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Metabolism of Ginsenoside Rc by Human Intestinal Bacteria and Its Related Antiallergic Activity
When ginsenoside Rc was anaerobically incubated with human fecal microflora, all specimens metabolized ginsenoside Rc to compound K and protopanaxadiol. The main metabolite was compound K. Among the bacteria isolated from human fecal microflora, most bacteria, such as Bacteroides sp., Eubacterium sp...
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Published in: | Biological & pharmaceutical bulletin 2002, Vol.25(6), pp.743-747 |
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creator | Bae, Eun-Ah Choo, Min-Kyung Park, Eun-Kyung Park, Sun-Young Shin, Ho-Young Kim, Dong-Hyun |
description | When ginsenoside Rc was anaerobically incubated with human fecal microflora, all specimens metabolized ginsenoside Rc to compound K and protopanaxadiol. The main metabolite was compound K. Among the bacteria isolated from human fecal microflora, most bacteria, such as Bacteroides sp., Eubacterium sp., and Bifidobacterium sp. potently transformed ginsenoside Rc to compound K. Bifidobacterium K-103 and Eubacterium A-44 transformed it to compound K via ginsenoside Rd, and Bacteroides HJ-15 and Bifidobacterium K-506 metabolized to compound K via ginsenoside Mb, which was isolated as a new metabolite (M.W. 940[+Na]). Among ginsenoside Rc and its metabolites, compound K exhibited the most potent antiallergic activity on the IgE-induced RBL cell line as well as potent cytotoxic activity against tumor cell lines. |
doi_str_mv | 10.1248/bpb.25.743 |
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Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bae, Eun-Ah</creatorcontrib><creatorcontrib>Choo, Min-Kyung</creatorcontrib><creatorcontrib>Park, Eun-Kyung</creatorcontrib><creatorcontrib>Park, Sun-Young</creatorcontrib><creatorcontrib>Shin, Ho-Young</creatorcontrib><creatorcontrib>Kim, Dong-Hyun</creatorcontrib><collection>Pascal-Francis</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><jtitle>Biological & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bae, Eun-Ah</au><au>Choo, Min-Kyung</au><au>Park, Eun-Kyung</au><au>Park, Sun-Young</au><au>Shin, Ho-Young</au><au>Kim, Dong-Hyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolism of Ginsenoside Rc by Human Intestinal Bacteria and Its Related Antiallergic Activity</atitle><jtitle>Biological & pharmaceutical bulletin</jtitle><date>2002</date><risdate>2002</risdate><volume>25</volume><issue>6</issue><spage>743</spage><epage>747</epage><pages>743-747</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>When ginsenoside Rc was anaerobically incubated with human fecal microflora, all specimens metabolized ginsenoside Rc to compound K and protopanaxadiol. The main metabolite was compound K. Among the bacteria isolated from human fecal microflora, most bacteria, such as Bacteroides sp., Eubacterium sp., and Bifidobacterium sp. potently transformed ginsenoside Rc to compound K. Bifidobacterium K-103 and Eubacterium A-44 transformed it to compound K via ginsenoside Rd, and Bacteroides HJ-15 and Bifidobacterium K-506 metabolized to compound K via ginsenoside Mb, which was isolated as a new metabolite (M.W. 940[+Na]). Among ginsenoside Rc and its metabolites, compound K exhibited the most potent antiallergic activity on the IgE-induced RBL cell line as well as potent cytotoxic activity against tumor cell lines.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><doi>10.1248/bpb.25.743</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | antiallergy Biological and medical sciences compound K General pharmacology ginsenoside Mb ginsenoside Rc intestinal bacteria Medical sciences Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments |
title | Metabolism of Ginsenoside Rc by Human Intestinal Bacteria and Its Related Antiallergic Activity |
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