Abstract |
Nitrosocarbaryl, nitroso-N-methylurethane and nitroso-N-ethylurethane were administered by gavage in olive oil solution to groups of 12 female Sprague-Dawley rats. The dose was 0.2 ml of 0.11 M solution once a week for 10 weeks, a total dose of 0.22 mmol. The rats given nitrosocarbaryl survived longer, but had as high an incidence of tumors (75%) as did rats given nitrosomethylurethane. Most of the tumors induced were invasive squamous carcinomas of the stomach. Nitrosoethylurethane appeared to be a little more potent than nitrosomethylurethane; all 12 animals in this group had squamous stomach tumors at death. A higher total dose of nitrosocarbaryl, 1.3 mmol, given to male rats twice weekly for 20 weeks did not produce a higher incidence of stomach tumors than did thelower dose in females, although the males died earlier with tumors.
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Authors | W Lijinsky, H W Taylor |
Journal | Cancer letters
(Cancer Lett)
Vol. 1
Issue 5
Pg. 275-9
(May 1976)
ISSN: 0304-3835 [Print] Ireland |
PMID | 828074
(Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Nitrosamines
- Nitroso Compounds
- Urethane
- Nitrosomethylurethane
- nitrosocarbaryl
- Carbaryl
|
Topics |
- Administration, Oral
- Administration, Topical
- Animals
- Carbaryl
(administration & dosage, analogs & derivatives, toxicity)
- Carcinoma, Squamous Cell
(chemically induced)
- Female
- Neoplasms, Experimental
(chemically induced)
- Nitrosamines
- Nitroso Compounds
(administration & dosage, toxicity)
- Nitrosomethylurethane
(analogs & derivatives, toxicity)
- Rats
- Skin Neoplasms
(chemically induced)
- Stomach Neoplasms
(chemically induced)
- Urethane
(analogs & derivatives)
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