Abstract
Long term inhalation studies and intraperitoneal injection studies in rats were undertaken with a series of chrysotile asbestos dusts. Three dust samples were generated from chrysotile modified by the wet dispersion process (WDC) and one was from unmodified chrysotile. Following a 1 year inhalation period, all the chrysotile samples proved extremely fibrogenic and carcinogenic and there were no significant differences between the WDC dusts and normal chrysotile. In all experimental groups approximately 25% of animals developed pulmonary carcinomas and in the oldest rats advanced interstitial fibrosis occupied on average 10% of all lung tissue. In the injection studies all the dust samples produced mesotheliomas in over 90% of animals. Very little chrysotile remained in the lungs of the animals that survived longest following dust inhalation and what there was was present as individual chrysotile fibrils. It is suggested that chrysotile is potentially the most harmful variety of asbestos as shown in these and other animal studies but that it is removed from lung tissue quite rapidly. In the long lived human species this may mean that except where exposure levels are very high and of long duration, chrysotile should be less hazardous than other asbestos types.
Full text
PDF
















Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bolton R. E., Davis J. M., Donaldson K., Wright A. Variations in the carcinogenicity of mineral fibres. Ann Occup Hyg. 1982;26(1-4):569–582. [PubMed] [Google Scholar]
- Davis J. M., Beckett S. T., Bolton R. E., Collings P., Middleton A. P. Mass and number of fibres in the pathogenesis of asbestos-related lung disease in rats. Br J Cancer. 1978 May;37(5):673–688. doi: 10.1038/bjc.1978.105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gylseth B., Mowé G., Wannag A. Fibre type and concentration in the lungs of workers in an asbestos cement factory. Br J Ind Med. 1983 Nov;40(4):375–379. doi: 10.1136/oem.40.4.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Middleton A. P., Beckett S. T., Davis J. M. Further observations on the short-term retention and clearance of asbestos by rats, using UICC reference samples. Ann Occup Hyg. 1979;22(2):141–152. doi: 10.1093/annhyg/22.2.141. [DOI] [PubMed] [Google Scholar]
- Stanton M. F., Laynard M., Tegeris A., Miller E., May M., Kent E. Carcinogenicity of fibrous glass: pleural response in the rat in relation to fiber dimension. J Natl Cancer Inst. 1977 Mar;58(3):587–603. doi: 10.1093/jnci/58.3.587. [DOI] [PubMed] [Google Scholar]
- Wagner J. C., Berry G., Skidmore J. W., Timbrell V. The effects of the inhalation of asbestos in rats. Br J Cancer. 1974 Mar;29(3):252–269. doi: 10.1038/bjc.1974.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wagner J. C., Berry G., Timbrell V. Mesotheliomata in rats after inoculation with asbestos and other materials. Br J Cancer. 1973 Aug;28(2):173–185. doi: 10.1038/bjc.1973.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walton W. H., Beckett S. T. A microscope eyepiece graticule for the evaluation of fibrous dusts. Ann Occup Hyg. 1977 Jul;20(1):19–23. doi: 10.1093/annhyg/20.1.19. [DOI] [PubMed] [Google Scholar]
- Weill H., Hughes J., Waggenspack C. Influence of dose and fiber type on respiratory malignancy risk in asbestos cement manufacturing. Am Rev Respir Dis. 1979 Aug;120(2):345–354. doi: 10.1164/arrd.1979.120.2.345. [DOI] [PubMed] [Google Scholar]