Objectives: The aim of the study was to evaluate urinary mutagenicity in workers employed in a major chemical plant located near Rouen (France) that produces dichlorobenzidine and azo dyes.
Materials And Methods: Samples were obtained from 47 male workers aged 38.9+/-11.3 years (range, 21-58 years), mean duration of employment 9.0+/-8.7 years (range, 1-32 years) for urinary mutagenicity determination with use of the Ames fluctuation test (strains TA 98 and TA 100 with and without metabolic activation) and gas chromatography/mass spectrometry. To assess occupational exposure of workers, urine samples were collected in two series. First, initial just after a one-month holiday (non-exposure). Second, four months later during regular occupational activity. During the same periods, workers completed a questionnaire, which sought information concerning their working conditions, non-occupational factors, and personal habits.
Results: Of the total 47 samples tested, 3 (6%) collected just after a one-month holiday and 6 (12%) samples collected during regular occupational activity were positive in at least one mutagenicity assay. Dichlorobenzidine traces ranging from 1.6 to 8.9 ppb were detected in 4 (8%) samples of the exposed as well as in 4 (8%) samples of non-exposed workers. No significant differences between biological and analytical responses obtained in the non-exposure period and after occupational exposure were observed, however, 5 (11%) workers in this group presented urinary mutagenicity that could be related to occupational exposure.
Conclusions: The study suggests that some industrial hygiene problems, revealed in the analysis of questionnaire responses and confirmed by our evaluation, could be undoubtedly and easily solved to improve working conditions of the employees.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.2478/v10001-007-0014-4 | DOI Listing |
Beijing Da Xue Xue Bao Yi Xue Ban
December 2024
Department of Rheumatology and Immunology, Peking University Shougang Hospital, Beijing 100144, China.
Monoclonal gammopathy of undetermined significance combined with renal damage is named monoclonal gammopathy of renal significance. There are few reports about IgA vasculitis in patients with monoclonal gammopathy of undetermined significance. Here, we report a case of monoclonal gammopathy of renal significance, who had manifestations of IgA vasculitis, including purpura, gastrointestinal bleeding and joint pain.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
Renal-Electrolyte Division, Department of Medicine, University of Pittsburgh, Pittsburg, PA 15261, USA.
Sensitization of primary afferents is essential for the development of pain, but the molecular events involved in this process and its reversal are poorly defined. Recent studies revealed that acid-sensing ion channels (ASICs) control the excitability of nociceptors in the urinary bladder. Using genetic and pharmacological tools we show that ASICs are functionally coupled with voltage-gated Ca channels to mediate Ca transients evoked by acidification in sensory neurons.
View Article and Find Full Text PDFInt Immunopharmacol
January 2025
Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia. Electronic address:
Systemic lupus erythematosus (SLE) is a classic autoimmune disorder that mostly affects young women and involves various organs, such as the skin, joints, central nervous system, and kidneys. WY14643, a selective agonist of peroxisome proliferator-activated receptor-α, has previously shown anti-inflammatory effects in various disease models. However, its effects on lupus nephritis are yet to be explored.
View Article and Find Full Text PDFAm J Physiol Renal Physiol
January 2025
Division of Nephrology and Hypertension, Department of Medicine, Stony Brook University, Stony Brook, New York, United States.
Acute kidney injury (AKI) is a major risk factor for chronic kidney disease (CKD), and there are currently no therapies for AKI. Proximal tubules (PTs) are particularly susceptible to AKI, due to nephrotoxins such as aristolochic acid I (AAI). Normal PTs use fatty acid oxidation and branched chain amino acid (BCAA; valine, leucine, and isoleucine) catabolism to generate ATP; however, in AKI, these pathways are downregulated.
View Article and Find Full Text PDFToxicol Rep
December 2024
Laboratory of Environmental Mutagenesis, Department of Biophysics and Biometry, IBRAG/UERJ (University of the State of Rio de Janeiro), 87 - Fundos, 4th floor, Vila Isabel, Rio de Janeiro, RJ 20551-030, Brazil.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!