Potentiation of lithocholic-acid-induced cholestasis by methyl isobutyl ketone.
Identifieur interne : 002196 ( PubMed/Corpus ); précédent : 002195; suivant : 002197Potentiation of lithocholic-acid-induced cholestasis by methyl isobutyl ketone.
Auteurs : L D Joseph ; I M Yousef ; G L Plaa ; M. SharkawiSource :
- Toxicology letters [ 0378-4274 ] ; 1992.
English descriptors
- KwdEn :
- Animals, Bile Acids and Salts (secretion), Bile Canaliculi (drug effects), Bile Canaliculi (secretion), Biological Transport (drug effects), Body Weight (drug effects), Cholestasis, Intrahepatic (chemically induced), Drug Synergism, Lithocholic Acid (toxicity), Male, Methyl n-Butyl Ketone (pharmacology), Organ Size (drug effects), Rats, Rats, Inbred Strains, Taurocholic Acid (metabolism).
- MESH :
- chemical , metabolism : Taurocholic Acid.
- chemical , pharmacology : Methyl n-Butyl Ketone.
- chemical , secretion : Bile Acids and Salts.
- chemically induced : Cholestasis, Intrahepatic.
- drug effects : Bile Canaliculi, Biological Transport, Body Weight, Organ Size.
- secretion : Bile Canaliculi.
- chemical , toxicity : Lithocholic Acid.
- Animals, Drug Synergism, Male, Rats, Rats, Inbred Strains.
Abstract
Methyl isobutyl ketone was found to potentiate intrahepatic cholestasis induced by taurolithocholate and the combination of manganese-bilirubin. The aim of this study was to elucidate the mechanism of this potentiation using the lithocholate-induced cholestasis model. Male rats were given methyl isobutyl ketone 7.5 mumol/kg body wt. daily for 3 days. The effect of this treatment on lithocholate-induced cholestasis, bile formation and taurocholic acid transport was examined. The data showed that methyl isobutyl ketone treatment potentiated lithocholate-induced cholestasis and reduced significantly bile salt, phospholipid and cholesterol secretion rates as well as the transport maximum of taurocholic acid. It is suggested that methyl isobutyl ketone potentiates lithocholate-induced cholestasis by reducing the bile salt pool and interfering with the haptic secretion rate of bile salts.
PubMed: 1609437
Links to Exploration step
pubmed:1609437Le document en format XML
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<author><name sortKey="Joseph, L D" sort="Joseph, L D" uniqKey="Joseph L" first="L D" last="Joseph">L D Joseph</name>
<affiliation><nlm:affiliation>Department of Pharmacology, University of Montreal, Canada.</nlm:affiliation>
</affiliation>
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<author><name sortKey="Yousef, I M" sort="Yousef, I M" uniqKey="Yousef I" first="I M" last="Yousef">I M Yousef</name>
</author>
<author><name sortKey="Plaa, G L" sort="Plaa, G L" uniqKey="Plaa G" first="G L" last="Plaa">G L Plaa</name>
</author>
<author><name sortKey="Sharkawi, M" sort="Sharkawi, M" uniqKey="Sharkawi M" first="M" last="Sharkawi">M. Sharkawi</name>
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<date when="1992">1992</date>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Potentiation of lithocholic-acid-induced cholestasis by methyl isobutyl ketone.</title>
<author><name sortKey="Joseph, L D" sort="Joseph, L D" uniqKey="Joseph L" first="L D" last="Joseph">L D Joseph</name>
<affiliation><nlm:affiliation>Department of Pharmacology, University of Montreal, Canada.</nlm:affiliation>
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<author><name sortKey="Yousef, I M" sort="Yousef, I M" uniqKey="Yousef I" first="I M" last="Yousef">I M Yousef</name>
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<author><name sortKey="Plaa, G L" sort="Plaa, G L" uniqKey="Plaa G" first="G L" last="Plaa">G L Plaa</name>
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<author><name sortKey="Sharkawi, M" sort="Sharkawi, M" uniqKey="Sharkawi M" first="M" last="Sharkawi">M. Sharkawi</name>
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<series><title level="j">Toxicology letters</title>
<idno type="ISSN">0378-4274</idno>
<imprint><date when="1992" type="published">1992</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Bile Acids and Salts (secretion)</term>
<term>Bile Canaliculi (drug effects)</term>
<term>Bile Canaliculi (secretion)</term>
<term>Biological Transport (drug effects)</term>
<term>Body Weight (drug effects)</term>
<term>Cholestasis, Intrahepatic (chemically induced)</term>
<term>Drug Synergism</term>
<term>Lithocholic Acid (toxicity)</term>
<term>Male</term>
<term>Methyl n-Butyl Ketone (pharmacology)</term>
<term>Organ Size (drug effects)</term>
<term>Rats</term>
<term>Rats, Inbred Strains</term>
<term>Taurocholic Acid (metabolism)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Taurocholic Acid</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Methyl n-Butyl Ketone</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="secretion" xml:lang="en"><term>Bile Acids and Salts</term>
</keywords>
<keywords scheme="MESH" qualifier="chemically induced" xml:lang="en"><term>Cholestasis, Intrahepatic</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Bile Canaliculi</term>
<term>Biological Transport</term>
<term>Body Weight</term>
<term>Organ Size</term>
</keywords>
<keywords scheme="MESH" qualifier="secretion" xml:lang="en"><term>Bile Canaliculi</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="toxicity" xml:lang="en"><term>Lithocholic Acid</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Drug Synergism</term>
<term>Male</term>
<term>Rats</term>
<term>Rats, Inbred Strains</term>
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<front><div type="abstract" xml:lang="en">Methyl isobutyl ketone was found to potentiate intrahepatic cholestasis induced by taurolithocholate and the combination of manganese-bilirubin. The aim of this study was to elucidate the mechanism of this potentiation using the lithocholate-induced cholestasis model. Male rats were given methyl isobutyl ketone 7.5 mumol/kg body wt. daily for 3 days. The effect of this treatment on lithocholate-induced cholestasis, bile formation and taurocholic acid transport was examined. The data showed that methyl isobutyl ketone treatment potentiated lithocholate-induced cholestasis and reduced significantly bile salt, phospholipid and cholesterol secretion rates as well as the transport maximum of taurocholic acid. It is suggested that methyl isobutyl ketone potentiates lithocholate-induced cholestasis by reducing the bile salt pool and interfering with the haptic secretion rate of bile salts.</div>
</front>
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<JournalIssue CitedMedium="Print"><Volume>61</Volume>
<Issue>1</Issue>
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<Month>Jun</Month>
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<Title>Toxicology letters</Title>
<ISOAbbreviation>Toxicol. Lett.</ISOAbbreviation>
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<ArticleTitle>Potentiation of lithocholic-acid-induced cholestasis by methyl isobutyl ketone.</ArticleTitle>
<Pagination><MedlinePgn>39-47</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Methyl isobutyl ketone was found to potentiate intrahepatic cholestasis induced by taurolithocholate and the combination of manganese-bilirubin. The aim of this study was to elucidate the mechanism of this potentiation using the lithocholate-induced cholestasis model. Male rats were given methyl isobutyl ketone 7.5 mumol/kg body wt. daily for 3 days. The effect of this treatment on lithocholate-induced cholestasis, bile formation and taurocholic acid transport was examined. The data showed that methyl isobutyl ketone treatment potentiated lithocholate-induced cholestasis and reduced significantly bile salt, phospholipid and cholesterol secretion rates as well as the transport maximum of taurocholic acid. It is suggested that methyl isobutyl ketone potentiates lithocholate-induced cholestasis by reducing the bile salt pool and interfering with the haptic secretion rate of bile salts.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Joseph</LastName>
<ForeName>L D</ForeName>
<Initials>LD</Initials>
<AffiliationInfo><Affiliation>Department of Pharmacology, University of Montreal, Canada.</Affiliation>
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<Author ValidYN="Y"><LastName>Plaa</LastName>
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