Mutagenic and cytotoxic effect of planifolin:: A naphthopyranone dimer isolated from Paepalanthus planifolius

被引:13
作者
Varanda, EA
Varella, SD
Rampazo, RA
Kitagawa, RR
Raddi, MSG
Vilegas, W
dos Santos, LC
机构
[1] UNESP, Fac Pharmaceut Sci, Dept Biol Sci, Estadual Paulist Univ, BR-14801902 Araraquara, SP, Brazil
[2] UNESP, Fac Pharmaceut Sci, Dept Clin Anal, Estadual Paulist Univ, BR-14801902 Araraquara, SP, Brazil
[3] UNESP, Chem Inst Araraquara, Estadual Paulist Univ, BR-14801970 Araraquara, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
planifolin; mutagenicity; Salmonella typhimurium;
D O I
10.1016/j.tiv.2005.09.010
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
A naphthopyranone dimer, named planifolin, was isolated from a methylene chloride extract of the capitula of Paepalanthus planifolius Koern. The molecule (C31H26O10) appeared to be made up of two monomeric portions, semi-vioxanthin and paepalantine (an isocoumarin), linked by an ether bond, and it may possess several kinds of biological activity that can be related to its polyphenolic structure. Short-term tests that detect genetic damage can afford the information needed to evaluate carcinogenic risks of chemicals to humans. The Ames test, recommended for testing the mutagenicity of chemical compounds with potential pharmacological application, was used in the present study. The mutagenic activity was evaluated in Salmonella typhimurium strains TA100, TA98, TA102 and TA97a and the cytotoxic effect in McCoy cells. The in vitro cytotoxicity of planifolin to McCoy cells, tested in microculture with neutral red, showed a significant cytotoxic index (CI50) of 12.83 mu g/mL. Planifolin showed mutagenic activity for TA100, TA98 and TA97a. The results indicate that this new naphthopyranone dimer causes mutations by substitution and by addition and deletion of bases in the sequence of DNA. Moreover, its mutagenic potential was increased by metabolic activation. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:664 / 668
页数:5
相关论文
共 27 条
[1]   Metabolism of 20(S)- and 20(R)-ginsenoside Rg3 by human intestinal bacteria and its relation to in vitro biological activities [J].
Bae, EA ;
Han, MJ ;
Choo, MK ;
Park, SY ;
Kim, DH .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2002, 25 (01) :58-63
[2]  
BARILE FA, 1994, INTRO IN VITRO CYTOT
[3]  
BENNETT WM, 1990, UROL CLIN N AM, V17, P145
[4]   AN EMPIRICAL-APPROACH TO THE STATISTICAL-ANALYSIS OF MUTAGENESIS DATA FROM THE SALMONELLA TEST [J].
BERNSTEIN, L ;
KALDOR, J ;
MCCANN, J ;
PIKE, MC .
MUTATION RESEARCH, 1982, 97 (04) :267-281
[5]   TOXICITY DETERMINED INVITRO BY MORPHOLOGICAL ALTERATIONS AND NEUTRAL RED ABSORPTION [J].
BORENFREUND, E ;
PUERNER, JA .
TOXICOLOGY LETTERS, 1985, 24 (2-3) :119-124
[6]  
Devienne KF, 2002, Z NATURFORSCH C, V57, P85
[7]  
EINHORN L, 1979, CANC TREATMENT REPOR, V63, P659
[8]   ANTICANCER DRUGS - AN UNDERESTIMATED RISK OR AN UNDERUTILIZED RESOURCE IN MUTAGENESIS [J].
FERGUSON, LR ;
DENNY, WA .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1995, 331 (01) :1-26
[9]  
Frisch M.J., 1995, GAUSSIAN 94
[10]   BIOACTIVITY IN PLANTS - THE LINK BETWEEN PHYTOCHEMISTRY AND MEDICINE [J].
HAMBURGER, M ;
HOSTETTMANN, K .
PHYTOCHEMISTRY, 1991, 30 (12) :3864-3874