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Title: Pulmonary carcinogenesis in the F344 and Wistar rat after inhalation of plutonium dioxide

Abstract

Pulmonary carcinogenesis was compared in female F344 and Wistar rats after inhalation of high-fired {sup 239}PuO{sub 2}. Plutonium particle aggregation, as determined by quantitative light and scanning electron microscopic autoradiography, was greater for the F344 strain than for the Wistar strain. The median survival times were similar in control and low-dose (0.8-1.0 Gy) groups of both strains, but were significantly decreased in the high-dose (34-37 Gy) groups of both strains. Squamous metaplasia was not found in control or low-dose groups of either strain, but was found in 62-65% of high-dose groups of both strains. Adenomatous metaplasia was considerably higher in control and low-dose groups of F344 rats than in Wistar rats. A total of 87 lung tumors were found in 140 exposed F344 rats and 46 lung tumors in 176 exposed Wistar rats. The incidence of lung tumors in F344 rats was 1.7% in controls, 20% in the low-dose group and 82% in the high-dose group. The incidence of lung tumors in Wistar rats was 0.1% in controls, nil in the low-dose group and 68% in the high-dose group. The median survival times of rats of both strains in the high-dose groups that died with lung tumors were greater comparedmore » with rats in these groups that died without lung tumors. In contrast, these differences did not occur among rats in the low-dose groups. The absolute risk was 1900 lung tumors per 10{sup 4} Rat-Gy for F344 rats but about 210 lung tumors per 10{sup 4} Rat-Gy for high-dose groups of both strains. The adenomatous tumor phenotype predominated in the F344 strain, while the squamous tumor phenotype predominated in the Wistar strain. Risk of squamous tumors was similar for both strains. Overall, the F344 strain appears to be more {open_quotes}sensitive{close_quotes} than the Wistar strain to formation of lung tumors at low to moderate doses from inhaled {sup 239}PuO{sub 2}. 31 refs., 1 fig., 7 tabs.« less

Authors:
 [1];  [1]
  1. Inhalation Toxicology Research Institute, Albuquerque, NM (United States)
Publication Date:
Sponsoring Org.:
USDOE
OSTI Identifier:
183327
DOE Contract Number:  
AC06-76RL01830; AC04-76EV01013
Resource Type:
Journal Article
Journal Name:
Radiation Research
Additional Journal Information:
Journal Volume: 144; Journal Issue: 2; Other Information: PBD: Nov 1995
Country of Publication:
United States
Language:
English
Subject:
56 BIOLOGY AND MEDICINE, APPLIED STUDIES; PLUTONIUM DIOXIDE; CARCINOGENESIS; DOSE-RESPONSE RELATIONSHIPS; RATS; RADIOSENSITIVITY; COMPARATIVE EVALUATIONS; LUNGS; NEOPLASMS; AUTORADIOGRAPHY; INHALATION

Citation Formats

Sanders, C L, Washington State Univ./Tri-Cities, Richland, WA, Pacific Northwest Labs., Richland, WA, and Lundgren, D L. Pulmonary carcinogenesis in the F344 and Wistar rat after inhalation of plutonium dioxide. United States: N. p., 1995. Web. doi:10.2307/3579260.
Sanders, C L, Washington State Univ./Tri-Cities, Richland, WA, Pacific Northwest Labs., Richland, WA, & Lundgren, D L. Pulmonary carcinogenesis in the F344 and Wistar rat after inhalation of plutonium dioxide. United States. https://doi.org/10.2307/3579260
Sanders, C L, Washington State Univ./Tri-Cities, Richland, WA, Pacific Northwest Labs., Richland, WA, and Lundgren, D L. 1995. "Pulmonary carcinogenesis in the F344 and Wistar rat after inhalation of plutonium dioxide". United States. https://doi.org/10.2307/3579260.
@article{osti_183327,
title = {Pulmonary carcinogenesis in the F344 and Wistar rat after inhalation of plutonium dioxide},
author = {Sanders, C L and Washington State Univ./Tri-Cities, Richland, WA and Pacific Northwest Labs., Richland, WA and Lundgren, D L},
abstractNote = {Pulmonary carcinogenesis was compared in female F344 and Wistar rats after inhalation of high-fired {sup 239}PuO{sub 2}. Plutonium particle aggregation, as determined by quantitative light and scanning electron microscopic autoradiography, was greater for the F344 strain than for the Wistar strain. The median survival times were similar in control and low-dose (0.8-1.0 Gy) groups of both strains, but were significantly decreased in the high-dose (34-37 Gy) groups of both strains. Squamous metaplasia was not found in control or low-dose groups of either strain, but was found in 62-65% of high-dose groups of both strains. Adenomatous metaplasia was considerably higher in control and low-dose groups of F344 rats than in Wistar rats. A total of 87 lung tumors were found in 140 exposed F344 rats and 46 lung tumors in 176 exposed Wistar rats. The incidence of lung tumors in F344 rats was 1.7% in controls, 20% in the low-dose group and 82% in the high-dose group. The incidence of lung tumors in Wistar rats was 0.1% in controls, nil in the low-dose group and 68% in the high-dose group. The median survival times of rats of both strains in the high-dose groups that died with lung tumors were greater compared with rats in these groups that died without lung tumors. In contrast, these differences did not occur among rats in the low-dose groups. The absolute risk was 1900 lung tumors per 10{sup 4} Rat-Gy for F344 rats but about 210 lung tumors per 10{sup 4} Rat-Gy for high-dose groups of both strains. The adenomatous tumor phenotype predominated in the F344 strain, while the squamous tumor phenotype predominated in the Wistar strain. Risk of squamous tumors was similar for both strains. Overall, the F344 strain appears to be more {open_quotes}sensitive{close_quotes} than the Wistar strain to formation of lung tumors at low to moderate doses from inhaled {sup 239}PuO{sub 2}. 31 refs., 1 fig., 7 tabs.},
doi = {10.2307/3579260},
url = {https://www.osti.gov/biblio/183327}, journal = {Radiation Research},
number = 2,
volume = 144,
place = {United States},
year = {Wed Nov 01 00:00:00 EST 1995},
month = {Wed Nov 01 00:00:00 EST 1995}
}