The effects of acute pesticide exposure on neuroblastoma cells chronically exposed to diazinon

被引:35
作者
Axelrad, JC
Howard, CV
McLean, WG
机构
[1] Univ Liverpool, Dept Pharmacol & Therapeut, Liverpool L69 3GE, Merseyside, England
[2] Univ Liverpool, Dept Human Anat & Cell Biol, Dev Toxicopathol Unit, Liverpool L69 3GE, Merseyside, England
关键词
organophosphate; neurotoxicity; in vitro; neurite; pesticide;
D O I
10.1016/S0300-483X(02)00592-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Speculation about potential neurotoxicity due to chronic exposure to low doses of organophosphate (OP) pesticides is not yet supported by experimental evidence. The objective of this work was to use a cell culture model of chronic OP exposure to determine if such exposure can alter the sensitivity of nerve cells to subsequent acute exposure to OPs or other compounds. NB2a neuroblastoma cells were grown in the presence of 25 muM diazinon for 8 weeks. The OP was then withdrawn and the cells were induced to differentiate in the presence of various other pesticides or herbicides, including OPs and OP-containing formulations. The resulting outgrowth of neurite-like structures was measured by light microscopy and quantitative image analysis and the IC50 for each OP or formulation was calculated. The IC50 values in diazinon-pre-exposed cells were compared with the equivalent values in cells not pre-exposed to diazinon. The IC50 for inhibition of neurite outgrowth by acute application of diazinon, pyrethrum, glyphosate or a commercial formulation of glyphosate was decreased by between 20 and 90% after pre-treatment with diazinon. In contrast, the IC50 for pirimiphos methyl was unaffected and those for phosmet or chlorpyrifos were increased by between 1.5- and 3-fold. Treatment of cells with chlorpyrifos or with a second glyphosate-containing formulation led to the formation of abnormal neurite-like structures in diazinon-pre-exposed cells. The data support the view that chronic exposure to an OP may reduce the threshold for toxicity of some, but by no means all, environmental agents. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:67 / 78
页数:12
相关论文
共 47 条
[1]   USE OF NEURITE OUTGROWTH AS AN IN-VITRO METHOD OF ASSESSING NEUROTOXICITY [J].
ABDULLA, EM ;
CAMPBELL, IC .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1993, 679 :276-279
[2]   Neurotoxicity resulting from coexposure to pyridostigmine bromide, DEET, and permethrin: Implications of Gulf War chemical exposures [J].
AbouDonia, MB ;
Wilmarth, KR ;
Jensen, KF ;
Oehme, FW ;
Kurt, TL .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1996, 48 (01) :35-56
[3]   Increased neurotoxicity following concurrent exposure to pyridostigmine bromide, DEET, and chlorpyrifos [J].
AbouDonia, MB ;
Wilmarth, KR ;
AbdelRahman, AA ;
Jensen, KF ;
Oehme, FW ;
Kurt, TL .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1996, 34 (02) :201-222
[4]  
[Anonymous], ORG
[5]  
AUDEGOND L, 1989, J TOXICOL CLIN EXPER, V9, P163
[6]   Interactions between pesticides and components of pesticide formulations in an in vitro neurotoxicity test [J].
Axelrad, JC ;
Howard, CV ;
McLean, WG .
TOXICOLOGY, 2002, 173 (03) :259-268
[7]   Comparative effectiveness of organophosphorus protoxicant activating systems in neuroblastoma cells and brain homogenates [J].
Barber, D ;
Correll, L ;
Ehrich, M .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A, 1999, 57 (01) :63-74
[8]  
BIGBEE JW, 1999, ENV HLTH PERSPECT, V107, pS81
[9]   Toxic effects of acetylcholinesterase on neuronal and glial-like cells in vitro [J].
Calderon, FH ;
von Bernhardi, R ;
De Ferrari, G ;
Luza, S ;
Aldunate, R ;
Inestrosa, NC .
MOLECULAR PSYCHIATRY, 1998, 3 (03) :247-255
[10]   ONE-YEAR DIETARY TOXICITY STUDY WITH METHIDATHION IN BEAGLE DOGS [J].
CHANG, JCF ;
WALBERG, JA ;
CAMPBELL, WR .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1992, 19 (02) :307-314