Organophosphorus pesticides: Do they all have the same mechanism of toxicity?

被引:495
作者
Pope, CN [1 ]
机构
[1] NE Louisiana Univ, Coll Pharm & Hlth Sci, Div Toxicol, Monroe, LA 71209 USA
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART B-CRITICAL REVIEWS | 1999年 / 2卷 / 02期
关键词
D O I
10.1080/109374099281205
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Organophosphorus (OP) pesticides are used extensively to control agricultural, household and structural pests. These pesticides constitute a diverse group of chemical structures exhibiting a wide range of physicochemical properties, with their primary toxicological action arising from inhibition of the enzyme acetylcholinesterase (AChE, EC 3.1.7.7). Historically, risk characterizations for these toxicants have been based on hazard and exposure data pertaining to individual chemicals. The Food Quality Protection Act of 1996 now requires, however, that combined risk assessments be performed with pesticides having a common mechanism of toxicity. It is therefore critical to consider whether OP pesticides ail exert toxicity through a common mechanism. This brief review evaluates the comparative toxicity of the 38 OP AChE inhibitors currently registered for use as pesticides in the United States and examines the data which suggest that some OP pesticides have toxicologically relevant sites of action in addition to AChE. It is concluded that all OP anticholinesterases potentially have a mechanism of toxicity in common, that is, phosphorylation of AChE causing accumulation of acetylcholine, overstimulation of cholinergic receptors, and consequent clinical signs of cholinergic toxicity. Additional macromolecular targets for some OP pesticides, however, may alter the cascade of events following AChE phosphorylation and thereby modify chat common mechanism. Furthermore, other macromolecular targets of some OP pesticides appear capable of altering noncholinergic neurochemical processes. These additional actions may contribute to qualitative and quantitative differences in toxicity sometimes noted in the presence of similar levels of AChE inhibition induced by different OP pesticides. Further investigation of these additional sites of action may allow subclassification and influence the decision to perform combined risk assessments on this class of pesticides based on common mechanism of toxicity.
引用
收藏
页码:161 / 181
页数:21
相关论文
共 65 条
[1]  
Albuquerque EX, 1997, J PHARMACOL EXP THER, V280, P1117
[2]   MUSCARINE RECEPTORS REGULATING ELECTRICALLY-EVOKED RELEASE OF ACETYLCHOLINE IN HIPPOCAMPUS ARE LINKED TO PERTUSSIS-TOXIN-SENSITIVE G-PROTEINS BUT NOT TO ADENYLATE-CYCLASE [J].
ALLGAIER, C ;
CHOI, BK ;
HERTTING, G .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (03) :1043-1049
[3]  
[Anonymous], ORGANOPHOSPHATES CHE
[4]   DIRECT ACTIONS OF ORGANO-PHOSPHATE ANTICHOLINESTERASES ON NICOTINIC AND MUSCARINIC ACETYLCHOLINE-RECEPTORS [J].
BAKRY, NMS ;
ELRASHIDY, AH ;
ELDEFRAWI, AT ;
ELDEFRAWI, ME .
JOURNAL OF BIOCHEMICAL TOXICOLOGY, 1988, 3 :235-259
[5]   REFERENCE DOSE (RFD) - DESCRIPTION AND USE IN HEALTH RISK ASSESSMENTS [J].
BARNES, DG ;
DOURSON, M .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1988, 8 (04) :471-486
[6]   INFLUENCE OF AGE ON TOXICITY AND METABOLISM OF METHYL PARATHION AND PARATHION IN MALE AND FEMALE RATS [J].
BENKE, GM ;
MURPHY, SD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1975, 31 (02) :254-269
[7]   THE MOLECULAR-BASIS OF MUSCARINIC RECEPTOR DIVERSITY [J].
BONNER, TI .
TRENDS IN NEUROSCIENCES, 1989, 12 (04) :148-151
[8]  
Camara AL, 1997, NEUROTOXICOLOGY, V18, P589
[9]   Chlorpyrifos interferes with cell development in rat brain regions [J].
Campbell, CG ;
Seidler, FJ ;
Slotkin, TA .
BRAIN RESEARCH BULLETIN, 1997, 43 (02) :179-189
[10]   INVOLVEMENT OF CAMP IN THE REGULATION OF HIGH-AFFINITY CHOLINE UPTAKE BY RAT-BRAIN SYNAPTOSOMES [J].
CANCELA, JM ;
BERTRAND, N ;
BELEY, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 213 (03) :944-949