Chemical properties of catechols and their molecular modes of toxic action in cells, from microorganisms to mammals

被引:477
作者
Schweigert, N
Zehnder, AJB
Eggen, RIL [1 ]
机构
[1] Swiss Fed Inst Environm Sci & Technol, CH-8600 Dubendorf, Switzerland
[2] Swiss Fed Inst Technol, CH-8600 Dubendorf, Switzerland
关键词
D O I
10.1046/j.1462-2920.2001.00176.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Catechols can undergo a variety of chemical reactions. In this review, we particularly focus on complex formations and the redox chemistry of catechols, which play an inportant role in the toxicity of catechols, In the presence of heavy metals, such as iron or copper, stable complexes can be formed. In the presence of oxidizing agents, catechols can be oxidized to semiquinone radicals and in a next step to o-benzoquinones. Heavy metals may catalyse redox reactions in which catechols are involved. Further chemical properties like the acidity constant and the lipophilicity of different catechols are shortly described as well. As a consequence of the chemical properties and the chemical reactions of catechols, many different reactions can occur with biomolecules such as DNA, proteins and membranes, ultimately leading to non-repairable damage. Reactions with nucleic acids such as adduct formation and strand breaks are discussed among others. Interactions with proteins causing protein and enzyme inactivation are described. The membrane-catechol interactions discussed here are lipid peroxidation and uncoupling. The deleterious effect of the interactions between catechols and the different biomolecules is discussed in the context of the observed toxicities, caused by catechols.
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收藏
页码:81 / 91
页数:11
相关论文
共 84 条
[1]   Estrogen-nucleic acid adducts: Reaction of 3,4-estrone o-quinone with nucleic acid bases [J].
Akanni, A ;
Tabakovic, K ;
AbulHajj, YJ .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (04) :477-481
[2]   Estrogen nucleic acid adducts: Reaction of 3,4-estrone-o-quinone radical anion with deoxyribonucleosides [J].
Akanni, A ;
AbulHajj, YJ .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (07) :760-766
[3]  
Anders MW, 1985, BIOACTIVATION FOREIG, P259
[4]  
Anderson NE, 1979, NEUROBIOLOGY DOPAMIN, P1
[5]  
[Anonymous], 1981, LIGNIN BIODEGRADATIO
[6]  
ATCHISON M, 1982, JNCI-J NATL CANCER I, V69, P503
[7]   COORDINATION CHEMISTRY OF MICROBIAL IRON TRANSPORT COMPOUNDS .9. STABILITY-CONSTANTS FOR CATECHOL MODELS OF ENTEROBACTIN [J].
AVDEEF, A ;
SOFEN, SR ;
BREGANTE, TL ;
RAYMOND, KN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1978, 100 (17) :5362-5370
[8]   IRREVERSIBLE BINDING OF ETHYNYL-ESTRADIOL METABOLITES TO PROTEIN AND NUCLEIC-ACIDS AS CATALYZED BY RAT-LIVER MICROSOMES AND MUSHROOM TYROSINASE [J].
BOLT, HM ;
KAPPUS, H .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1974, 5 (02) :179-184
[9]   Role of quinoids in estrogen carcinogenesis [J].
Bolton, JL ;
Pisha, E ;
Zhang, FG ;
Qiu, SX .
CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (10) :1113-1127
[10]  
Boyd EM, 1997, ENVIRON TOXICOL CHEM, V16, P849, DOI [10.1002/etc.5620160503, 10.1897/1551-5028(1997)016&lt