Abstract | BACKGROUND: METHODS: Male Wistar rats were given daily dose of 500, 1000, 1500, 2000, 4000 mg/kg bw n-hexane by gavage for 24 weeks. The levels of pyrrole adducts in serum and urine were determined at 8, 24 hours postdose once a week. The Biological Exposure Indices was evaluated by neurological evaluation and the levels of pyrrole adducts. The difference in pyrrole adducts formation between humans and rats were estimated by using in vitro test. RESULTS: Dose-dependent effects were observed between the doses of n-hexane and pyrrole adducts in serum and urine, and the levels of pyrrole adduct in serum and urine approached a plateau at week 4. There was a significantly negative correlation between the time to paralysis and the level of pyrrole adducts in serum and urine, while a positive correlation between gait score and levels of pyrrole adducts in serum and urine was observed. In vitro, pyrrole adducts formed in human serum was about two times more than those in rat serum at the same level of 2,5-HD. CONCLUSION: It was concluded that the BEIs of pyrrole adducts in humans were 23.1 ± 5.91 nmol/ml in serum 8 h postdose, 11.7 ± 2.64 nmol/ml in serum 24 h postdose, 253.8 ± 36.3 nmol/ml in urine 8 h postdose and 54.6 ± 15.42 nmol/ml in urine 24 h postdose.
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Authors | Hongyin Yin, Chunling Zhang, Ying Guo, Xiaoying Shao, Tao Zeng, Xiulan Zhao, Keqin Xie |
Journal | PloS one
(PLoS One)
Vol. 9
Issue 1
Pg. e86108
( 2014)
ISSN: 1932-6203 [Electronic] United States |
PMID | 24465904
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biomarkers
- Hexanes
- Pyrroles
- n-hexane
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Topics |
- Adult
- Animals
- Biomarkers
(blood, urine)
- Body Weight
(drug effects)
- Female
- Gait
(drug effects)
- Hexanes
(administration & dosage, adverse effects)
- Humans
- Male
- Middle Aged
- Occupational Exposure
(adverse effects)
- Paralysis
(etiology)
- Presynaptic Terminals
(drug effects)
- Pyrroles
(blood, chemistry, urine)
- Rats
- Time Factors
- Young Adult
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