Source:http://linkedlifedata.com/resource/pubmed/id/15650337
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2005-1-14
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pubmed:abstractText |
Ginsenosides, active ingredients of Panax ginseng, exist as stereoisomers depending on the position of the hydroxyl group on carbon-20; i.e. 20(R)-ginsenoside and 20(S)-ginsenoside are epimers. We have shown previously that the mixture of 20(R)- and 20(S)-ginsenosides regulates ion channel activity. However, it was not clear which epimer was responsible. We investigated the structure-activity relationship of the ginsenoside Rg3 stereoisomers, 20-R-protopanaxatriol-3-[O-beta-D-glucopyranosyl (1-->2)-beta-glucopyranoside], (20(R)-Rg3) and 20-S-proto-panaxatriol-3-[O-beta-D-glucopyranosyl (1-->2)-beta-glucopyr-anoside], (20(S)-Rg3) in regulating voltage-dependent Ca2+, K+ or Na+ channel currents and 5-HT3A and a3b4 nicotinic acetylcholine (nACh) receptor channel currents expressed in Xenopus oocytes. 20(S)-Rg3 but not 20(R)-Rg3 inhibited the Ca2+, K+ and Na+ channel currents in a dose- and voltage-dependent manner. The fact that only 20(S)-Rg3 is active indicates that its hydroxyl group may be geometrically better aligned with the hydroxyl acceptor group in the ion channels than that of 20(R)-Rg3. However, both Rg3 stereoisomers inhibited 5-HT3A and a3beta4 nACh receptor channel currents. These results indicate that the selectivity of action of the Rg3 stereoisomers differs between voltage-dependent and ligand-gated ion channels.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Ginsenosides,
http://linkedlifedata.com/resource/pubmed/chemical/Ions,
http://linkedlifedata.com/resource/pubmed/chemical/Oxygen,
http://linkedlifedata.com/resource/pubmed/chemical/ginsenoside Rg3
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1016-8478
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
31
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
383-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15650337-Animals,
pubmed-meshheading:15650337-DNA, Complementary,
pubmed-meshheading:15650337-Dose-Response Relationship, Drug,
pubmed-meshheading:15650337-Electrophysiology,
pubmed-meshheading:15650337-Ginsenosides,
pubmed-meshheading:15650337-Ions,
pubmed-meshheading:15650337-Models, Chemical,
pubmed-meshheading:15650337-Oocytes,
pubmed-meshheading:15650337-Oxygen,
pubmed-meshheading:15650337-Panax,
pubmed-meshheading:15650337-Patch-Clamp Techniques,
pubmed-meshheading:15650337-Stereoisomerism,
pubmed-meshheading:15650337-Transcription, Genetic,
pubmed-meshheading:15650337-Xenopus laevis
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pubmed:year |
2004
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pubmed:articleTitle |
Stereospecificity of ginsenoside Rg3 action on ion channels.
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pubmed:affiliation |
Research Laboratory for the Study of Ginseng Signal Transduction and Department of Physiology, College of Veterinary Medicine, Konkuk University, Seoul 143-701, Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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