Identification of two cardiac glycosides as Na(+)-pump inhibitors in rat urine and diet
Endogenous Na(+)-pump specific inhibitors are present in the plasma, urine, and tissues of humans and animals. To date, the source of these inhibitors has not been rigorously defined. In the present study, large amounts of several Na(+)-pump specific inhibitors have been demonstrated to exist in the...
Gespeichert in:
Veröffentlicht in: | The Journal of biological chemistry 1994-04, Vol.269 (16), p.11972-11979 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 11979 |
---|---|
container_issue | 16 |
container_start_page | 11972 |
container_title | The Journal of biological chemistry |
container_volume | 269 |
creator | TAMURA, M HARRIS, T. M PHILLIPS, D BLAIR, I. A YUE FEN WANG HELLERQVIST, C. G SAU KUEN LAM INAGAMI, T |
description | Endogenous Na(+)-pump specific inhibitors are present in the plasma, urine, and tissues of humans and animals. To date, the
source of these inhibitors has not been rigorously defined. In the present study, large amounts of several Na(+)-pump specific
inhibitors have been demonstrated to exist in the urine of rats raised on a regular chow diet and tap water. All of the inhibitor
levels have been found to increase 1.5-8-fold by the surgical preparation of reduced renal mass (RRM) and one-kidney, one-clip
(IK, IC) hypertension. These urinary inhibitors, however, except for the ouabain-like inhibitor which eluted from a high performance
liquid chromatography C18 column at the same retention time as [3H]ouabain, disappeared within a week after switching the
diet from regular diet (number 5001, PMI Feeds, Inc.) to pure synthetic diet (number 5755). The urinary level of the ouabain-like
inhibitor decreased to only one-half of the level in the control rat raised on a regular diet. Two of these inhibitors were
purified from both urine and diet by a combination of Amberlite XAD-2 adsorption chromatography, reverse phase low pressure
liquid chromatography, and several high performance liquid chromatographies. Reverse phase high performance liquid chromatography,
liquid secondary ion and gas-liquid mass spectrometries, and proton nuclear magnetic resonance spectroscopy identified these
inhibitors as a stereoisomer of convalloside, probably neoconvalloside, and a mono-rhamnoside of periplogenin or its stereoisomer.
These cardiac glycosides exhibited inhibitory potencies comparable to ouabain against ouabain-displacement from Na+,K(+)-ATPase
and against 86Rb uptake into human erythrocytes, and they also exhibited cross-reactivity to anti-ouabain antibodies and anti-digoxin
antibodies. These results clearly demonstrate that the principal source of most of the inhibitors in rat urine is the diet.
The results suggest that the ouabain-like inhibitor may be derived from an endogenous origin. |
doi_str_mv | 10.1016/S0021-9258(17)32669-8 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76447483</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76447483</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3248-1139434938f91da3d0a0b89874fdfe0c6497b4f275cc70b0ead4994744b057af3</originalsourceid><addsrcrecordid>eNpFkF1LHTEQhoNU9FT9CUIupChlbWaT3SSXRfohSHthpb0Ls_nwRHY3x2QX8d931cNxbmZgnpkXHkJOgV0Cg_bLLWM1VLpu1DnIC163ra7UHlkBU7ziDfz7QFY75JB8LOWBLSU0HJADBS1vGFuRv9fOj1MM0eIU00hToNNTohazi2jpff9sU4nOF4qF_sLzzxfVZh42NI7r2MUp5bKMNONE5xxHT3F01EU_HZP9gH3xJ9t-RO6-f_tz9bO6-f3j-urrTWV5LVQFwLXgQnMVNDjkjiHrlFZSBBc8s63QshOhlo21knXMoxNaCylExxqJgR-RT29_Nzk9zr5MZojF-r7H0ae5GNmKhVZ8AZs30OZUSvbBbHIcMD8bYOZFqHkVal5sGZDmVahRy93pNmDuBu92V1uDy_5su8disQ8ZRxvLDhPQ8Lbh79g63q-fYvami8mu_WDqJWZJB9Cy5v8BpFOITg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>76447483</pqid></control><display><type>article</type><title>Identification of two cardiac glycosides as Na(+)-pump inhibitors in rat urine and diet</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>TAMURA, M ; HARRIS, T. M ; PHILLIPS, D ; BLAIR, I. A ; YUE FEN WANG ; HELLERQVIST, C. G ; SAU KUEN LAM ; INAGAMI, T</creator><creatorcontrib>TAMURA, M ; HARRIS, T. M ; PHILLIPS, D ; BLAIR, I. A ; YUE FEN WANG ; HELLERQVIST, C. G ; SAU KUEN LAM ; INAGAMI, T</creatorcontrib><description>Endogenous Na(+)-pump specific inhibitors are present in the plasma, urine, and tissues of humans and animals. To date, the
source of these inhibitors has not been rigorously defined. In the present study, large amounts of several Na(+)-pump specific
inhibitors have been demonstrated to exist in the urine of rats raised on a regular chow diet and tap water. All of the inhibitor
levels have been found to increase 1.5-8-fold by the surgical preparation of reduced renal mass (RRM) and one-kidney, one-clip
(IK, IC) hypertension. These urinary inhibitors, however, except for the ouabain-like inhibitor which eluted from a high performance
liquid chromatography C18 column at the same retention time as [3H]ouabain, disappeared within a week after switching the
diet from regular diet (number 5001, PMI Feeds, Inc.) to pure synthetic diet (number 5755). The urinary level of the ouabain-like
inhibitor decreased to only one-half of the level in the control rat raised on a regular diet. Two of these inhibitors were
purified from both urine and diet by a combination of Amberlite XAD-2 adsorption chromatography, reverse phase low pressure
liquid chromatography, and several high performance liquid chromatographies. Reverse phase high performance liquid chromatography,
liquid secondary ion and gas-liquid mass spectrometries, and proton nuclear magnetic resonance spectroscopy identified these
inhibitors as a stereoisomer of convalloside, probably neoconvalloside, and a mono-rhamnoside of periplogenin or its stereoisomer.
These cardiac glycosides exhibited inhibitory potencies comparable to ouabain against ouabain-displacement from Na+,K(+)-ATPase
and against 86Rb uptake into human erythrocytes, and they also exhibited cross-reactivity to anti-ouabain antibodies and anti-digoxin
antibodies. These results clearly demonstrate that the principal source of most of the inhibitors in rat urine is the diet.
The results suggest that the ouabain-like inhibitor may be derived from an endogenous origin.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/S0021-9258(17)32669-8</identifier><identifier>PMID: 8163500</identifier><identifier>CODEN: JBCHA3</identifier><language>eng</language><publisher>Bethesda, MD: American Society for Biochemistry and Molecular Biology</publisher><subject>Analysis of Variance ; Analytical, structural and metabolic biochemistry ; Animal Feed ; Animals ; Biological and medical sciences ; Brain - enzymology ; Cardiac Glycosides - analysis ; Cardiac Glycosides - pharmacology ; Cardiac Glycosides - urine ; Cell Membrane - enzymology ; Diet ; Digitoxigenin - analogs & derivatives ; Digitoxigenin - analysis ; Digitoxigenin - pharmacology ; Digitoxigenin - urine ; Enzymes and enzyme inhibitors ; Fundamental and applied biological sciences. Psychology ; Glycosides - analysis ; Glycosides - pharmacology ; Glycosides - urine ; Humans ; Hydrolases ; Hypertension, Renovascular - urine ; Magnetic Resonance Spectroscopy ; Male ; Mass Spectrometry ; Molecular Structure ; Rats ; Rats, Sprague-Dawley ; Reference Values ; Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors</subject><ispartof>The Journal of biological chemistry, 1994-04, Vol.269 (16), p.11972-11979</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3248-1139434938f91da3d0a0b89874fdfe0c6497b4f275cc70b0ead4994744b057af3</citedby><cites>FETCH-LOGICAL-c3248-1139434938f91da3d0a0b89874fdfe0c6497b4f275cc70b0ead4994744b057af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4153653$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8163500$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TAMURA, M</creatorcontrib><creatorcontrib>HARRIS, T. M</creatorcontrib><creatorcontrib>PHILLIPS, D</creatorcontrib><creatorcontrib>BLAIR, I. A</creatorcontrib><creatorcontrib>YUE FEN WANG</creatorcontrib><creatorcontrib>HELLERQVIST, C. G</creatorcontrib><creatorcontrib>SAU KUEN LAM</creatorcontrib><creatorcontrib>INAGAMI, T</creatorcontrib><title>Identification of two cardiac glycosides as Na(+)-pump inhibitors in rat urine and diet</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Endogenous Na(+)-pump specific inhibitors are present in the plasma, urine, and tissues of humans and animals. To date, the
source of these inhibitors has not been rigorously defined. In the present study, large amounts of several Na(+)-pump specific
inhibitors have been demonstrated to exist in the urine of rats raised on a regular chow diet and tap water. All of the inhibitor
levels have been found to increase 1.5-8-fold by the surgical preparation of reduced renal mass (RRM) and one-kidney, one-clip
(IK, IC) hypertension. These urinary inhibitors, however, except for the ouabain-like inhibitor which eluted from a high performance
liquid chromatography C18 column at the same retention time as [3H]ouabain, disappeared within a week after switching the
diet from regular diet (number 5001, PMI Feeds, Inc.) to pure synthetic diet (number 5755). The urinary level of the ouabain-like
inhibitor decreased to only one-half of the level in the control rat raised on a regular diet. Two of these inhibitors were
purified from both urine and diet by a combination of Amberlite XAD-2 adsorption chromatography, reverse phase low pressure
liquid chromatography, and several high performance liquid chromatographies. Reverse phase high performance liquid chromatography,
liquid secondary ion and gas-liquid mass spectrometries, and proton nuclear magnetic resonance spectroscopy identified these
inhibitors as a stereoisomer of convalloside, probably neoconvalloside, and a mono-rhamnoside of periplogenin or its stereoisomer.
These cardiac glycosides exhibited inhibitory potencies comparable to ouabain against ouabain-displacement from Na+,K(+)-ATPase
and against 86Rb uptake into human erythrocytes, and they also exhibited cross-reactivity to anti-ouabain antibodies and anti-digoxin
antibodies. These results clearly demonstrate that the principal source of most of the inhibitors in rat urine is the diet.
The results suggest that the ouabain-like inhibitor may be derived from an endogenous origin.</description><subject>Analysis of Variance</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animal Feed</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain - enzymology</subject><subject>Cardiac Glycosides - analysis</subject><subject>Cardiac Glycosides - pharmacology</subject><subject>Cardiac Glycosides - urine</subject><subject>Cell Membrane - enzymology</subject><subject>Diet</subject><subject>Digitoxigenin - analogs & derivatives</subject><subject>Digitoxigenin - analysis</subject><subject>Digitoxigenin - pharmacology</subject><subject>Digitoxigenin - urine</subject><subject>Enzymes and enzyme inhibitors</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glycosides - analysis</subject><subject>Glycosides - pharmacology</subject><subject>Glycosides - urine</subject><subject>Humans</subject><subject>Hydrolases</subject><subject>Hypertension, Renovascular - urine</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Male</subject><subject>Mass Spectrometry</subject><subject>Molecular Structure</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reference Values</subject><subject>Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkF1LHTEQhoNU9FT9CUIupChlbWaT3SSXRfohSHthpb0Ls_nwRHY3x2QX8d931cNxbmZgnpkXHkJOgV0Cg_bLLWM1VLpu1DnIC163ra7UHlkBU7ziDfz7QFY75JB8LOWBLSU0HJADBS1vGFuRv9fOj1MM0eIU00hToNNTohazi2jpff9sU4nOF4qF_sLzzxfVZh42NI7r2MUp5bKMNONE5xxHT3F01EU_HZP9gH3xJ9t-RO6-f_tz9bO6-f3j-urrTWV5LVQFwLXgQnMVNDjkjiHrlFZSBBc8s63QshOhlo21knXMoxNaCylExxqJgR-RT29_Nzk9zr5MZojF-r7H0ae5GNmKhVZ8AZs30OZUSvbBbHIcMD8bYOZFqHkVal5sGZDmVahRy93pNmDuBu92V1uDy_5su8disQ8ZRxvLDhPQ8Lbh79g63q-fYvami8mu_WDqJWZJB9Cy5v8BpFOITg</recordid><startdate>19940422</startdate><enddate>19940422</enddate><creator>TAMURA, M</creator><creator>HARRIS, T. M</creator><creator>PHILLIPS, D</creator><creator>BLAIR, I. A</creator><creator>YUE FEN WANG</creator><creator>HELLERQVIST, C. G</creator><creator>SAU KUEN LAM</creator><creator>INAGAMI, T</creator><general>American Society for Biochemistry and Molecular Biology</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>19940422</creationdate><title>Identification of two cardiac glycosides as Na(+)-pump inhibitors in rat urine and diet</title><author>TAMURA, M ; HARRIS, T. M ; PHILLIPS, D ; BLAIR, I. A ; YUE FEN WANG ; HELLERQVIST, C. G ; SAU KUEN LAM ; INAGAMI, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3248-1139434938f91da3d0a0b89874fdfe0c6497b4f275cc70b0ead4994744b057af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Analysis of Variance</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animal Feed</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain - enzymology</topic><topic>Cardiac Glycosides - analysis</topic><topic>Cardiac Glycosides - pharmacology</topic><topic>Cardiac Glycosides - urine</topic><topic>Cell Membrane - enzymology</topic><topic>Diet</topic><topic>Digitoxigenin - analogs & derivatives</topic><topic>Digitoxigenin - analysis</topic><topic>Digitoxigenin - pharmacology</topic><topic>Digitoxigenin - urine</topic><topic>Enzymes and enzyme inhibitors</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycosides - analysis</topic><topic>Glycosides - pharmacology</topic><topic>Glycosides - urine</topic><topic>Humans</topic><topic>Hydrolases</topic><topic>Hypertension, Renovascular - urine</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Male</topic><topic>Mass Spectrometry</topic><topic>Molecular Structure</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reference Values</topic><topic>Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAMURA, M</creatorcontrib><creatorcontrib>HARRIS, T. M</creatorcontrib><creatorcontrib>PHILLIPS, D</creatorcontrib><creatorcontrib>BLAIR, I. A</creatorcontrib><creatorcontrib>YUE FEN WANG</creatorcontrib><creatorcontrib>HELLERQVIST, C. G</creatorcontrib><creatorcontrib>SAU KUEN LAM</creatorcontrib><creatorcontrib>INAGAMI, T</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>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TAMURA, M</au><au>HARRIS, T. M</au><au>PHILLIPS, D</au><au>BLAIR, I. A</au><au>YUE FEN WANG</au><au>HELLERQVIST, C. G</au><au>SAU KUEN LAM</au><au>INAGAMI, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of two cardiac glycosides as Na(+)-pump inhibitors in rat urine and diet</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1994-04-22</date><risdate>1994</risdate><volume>269</volume><issue>16</issue><spage>11972</spage><epage>11979</epage><pages>11972-11979</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><coden>JBCHA3</coden><abstract>Endogenous Na(+)-pump specific inhibitors are present in the plasma, urine, and tissues of humans and animals. To date, the
source of these inhibitors has not been rigorously defined. In the present study, large amounts of several Na(+)-pump specific
inhibitors have been demonstrated to exist in the urine of rats raised on a regular chow diet and tap water. All of the inhibitor
levels have been found to increase 1.5-8-fold by the surgical preparation of reduced renal mass (RRM) and one-kidney, one-clip
(IK, IC) hypertension. These urinary inhibitors, however, except for the ouabain-like inhibitor which eluted from a high performance
liquid chromatography C18 column at the same retention time as [3H]ouabain, disappeared within a week after switching the
diet from regular diet (number 5001, PMI Feeds, Inc.) to pure synthetic diet (number 5755). The urinary level of the ouabain-like
inhibitor decreased to only one-half of the level in the control rat raised on a regular diet. Two of these inhibitors were
purified from both urine and diet by a combination of Amberlite XAD-2 adsorption chromatography, reverse phase low pressure
liquid chromatography, and several high performance liquid chromatographies. Reverse phase high performance liquid chromatography,
liquid secondary ion and gas-liquid mass spectrometries, and proton nuclear magnetic resonance spectroscopy identified these
inhibitors as a stereoisomer of convalloside, probably neoconvalloside, and a mono-rhamnoside of periplogenin or its stereoisomer.
These cardiac glycosides exhibited inhibitory potencies comparable to ouabain against ouabain-displacement from Na+,K(+)-ATPase
and against 86Rb uptake into human erythrocytes, and they also exhibited cross-reactivity to anti-ouabain antibodies and anti-digoxin
antibodies. These results clearly demonstrate that the principal source of most of the inhibitors in rat urine is the diet.
The results suggest that the ouabain-like inhibitor may be derived from an endogenous origin.</abstract><cop>Bethesda, MD</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>8163500</pmid><doi>10.1016/S0021-9258(17)32669-8</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9258 |
ispartof | The Journal of biological chemistry, 1994-04, Vol.269 (16), p.11972-11979 |
issn | 0021-9258 1083-351X |
language | eng |
recordid | cdi_proquest_miscellaneous_76447483 |
source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Analysis of Variance Analytical, structural and metabolic biochemistry Animal Feed Animals Biological and medical sciences Brain - enzymology Cardiac Glycosides - analysis Cardiac Glycosides - pharmacology Cardiac Glycosides - urine Cell Membrane - enzymology Diet Digitoxigenin - analogs & derivatives Digitoxigenin - analysis Digitoxigenin - pharmacology Digitoxigenin - urine Enzymes and enzyme inhibitors Fundamental and applied biological sciences. Psychology Glycosides - analysis Glycosides - pharmacology Glycosides - urine Humans Hydrolases Hypertension, Renovascular - urine Magnetic Resonance Spectroscopy Male Mass Spectrometry Molecular Structure Rats Rats, Sprague-Dawley Reference Values Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors |
title | Identification of two cardiac glycosides as Na(+)-pump inhibitors in rat urine and diet |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T05%3A44%3A25IST&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=Identification%20of%20two%20cardiac%20glycosides%20as%20Na(+)-pump%20inhibitors%20in%20rat%20urine%20and%20diet&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=TAMURA,%20M&rft.date=1994-04-22&rft.volume=269&rft.issue=16&rft.spage=11972&rft.epage=11979&rft.pages=11972-11979&rft.issn=0021-9258&rft.eissn=1083-351X&rft.coden=JBCHA3&rft_id=info:doi/10.1016/S0021-9258(17)32669-8&rft_dat=%3Cproquest_cross%3E76447483%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=76447483&rft_id=info:pmid/8163500&rfr_iscdi=true |