Occupational exposure tocis-1,3-dichloropropene: biological effect monitoring of kidney and liver function

OBJECTIVES To investigate the possible effects of occupational exposure to the nematocide cis-1,3-dichloropropene (cis-DCP) on function of the kidney and liver in the starch potato growing region in The Netherlands. METHODS The study involved 13 commercial application workers exposed tocis-DCP for 117 days, and 22 matched control workers. The inhalatory exposure of the application workers was estimated from biological monitoring data. All workers collected urine and serum samples before, during, and after the fumigation season for monitoring of variables for kidney and liver function. Renal effect variables were alanine aminopeptidase (AAP), N-acetyl-β-D-glucosaminidase (NAG), retinol binding protein (RBP), and albumin (ALB) in urine, and β2-microglobulin (β2M-S) and creatinine in serum (Creat-S). Liver variables were alanine aminotransferase (ALAT), aspartate aminotransferase (ASAT), γ-glutamyltranspeptidase (GGT), alkaline phosphatase (ALP), and total bilirubin (TBIL) in serum and the urinary ratio of 6-β-hydroxycortisol to free cortisol (βOHC/COR). RESULTS The geometric mean exposure of the application workers was 2.7 mg/m3 (8 hour time weighted average (8 hour TWA)); range 0.1–9.5 mg/m3. No differences were found between the values of the renal effect variables or the liver variables of the exposed group and the control group, except a lower urinary ratio of βOHC/COR in the exposed group. This was not considered to be related to the exposure tocis-DCP. No dose-effect relations were found between the exposure indices and the effect variables. CONCLUSIONS The present study does not provide evidence that occupational exposure tocis-DCP in the starch potato growing region causes adverse effects on the kidney or liver at 8 hour TWA exposure concentrations below 9.5 mg/m3 (2 ppm).

[1]  L. Bloemen,et al.  Personal air sampling and biological monitoring of occupational exposure to the soil fumigantcis-1,3-dichloropropene , 2000, Occupational and environmental medicine.

[2]  K. Schaller,et al.  Standardized method for the estimation of β2-microglobulin, retinol-binding protein and albumin in urine (Technical Report) , 1994 .

[3]  J. Osterloh,et al.  Urinary protein markers in pesticide applicators during a chlorinated hydrocarbon exposure. , 1993, Environmental research.

[4]  D. Young Effects of Preanalytical Variables on Clinical Laboratory Tests , 1993 .

[5]  Y. Horsmans,et al.  Absence of CYP3A genetic polymorphism assessed by urinary excretion of 6 beta-hydroxycortisol in 102 healthy subjects on rifampicin. , 1992, Pharmacology & toxicology.

[6]  W. F. Tordoir,et al.  Biological effect monitoring of occupational exposure to 1,3-dichloropropene: effects on liver and renal function and on glutathione conjugation. , 1991, British journal of industrial medicine.

[7]  C. Evelo,et al.  Biological effect monitoring of occupational exposure to 1,3-dichloropropene: effects on liver and renal function and on glutathione conjugation. , 1991, British journal of industrial medicine.

[8]  S. Loft,et al.  Prediction of xenobiotic metabolism by non-invasive methods. , 1990, Pharmacology & toxicology.

[9]  P. Beaune,et al.  The increase in urinary excretion of 6 beta-hydroxycortisol as a marker of human hepatic cytochrome P450IIIA induction. , 1989, British journal of clinical pharmacology.

[10]  J. Osterloh,et al.  Biological monitoring of dichloropropene: air concentrations, urinary metabolite, and renal enzyme excretion. , 1989, Archives of environmental health.

[11]  W. Stott,et al.  The chronic toxicity and oncogenicity of inhaled technical-grade 1,3-dichloropropene in rats and mice. , 1989, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[12]  Y. Nagamachi,et al.  Urinary excretion of beta 2-microglobulin and N-acetyl-beta-D-glucosaminidase in advanced neuroblastoma patients receiving cis-diamminedichloroplatinum(II). , 1988, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.

[13]  M. Vahter,et al.  Assessment of exposure to lead and cadmium through biological monitoring: results of a UNEP/WHO global study. , 1983, Environmental research.

[14]  K. Jung,et al.  An optimized assay of alanine aminopeptidase activity in urine. , 1980, Clinical chemistry.

[15]  F. Oyen,et al.  The toxicity of 1,3-dichloropropene as determined by repeated exposure of laboratory animals. , 1977, American Industrial Hygiene Association journal.

[16]  D. Maruhn Rapid colorimetric assay of -galactosidase and N-acetyl--glucosaminidase in human urine , 1976 .

[17]  D. Young,et al.  Effects of drugs on clinical laboratory tests. , 1972, Clinical chemistry.

[18]  R. de Wit,et al.  Comparison of renal function parameters in the assessment of cis-platin induced nephrotoxicity. , 1994, Nephron.

[19]  N. Vermeulen,et al.  Inhalation exposure to 1,3-dichloropropene in the Dutch flower-bulb culture. Part II. Biological monitoring by measurement of urinary excretion of two mercapturic acid metabolites , 1991, Archives of environmental contamination and toxicology.

[20]  W. Breslin,et al.  1,3-dichloropropene: two-generation inhalation reproduction study in Fischer 344 rats. , 1989, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[21]  W. Stott,et al.  Subchronic toxicity of inhaled technical grade 1,3-dichloropropene in rats and mice. , 1988, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[22]  I. J. Climie,et al.  Glutathione conjugation in the detoxication of (Z)-1,3-dichloropropene (a component of the nematocide D-D) in the rat. , 1979, Xenobiotica; the fate of foreign compounds in biological systems.