Comparison of Calidria chrysotile asbestos to pure tremolite: inhalation biopersistence and histopathology following short-term exposure
- PMID: 14648356
- DOI: 10.1080/08958370390248888
Comparison of Calidria chrysotile asbestos to pure tremolite: inhalation biopersistence and histopathology following short-term exposure
Abstract
The differences between chrysotile asbestos, a serpentine mineral, and amphibole asbestos have been debated extensively. Many studies have shown that chrysotile is cleared from the lung more rapidly than amphibole. In order to quantify the comparative clearance of chrysotile and the amphibole asbestos tremolite, both fibers were evaluated in an inhalation biopersistence study that followed the European Commission recommended guidelines. In addition, the histopathological response in the lung was evaluated following the short-term exposure. This article presents the results of this study through 90 days after cessation of exposure. Following the termination of the study, a subsequent article will provide the complete results through 12 mo after cessation of exposure. In order to quantify the dynamics and rate by which these fibers are removed from the lung, the biopersistence of a sample of commercial grade chrysotile from the Coalinga mine in New Idria, CA, of the type Calidria RG144 and of a long-fiber tremolite were studied. For synthetic vitreous fibers, the biopersistence of the fibers longer than 20 microm has been found to be directly related to their potential to cause disease. This study was designed to determine lung clearance (biopersistence) and the histopathological response. As the long fibers have been shown to have the greatest potential for pathogenicity, the aerosol generation technique was designed to maximize the number of long respirable fibers. The chrysotile samples were specifically chosen to have 200 fibers/cm3 longer than 20 microm in length present in the exposure aerosol. These longer fibers were found to be largely composed of multiple shorter fibrils. The tremolite samples were chosen to have 100 fibers/cm3 longer than 20 microm in length present in the exposure aerosol. Calidria chrysotile fibers clear from the lung more rapidly (T1/2, fibers L > 20 microm = 7 h) than any other commercial fiber tested including synthetic vitreous fibers. With such rapidly clearing fibers, the 5-day exposure would not be expected to result in any pathological change in the lung, and the lungs of animals that inhaled Calidria chrysotile showed no sign of inflammation or pathology and were no different than the lungs of those animals that breathed filtered air. Following this 5-day exposure to tremolite, the tremolite fibers once deposited in the lung parenchyma do not clear and almost immediately result in inflammation and a pathological response in the lung. At the first time point examined, 1 day after cessation of exposure, inflammation was observed and granulomas were already formed. By 14 days postexposure these microgranulomas had turned fibrotic, and by 90 days postexposure the severity of the collagen deposits had increased and interstitial fibrosis was observed in one of the rats. These findings provide an important basis for substantiating both kinetically and pathologically the differences between chrysotile and the amphibole tremolite. As Calidria chrysotile has been certified to have no tremolite fiber, the results of the current study together with the results from toxicological and epidemiological studies indicate that this fiber is not associated with lung disease.
Similar articles
-
Comparison of Calidria chrysotile asbestos to pure tremolite: final results of the inhalation biopersistence and histopathology examination following short-term exposure.Inhal Toxicol. 2005 Aug;17(9):427-49. doi: 10.1080/08958370591002012. Inhal Toxicol. 2005. PMID: 16020039
-
The biopersistence of brazilian chrysotile asbestos following inhalation.Inhal Toxicol. 2004 Oct-Nov;16(11-12):745-61. doi: 10.1080/08958370490490176. Inhal Toxicol. 2004. PMID: 16036745
-
The biopersistence of Canadian chrysotile asbestos following inhalation.Inhal Toxicol. 2003 Nov;15(13):1247-74. doi: 10.1080/08958370390241713. Inhal Toxicol. 2003. PMID: 14569492
-
The health risk of chrysotile asbestos.Curr Opin Pulm Med. 2014 Jul;20(4):366-70. doi: 10.1097/MCP.0000000000000064. Curr Opin Pulm Med. 2014. PMID: 24811832 Review.
-
The health effects of chrysotile: current perspective based upon recent data.Regul Toxicol Pharmacol. 2006 Aug;45(3):252-64. doi: 10.1016/j.yrtph.2006.04.008. Epub 2006 Jul 11. Regul Toxicol Pharmacol. 2006. PMID: 16814911 Review.
Cited by
-
Dissolution Reaction and Surface Modification of UICC Amosite in Mimicked Gamble's Solution: A Step towards Filling the Gap between Asbestos Toxicity and Its Crystal Chemical Features.Nanomaterials (Basel). 2023 Nov 12;13(22):2933. doi: 10.3390/nano13222933. Nanomaterials (Basel). 2023. PMID: 37999287 Free PMC article.
-
Adverse health effects of asbestos: solving mysteries regarding asbestos carcinogenicity based on follow-up survey of a Chinese factory.Environ Health Prev Med. 2018 Aug 8;23(1):35. doi: 10.1186/s12199-018-0726-z. Environ Health Prev Med. 2018. PMID: 30089452 Free PMC article. Review.
-
Subchronic pulmonary pathology, iron overload, and transcriptional activity after Libby amphibole exposure in rat models of cardiovascular disease.Environ Health Perspect. 2012 Jan;120(1):85-91. doi: 10.1289/ehp.1103990. Epub 2011 Oct 6. Environ Health Perspect. 2012. PMID: 21979745 Free PMC article.
-
Pulmonary endpoints (lung carcinomas and asbestosis) following inhalation exposure to asbestos.J Toxicol Environ Health B Crit Rev. 2011;14(1-4):76-121. doi: 10.1080/10937404.2011.556047. J Toxicol Environ Health B Crit Rev. 2011. PMID: 21534086 Free PMC article. Review.
-
Erionite induces production of autoantibodies and IL-17 in C57BL/6 mice.Toxicol Appl Pharmacol. 2014 Mar 15;275(3):257-64. doi: 10.1016/j.taap.2014.01.018. Epub 2014 Feb 9. Toxicol Appl Pharmacol. 2014. PMID: 24518925 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials