Chelating and antioxidant activity of lignans from Chilean woods (Cupressaceae)

被引:25
作者
Donoso-Fierro, Cesar [1 ]
Becerra, Jose [1 ]
Bustos-Concha, Evelyn [1 ]
Silva, Mario [1 ]
机构
[1] Univ Concepcion, Fac Ciencias Nat & Oceanog, Dept Bot, Lab Quim Prod Nat, Concepcion, Chile
关键词
antioxidant; Austrocedrus chilensis; Cupressaceae; Fitzroya cupressoides; iron-chelating; lignans; natural durability; Pilgerodendron uviferum; NATURAL DURABILITY; POLYPHENOLS; PLANT; STILBENES; TANNINS;
D O I
10.1515/HF.2009.123
中图分类号
S7 [林业];
学科分类号
0829 ; 0907 ;
摘要
Wood species resistant to biodegradation by fungi contain phenolic compounds with proven fungicidal activity. Saprophytic fungi are able to colonize wood and later begin to break down its polymeric components through metal-dependent reactions. These generate free radicals at the onset of the degradation process. Later on, extracellular enzymes are active that use metallic cofactors. Five lignans were isolated from the methanolic extracts of the Chilean heartwoods (Austrocedrus chilensis, Fitzroya cupressoides, and Pilgerodendron uviferum) belonging to the Cupressaceae: isotaxiresinol, secoisolariciresinol, isolariciresinol, didemethylmatairesinol, and matairesinol. Their structures were determined spectroscopically. The antioxidant activity of the methanolic extracts and the isolated compounds was determined in vitro against the radical 1,1-diphenyl-2-picrylhydrazyl (DPPH) and their iron-chelating capacity was evaluated by the Chrome Azurol S assay. All isolated methanolic extracts and lignans exhibited antioxidant activity against DPPH and Fe-chelating capacity with values greater than 87%. This may be interpreted that the antioxidant properties and metal-chelating capacity of these compounds have a protective effect on the wood of these species when exposed to attacks by saprophytic fungi.
引用
收藏
页码:559 / 563
页数:5
相关论文
共 41 条
[1]   Iron-chelation properties of phenolic acids bearing catechol and galloyl groups [J].
Andjelkovic, M ;
Van Camp, J ;
De Meulenaer, B ;
Depaemelaere, G ;
Socaciu, C ;
Verloo, M ;
Verhe, R .
FOOD CHEMISTRY, 2006, 98 (01) :23-31
[2]  
Ayres D. C., 1990, LIGNANS CHEM BBIOLOG
[3]   HYDROXYL RADICAL ACTIVITY IN BROWN-ROT FUNGI STUDIED BY A NEW CHEMILUMINESCENCE METHOD [J].
BACKA, S ;
GIERER, J ;
REITBERGER, T ;
NILSSON, T .
HOLZFORSCHUNG, 1992, 46 (01) :61-67
[4]  
Banskota AH, 2003, PLANTA MED, V69, P500, DOI 10.1055/s-2003-40641
[5]   Structure-radical scavenging activity relationships of phenolic compounds from traditional Chinese medicinal plants [J].
Cai, Yi-Zhong ;
Sun, Mei ;
Xing, Jie ;
Luo, Qiong ;
Corke, Harold .
LIFE SCIENCES, 2006, 78 (25) :2872-2888
[6]  
Cassidy A, 2000, J SCI FOOD AGR, V80, P1044, DOI 10.1002/(SICI)1097-0010(20000515)80:7<1044::AID-JSFA586>3.3.CO
[7]  
2-E
[8]   Antiviral activity of lignans [J].
Charlton, JL .
JOURNAL OF NATURAL PRODUCTS, 1998, 61 (11) :1447-1451
[9]   Tannins and human health: A review [J].
Chung, KT ;
Wong, TY ;
Wei, CI ;
Huang, YW ;
Lin, Y .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1998, 38 (06) :421-464
[10]  
Cooper-Driver GA, 1998, PHYTOCHEMISTRY, V49, P1165, DOI 10.1016/S0031-9422(98)00054-5