In order to observe the health effects of diesel exhaust, long-term inhalation experiments were carried out on F344 rats. The inhalation experiments consisted of a carcinogenicity test with emphasis on the respiratory system and a long-term inhalation test in which the health effects of diesel exhausts on rats were evaluated every six months from the start of inhalation.
LD and HD diesel engines were used in these tests and the engines were operated at a constant speed.
Experimental animals used for these tests were Fischer 344 rats (SPF), 5 weeks old. For the carcinogenicity and long-term inhalation tests, five experimental groups were used in the LD (2.3, 1.1, 0.4, 0.1 and 0 mg/m
3) and HD (3.7, 1.8, 1.0, 0.5 and 0mg/m
3) series, respectively. Each experimental group of rats consisted of 120 males and 95 females. The inhalations were carried out 16 hours a day, 6 days a week for 30 months at the longest. The living environments in the barrier were strictly controlled from the microbiological standpoint in order to protect animals from infection and other diseases. As the result, the average number of airborne bacteria in the barrier was less than 3 colonies per plate during the experimental period. Antibody-titers of specific pathogens were not detected at all. The results obtained from these experiments as follows:
(1) The survival rates of both sexes in all experimental groups after 30 months inhalation were in the range of 30%-40%.
(2) Diesel particles were histologically observed to be deposited mainly in the alveolar cavities in short duration and low particle concentration groups, but the degree of interstitial deposition increased gradually, with inhaled duration and particle concentration.
(3) The swelling of type II alveolar epithelium and the extension of respiratory bronchiole epithelium toward the alveolar ducts were caused by the anthracosis.
These hyperplastic lesions have a tendency to increase in relation to the particle concentrations and inhalation time, particularly, the focus of adenomatous hyperplasia which fused the each lesions observed in the high concentration and longer duration groups.
(4) All primary lung tumors observed in this test were epithelial tumors; nonepithelial tumors did not occur. Histological types of the carcinomas showed no particular tendencies.
(5) The incidence of lung tumors was low and showed a significant difference (P-0.05) between the 3.7mg/m
3 group and the control group in the HD series.
(6) No remarkable changes were seen in the trachea, the bronchi, the bronchial gland or the nasal cavity.Leukemia, breast tumors and other tumors were not significantly increased in the experimental groups compared with the control group after 30 months inhalation.
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