Loading…
Hepatic injury induced by bile salts: Correlation between biochemical and morphological events
Continuous intravenous infusion of taurochenodeoxycholate at a rate of 0.4 μmol · min−1 · 100 gm−1 for only 30 min in rats caused threefold to tenfold greater release of proteins (alkaline phosphatase, lactate dehydrogenase and albumin) into bile in comparison with animals infused with tauroursodeox...
Saved in:
Published in: | Hepatology (Baltimore, Md.) Md.), 1990-11, Vol.12 (5), p.1216-1221 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c4753-5891240c0f530aef9dcd38a7fdacd5181a4906a394774f1392a87b04a8908cfa3 |
---|---|
cites | cdi_FETCH-LOGICAL-c4753-5891240c0f530aef9dcd38a7fdacd5181a4906a394774f1392a87b04a8908cfa3 |
container_end_page | 1221 |
container_issue | 5 |
container_start_page | 1216 |
container_title | Hepatology (Baltimore, Md.) |
container_volume | 12 |
creator | Schmucker, Douglas L. Ohta, Minoru Kanai, Setsuko Sato, Yuko Kitani, Kenichi |
description | Continuous intravenous infusion of taurochenodeoxycholate at a rate of 0.4 μmol · min−1 · 100 gm−1 for only 30 min in rats caused threefold to tenfold greater release of proteins (alkaline phosphatase, lactate dehydrogenase and albumin) into bile in comparison with animals infused with tauroursodeoxycholate at much higher rates (1.8 μmol · min−1 · 100 gm−1) for 2 hr. The simultaneous infusion of tauroursodeoxycholate and taurochenodeoxycholate (0.6 and 0.4 μmol · min−1 · 100 gm−1, respectively) for 2 hr prevented the marked biochemical changes in the bile induced by taurochenodeoxycholate infusion alone. Livers infused with taurochenodeoxycholate for 15 to 60 min exhibited significantly more necrotic hepatocytes, especially in zone 1, in comparison with animals infused with tauroursodeoxycholate or a combination of taurochenodeoxycholate and tauroursodeoxycholate. A good correlation was observed between biochemical and morphological indices of bile acid—induced hepatocyte injury. These data suggest that (a) primary events induced by the acute infusion of toxic bile salts responsible for cholestasis include zone 1 hepatocellular necrosis and (b) this can be prevented by the simultaneous infusion of tauroursodeoxycholate (HEPATOLOGY 1990;12:1216–1221). |
doi_str_mv | 10.1002/hep.1840120523 |
format | article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_hep_1840120523</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>HEP1840120523</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4753-5891240c0f530aef9dcd38a7fdacd5181a4906a394774f1392a87b04a8908cfa3</originalsourceid><addsrcrecordid>eNqFkD1PwzAQhi0EKqWwsiF5YE05fwTbbKgqFKkSDLASOY5NU-VLdkqVf4-hVWFjeiXfc3e-B6FLAlMCQG9WtpsSyYFQSCk7QmOSUpEwlsIxGgMVkCjC1Ck6C2ENAIpTOUIjSqmQlIzR-8J2ui8NLpv1xg8xio2xBc4HnJeVxUFXfbjDs9Z7W0WwbXBu-621McvWrGxdGl1h3RS4bn23aqv24-fFftqmD-foxOkq2It9TtDbw_x1tkiWz49Ps_tlYrhIWZJKRSgHAy5loK1ThSmY1MIV2hQpkURzBbeaKS4Ed_EeqqXIgWupQBqn2QRNd3ONb0Pw1mWdL2vth4xA9u0pi56yX0-x4WrX0G3y2hYHfC8m1q_3dR3iOc7rxpThgHElU8VlxNQO20ZZwz9Ls8X85c8XvgCSsIGU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Hepatic injury induced by bile salts: Correlation between biochemical and morphological events</title><source>Alma/SFX Local Collection</source><creator>Schmucker, Douglas L. ; Ohta, Minoru ; Kanai, Setsuko ; Sato, Yuko ; Kitani, Kenichi</creator><creatorcontrib>Schmucker, Douglas L. ; Ohta, Minoru ; Kanai, Setsuko ; Sato, Yuko ; Kitani, Kenichi</creatorcontrib><description>Continuous intravenous infusion of taurochenodeoxycholate at a rate of 0.4 μmol · min−1 · 100 gm−1 for only 30 min in rats caused threefold to tenfold greater release of proteins (alkaline phosphatase, lactate dehydrogenase and albumin) into bile in comparison with animals infused with tauroursodeoxycholate at much higher rates (1.8 μmol · min−1 · 100 gm−1) for 2 hr. The simultaneous infusion of tauroursodeoxycholate and taurochenodeoxycholate (0.6 and 0.4 μmol · min−1 · 100 gm−1, respectively) for 2 hr prevented the marked biochemical changes in the bile induced by taurochenodeoxycholate infusion alone. Livers infused with taurochenodeoxycholate for 15 to 60 min exhibited significantly more necrotic hepatocytes, especially in zone 1, in comparison with animals infused with tauroursodeoxycholate or a combination of taurochenodeoxycholate and tauroursodeoxycholate. A good correlation was observed between biochemical and morphological indices of bile acid—induced hepatocyte injury. These data suggest that (a) primary events induced by the acute infusion of toxic bile salts responsible for cholestasis include zone 1 hepatocellular necrosis and (b) this can be prevented by the simultaneous infusion of tauroursodeoxycholate (HEPATOLOGY 1990;12:1216–1221).</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.1840120523</identifier><identifier>PMID: 2227821</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Philadelphia, PA: W.B. Saunders</publisher><subject>Animals ; Bile - drug effects ; Bile - metabolism ; Bile - physiology ; Bile Acids and Salts - pharmacology ; Biological and medical sciences ; Gastroenterology. Liver. Pancreas. Abdomen ; Liver - drug effects ; Liver - metabolism ; Liver - pathology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Necrosis ; Other diseases. Semiology ; Proteins - metabolism ; Rats ; Rats, Inbred Strains ; Taurochenodeoxycholic Acid - pharmacology ; Taurocholic Acid - pharmacology</subject><ispartof>Hepatology (Baltimore, Md.), 1990-11, Vol.12 (5), p.1216-1221</ispartof><rights>Copyright © 1990 American Association for the Study of Liver Diseases</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4753-5891240c0f530aef9dcd38a7fdacd5181a4906a394774f1392a87b04a8908cfa3</citedby><cites>FETCH-LOGICAL-c4753-5891240c0f530aef9dcd38a7fdacd5181a4906a394774f1392a87b04a8908cfa3</cites></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=4985948$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2227821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schmucker, Douglas L.</creatorcontrib><creatorcontrib>Ohta, Minoru</creatorcontrib><creatorcontrib>Kanai, Setsuko</creatorcontrib><creatorcontrib>Sato, Yuko</creatorcontrib><creatorcontrib>Kitani, Kenichi</creatorcontrib><title>Hepatic injury induced by bile salts: Correlation between biochemical and morphological events</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>Continuous intravenous infusion of taurochenodeoxycholate at a rate of 0.4 μmol · min−1 · 100 gm−1 for only 30 min in rats caused threefold to tenfold greater release of proteins (alkaline phosphatase, lactate dehydrogenase and albumin) into bile in comparison with animals infused with tauroursodeoxycholate at much higher rates (1.8 μmol · min−1 · 100 gm−1) for 2 hr. The simultaneous infusion of tauroursodeoxycholate and taurochenodeoxycholate (0.6 and 0.4 μmol · min−1 · 100 gm−1, respectively) for 2 hr prevented the marked biochemical changes in the bile induced by taurochenodeoxycholate infusion alone. Livers infused with taurochenodeoxycholate for 15 to 60 min exhibited significantly more necrotic hepatocytes, especially in zone 1, in comparison with animals infused with tauroursodeoxycholate or a combination of taurochenodeoxycholate and tauroursodeoxycholate. A good correlation was observed between biochemical and morphological indices of bile acid—induced hepatocyte injury. These data suggest that (a) primary events induced by the acute infusion of toxic bile salts responsible for cholestasis include zone 1 hepatocellular necrosis and (b) this can be prevented by the simultaneous infusion of tauroursodeoxycholate (HEPATOLOGY 1990;12:1216–1221).</description><subject>Animals</subject><subject>Bile - drug effects</subject><subject>Bile - metabolism</subject><subject>Bile - physiology</subject><subject>Bile Acids and Salts - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Liver - pathology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Necrosis</subject><subject>Other diseases. Semiology</subject><subject>Proteins - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Taurochenodeoxycholic Acid - pharmacology</subject><subject>Taurocholic Acid - pharmacology</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAQhi0EKqWwsiF5YE05fwTbbKgqFKkSDLASOY5NU-VLdkqVf4-hVWFjeiXfc3e-B6FLAlMCQG9WtpsSyYFQSCk7QmOSUpEwlsIxGgMVkCjC1Ck6C2ENAIpTOUIjSqmQlIzR-8J2ui8NLpv1xg8xio2xBc4HnJeVxUFXfbjDs9Z7W0WwbXBu-621McvWrGxdGl1h3RS4bn23aqv24-fFftqmD-foxOkq2It9TtDbw_x1tkiWz49Ps_tlYrhIWZJKRSgHAy5loK1ThSmY1MIV2hQpkURzBbeaKS4Ed_EeqqXIgWupQBqn2QRNd3ONb0Pw1mWdL2vth4xA9u0pi56yX0-x4WrX0G3y2hYHfC8m1q_3dR3iOc7rxpThgHElU8VlxNQO20ZZwz9Ls8X85c8XvgCSsIGU</recordid><startdate>199011</startdate><enddate>199011</enddate><creator>Schmucker, Douglas L.</creator><creator>Ohta, Minoru</creator><creator>Kanai, Setsuko</creator><creator>Sato, Yuko</creator><creator>Kitani, Kenichi</creator><general>W.B. Saunders</general><general>Wiley</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></search><sort><creationdate>199011</creationdate><title>Hepatic injury induced by bile salts: Correlation between biochemical and morphological events</title><author>Schmucker, Douglas L. ; Ohta, Minoru ; Kanai, Setsuko ; Sato, Yuko ; Kitani, Kenichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4753-5891240c0f530aef9dcd38a7fdacd5181a4906a394774f1392a87b04a8908cfa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Animals</topic><topic>Bile - drug effects</topic><topic>Bile - metabolism</topic><topic>Bile - physiology</topic><topic>Bile Acids and Salts - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Liver - pathology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Necrosis</topic><topic>Other diseases. Semiology</topic><topic>Proteins - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Taurochenodeoxycholic Acid - pharmacology</topic><topic>Taurocholic Acid - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schmucker, Douglas L.</creatorcontrib><creatorcontrib>Ohta, Minoru</creatorcontrib><creatorcontrib>Kanai, Setsuko</creatorcontrib><creatorcontrib>Sato, Yuko</creatorcontrib><creatorcontrib>Kitani, Kenichi</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><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schmucker, Douglas L.</au><au>Ohta, Minoru</au><au>Kanai, Setsuko</au><au>Sato, Yuko</au><au>Kitani, Kenichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatic injury induced by bile salts: Correlation between biochemical and morphological events</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>1990-11</date><risdate>1990</risdate><volume>12</volume><issue>5</issue><spage>1216</spage><epage>1221</epage><pages>1216-1221</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>Continuous intravenous infusion of taurochenodeoxycholate at a rate of 0.4 μmol · min−1 · 100 gm−1 for only 30 min in rats caused threefold to tenfold greater release of proteins (alkaline phosphatase, lactate dehydrogenase and albumin) into bile in comparison with animals infused with tauroursodeoxycholate at much higher rates (1.8 μmol · min−1 · 100 gm−1) for 2 hr. The simultaneous infusion of tauroursodeoxycholate and taurochenodeoxycholate (0.6 and 0.4 μmol · min−1 · 100 gm−1, respectively) for 2 hr prevented the marked biochemical changes in the bile induced by taurochenodeoxycholate infusion alone. Livers infused with taurochenodeoxycholate for 15 to 60 min exhibited significantly more necrotic hepatocytes, especially in zone 1, in comparison with animals infused with tauroursodeoxycholate or a combination of taurochenodeoxycholate and tauroursodeoxycholate. A good correlation was observed between biochemical and morphological indices of bile acid—induced hepatocyte injury. These data suggest that (a) primary events induced by the acute infusion of toxic bile salts responsible for cholestasis include zone 1 hepatocellular necrosis and (b) this can be prevented by the simultaneous infusion of tauroursodeoxycholate (HEPATOLOGY 1990;12:1216–1221).</abstract><cop>Philadelphia, PA</cop><pub>W.B. Saunders</pub><pmid>2227821</pmid><doi>10.1002/hep.1840120523</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0270-9139 |
ispartof | Hepatology (Baltimore, Md.), 1990-11, Vol.12 (5), p.1216-1221 |
issn | 0270-9139 1527-3350 |
language | eng |
recordid | cdi_crossref_primary_10_1002_hep_1840120523 |
source | Alma/SFX Local Collection |
subjects | Animals Bile - drug effects Bile - metabolism Bile - physiology Bile Acids and Salts - pharmacology Biological and medical sciences Gastroenterology. Liver. Pancreas. Abdomen Liver - drug effects Liver - metabolism Liver - pathology Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Necrosis Other diseases. Semiology Proteins - metabolism Rats Rats, Inbred Strains Taurochenodeoxycholic Acid - pharmacology Taurocholic Acid - pharmacology |
title | Hepatic injury induced by bile salts: Correlation between biochemical and morphological events |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T22%3A26%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hepatic%20injury%20induced%20by%20bile%20salts:%20Correlation%20between%20biochemical%20and%20morphological%20events&rft.jtitle=Hepatology%20(Baltimore,%20Md.)&rft.au=Schmucker,%20Douglas%20L.&rft.date=1990-11&rft.volume=12&rft.issue=5&rft.spage=1216&rft.epage=1221&rft.pages=1216-1221&rft.issn=0270-9139&rft.eissn=1527-3350&rft.coden=HPTLD9&rft_id=info:doi/10.1002/hep.1840120523&rft_dat=%3Cwiley_cross%3EHEP1840120523%3C/wiley_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4753-5891240c0f530aef9dcd38a7fdacd5181a4906a394774f1392a87b04a8908cfa3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/2227821&rfr_iscdi=true |