Antioxidant and antimutagenic activity of N-(2-carboxyethyl)chitosan

被引:89
作者
Kogan, G
Skorik, YA
Zitnanová, I
Krizková, L
Duracková, Z
Gomes, CAR
Yatluk, YG
Krajcovic, J
机构
[1] Slovak Acad Sci, Inst Chem, Ctr Excellence CEDEBIPO, SK-84538 Bratislava, Slovakia
[2] Univ Porto, Fac Ciencias, LAQUIPAI, Oporto, Portugal
[3] Urals State Univ, Dept Chem, Ekaterinburg, Russia
[4] Comenius Univ, Fac Med, Inst Med Chem Biochem & Clin Biochem, Bratislava, Slovakia
[5] Comenius Univ, Inst Cell Biol, Fac Nat Sci, Bratislava, Slovakia
[6] Russian Acad Sci, Inst Organ Synth, Urals Div, Ekaterinburg, Russia
关键词
carboxyethylation; chitosan; Euglena gracilis; ofloxacin; acridine orange; antioxidant; antimutagenicity;
D O I
10.1016/j.taap.2004.05.009
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The antioxidant and antimutagenic activities of the novel carboxyethyl derivatives of chitosan with three different degrees of substitution have been assayed in vitro in the unicellular flagellate Euglena gracilis subjected to the action of genotoxic agents acridine orange and ofloxacin. It has been demonstrated that chitosan derivatives exhibit concentration-dependent protective antigenotoxic activity against both mutagens. It is suggested that different mechanisms may be involved in its protective action-antioxidant activity in case of ofloxacin-induced DNA damage, as well as possible interaction with the cell membrane that prevents acridine orange from reaching the genetic compartments and subsequent damaging DNA through intercalative binding. Direct adsorption of acridine orange on chitosan derivatives was ruled out as a possible mechanism of protection on the basis of spectrophotometric measurements. Dependence of the antimutagenic proper-ties of the studied chitosan derivatives on the degree of substitution was reversed in experiments involving acridine orange and ofloxacin. which also indicated different mechanisms of protection involved in these two cases. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:303 / 310
页数:8
相关论文
共 49 条
[1]
AMINO AND CARBOXY TERMINAL SEQUENCES OF THE DNA-BINDING PROTEIN HU FROM THE CYANOBACTERIUM SYNECHOCYSTIS PCC-6701 (ATCC-27170) [J].
AITKEN, A ;
ROUVIEREYANIV, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1979, 91 (02) :461-467
[2]
Antioxidant capacity of reaction products limits the applicability of the Trolox Equivalent Antioxidant Capacity (TEAC) assay [J].
Arts, MJTJ ;
Haenen, GRMM ;
Voss, HP ;
Bast, A .
FOOD AND CHEMICAL TOXICOLOGY, 2004, 42 (01) :45-49
[3]
SIMILARITY BETWEEN THE BACTERIAL HISTONE-LIKE PROTEIN HU AND A PROTEIN FROM SPINACH-CHLOROPLASTS [J].
BRIAT, JF ;
LETOFFE, S ;
MACHE, R ;
ROUVIEREYANIV, J .
FEBS LETTERS, 1984, 172 (01) :75-79
[4]
CHARACTERIZATION OF A HISTONE-LIKE PROTEIN EXTRACTED FROM YEAST MITOCHONDRIA [J].
CARON, F ;
JACQ, C ;
ROUVIEREYANIV, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (09) :4265-4269
[5]
Evaluation of the biological properties of soluble chitosan and chitosan microspheres [J].
CarrenoGomez, B ;
Duncan, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 148 (02) :231-240
[6]
GROWTH AND PHOTOSYNTHETIC CHARACTERISTICS OF EUGLENA GRACILIS [J].
CRAMER, M ;
MYERS, J .
ARCHIV FUR MIKROBIOLOGIE, 1952, 17 (04) :384-402
[7]
SEPARATION OF CELIAC-ACTIVE PEPTIDES FROM BREAD WHEAT WITH THE AID OF METHYLPYRROLIDINONE CHITOSAN [J].
DEVINCENZI, M ;
DESSI, MR ;
MUZZARELLI, RAA .
CARBOHYDRATE POLYMERS, 1993, 21 (04) :295-298
[8]
Durackova Z, 1998, FREE RADICALS ANTIOX
[9]
Antimutagens reduce ofloxacin-induced bleaching in Euglena gracilis [J].
Ebringer, L ;
Dobias, J ;
Krajcovic, J ;
Polonyi, J ;
Krizkova, L ;
Lahitova, N .
MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS, 1996, 359 (02) :85-93
[10]
Studies on applications of chitin and its derivatives [J].
Felse, PA ;
Panda, T .
BIOPROCESS ENGINEERING, 1999, 20 (06) :505-512