oblDYxFVeKz89KVQsElbbaNCX1WZDFq0avNn-ck125_J2vLCofybjQ92Pk8N41SLlvJASZPoX9AXM3Ttb</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>230098818</pqid></control><display><type>article</type><title>Urine concentrating defect in prostaglandin EP^sub 1^-deficient mice</title><source>American Physiological Society Free</source><creator>Kennedy, Chris R J ; Xiong, Huaqi ; Rahal, Sherine ; Vanderluit, Jacqueline</creator><creatorcontrib>Kennedy, Chris R J ; Xiong, Huaqi ; Rahal, Sherine ; Vanderluit, Jacqueline</creatorcontrib><description>We investigated the role of the prostaglandin E... (PGE...) EP... receptor in modulating urine concentration as it is expressed along the renal collecting duct where arginine-vasopressin (AVP) exerts its anti-diuretic activity, and in the paraventricular and supraoptic nuclei of the hypothalamus where AVP is synthesized. The urine osmolality of EP...-null mice (EP...) failed to match levels achieved by wild-type (WT) counterparts upon water deprivation (WD) for 24 h. This difference was reflected by higher plasma osmolality in WD EP... mice. Along the collecting duct, the induction and subapical to plasma membrane translocation of the aquaporin-2 water channel in WD EP... mice appeared equivalent to that of WD WT mice as determined by quantitative RT-PCR and immunohistochemistry. However, medullary interstitial osmolalities dropped significantly in EP... mice following WD. Furthermore, urinary AVP levels of WD EP... mice were significantly lower than those of WD WT mice. This deficit could be traced back to a blunted induction of hypothalamic AVP mRNA expression in WD EP... mice as determined by quantitative RT-PCR. Administration of the AVP mimetic [deamino-Cys...,D-Arg...]-vasopressin restored a significant proportion of the urine concentrating ability of WD EP... mice. When mice were water loaded to suppress endogenous AVP production, urine osmolalities increased equally for WT and EP... mice. These data suggest that PGE... modulates urine concentration by acting at EP... receptors, not in the collecting duct, but within the hypothalamus to promote AVP synthesis in response to acute WD. (ProQuest Information and Learning: ... denotes formulae/symbols omitted.)</description><identifier>ISSN: 1931-857X</identifier><identifier>EISSN: 1522-1466</identifier><language>eng</language><publisher>Bethesda: American Physiological Society</publisher><subject>Fatty acids ; Nephrology ; Rodents ; Urine</subject><ispartof>American journal of physiology. Renal physiology, 2007-02, Vol.292 (2), p.F868</ispartof><rights>Copyright American Physiological Society Feb 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Kennedy, Chris R J</creatorcontrib><creatorcontrib>Xiong, Huaqi</creatorcontrib><creatorcontrib>Rahal, Sherine</creatorcontrib><creatorcontrib>Vanderluit, Jacqueline</creatorcontrib><title>Urine concentrating defect in prostaglandin EP^sub 1^-deficient mice</title><title>American journal of physiology. Renal physiology</title><description>We investigated the role of the prostaglandin E... (PGE...) EP... receptor in modulating urine concentration as it is expressed along the renal collecting duct where arginine-vasopressin (AVP) exerts its anti-diuretic activity, and in the paraventricular and supraoptic nuclei of the hypothalamus where AVP is synthesized. The urine osmolality of EP...-null mice (EP...) failed to match levels achieved by wild-type (WT) counterparts upon water deprivation (WD) for 24 h. This difference was reflected by higher plasma osmolality in WD EP... mice. Along the collecting duct, the induction and subapical to plasma membrane translocation of the aquaporin-2 water channel in WD EP... mice appeared equivalent to that of WD WT mice as determined by quantitative RT-PCR and immunohistochemistry. However, medullary interstitial osmolalities dropped significantly in EP... mice following WD. Furthermore, urinary AVP levels of WD EP... mice were significantly lower than those of WD WT mice. This deficit could be traced back to a blunted induction of hypothalamic AVP mRNA expression in WD EP... mice as determined by quantitative RT-PCR. Administration of the AVP mimetic [deamino-Cys...,D-Arg...]-vasopressin restored a significant proportion of the urine concentrating ability of WD EP... mice. When mice were water loaded to suppress endogenous AVP production, urine osmolalities increased equally for WT and EP... mice. These data suggest that PGE... modulates urine concentration by acting at EP... receptors, not in the collecting duct, but within the hypothalamus to promote AVP synthesis in response to acute WD. (ProQuest Information and Learning: ... denotes formulae/symbols omitted.)</description><subject>Fatty acids</subject><subject>Nephrology</subject><subject>Rodents</subject><subject>Urine</subject><issn>1931-857X</issn><issn>1522-1466</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqNi8sOgjAURBujifj4h8Z9k94iWNaKcelCE1eQWgopwYu25f_twg9wNTOZc2YkgUwIBvs8n8depMBkdngsycr7nnMOICAhp7uzaKgeURsMTgWLHW1Ma3SgFunbjT6oblDYxFVeKz89KVQsElbbaNCX1WZDFq0avNn-ck125_J2vLCofybjQ92Pk8N41SLlvJASZPoX9AXM3Ttb</recordid><startdate>20070201</startdate><enddate>20070201</enddate><creator>Kennedy, Chris R J</creator><creator>Xiong, Huaqi</creator><creator>Rahal, Sherine</creator><creator>Vanderluit, Jacqueline</creator><general>American Physiological Society</general><scope/></search><sort><creationdate>20070201</creationdate><title>Urine concentrating defect in prostaglandin EP^sub 1^-deficient mice</title><author>Kennedy, Chris R J ; Xiong, Huaqi ; Rahal, Sherine ; Vanderluit, Jacqueline</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_2300988183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Fatty acids</topic><topic>Nephrology</topic><topic>Rodents</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kennedy, Chris R J</creatorcontrib><creatorcontrib>Xiong, Huaqi</creatorcontrib><creatorcontrib>Rahal, Sherine</creatorcontrib><creatorcontrib>Vanderluit, Jacqueline</creatorcontrib><jtitle>American journal of physiology. Renal physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kennedy, Chris R J</au><au>Xiong, Huaqi</au><au>Rahal, Sherine</au><au>Vanderluit, Jacqueline</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Urine concentrating defect in prostaglandin EP^sub 1^-deficient mice</atitle><jtitle>American journal of physiology. Renal physiology</jtitle><date>2007-02-01</date><risdate>2007</risdate><volume>292</volume><issue>2</issue><spage>F868</spage><pages>F868-</pages><issn>1931-857X</issn><eissn>1522-1466</eissn><abstract>We investigated the role of the prostaglandin E... (PGE...) EP... receptor in modulating urine concentration as it is expressed along the renal collecting duct where arginine-vasopressin (AVP) exerts its anti-diuretic activity, and in the paraventricular and supraoptic nuclei of the hypothalamus where AVP is synthesized. The urine osmolality of EP...-null mice (EP...) failed to match levels achieved by wild-type (WT) counterparts upon water deprivation (WD) for 24 h. This difference was reflected by higher plasma osmolality in WD EP... mice. Along the collecting duct, the induction and subapical to plasma membrane translocation of the aquaporin-2 water channel in WD EP... mice appeared equivalent to that of WD WT mice as determined by quantitative RT-PCR and immunohistochemistry. However, medullary interstitial osmolalities dropped significantly in EP... mice following WD. Furthermore, urinary AVP levels of WD EP... mice were significantly lower than those of WD WT mice. This deficit could be traced back to a blunted induction of hypothalamic AVP mRNA expression in WD EP... mice as determined by quantitative RT-PCR. Administration of the AVP mimetic [deamino-Cys...,D-Arg...]-vasopressin restored a significant proportion of the urine concentrating ability of WD EP... mice. When mice were water loaded to suppress endogenous AVP production, urine osmolalities increased equally for WT and EP... mice. These data suggest that PGE... modulates urine concentration by acting at EP... receptors, not in the collecting duct, but within the hypothalamus to promote AVP synthesis in response to acute WD. (ProQuest Information and Learning: ... denotes formulae/symbols omitted.)</abstract><cop>Bethesda</cop><pub>American Physiological Society</pub></addata></record>
fulltext fulltext
identifier ISSN: 1931-857X
ispartof American journal of physiology. Renal physiology, 2007-02, Vol.292 (2), p.F868
issn 1931-857X
1522-1466
language eng
recordid cdi_proquest_journals_230098818
source American Physiological Society Free
subjects Fatty acids
Nephrology
Rodents
Urine
title Urine concentrating defect in prostaglandin EP^sub 1^-deficient mice
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T01%3A40%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Urine%20concentrating%20defect%20in%20prostaglandin%20EP%5Esub%201%5E-deficient%20mice&rft.jtitle=American%20journal%20of%20physiology.%20Renal%20physiology&rft.au=Kennedy,%20Chris%20R%20J&rft.date=2007-02-01&rft.volume=292&rft.issue=2&rft.spage=F868&rft.pages=F868-&rft.issn=1931-857X&rft.eissn=1522-1466&rft_id=info:doi/&rft_dat=%3Cproquest%3E1214286491%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_journals_2300988183%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=230098818&rft_id=info:pmid/&rfr_iscdi=true