Depression of Hepatic Microsomal Enzyme Systems by Lentinan in Mice
Studies were performed to determine the effects of an immunopotentiating agent, lentinan, on the hepatic drug-metabolizing enzymes in mice. Lentinan was injected twice a day for two days, and the enzyme activities were determined 12 hr after the last injection of lentinan. A lentinan dose of over 0....
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Veröffentlicht in: | Japanese journal of pharmacology 1985, Vol.37(1), pp.107-115 |
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creator | SASAKI, Ken-ichi SASAKI, Minoru ISHIKAWA, Masaaki TAKAYANAGI, Giichi |
description | Studies were performed to determine the effects of an immunopotentiating agent, lentinan, on the hepatic drug-metabolizing enzymes in mice. Lentinan was injected twice a day for two days, and the enzyme activities were determined 12 hr after the last injection of lentinan. A lentinan dose of over 0.25 mg/kg was required to cause a significant decrease (20–40%) in the hepatic microsomal aminopyrine N-demethylase and aniline hydroxylase activities. The loss of drug-metabolizing activity by the treatment with lentinan agreed with the loss of cytochrome P-450 content in many cases. Strain and substrate differences concerning the effect of lentinan on the metabolism of drug were also observed. That is to say, the loss of cytochrome P-450 content by the treatment with lentinan was observed in the ddY, C57BL/6 and BDF1 strain mice, but was not observed in the DBA/2, C3H/He and C57BL/10 strain mice. The decrease in the activities of 7-ethoxycoumarin O-deethylase and biphenyl 2-hydroxylase by the treatment with lentinan was considerably less than that of aminopyrine N-demethylase and aniline hydroxylase in ddY mice. |
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Lentinan was injected twice a day for two days, and the enzyme activities were determined 12 hr after the last injection of lentinan. A lentinan dose of over 0.25 mg/kg was required to cause a significant decrease (20–40%) in the hepatic microsomal aminopyrine N-demethylase and aniline hydroxylase activities. The loss of drug-metabolizing activity by the treatment with lentinan agreed with the loss of cytochrome P-450 content in many cases. Strain and substrate differences concerning the effect of lentinan on the metabolism of drug were also observed. That is to say, the loss of cytochrome P-450 content by the treatment with lentinan was observed in the ddY, C57BL/6 and BDF1 strain mice, but was not observed in the DBA/2, C3H/He and C57BL/10 strain mice. The decrease in the activities of 7-ethoxycoumarin O-deethylase and biphenyl 2-hydroxylase by the treatment with lentinan was considerably less than that of aminopyrine N-demethylase and aniline hydroxylase in ddY mice.</description><identifier>ISSN: 0021-5198</identifier><identifier>EISSN: 1347-3506</identifier><identifier>DOI: 10.1254/jjp.37.107</identifier><identifier>PMID: 3990039</identifier><identifier>CODEN: JJPAAZ</identifier><language>eng</language><publisher>Kyoto: The Japanese Pharmacological Society</publisher><subject>Aminopyrine N-Demethylase - metabolism ; Aniline Compounds - metabolism ; Animals ; Antipyrine - metabolism ; BCG Vaccine - pharmacology ; Biological and medical sciences ; Body Weight - drug effects ; Cytochrome P-450 Enzyme System - metabolism ; Depression, Chemical ; Immunomodulators ; Ketamine - pharmacology ; Lentinan - pharmacology ; Liver - drug effects ; Male ; Medical sciences ; Mice ; Mice, Inbred Strains ; Microsomes, Liver - enzymology ; Mixed Function Oxygenases - antagonists & inhibitors ; Organ Size - drug effects ; Pentobarbital - pharmacology ; Pharmacology. Drug treatments ; Polysaccharides - pharmacology ; Sleep - drug effects ; Species Specificity ; Time Factors</subject><ispartof>The Japanese Journal of Pharmacology, 1985, Vol.37(1), pp.107-115</ispartof><rights>1985 Elsevier B.V.</rights><rights>The Japanese PharmacologicalSociety</rights><rights>1985 INIST-CNRS</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c550t-a2a2da1d3896b4eed538e0d74de2b0f78d317913dd9980b2abcc3ff5b3d9cd3d3</citedby><cites>FETCH-LOGICAL-c550t-a2a2da1d3896b4eed538e0d74de2b0f78d317913dd9980b2abcc3ff5b3d9cd3d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1883,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9298687$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3990039$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SASAKI, Ken-ichi</creatorcontrib><creatorcontrib>SASAKI, Minoru</creatorcontrib><creatorcontrib>ISHIKAWA, Masaaki</creatorcontrib><creatorcontrib>TAKAYANAGI, Giichi</creatorcontrib><title>Depression of Hepatic Microsomal Enzyme Systems by Lentinan in Mice</title><title>Japanese journal of pharmacology</title><addtitle>Jpn.J.Pharmacol.</addtitle><description>Studies were performed to determine the effects of an immunopotentiating agent, lentinan, on the hepatic drug-metabolizing enzymes in mice. Lentinan was injected twice a day for two days, and the enzyme activities were determined 12 hr after the last injection of lentinan. A lentinan dose of over 0.25 mg/kg was required to cause a significant decrease (20–40%) in the hepatic microsomal aminopyrine N-demethylase and aniline hydroxylase activities. The loss of drug-metabolizing activity by the treatment with lentinan agreed with the loss of cytochrome P-450 content in many cases. Strain and substrate differences concerning the effect of lentinan on the metabolism of drug were also observed. That is to say, the loss of cytochrome P-450 content by the treatment with lentinan was observed in the ddY, C57BL/6 and BDF1 strain mice, but was not observed in the DBA/2, C3H/He and C57BL/10 strain mice. The decrease in the activities of 7-ethoxycoumarin O-deethylase and biphenyl 2-hydroxylase by the treatment with lentinan was considerably less than that of aminopyrine N-demethylase and aniline hydroxylase in ddY mice.</description><subject>Aminopyrine N-Demethylase - metabolism</subject><subject>Aniline Compounds - metabolism</subject><subject>Animals</subject><subject>Antipyrine - metabolism</subject><subject>BCG Vaccine - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Cytochrome P-450 Enzyme System - metabolism</subject><subject>Depression, Chemical</subject><subject>Immunomodulators</subject><subject>Ketamine - pharmacology</subject><subject>Lentinan - pharmacology</subject><subject>Liver - drug effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Microsomes, Liver - enzymology</subject><subject>Mixed Function Oxygenases - antagonists & inhibitors</subject><subject>Organ Size - drug effects</subject><subject>Pentobarbital - pharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Polysaccharides - pharmacology</subject><subject>Sleep - drug effects</subject><subject>Species Specificity</subject><subject>Time Factors</subject><issn>0021-5198</issn><issn>1347-3506</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEFv1DAQhS1EVbaFC3ekHBCHSlns2FnbR7QttNJWHICz5dgT6ihxgieLtP31eMlqT0hcZjR6n97oPULeMrpmVS0-dt205nLNqHxBVowLWfKabl6SFaUVK2um1StyhdjlU1EmLskl15pSrldkewtTAsQwxmJsi3uY7Bxc8RhcGnEcbF_cxefDAMW3A84wYNEcih3EOUQbixCPILwmF63tEd6c9jX58fnu-_a-3H398rD9tCtdXdO5tJWtvGWeK71pBICvuQLqpfBQNbSVynMmNePea61oU9nGOd62dcO9dp57fk0-LL5TGn_tAWczBHTQ9zbCuEcjN1TqmtH_gkwIQaUSGbxZwGNaTNCaKYXBpoNh1ByrNblaw2U-ZYbfnVz3zQD-jJ66zPr7k27R2b5NNrqAZ0xXWm3U0eZ2wTqc7U846zbl4nsw3fSELMf4-3YZ-ftZdk82GYjZRiw2kBv_HSAZdAGiAx8SuNn4MfwrxB_Pkqsx</recordid><startdate>1985</startdate><enddate>1985</enddate><creator>SASAKI, Ken-ichi</creator><creator>SASAKI, Minoru</creator><creator>ISHIKAWA, Masaaki</creator><creator>TAKAYANAGI, Giichi</creator><general>The Japanese Pharmacological Society</general><general>Japanese Pharmacological Society</general><scope>6I.</scope><scope>AAFTH</scope><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>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>1985</creationdate><title>Depression of Hepatic Microsomal Enzyme Systems by Lentinan in Mice</title><author>SASAKI, Ken-ichi ; SASAKI, Minoru ; ISHIKAWA, Masaaki ; TAKAYANAGI, Giichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c550t-a2a2da1d3896b4eed538e0d74de2b0f78d317913dd9980b2abcc3ff5b3d9cd3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Aminopyrine N-Demethylase - metabolism</topic><topic>Aniline Compounds - metabolism</topic><topic>Animals</topic><topic>Antipyrine - metabolism</topic><topic>BCG Vaccine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Cytochrome P-450 Enzyme System - metabolism</topic><topic>Depression, Chemical</topic><topic>Immunomodulators</topic><topic>Ketamine - pharmacology</topic><topic>Lentinan - pharmacology</topic><topic>Liver - drug effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Microsomes, Liver - enzymology</topic><topic>Mixed Function Oxygenases - antagonists & inhibitors</topic><topic>Organ Size - drug effects</topic><topic>Pentobarbital - pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Polysaccharides - pharmacology</topic><topic>Sleep - drug effects</topic><topic>Species Specificity</topic><topic>Time Factors</topic><toplevel>online_resources</toplevel><creatorcontrib>SASAKI, Ken-ichi</creatorcontrib><creatorcontrib>SASAKI, Minoru</creatorcontrib><creatorcontrib>ISHIKAWA, Masaaki</creatorcontrib><creatorcontrib>TAKAYANAGI, Giichi</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Japanese journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SASAKI, Ken-ichi</au><au>SASAKI, Minoru</au><au>ISHIKAWA, Masaaki</au><au>TAKAYANAGI, Giichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Depression of Hepatic Microsomal Enzyme Systems by Lentinan in Mice</atitle><jtitle>Japanese journal of pharmacology</jtitle><addtitle>Jpn.J.Pharmacol.</addtitle><date>1985</date><risdate>1985</risdate><volume>37</volume><issue>1</issue><spage>107</spage><epage>115</epage><pages>107-115</pages><issn>0021-5198</issn><eissn>1347-3506</eissn><coden>JJPAAZ</coden><abstract>Studies were performed to determine the effects of an immunopotentiating agent, lentinan, on the hepatic drug-metabolizing enzymes in mice. Lentinan was injected twice a day for two days, and the enzyme activities were determined 12 hr after the last injection of lentinan. A lentinan dose of over 0.25 mg/kg was required to cause a significant decrease (20–40%) in the hepatic microsomal aminopyrine N-demethylase and aniline hydroxylase activities. The loss of drug-metabolizing activity by the treatment with lentinan agreed with the loss of cytochrome P-450 content in many cases. Strain and substrate differences concerning the effect of lentinan on the metabolism of drug were also observed. That is to say, the loss of cytochrome P-450 content by the treatment with lentinan was observed in the ddY, C57BL/6 and BDF1 strain mice, but was not observed in the DBA/2, C3H/He and C57BL/10 strain mice. The decrease in the activities of 7-ethoxycoumarin O-deethylase and biphenyl 2-hydroxylase by the treatment with lentinan was considerably less than that of aminopyrine N-demethylase and aniline hydroxylase in ddY mice.</abstract><cop>Kyoto</cop><pub>The Japanese Pharmacological Society</pub><pmid>3990039</pmid><doi>10.1254/jjp.37.107</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aminopyrine N-Demethylase - metabolism Aniline Compounds - metabolism Animals Antipyrine - metabolism BCG Vaccine - pharmacology Biological and medical sciences Body Weight - drug effects Cytochrome P-450 Enzyme System - metabolism Depression, Chemical Immunomodulators Ketamine - pharmacology Lentinan - pharmacology Liver - drug effects Male Medical sciences Mice Mice, Inbred Strains Microsomes, Liver - enzymology Mixed Function Oxygenases - antagonists & inhibitors Organ Size - drug effects Pentobarbital - pharmacology Pharmacology. Drug treatments Polysaccharides - pharmacology Sleep - drug effects Species Specificity Time Factors |
title | Depression of Hepatic Microsomal Enzyme Systems by Lentinan in Mice |
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