國家衛生研究院 NHRI:Item 3990099045/4669
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 907510      Online Users : 955
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/4669


    Title: Protective effects of Polyporus umbellatus polysaccharides alone and in combination with WR-2721 on radiation- and cyclophosphamide-induced genotoxicity in vitro and in vivo
    Authors: Wu, HC;Lin, FJ;Pei, SY;Wu, KY;Huang, HF;Chiang, SY
    Contributors: Division of Environmental Health and Occupational Medicine
    Abstract: Polyporus umbellatus Polysaccharides (PUPs) are the main active components of Polyporus umbellatus, one of the commonly used traditional chinese medicines. In this study, the radioprotective and chemopreventive effects of PUPs were studied in vitro and in vivo. In human lymphoblastoid Tk6 cells, pretreatment of PUPs at a dose of 100 Ag/ml and 300 Ag/ml 30 min before irradiation significantly reduced radiation-induced micronuclei (MN) and tk mutant frequencies. Pretreatments of PUPs at a dose of 50 mg/Kg by i.p. injection 30 min or 45 min before 6 Gy irradiation resulted in statistically significant decrease of MN frequencies in the peripheral blood erythrocytes of irradiated mice. Comparative studies with a known radioprotective agent WR-2721 showed that PUPs may be a better radioprotective agent with a higher inhibition ratio of radiation-induced micronuclei and tk mutant frequencies. Mechanistic study showed that administration of PUPs at a dose of 50 mg/kg 30 min before irradiation significantly reduced the formation of the oxidative DNA damage (8-hydroxy-2V-deoxyguanosine) and lipid peroxidation in irradiated mouse liver. The antioxidant activity of PUPs may contribute to its radioprotective effect. Furthermore, PUPs caused a dose-dependent inhibition of cyclophosphamide-induced MN formation in TK6 cells. PUPs also inhibited MN frequencies in cyclophosphamide-treated mice. Since PUPs are natural, relatively nontoxic and less-expensive; these data suggest that PUPs may be a useful radioprotective agent and chemopreventive agent.
    Date: 2004-06
    Relation: Toxicology and Applied Pharmacology. 2004 Jun;197(3):347-348.
    Link to: http://dx.doi.org/10.1016/j.taap.2004.04.002
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0041-008X&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000222348900765
    Appears in Collections:[Kuen-Yuh Wu(2001-2008)] Conference Papers/Meeting Abstract

    Files in This Item:

    File Description SizeFormat
    ISI000222348900765.pdf53KbAdobe PDF483View/Open


    All items in NHRI are protected by copyright, with all rights reserved.

    Related Items in TAIR

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback