Chlorfenvinphos Research Articles

Evolution of acaricide resistance of Rhipicephalus decoloratus on commercial farms in South Africa.

The development of tick resistance to chemical control plays a major role in the increasing global economic impact of ticks on cattle farming. Reports on acaricide resistance of Rhipicephalus decoloratus, endemic to Africa and South Africa, are relatively few compared to the closely related and globally distributed Rhipicephalus microplus. In South Africa, ectoparasite control became the sole responsibility of each commercial producer when compulsory dipping was phased out from 1984. Different acaricidal management strategies resulted in the simultaneous development of resistance to various acaricide groups. The establishment of a Pesticide Resistance Testing Facility provided the opportunity to test Rhipicephalus (Boophilus) populations, submitted from all over South Africa, for resistance where failure of chemical control was experienced. The number of populations resistant to cypermethrin (CM) was significantly higher than those tested as resistant to amitraz (AM), or chlorfenvinphos (CFVP). No significant difference was found between the number of populations resistant to AM and CFVP. The evolution of R. decoloratus resistance at the end of a 12year period indicated a stable but high prevalence of 90% overall resistance to CM. The same trend was seen for AM-resistant R. decoloratus populations but at a lower level of just over 40%. In contrast, CFVP resistant R. decoloratus populations showed a decreasing trend with near-total reversion to susceptibility. Multi-resistance was present in more than 50% of populations tested with the highest incidence in the Eastern Cape, KwaZulu-Natal, and Western Cape provinces.

Fate and removal of pesticides in solid and liquid phases of metropolitan, urban and rural-scale wastewater treatment plants

In this study, the change of occurrence, distribution, seasonal variation and removal of pesticides, atrazine (ATZ), chlorpyriphos (CPR) and chlorfenvinphos (CFV), were investigated both in liquid and solid phases of three different types of wastewater treatment plants (WWTPs). Treatment configurations of the studied WWTPs consist of a metropolitan advanced biological treatment system (4-stage Bardenpho), urban-scale waste stabilization pond (WSP) and rural-scale horizontal subsurface flow constructed wetland (HSSCW).ATZ removal efficiencies (59.8 %–92.4 %) were higher than CPR and CFV removal efficiencies at all WWTPs. CPR and CFV are removed at 78.5 % and 53.1 % efficiency, respectively, from the influent of advanced biological treatment system. CPR and CFV removals were 21.6 and 22.7 % at WSP, respectively.One of the important findings is that ATZ and CFV were removed at higher percentages in primary treatment than in biological treatment in advanced biological WWTP. Sorption onto sludge has been evaluated as an effective removal mechanism for pesticide elimination, at least as much as biodegradation/biotransformation. All investigated pesticides were detected in higher concentrations in primary sludge (168.8–399.5 μg/kg) compared to secondary sludge (21.9–146.3 μg/kg) in advanced biological WWTP and in facultative sludge (447.8–1044.7 μg/kg) compared to anaerobic sludge (250.0–613.0 μg/kg) in WSP. It was determined that ATZ was the most treated compound in the liquid phase under anaerobic conditions among the studied pesticides. In line with these results, approximately 45 % removal efficiency was determined for CPR and CFV in the anaerobic digestion process present in advanced biological WWTP.

Study of the chlorfenvinphos pesticide removal under different anodic materials and different reactor configuration

The present manuscript focuses on the study of the electrochemical oxidation of the insecticide Chlorfenvinphos (CVP). The assays were carried out under galvanostatic conditions using boron-doped diamond (BDD) and low-cost tin dioxide doped with antimony (Sb-doped SnO2) as anodes. The influence of the operating variables, such as applied current density, presence or absence of a cation-exchange membrane and concentration of supporting electrolyte, was discussed. The results revealed that the higher applied current density the higher degradation and mineralization of the insecticide for both anodes. The presence of the membrane and the highest concentration of Na2SO4 studied (0.1 M) as a supporting electrolyte benefited the oxidation process of CVP using the BDD electrode, while with the ceramic anode the elimination of CVP was lower under these experimental conditions. Although the BDD electrode showed the best performance, ceramic anodes appear as an interesting alternative as they were able to degrade CVP completely for the highest applied current density values. Toxicity tests revealed that the initial solution of CVP was more toxic than the samples treated with the ceramic electrode, while using the BDD electrode the toxicity of the sample increased.

TiO2 Modified with Organic Acids for the Decomposition of Chlorfenvinphos under the Influence of Visible Light: Activity, Performance, Adsorption, and Kinetics.

Photocatalytic decomposition of chlorfenvinphos (CFVP) in the presence of titanium dioxide (TiO2) modified with organic acids: pyruvic (PA) and succinic (SA) under the visible light radiation has been studied. The following tests were examined: dose of photocatalysts, adsorption time, pH of the model solution, deactivation of catalysts, the role of oxygen, identification of free radicals for the CFVP decomposition, Langmuir-Hinshelwood kinetics. The synthesized materials were characterized by Scanning Electron Microscopy (SEM) and UV-Vis. At 10 wt.% of acid (90:10) decomposition of chlorfenvinphos was the most effective in the following conditions: dose of catalyst 50.0 mg/L, time of adsorption = 20 min, pH of model solution = 3.0. Under these conditions the order of photocatalyst efficiency has been proposed: TiO2/PA/90:10 > TiO2/SA/90:10 > TiO2 with the removal degree of 85, 72 and 48%. The mathematically calculated half-life at this conditions was 27.0 min and 39.0 min for TiO2/PA/90:10 and TiO2/SA/90:10 respectively, compared to 98 min for pure TiO2. It has been determined that the O2•− radicals and holes (h+) are the main reactive species involved in the photodegradation of chlorfenvinphos. The results of this study showed that method may be an interesting alternative for the treatment of chlorfenvinphos contaminated wastewater.

Determination of Organophosphorous Pesticides in Blood Using Microextraction in Packed Sorbent and Gas Chromatography-Tandem Mass Spectrometry.

The aim of our work was to develop a method for the determination of six organophosphorous pesticides (Ops) (azynphos-ethyl (AZP), diazinon (DZN), chlorpyrifos (CLP), chlorfenvinfos (CLF), parathion-ethyl (PRT) and quinalphos (QLP)) in whole blood using microextraction by packed sorbent (MEPS) and analysis by gas chromatography-tandem mass spectrometry (GC-MS/MS). The optimization of the MEPS procedure was performed using a design of experiments (DOE) approach, assessing different factors that significantly affected the extraction efficiency. Ultimately, the number of sample strokes, wash volume, percentage of 2-propanol in the wash solvent and the number of elution strokes were successfully optimized using a response surface methodology (RSM). The developed and optimized method was fully validated according to international guidelines. Linearity was established from 2.5 to 50 μg/mL for AZP and from 0.5 to 50 μg/mL for the remaining compounds, with coefficients of determination (R2) higher than 0.99 in all cases. The lower limit of quantification were 2.5 μg/mL (AZP) and 0.5 μg/mL (remaining compounds). Recoveries ranged from 61% to 77%. Intra- and inter-day precision and accuracy were considered adequate according to the guidelines. This is the first method employing MEPS as a sample preparation procedure for the analysis of these OPs in whole blood.

Partitioning of organophosphorus pesticides into phosphatidylcholine small unilamellar vesicles studied by second-derivative spectrophotometry

In order to quantitatively examine the lipophilicity of the widely used organophosphorus pesticides (OPs) chlorfenvinphos (CFVP), chlorpyrifos-methyl (CPFM), diazinon (DZN), fenitrothion (FNT), fenthion (FT), isofenphos (IFP), profenofos (PFF) and pyraclofos (PCF), their partition coefficient (Kp) values between phosphatidylcholine (PC) small unilamellar vesicles (SUVs) and water (liposome–water system) were determined by second-derivative spectrophotometry. The second-derivative spectra of these OPs in the presence of PC SUV showed a bathochromic shift according to the increase in PC concentration and distinct derivative isosbestic points, demonstrating the complete elimination of the residual background signal effects that were observed in the absorption spectra. The Kp values were calculated from the second-derivative intensity change induced by addition of PC SUV and obtained with a good precision of R.S.D. below 10%. The Kp values were in the order of CPFM>FT>PFF>PCF>IFP>CFVP>FNT⩾DZN and did not show a linear correlation relationship with the reported partition coefficients obtained using an n-octanol–water system (R2=0.530). Also, the results quantitatively clarified the effect of chemical-group substitution in OPs on their lipophilicity. Since the partition coefficient for the liposome–water system is more effective for modeling the quantitative structure–activity relationship than that for the n-octanol–water system, the obtained results are toxicologically important for estimating the accumulation of these OPs in human cell membranes.

Treatment of water networks (waters and deposits) contaminated with chlorfenvinphos by oxidation with Fenton’s reagent

The treatment of waters/deposits from drinking water networks contaminated with chlorfenvinphos (CFVP) was performed through the Fenton’s process. Concerning the CFVP degradation in water matrices, the mineralization and CFVP concentration in a batch reactor were analysed along time for several operating conditions. A detailed parametric study was done to analyse the effect of the initial concentrations of oxidant (H2O2) and catalyst (Fe2+), temperature and initial pH, allowing concluding that temperature significantly affects the degradation process. In fact, in the range from 10 to 70°C, the time for complete degradation of CFVP decreased from 3h to only 5min. In the same temperature range, the mineralization after 3h increased from 5% to 35%. The effect of other parameters is not so significant; depending on their values they can affect positively or negatively the responses.The degradation of the pesticide was assessed for the first time using deposits from water networks as catalysts. These deposits result from the natural deposition of small particles in suspension, being in some cases highly rich in iron, and therefore it is envisaged the valorisation of these materials for off-line applications and the possibility of avoiding the use of some reagents –catalyst – if an in situ treatment is required.The decontamination of deposits was assessed in a slurry batch system, showing to be possible to use iron-rich deposits as catalysts in the oxidation process, as well as to decontaminate them using as catalyst the iron present in their composition. Results showed that oxidation is fast and effective in the liquid phase (conversion >95% in 1h); the pesticide was also removed from the solid, although apparently not always in a complete manner, in the conditions tested.

Partial protection from organophosphate-induced cholinesterase inhibition by metyrapone treatment

Organophosphates are cholinesterase (ChE) inhibitors with worldwide use as insecticides. Stress response, evidenced by a dramatic and relatively long-lasting (several hours) rise in the plasma glucocorticoid concentration is an integral element of the organophosphate (OP) poisoning symptomatology. In rodents, corticosterone (CORT) is the main glucocorticoid. There are several reports suggesting a relationship between the stressor-induced rise in CORT concentration (the CORT response) and the activity of the cerebral and peripheral ChE. Thus, it seems reasonable to presume that, in OP intoxication, the rise in plasma CORT concentration may somehow affect the magnitude of the OP-induced ChE inhibition. Metyrapone (MET) [2-methyl-1,2-di(pyridin-3-yl)propan-1-one] blocks CORT synthesis by inhibiting steroid 11β-hydroxylase, thereby preventing the CORT response. Chlorfenvinphos (CVP) [2-chloro-1-(2,4-dichlorophenyl) ethenyl diethyl phosphate] is an organophosphate insecticide still in use in some countries. The purpose of the present work was to compare the CVP-induced effects - the rise of the plasma CORT concentration and the reduction in ChE activity - in MET-treated and MET-untreated rats. Chlorfenvinphos was administered once at 0.0, 0.5, 1.0 and 3.0 mg/kg i.p. Metyrapone, at 100 mg/kg i.p., was administered five times, at 24-h intervals. The first MET dose was given two hours before CVP. The following was observed in the MET-treated rats: i) no rise in plasma CORT concentration after the CVP administration, ii) a reduced inhibition and a faster restitution of blood and brain ChE activities. The results suggest that MET treatment may confer significant protection against at least some effects of OP poisoning. The likely mechanism of the protective MET action has been discussed.

Rapid determination of pesticide mixtures using disposable biosensors based on genetically modified enzymes and artificial neural networks

We present a one-step inhibition biosensor method that can be used to determine mixtures of three organophosphorus compounds. We propose to calculate the rate of irreversible inactivation of the enzyme (kp) to demonstrate the direct relationship between enzymatic biosensors and Chlorpyriphos-oxon (CPO), Chlorfenvinphos (CFV) and Azinphos-methyl oxon (AZMO) insecticides. The array of biosensors was designed using only two acetylcholinesterases from Drosophila melanogaster (wild-type and genetically modified). We used the values the slope of inhibitions mi from an array of biosensors and an artificial neural network to solve mixtures of CPO, CFV and AZMO insecticides The errors were low between the obtained and expected values for a set of 20 external test samples.

Two Suicidal Fatalities Due to the Ingestion of Chlorfenvinphos Formulations: Simultaneous Determination of the Pesticide and the Petroleum Distillates in Tissues by Gas Chromatography–Flame-Ionization Detection and Gas Chromatography–Mass Spectrometry

Chlorfenvinphos (CFVP) is an organophosporus insecticide designated as a threat agent by the National Institutes of Health (NIH). However, there are very few reported cases of poisonings in humans and none with postmortem toxicological analysis. We report the first two fatalities due to suicidal massive ingestion of a veterinary formulation containing CFVP and petroleum distillates. Case 1: A 24-year-old woman was found dead by her mother. According to the police records, the room was filled with an odor of solvents or pesticides and feces. There was an empty bottle of Supona(®) near the body and a suicide note on a Bible on a table. The only relevant postmortem finding was that the lungs appeared congested and edematous. Case 2: A 60-year-old man committed in his van by ingesting an unknown product. The vehicle was locked and had an odor that resembled an acid, sulfate, or solvent according to different witnesses. There was a suicide note as well as multiple containers containing automobile products nearby. The stomach of the victim was filled with abundant pale greenish fluid with a similar odor to that presented in the vehicle. The simultaneous toxicological screening and quantitation of CFVP and petroleum distillates [a mixture of trimethylbenzene isomers (TMBs)] was performed by means of gas chromatography with flame-ionization detection (GC-FID) and confirmation was performed using gas chromatography-mass spectrometry (GC-MS). Disposition of CFVP and TMBs in different tissues were, respectively, as follows: Case 1: heart blood, 8.6 and 3.7 mg/L; liver, 60.0 and 33.4 mg/kg; and stomach contents, 1132 mg/L (792.4 mg total) and 377.0 mg/L (263.9 mg total). Case 2: heart blood, 4.4 and 6.5 mg/L; urine, 1.4 and detected (< LOQ); bile 7.8 and 12.2 mg/L; vitreous 0.3 mg/L and detected (< LOQ); liver, 139.2 and 172.1 mg/kg; and stomach contents, 76,168 mg/L (72,359 mg total) and 108,109 mg/L (102,703 mg total). Results of alcohol, other volatiles, abused and therapeutic drugs were negative in both cases. The proposed analytical method allows the simultaneous determination of a wide variety of pesticides and additives, including petroleum distillates suitable for toxicological investigation in forensic and clinical cases. This is crucial to solving poisoning cases in which the poisoning source is uncertain.

Analysis of Some Selected Persistent Organic Chlorinated Pesticides in Marine Water and Food Stuffs by Differential Pulse‐Cathodic Stripping Voltammetry

AbstractBased on the redox characteristics of two selected organochlorine pesticides namely alachlor (ALC) and chlorfenvinphos (CHL) in Britton–Robinson (B–R) buffer at a hanging mercury drop, Pt and Au working electrode (HMDE), a fast, simple and selective differential pulse cathodic stripping voltammetric (DP CSV) method was developed for their determination. The cathodic stripping peak currents for ALC versus concentrations was linear in the range from 7.4×10−9 to 1.4×10−7 mol L−1 and in the range from 2.7×10−9 to 1.6×10−8 mol L−1 for CHL. The method was applied for the analysis of trace concentrations of ALC and CHL in fresh‐ and marine water (Atlantic and Red Sea) and sediment samples and food stuffs.

An Approach to an Inhibition Electronic Tongue to Detect On-Line Organophosphorus Insecticides Using a Computer Controlled Multi-Commuted Flow System

An approach to an inhibition bioelectronic tongue is presented. The work is focused on development of an automated flow system to carry out experimental assays, a custom potentiostat to measure the response from an enzymatic biosensor, and an inhibition protocol which allows on-line detections. A Multi-commuted Flow Analysis system (MCFA) was selected and developed to carry out assays with an improved inhibition method to detect the insecticides chlorpyrifos oxon (CPO), chlorfenvinfos (CFV) and azinphos methyl-oxon (AZMO). The system manifold comprised a peristaltic pump, a set of seven electronic valves controlled by a personal computer electronic interface and software based on LabView® to control the sample dilutions into the cell. The inhibition method consists in the injection of the insecticide when the enzyme activity has reached the plateau of the current; with this method the incubation time is avoided. A potentiostat was developed to measure the response from the enzymatic biosensor. Low limits of detection of 10 nM for CPO, CFV, and AZMO were achieved.

Artificial neural network implementation in single low-cost chip for the detection of insecticides by modeling of screen-printed enzymatic sensors response

This work presents a hardware implementation of artificial neural networks (ANNs) using a dsPIC ® microcontroller to resolve mixtures of pesticides measured by amperometric acetylcholinesterase (AChE) biosensors. The response of three biosensors with different concentrations of Chlorpyrifos Oxon (CPO) and Chlorfenvinfos (CFV) was modeled by two ANNs, which were implemented on the dsPIC ®. The performance of the ANNs was good, the prediction ability was better than 0.986 when the obtained values were compared with those expected for a set of eight external test samples, which were not used for training. This implementation is proposed to develop low-cost analytical chemical specialized tools.

Structure-Based Rational Design of a Phosphotriesterase

In silico substrate docking of both stereoisomers of the pesticide chlorfenvinphos (CVP) in the phosphotriesterase from Agrobacterium radiobacter identified two residues (F131 and W132) that prevent productive substrate binding and cause stereospecificity. A variant (W131H/F132A) was designed that exhibited ca. 480-fold and 8-fold increases in the rate of Z-CVP and E-CVP hydrolysis, respectively, eliminating stereospecificity.

The use of Artificial Neural Networks for the selective detection of two organophosphate insecticides: Chlorpyrifos and chlorfenvinfos

Amperometric acetylcholinesterase (AChE) biosensors have been developed to resolve mixtures of chlorpyrifos oxon (CPO) and chlorfenvinfos (CFV) pesticides. Three different biosensors were built using the wild type from electric eel (EE), the genetically modified Drosophila melanogaster AChE B394 and B394 co-immobilized with a phosphotriesterase (PTE). Artificial Neural Networks (ANNs) were used to model the combined response of the two pesticides. Specifically two different ANNs were constructed. The first one was used to model the combined response of B394 + PTE and EE biosensors and was applied when the concentration of CPO was high and the other, modelling the combined response of B394 + PTE and B394 biosensors, was applied with low concentrations of CPO. In both cases, good prediction ability was obtained with correlation coefficients better than 0.986 when the obtained values were compared with those expected for a set of six external test samples not used for training.

Impact of Biotransformation and Bioavailability on the Toxicity of the Insecticides α-Cypermethrin and Chlorfenvinphos in Earthworm

Knowledge about the bioavailability and metabolism of pesticides in soil organisms facilitates interpretation of its toxicity in soil. The present study relates uptake kinetics and metabolism of two insecticides, the pyrethroid alpha-cypermethrin (alpha-CYP) and the organophosphate chlorfenvinphos (CFVP), in the earthworm Eisenia fetida to their lethal and sublethal toxicity. Experiments were conducted in two soils with different organic matter contents to provide media with contrasting sorption capacity for the insecticides. The results showed that organophosphate CFVP was, when taken up by earthworms, rapidly and irreversibly bound to biomolecules and the fraction of extractable parent insecticide and metabolites was low. In contrast, alpha-CYP was rapidly metabolized by earthworms but did not form conjugates. It seems that the phase II metabolism of alpha-CYP is inhibited in earthworms, resulting in an increasing accumulation of its metabolites. Instantaneous binding of non-altered CFVP to the target site presumably resulted in a higher toxicity compared to alpha-CYP and explains the small difference between lethal and reproduction toxicity. For alpha-CYP, however, accumulation of alpha-CYP metabolites in earthworms during chronic exposure may explain the large observed difference between lethal and sublethal toxicity. Bioaccumulation and toxicity of either insecticide decreased with increasing organic matter content in soil, emphasizing the role of compound sorption on bioavailability and toxicity for soil organisms.

Nonexhaustive β-Cyclodextrin Extraction as a Chemical Tool To Estimate Bioavailability of Hydrophobic Pesticides for Earthworms

Chemical methods to assess bioavailability in soil and sediment often use synthetic polymers that mimic uptake of organic compounds in organisms or microbial degradation. In this paper we have assessed a biomimetic extraction method using hydroxyl-beta-cyclodextrin (HP-beta-CD) to estimate uptake of the two insecticides alpha-cypermethrin (alpha-CYP) and chlorfenvinphos (CFVP) in the earthworm Eisenia fetida. Additionally, a novel approach was developed to estimate the efficiency of biomimetic extractions. The study revealed that HP-beta-CD is a suitable surrogate for estimating the bioaccessibility of hydrophobic chemicals in soil. If one uses a 3.5 times higher amount of HP-beta-CD than soil, effective and reproducible extractions can be achieved within 48 h. Atthese conditions, inclusion of dissolved chemicals by HP-beta-CD mimics uptake of a given compound into earthworms and takes into account sorption-related aspects that control biological uptake. The data indicate that, with increasing hydrophobicity, the affinity of organic chemicals to HP-beta-CD does not increase to the same degree as to soil organic matter. Therefore, a high surplus of HP-beta-CD is necessaryto provide a sufficient extraction capacity in biomimetic extractions.

Photo-Fenton decomposition of chlorfenvinphos: Determination of reaction pathway

The purpose of this work was to determine the degradation products and pathway of chlorfenvinphos (CFVP) in water treated by photo-Fenton driven by solar irradiation, as well as to develop an analytical procedure for the degradation experiments. Degradation products and pathway were determined in a laboratory experimental setup. Routine water sample analysis was done by standard laboratory wet chemistry procedures and the use of laboratory equipment such as HPLC–UV and ionic chromatography (IC). Solid-phase extraction (SPE) was used to extract analytes from an aqueous matrix, and GC–MS was used to identify intermediate degradation products. The use of an HPLC–TOF-MS provided more results on degradation products and more insight was gained into how degradation takes place. In all experiments, strong mineralisation and degradation of CFVP was observed. CFVP and its degradation products, like 2,4-dichlorophenol, 2,4-dichlorobenzoic acid and triethylphosphate were decomposed into organic substances like acetate, formate, maleate, and inorganic ions like chloride and phosphate, within the detection limits (12.5 μg/L for CFVP in the GC–MS and 40 μg/L in HPLC–UV) of the equipment used. In fact, Cl − emerges in nearly stoichiometric concentrations and PO 4 3 − is precipitated as FePO 4. The remarkably complete absence of chlorinated aliphatic substances and chlorinated acids leads to the conclusion that chlorine is removed very quickly, and that residual DOC does not correspond to any chlorinated compound.

Pretreatment With Footshock Alters Some Effects Of Subsequent Organophosphate Exposure

Pre-exposure to non-chemical stressors may alter a subject's vulnerability to chemical stressors. We found recently that rats given a subtoxic dose of chlorfenvinphos (CVP), an organophosphorus pesticide, develop behavioral hyposensitivity to amphetamine (AMPH). The present experiments were performed in order to find out whether pre-exposure to a non-chemical stressor several days prior to CVP exposure could influence this effect of the pesticide. In experiment 1 adult male Wistar rats were subjected once to either a short, 5 min (SFS) or long, 20 min (LFS) series of unavoidable footshocks (FS). Twenty-four hours or 14 days after the FS, their open field behavior was tested before and after a test dose of AMPH (0.5 mg/kg. i.p). In experiment 2, the rats were subjected to LFS and 14 days later they were injected intraperitoneally with CVP (1.0 mg/kg) or vehicle (corn oil). In both experiments, serum corticosterone (CORT) levels were determined in separate groups of rats in order to assess the magnitude of the stress response induced by the applied stressors. It was found that: (i) the rise in serum CORT concentration after SFS or LFS was similar in magnitude, while that following LFS was more persistent; (ii) exposure to LFS, but not to SFS, resulted in a decreased response to AMPH on day 14 after the experience; (iii) in rats not pretreated with LFS, CVP exposure resulted in a profound increase in serum CORT concentration. In LFS pretreated rats, however, this effect was significantly reduced; (iv) three weeks after the exposure to CVP, the psychomotor response to AMPH was diminished in control rats but was normal in LFS pretreated animals. The results indicate that pretreatment with a non-chemical stressor may protect the rat against at least some of the effects of an organophosphate pesticide.

On the interactions between antimuscarinic atropine and NMDA receptor antagonists in anticholinesterase-treated mice.

Both organophosphate (OP) and carbamate pesticides may produce seizures and death commonly attributed to the inhibition of acetylcholinesterase (AChE) and subsequent excess of acetylcholine (ACh). The anticonvulsant and neuroprotective properties of N-methyl-D-aspartate (NMDA) receptor antagonists in animals encouraged us to investigate their effects on the toxic and convulsant properties of OP and carbamate pesticides. Adult Swiss mice were systemically injected with the OP pesticide, chlorfenvinphos (CVP), or the carbamate pesticide, methomyl (MET). Both CVP and MET induced dose-dependent seizure activity and death in mice. Pretreatment with the muscarinic antagonist, atropine (ATR), at a dose of 1.8 mg/kg did not prevent seizures but decreased the lethal effects of CVP and MET. Pretreatment with the NMDA antagonists, dizocilpine (MK-801) at a dose of 1 mg/kg or 3-((R,S)-2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP) at a dose of 10 mg/kg, influenced neither MET-induced seizures nor CVP- or MET-induced death. However, both MK-801 and CPP blocked CVP-induced seizures. Concurrent administration of ATR and the NMDA antagonists prevented seizures produced by CVP, but not those produced by MET. Nevertheless, both MK801 and CPP coadministered with ATR markedly enhanced its antilethal effects in CVP- and MET-intoxicated mice. The antidotes had no influence upon brain AChE activities in mice treated with saline or CVP or MET. It seems that combined treatment with ATR and NMDA receptor antagonists might be of clinical relevance.