ABSTRACT
Inorganic forms of As (arsenite - As(III) and arsenate - As(V)) are prevalent in soil and recognized for their high toxicity. Once in the soil, these forms of As can compromise key organisms for ecological processes, such as earthworms. The aim of the study was to evaluate the toxicity of arsenite and arsenate in the Californian earthworm Eisenia andrei exposed in natural soil and tropical artificial soil (TAS). Adverse effects were evaluated using avoidance test, acute toxicity test, and a sublethal concentration test to assess biochemical parameters. LC50 values for arsenite were 21.27 mg/kg in natural soil and 19.0 mg/kg in TAS and for arsenate were 76.18 mg/kg in natural soil and above 120 mg/kg in TAS. In the avoidance test, this behavior was shown to be significantly higher in the natural soil and for earthworms exposed to arsenite, while total antioxidant capacity, glutathione levels, lipid damage, and DNA damage were significantly higher in animals exposed to arsenite, but without differences in relation to the two types of soil tested. Animals exposed to As(V) showed increased activity of enzymes related to glutathione metabolism. The results obtained in the present study show the impact of As exposure on the health of the Californian earthworm E. andrei, especially in the form of arsenite, and alert the public authorities that legal limits should, whenever possible, consider the soil properties and also the different chemical species of the contaminants.
Subject(s)
Arsenites , Oligochaeta , Soil Pollutants , Animals , Soil/chemistry , Arsenates/toxicity , Arsenates/metabolism , Arsenites/toxicity , Arsenites/metabolism , Soil Pollutants/analysisABSTRACT
Previous studies have suggested that arsenic crosses the placenta and affects the fetus development. The study under consideration aims to show comparative ameliorative effect of Moringa oleifera leaf and flower extracts against sodium arsenate induced fetus toxicity of mice. Pregnant mice (N=44) were kept in lab and divided into eleven group from (A to K) and were orally administered the doses 6 mg/kg, 12 mg/kg for sodium arsenate, 150 mg/kg and 300 mg/kg for Moringa oleifera leaf extracts (MOLE) and 150 mg/kg and 300 mg/kg for Moringa oleifera flower extracts (MOFE) comparing with control. The investigation revealed evident reduction in the fetuses weight, hind limb, fore limb, tail and snout length, crown rump and head circumferences well as malformations in tail, feet, arms, legs, skin and eyes in the negative control group (only administered with sodium arsenate). Co-administration of sodium arsenate with MOLE and MOFE ameliorate the reversed effect of sodium arsenate on the shape, length, body weight and DNA damage of fetus significantly at 95% confidence interval. However, Moringa oleifera leaf extract showed more significant results in comparison to Moringa oleifera flower extract. Hence concluded that Moringa oleifera leaf extract ameliorated the embryo toxic effects of sodium arsenate and can be used against environmental teratogens.(AU)
Estudos anteriores sugeriram que o arsênio atravessa a placenta e afeta o desenvolvimento do feto. O estudo em consideração visa mostrar o efeito melhorador comparativo de extratos de folhas e flores de Moringa oleifera contra a toxicidade fetal induzida por arseniato de sódio em camundongos. Camundongos grávidas (N = 44) foram mantidos em laboratório e divididos em 11 grupos (de A a K) e foram administrados por via oral nas doses de 6 mg/kg, 12 mg/kg para arseniato de sódio, 150 mg/kg e 300 mg/kg para extratos de folhas de Moringa oleifera (MOLE) e 150 mg/kg e 300 mg/kg para extratos de flores de Moringa oleifera (MOFE) em comparação com o controle. A investigação revelou redução evidente no peso do feto, membro posterior, membro anterior, comprimento da cauda e focinho, coroa, nádega e circunferência da cabeça, bem como malformações na cauda, pés, braços, pernas, pele e olhos no grupo de controle negativo (apenas administrado com arseniato de sódio). A coadministração de arseniato de sódio com MOLE e MOFE melhora significativamente o efeito reverso do arseniato de sódio na forma, comprimento, peso corporal e dano ao DNA do feto, com intervalo de confiança de 95%. No entanto, o extrato da folha da Moringa oleifera apresentou resultados mais significativos em comparação ao extrato da flor da Moringa oleifera. Portanto, concluiu que o extrato da folha de Moringa oleifera melhorou os efeitos tóxicos do arseniato de sódio para o embrião e pode ser usado contra teratógenos ambientais.(AU)
Subject(s)
Animals , Female , Pregnancy , Mice , Moringa oleifera/embryology , Comet Assay/veterinary , Fetus/abnormalities , Fetus/drug effects , Prenatal Injuries/veterinary , Arsenates/toxicityABSTRACT
Previous studies have suggested that arsenic crosses the placenta and affects the fetus development. The study under consideration aims to show comparative ameliorative effect of Moringa oleifera leaf and flower extracts against sodium arsenate induced fetus toxicity of mice. Pregnant mice (N=44) were kept in lab and divided into eleven group from (A to K) and were orally administered the doses 6 mg/kg, 12 mg/kg for sodium arsenate, 150 mg/kg and 300 mg/kg for Moringa oleifera leaf extracts (MOLE) and 150 mg/kg and 300 mg/kg for Moringa oleifera flower extracts (MOFE) comparing with control. The investigation revealed evident reduction in the fetuses weight, hind limb, fore limb, tail and snout length, crown rump and head circumferences well as malformations in tail, feet, arms, legs, skin and eyes in the negative control group (only administered with sodium arsenate). Co-administration of sodium arsenate with MOLE and MOFE ameliorate the reversed effect of sodium arsenate on the shape, length, body weight and DNA damage of fetus significantly at 95% confidence interval. However, Moringa oleifera leaf extract showed more significant results in comparison to Moringa oleifera flower extract. Hence concluded that Moringa oleifera leaf extract ameliorated the embryo toxic effects of sodium arsenate and can be used against environmental teratogens.
Estudos anteriores sugeriram que o arsênio atravessa a placenta e afeta o desenvolvimento do feto. O estudo em consideração visa mostrar o efeito melhorador comparativo de extratos de folhas e flores de Moringa oleifera contra a toxicidade fetal induzida por arseniato de sódio em camundongos. Camundongos grávidas (N = 44) foram mantidos em laboratório e divididos em 11 grupos (de A a K) e foram administrados por via oral nas doses de 6 mg/kg, 12 mg/kg para arseniato de sódio, 150 mg/kg e 300 mg/kg para extratos de folhas de Moringa oleifera (MOLE) e 150 mg/kg e 300 mg/kg para extratos de flores de Moringa oleifera (MOFE) em comparação com o controle. A investigação revelou redução evidente no peso do feto, membro posterior, membro anterior, comprimento da cauda e focinho, coroa, nádega e circunferência da cabeça, bem como malformações na cauda, pés, braços, pernas, pele e olhos no grupo de controle negativo (apenas administrado com arseniato de sódio). A coadministração de arseniato de sódio com MOLE e MOFE melhora significativamente o efeito reverso do arseniato de sódio na forma, comprimento, peso corporal e dano ao DNA do feto, com intervalo de confiança de 95%. No entanto, o extrato da folha da Moringa oleifera apresentou resultados mais significativos em comparação ao extrato da flor da Moringa oleifera. Portanto, concluiu que o extrato da folha de Moringa oleifera melhorou os efeitos tóxicos do arseniato de sódio para o embrião e pode ser usado contra teratógenos ambientais.
Subject(s)
Female , Animals , Pregnancy , Mice , Arsenates/toxicity , Comet Assay/veterinary , Fetus/abnormalities , Fetus/drug effects , Prenatal Injuries/veterinary , Moringa oleifera/embryologyABSTRACT
Aquatic hyphomycetes are fungi with a fundamental ecological role in forested streams. These organisms are responsible for cycling of nutrients in aquatic environments. However, their structure and composition can be affected when exposed to certain pollutants. Arsenic (As) is a trace element with high toxicity for the aquatic biota. Here we evaluated the effects of different concentrations of Arsenite (AsIII) and Arsenate (AsV) on aquatic hyphomycetes assemblages. To test As toxicity, we conditioned Nectandra megapotamica leaves in a stream and after this period, we incubated leaf discs with stream water and different concentrations of AsIII and AsV. Species richness was negatively affected by both As form. Likewise, the hyphomycetes assemblages presented variation in the composition of species. However, the sporulation rates were not influenced by As. The As showed toxicity on species of hyphomycetes more sensitive, remaining only in species tolerant to its toxicity. In this way, As generated a change in the aquatic hyphomycetes composition. We observed that As had a negative effect on the aquatic hyphomycetes assemblages, regardless of the chemical form. Our results point to the toxicity of this element and its effects on a group that is fundamental to the streams ecosystems functioning.
Subject(s)
Arsenic , Mitosporic Fungi , Rivers , Water Pollution, Chemical , Arsenates/toxicity , Arsenic/toxicity , Arsenites/toxicity , Ecosystem , Plant Leaves , Rivers/chemistry , Trace Elements/toxicity , Water Pollution, Chemical/adverse effects , Water Pollution, Chemical/analysisABSTRACT
Preservative treatments increase the durability of wood, and one of the alternative treatments involves the use of chromated copper arsenate (CCA). Due to the toxicity of CCA, the disposal of CCA-treated wood residues is problematic, and burning is considered to provide a solution. The ecotoxicological potential of ash can be high when these components are toxic and mutagenic. The aim of this study was to evaluate the toxicity and genotoxicity of bottom ash leachates originating from CCA-treated wood burning. Physical-chemical analysis of the leachates revealed that in treated wood ashes leachate (CCA-TWBAL), the contents of arsenic and chromium were 59.45 mg.L-1 and 54.28 mg.L-1, respectively. In untreated wood ashes leachate (UWBAL), these contents were 0.70 mg.L-1 and 0.30 mg.L-1, respectively. CCA-TWBAL caused significant toxicity in Lactuca sativa, Allium cepa, and microcrustacean Artemia spp. (LC50 = 12.12 mg.mL-1). Comet assay analyses using NIH3T3 cells revealed that concentrations ranging from 1.0 and 2.5 mg.mL-1 increase the damage frequency (DF) and damage index (DI). According to MTT assay results, CCA-TWBAL at concentrations as low as 1 mg.mL-1 caused a significant decrease in cellular viability. Hemolysis assay analyses suggest that the arsenic and chromium leachate contents are important for the ecotoxic, cytotoxic, and genotoxic effects of CCA-TWBAL.
Subject(s)
Antineoplastic Agents , Arsenic , Refuse Disposal , Animals , Arsenates/chemistry , Arsenates/toxicity , Arsenic/analysis , Chromium/analysis , Copper/chemistry , DNA Damage , Mice , NIH 3T3 Cells , Refuse Disposal/methods , Wood/chemistryABSTRACT
In order to evaluate the differential absorption and toxicity of arsenate (AsV) and arsenite (AsIII), Lemna valdiviana plants were grown in a nutrient solution and subjected to 0.0 (control); 0.5; 1.0; 1.5; 2.0; 3.0; 4.0; 5.0 and 7.5 mg L-1 of AsIII or AsV for three days. Exposure to both chemical forms resulted in As bioaccumulation, although AsIII-grown plants showed higher As content in tissues. In AsV-grown plants, the relative growth rate (RGR) decreased to 50%, at a concentration of 4.0 mg L-1, while for treatments with AsIII, the same decrease was observed at 1.0 mg L-1. The tolerance index decreased with increasing concentrations, with lower values for AsIII. Plants treated with AsIII showed increased superoxide anion levels, whilst higher levels of hydrogen peroxide were present in AsV-treated plants. Moreover, malondialdehyde (MDA) levels were higher for plants subjected to AsIII when compared to AsV at lower concentrations. Concentrations of 1 mg L-1 of AsIII and 4 mg L-1 of AsV showed equivalent MDA levels. Superoxide dismutase and catalase activities were increased at low concentrations and were inhibited at higher concentrations of AsIII and AsV, whereas peroxidase activity was positively modulated by increased AsIII or AsV concentrations. In conclusion, L. valdiviana plants took up and accumulated arsenic as AsIII or AsV, demonstrating the potential for phytoremediation of this metalloid. Furthermore, AsIII-exposed plants showed enhanced toxicity when compared to AsV, at the same applied concentration, although toxicity was more related to internal As concentrations, regardless of the chemical form applied.
Subject(s)
Arsenates/toxicity , Arsenites/toxicity , Environmental Pollutants/toxicity , Plants/drug effects , Araceae/physiology , Biodegradation, Environmental , Malondialdehyde , Superoxide Dismutase/metabolismABSTRACT
The Burkholderia xenovorans LB400 multireplicon genome displays a relatively high proportion of redundant genes, including several genes predicted to be related to arsenic resistance. These comprise an ars gene cluster, composed of the arsR3, acr3, arsC1 and arsH genes, as well as two arsB, arsC2, and seven individual arsR genes. The objective of this work was to elucidate the involvement of the ars gene cluster in arsenic resistance by the LB400 strain. Susceptibility tests showed that B. xenovorans LB400 is highly resistant to arsenate and arsenite. Arsenic resistance was induced by prior exposure of LB400 to arsenate or arsenite. reverse transcription-polymerase chain reaction assays using total RNA from LB400 showed arsenite-induced transcription of the arsR3 gene, suggesting that the ars gene cluster constitutes an arsenite-responsive operon. Transfer of cloned LB400 ars genes to heterologous Escherichia coli or Pseudomonas aeruginosa strains demonstrated that the ArsR3 transcriptional repressor, ArsC1 arsenate reductase, and the Acr3 arsenite efflux pump encoded in the LB400 ars gene cluster, are all associated to the arsenic resistance phenotype of this strain. The ars gene cluster from Burkholderia xenovorans LB400 is responsible for the inducible arsenic-resistance phenotype of the bacterium.
Subject(s)
Arsenic/metabolism , Bacterial Proteins/genetics , Burkholderia/genetics , Drug Resistance, Bacterial/genetics , Multigene Family/genetics , Arsenate Reductases/genetics , Arsenates/metabolism , Arsenates/toxicity , Arsenic/toxicity , Arsenites/metabolism , Arsenites/toxicity , Bacterial Proteins/metabolism , Base Sequence , Burkholderia/drug effects , Burkholderia/growth & development , Cloning, Molecular , DNA, Bacterial/analysis , Escherichia coli/genetics , Gene Expression Regulation, Bacterial , Microbial Sensitivity Tests , Operon , Phenotype , Phylogeny , Pseudomonas aeruginosa/genetics , Sequence Alignment , Sequence Analysis, Protein , Trans-Activators/geneticsABSTRACT
Arsenic impairs male reproductive functions. However, it is not clear whether different arsenic compounds similarly affect fertility. In this study, we compared the impact of sodium arsenite and arsenate on sperm quality and fertility. After 56â¯d exposure, male Wistar rats were mated and pregnant females were evaluated by fertility indexes. Clearly, exposure to 10â¯mg/L arsenite reduced daily sperm production via H2O2 overproduction and germ cells loss. Animals from this group also showed a decrease in epididymal sperm counts and percentage of sperm with intact membranes. Moreover, they presented low fertility potential and high preimplantation loss. In contrast, 10â¯mg/L arsenate caused oxidative stress in testis, mineral imbalance in epididymis, and sperm membranes damage, with no effects on fertility. Both arsenic compounds at 0.01â¯mg/L altered reproductive parameters. We concluded that arsenite is more harmful than arsenate to sperm quality and male fertility, with negative influences in early pregnancy.
Subject(s)
Arsenates/toxicity , Arsenites/toxicity , Fertility/drug effects , Sodium Compounds/toxicity , Animals , Catalase/metabolism , Female , Glutathione Transferase/metabolism , Male , Malondialdehyde/metabolism , Rats, Wistar , Sperm Count , Sperm Motility/drug effects , Spermatozoa/drug effects , Testis/drug effects , Testis/metabolism , Testis/pathology , Testosterone/bloodABSTRACT
Arsenic (As), in the form of trivalent arsenite or pentavalent arsenate, is a ubiquitous toxic compound naturally occurring in the environment. This study aimed to evaluate the impact of two different forms of inorganic As on reproductive parameters following oral exposure. Adult Wistar male rats were exposed to sodium arsenite or arsenate at concentrations of 0.01 mg/L or 10 mg/L for 56 d in drinking water. Sodium arsenite at both concentrations and sodium arsenate at 10 mg/L produced reduction in daily sperm production, in number of spermatids in the testis, and in sperm in the epididymal caput/corpus regions. Changes in epididymal morphometry were variable and region specific. Total and progressive sperm motility and sperm morphology did not differ markedly between controls and animals exposed to As. The body and reproductive organs weights, as well as testosterone concentration, remained unchanged among all groups. In conclusion, As exposure in drinking water over 56 d produced damage in male reproductive functions in adult rats, suggesting that fertility problems might occur. Therefore, additional studies need to be undertaken to investigate potential mechanisms underlying sodium arsenite- and arsenate-induced disturbances in fertility and reproductive performance.
Subject(s)
Arsenates/toxicity , Arsenites/toxicity , Fertility/drug effects , Reproduction/drug effects , Animals , Body Weight/drug effects , Drinking Water , Epididymis/pathology , Male , Organ Size/drug effects , Rats , Rats, Wistar , Sperm Count , Sperm Motility/drug effects , Spermatozoa/drug effects , Spermatozoa/ultrastructure , Testosterone/metabolismABSTRACT
Arsenic is an ametal ubiquitous in nature and known by its high toxicity. Many studies have tried to elucidate the arsenic metabolism in the cell and its impact to plants, animals and human health. In aqueous phase, inorganic arsenic is more common and its oxidation state (As III and As V) depends on physical and chemical environmental conditions. The aim of this study was to evaluate toxicity of arsenic to Daphnia similis and Ceriodaphnia silvestrii, isolated and associated with iron. The results showed differences in toxicity of As III and As V to both species. Effective concentration (EC50) mean values were 0.45 mg L-1 (As III) and 0.54 mg L-1 (As V) for D. similis, and 0.44 mg L-1 (As III) and 0.69 mg L-1 (As V) for C. silvestrii. However, As V IC25 mean value was 0.59 mg L-1, indicating that C. silvestrii has mechanisms to reduce arsenic toxicity. On the other hand, when associated with iron at 0.02 and 2.00 mg L-1, EC50 values decreased for D. similis (0.34 and 0.38 mg L-1) as well as C. silvestrii (0.37 and 0.37 mg L-1), showing synergistic effect of these substances.
Subject(s)
Arsenates/toxicity , Arsenites/toxicity , Cladocera/drug effects , Daphnia/drug effects , Iron , Animals , Arsenic/toxicity , Toxicity Tests, Acute , Toxicity Tests, ChronicABSTRACT
Acacia farnesiana is a shrub widely distributed in soils heavily polluted with arsenic in Mexico. However, the mechanisms by which this species tolerates the phytotoxic effects of arsenic are unknown. This study aimed to investigate the tolerance and bioaccumulation of As by A. farnesiana seedlings exposed to high doses of arsenate (AsV) and the role of peroxidases (POX) and glutathione S-transferases (GST) in alleviating As-stress. For that, long-period tests were performed in vitro under different AsV treatments. A. farnesiana showed a remarkable tolerance to AsV, achieving a half-inhibitory concentration (IC50) of about 2.8 mM. Bioaccumulation reached about 940 and 4380 mg As·kg(-1) of dry weight in shoots and roots, respectively, exposed for 60 days to 0.58 mM AsV. Seedlings exposed to such conditions registered a growth delay during the first 15 days, when the fastest As uptake rate (117 mg kg(-1) day(-1)) occurred, coinciding with both the highest rate of lipid peroxidation and the strongest up-regulation of enzyme activities. GST activity showed a strong correlation with the As bioaccumulated, suggesting its role in imparting AsV tolerance. This study demonstrated that besides tolerance to AsV, A. farnesiana bioaccumulates considerable amounts of As, suggesting that it may be useful for phytostabilization purposes.
Subject(s)
Acacia/drug effects , Acacia/metabolism , Arsenates/toxicity , Soil Pollutants/toxicity , Acacia/enzymology , Acacia/genetics , Arsenates/metabolism , Arsenic/metabolism , Arsenic/toxicity , Biodegradation, Environmental , Glutathione Transferase/metabolism , Lipid Peroxidation/drug effects , Oxidative Stress , Peroxidases/metabolism , Plant Proteins/metabolism , Seedlings/drug effects , Seedlings/enzymology , Seedlings/growth & development , Seedlings/metabolism , Soil Pollutants/metabolismABSTRACT
Arsenate (As(V)) and arsenite (As(III)) contamination is able to interfere negatively on plant metabolism, promoting a reduction of nutrients uptake and transport and also an increase of reactive oxygen species (ROS) generation. However, some plants are considered tolerant against As exposure through the activation of defense mechanisms. Therefore, this study aimed to evaluate the effects of different As(V) and As(III) concentrations (0.0, 6.6, 13.2, 26.4 and 52.8 µmol L(-1)), on mineral nutrients concentration [calcium (Ca), magnesium (Mg), phosphorous (P), iron (Fe), manganese (Mg) and copper (Cu)], on membrane lipid peroxidation and also on the enzymes belonging to the antioxidant defense system [superoxide dismutase (SOD), total peroxidase (POX), catalase (CAT), glutathione reductase (GR) and ascorbate peroxidase (APX)] of plants of Lactuca sativa L. cv Hanson. As(V) and As(III), showed, in general, the same toxic effects in leaves and roots with significant changes in essential macro- and micronutrients concentration. Lipid peroxidation of cellular membranes was also observed in tested plants, probably resulted from an action of ROS generated by this metalloid. The increase of ROS generation and their scavenge were evident since an increase of SOD, POX, CAT and APX activity in leaves, and SOD, CAT and GR activity in roots were observed. Therefore, As(V) and As(III) exposure resulted in toxic effects in leaves and roots of lettuce plants; however, this plant species was able to attenuate these potential As damages through the activation of defense mechanisms, keeping its metabolism. Arsenic-tolerant plants are considered a great risk to the public health since it results in As insertion to the food chain.
Subject(s)
Arsenates/toxicity , Arsenites/toxicity , Lactuca/drug effects , Lactuca/metabolism , Antioxidants/metabolism , Ascorbate Peroxidases/metabolism , Catalase/metabolism , Glutathione Reductase/metabolism , Lipid Peroxidation/drug effects , Peroxidase/metabolism , Superoxide Dismutase/metabolismABSTRACT
It is useful to test ecotoxicity and genotoxicity endpoints in the environmental impact assessment. Here, we compare and discuss ecotoxicity and genotoxicity effects in organisms in response to exposure to arsenate (As V) in solution. Eco(geno)toxicity responses in Aliivibrio fischeri, Lytechinus variegatus, Daphnia magna, Skeletonema costatum and Vicia faba were analyzed by assessing different endpoints: biomass growth, peroxidase activity, mitotic index, micronucleus frequency, and lethality in accordance with the international protocols. Quantitative sensitivity relationships (QSR) between these endpoints were established in order to rank endpoint sensitivity. The results for the QSR values based on the lowest observed effect concentration (LOEC) ratios varied from 2 (for ratio of root peroxidase activity to leaf peroxidase activity) to 2286 (for ratio of higher plant biomass growth to root peroxidase activity). The QSR values allowed the following sensitivity ranking to be established: higher plant enzymatic activity>daphnids≈echinoderms>bacteria≈algae>higher plant biomass growth. The LOEC values for the mitotic index and micronucleus frequency (LOEC=0.25mgAsL(-1)) were similar to the lowest LOEC values observed in aquatic organisms. This approach to the QSR of different endpoints could form the basis for monitoring and predicting early effects of pollutants before they give rise to significant changes in natural community structures.
Subject(s)
Arsenates/toxicity , Water Pollutants, Chemical/toxicity , Aliivibrio fischeri , Animals , Aquatic Organisms , Arsenates/standards , Biomarkers/metabolism , Biomass , Daphnia , Mutagens/standards , Mutagens/toxicity , Plant Roots/growth & development , Risk Assessment , Vicia faba , Water Pollutants, Chemical/standardsABSTRACT
Arsenic (As) exposure has been associated with serious chronic health risk to humans including cancer and neurological disturbances. However, there are limited studies about the mechanisms behind its toxicity. In this study, adult zebrafish were exposed to several concentrations of As (0.05, 5, and 15 mg As/L; Na(2)HAsO(4) as As(V)) during 96 h to evaluate the zebrafish locomotor activity, anxiety, and brain extracellular nucleotide hydrolysis. We showed that 5 mg/L As is able to promote significant decrease in the locomotor activity as evaluated by the number of line crossings. In addition, animals treated with 5mg/L As presented an increase in time spent in the lower zone of the tank test, suggesting an anxiogenic effect. Considering that behavioral parameters, such as anxiety and locomotion, might be modulated by the purinergic system, we also evaluated the ectonucleotidase activities in zebrafish brain after a 96-h As exposure. A significant decrease in ATP, ADP, and AMP hydrolysis was observed at 0.05, 5, and 15 mg/L when compared to control group. These findings demonstrated that As might affect behavioral parameters and the ectonucleotidase activities in zebrafish, suggesting this enzyme pathway is a target for neurotoxic effects induced by As.
Subject(s)
Arsenates/toxicity , Behavior, Animal/drug effects , Brain/drug effects , Nucleoside-Triphosphatase/metabolism , Water Pollutants, Chemical/toxicity , Zebrafish/physiology , Adenosine Diphosphate/metabolism , Adenosine Monophosphate/metabolism , Adenosine Triphosphate/metabolism , Animals , Anxiety/chemically induced , Brain/enzymology , Female , Hydrolysis , Locomotion/drug effects , Male , Toxicity TestsABSTRACT
INTRODUCTION: This study aimed to analyze antioxidant responses and oxidative damage induced by two inorganic forms of arsenic (As; As(III) and As(V)) in an estuarine polychaete species, Laeonereis acuta (Nereididae). The capacity of arsenic biotransformation was also evaluated through the methylation process considering the activity of a key enzyme involved in the metabolization process. MATERIALS AND METHODS: Worms were exposed to 50 µg (As(III) or As(V))/l during 2 or 7 days, plus a control group. Endpoints analyzed included concentration of reactive oxygen species (ROS), activities of antioxidant enzymes such as glutathione reductase (GR), total glutathione-S-transferase (GST), and omega isoform (GST Ω), glucose-6-phosphate deshydrogenase (G6PDH), levels of the antioxidant glutathione (GSH), and lipid peroxides concentration (TBARS). RESULTS AND DISCUSSION: Results showed: (1) GR inhibition after 2-day exposure to both As forms (p < 0.05); (2) GST Ω inhibition after 7-day exposure to As(III) paralleled by an increase in total GST activity (p < 0.05); (3) augmented G6PDH activity after 7-day exposure to both As forms (p < 0.05); (4) no differences in terms of ROS and TBARS; and (5) inhibition of GST Ω activity in As(III) exposed worms, which was concomitant with a lowering of mono- and dymethylated arsenic species. CONCLUSION: These results confirm the reactivity of some biochemical variables of L. acuta to As and indicates its importance as a sentinel species in estuarine regions with presence of arsenic.
Subject(s)
Arsenates/metabolism , Arsenites/metabolism , Polychaeta/metabolism , Water Pollutants/metabolism , Animals , Antioxidants/metabolism , Arsenates/chemistry , Arsenates/toxicity , Arsenites/chemistry , Arsenites/toxicity , Biotransformation , Environmental Monitoring , Glucosephosphate Dehydrogenase/metabolism , Glutathione/metabolism , Glutathione Reductase/metabolism , Glutathione Transferase/metabolism , Lipid Peroxidation , Oxidative Stress/drug effects , Polychaeta/drug effects , Polychaeta/enzymology , Reactive Oxygen Species/metabolism , Water Pollutants/toxicityABSTRACT
Epidemiological evidence has associated exposure to arsenic (As) in drinking water with an increased incidence of human cancers in the skin, bladder, liver, kidney and lung. Sodium arsenite mimics the effects of estradiol and induces cell proliferation in the estrogen responsive breast cancer cell line MCF-7. Therefore, our aim was to further explore the ability of sodium arsenite to induce MCF-7 epithelial breast cell proliferation and some of its underlying mechanisms by studying ROS production, c-Myc and HO-1 protein levels, 8-OHdG formation and NF-kappaB activation. Low arsenite concentrations (0.5-5 microM) induced ROS production and ROS-related depolarization of the mitochondrial membrane suggesting that mitochondria played an important role in the oxidative effects of As. ROS-mediated DNA damage as measured by the presence of 8-OHdG DNA-adducts in their nuclei, IkappaB phosphorylation, NF-kappaB activation and increases in c-Myc and HO-1 protein levels were also observed, suggesting that these factors play a relevant role in the arsenite induced MCF-7 cell recruitment into the S-phase of the cell cycle and cell proliferation observed. In conclusion, arsenite activates several pathways involved in MCF-7 cell proliferation suggesting that arsenite exposure may pose a risk for breast cancer in human exposed populations notwithstanding that most studies to date have not yet implicated this metalloid as a cofactor in the etiology of this disease.
Subject(s)
Arsenates/toxicity , Breast Neoplasms/pathology , Cell Proliferation/drug effects , DNA Damage , Heme Oxygenase-1/metabolism , NF-kappa B/metabolism , Proto-Oncogene Proteins c-myc/metabolism , Reactive Oxygen Species/metabolism , Cell Cycle/drug effects , Cell Line, Tumor , DNA Adducts/metabolism , DNA Damage/physiology , Drug Evaluation, Preclinical , Humans , Mitochondria/drug effects , Mitochondria/metabolism , Oxidative Stress/drug effects , Oxidative Stress/geneticsABSTRACT
Numerous epidemiological studies suggest that arsenic (As) compounds are carcinogens, however, recent data have renewed the interest in their anticarcinogenic properties. The cytotoxic effects of three arsenic compounds were assessed: sodium arsenite, sodium arsenate and sodium cacodylate, representing the trivalent and pentavalent species of arsenic, along with a dimethylated pentavalent arsenic species. HeLa cells and Salmonella typhimurium (strains TA98 and TA100) were exposed to As compounds and the cytotoxic effects were evaluated. Alterations on RNA and DNA synthesis in HeLa cells were also examined. All arsenic compounds produced a dose-dependent inhibition on colony formation and DNA synthesis in HeLa cells, yet any of them significantly influenced RNA synthesis in these cells. No evidence of arsenic-induced mutagenicity or antimutagenicity was observed using the Ames assay. In bacterial cells, only sodium arsenite caused a dose-dependent inhibition of colony formation.Collectively, these results indicate that in both, HeLa and S. typhimurium cell systems, only trivalent sodium arsenite can act as an effective inhibitor of cell growth. The possible mechanism(s) of the cytotoxic effect of arsenite in these two different cell systems might be due to its reactivity with intracellular sulfhydryl groups.
Subject(s)
Antineoplastic Agents/pharmacology , Arsenates/pharmacology , Arsenates/toxicity , Arsenites/pharmacology , Arsenites/toxicity , Cacodylic Acid/pharmacology , Cacodylic Acid/toxicity , Salmonella typhimurium/drug effects , Sodium Compounds/pharmacology , Sodium Compounds/toxicity , Antimutagenic Agents/pharmacology , Cell Division/drug effects , Colony-Forming Units Assay , DNA/biosynthesis , HeLa Cells , Humans , Mutagenicity Tests , Mutagens/toxicity , RNA/biosynthesis , Salmonella typhimurium/geneticsABSTRACT
Two arsenic compounds, sodium arsenite (NaAsO2) and sodium arsenate (Na2HAsO4), were tested for their possible genotoxicity in germinal and somatic cells of Drosophila melanogaster. For germinal cells, the sex-linked recessive lethal test (SLRLT) and the sex chromosome loss test (SCLT) were used. In both tests, a brood scheme of 2-3-3 days was employed. Two routes of administration were used for the SLRLT: adult male injection (0.38, 0.77 mM for sodium arsenite; and 0.54, 1.08 mM for sodium arsenate) and larval feeding (0.008, 0.01, 0.02 mM for sodium arsenite; and 0.01, 0.02 mM for sodium arsenate). For the SCLT the compounds were injected into males. Controls were treated with a solution of 5% sucrose which was employed as solvent. The somatic mutation and recombination test (SMART) was run in the w+/w eye assay as well as in the mwh +/+ flr3 wing test, employing the standard and insecticide-resistant strains. In both tests, third instar larvae were treated for 6 hr with sodium arsenite (0.38, 0.77, 1.15 mM), and sodium arsenate (0.54, 1.34, 2.69 mM). In the SLRLT, both compounds were positive, but they were negative in the SCLT. The genotoxicity of both compounds was localized mainly in somatic cells, in agreement with reports on the carcinogenic potential of arsenical compounds. Sodium arsenite was an order of magnitude more toxic and mutagenic than sodium arsenate. This study confirms the reliability of the Drosophila in vivo system to test the genotoxicity of environmental compounds.