TY - JOUR
T1 - Alkylation of rat liver dna by dimethylnitrosamine
T2 - Effect of dosage on o6-methyiguanine levels
AU - Pegg, Anthony E.
N1 - Funding Information:
ABBREVIATION USED: DMN = dimethylnitrosamine. 1 Received April 19, 1976; accepted July 2, 1976. 2 Supported by Public Health Service grants CA18137 and CA18450 from the National Cancer Institute. 3 Department of Physiology and Specialized Cancer Research Center, The Milton S. Hershey Medical Center, The Pennsylvania State University, 500 University Drive, Hershey, Pa. 17033. 4 The author acknowledges the technical assistance of Ms. G. Hui.
PY - 1977/3
Y1 - 1977/3
N2 - Alkylation of liver DNA was studied following administration to Sprague-Dawley rats of doses of dimethylnitrosa-mine (DMN) varying from 0.25 to 20 mg/kg body weight. Measurements were made of the amounts of O6-methyiguanine and 7-methylguanine present in liver DNA at 4 and 24 hours after treatment with the carcinogen. There was a linear relationship between 7-methylguanine levels and dose of the nitrosamine at both of these times, in contrast, the corresponding levels of O6-methylguanine were not directly proportional to dosage but were less than expected, particularly at low doses below 2.5 mg/kg. This discrepancy was significant at 4 hours, but was even more marked at 24 hours. Only doses above 4 mg/kg at the 4-hour time point gave rise to a 0.11 ratio of alkylation of guanine at the O6-position to that at the 7-position. This ratio was that expected for the initial interaction of the alkylating species derived from DMN with DNA. Evidence was obtained to support the hypothesis that these results were due to an enzymatic removal of O6-methyl-guanine from liver DNA, which occurred much more efficiently at lower initial levels of alkylation. Repeated daily injections of DMN up to 11 days also gave rise to O6-methyiguanine levels that were not proportional to dosage but were relatively greater at higher dose levels. The significance of these findings in the induction of liver cancer by feeding or repeated injection of DMN was explored.
AB - Alkylation of liver DNA was studied following administration to Sprague-Dawley rats of doses of dimethylnitrosa-mine (DMN) varying from 0.25 to 20 mg/kg body weight. Measurements were made of the amounts of O6-methyiguanine and 7-methylguanine present in liver DNA at 4 and 24 hours after treatment with the carcinogen. There was a linear relationship between 7-methylguanine levels and dose of the nitrosamine at both of these times, in contrast, the corresponding levels of O6-methylguanine were not directly proportional to dosage but were less than expected, particularly at low doses below 2.5 mg/kg. This discrepancy was significant at 4 hours, but was even more marked at 24 hours. Only doses above 4 mg/kg at the 4-hour time point gave rise to a 0.11 ratio of alkylation of guanine at the O6-position to that at the 7-position. This ratio was that expected for the initial interaction of the alkylating species derived from DMN with DNA. Evidence was obtained to support the hypothesis that these results were due to an enzymatic removal of O6-methyl-guanine from liver DNA, which occurred much more efficiently at lower initial levels of alkylation. Repeated daily injections of DMN up to 11 days also gave rise to O6-methyiguanine levels that were not proportional to dosage but were relatively greater at higher dose levels. The significance of these findings in the induction of liver cancer by feeding or repeated injection of DMN was explored.
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U2 - 10.1093/jnci/58.3.681
DO - 10.1093/jnci/58.3.681
M3 - Article
C2 - 839563
AN - SCOPUS:0017356358
SN - 0027-8874
VL - 58
SP - 681
EP - 687
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 3
ER -