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1.
Food Chem Toxicol ; 47(7): 1521-9, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19358871

ABSTRACT

Drinking hot maté has been associated with risk for esophageal cancer in South America. Thus, the aims of this study were to evaluate the modifying effects of maté intake on DNA damage and esophageal carcinogenesis induced by diethylnitrosamine (DEN) and thermal injury (TI) in male Wistar rats. At the initiation phase of carcinogenesis, rats were treated with DEN (8 x 80 mg/kg) and submitted to TI (water at 65 degrees C, 1 ml/rat, instilled into the esophagus). Concomitantly, the animals received maté (2.0%w/v) for 8 weeks. Samples of peripheral blood were collected 4h after the last DEN application for DNA damage analysis. At weeks 8 and 20, samples from esophagus and liver were also collected for histological and immunohistochemical analysis. Maté significantly decreased DNA damage in leukocytes, cell proliferation rates in both esophagus and liver and the number of preneoplastic liver lesions from DEN/TI-treated animals at week 8. A significant lower incidence of esophageal papillomas and liver adenomas and tumor multiplicity was observed in the animals previously treated with maté at week 20. Thus, maté presented protective effects against DNA damage and esophageal and liver carcinogenesis induced by DEN.


Subject(s)
Anticarcinogenic Agents , Aquifoliaceae/chemistry , Burns/complications , DNA Damage , Diethylnitrosamine/antagonists & inhibitors , Esophageal Neoplasms/prevention & control , Esophagus/injuries , Protective Agents , Animals , Aspartate Aminotransferases/blood , Beverages , Body Weight/drug effects , Burns/pathology , Caffeine/pharmacology , Comet Assay , Diethylnitrosamine/toxicity , Esophageal Neoplasms/pathology , Glutathione Peroxidase/metabolism , Immunohistochemistry , Leukocytes/drug effects , Leukocytes/pathology , Leukocytes/ultrastructure , Male , Organ Size/drug effects , Proliferating Cell Nuclear Antigen/analysis , Rats , Rats, Wistar , Tea
2.
Food Chem Toxicol ; 41(11): 1543-50, 2003 Nov.
Article in English | MEDLINE | ID: mdl-12963007

ABSTRACT

The chemopreventive potential of an Agaricus blazei (Ab) Murrill mushroom meal was investigated in a medium-term rat liver carcinogenesis assay. Male Wistar rats initiated for hepatocarcinogenesis with diethylnitrosamine (DEN, 200 mg/kg i.p.) were fed during a 6-week period with the dry powdered mushroom strains Ab 29 or 26, each one with opened (OB) or closed basidiocarp (CB), mixed at 10% level in a basal diet. All experimental animals and controls were subjected to partial hepatectomy at week 3 and killed at week 8. Chemopreventive activity of the mushroom meal was observed for the Ab 29 (OB and CB) and Ab 26 (CB) strains in terms of the number of putative preneoplastic altered foci of hepatocytes which express either the enzyme glutathione S-transferase, placental form (GST-P+) or the transforming growth factor-alpha, and for the Ab 29 (OB) and Ab 26 (CB) strains on the size of GST-P+ foci. This was associated with inhibition of foci cell proliferation in the animals fed the Ab 29 (OB) and Ab 26 (CB) strains. The results suggest that the protective influence of the Ab meal against the DEN potential for rat liver carcinogenicity depends on both the strain and period of mushroom harvest.


Subject(s)
Agaricus/chemistry , Anticarcinogenic Agents/pharmacology , Liver Neoplasms, Experimental/prevention & control , Precancerous Conditions/prevention & control , Animals , Anticarcinogenic Agents/chemistry , Body Weight/drug effects , Carcinogens/antagonists & inhibitors , Carcinogens/toxicity , Diet , Diethylnitrosamine/antagonists & inhibitors , Diethylnitrosamine/toxicity , Eating , Glutathione Peroxidase/metabolism , Immunohistochemistry , Liver/drug effects , Liver/enzymology , Liver/pathology , Liver Neoplasms, Experimental/chemically induced , Male , Organ Size/drug effects , Precancerous Conditions/chemically induced , Proliferating Cell Nuclear Antigen/metabolism , Rats , Rats, Wistar , Transforming Growth Factor alpha/metabolism , Weight Gain/drug effects
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