Possible Role of Ginsenoside Rb1 on Regulation of Rat Liver Triglycerides
We have studied the effects of ginsenoside Rb1 (GRb1) on the change in lipid contents in rat liver. When GRb1 was administered intraperitoneally to rats, liver microsomal cytochrome P-450 content and NADPH-cytochrome P-450 reductase activity were lower than those in control rats. The contents of tri...
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Veröffentlicht in: | Biological & pharmaceutical bulletin 2002, Vol.25(4), pp.457-460 |
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creator | Park, Ki-Hyun Shin, Han-Jae Song, Young-Bum Hyun, Hak-Chul Cho, Hyun-Jeong Ham, Hye-Seon Yoo, Young-Bin Ko, Young-Chul Jun, Woong-Tak Park, Hwa-Jin |
description | We have studied the effects of ginsenoside Rb1 (GRb1) on the change in lipid contents in rat liver. When GRb1 was administered intraperitoneally to rats, liver microsomal cytochrome P-450 content and NADPH-cytochrome P-450 reductase activity were lower than those in control rats. The contents of triglyceride (TG) and cholesterol were decreased, but those of total phospholipid, phosphatidylcholine, and phosphatidylethanolamine were increased in the GRb1-treated group compared with controls. These results indicate that GRb1 might be involved in lipid metabolism by regulating the activity of microsomal cytochrome P-450 monooxygenase. Although liver TG levels were reduced by GRb1, the levels of TG and β-lipoprotein in serum from the GRb1-treated group did not change as compared with those in controls. Thus we suggest that the decrease in liver TG levels with GRb1-treatment is not associated with the secretion of TG-rich very low-density lipoprotein. Furthermore, the level of cAMP was also significantly increased in the GRb1-treated group as compared with that in controls. Additionally, the cAMP level was more markedly increased as compared with that in the GRb1-treated group or control group when GRb1 was exogenously added to the reaction system for measuring cAMP production in homogenates from control group liver. Accordingly, these results demonstrate that GRb1 might lower TG levels via cAMP-production in the liver, and GRb1 might be an interesting candidate to for a modulator of cAMP-mediated effects, especially within the liver steatosis system. |
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When GRb1 was administered intraperitoneally to rats, liver microsomal cytochrome P-450 content and NADPH-cytochrome P-450 reductase activity were lower than those in control rats. The contents of triglyceride (TG) and cholesterol were decreased, but those of total phospholipid, phosphatidylcholine, and phosphatidylethanolamine were increased in the GRb1-treated group compared with controls. These results indicate that GRb1 might be involved in lipid metabolism by regulating the activity of microsomal cytochrome P-450 monooxygenase. Although liver TG levels were reduced by GRb1, the levels of TG and β-lipoprotein in serum from the GRb1-treated group did not change as compared with those in controls. Thus we suggest that the decrease in liver TG levels with GRb1-treatment is not associated with the secretion of TG-rich very low-density lipoprotein. Furthermore, the level of cAMP was also significantly increased in the GRb1-treated group as compared with that in controls. Additionally, the cAMP level was more markedly increased as compared with that in the GRb1-treated group or control group when GRb1 was exogenously added to the reaction system for measuring cAMP production in homogenates from control group liver. Accordingly, these results demonstrate that GRb1 might lower TG levels via cAMP-production in the liver, and GRb1 might be an interesting candidate to for a modulator of cAMP-mediated effects, especially within the liver steatosis system.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.25.457</identifier><identifier>PMID: 11995924</identifier><language>eng</language><publisher>Tokyo: The Pharmaceutical Society of Japan</publisher><subject>Animals ; Biological and medical sciences ; Cyclic AMP - metabolism ; cyclic-adenosine monophosphate ; Cytochrome P-450 Enzyme System - metabolism ; cytochrome P-450 monooxygenase ; General pharmacology ; ginsenoside Rb1 ; Ginsenosides - administration & dosage ; Ginsenosides - pharmacology ; Injections, Intraperitoneal ; Liver - drug effects ; Liver - metabolism ; Male ; Medical sciences ; Microsomes, Liver - drug effects ; Microsomes, Liver - metabolism ; Panax - chemistry ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. Drug treatments ; Rats ; Rats, Sprague-Dawley ; triglyceride ; Triglycerides - metabolism</subject><ispartof>Biological and Pharmaceutical Bulletin, 2002, Vol.25(4), pp.457-460</ispartof><rights>2002 The Pharmaceutical Society of Japan</rights><rights>2002 INIST-CNRS</rights><rights>Copyright Japan Science and Technology Agency 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5667-83b39938b44cbd40109db419131ab73a464d5c1e8e3edd7cd96b78a7383c122a3</citedby><cites>FETCH-LOGICAL-c5667-83b39938b44cbd40109db419131ab73a464d5c1e8e3edd7cd96b78a7383c122a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13642718$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11995924$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Ki-Hyun</creatorcontrib><creatorcontrib>Shin, Han-Jae</creatorcontrib><creatorcontrib>Song, Young-Bum</creatorcontrib><creatorcontrib>Hyun, Hak-Chul</creatorcontrib><creatorcontrib>Cho, Hyun-Jeong</creatorcontrib><creatorcontrib>Ham, Hye-Seon</creatorcontrib><creatorcontrib>Yoo, Young-Bin</creatorcontrib><creatorcontrib>Ko, Young-Chul</creatorcontrib><creatorcontrib>Jun, Woong-Tak</creatorcontrib><creatorcontrib>Park, Hwa-Jin</creatorcontrib><title>Possible Role of Ginsenoside Rb1 on Regulation of Rat Liver Triglycerides</title><title>Biological & pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>We have studied the effects of ginsenoside Rb1 (GRb1) on the change in lipid contents in rat liver. When GRb1 was administered intraperitoneally to rats, liver microsomal cytochrome P-450 content and NADPH-cytochrome P-450 reductase activity were lower than those in control rats. The contents of triglyceride (TG) and cholesterol were decreased, but those of total phospholipid, phosphatidylcholine, and phosphatidylethanolamine were increased in the GRb1-treated group compared with controls. These results indicate that GRb1 might be involved in lipid metabolism by regulating the activity of microsomal cytochrome P-450 monooxygenase. Although liver TG levels were reduced by GRb1, the levels of TG and β-lipoprotein in serum from the GRb1-treated group did not change as compared with those in controls. Thus we suggest that the decrease in liver TG levels with GRb1-treatment is not associated with the secretion of TG-rich very low-density lipoprotein. Furthermore, the level of cAMP was also significantly increased in the GRb1-treated group as compared with that in controls. Additionally, the cAMP level was more markedly increased as compared with that in the GRb1-treated group or control group when GRb1 was exogenously added to the reaction system for measuring cAMP production in homogenates from control group liver. Accordingly, these results demonstrate that GRb1 might lower TG levels via cAMP-production in the liver, and GRb1 might be an interesting candidate to for a modulator of cAMP-mediated effects, especially within the liver steatosis system.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cyclic AMP - metabolism</subject><subject>cyclic-adenosine monophosphate</subject><subject>Cytochrome P-450 Enzyme System - metabolism</subject><subject>cytochrome P-450 monooxygenase</subject><subject>General pharmacology</subject><subject>ginsenoside Rb1</subject><subject>Ginsenosides - administration & dosage</subject><subject>Ginsenosides - pharmacology</subject><subject>Injections, Intraperitoneal</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microsomes, Liver - drug effects</subject><subject>Microsomes, Liver - metabolism</subject><subject>Panax - chemistry</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>triglyceride</subject><subject>Triglycerides - metabolism</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0E1rGzEQBmARWhIn7aU_oCyU5BBYV6OPlXQKITRpwNBi0rOQtGNXZr3rSruB_Psq2DiQy0hIDzPDS8gXoHNgQn_3Oz9nci6kOiEz4ELVkoH8QGbUgK4bkPqMnOe8oZQqyvgpOQMwRhomZuTx95Bz9B1Wy6GUYVU9xD5jP-TYljcP1dBXS1xPnRtjuRawdGO1iM-YqqcU191LwFRs_kQ-rlyX8fPhvCB_7n883f2sF78eHu9uF3WQTaNqzT03hmsvRPCtoEBN6wUY4OC84k40opUBUCPHtlWhNY1X2imueQDGHL8gV_u-uzT8mzCPdhtzwK5zPQ5TtgoaCVJAgd_ewc0wpb7sZkEIUyKgzau63quQShIJV3aX4talFwvUvsZrS7yWSVviLfjroeXkt9i-0UOeBVwegMvBdavk-hDzm-ONYAp0cTd7t8mjW-MRuDTG0OFx5r6U0cef8Ncliz3_D8b6lxY</recordid><startdate>200204</startdate><enddate>200204</enddate><creator>Park, Ki-Hyun</creator><creator>Shin, Han-Jae</creator><creator>Song, Young-Bum</creator><creator>Hyun, Hak-Chul</creator><creator>Cho, Hyun-Jeong</creator><creator>Ham, Hye-Seon</creator><creator>Yoo, Young-Bin</creator><creator>Ko, Young-Chul</creator><creator>Jun, Woong-Tak</creator><creator>Park, Hwa-Jin</creator><general>The Pharmaceutical Society of Japan</general><general>Maruzen</general><general>Japan Science and Technology Agency</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><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200204</creationdate><title>Possible Role of Ginsenoside Rb1 on Regulation of Rat Liver Triglycerides</title><author>Park, Ki-Hyun ; Shin, Han-Jae ; Song, Young-Bum ; Hyun, Hak-Chul ; Cho, Hyun-Jeong ; Ham, Hye-Seon ; Yoo, Young-Bin ; Ko, Young-Chul ; Jun, Woong-Tak ; Park, Hwa-Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5667-83b39938b44cbd40109db419131ab73a464d5c1e8e3edd7cd96b78a7383c122a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cyclic AMP - metabolism</topic><topic>cyclic-adenosine monophosphate</topic><topic>Cytochrome P-450 Enzyme System - metabolism</topic><topic>cytochrome P-450 monooxygenase</topic><topic>General pharmacology</topic><topic>ginsenoside Rb1</topic><topic>Ginsenosides - administration & dosage</topic><topic>Ginsenosides - pharmacology</topic><topic>Injections, Intraperitoneal</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microsomes, Liver - drug effects</topic><topic>Microsomes, Liver - metabolism</topic><topic>Panax - chemistry</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>triglyceride</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Ki-Hyun</creatorcontrib><creatorcontrib>Shin, Han-Jae</creatorcontrib><creatorcontrib>Song, Young-Bum</creatorcontrib><creatorcontrib>Hyun, Hak-Chul</creatorcontrib><creatorcontrib>Cho, Hyun-Jeong</creatorcontrib><creatorcontrib>Ham, Hye-Seon</creatorcontrib><creatorcontrib>Yoo, Young-Bin</creatorcontrib><creatorcontrib>Ko, Young-Chul</creatorcontrib><creatorcontrib>Jun, Woong-Tak</creatorcontrib><creatorcontrib>Park, Hwa-Jin</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><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Ki-Hyun</au><au>Shin, Han-Jae</au><au>Song, Young-Bum</au><au>Hyun, Hak-Chul</au><au>Cho, Hyun-Jeong</au><au>Ham, Hye-Seon</au><au>Yoo, Young-Bin</au><au>Ko, Young-Chul</au><au>Jun, Woong-Tak</au><au>Park, Hwa-Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Possible Role of Ginsenoside Rb1 on Regulation of Rat Liver Triglycerides</atitle><jtitle>Biological & pharmaceutical bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2002-04</date><risdate>2002</risdate><volume>25</volume><issue>4</issue><spage>457</spage><epage>460</epage><pages>457-460</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>We have studied the effects of ginsenoside Rb1 (GRb1) on the change in lipid contents in rat liver. When GRb1 was administered intraperitoneally to rats, liver microsomal cytochrome P-450 content and NADPH-cytochrome P-450 reductase activity were lower than those in control rats. The contents of triglyceride (TG) and cholesterol were decreased, but those of total phospholipid, phosphatidylcholine, and phosphatidylethanolamine were increased in the GRb1-treated group compared with controls. These results indicate that GRb1 might be involved in lipid metabolism by regulating the activity of microsomal cytochrome P-450 monooxygenase. Although liver TG levels were reduced by GRb1, the levels of TG and β-lipoprotein in serum from the GRb1-treated group did not change as compared with those in controls. Thus we suggest that the decrease in liver TG levels with GRb1-treatment is not associated with the secretion of TG-rich very low-density lipoprotein. Furthermore, the level of cAMP was also significantly increased in the GRb1-treated group as compared with that in controls. Additionally, the cAMP level was more markedly increased as compared with that in the GRb1-treated group or control group when GRb1 was exogenously added to the reaction system for measuring cAMP production in homogenates from control group liver. Accordingly, these results demonstrate that GRb1 might lower TG levels via cAMP-production in the liver, and GRb1 might be an interesting candidate to for a modulator of cAMP-mediated effects, especially within the liver steatosis system.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>11995924</pmid><doi>10.1248/bpb.25.457</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Cyclic AMP - metabolism cyclic-adenosine monophosphate Cytochrome P-450 Enzyme System - metabolism cytochrome P-450 monooxygenase General pharmacology ginsenoside Rb1 Ginsenosides - administration & dosage Ginsenosides - pharmacology Injections, Intraperitoneal Liver - drug effects Liver - metabolism Male Medical sciences Microsomes, Liver - drug effects Microsomes, Liver - metabolism Panax - chemistry Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Rats Rats, Sprague-Dawley triglyceride Triglycerides - metabolism |
title | Possible Role of Ginsenoside Rb1 on Regulation of Rat Liver Triglycerides |
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