Inhibition and induction of glutathione S-transferases by flavonoids: possible pharmacological and toxicological consequences

被引:54
作者
Bousova, Iva [1 ]
Skalova, Lenka [1 ]
机构
[1] Charles Univ Prague, Fac Pharm, Dept Biochem Sci, CZ-50005 Hradec Kralove, Czech Republic
关键词
GST; drug-flavonoid interaction; dietary supplement; cytostatics; detoxification; ANTIOXIDANT-RESPONSE ELEMENT; DRUG-METABOLIZING-ENZYMES; INDUCED OXIDATIVE STRESS; PHASE-II ENZYMES; RAT-LIVER; BREAST-CANCER; GREEN TEA; GASTROINTESTINAL GLUTATHIONE; STRUCTURAL-CHARACTERIZATION; INDUCED HEPATOTOXICITY;
D O I
10.3109/03602532.2012.713969
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Many studies reviewed herein demonstrated the potency of some flavonoids to modulate the activity and/or expression of glutathione S-transferases (GSTs). Because GSTs play a crucial role in the detoxification of xenobiotics, their inhibition or induction may significantly affect metabolism and biological effects of many drugs, industrials, and environmental contaminants. The effect of flavonoids on GSTs strongly depends on flavonoid structure, concentration, period of administration, as well as on GST isoform and origin. Moreover, the results obtained in vitro are often contrary to the vivo results. Based on these facts, the revelation of important flavonoid-drug or flavonoid-pollutant interaction has been complicated. However, it should be borne in mind that ingestion of certain flavonoids in combination with drugs or pollutants (e.g., acetaminophen, simvastatin, cyclophosphamide, cisplatine, polycyclic aromatic hydrocarbons, chlorpyrifos, acrylamide, and isocyanates), which are GST substrates, could have significant pharmacological and toxicological consequences. Although reasonable consumptions of a flavonoids-rich diet (that may lead to GST induction) are mostly beneficial, the uncontrolled intake of high concentrations of certain flavonoids (e.g., quercetin and catechins) in dietary supplements (that may cause GST inhibition) may threaten human health.
引用
收藏
页码:267 / 286
页数:20
相关论文
共 187 条
[1]   CHARACTERIZATION AND LOCALIZATION OF GLUTATHIONE-S-TRANSFERASES IN RAT-BRAIN AND BINDING OF HORMONES, NEUROTRANSMITTERS, AND DRUGS [J].
ABRAMOVITZ, M ;
HOMMA, H ;
ISHIGAKI, S ;
TANSEY, F ;
CAMMER, W ;
LISTOWSKY, I .
JOURNAL OF NEUROCHEMISTRY, 1988, 50 (01) :50-57
[2]   Regulation of JNK signaling by GSTp [J].
Adler, V ;
Yin, ZM ;
Fuchs, SY ;
Benezra, M ;
Rosario, L ;
Tew, KD ;
Pincus, MR ;
Sardana, M ;
Henderson, CJ ;
Wolf, CR ;
Davis, RJ ;
Ronai, Z .
EMBO JOURNAL, 1999, 18 (05) :1321-1334
[3]   Dietary flavonols: Chemistry, food content, and metabolism [J].
Aherne, SA ;
O'Brien, NM .
NUTRITION, 2002, 18 (01) :75-81
[4]  
Ahmad H, 2006, ACS SYM SER, V936, P130
[5]   Inhibition of Filarial Glutathione-S-transferase by various classes of compounds and their evaluation as novel antifilarial agents [J].
Ahmad, R. ;
Srivastava, A. K. .
HELMINTHOLOGIA, 2008, 45 (03) :114-120
[6]   In vitro and in vivo regulation of antioxidant response element-dependent gene expression by estrogens [J].
Ansell, PJ ;
Espinosa-Nicholas, C ;
Curran, EM ;
Judy, BM ;
Philips, BJ ;
Hannink, M ;
Lubahn, DB .
ENDOCRINOLOGY, 2004, 145 (01) :311-317
[7]   In-vitro effect of flavonoids from Solidago canadensis extract on glutathione S-transferase [J].
Apáti, P ;
Houghton, PJ ;
Kite, G ;
Steventon, GB ;
Kéry, A .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2006, 58 (02) :251-256
[8]   Soy induces phase II enzymes but does not inhibit dimethylbenz[a]anthracene-induced carcinogenesis in female rats [J].
Appelt, LC ;
Reicks, MM .
JOURNAL OF NUTRITION, 1999, 129 (10) :1820-1826
[9]   Structure, catalytic mechanism, and evolution of the glutathione transferases [J].
Armstrong, RN .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (01) :2-18
[10]  
Artali R, 2009, J ENZYM INHIB MED CH, V24, P287, DOI [10.1080/14756360802177282, 10.1080/14756360802177282 ]