Skip to main content
Thorax logoLink to Thorax
. 1970 Sep;25(5):612–614. doi: 10.1136/thx.25.5.612

Effect of sulphur dioxide on the enzyme activity of the alveolar macrophage of rats

David H Barry 1, Lionel E Mawdesley-Thomas 1
PMCID: PMC472198  PMID: 4249883

Abstract

Adult rats were exposed to sulphur dioxide to induce hypersecretion of mucus and so increase the amount of mucus reaching the alveoli. The comparative activity of four lysosomal hydrolytic enzymes was studied histochemically in free alveolar cells, thought to be macrophages, from the lungs of the exposed and control animals. Although the activity of β-glucuronidase, β-galactosidase, and N-acetyl-β-glucosaminidase appeared increased in some free alveolar cells in the peribronchiolar region, a marked increase of acid phosphatase activity was seen in the free alveolar cells throughout the lung parenchyma. It is suggested that in rats acid phosphatase in alveolar macrophages is connected with the catabolism and removal of mucopolysaccharide and increases in response to the extra amount of mucus reaching the alveoli after respiratory irritation with sulphur dioxide.

Full text

PDF
612

Images in this article

Selected References

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

  1. BURSTONE M. S. Histochemical demonstration of phosphatases in frozen sections with naphthol AS-phosphates. J Histochem Cytochem. 1961 Mar;9:146–153. doi: 10.1177/9.2.146. [DOI] [PubMed] [Google Scholar]
  2. Barry D. H., Robinson W. E. Enzyme histochemical studies on rat lungs. I. An improved technique for the demonstration of enzyme activity in alveolar tissue. Histochem J. 1969 Nov;1(6):497–504. doi: 10.1007/BF01012856. [DOI] [PubMed] [Google Scholar]
  3. FELL H. B., DINGLE J. T. Studies on the mode of action of excess of vitamin A. 6. Lysosomal protease and the degradation of cartilage matrix. Biochem J. 1963 May;87:403–408. doi: 10.1042/bj0870403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. HAYASHI M., NAKAJIMA Y., FISHMAN W. H. THE CYTOLOGIC DEMONSTRATION OF BETA-GLUCURONIDASE EMPLOYING NAPHTHOL AS-BI GLUCURONIDE AND HEXAZONIUM PARAROSANILIN; A PRELIMINARY REPORT. J Histochem Cytochem. 1964 Apr;12:293–297. doi: 10.1177/12.4.293. [DOI] [PubMed] [Google Scholar]
  5. KARRER H. E. The ultrastructure of mouse lung: the alveolar macrophage. J Biophys Biochem Cytol. 1958 Nov 25;4(6):693–700. doi: 10.1083/jcb.4.6.693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. LEAKE E. S., GONZALEZ-OJEDA D., MYRVIK Q. N. ENZYMATIC DIFFERENCES BETWEEN NORMAL ALVEOLAR MACROPHAGES AND OIL-INDUCED PERITONEAL MACROPHAGES OBTAINED FROM RABBITS. Exp Cell Res. 1964 Feb;33:553–561. doi: 10.1016/0014-4827(64)90020-5. [DOI] [PubMed] [Google Scholar]
  7. MCCARTHY C., REID L., GIBBONS R. A. INTRA-ALVEOLAR MUCUS--REMOVAL BY MACROPHAGES: WITH IRON ACCUMULATION. J Pathol Bacteriol. 1964 Jan;87:39–47. [PubMed] [Google Scholar]
  8. Mawdesley-Thomas L. E., Healey P. The quantitative evaluation of experimental chronic bronchitis. A preliminary study. Am Rev Respir Dis. 1969 Aug;100(2):231–233. doi: 10.1164/arrd.1969.100.2.231. [DOI] [PubMed] [Google Scholar]
  9. PUGH D., WALKER P. G. The localization of N-acetyl-beta-glucosaminidase in tissues. J Histochem Cytochem. 1961 May;9:242–250. doi: 10.1177/9.3.242. [DOI] [PubMed] [Google Scholar]
  10. REID L. AN EXPERIMENTAL STUDY OF HYPERSECRETION OF MUCUS IN THE BRONCHIAL TREE. Br J Exp Pathol. 1963 Aug;44:437–445. [PMC free article] [PubMed] [Google Scholar]
  11. RUTENBURG A. M., RUTENBURG S. H., MONIS B., TEAGUE R., SELIGMAN A. M. Histochemical demonstration of beta-D-galactosidase in the rat. J Histochem Cytochem. 1958 Mar;6(2):122–129. doi: 10.1177/6.2.122. [DOI] [PubMed] [Google Scholar]
  12. SELIGMAN A. M., TSOU K. C., RUTENBURG S. H., COHEN R. B. Histochemical demonstration of beta-d-glucuronidase with a synthetic substrate. J Histochem Cytochem. 1954 May;2(3):209–229. doi: 10.1177/2.3.209. [DOI] [PubMed] [Google Scholar]

Articles from Thorax are provided here courtesy of BMJ Publishing Group

RESOURCES