Chloride transport by the rabbit cortical collecting duct : Dependence on H, K-ATPase
The rabbit cortical collecting duct (CCD) exhibits the capacity for active chloride absorption when basolateral Na-K-ATPase is inhibited by ouabain. The present studies examine the contribution of H,K-ATPase to this ouabain-insensitive Cl absorption and to related ion fluxes. Rabbits were fed a KCl-...
Gespeichert in:
Veröffentlicht in: | Journal of the American Society of Nephrology 1998-12, Vol.9 (12), p.2194-2202 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2202 |
---|---|
container_issue | 12 |
container_start_page | 2194 |
container_title | Journal of the American Society of Nephrology |
container_volume | 9 |
creator | XIAOMING ZHOU XIA, S.-L WINGO, C. S |
description | The rabbit cortical collecting duct (CCD) exhibits the capacity for active chloride absorption when basolateral Na-K-ATPase is inhibited by ouabain. The present studies examine the contribution of H,K-ATPase to this ouabain-insensitive Cl absorption and to related ion fluxes. Rabbits were fed a KCl-rich diet with no measurable Na for 4 to 13 d before isolation of the CCD for microperfusion. Application of peritubular ouabain (0.1 mM) significantly increased (P < 0.001) net luminal absorptive chloride flux (J(N)Cl) without an effect on lumen-to-bath isotopic 36Cl flux (J(lb)Cl). The H,K-ATPase inhibitor Sch 28080 (1 to 10 microM) abolished ouabain-insensitive J(N)Cl, but transepithelial voltage (V(T)) was not significantly affected. The contribution of H,K-ATPase activity on active Cl flux (J(A)Cl) and passive Cl flux (J(P)Cl) was also assessed. Ouabain significantly increased J(A)Cl and Sch 28080 inhibited J(A)Cl, but J(P)Cl was not affected by Sch 28080. To assess the contribution of changes in net bicarbonate flux (JtCO2) to changes in J(N)Cl, JtCO2 was measured under identical conditions as for J(N)Cl. Ouabain significantly increased JtCO2, and this ouabain-insensitive bicarbonate flux was inhibited by Sch 28080 without significantly affecting V(T). To assess the possibility that the CCD may possess mechanisms for neutral salt absorption, lumen-to-bath 86Rb efflux (K(Rb)), and 22Na efflux (K(Na)) were also measured. Ouabain significantly increased K(Rb), and Sch 28080 inhibited this ouabain-insensitive K(Rb). Furthermore, Sch 28080 and A80915a (a structurally distinct H,K-ATPase inhibitor) significantly inhibited K(Na) in the presence of 1 mM luminal amiloride. These observations suggest that, in addition to potassium, sodium can be transported via the H,K-ATPase. Although the CCD contains more than one cell population, the data could be fitted very well to the function of the B-type intercalated cell. A cell model is proposed for the hypothesis that ouabain-insensitive chloride absorption is mediated by the parallel operation of an apical H,K-ATPase with an apical Cl-HCO3 exchanger and that the H,K-ATPase can function, under certain conditions, as a mechanism of Na absorption. |
doi_str_mv | 10.1681/ASN.V9122194 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70101516</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70101516</sourcerecordid><originalsourceid>FETCH-LOGICAL-c272t-26283c8cc07f8b29214017076d7aef47a2146848f9de8d258c68eaaff37e3603</originalsourceid><addsrcrecordid>eNpFkEtPwzAQhC0EKqVw44rkA-LUFL9iO9yq8hQVIFG4Ro6zoUFpEuzk0H-PUQOcdrQzGu1-CJ1SMqNS08v569PsPaGM0UTsoTGNOY-4iMl-0ETISErFD9GR95-E0JgpNUKjRAutFB-jt8W6alyZA-6cqX3buA5nW9ytATuTZWWHbViV1lRBVBXYrqw_cN7bDl_ha2ihzqG2gJsa30_xYzRfvRgPx-igMJWHk2FO0Or2ZrW4j5bPdw-L-TKyTLEuYpJpbrW1RBU6YwmjglBFlMyVgUIoExYyXFokOeicxdpKDcYUBVfAJeETdLGrbV3z1YPv0k3pLVSVqaHpfaoIDR9TGYLTXdC6xnsHRdq6cmPcNqUk_YGYBojpL8QQPxt6-2wD-V94oBb888E3PpApAjlb-v9OKYTklH8DO713uA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70101516</pqid></control><display><type>article</type><title>Chloride transport by the rabbit cortical collecting duct : Dependence on H, K-ATPase</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>XIAOMING ZHOU ; XIA, S.-L ; WINGO, C. S</creator><creatorcontrib>XIAOMING ZHOU ; XIA, S.-L ; WINGO, C. S</creatorcontrib><description>The rabbit cortical collecting duct (CCD) exhibits the capacity for active chloride absorption when basolateral Na-K-ATPase is inhibited by ouabain. The present studies examine the contribution of H,K-ATPase to this ouabain-insensitive Cl absorption and to related ion fluxes. Rabbits were fed a KCl-rich diet with no measurable Na for 4 to 13 d before isolation of the CCD for microperfusion. Application of peritubular ouabain (0.1 mM) significantly increased (P < 0.001) net luminal absorptive chloride flux (J(N)Cl) without an effect on lumen-to-bath isotopic 36Cl flux (J(lb)Cl). The H,K-ATPase inhibitor Sch 28080 (1 to 10 microM) abolished ouabain-insensitive J(N)Cl, but transepithelial voltage (V(T)) was not significantly affected. The contribution of H,K-ATPase activity on active Cl flux (J(A)Cl) and passive Cl flux (J(P)Cl) was also assessed. Ouabain significantly increased J(A)Cl and Sch 28080 inhibited J(A)Cl, but J(P)Cl was not affected by Sch 28080. To assess the contribution of changes in net bicarbonate flux (JtCO2) to changes in J(N)Cl, JtCO2 was measured under identical conditions as for J(N)Cl. Ouabain significantly increased JtCO2, and this ouabain-insensitive bicarbonate flux was inhibited by Sch 28080 without significantly affecting V(T). To assess the possibility that the CCD may possess mechanisms for neutral salt absorption, lumen-to-bath 86Rb efflux (K(Rb)), and 22Na efflux (K(Na)) were also measured. Ouabain significantly increased K(Rb), and Sch 28080 inhibited this ouabain-insensitive K(Rb). Furthermore, Sch 28080 and A80915a (a structurally distinct H,K-ATPase inhibitor) significantly inhibited K(Na) in the presence of 1 mM luminal amiloride. These observations suggest that, in addition to potassium, sodium can be transported via the H,K-ATPase. Although the CCD contains more than one cell population, the data could be fitted very well to the function of the B-type intercalated cell. A cell model is proposed for the hypothesis that ouabain-insensitive chloride absorption is mediated by the parallel operation of an apical H,K-ATPase with an apical Cl-HCO3 exchanger and that the H,K-ATPase can function, under certain conditions, as a mechanism of Na absorption.</description><identifier>ISSN: 1046-6673</identifier><identifier>EISSN: 1533-3450</identifier><identifier>DOI: 10.1681/ASN.V9122194</identifier><identifier>PMID: 9848773</identifier><identifier>CODEN: JASNEU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Animals ; Antiporters - metabolism ; Bicarbonates - metabolism ; Biological and medical sciences ; Cell Polarity ; Chloride-Bicarbonate Antiporters ; Chlorides - metabolism ; Enzyme Inhibitors - pharmacology ; Female ; H(+)-K(+)-Exchanging ATPase - metabolism ; Imidazoles - pharmacology ; Investigative techniques, diagnostic techniques (general aspects) ; Ion Transport - drug effects ; Kidney Cortex - drug effects ; Kidney Cortex - metabolism ; Kidney Tubules, Collecting - drug effects ; Kidney Tubules, Collecting - metabolism ; Medical sciences ; Models, Biological ; Naphthoquinones - pharmacology ; Ouabain - pharmacology ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Potassium - administration & dosage ; Proton Pump Inhibitors ; Rabbits ; Rubidium - metabolism ; Sodium - metabolism ; Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors ; Urinary system</subject><ispartof>Journal of the American Society of Nephrology, 1998-12, Vol.9 (12), p.2194-2202</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1644631$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9848773$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>XIAOMING ZHOU</creatorcontrib><creatorcontrib>XIA, S.-L</creatorcontrib><creatorcontrib>WINGO, C. S</creatorcontrib><title>Chloride transport by the rabbit cortical collecting duct : Dependence on H, K-ATPase</title><title>Journal of the American Society of Nephrology</title><addtitle>J Am Soc Nephrol</addtitle><description>The rabbit cortical collecting duct (CCD) exhibits the capacity for active chloride absorption when basolateral Na-K-ATPase is inhibited by ouabain. The present studies examine the contribution of H,K-ATPase to this ouabain-insensitive Cl absorption and to related ion fluxes. Rabbits were fed a KCl-rich diet with no measurable Na for 4 to 13 d before isolation of the CCD for microperfusion. Application of peritubular ouabain (0.1 mM) significantly increased (P < 0.001) net luminal absorptive chloride flux (J(N)Cl) without an effect on lumen-to-bath isotopic 36Cl flux (J(lb)Cl). The H,K-ATPase inhibitor Sch 28080 (1 to 10 microM) abolished ouabain-insensitive J(N)Cl, but transepithelial voltage (V(T)) was not significantly affected. The contribution of H,K-ATPase activity on active Cl flux (J(A)Cl) and passive Cl flux (J(P)Cl) was also assessed. Ouabain significantly increased J(A)Cl and Sch 28080 inhibited J(A)Cl, but J(P)Cl was not affected by Sch 28080. To assess the contribution of changes in net bicarbonate flux (JtCO2) to changes in J(N)Cl, JtCO2 was measured under identical conditions as for J(N)Cl. Ouabain significantly increased JtCO2, and this ouabain-insensitive bicarbonate flux was inhibited by Sch 28080 without significantly affecting V(T). To assess the possibility that the CCD may possess mechanisms for neutral salt absorption, lumen-to-bath 86Rb efflux (K(Rb)), and 22Na efflux (K(Na)) were also measured. Ouabain significantly increased K(Rb), and Sch 28080 inhibited this ouabain-insensitive K(Rb). Furthermore, Sch 28080 and A80915a (a structurally distinct H,K-ATPase inhibitor) significantly inhibited K(Na) in the presence of 1 mM luminal amiloride. These observations suggest that, in addition to potassium, sodium can be transported via the H,K-ATPase. Although the CCD contains more than one cell population, the data could be fitted very well to the function of the B-type intercalated cell. A cell model is proposed for the hypothesis that ouabain-insensitive chloride absorption is mediated by the parallel operation of an apical H,K-ATPase with an apical Cl-HCO3 exchanger and that the H,K-ATPase can function, under certain conditions, as a mechanism of Na absorption.</description><subject>Animals</subject><subject>Antiporters - metabolism</subject><subject>Bicarbonates - metabolism</subject><subject>Biological and medical sciences</subject><subject>Cell Polarity</subject><subject>Chloride-Bicarbonate Antiporters</subject><subject>Chlorides - metabolism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>H(+)-K(+)-Exchanging ATPase - metabolism</subject><subject>Imidazoles - pharmacology</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Ion Transport - drug effects</subject><subject>Kidney Cortex - drug effects</subject><subject>Kidney Cortex - metabolism</subject><subject>Kidney Tubules, Collecting - drug effects</subject><subject>Kidney Tubules, Collecting - metabolism</subject><subject>Medical sciences</subject><subject>Models, Biological</subject><subject>Naphthoquinones - pharmacology</subject><subject>Ouabain - pharmacology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Potassium - administration & dosage</subject><subject>Proton Pump Inhibitors</subject><subject>Rabbits</subject><subject>Rubidium - metabolism</subject><subject>Sodium - metabolism</subject><subject>Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors</subject><subject>Urinary system</subject><issn>1046-6673</issn><issn>1533-3450</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtPwzAQhC0EKqVw44rkA-LUFL9iO9yq8hQVIFG4Ro6zoUFpEuzk0H-PUQOcdrQzGu1-CJ1SMqNS08v569PsPaGM0UTsoTGNOY-4iMl-0ETISErFD9GR95-E0JgpNUKjRAutFB-jt8W6alyZA-6cqX3buA5nW9ytATuTZWWHbViV1lRBVBXYrqw_cN7bDl_ha2ihzqG2gJsa30_xYzRfvRgPx-igMJWHk2FO0Or2ZrW4j5bPdw-L-TKyTLEuYpJpbrW1RBU6YwmjglBFlMyVgUIoExYyXFokOeicxdpKDcYUBVfAJeETdLGrbV3z1YPv0k3pLVSVqaHpfaoIDR9TGYLTXdC6xnsHRdq6cmPcNqUk_YGYBojpL8QQPxt6-2wD-V94oBb888E3PpApAjlb-v9OKYTklH8DO713uA</recordid><startdate>19981201</startdate><enddate>19981201</enddate><creator>XIAOMING ZHOU</creator><creator>XIA, S.-L</creator><creator>WINGO, C. S</creator><general>Lippincott Williams & Wilkins</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><scope>7X8</scope></search><sort><creationdate>19981201</creationdate><title>Chloride transport by the rabbit cortical collecting duct : Dependence on H, K-ATPase</title><author>XIAOMING ZHOU ; XIA, S.-L ; WINGO, C. S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c272t-26283c8cc07f8b29214017076d7aef47a2146848f9de8d258c68eaaff37e3603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Antiporters - metabolism</topic><topic>Bicarbonates - metabolism</topic><topic>Biological and medical sciences</topic><topic>Cell Polarity</topic><topic>Chloride-Bicarbonate Antiporters</topic><topic>Chlorides - metabolism</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Female</topic><topic>H(+)-K(+)-Exchanging ATPase - metabolism</topic><topic>Imidazoles - pharmacology</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Ion Transport - drug effects</topic><topic>Kidney Cortex - drug effects</topic><topic>Kidney Cortex - metabolism</topic><topic>Kidney Tubules, Collecting - drug effects</topic><topic>Kidney Tubules, Collecting - metabolism</topic><topic>Medical sciences</topic><topic>Models, Biological</topic><topic>Naphthoquinones - pharmacology</topic><topic>Ouabain - pharmacology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Potassium - administration & dosage</topic><topic>Proton Pump Inhibitors</topic><topic>Rabbits</topic><topic>Rubidium - metabolism</topic><topic>Sodium - metabolism</topic><topic>Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors</topic><topic>Urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>XIAOMING ZHOU</creatorcontrib><creatorcontrib>XIA, S.-L</creatorcontrib><creatorcontrib>WINGO, C. S</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><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Society of Nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>XIAOMING ZHOU</au><au>XIA, S.-L</au><au>WINGO, C. S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chloride transport by the rabbit cortical collecting duct : Dependence on H, K-ATPase</atitle><jtitle>Journal of the American Society of Nephrology</jtitle><addtitle>J Am Soc Nephrol</addtitle><date>1998-12-01</date><risdate>1998</risdate><volume>9</volume><issue>12</issue><spage>2194</spage><epage>2202</epage><pages>2194-2202</pages><issn>1046-6673</issn><eissn>1533-3450</eissn><coden>JASNEU</coden><abstract>The rabbit cortical collecting duct (CCD) exhibits the capacity for active chloride absorption when basolateral Na-K-ATPase is inhibited by ouabain. The present studies examine the contribution of H,K-ATPase to this ouabain-insensitive Cl absorption and to related ion fluxes. Rabbits were fed a KCl-rich diet with no measurable Na for 4 to 13 d before isolation of the CCD for microperfusion. Application of peritubular ouabain (0.1 mM) significantly increased (P < 0.001) net luminal absorptive chloride flux (J(N)Cl) without an effect on lumen-to-bath isotopic 36Cl flux (J(lb)Cl). The H,K-ATPase inhibitor Sch 28080 (1 to 10 microM) abolished ouabain-insensitive J(N)Cl, but transepithelial voltage (V(T)) was not significantly affected. The contribution of H,K-ATPase activity on active Cl flux (J(A)Cl) and passive Cl flux (J(P)Cl) was also assessed. Ouabain significantly increased J(A)Cl and Sch 28080 inhibited J(A)Cl, but J(P)Cl was not affected by Sch 28080. To assess the contribution of changes in net bicarbonate flux (JtCO2) to changes in J(N)Cl, JtCO2 was measured under identical conditions as for J(N)Cl. Ouabain significantly increased JtCO2, and this ouabain-insensitive bicarbonate flux was inhibited by Sch 28080 without significantly affecting V(T). To assess the possibility that the CCD may possess mechanisms for neutral salt absorption, lumen-to-bath 86Rb efflux (K(Rb)), and 22Na efflux (K(Na)) were also measured. Ouabain significantly increased K(Rb), and Sch 28080 inhibited this ouabain-insensitive K(Rb). Furthermore, Sch 28080 and A80915a (a structurally distinct H,K-ATPase inhibitor) significantly inhibited K(Na) in the presence of 1 mM luminal amiloride. These observations suggest that, in addition to potassium, sodium can be transported via the H,K-ATPase. Although the CCD contains more than one cell population, the data could be fitted very well to the function of the B-type intercalated cell. A cell model is proposed for the hypothesis that ouabain-insensitive chloride absorption is mediated by the parallel operation of an apical H,K-ATPase with an apical Cl-HCO3 exchanger and that the H,K-ATPase can function, under certain conditions, as a mechanism of Na absorption.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>9848773</pmid><doi>10.1681/ASN.V9122194</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1046-6673 |
ispartof | Journal of the American Society of Nephrology, 1998-12, Vol.9 (12), p.2194-2202 |
issn | 1046-6673 1533-3450 |
language | eng |
recordid | cdi_proquest_miscellaneous_70101516 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Animals Antiporters - metabolism Bicarbonates - metabolism Biological and medical sciences Cell Polarity Chloride-Bicarbonate Antiporters Chlorides - metabolism Enzyme Inhibitors - pharmacology Female H(+)-K(+)-Exchanging ATPase - metabolism Imidazoles - pharmacology Investigative techniques, diagnostic techniques (general aspects) Ion Transport - drug effects Kidney Cortex - drug effects Kidney Cortex - metabolism Kidney Tubules, Collecting - drug effects Kidney Tubules, Collecting - metabolism Medical sciences Models, Biological Naphthoquinones - pharmacology Ouabain - pharmacology Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Potassium - administration & dosage Proton Pump Inhibitors Rabbits Rubidium - metabolism Sodium - metabolism Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors Urinary system |
title | Chloride transport by the rabbit cortical collecting duct : Dependence on H, K-ATPase |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T18%3A45%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Chloride%20transport%20by%20the%20rabbit%20cortical%20collecting%20duct%20:%20Dependence%20on%20H,%20K-ATPase&rft.jtitle=Journal%20of%20the%20American%20Society%20of%20Nephrology&rft.au=XIAOMING%20ZHOU&rft.date=1998-12-01&rft.volume=9&rft.issue=12&rft.spage=2194&rft.epage=2202&rft.pages=2194-2202&rft.issn=1046-6673&rft.eissn=1533-3450&rft.coden=JASNEU&rft_id=info:doi/10.1681/ASN.V9122194&rft_dat=%3Cproquest_cross%3E70101516%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70101516&rft_id=info:pmid/9848773&rfr_iscdi=true |