Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 1994 Oct;102(Suppl 5):201–203. doi: 10.1289/ehp.102-1567276

One-year follow-up of the phagocytic activity of leukocytes after exposure of rats to asbestos and basalt fibers.

M Hurbánková 1
PMCID: PMC1567276  PMID: 7882931

Abstract

The phagocytic activity of leukocytes in peripheral blood was investigated after 2, 24, and 48 hr; 1, 2, 4, and 8 weeks; and 6 and 12 months following intraperitoneal administration of asbestos and basalt fibers to Wistar rats. Asbestos and basalt fibers differed in their effects on the parameters studied. Both granulocyte count and phagocytic activity of leukocytes during the 1-year dynamic follow-up in both dust-exposed groups of animals changed in two phases, characterized by the initial stimulation of the acute phase I, followed by the suppression of the parameters in the chronic phase II. Exposure to asbestos and basalt fibers led, in phase II, to impairment of the phagocytic activity of granulocytes. Asbestos fibers also significantly decreased phagocytic activity of monocytes. Exposure to basalt fibers did not affect the phagocytic activity of monocytes in phase II. Results suggest that the monocytic component of leukocytes plays an important role in the development of diseases caused by exposure to fibrous dusts, but basalt fibers have lesser biological effects than asbestos fibers.

Full text

PDF
201

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Botham S. K., Holt P. F. Comparison of effects of glass fibre and glass powder on guinea-pig lungs. Br J Ind Med. 1973 Jul;30(3):232–236. doi: 10.1136/oem.30.3.232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bozelka B. E., Sestini P., Gaumer H. R., Hammad Y., Heather C. J., Salvaggio J. E. A murine model of asbestosis. Am J Pathol. 1983 Sep;112(3):326–337. [PMC free article] [PubMed] [Google Scholar]
  3. Hartmann D. P. Immunological consequences of asbestos exposure. Surv Immunol Res. 1985;4(1):65–68. doi: 10.1007/BF02918587. [DOI] [PubMed] [Google Scholar]
  4. Kuschner M. The effects of MMMF on animal systems: some reflections on their pathogenesis. Ann Occup Hyg. 1987;31(4B):791–797. doi: 10.1093/annhyg/31.4b.791. [DOI] [PubMed] [Google Scholar]
  5. Lew F., Tsang P., Holland J. F., Warner N., Selikoff I. J., Bekesi J. G. High frequency of immune dysfunctions in asbestos workers and in patients with malignant mesothelioma. J Clin Immunol. 1986 May;6(3):225–233. doi: 10.1007/BF00918702. [DOI] [PubMed] [Google Scholar]
  6. Manning L. S., Davis M. R., Robinson B. W. Asbestos fibres inhibit the in vitro activity of lymphokine-activated killer (LAK) cells from healthy individuals and patients with malignant mesothelioma. Clin Exp Immunol. 1991 Jan;83(1):85–91. doi: 10.1111/j.1365-2249.1991.tb05593.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. deShazo R. D. Current concepts about the pathogenesis of silicosis and asbestosis. J Allergy Clin Immunol. 1982 Jul;70(1):41–49. doi: 10.1016/0091-6749(82)90200-7. [DOI] [PubMed] [Google Scholar]

Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES