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Solid-phase microextraction for gas chromatographic/mass spectrometric analysis of dimethoate in human biological samples.

A new, simple and rapid procedure for the determination of dimethoate in urine and blood samples was developed using direct immersion solid-phase microextraction and gas chromatography/mass spectrometry. This technique required only 0.1 mL of sample, and ethion was used as internal standard. Two types of coated fibre were compared (100 microm polydimethylsiloxane, and 65 microm Carbowax/divinylbenzene). Other parameters, such as extraction temperature, adsorption and desorption time, salt addition, agitation and pH, were optimized to enhance the sensitivity of the method. Limits of detection (LODs) and quantitation (LOQs) were 50 and 100 ng/mL for urine and 200 and 500 ng/mL for blood, respectively. The method was found to be linear between the LOQ and 40 microg/mL for urine, and between the LOQ and 50 microg/mL for blood, with correlation coefficients ranging from 0.9923-0.9996. Precision (intra- and interday) and accuracy were in conformity with the criteria normally accepted in bioanalytical method validation. The mean absolute recoveries of dimethoate were 1.24 and 0.50% for urine and blood, respectively. Because of its simplicity and the fact that small volumes of sample are used, the described method can be successfully used in the diagnosis of poisoning by this pesticide, namely in those situations where the sample volume is limited, as frequently occurs in forensic toxicology.

Dimethoate↗

Effect of dimethoate on body growth of representatives of the soil living mesofauna.

For the elucidation of effects of a pesticide on life-cycle parameters of arthropods, applicable in the development of ecotoxicological test procedures with soil living animals, attention was drawn to body growth, which has previously been described as a sensitive parameter in Collembola. Body growth of the following three soil-dwelling arthropods was studied under the influence of dimethoate: Folsomia fimetaria (L.), Hypogastrura assimilis Krausbauer, and Hypoaspis aculeifer Canestrini. The effect of this insecticide and acaricide proved to be sex and species specific. Two models were compared for modeling individual body length. The logistic growth model fitted data for all species, whereas the growth model of von Bertalanffy was less applicable for F. fimetaria and H. aculeifer. The growth rate coefficient of the logistic model proved to be a robust parameter useful for predicting effects of dimethoate on juvenile growth of F. fimetaria and H. aculeifer. Adverse effect concentrations on growth for these species were the following: EC10 = 0.11 mg dimethoate/kg dry soil for F. fimetaria and EC10 = 0.59 mg dimethoate/kg dry soil for H. aculeifer. For H. assimilis, no adverse effects on growth were observed at the tested concentrations. The results are compared to other life-cycle parameters (end-points).

Analysis of Variance↗

Effect of dimethoate on photosynthesis and pigment fluorescence of Synechocystis sp. PCC 6803.

The organophosphorus (OP) insecticides are powerful inhibitors of esterases, and their toxic actions are commonly explained in terms of acetylcholinesterase (EC 3.1.1.7) inhibition but their phytotoxic effects remain unexplained. In this study the effects of an OP insecticide, dimethoate, on cyanobacterial photosynthesis and respiration were measured using the cyanobacterium Synechocystis sp. PCC 6803 as test organism. The insecticide caused enhancement of respiratory O2 consumption at all tested concentrations (10-300 microM) while photosynthesis was found to be significantly affected at concentrations > or = 50 microM. From fluorescence emission analysis, oxygen exchange measurement, and determination of 14CO2 incorporation, it was found that dimethoate caused inhibition of photosynthetic electron transport, resulting in increase of PS II fluorescence and reduction in photosynthetic carbon fixation. An increase of nonphotochemical quenching was caused by the insecticide through the increase in acidity of the thylakoid lumen. Furthermore, detachment of phycobilisomes (PBS) from the PS II reaction centers was observed in terms of increase in PBS fluorescence in treated cultures. This detachment is expected to be caused by membrane fluidity changes. The fluorescence enhancement of PS II was more than that of the PBS.

Carbon Dioxide↗

Dimethoate-induced toxic cardiac failure in the guinea pig.

In anaesthetized guinea-pigs treated with lethal doses of dimethoate, cardiac failure and serious ECG disturbances developed in the early phase of intoxication. The toxic cardiac phenomena appeared to be unrelated to the degree of cholinesterase inhibition, but showed a close correlation with myocardial dimethoate concentration. Cardiac failure and mortality were first observed at a critical pesticide level of about 110 micrograms/g, while a level of 221 micrograms/g resulted in death in all cases. The present investigation refers to the direct effect of the pesticide on the myocardium, independent of its anticholinesterase action.

Animals↗

Organophosphate poisonings with parathion and dimethoate.

OBJECTIVE: Organophosphate toxicity is the leading cause of morbidity and death in poisoning by insecticides. The clinical symptoms of pesticide toxicity range from the classic cholinergic syndrome to flaccid paralysis and intractable seizures. The mainstays of therapy are atropine, oximes, benzodiazepines and supportive care. The toxicokinetics vary not only with the extent of exposure, but also with the chemical structure of the agent. PATIENTS: We report two cases of poisoning with parathion-ethyl and dimethoate. The patients developed a cholinergic syndrome immediately, accompanied by bradycardia and hypotension. INTERVENTIONS: The patients were admitted to the intensive care unit (ICU) a few hours after ingestion. Atropine was administered according to the cholinergic symptoms. The patients recovered in the ICU after 10-12 days and were discharged after 3 and 4 weeks. MEASUREMENTS AND RESULTS: Organophosphate blood and urine levels were determined on admission and during hospitalisation. The pesticides were rapidly distributed and slow elimination rate of the poisons was documented. In the case of parathion-ethyl the distribution half-life estimated was t(1/2alpha) = 3.1h while the terminal half-life was t(1/2beta) = 17.9 h. Using a one-compartment model for dimethoate the elimination half-life was t(1/2beta) = 30.4 h in plasma and 23.8 h in urine. The serum pseudo-cholinesterase activity was below the limit of detection at admission and recovered during the following 3weeks.

Aged↗

Alterations in the levels of ions in blood and liver of freshwater fish, Cyprinus carpio var. communis exposed to dimethoate.

The fingerlings of Cyprinus carpio var. communis were exposed to sublethal concentration of dimethoate for 7, 14 days to evaluate the impact of the pesticide dimethoate on different ions namely sodium, potassium, chloride, calcium, magnesium. The blood potassium, calcium, magnesium and liver chloride and magnesium levels were elevated under sublethal condition. The blood sodium, chloride and liver sodium, potassium, and calcium levels were found to be significantly decreased.

Animals↗

The effect of dimethoate, dichlorvos, and parathion-methyl on bone marrow cell chromosomes of rats in subchronic experiments in vivo.

The three organophosphorous insecticides dimethoate, dichlorvos, and parathion-methyl were investigated in subchronic experiments on bone marrow cell chromosomes. In the literature these compounds were reported to exhibit both positive and negative results in mutagenicity tests demanding further investigations in subchronic tests. The treatment of different groups of male Wistar rats lasted for 6 weeks with 5 treatment days per week at doses of 1/100, 1/75, and 1/50 of the LD50. Following the last treatment, bone marrow cell chromosomes were prepared. The frequency of cells revealing any aberrations as well as numeric and structural aberrations were evaluated. In this test both dimethoate and dichlorvos demonstrated mutagenic effects following subchronic treatment of Wistar rats, while parathion-methyl at doses of 1/100, 1/75, and 1/50 of LD50 displayed no significant mutagenicity.

Animals↗

Indication for weak mutagenicity of the organophosphorus insecticide dimethoate in Drosophila melanogaster.

The organophosphorus insecticide dimethoate was tested for induction of genetic damage in male germ cells of Drosophila melanogaster. Sex-linked recessive lethals, sex-chromosome loss and non-disjunction induction were studied following different routes of administration: adult feeding, injection and larval feeding. Our results show that, after injection, dimethoate induces a slight but significant increase in the frequency of point mutations.

Animals↗

Genotoxicity of an organophosphorus insecticide, dimethoate, in the mouse.

The effects of dimethoate were investigated in the mouse after acute (10 mg/kg i.p.) or chronic treatment (0.6 ppm, 5 days a week for 7 weeks). Dominant lethal mutations were scored for a 7-week period after the acute dose, and immediately after exposure for the chronic dose. Chromosome damage was also analysed in bone marrow and spermatogonial cells at the same dose levels (from 12 to 48 h after treatment). MMS (60 mg/kg i.p.) was chosen as the positive control. In no experiment did dimethoate show any genotoxicity.

Animals↗

Sister-chromatid exchanges in human lymphocytes induced by dimethoate, omethoate, deltamethrin, benomyl and their mixture.

Dimethoate and omethoate, two common organophosphorus insecticides, induced a dose-related increase in the frequency of sister-chromatid exchanges (SCEs) in human lymphocytes in vitro (P of the regression lines less than 0.01). Two other common pesticides, the pyrethroid insecticide deltamethrin and the systemic fungicide benomyl, induced a modest increase in SCEs which bordered on statistical significance (P = 0.053 and 0.055, respectively). Mixtures of the four pesticides at total concentrations of 41.5 and 83 micrograms/ml (composed of 43% dimethoate, 43% omethoate, 12% deltamethrin and 1.2% benomyl) induced a dose-dependent increase in SCEs (P less than 0.01). The effects of these mixtures of pesticides were variable using lymphocytes from different individuals, although these differences did not attain statistical significance. Moreover, low concentrations of the four pesticides that did not increase SCEs significantly when tested alone, were positive for SCE induction when tested as a mixture. The experiments show that sub-threshold doses of pesticides may increase SCEs when present in a mixture.

Adult↗

Study of the removal of dichlorvos and dimethoate in a titanium dioxide mediated photocatalytic process through the examination of intermediates and the reaction mechanism.

The photocatalytic oxidation of two selected organophosphorous insecticides (dichlorvos and dimethoate) has been investigated. The aim of the study was the identification of the intermediates that are formed during photocatalytic treatment. Intermediate products from the slurry system were identified by means of solid-phase extraction (SPE) coupled to gas chromatography-mass spectroscopy techniques (GC-MS). Nine possible by-products were identified for dimethoate and three for dichlorvos. A proposed degradation pathway for each insecticide is presented, involving mainly oxidation and dealkylation reactions. The results demonstrated that some of the transient intermediates formed (oxon derivatives, disulfide, chlorinated fragments), were more toxic compared to parent compounds whereas most of them are less toxic than the parent compounds.

Catalysis↗

Effects of dimethoate on spiders from metal pollution gradient.

In this study, an attempt has been made to assess whether a chronic exposure to metals in habitats under a strong industrial pressure might have equipped spiders with biochemical defensive mechanisms enabling them to survive an additional chemical stress. To check this, non-web-building wolf spiders Pardosa lugubris (Lycosidae) and funnel web Agelena labyrinthica (Agelenidae) were collected at five variously polluted meadows and, under laboratory conditions, intoxicated with either single or multiple dose of dimethoate (OP pesticide). Then the activities of detoxifying (carboxylesterase: CarE, glutathione S-transferase: GST), antioxidative (selene-dependent and selene-independent glutathione peroxidases: GPOX and GSTPx) enzymes as well as acetylcholinesterase as a biomarker of exposure to OP pesticides were measured. In web-building A. labyrinthica, even a single application of the pesticide caused the inhibition of CarE, GSTPx and GPOX in individuals from less polluted sites and AChE and GST in specimens pre-exposed to high metal concentrations. Multiple intoxication, irrespectively of the site, caused significant, in comparison to controls, decrease in CarE, AChE and GSTPx activities. Actively hunting P. lugubris seem more resistant to acute pesticide intoxication, since the spiders from each site had a constant level of GST and AChE. In individuals of this species from heavily polluted sites, the inhibition caused by multiple intoxication with dimethoate was stated only for glutathione peroxidases.

Acetylcholinesterase↗

Effects of acute dimethoate administration on antioxidant status of liver and brain of experimental rats.

Organophosphorus compounds may induce oxidative stress leading to generation of free radicals and alterations in antioxidant and scavengers of oxygen free radicals. The present study demonstrates effect of acute exposure of dimethoate in causation of oxidative stress in male Wistar rats. Dimethoate was administered orally at doses 45, 75 and 90 mg/kg of body weight on the basis of LD(50) for 24 h. After administration of doses, the liver and brain homogenates were analyzed for various parameters of oxidative stress. The results indicated an increase in hepatic cytochrome P450, lipid peroxidation, catalase, superoxide dismutase, glutathione peroxidase, glutathione reductase in liver and brain at 90 and 75 mg/kg doses. There were no significant changes in the levels of glucose-6-phosphate dehydrogenase activity in both liver and brain. Similarly, there were no significant changes in hepatic glutathione and glutathione-S-transferase activities. However, there was a significant increase in glutathione and glutathione-S-transferase in brain at 90 mg/kg dose only. Erythrocyte acetylcholinesterase was inhibited at all doses used. Dose-dependent histopathological changes, observed in both liver and brain, are also described.

Administration, Oral↗

Altered glucose homeostasis and oxidative impairment in pancreas of rats subjected to dimethoate intoxication.

The primary objective of this study was to investigate the effect of repeated sublethal doses of dimethoate (DM), an organophosphorus insecticide on glucose homeostasis, oxidative stress induction in pancreas and pancreatic damage in adult rats. Daily oral administration of DM (20 and 40 mg/kg b.w.) for 30 days induced a significant increase in blood glucose levels which was associated with impaired glucose tolerance. DM treatment resulted in elevated levels of pancreatic tissue specific markers such as activities of amylase and lipase in serum and pancreatic tissue indicating pancreatic dysfunction. Further, the activities of DT-diaphorase and NADPH-diaphorase in pancreas of DM treated rats were also found to be elevated. Interestingly, these biochemical dysfunctions were accompanied by a marked dose-related enhancement of lipid peroxidation and ROS levels in the pancreatic tissue indicating significant induction of oxidative damage. Additional evidence such as depletion in reduced glutathione levels and significant alterations in enzymic antioxidant defenses in pancreas among DM treated rats suggested induction of oxidative stress. Taken together, these findings provide experimental evidence that dimethoate at subchronic oral doses has the propensity to impair glucose homeostasis, induce significant pancreatic damage and also provide an account of the associated oxidative damage to pancreatic tissue in adult rats.

Administration, Oral↗

Rapid multi-residue method for the determination of azinphos methyl, bromopropylate, chlorpyrifos, dimethoate, parathion methyl and phosalone in apricots and peaches by using negative chemical ionization ion trap technology.

A rapid, selective and sensitive multi-residue method for the determination of six common pesticides in stone fruit samples is described. The proposed method involves the extraction of the pesticides with the use of acetone solvent followed by liquid-liquid partition with a mixture of dichloromethane and light petroleum (40-60 degrees C) and subsequent determination by a gas chromatographic-mass spectrometry system using ion trap technology in negative ion chemical ionization mode. The average percent recoveries of bromopropylate and phosalone in the concentration range 0.2-2.0 mg/kg were 97.3 +/- 6.7 to 120 +/- 1.0%, while the recoveries of chlorpyrifos and parathion methyl examined in the concentration range 0.02-0.2 mg/kg were 95.5 +/- 7.5 to 145 +/- 3.6%, the recoveries of azinphos methyl in the range 0.05-0.5 mg/kg were 74.8 +/- 29.6 to 96.5 +/- 13% and those of dimethoate in the range 0.1-1.0 mg/kg were 73.1 +/- 5.7 to 92.8 +/- 2.8% for n = 3 for all the above pesticides. The high mean recovery (145%) for chlorpyrifos is attributed to a matrix enhancement effect. The limits of quantitation in apricots were 0.01 mg/kg for chlorpyrifos, 0.02 mg/kg for dimethoate and parathion methyl, 0.05 mg/kg for azinphos methyl and phosalone and 0.1 mg/kg for bromopropylate. The usefulness of tandem mass spectrometry for confirmation purposes was also examined. The method was applied successfully to the determination of the target pesticides in 32 samples of stone fruits (apricots and peaches).

Azinphosmethyl↗

The thermal decomposition of dimethoate.

The thermal decomposition of dimethoate, an organophosphorus pesticide, has been studied with the aim at assessing the reaction kinetics, the energy released during the process and the decomposition products. Dimethoate shows a marked tendency to undergo thermal decomposition at temperature higher than 369 K. A moderate pressure increase has been recorded at the end of all runs. Many thiophosphoric compounds have been identified among the decomposition products.

Biodegradation, Environmental↗

Electroneurophysiological studies in rats of acute dimethoate poisoning.

In order to investigate the mechanism of muscular weakness in the intermediate myasthenia syndrome (IMS) following acute organophosphate poisoning, the effect of dimethoate on the neuromuscular transmission was studied in rats by using the electrical stimulation single fiber electromyography (SSFEMG) and repetitive nerve stimulation (RNS). The results showed that there was a prolongation of mean consecutive difference (MCD) of the latencies of single fiber potential shown by SSFEMG in dimethoate intoxicated rats during the presence of muscle weakness when the stimuli were given at 10 or 20 Hz, and there was a remarkable decrement of compound muscle action potential (CMAP) of gastrocnemius muscle evoked by RNS on the sciatic nerve at 20 Hz in some rats with myasthenia. The frequency of neuromuscular transmission abnormalities detected by SSFEMG was significantly higher than those detected by RNS. This study demonstrates that the SSFEMG is a more sensitive electrophysiological method in the detection of neuromuscular transmission block occurred in rats of acute organophosphate poisoning with muscle weakness.

Acute Disease↗

Effect of organophosphorus (dimethoate) and pyrethroid (deltamethrin) pesticides on semen characteristics in rabbits.

The present study was undertaken to determine the effect of chronic treatment with two sublethal doses of Dimethoate (organo-phosphorus) or Deltamethrin (pyrethroid) on body weight and semen characteristics in adult male rabbits. Pesticide treatment resulted in a decline in body weight, libido, ejaculate volume, sperm concentration and semen initial fructose; and an increase in abnormal and dead sperm and methylene blue reduction time. In this regard Dimethoate showed greater effects than Deltamethrin. The hazardous effect of these pesticides on semen quality continued during the post-treatment period, and was dose-dependent. This deleterious effect on sperm formation together with the decline in libido suggest a decrease in testosterone secretion by pesticide treatment.

Animals↗