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The potent protective effect of wild ginseng (Panax ginseng C.A. Meyer) against benzo[alpha]pyrene-induced toxicity through metabolic regulation of CYP1A1 and GSTs

Cited 45 time in Web of Science Cited 53 time in Scopus
Authors
Gum, Sang Il; Jo, Sung Jun; Ahn, Sang Hyun; Kim, Sang Geon; Kim, Jin-Taek; Shin, Heung Mook; Cho, Min Kyung
Issue Date
2007-06-26
Publisher
Elsevier
Citation
J Ethnopharmacol. 2007 Jul 25;112(3):568-76. Epub 2007 May 18.
Keywords
Administration, OralAlanine Transaminase/bloodAnimalsAspartate Aminotransferases/bloodBenzo(a)pyrene/administration & dosage/toxicityBlotting, WesternCell LineCytochrome P-450 CYP1A1/*genetics/metabolismGene Expression/drug effectsGlutathione Transferase/*genetics/metabolismInjections, IntraperitonealIsoenzymes/genetics/metabolismLipid Peroxidation/drug effectsLiver/drug effects/metabolism/pathologyLiver Diseases/chemically induced/enzymology/*prevention & controlMetabolic Networks and Pathways/drug effectsPanax/*chemistryPlant Extracts/administration & dosage/chemistry/*pharmacologyPlant Roots/chemistryRNA, Messenger/genetics/metabolismRatsRats, Sprague-DawleyReverse Transcriptase Polymerase Chain Reaction
Abstract
Wild Panax ginseng C.A. Meyer (WG) is a well-known medicinal herb. In this study, the protective effects of a water extract from the root of WG on benzo[alpha]pyrene (BP)-induced hepatotoxicity and the mechanism of these effects were investigated for the first time. The effects of WG on liver toxicities induced by BP were assessed by blood biochemical and histopathological analyses. BP caused severe liver injury in rats, as indicated by elevated plasma ALT, AST and LPO levels. Pretreatment with WG for 4 weeks completely abrogated increases in the ALT, AST and LPO levels when challenged with BP. Reductions in GSH content and GST activity by BP were reversed by WG. These protective effects of WG against BP-induced toxicity were consistent with the results of histopathological examinations. We next examined the effects of WG on the gene expression of the enzymes that metabolize BP in H4IIE cells. CYP1A1 mRNA and protein expression were increased by BP. WG moderately inhibited BP-induced CYP1A1 gene expression. Moreover, GSTA2, GSTA3 and GSTM2 gene expressions were significantly increased by WG through the Nrf2/antioxidant responsive element pathway for enzyme induction. In summary, WG is efficacious in protecting against BP-induced hepatotoxicity as results of metabolic regulations through both the inhibition of metabolic enzyme activation and the enhancement of electrophilic detoxification, implying that WG should be considered a potential chemopreventive agent.
ISSN
0378-8741 (Print)
Language
English
URI
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T8D-4NS0KS5-2&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&_docanchor=&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=90c72d3f669829d3f07dc1a67dd82cee

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=17590295

http://hdl.handle.net/10371/21379
DOI
https://doi.org/10.1016/j.jep.2007.05.014
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College of Medicine/School of Medicine (의과대학/대학원)Program in Clinical Pharmacology (협동과정-임상약리학전공)Journal Papers (저널논문_협동과정-임상약리학전공)
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