TY - JOUR
T1 - Effect of chronic dietary ethanol consumption on colonic cancer in rats induced by 1,1-dimethylhydrazine
AU - Hayashi, Nobuhiko
AU - Tsutsumi, Mikihiro
AU - Fukura, Masayuki
AU - Yano, Hirokazu
AU - Tsuchishima, Mutsumi
AU - Takase, Shujiro
PY - 2007/1
Y1 - 2007/1
N2 - Background: The pathogenetic correlation between chronic alcohol consumption and development of colon cancer is not clear. The role of alcohol abuse in the carcinogenic action of 1,1-dimethylhydrazine (DMH), which induces tumors in the colon, was evaluated. Methods: Twenty male rats were fed liquid diets containing ethanol or carbohydrates for 39 weeks. DMH (20 mg/kg body weight, once a week) was injected subcutaneously from the 5th to the 20th week. Pair feeding was stopped at 10:00 am and DMH was administered at 02:00 pm. Ethanol was not detected in the blood at the time of injection. Liquid diets were provided again at 05:00 pm until 10:00 am next day. The animals were killed at the end of the 39th week, and the colons were removed for examination for the number of aberrant crypt foci (ACF) by methylene blue staining. Tissue sections were stained for histology and cytochrome P4502E1 (CYP2E1) expression. Results: The number of ACF in colons obtained from ethanol-fed rats with DMH was 24 (n=5, 4.4±2.5/rat), which was significantly (p<0.001) more than that of the other treated rats: only 3 (n=5, 0.6±0.5/rat) in the pair-fed control rats with DMH, and none in the ethanol-fed or control-fed rats without DMH. Cytochrome P4502E1 staining demonstrated marked expression in the colon mucosa from ethanol-fed rats, but not in the pair-fed control rats. Conclusions: The increased expression of CYP2E1 induced by chronic ethanol consumption promotes the development of DMH-induced colon cancer.
AB - Background: The pathogenetic correlation between chronic alcohol consumption and development of colon cancer is not clear. The role of alcohol abuse in the carcinogenic action of 1,1-dimethylhydrazine (DMH), which induces tumors in the colon, was evaluated. Methods: Twenty male rats were fed liquid diets containing ethanol or carbohydrates for 39 weeks. DMH (20 mg/kg body weight, once a week) was injected subcutaneously from the 5th to the 20th week. Pair feeding was stopped at 10:00 am and DMH was administered at 02:00 pm. Ethanol was not detected in the blood at the time of injection. Liquid diets were provided again at 05:00 pm until 10:00 am next day. The animals were killed at the end of the 39th week, and the colons were removed for examination for the number of aberrant crypt foci (ACF) by methylene blue staining. Tissue sections were stained for histology and cytochrome P4502E1 (CYP2E1) expression. Results: The number of ACF in colons obtained from ethanol-fed rats with DMH was 24 (n=5, 4.4±2.5/rat), which was significantly (p<0.001) more than that of the other treated rats: only 3 (n=5, 0.6±0.5/rat) in the pair-fed control rats with DMH, and none in the ethanol-fed or control-fed rats without DMH. Cytochrome P4502E1 staining demonstrated marked expression in the colon mucosa from ethanol-fed rats, but not in the pair-fed control rats. Conclusions: The increased expression of CYP2E1 induced by chronic ethanol consumption promotes the development of DMH-induced colon cancer.
KW - 1,1-Dimethylhydrazine
KW - CYP2E1
KW - Chronic Alcohol Consumption
KW - Colon Cancer
UR - http://www.scopus.com/inward/record.url?scp=33846272367&partnerID=8YFLogxK
U2 - 10.1111/j.1530-0277.2006.00290.x
DO - 10.1111/j.1530-0277.2006.00290.x
M3 - 学術論文
C2 - 17331170
AN - SCOPUS:33846272367
SN - 0145-6008
VL - 31
SP - 72S-76S
JO - Alcoholism: Clinical and Experimental Research
JF - Alcoholism: Clinical and Experimental Research
IS - SUPPL. 1
ER -
