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
[51]  
Rocha ES, 1996, J PHARMACOL EXP THER, V278, P1175
[52]   NEUROTOXIC EFFECTS OF ORGANOPHOSPHORUS INSECTICIDES - AN INTERMEDIATE SYNDROME [J].
SENANAYAKE, N ;
KARALLIEDDE, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (13) :761-763
[53]   Subchronic neurotoxicity screening studies with six organophosphate insecticides: An assessment of behavior and morphology relative to cholinesterase inhibition [J].
Sheets, LP ;
Hamilton, BF ;
Sangha, GK ;
Thyssen, JH .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1997, 35 (01) :101-119
[54]   PUTATIVE M2 MUSCARINIC RECEPTORS OF RAT-HEART HAVE HIGH-AFFINITY FOR ORGANOPHOSPHORUS ANTICHOLINESTERASES [J].
SILVEIRA, CLP ;
ELDEFRAWI, AT ;
ELDERFRAWI, ME .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 103 (03) :474-481
[55]   Cellular mechanisms for developmental toxicity of chlorpyrifos: Targeting the adenylyl cyclase signaling cascade [J].
Song, X ;
Seidler, FJ ;
Saleh, JL ;
Zhang, J ;
Padilla, S ;
Slotkin, TA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1997, 145 (01) :158-174
[56]  
*US EPA, 1984, AN REF STAND SUPPL D
[57]  
*US EPA, 1997, GUID EST COMM MECH T
[58]  
vandenBeukel I, 1997, J PHARMACOL EXP THER, V281, P1113
[59]  
Vogelsberg V, 1997, J NEUROCHEM, V68, P1062
[60]   INVITRO MODULATION OF BOVINE CAUDATE MUSCARINIC RECEPTOR NUMBER BY ORGANOPHOSPHATES AND CARBAMATES [J].
VOLPE, LS ;
BIAGIONI, TM ;
MARQUIS, JK .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1985, 78 (02) :226-234