DNA damage and aberrant crypt foci as putative biomarkers to evaluate the chemopreventive effect of annatto (Bixa orellana L.) in rat colon carcinogenesis

被引:43
作者
Agner, AR [1 ]
Bazo, AP [1 ]
Ribeiro, LR [1 ]
Salvadori, DMF [1 ]
机构
[1] Univ Estadual Paulista, UNESP, Fac Med, Dept Patol,TOXICAN,Nucleo Avaliacao Toxicgenet &, BR-18618 Botucatu, SP, Brazil
关键词
aberrant crypt foci; annatto; chemoprevention; comet assay dimethylhidrazine;
D O I
10.1016/j.mrgentox.2005.01.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chemoprevention opens new perspectives in the prevention of cancer and other degenerative diseases. Use of target-organ biological models at the histological and genetic levels can markedly facilitate the identification of such potential chemopreventive agents. Colon cancer is one of the highest incidence rates throughout the world and some evidences have indicated carotenoids as possible agents that decrease the risk of colorectal cancer. In the present study, we evaluate the activity of annatto (Bixa orellaria L.), a natural food colorant rich in carotenoid, on the formation of aberrant crypt foci (ACF) induced by dimethy1hydrazine (DMH) in rat colon. Further, we investigate, the effect of annatto on DMH-induced DNA damage, by the comet assay. Male Wistar rats were given s.c. injections of DMH (40 mg/kg body wt.) twice a week for 2 weeks to induce ACE They also received experimental diets containing annatto at 20, 200 or 1000 ppm for five 5 weeks before (pre-treatment), or 10 weeks after (post-treatment) DMH treatment. In both protocols the rats were sacrificed on week 15th. For the comet assay, the animals were fed with the same experimental diets for 2 weeks. Four hours before the sacrifice, the animals received an s.c. injection of DMH (40 mg/kg body wt.). Under such conditions, dietary administration of 1000 ppm annatto neither induce DNA damage in blood and colon cells nor aberrant crypt foci in rat distal colon. Conversely, annatto was successful in inhibiting the number of crypts/colon (animal), but not in the incidence of DMH-induced ACF, mainly when administered after DMH. However, no antigenotoxic effect was observed in colon cells. These findings suggest possible chemopreventive effects of annatto through their modulation of the cryptal cell proliferation but not at the initiation stage of colon carcinogenesis. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 154
页数:9
相关论文
共 41 条
  • [1] Protective action of propolis on the rat colon carcinogenesis
    Bazo, AP
    Rodrigues, MAM
    Sforcin, JM
    de Camargo, JLV
    Ribeiro, LR
    Salvadori, DMF
    [J]. TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS, 2002, 22 (03): : 183 - 194
  • [2] The second National Toxicology Program comparative exercise on the prediction of rodent carcinogenicity: definitive results
    Benigni, R
    Zito, R
    [J]. MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2004, 566 (01) : 49 - 63
  • [3] OBSERVATION AND QUANTIFICATION OF ABERRANT CRYPTS IN THE MURINE COLON TREATED WITH A COLON CARCINOGEN - PRELIMINARY FINDINGS
    BIRD, RP
    [J]. CANCER LETTERS, 1987, 37 (02) : 147 - 151
  • [4] ROLE OF ABERRANT CRYPT FOCI IN UNDERSTANDING THE PATHOGENESIS OF COLON-CANCER
    BIRD, RP
    [J]. CANCER LETTERS, 1995, 93 (01) : 55 - 71
  • [5] Study on the mutagenicity and antimutagenicity of a natural food colour (annatto) in mouse bone marrow cells
    de Lima, ROA
    Azevedo, L
    Ribeiro, LR
    Salvadori, DMF
    [J]. FOOD AND CHEMICAL TOXICOLOGY, 2003, 41 (02) : 189 - 192
  • [6] Induction of liver monooxygenases by annatto and bixin in female rats
    De-Oliveira, ACAX
    Silva, IB
    Manhaes-Rocha, DA
    Paumgartten, FJR
    [J]. BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2003, 36 (01) : 113 - 118
  • [7] DI MASCIO P, 1990, BIOCHEM SOC T, V18, P1054
  • [8] Aberrant crypt foci: A review
    Fenoglio-Preiser, CM
    Noffsinger, A
    [J]. TOXICOLOGIC PATHOLOGY, 1999, 27 (06) : 632 - 642
  • [9] Norbixin ingestion did not induce any detectable DNA breakage in liver and kidney but caused a considerable impairment in plasma glucose levels of rats and mice
    Fernandes, ACS
    Almeida, CA
    Albano, F
    Laranja, GAT
    Felzenszwalb, I
    Lage, CLS
    de Sa, CCNF
    Moura, AS
    Kovary, K
    [J]. JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2002, 13 (07) : 411 - 420
  • [10] Chemoprevention of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-induced colon carcinogenesis by 1-O-hexyl-2,3,5-trimethylhydroquinone after initiation with 1,2-dimethylhydrazine in F344 rats
    Futakuchi, M
    Hirose, M
    Imaida, K
    Takahashi, S
    Ogawa, K
    Asamoto, M
    Miki, T
    Shirai, T
    [J]. CARCINOGENESIS, 2002, 23 (02) : 283 - 287