Literature DB >> 6731470

Increased urinary enzyme excretion in workers exposed to nephrotoxic chemicals.

B R Meyer, A Fischbein, K Rosenman, Y Lerman, D E Drayer, M M Reidenberg.   

Abstract

Nephrotoxic chemicals are commonly present in the environment, particularly in the workplace. The level of occupational exposure to these chemicals has been so reduced that exposure to these agents now rarely causes clinically evident acute renal disease. A sensitive indicator of renal injury, urinary excretion of N-acetyl-beta-glucosaminidase, was utilized to evaluate persons exposed in the workplace to lead, mercury, or organic solvents, for evidence of renal effects from this exposure. None of the persons had clinically evident renal disease by history, none had hypertension, and all had normal findings on urinalysis. When compared with appropriate control populations, workers exposed to lead, workers exposed to mercury, and two of three groups of workers exposed to organic solvents had significant increases in urinary acetyl glucosaminidase activity. The third group of laboratory workers with low exposure to organic solvents had no increase in urinary acetyl glucosaminidase activity. It is concluded that exposure to environmental nephrotoxins at levels currently considered safe can produce renal effects as manifested by elevations of urinary acetyl glucosaminidase excretion. It is speculated that these renal effects are not always innocuous.

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Year:  1984        PMID: 6731470     DOI: 10.1016/0002-9343(84)90847-7

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  21 in total

Review 1.  Assessment of thyroid, testes, kidney and autonomic nervous system function in lead-exposed workers.

Authors:  J P Gennart; A Bernard; R Lauwerys
Journal:  Int Arch Occup Environ Health       Date:  1992       Impact factor: 3.015

2.  Detection of sub-clinical lead toxicity in monocasters.

Authors:  B D Kumar; K Krishnaswamy
Journal:  Bull Environ Contam Toxicol       Date:  1995-06       Impact factor: 2.151

3.  Stabilization of alanine aminopeptidase, gamma glutamyltranspeptidase, and N-acetyl-beta-D-glucosaminidase activity in normal urines.

Authors:  P W Mueller; M L MacNeil; K K Steinberg
Journal:  Arch Environ Contam Toxicol       Date:  1986-07       Impact factor: 2.804

4.  Enzymuria in workers exposed to inorganic mercury.

Authors:  L Barregård; B Hultberg; A Schütz; G Sällsten
Journal:  Int Arch Occup Environ Health       Date:  1988       Impact factor: 3.015

5.  Trichloroethylene exposure in vapour degreasing and the urinary excretion of N-acetyl-beta-D-glucosaminidase.

Authors:  A Seldén; B Hultberg; A Ulander; G Ahlborg
Journal:  Arch Toxicol       Date:  1993       Impact factor: 5.153

6.  Effects of exposure to low concentrations of chlorinated hydrocarbons on the kidney and liver of industrial workers.

Authors:  P J Boogaard; P S Rocchi; N J van Sittert
Journal:  Br J Ind Med       Date:  1993-04

7.  Occupational exposures and chronic kidney disease: Possible associations with endotoxin and ultrafine particles.

Authors:  Todd R Sponholtz; Dale P Sandler; Christine G Parks; Katie M Applebaum
Journal:  Am J Ind Med       Date:  2015-11-17       Impact factor: 2.214

8.  Associations of lead biomarkers with renal function in Korean lead workers.

Authors:  V M Weaver; B-K Lee; K-D Ahn; G-S Lee; A C Todd; W F Stewart; J Wen; D J Simon; P J Parsons; B S Schwartz
Journal:  Occup Environ Med       Date:  2003-08       Impact factor: 4.402

9.  Urinary N-acetyl-beta-D-glucosaminidase and beta-aminoisobutyric acid in workers occupationally exposed to metals such as chromium, nickel, and iron.

Authors:  K Tomokuni; M Ichiba; Y Hirai
Journal:  Int Arch Occup Environ Health       Date:  1993       Impact factor: 3.015

10.  Markers of early renal changes induced by industrial pollutants. I. Application to workers exposed to mercury vapour.

Authors:  A Cárdenas; H Roels; A M Bernard; R Barbon; J P Buchet; R R Lauwerys; J Roselló; G Hotter; A Mutti; I Franchini
Journal:  Br J Ind Med       Date:  1993-01
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