TY - JOUR
T1 - Chemopreventive properties of chlorophylls towards aflatoxin B1
T2 - A review of the antimutagenicity and anticarcinogenicity data in rainbow trout
AU - Dashwood, Roderick
AU - Negishi, Tomoe
AU - Hayatsu, Hikoya
AU - Breinholt, Vibeke
AU - Hendricks, Jerry
AU - Bailey, George
N1 - Funding Information:
The work reviewed here was supported in part by the following Public Health Service grants: CA65525, CA34732, ES03850 and ES00210.
PY - 1998/3/20
Y1 - 1998/3/20
N2 - The anticarcinogenic activity of chlorophyllin (CHL), a water-soluble derivative of chlorophyll, was first reported in rainbow trout. This review describes certain experiments which set the stage for long-term tumor bioassays, in trout and other species, using CHL and various food-borne carcinogens. Initial work with trout and rat liver enzymes in the Salmonella assay showed that CHL was a potent antimutagen towards heterocyclic amines, polycyclic aromatic hydrocarbons, aflatoxins and other classes of mutagen. Antimutagenic activity was further demonstrated using the corresponding direct-acting mutagens in the absence of an exogenous metabolizing system. Mutagen-inhibitor interaction (molecular complex formation) was identified in spectrophotometry studies, suggesting that CHL acts as an 'interceptor molecule'. In vivo, CHL reduced hepatic AFB1-DNA adducts and hepatocarcinogenesis when the inhibitor and carcinogen were co-administered in the diet. Finally, co-injection of inhibitor and AFB1 into trout embryos established that CHL was more effective than chlorophyll a in reducing AFB1- DNA adducts 2 weeks after injection, and liver tumors after 1 year.
AB - The anticarcinogenic activity of chlorophyllin (CHL), a water-soluble derivative of chlorophyll, was first reported in rainbow trout. This review describes certain experiments which set the stage for long-term tumor bioassays, in trout and other species, using CHL and various food-borne carcinogens. Initial work with trout and rat liver enzymes in the Salmonella assay showed that CHL was a potent antimutagen towards heterocyclic amines, polycyclic aromatic hydrocarbons, aflatoxins and other classes of mutagen. Antimutagenic activity was further demonstrated using the corresponding direct-acting mutagens in the absence of an exogenous metabolizing system. Mutagen-inhibitor interaction (molecular complex formation) was identified in spectrophotometry studies, suggesting that CHL acts as an 'interceptor molecule'. In vivo, CHL reduced hepatic AFB1-DNA adducts and hepatocarcinogenesis when the inhibitor and carcinogen were co-administered in the diet. Finally, co-injection of inhibitor and AFB1 into trout embryos established that CHL was more effective than chlorophyll a in reducing AFB1- DNA adducts 2 weeks after injection, and liver tumors after 1 year.
KW - Aflatoxin B1
KW - Anticarcinogen
KW - Chlorophyllin
KW - DNA adduct
KW - Heterocyclic amine
KW - Salmonella assay
KW - Trout
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U2 - 10.1016/S0027-5107(97)00259-5
DO - 10.1016/S0027-5107(97)00259-5
M3 - Article
C2 - 9672663
AN - SCOPUS:0032549474
SN - 0027-5107
VL - 399
SP - 245
EP - 253
JO - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
JF - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
IS - 2
ER -