Effect of chronic administration of alcoholic beverages and seasoning containing alcohol on hepatic ethanol metabolism in mice
Five-week-old male mice, C3H/HeNCrj (C3H/He), were given a 5% (v/v) ethanol solution, commercial alcoholic beverages (Japanese sake (sake) or red wine) or a Japanese seasoning (mirin [containing ethanol and a large amount of glucose]) ad libitum for 45 d, and were then examined for changes n the hep...
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Veröffentlicht in: | Journal of Nutritional Science and Vitaminology 1997, Vol.43(6), pp.613-626 |
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description | Five-week-old male mice, C3H/HeNCrj (C3H/He), were given a 5% (v/v) ethanol solution, commercial alcoholic beverages (Japanese sake (sake) or red wine) or a Japanese seasoning (mirin [containing ethanol and a large amount of glucose]) ad libitum for 45 d, and were then examined for changes n the hepatic enzymes related to ethanol metabolism 2 h after oral administration of 5 g of ethanol/kg body weight. The specific activity of aniline hydroxylase (ANH) in the hepatic microsome increase significantly in all groups chronically administered ethanol solution, sake, red wine or mirin, and the greatest increase was in the hepatic microsome of mirin-administered mice. The cytochrome P-450 (CYP) 2E1 increased in the hepatic microsome of the mice administered ethanol solution, red wine or mirin where accompanied by high ANH activity. The immunoreactive band for CYP1A1 showed high specificity in the microsome of mice given sake,red wine or mirin. It was assumed that CYP1A1 was induced by unknown component(s) other than ethanol in these solutions. In the cytosolic fraction, following the chronic administration of sake and mirin, the total aldehyde dehydrogenase (A1DH) activity with high-Km decreased significantly. In the mitochondrial fraction, the activity of high-Km A1DH increased significantly in the mirin-administered mice which drank a large amount of ethanol, whereas that in the red wine-administered group tended to decrease. These results indicate that the enzyme activities related to the oxidation of both ethanol and acetaldehyde in the cytosolic, mitochondrial and microsomal fractions of the liver were affected by either the action of ethanol or its interaction with other constituents of sake, red wine and mirin |
doi_str_mv | 10.3177/jnsv.43.613 |
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(Kobe Gakuin Univ. (Japan). Faculty of Nutrition) ; Ueda, M ; Kawakami, M ; Goda, K ; Park, S.S ; Nakata, Y</creator><creatorcontrib>Kishimoto, R. (Kobe Gakuin Univ. (Japan). Faculty of Nutrition) ; Ueda, M ; Kawakami, M ; Goda, K ; Park, S.S ; Nakata, Y</creatorcontrib><description>Five-week-old male mice, C3H/HeNCrj (C3H/He), were given a 5% (v/v) ethanol solution, commercial alcoholic beverages (Japanese sake (sake) or red wine) or a Japanese seasoning (mirin [containing ethanol and a large amount of glucose]) ad libitum for 45 d, and were then examined for changes n the hepatic enzymes related to ethanol metabolism 2 h after oral administration of 5 g of ethanol/kg body weight. The specific activity of aniline hydroxylase (ANH) in the hepatic microsome increase significantly in all groups chronically administered ethanol solution, sake, red wine or mirin, and the greatest increase was in the hepatic microsome of mirin-administered mice. The cytochrome P-450 (CYP) 2E1 increased in the hepatic microsome of the mice administered ethanol solution, red wine or mirin where accompanied by high ANH activity. The immunoreactive band for CYP1A1 showed high specificity in the microsome of mice given sake,red wine or mirin. It was assumed that CYP1A1 was induced by unknown component(s) other than ethanol in these solutions. In the cytosolic fraction, following the chronic administration of sake and mirin, the total aldehyde dehydrogenase (A1DH) activity with high-Km decreased significantly. In the mitochondrial fraction, the activity of high-Km A1DH increased significantly in the mirin-administered mice which drank a large amount of ethanol, whereas that in the red wine-administered group tended to decrease. These results indicate that the enzyme activities related to the oxidation of both ethanol and acetaldehyde in the cytosolic, mitochondrial and microsomal fractions of the liver were affected by either the action of ethanol or its interaction with other constituents of sake, red wine and mirin</description><identifier>ISSN: 0301-4800</identifier><identifier>EISSN: 1881-7742</identifier><identifier>DOI: 10.3177/jnsv.43.613</identifier><identifier>PMID: 9530614</identifier><language>eng</language><publisher>Tokyo: Center for Academic Publications Japan</publisher><subject>Alcohol Dehydrogenase - metabolism ; ALCOHOLIC BEVERAGES ; Aldehyde Dehydrogenase - metabolism ; Aniline Hydroxylase - metabolism ; Animals ; AROMATISANT ; AROMATIZANTES ; BEBIDAS ALCOHOLICAS ; Biological and medical sciences ; Blotting, Western ; BOISSON ALCOOLISEE ; C3H/He mice ; CYP1A1 ; CYP2E1 ; Cytochrome P-450 CYP1A1 - biosynthesis ; Cytochrome P-450 CYP1A1 - metabolism ; Enzyme Induction ; ETANOL ; ETHANOL ; Ethanol - administration & dosage ; Ethanol - metabolism ; FLAVOURINGS ; FOIE ; Fundamental and applied biological sciences. Psychology ; HIGADO ; Intermediate and energetic metabolism ; LIVER ; Male ; METABOLISM ; METABOLISME ; METABOLISMO ; Metabolisms and neurohumoral controls ; MICE ; Mice, Inbred C3H ; Microsomes, Liver - enzymology ; Microsomes, Liver - metabolism ; mirin ; RATON ; SOURIS ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>Journal of Nutritional Science and Vitaminology, 1997, Vol.43(6), pp.613-626</ispartof><rights>the Center for Academic Publications Japan</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c581t-4d6f7b5c681e7298876124a63a3ac2155c74e0142dc65795e5c4214c12cf03473</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1883,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2239948$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9530614$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kishimoto, R. (Kobe Gakuin Univ. (Japan). Faculty of Nutrition)</creatorcontrib><creatorcontrib>Ueda, M</creatorcontrib><creatorcontrib>Kawakami, M</creatorcontrib><creatorcontrib>Goda, K</creatorcontrib><creatorcontrib>Park, S.S</creatorcontrib><creatorcontrib>Nakata, Y</creatorcontrib><title>Effect of chronic administration of alcoholic beverages and seasoning containing alcohol on hepatic ethanol metabolism in mice</title><title>Journal of Nutritional Science and Vitaminology</title><addtitle>J Nutr Sci Vitaminol</addtitle><description>Five-week-old male mice, C3H/HeNCrj (C3H/He), were given a 5% (v/v) ethanol solution, commercial alcoholic beverages (Japanese sake (sake) or red wine) or a Japanese seasoning (mirin [containing ethanol and a large amount of glucose]) ad libitum for 45 d, and were then examined for changes n the hepatic enzymes related to ethanol metabolism 2 h after oral administration of 5 g of ethanol/kg body weight. The specific activity of aniline hydroxylase (ANH) in the hepatic microsome increase significantly in all groups chronically administered ethanol solution, sake, red wine or mirin, and the greatest increase was in the hepatic microsome of mirin-administered mice. The cytochrome P-450 (CYP) 2E1 increased in the hepatic microsome of the mice administered ethanol solution, red wine or mirin where accompanied by high ANH activity. The immunoreactive band for CYP1A1 showed high specificity in the microsome of mice given sake,red wine or mirin. It was assumed that CYP1A1 was induced by unknown component(s) other than ethanol in these solutions. In the cytosolic fraction, following the chronic administration of sake and mirin, the total aldehyde dehydrogenase (A1DH) activity with high-Km decreased significantly. In the mitochondrial fraction, the activity of high-Km A1DH increased significantly in the mirin-administered mice which drank a large amount of ethanol, whereas that in the red wine-administered group tended to decrease. These results indicate that the enzyme activities related to the oxidation of both ethanol and acetaldehyde in the cytosolic, mitochondrial and microsomal fractions of the liver were affected by either the action of ethanol or its interaction with other constituents of sake, red wine and mirin</description><subject>Alcohol Dehydrogenase - metabolism</subject><subject>ALCOHOLIC BEVERAGES</subject><subject>Aldehyde Dehydrogenase - metabolism</subject><subject>Aniline Hydroxylase - metabolism</subject><subject>Animals</subject><subject>AROMATISANT</subject><subject>AROMATIZANTES</subject><subject>BEBIDAS ALCOHOLICAS</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>BOISSON ALCOOLISEE</subject><subject>C3H/He mice</subject><subject>CYP1A1</subject><subject>CYP2E1</subject><subject>Cytochrome P-450 CYP1A1 - biosynthesis</subject><subject>Cytochrome P-450 CYP1A1 - metabolism</subject><subject>Enzyme Induction</subject><subject>ETANOL</subject><subject>ETHANOL</subject><subject>Ethanol - administration & dosage</subject><subject>Ethanol - metabolism</subject><subject>FLAVOURINGS</subject><subject>FOIE</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>HIGADO</subject><subject>Intermediate and energetic metabolism</subject><subject>LIVER</subject><subject>Male</subject><subject>METABOLISM</subject><subject>METABOLISME</subject><subject>METABOLISMO</subject><subject>Metabolisms and neurohumoral controls</subject><subject>MICE</subject><subject>Mice, Inbred C3H</subject><subject>Microsomes, Liver - enzymology</subject><subject>Microsomes, Liver - metabolism</subject><subject>mirin</subject><subject>RATON</subject><subject>SOURIS</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0301-4800</issn><issn>1881-7742</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc2P0zAUxC0EWroLJ85IPiAuKMVfiZ0j2l0W0EpwgLP1-uI0rhK72OlKXPjbcduoXGzL83sz1piQN5ytJdf64y7kp7WS64bLZ2TFjeGV1ko8JysmGa-UYewluc55x5hqjTJX5KqtJWu4WpG_933vcKaxpzikGDxS6CYffJ4TzD6GowIjxiGORdu4J5dg6zKF0NHsIJeRsKUYwwz-dFxgWkYHty8eSN08QChXk5thU3zyRH2gk0f3irzoYczu9bLfkF-f73_efqkevz98vf30WGFt-Fyprun1psbGcKdFa4xuuFDQSJCAgtc1auUYV6LDptZt7WpUgivkAnsmlZY35P3Zd5_i74PLs518RjeOEFw8ZFtmjGgkL-CHM4gp5pxcb_fJT5D-WM7ssW17bNsqaUvbhX672B42k-su7FJv0d8tOmSEsU8Q0OcLJoRsW2UKdnfGdnku5V50SKW90Z0ieavlKfa8lPSLjAMk68L_1_QQLWxTSfr2g7dt-X8pjZD_AAAkqk8</recordid><startdate>19971201</startdate><enddate>19971201</enddate><creator>Kishimoto, R. (Kobe Gakuin Univ. (Japan). Faculty of Nutrition)</creator><creator>Ueda, M</creator><creator>Kawakami, M</creator><creator>Goda, K</creator><creator>Park, S.S</creator><creator>Nakata, Y</creator><general>Center for Academic Publications Japan</general><scope>FBQ</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>7X8</scope></search><sort><creationdate>19971201</creationdate><title>Effect of chronic administration of alcoholic beverages and seasoning containing alcohol on hepatic ethanol metabolism in mice</title><author>Kishimoto, R. (Kobe Gakuin Univ. (Japan). Faculty of Nutrition) ; Ueda, M ; Kawakami, M ; Goda, K ; Park, S.S ; Nakata, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c581t-4d6f7b5c681e7298876124a63a3ac2155c74e0142dc65795e5c4214c12cf03473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Alcohol Dehydrogenase - metabolism</topic><topic>ALCOHOLIC BEVERAGES</topic><topic>Aldehyde Dehydrogenase - metabolism</topic><topic>Aniline Hydroxylase - metabolism</topic><topic>Animals</topic><topic>AROMATISANT</topic><topic>AROMATIZANTES</topic><topic>BEBIDAS ALCOHOLICAS</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>BOISSON ALCOOLISEE</topic><topic>C3H/He mice</topic><topic>CYP1A1</topic><topic>CYP2E1</topic><topic>Cytochrome P-450 CYP1A1 - biosynthesis</topic><topic>Cytochrome P-450 CYP1A1 - metabolism</topic><topic>Enzyme Induction</topic><topic>ETANOL</topic><topic>ETHANOL</topic><topic>Ethanol - administration & dosage</topic><topic>Ethanol - metabolism</topic><topic>FLAVOURINGS</topic><topic>FOIE</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>HIGADO</topic><topic>Intermediate and energetic metabolism</topic><topic>LIVER</topic><topic>Male</topic><topic>METABOLISM</topic><topic>METABOLISME</topic><topic>METABOLISMO</topic><topic>Metabolisms and neurohumoral controls</topic><topic>MICE</topic><topic>Mice, Inbred C3H</topic><topic>Microsomes, Liver - enzymology</topic><topic>Microsomes, Liver - metabolism</topic><topic>mirin</topic><topic>RATON</topic><topic>SOURIS</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kishimoto, R. (Kobe Gakuin Univ. (Japan). Faculty of Nutrition)</creatorcontrib><creatorcontrib>Ueda, M</creatorcontrib><creatorcontrib>Kawakami, M</creatorcontrib><creatorcontrib>Goda, K</creatorcontrib><creatorcontrib>Park, S.S</creatorcontrib><creatorcontrib>Nakata, Y</creatorcontrib><collection>AGRIS</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>MEDLINE - Academic</collection><jtitle>Journal of Nutritional Science and Vitaminology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kishimoto, R. (Kobe Gakuin Univ. (Japan). Faculty of Nutrition)</au><au>Ueda, M</au><au>Kawakami, M</au><au>Goda, K</au><au>Park, S.S</au><au>Nakata, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of chronic administration of alcoholic beverages and seasoning containing alcohol on hepatic ethanol metabolism in mice</atitle><jtitle>Journal of Nutritional Science and Vitaminology</jtitle><addtitle>J Nutr Sci Vitaminol</addtitle><date>1997-12-01</date><risdate>1997</risdate><volume>43</volume><issue>6</issue><spage>613</spage><epage>626</epage><pages>613-626</pages><issn>0301-4800</issn><eissn>1881-7742</eissn><abstract>Five-week-old male mice, C3H/HeNCrj (C3H/He), were given a 5% (v/v) ethanol solution, commercial alcoholic beverages (Japanese sake (sake) or red wine) or a Japanese seasoning (mirin [containing ethanol and a large amount of glucose]) ad libitum for 45 d, and were then examined for changes n the hepatic enzymes related to ethanol metabolism 2 h after oral administration of 5 g of ethanol/kg body weight. The specific activity of aniline hydroxylase (ANH) in the hepatic microsome increase significantly in all groups chronically administered ethanol solution, sake, red wine or mirin, and the greatest increase was in the hepatic microsome of mirin-administered mice. The cytochrome P-450 (CYP) 2E1 increased in the hepatic microsome of the mice administered ethanol solution, red wine or mirin where accompanied by high ANH activity. The immunoreactive band for CYP1A1 showed high specificity in the microsome of mice given sake,red wine or mirin. It was assumed that CYP1A1 was induced by unknown component(s) other than ethanol in these solutions. In the cytosolic fraction, following the chronic administration of sake and mirin, the total aldehyde dehydrogenase (A1DH) activity with high-Km decreased significantly. In the mitochondrial fraction, the activity of high-Km A1DH increased significantly in the mirin-administered mice which drank a large amount of ethanol, whereas that in the red wine-administered group tended to decrease. These results indicate that the enzyme activities related to the oxidation of both ethanol and acetaldehyde in the cytosolic, mitochondrial and microsomal fractions of the liver were affected by either the action of ethanol or its interaction with other constituents of sake, red wine and mirin</abstract><cop>Tokyo</cop><pub>Center for Academic Publications Japan</pub><pmid>9530614</pmid><doi>10.3177/jnsv.43.613</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese |
subjects | Alcohol Dehydrogenase - metabolism ALCOHOLIC BEVERAGES Aldehyde Dehydrogenase - metabolism Aniline Hydroxylase - metabolism Animals AROMATISANT AROMATIZANTES BEBIDAS ALCOHOLICAS Biological and medical sciences Blotting, Western BOISSON ALCOOLISEE C3H/He mice CYP1A1 CYP2E1 Cytochrome P-450 CYP1A1 - biosynthesis Cytochrome P-450 CYP1A1 - metabolism Enzyme Induction ETANOL ETHANOL Ethanol - administration & dosage Ethanol - metabolism FLAVOURINGS FOIE Fundamental and applied biological sciences. Psychology HIGADO Intermediate and energetic metabolism LIVER Male METABOLISM METABOLISME METABOLISMO Metabolisms and neurohumoral controls MICE Mice, Inbred C3H Microsomes, Liver - enzymology Microsomes, Liver - metabolism mirin RATON SOURIS Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Effect of chronic administration of alcoholic beverages and seasoning containing alcohol on hepatic ethanol metabolism in mice |
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