COMPARISON OF INVIVO CHOLINESTERASE INHIBITION IN NEONATAL AND ADULT-RATS BY 3 ORGANOPHOSPHOROTHIOATE INSECTICIDES

被引:221
作者
POPE, CN
CHAKRABORTI, TK
CHAPMAN, ML
FARRAR, JD
ARTHUN, D
机构
[1] Department of Pharmacology and Toxicology, School of Pharmacy, Northeast Louisiana University, Monroe
关键词
ORGANOPHOSPHATE; DEVELOPMENTAL; CHOLINESTERASE INHIBITION; PARATHION; METHYL PARATHION; CHLORPYRIFOS;
D O I
10.1016/0300-483X(91)90061-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Developing mammals are more sensitive than adults to a variety of organophosphorothioate insecticides (OPs), compounds which act in vivo by inhibition of cholinesterase (ChE). Little is known, however, regarding age-related differences in biochemical responses to these toxicants. The time course of ChE inhibition and recovery in whole brain was compared in neonatal (7 days of age) and adult (80-100 days of age) rats after treatment with maximal tolerated doses (MTDs) of either methyl parathion (MPS), parathion (PS) or chlorpyrifos (CPF). Neonatal rats were more sensitive than adults in all cases (MTDs for MPS, PS and CPF: neonates = 7.8, 2.1 and 45 mg/kg, s.c.; adults = 18, 18, and 279 mg/kg. s.c., respectively). In general, maximal brain ChE inhibition was similar (> 78%) in both age groups but ChE activity recovered faster in neonates. Plasma and erythrocyte ChE activities correlated relatively well (r = 0.794-0.943) with brain ChE activity in neonatal rats at all time points between 4 h and 7 days after treatment but similar correlations between circulating and brain ChE activities in adults were more variable (r = 0.211-0.917). The results indicate that neonatal rats are more sensitive to acute lethality from these compounds and that MTD exposures produce extensive brain ChE inhibition in both age groups. Significant inhibitor-related and age-related differences in the duration of ChE inhibition can ensue, however, following such OP exposures.
引用
收藏
页码:51 / 61
页数:11
相关论文
共 27 条
[1]  
ADAMS GK, 1976, EUR J PHARMACOL, V38, P101
[2]  
[Anonymous], 1988, SAS STAT USERS GUIDE
[3]   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
[4]  
BISSO GM, 1985, CAN J PHYSIO PHARM, V64, P376
[5]   A CONFIRMATORY STUDY OF THE UP-AND-DOWN METHOD FOR ACUTE ORAL TOXICITY TESTING [J].
BRUCE, RD .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1987, 8 (01) :97-100
[6]   NEUROCHEMICAL ASPECTS OF ONTOGENESIS OF CHOLINERGIC NEURONS IN RAT-BRAIN [J].
COYLE, JT ;
YAMAMURA, HI .
BRAIN RESEARCH, 1976, 118 (03) :429-440
[7]  
ETO M, 1974, ORGANOPHOSPHORUS PES, P138
[8]   POSTNATAL-DEVELOPMENT OF CHOLINERGIC ENZYMES AND RECEPTORS IN MOUSE-BRAIN [J].
FIEDLER, EP ;
MARKS, MJ ;
COLLINS, AC .
JOURNAL OF NEUROCHEMISTRY, 1987, 49 (03) :983-990
[9]   THE ACUTE TOXICITY OF PESTICIDES TO RATS [J].
GAINES, TB .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1960, 2 (01) :88-99
[10]   ACUTE TOXICITY OF PESTICIDES [J].
GAINES, TB .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1969, 14 (03) :515-&