Urinary S-phenylmercapturic acid variation in benzene exposed.
- Author:
Yi-min LIU
1
;
Hao CHEN
;
Xu-dong LI
;
Jian-xun HUANG
;
Zhao-fa HUANG
;
Min CAO
Author Information
- Publication Type:Journal Article
- MeSH: Acetylcysteine; analogs & derivatives; urine; Adult; Animals; Benzene; administration & dosage; toxicity; Environmental Exposure; adverse effects; Female; Humans; Male; Middle Aged; Rats; Rats, Wistar; Young Adult
- From: Chinese Journal of Industrial Hygiene and Occupational Diseases 2008;26(3):151-153
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo observe the urinary S-phenylmercapturic acid (S-PMA) variation in the benzene dynamic exposed rat models and benzene exposed workers, and study the feasibility of use of urinary S-PMA as the biomarker in benzene exposed.
METHODSIn an animal model study, forty-eight adult Wistar rats were randomly divided into 4 groups: the control group, low-dose group, middle-dose group and high-dose group. The exposed groups were dynamically exposed for 28 days (4 periods) by benzene and the concentration was monitored. The urine was immediately collected after every exposure period and detected by the liquid chromatographic/mass spectrometry methods. In a cohort study, eighty benzene exposed workers in a ship-yard in Guangzhou were selected as the exposed subjects while forty healthy officers in the same shipyard who were not occupationally exposed to benzene were treated as the control. The urine was collected after work shift. The urinary S-PMA and the benzene in the workplace was treated as the rat model.
RESULTSIn the animal model study, the urinary S-PMA increased along with the environment benzene in every period and had significantly difference in the different exposed groups (P < 0.01 or P < 0.05), but did not change along with the exposed time course (P > 0.05). In the cohort study, the urinary S-PMA in the high-dose group [(27.2 +/- 7.9)microg/L] was significantly higher than the low-dose group [(13.6 +/- 3.4)microg/L] (P < 0.01). Otherwise, the background of urinary S-PMA was lower than 5microg/L in both workers and rat models.
CONCLUSIONThe urinary S-PMA can be proposed as a sensitive biomarker of occupational benzene exposure.