Cordyceps sinensis extracts do not prevent Fas-receptor and hydrogen peroxide-induced T-cell apoptosis

被引:19
作者
Buenz, EJ
Weaver, JG
Bauer, BA
Chalpin, SD
Badley, AD [1 ]
机构
[1] Mayo Clin & Mayo Fdn, Div Infect Dis, Rochester, MN 55905 USA
[2] Ottawa Civic Hosp, Div Gen Surg, Ottawa, ON K1Y 4E9, Canada
[3] HiHlth, Scottsdale, AZ USA
[4] Mayo Clin & Mayo Fdn, Translat Immunovirol & Biodef Program, Rochester, MN 55905 USA
关键词
Cordyceps sinensis; apoptosis; reactive oxygen species; traditional medicine;
D O I
10.1016/j.jep.2003.09.025
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aqueous and alcohol extracts of Cordyceps sinensis (Berk) Succ. are used as a traditional medicine in China for the treatment of a wide range of diseases and are reported to have antioxidant and antiapoptotic properties. We therefore examined the ability of aqueous, organic, and alcohol extracts of Cordyceps sinensis to inhibit apoptosis induced either by hydrogen peroxide or Fas-receptor ligation; both stimuli induce apoptosis dependent on reactive oxygen species. Cells pre-incubated with Cordyceps sinensis extracts were equally sensitive to hydrogen peroxide and Fas-mediated apoptosis. Thus, the putative antioxidant and antiapoptotic properties of Cordyceps sinensis are insufficient to rescue cells from apoptosis induced by these stimuli in vitro. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:57 / 62
页数:6
相关论文
共 48 条
[1]   Cellular titration of apoptosis with steady state concentrations of H2O2:: Submicromolar levels of H2O2 induce apoptosis through Fenton chemistry independent of the cellular thiol state [J].
Antunes, F ;
Cadenas, E .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 30 (09) :1008-1018
[2]   Selection of lymphocyte gating protocol has an impact on the level of reliability of T-cell subsets in aging specimens [J].
Bergeron, M ;
Nicholson, JKA ;
Phaneuf, S ;
Ding, T ;
Soucy, N ;
Badley, AD ;
Foss, NCH ;
Mandy, F .
CYTOMETRY, 2002, 50 (02) :53-61
[3]   HYDROGEN-PEROXIDE AND THE PROLIFERATION OF BHK-21-CELLS [J].
BURDON, RH ;
ALLIANGANA, D ;
GILL, V .
FREE RADICAL RESEARCH, 1995, 23 (05) :471-486
[4]   Incorporation of sodium channel blocking and free radical scavenging activities into a single drug, AM-36, results in profound inhibition of neuronal apoptosis [J].
Callaway, JK ;
Beart, PM ;
Jarrott, B ;
Giardina, SF .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 132 (08) :1691-1698
[5]   Oxidative stress signalling in the apoptosis of jurkat T-lymphocytes [J].
Chiaramonte, R ;
Bartolini, E ;
Riso, P ;
Calzavara, E ;
Erba, D ;
Testolin, G ;
Comi, P ;
Sherbet, GV .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2001, 82 (03) :437-444
[6]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[7]   Inhibition of intestinal epithelial apoptosis and survival in a murine model of pneumonia-induced sepsis [J].
Coopersmith, CM ;
Stromberg, PE ;
Dunne, WM ;
Davis, CG ;
Amiot, DM ;
Buchman, TG ;
Karl, IE ;
Hotchkiss, RS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (13) :1716-1721
[8]   Oxidative damage to DNA in diabetes mellitus [J].
Dandona, P ;
Thusu, K ;
Cook, S ;
Snyder, B ;
Makowski, J ;
Armstrong, D ;
Nicotera, T .
LANCET, 1996, 347 (8999) :444-445
[9]   Chemotherapy: targeting the mitochondrial cell death pathway [J].
Debatin, KM ;
Poncet, D ;
Kroemer, G .
ONCOGENE, 2002, 21 (57) :8786-8803
[10]  
Decaudin D, 1998, INT J ONCOL, V12, P141