Effects of single or repeated dermal exposure to methyl parathion on behavior and blood cholinesterase activity in rats

Citation
H. Zhu et al., Effects of single or repeated dermal exposure to methyl parathion on behavior and blood cholinesterase activity in rats, J BIOMED SC, 8(6), 2001, pp. 467-474
Citations number
45
Categorie Soggetti
Medical Research General Topics
Journal title
JOURNAL OF BIOMEDICAL SCIENCE
ISSN journal
10217770 → ACNP
Volume
8
Issue
6
Year of publication
2001
Pages
467 - 474
Database
ISI
SICI code
1021-7770(200111/12)8:6<467:EOSORD>2.0.ZU;2-0
Abstract
The effects of a single or repeated dermal administration of methyl parathi on on motor function, learning and memory were investigated in adult female rats and correlated with blood cholinesterase activity. Exposure to a sing le dose of 50 mg/kg methyl parathion (75% of the dermal LD50) resulted in a n 88% inhibition of blood cholinesterase activity and was associated with s evere acute toxicity. Spontaneous locomotor activity and neuromuscular coor dination were also depressed. Rats treated with a lower dose of methyl para thion, Le. 6.25 or 12.5 mg/kg, displayed minimal signs of acute toxicity. B lood cholinesterase activity and motor function, however, were depressed in itially but recovered fully within 1-3 weeks. There were no delayed effects of a single dose of methyl parathion on learning acquisition or memory as assessed by a step-down inhibitory avoidance learning task. Repeated treatm ent with 1 mg/kg/day methyl parathion resulted in a 50% inhibition of blood cholinesterase activity. A decrease in locomotor activity and impairment o f memory were also observed after 28 days of repeated treatment. Thus, a si ngle dermal exposure of rats to doses of methyl parathion which are lower t han those that elicit acute toxicity can cause decrements in both cholinest erase activity and motor function which are reversible. In contrast, repeat ed low-dose dermal treatment results in a sustained inhibition of cholinest erase activity and impairment of both motor function and memory. Copyright (C) 2001 National Science Council, ROC and S. Karger AG, Basel.