Skip to main content
British Journal of Industrial Medicine logoLink to British Journal of Industrial Medicine
. 1991 Mar;48(3):167–172. doi: 10.1136/oem.48.3.167

Biological effect monitoring of occupational exposure to 1,3-dichloropropene: effects on liver and renal function and on glutathione conjugation.

E J Brouwer 1, C T Evelo 1, A J Verplanke 1, R T van Welie 1, F A de Wolff 1
PMCID: PMC1035344  PMID: 2015207

Abstract

A prospective study was performed in the Dutch flower bulb culture to investigate the possible effects of subchronic exposure to the soil fumigant 1,3-dichloropropene (DCP) on liver and kidney function and on glutathione conjugation capacity in blood. Urine spot samples and venous blood samples from 14 workers applying DCP (applicators) were taken at the start of the season in July, and after the season in October. The parameters of liver function measured were: alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, lactate dehydrogenase, gamma-glutamyltranspeptidase, and total bilirubin (conjugated and unconjugated). Total bilirubin was significantly decreased from 9.5 before to 7.0 mumol/l after the season. In combination with an increase in serum gamma-glutamyltranspeptidase activity from 12.5 to 19.5 U/l this indicates moderate hepatic enzyme induction. To study renal function, creatinine and beta 2-microglobulin in serum, and beta 2-microglobulin, albumin, alanine aminopeptidase, beta-galactosidase, and retinol binding protein in urine were measured. The glomerular function parameters albumin in urine and creatinine in serum changed significantly during the season: albumin concentration increased from 5.2 to 7.6 mg/l, whereas creatinine concentration [corrected] decreased from 93.0 to 87.5 mumol/l. The tubular function parameter retinol binding protein also increased in concentration from 20.0 to 26.9 micrograms/l. Therefore, a subclinical nephrotoxic effect of subchronic exposure to DCP cannot be excluded. Effects on glutathione conjugation capacity were studied by measuring erythrocyte glutathione S-transferase activity and blood glutathione concentrations. The activity of glutathione S-transferase in erythrocytes was significantly decreased from 4.7 before to 3.3 U/g haemoglobin after the season. The same was true for the blood glutathione concentrations, which decreased from 0.93 to 0.82 mM.(ABSTRACT TRUNCATED AT 250 WORDS)

Full text

PDF
167

Selected References

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

  1. Al-Turk W. A., Stohs S. J., el-Rashidy F. H., Othman S. Changes in glutathione and its metabolizing enzymes in human erythrocytes and lymphocytes with age. J Pharm Pharmacol. 1987 Jan;39(1):13–16. doi: 10.1111/j.2042-7158.1987.tb07154.x. [DOI] [PubMed] [Google Scholar]
  2. Albrecht W. N. Toxicology and hazard assessment of 1,3-dichloropropene (Telone II). Arch Environ Health. 1987 Sep-Oct;42(5):292–296. doi: 10.1080/00039896.1987.9935823. [DOI] [PubMed] [Google Scholar]
  3. Anderson M. E. Determination of glutathione and glutathione disulfide in biological samples. Methods Enzymol. 1985;113:548–555. doi: 10.1016/s0076-6879(85)13073-9. [DOI] [PubMed] [Google Scholar]
  4. Ansari G. A., Singh S. V., Gan J. C., Awasthi Y. C. Human erythrocyte glutathione S-transferase: a possible marker of chemical exposure. Toxicol Lett. 1987 Jun;37(1):57–62. doi: 10.1016/0378-4274(87)90167-6. [DOI] [PubMed] [Google Scholar]
  5. Gidlow D. A., Church J. F., Clayton B. E. Haematological and biochemical parameters in an industrial workforce. Ann Clin Biochem. 1983 Nov;20(Pt 6):341–348. doi: 10.1177/000456328302000603. [DOI] [PubMed] [Google Scholar]
  6. Habig W. H., Jakoby W. B. Assays for differentiation of glutathione S-transferases. Methods Enzymol. 1981;77:398–405. doi: 10.1016/s0076-6879(81)77053-8. [DOI] [PubMed] [Google Scholar]
  7. Henderson R. F., Bechtold W. E., Bond J. A., Sun J. D. The use of biological markers in toxicology. Crit Rev Toxicol. 1989;20(2):65–82. doi: 10.3109/10408448909017904. [DOI] [PubMed] [Google Scholar]
  8. Jung K., Scholz D. An optimized assay of alanine aminopeptidase activity in urine. Clin Chem. 1980 Aug;26(9):1251–1254. [PubMed] [Google Scholar]
  9. Kilpikari I., Savolainen H. Decreased erythrocyte glutathione s-transferase activity in rubber workers. Int Arch Occup Environ Health. 1984;53(4):299–302. doi: 10.1007/BF00380668. [DOI] [PubMed] [Google Scholar]
  10. Lauwerys R. R., Bernard A. Early detection of the nephrotoxic effects of industrial chemicals: state of the art and future prospects. Am J Ind Med. 1987;11(3):275–285. doi: 10.1002/ajim.4700110305. [DOI] [PubMed] [Google Scholar]
  11. Maruhn D. Rapid colorimetric assay of beta-galactosidase and N-acetyl-beta-glucosaminidase in human urine. Clin Chim Acta. 1976 Dec;73(3):453–461. doi: 10.1016/0009-8981(76)90147-9. [DOI] [PubMed] [Google Scholar]
  12. Osterloh J. D., Wang R., Schneider F., Maddy K. Biological monitoring of dichloropropene: air concentrations, urinary metabolite, and renal enzyme excretion. Arch Environ Health. 1989 Jul-Aug;44(4):207–213. doi: 10.1080/00039896.1989.9935885. [DOI] [PubMed] [Google Scholar]
  13. Peter H., Deutschmann S., Reichel C., Hallier E. Metabolism of methyl chloride by human erythrocytes. Arch Toxicol. 1989;63(5):351–355. doi: 10.1007/BF00303122. [DOI] [PubMed] [Google Scholar]
  14. Strange R. C., Johnson P. H., Lawton A., Moult J. A., Tector M. J., Tyminski R. J., Cotton W. Studies on the variability of glutathione S-transferase from human erythrocytes. Clin Chim Acta. 1982 Apr 8;120(2):251–260. doi: 10.1016/0009-8981(82)90162-0. [DOI] [PubMed] [Google Scholar]
  15. Torkelson T. R., Oyen F. The toxicity of 1,3-dichloropropene as determined by repeated exposure of laboratory animals. Am Ind Hyg Assoc J. 1977 May;38(5):217–223. doi: 10.1080/0002889778507603. [DOI] [PubMed] [Google Scholar]
  16. Van Kampen E. J., Zijlstra W. G. Determination of hemoglobin and its derivatives. Adv Clin Chem. 1965;8:141–187. doi: 10.1016/s0065-2423(08)60414-x. [DOI] [PubMed] [Google Scholar]
  17. Warholm M., Guthenberg C., Mannervik B. Molecular and catalytic properties of glutathione transferase mu from human liver: an enzyme efficiently conjugating epoxides. Biochemistry. 1983 Jul 19;22(15):3610–3617. doi: 10.1021/bi00284a011. [DOI] [PubMed] [Google Scholar]
  18. Zielhuis R. L., Henderson P. T. Definitions of monitoring activities and their relevance for the practice of occupational health. Int Arch Occup Environ Health. 1986;57(4):249–257. doi: 10.1007/BF00406181. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Industrial Medicine are provided here courtesy of BMJ Publishing Group

RESOURCES