Pharmacological studies on schizandra fruits. III: Effects of wuweizisu C, a lignan component of schizandra fruits, on experimental liver injuries in rats
The effects of wuweizisu C, a lignan component of schizandra fruits, on liver injuries induced by carbon tetrachloride (CCl4), d-galactosamine and dl-ethionine were investigated by means of serum-biochemical and histopathological examinations in rats. Pretreatment or combined administration of wuwei...
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Veröffentlicht in: | Folia Pharmacologica Japonica 1985, Vol.85(3), pp.193-208 |
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creator | TAKEDA, Shigefumi FUNO, Shyuji IIZUKA, Akira KASE, Yoshio ARAI, Ichiro OHKURA, Yasufumi SUDO, Kazuhiko KIUCHI, Noriko YOSHIDA, Chizuru MAEDA, Shinya ABURADA, Masaki HOSOYA, Eikichi |
description | The effects of wuweizisu C, a lignan component of schizandra fruits, on liver injuries induced by carbon tetrachloride (CCl4), d-galactosamine and dl-ethionine were investigated by means of serum-biochemical and histopathological examinations in rats. Pretreatment or combined administration of wuweizisu C dose-dependently reduced the elevation of serum transaminase activity and histological changes such as fatty degeneration, cell necrosis, inflammatory cell infiltration, etc., which were caused by the single administration of 1 ml/kg, p.o., or the repeated administration of 0.2 ml/kg, s.c., daily for 4 days of CCl4, respectively. The effects of wuweizisu C on the liver injuries induced by a low dose (200 mg/kg, i.p.) and a high dose (400 mg/kg, i.p.) of d-galactosamine were compared with those of uridine. Wuweizisu C significantly lowered the rise of serum transaminase activity after the administration of a low dose of d-galactosamine in the serum-biochemical analysis. A tendency was also shown to inhibit cell necrosis and inflammatory cell infiltration caused by both doses of d-galactosamine in the histopathological examination. On the other hand, uridine markedly repaired the serum-biochemical and histopathological changes after the administrations of both doses of d-galactosamine. Also wuweizisu C cured the liver injury by the repeated administration of 150 mg/kg, i.p., daily for 4 days of d-galactosamine. After the repeated administration of 250 mg/kg, s.c., daily for 4 days of ethionine, liver cell atrophy, diffuse fatty degeneration and decrease of serum triglyceride were observed, but not cell necrosis. Wuweizisu C dose-dependently inhibited fatty degeneration and decrease of serum triglyceride. These findings suggest that wuweizisu C can be protective and/or therapeutic on hepatocellular phenomena such as cell necrosis, fatty degeneration, inflammatory cell infiltration, etc., in human hepatitis. |
doi_str_mv | 10.1254/fpj.85.193 |
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III: Effects of wuweizisu C, a lignan component of schizandra fruits, on experimental liver injuries in rats</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>TAKEDA, Shigefumi ; FUNO, Shyuji ; IIZUKA, Akira ; KASE, Yoshio ; ARAI, Ichiro ; OHKURA, Yasufumi ; SUDO, Kazuhiko ; KIUCHI, Noriko ; YOSHIDA, Chizuru ; MAEDA, Shinya ; ABURADA, Masaki ; HOSOYA, Eikichi</creator><creatorcontrib>TAKEDA, Shigefumi ; FUNO, Shyuji ; IIZUKA, Akira ; KASE, Yoshio ; ARAI, Ichiro ; OHKURA, Yasufumi ; SUDO, Kazuhiko ; KIUCHI, Noriko ; YOSHIDA, Chizuru ; MAEDA, Shinya ; ABURADA, Masaki ; HOSOYA, Eikichi</creatorcontrib><description>The effects of wuweizisu C, a lignan component of schizandra fruits, on liver injuries induced by carbon tetrachloride (CCl4), d-galactosamine and dl-ethionine were investigated by means of serum-biochemical and histopathological examinations in rats. Pretreatment or combined administration of wuweizisu C dose-dependently reduced the elevation of serum transaminase activity and histological changes such as fatty degeneration, cell necrosis, inflammatory cell infiltration, etc., which were caused by the single administration of 1 ml/kg, p.o., or the repeated administration of 0.2 ml/kg, s.c., daily for 4 days of CCl4, respectively. The effects of wuweizisu C on the liver injuries induced by a low dose (200 mg/kg, i.p.) and a high dose (400 mg/kg, i.p.) of d-galactosamine were compared with those of uridine. Wuweizisu C significantly lowered the rise of serum transaminase activity after the administration of a low dose of d-galactosamine in the serum-biochemical analysis. A tendency was also shown to inhibit cell necrosis and inflammatory cell infiltration caused by both doses of d-galactosamine in the histopathological examination. On the other hand, uridine markedly repaired the serum-biochemical and histopathological changes after the administrations of both doses of d-galactosamine. Also wuweizisu C cured the liver injury by the repeated administration of 150 mg/kg, i.p., daily for 4 days of d-galactosamine. After the repeated administration of 250 mg/kg, s.c., daily for 4 days of ethionine, liver cell atrophy, diffuse fatty degeneration and decrease of serum triglyceride were observed, but not cell necrosis. Wuweizisu C dose-dependently inhibited fatty degeneration and decrease of serum triglyceride. These findings suggest that wuweizisu C can be protective and/or therapeutic on hepatocellular phenomena such as cell necrosis, fatty degeneration, inflammatory cell infiltration, etc., in human hepatitis.</description><identifier>ISSN: 0015-5691</identifier><identifier>EISSN: 1347-8397</identifier><identifier>DOI: 10.1254/fpj.85.193</identifier><identifier>PMID: 2989131</identifier><language>eng ; jpn</language><publisher>Japan: The Japanese Pharmacological Society</publisher><subject>Animals ; Carbon Tetrachloride Poisoning - drug therapy ; Chemical and Drug Induced Liver Injury ; Cyclooctanes ; Ethionine - antagonists & inhibitors ; Fatty Liver - prevention & control ; Galactosamine - antagonists & inhibitors ; Hepatitis - prevention & control ; Lignans ; Liver Diseases - drug therapy ; Liver Diseases - prevention & control ; Male ; Plant Extracts - therapeutic use ; Plants, Medicinal ; Polycyclic Compounds - therapeutic use ; Rats ; Rats, Inbred Strains</subject><ispartof>Folia Pharmacologica Japonica, 1985, Vol.85(3), pp.193-208</ispartof><rights>The Japanese PharmacologicalSociety</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2933-391e6c36d2c3d8b667f90f84dd6be88fb0511cf2500ff449e67f3e6a7d41a4d93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,4025,27928,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2989131$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TAKEDA, Shigefumi</creatorcontrib><creatorcontrib>FUNO, Shyuji</creatorcontrib><creatorcontrib>IIZUKA, Akira</creatorcontrib><creatorcontrib>KASE, Yoshio</creatorcontrib><creatorcontrib>ARAI, Ichiro</creatorcontrib><creatorcontrib>OHKURA, Yasufumi</creatorcontrib><creatorcontrib>SUDO, Kazuhiko</creatorcontrib><creatorcontrib>KIUCHI, Noriko</creatorcontrib><creatorcontrib>YOSHIDA, Chizuru</creatorcontrib><creatorcontrib>MAEDA, Shinya</creatorcontrib><creatorcontrib>ABURADA, Masaki</creatorcontrib><creatorcontrib>HOSOYA, Eikichi</creatorcontrib><title>Pharmacological studies on schizandra fruits. III: Effects of wuweizisu C, a lignan component of schizandra fruits, on experimental liver injuries in rats</title><title>Folia Pharmacologica Japonica</title><addtitle>Nihon Yakurigaku Zasshi</addtitle><description>The effects of wuweizisu C, a lignan component of schizandra fruits, on liver injuries induced by carbon tetrachloride (CCl4), d-galactosamine and dl-ethionine were investigated by means of serum-biochemical and histopathological examinations in rats. Pretreatment or combined administration of wuweizisu C dose-dependently reduced the elevation of serum transaminase activity and histological changes such as fatty degeneration, cell necrosis, inflammatory cell infiltration, etc., which were caused by the single administration of 1 ml/kg, p.o., or the repeated administration of 0.2 ml/kg, s.c., daily for 4 days of CCl4, respectively. The effects of wuweizisu C on the liver injuries induced by a low dose (200 mg/kg, i.p.) and a high dose (400 mg/kg, i.p.) of d-galactosamine were compared with those of uridine. Wuweizisu C significantly lowered the rise of serum transaminase activity after the administration of a low dose of d-galactosamine in the serum-biochemical analysis. A tendency was also shown to inhibit cell necrosis and inflammatory cell infiltration caused by both doses of d-galactosamine in the histopathological examination. On the other hand, uridine markedly repaired the serum-biochemical and histopathological changes after the administrations of both doses of d-galactosamine. Also wuweizisu C cured the liver injury by the repeated administration of 150 mg/kg, i.p., daily for 4 days of d-galactosamine. After the repeated administration of 250 mg/kg, s.c., daily for 4 days of ethionine, liver cell atrophy, diffuse fatty degeneration and decrease of serum triglyceride were observed, but not cell necrosis. Wuweizisu C dose-dependently inhibited fatty degeneration and decrease of serum triglyceride. These findings suggest that wuweizisu C can be protective and/or therapeutic on hepatocellular phenomena such as cell necrosis, fatty degeneration, inflammatory cell infiltration, etc., in human hepatitis.</description><subject>Animals</subject><subject>Carbon Tetrachloride Poisoning - drug therapy</subject><subject>Chemical and Drug Induced Liver Injury</subject><subject>Cyclooctanes</subject><subject>Ethionine - antagonists & inhibitors</subject><subject>Fatty Liver - prevention & control</subject><subject>Galactosamine - antagonists & inhibitors</subject><subject>Hepatitis - prevention & control</subject><subject>Lignans</subject><subject>Liver Diseases - drug therapy</subject><subject>Liver Diseases - prevention & control</subject><subject>Male</subject><subject>Plant Extracts - therapeutic use</subject><subject>Plants, Medicinal</subject><subject>Polycyclic Compounds - therapeutic use</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><issn>0015-5691</issn><issn>1347-8397</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kDtrwzAURkVpSUOapXvBc8GurvWwNJbQhyHQDu0sZD0SFScOkjO0v74KDll0h3P44Aihe8AV1Iw--cNPJVgFklyhORDalILI5hrNMQZWMi7hFi1TCh3GrKkbTmCGZrUUEgjMEXxuddxpM_TDJhjdF2k82uBSMeyLZLbhT-9t1IWPxzCmqmjb9g7deN0ntzzfBfp-fflavZfrj7d29bwuTS0JKYkExw3htjbEio7zxkvsBbWWd04I32EGYHzNMPaeUumyQBzXjaWgqZVkgR6nXROHlKLz6hDDTsdfBVidylUuV4KpXJ7lh0k-HLudsxf13Jn5auI_adQbd-E6jsH07jQFktLTHJmevHqhJv-RcnvyDymYauU</recordid><startdate>1985</startdate><enddate>1985</enddate><creator>TAKEDA, Shigefumi</creator><creator>FUNO, Shyuji</creator><creator>IIZUKA, Akira</creator><creator>KASE, Yoshio</creator><creator>ARAI, Ichiro</creator><creator>OHKURA, Yasufumi</creator><creator>SUDO, Kazuhiko</creator><creator>KIUCHI, Noriko</creator><creator>YOSHIDA, Chizuru</creator><creator>MAEDA, Shinya</creator><creator>ABURADA, Masaki</creator><creator>HOSOYA, Eikichi</creator><general>The Japanese Pharmacological Society</general><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>1985</creationdate><title>Pharmacological studies on schizandra fruits. III</title><author>TAKEDA, Shigefumi ; FUNO, Shyuji ; IIZUKA, Akira ; KASE, Yoshio ; ARAI, Ichiro ; OHKURA, Yasufumi ; SUDO, Kazuhiko ; KIUCHI, Noriko ; YOSHIDA, Chizuru ; MAEDA, Shinya ; ABURADA, Masaki ; HOSOYA, Eikichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2933-391e6c36d2c3d8b667f90f84dd6be88fb0511cf2500ff449e67f3e6a7d41a4d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Carbon Tetrachloride Poisoning - drug therapy</topic><topic>Chemical and Drug Induced Liver Injury</topic><topic>Cyclooctanes</topic><topic>Ethionine - antagonists & inhibitors</topic><topic>Fatty Liver - prevention & control</topic><topic>Galactosamine - antagonists & inhibitors</topic><topic>Hepatitis - prevention & control</topic><topic>Lignans</topic><topic>Liver Diseases - drug therapy</topic><topic>Liver Diseases - prevention & control</topic><topic>Male</topic><topic>Plant Extracts - therapeutic use</topic><topic>Plants, Medicinal</topic><topic>Polycyclic Compounds - therapeutic use</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAKEDA, Shigefumi</creatorcontrib><creatorcontrib>FUNO, Shyuji</creatorcontrib><creatorcontrib>IIZUKA, Akira</creatorcontrib><creatorcontrib>KASE, Yoshio</creatorcontrib><creatorcontrib>ARAI, Ichiro</creatorcontrib><creatorcontrib>OHKURA, Yasufumi</creatorcontrib><creatorcontrib>SUDO, Kazuhiko</creatorcontrib><creatorcontrib>KIUCHI, Noriko</creatorcontrib><creatorcontrib>YOSHIDA, Chizuru</creatorcontrib><creatorcontrib>MAEDA, Shinya</creatorcontrib><creatorcontrib>ABURADA, Masaki</creatorcontrib><creatorcontrib>HOSOYA, Eikichi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Folia Pharmacologica Japonica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TAKEDA, Shigefumi</au><au>FUNO, Shyuji</au><au>IIZUKA, Akira</au><au>KASE, Yoshio</au><au>ARAI, Ichiro</au><au>OHKURA, Yasufumi</au><au>SUDO, Kazuhiko</au><au>KIUCHI, Noriko</au><au>YOSHIDA, Chizuru</au><au>MAEDA, Shinya</au><au>ABURADA, Masaki</au><au>HOSOYA, Eikichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacological studies on schizandra fruits. III: Effects of wuweizisu C, a lignan component of schizandra fruits, on experimental liver injuries in rats</atitle><jtitle>Folia Pharmacologica Japonica</jtitle><addtitle>Nihon Yakurigaku Zasshi</addtitle><date>1985</date><risdate>1985</risdate><volume>85</volume><issue>3</issue><spage>193</spage><epage>208</epage><pages>193-208</pages><issn>0015-5691</issn><eissn>1347-8397</eissn><abstract>The effects of wuweizisu C, a lignan component of schizandra fruits, on liver injuries induced by carbon tetrachloride (CCl4), d-galactosamine and dl-ethionine were investigated by means of serum-biochemical and histopathological examinations in rats. Pretreatment or combined administration of wuweizisu C dose-dependently reduced the elevation of serum transaminase activity and histological changes such as fatty degeneration, cell necrosis, inflammatory cell infiltration, etc., which were caused by the single administration of 1 ml/kg, p.o., or the repeated administration of 0.2 ml/kg, s.c., daily for 4 days of CCl4, respectively. The effects of wuweizisu C on the liver injuries induced by a low dose (200 mg/kg, i.p.) and a high dose (400 mg/kg, i.p.) of d-galactosamine were compared with those of uridine. Wuweizisu C significantly lowered the rise of serum transaminase activity after the administration of a low dose of d-galactosamine in the serum-biochemical analysis. A tendency was also shown to inhibit cell necrosis and inflammatory cell infiltration caused by both doses of d-galactosamine in the histopathological examination. On the other hand, uridine markedly repaired the serum-biochemical and histopathological changes after the administrations of both doses of d-galactosamine. Also wuweizisu C cured the liver injury by the repeated administration of 150 mg/kg, i.p., daily for 4 days of d-galactosamine. After the repeated administration of 250 mg/kg, s.c., daily for 4 days of ethionine, liver cell atrophy, diffuse fatty degeneration and decrease of serum triglyceride were observed, but not cell necrosis. Wuweizisu C dose-dependently inhibited fatty degeneration and decrease of serum triglyceride. These findings suggest that wuweizisu C can be protective and/or therapeutic on hepatocellular phenomena such as cell necrosis, fatty degeneration, inflammatory cell infiltration, etc., in human hepatitis.</abstract><cop>Japan</cop><pub>The Japanese Pharmacological Society</pub><pmid>2989131</pmid><doi>10.1254/fpj.85.193</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Carbon Tetrachloride Poisoning - drug therapy Chemical and Drug Induced Liver Injury Cyclooctanes Ethionine - antagonists & inhibitors Fatty Liver - prevention & control Galactosamine - antagonists & inhibitors Hepatitis - prevention & control Lignans Liver Diseases - drug therapy Liver Diseases - prevention & control Male Plant Extracts - therapeutic use Plants, Medicinal Polycyclic Compounds - therapeutic use Rats Rats, Inbred Strains |
title | Pharmacological studies on schizandra fruits. III: Effects of wuweizisu C, a lignan component of schizandra fruits, on experimental liver injuries in rats |
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