Rat brain acetylcholinesterase activity: developmental profile and maturational sensitivity to carbamate and organophosphorus inhibitors

被引:60
作者
Mortensen, SR
Hooper, MJ
Padilla, S
机构
[1] US EPA, Div Neurotoxicol, Cellular & Mol Toxicol Branch, Res Triangle Pk, NC 27711 USA
[2] Clemson Univ, Dept Environm Toxicol, Pendleton, SC 29670 USA
[3] Clemson Univ, Inst Wildlife & Environm Toxicol, Pendleton, SC 29670 USA
关键词
rat brain; carbamate; organophosphorus inhibitors;
D O I
10.1016/S0300-483X(97)00157-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A growing body of evidence indicates that young animals exhibit an increased susceptibility to the lethal effects of cholinesterase (ChE)-inhibiting insecticides. Our laboratory is engaged in defining factors which may explain this age-related sensitivity. This report includes results from experiments designed to compare the developmental profiles, kinetic parameters and intrinsic (i.e, in vitro) sensitivity of developing male rat brain acetylcholinesterase (AChE) activity to carbamate and organophosphorus anticholinesterases. Total ChE activity in whole brain for each age was composed of about 90% AChE and 10% butyrylcholinesterase (BuChE) activity for the six ages examined. Brain AChE activity showed an age-related increase in V-max until postnatal day 17 with no change in K-m (average of all six ages similar to 72 mu M). Optimal substrate (acetylthiocholine) concentration for each age was 1 mM, and there was substrate inhibition (approximate to 10%) at 2.5 mM. IC(50)s (the concentration of compound that inhibits 50% of the AChE activity in 30 min at 26 degrees C) defined concomitantly for postnatal day 4 and adult brain AChE using either aldicarb, carbaryl, chlorpyrifos-oxon or malaoxon were virtually identical at both ages with average IC50 values being: aldicarb = 2.4 mu M, carbaryl = 1.7 mu M, chlorpyrifos-oxon = 4.9 nM and malaoxon = 140 nM. In summary, AChE in young and adult brain differs mostly in specific activity while the K(m)s, substrate profiles, and in vitro sensitivity to selected anticholinesterase insecticides are not different. Therefore, these data support the hypothesis that the greater sensitivity of the young animals to anticholinesterase pesticides is not due to the greater sensitivity of the target molecule AChE to these inhibitors. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:13 / 19
页数:7
相关论文
共 30 条
[1]  
ALDRIDGE WN, 1975, ENZYME INHIBITORS SU, P91
[2]  
ASPELIN AL, 1994, 733K94001 EPA
[3]  
BENJAMINS JA, 1981, BASIC NEUROCHEMISTRY, P445
[4]   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
[5]   DEVELOPMENTAL FACTORS AFFECTING BRAIN ACETYLCHOLINESTERASE INHIBITION AND RECOVERY IN DFP-TREATED RATS [J].
BISSO, GM ;
MENEGUZ, A ;
MICHALEK, H .
DEVELOPMENTAL NEUROSCIENCE, 1982, 5 (5-6) :508-519
[6]  
BRODEUR J, 1963, P SOC EXP BIOL MED, V114, P509, DOI 10.3181/00379727-114-28716
[7]   BIDRIN - PERINATAL TOXICITY AND EFFECT ON DEVELOPMENT OF BRAIN ACETYLCHOLINESTERASE AND CHOLINE-ACETYLTRANSFERASE IN MICE [J].
BUS, JS ;
GIBSON, JE .
FOOD AND COSMETICS TOXICOLOGY, 1974, 12 (03) :313-322
[8]   COMPARATIVE DEVELOPMENTAL AND MATERNAL NEUROTOXICITY FOLLOWING ACUTE GESTATIONAL EXPOSURE TO CHLORPYRIFOS IN RATS [J].
CHANDA, SM ;
HARP, P ;
LIU, J ;
POPE, CN .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1995, 44 (02) :189-202
[9]  
ECOBICHON DJ, 1991, CASARETT DOULLS TOXI, P565
[10]   A NEW AND RAPID COLORIMETRIC DETERMINATION OF ACETYLCHOLINESTERASE ACTIVITY [J].
ELLMAN, GL ;
COURTNEY, KD ;
ANDRES, V ;
FEATHERSTONE, RM .
BIOCHEMICAL PHARMACOLOGY, 1961, 7 (02) :88-&