The effect of chlorpyrifos and chlorpyrifos-oxon on brain cholinesterase, muscarinic receptor binding, and neurotrophin levels in rats following early postnatal exposure

被引:61
作者
Betancourt, AM [1 ]
Carr, RL [1 ]
机构
[1] Mississippi State Univ, Coll Vet Med, Environm Hlth Sci Ctr, Mississippi State, MS 39762 USA
关键词
chlorpyrifos; chlorpyrifos-oxon; neonatal; cholinesterase inhibition; neurotrophins; muscarinic receptors;
D O I
10.1093/toxsci/kfh003
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Chlorpyrifos (CPS) is a widely used diethyl organophosphorus insecticide in agricultural settings. Household and urinary residue analysis has suggested that children in agricultural communities are at risk of exposure to diethyl organophosphorus insecticides. The effects of repeated postnatal exposure to CPS and its metabolite chlorpyrifos-oxon (CPO) on total muscarinic acetylcholine receptor (mAChR) binding, nerve growth factor (NGF) levels, and brain derived neurotrophic factor (BDNF) levels in the forebrain of neonatal rats were investigated. Peak inhibition of brain cholinesterase (ChE) for CPS and CPO was determined after acute exposure to dosages of each compound (a low and a high for each), which produced similar degrees of initial ChE inhibition. Pups were administered CPS (1.5 or 3.0 mg/kg), CPO (0.25 or 0.35 mg/kg), or the corn oil vehicle by daily gavage from postnatal day 1 (PND 1) through PND 6. This exposure paradigm resulted in persistent ChE inhibition by CPS but only transient inhibition by CPO, suggesting that, even though the initial ChE inhibition is similar between compounds, the effects of repeated exposure differ significantly. Forebrain mAChR density, as measured by the binding of H-3-QNB, and NGF levels were significantly reduced on PND 4 and 7 after CPS but not on PND 12. No effects on mAChR density or NGF levels were observed with CPO. No effects on BDNF levels were observed with either compound. The data suggest that the persistent ChE inhibition and decreased mAChR binding may play a role in the decreased NGF levels following CPS exposure.
引用
收藏
页码:63 / 71
页数:9
相关论文
共 57 条
[11]   INHIBITION PATTERNS OF BRAIN ACETYLCHOLINESTERASE AND HEPATIC AND PLASMA ALIESTERASES FOLLOWING EXPOSURES TO 3 PHOSPHOROTHIONATE INSECTICIDES AND THEIR OXONS IN RATS [J].
CHAMBERS, JE ;
CARR, RL .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1993, 21 (01) :111-119
[12]  
CHAMBERS JE, 1988, NEUROSCI RES COMMUN, V3, P85
[13]   SHORT-TERM EFFECTS OF PARAOXON AND ATROPINE ON SCHEDULE-CONTROLLED BEHAVIOR IN RATS [J].
CHAMBERS, JE ;
CHAMBERS, HW .
NEUROTOXICOLOGY AND TERATOLOGY, 1989, 11 (05) :427-432
[14]  
Chen KS, 1997, J NEUROSCI, V17, P7288
[15]   Developmental neurotoxicity of chlorpyrifos in vivo and in vitro: effects on nuclear transcription factors involved in cell replication and differentiation [J].
Crumpton, TL ;
Seidler, FJ ;
Slotkin, TA .
BRAIN RESEARCH, 2000, 857 (1-2) :87-98
[16]   Neonatal chlorpyrifos exposure alters synaptic development and neuronal activity in cholinergic and catecholaminergic pathways [J].
Dam, K ;
Garcia, SJ ;
Seidler, FJ ;
Slotkin, TA .
DEVELOPMENTAL BRAIN RESEARCH, 1999, 116 (01) :9-20
[17]   Developmental neurotoxicity of chlorpyrifos: delayed targeting of DNA synthesis after repeated administration [J].
Dam, K ;
Seidler, FJ ;
Slotkin, TA .
DEVELOPMENTAL BRAIN RESEARCH, 1998, 108 (1-2) :39-45
[18]   Neuronal differentiation in PC12 cells is inhibited by chlorpyrifos and its metabolites: Is acetylcholinesterase inhibition the site of action? [J].
Das, KP ;
Barone, S .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1999, 160 (03) :217-230
[19]   COMPARATIVE ASPECTS OF THE BRAIN GROWTH SPURT [J].
DOBBING, J ;
SANDS, J .
EARLY HUMAN DEVELOPMENT, 1979, 3 (01) :79-83
[20]  
Dreyfus CF, 1998, PERSPECT DEV NEUROBI, V5, P389