Effects of mercury graded doses on redox status,metallothionein levels and genotoxicity in the intestine of sea cucumber Holothuria forskali

Mercury (Hg) is a ubiquitous and a major environmental metal pollutant in the aquatic ecosystem. The present study was performed to evaluate the effect of mercury graded doses exposure on oxidative stress, redox status, metallothionein levels and genotoxicity in the intestine of sea cucumber Holothuria forskali. Specimens were exposed for 96?h to three concentrations of Hg (40, 80 and 160?µg/L). Exposure of H. forskali to Hg promoted oxidative stress with an increase in malondialdehyde (MDA), protein carbonyl (PCO) and advanced oxidation protein products (AOPP) levels. An increase of glutathione (GSH), vitamin C (ViteC) and non-protein thiols (NPSH) contents was also observed. Additionally, antioxidant activities of catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GPx) increased especially with the highest doses of Hg indicating a great defense of the antioxidant system. Our investigation revealed an increase in total Metallothionein (MT) content which was more pronounced at the sharpest concentrations of Hg. A significant decline of AChE activity was also observed. In the intestine of Hg-treated H. forskali genotoxicity was confirmed by DNA degradation.     

Genotoxicity in the freshwater gastropod Lymnaea luteola L: assessment of cell type sensitivities to lead nitrate

The aquatic ecosystems are converting into the highly contaminated site due to environmental pollutants. The present study explores the oxidative stress and toxic potential of lead nitrate in freshwater snail Lymnaea luteola (L. luteola) L. The snails were exposed to an environmentally relevant concentration of lead nitrate for 24 and 96?h. Later exposure to lead nitrate (0, 10, 20 and 40?µg/mL) to the freshwater snail, the level of reactive oxygen species, malondialdehyde and nitric oxide (NO) were increased and glutathione, glutathione-S-transferase were decreased. Lead-nitrate-induced haemocyte cell death and it was observed by using Annexin-V FITC/PI through a flow cytometer. DNA damage in haemocyte cells was measured at above doses of lead-nitrate exposure for 24 and 96?h and it was compared to the untreated snail. Average tail DNA (%) and olive tail moment in single-cell gel test were increased dose and duration fashion and maximum DNA damage was measured at 96?h. These results indicate the potential toxicity and genotoxicity of lead nitrate in acute treatment to L. luteola and single-cell gel test are the assay for rapid detection of genetic effects.     

Neurotoxicity and oxidative stress induced by permethrin in gills of the freshwater mussel Unio ravoisieri

Pyrethroids are contaminants found in the aquatic environment, and their toxicological effects on aquatic organisms have received extensive attention. However, the impact on freshwater bivalve of exposure to these chemicals is still largely unknown. Freshwater mussels Unio ravoisieri were exposed to two nominal permethrin (PM) concentrations C1?=?50?µg/L and C2?=?100?µg/L during 7 days. The measured concentrations of PM using gas chromatography (GC/ECD) in the treated aquariums were, respectively, 28.7–62.3?µg/L. Catalase (CAT), Glutathione-S-transferase (GST), and Acetylcholinesterase (AChE) activities, Glutatione (GSH) and Malondialdehyde (MDA) levels were determined in gills of U. ravoisieri. Significant increase in CAT activity by the lowest concentration and decrease by highest concentration were observed. Additionally, GST activity was increased in a concentration-dependent manner. However, statistically significant decrease in GSH levels (about 39%) was observed only at high concentration of this compound (100?µg/L). PM generated an increase in MDA levels reaching the highest value at the high concentration. AChE activity of mussel ranging from 51% inhibition at lowest concentration 50?µg/L to 89% inhibition at highest concentration 100?µg/L. The results indicated that oxidative stress and cell damage might be one of the main mechanisms of PM toxicity to freshwater mussels.     

Induction of micronuclei in tadpoles of Odontophrynus americanus (Amphibia: Leptodactylidae) by the pyrethroid insecticide cypermethrin

Cypermethrin (CY) is an active cyano pyrethroid effective against a wide range of pests encountered in agriculture and forestry. Although CY is not mutagenic in in vitro assays for gene mutation, in vivo assays showed conflicting results. In vivo genotoxicity of the synthetic pyrethroid CY in erythrocytes of Odontophrynus americanus tadpoles was examined. The frequency of micronuclei (MN) was recorded in blood smears obtained from tadpoles exposed in vivo to four different nominal concentrations 5, 10, 20 or 40?µg?L^?1 of the compound and fixed at two sampling times 48 and 96?h. As a positive control larvae were exposed to 40?mg?L^?1 of cyclophosphamide (CP). Tadpoles exposed to all CY treatments showed a significant increase in single small MN compared to the negative control group after 48?h and at 5 and 10?µg?L^?1 of CY at 96?h. Results obtained here demonstrated the genotoxic effects of the commercial formulation CY in the anuran larvae analyzed. Thus, data suggest that measurements of MN and other erythrocytes morphological aberrations performed in circulating blood samples of O. americanus tadpoles is a method for detecting cytogenetic damage in other native species.     

Effects of subchronic exposure to carbofuran on antioxidant defence system and malondialdehyde levels in common carp (Cyprinus carpio L.)

The present study focused on the assessment of oxidative stress induction by pesticides such as carbamates which are widely used as insecticides and nematicides and contaminate aquatic ecosystems on certain biomarkers in liver of common carp (Cyprinus carpio L.). Biomarkers selected for stress monitoring were malondialdehyde (MDA), an index of lipid peroxidation, and antioxidant defence system enzymes, mainly catalase (CAT), glutathione reductase (GR), and glutathione-S-transferase (GST) activities in liver of fish exposed to 0, 10, 50, or 100?µg?L^?1 of carbofuran for 4, 15, or 30 days. Oxidative stress was found in liver of common carp exposed to carbofuran which was manifested by a decrease in CAT and GR activities after 4 and 30 days of exposure. An adaptive response was probably produced since at day 15 no modifications in the CAT activity and increased GR activity were observed. In addition, a decrease in MDA content with the highest concentration of carbofuran used was found after 30 days of exposure. However, no significant changes were found in GST activity showing a varied response. The results concerning oxidative and antioxidant profiles indicate that subchronic exposure to the insecticide carbofuran is capable of inducing oxidative stress in fish.     

Indium tin oxide nanoparticles-mediated DNA fragmentation and cell death by apoptosis in human lung epithelial cells

Indium tin oxide (ITO) nanoparticles (NP) have extensive applications in industrial fields, and concerns regarding their potential toxicity in humans and environmental impact have increased. Since exposure to ITO NP is mainly via skin and inhalation, this study was conducted utilizing human lung epithelial (A549) cell line. Cells were exposed to different concentrations of the ITO NP for 24 and 48 hr. A severe cytotoxic response of ITO NP was observed as evident by the (3-4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and neutral red uptake assays after 48 hr exposure. ITO NP significantly reduced glutathione levels with a concomitant increase in lipid hydroperoxide levels, superoxide activity, and reactive oxygen species (ROS) generation after exposure. A significant induction in caspase activity and formation of condensed chromosomal bodies was also observed after ITO NP (10 or 25 µg/ml) exposure. Furthermore, a significant induction in DNA damage was observed by the Comet assay in cells exposed to ITO NP. Our data demonstrate that ITO NP display cytotoxic and genotoxic potential. However, increase in ROS levels and oxidative stress leading to oxidative DNA damage and condensed chromosomal bodies formation, suggests involvement of apotosis. Thus, ITO NP-mediated effects on cell viability indicate cytotoxicity, and therefore, exposures need to be carefully monitored in the industrial sector.     

Deltamethrin-induced alterations in serum calcium and prolactin cells of a freshwater teleost,Heteropneustes fossilis

Deltamethrin, a pyrethroid insecticide widely used in many countries, causes significant adverse effects in aquatic ecosystems. The concentration of deltamethrin in water reservoirs and the run off from agricultural areas (in water) in many countries range up to 24.0?µg?L^?1 which is higher than the recommendation of the European Union standard. Hence, in this study the effects of deltamethrin were investigated, i.e. its toxic impacts on the freshwater catfish Heteropneustes fossilis in terms of serum calcium and prolactin cells (located in the rostral pars distalis region of the pituitary). The fish were subjected to deltamethrin for a short-term experiment (96?h; 1.5?µg?L^?1 e.0.8 of 96?h LC₅₀) and a long-term experiment (28 days; 0.37?µg?L^?1 e.0.2 of 96?h LC₅₀). After short-term deltamethrin exposure, serum calcium levels decrease. No histological change in prolactin cells is noticed throughout the short-term experiment. Fish exposed to deltamethrin for 7 days also exhibit a decrease in serum calcium level. This decrease persisted until the end of the experiment (28 days). Prolactin cells of fish treated for 14 days with deltamethrin exhibit increased nuclear volume and degranulation, increasing progressively from the 21st day onwards. After 28 days, a few degenerated cells are discerned. The results of this study show that deltamethrin is moderately toxic for the freshwater fish H. fossilis by producing adverse effects on serum calcium and prolactin cells. Hence, it should be used with caution in areas near fish-inhabited waters.     

Antioxidant enzymatic activities and lipid peroxidation in liver and ovary of zebrafish (Danio rerio) exposed to deltamethrin

Deltamethrin (DM) is being used as a substitute for organochlorines and organophosphates in pest control because of its low environmental persistence and toxicity. But it has become an environmental contaminant as it has been used widely. In this study, we investigated the effect of DM (technical grade) on the antioxidant system of adult zebrafish. For this, six-month-old fish were exposed to 2, 4 and 6?μg/L of DM for 96?h. The tissues selected were liver and ovary. Our data showed that exposure to DM increases CAT (catalase), SOD (superoxide dismutase), GPx (glutathione peroxidase, antioxidant enzymes), LPO (lipid peroxidation, non-enzymatic antioxidant) and GST (glutathione S-transferase, detoxifying enzyme) in liver and ovary. Increased GST could detoxify the toxicant; still there could be enough DM to cause oxidative stress. It appears from our study that zebrafish used compensatory mechanisms in eliminating reactive oxygen species. These data will be useful as oxidative stress is being used as a biomarker for aquatic pollution.     

Bisphenol S induces oxidative stress and DNA damage in rat spermatozoa in vitro and disrupts daily sperm production in vivo

Bisphenol S has been introduced into some industrial applications and it may act as a xeno-estrogen that can alter endocrine functions and reproduction. The present study was carried out to examine the effect of bisphenol S exposure on oxidative stress, generation of reactive oxygen species, and DNA integrity in rat spermatozoa in vitro and daily sperm production and sperm DNA damage in vivo. Sperm were incubated with bisphenol S at concentrations of 0.5, 1, 10, and 100 µg/L. At the highest concentration, bisphenol S induced formation of reactive oxygen species, caused lipid peroxidation, affected superoxide dismutase levels, and increased DNA fragmentation. Adult rats were exposed to doses of 0.5, 5, 25, and 50 µg/kg/d for 28 days. Decrease in daily sperm production and an increase in sperm DNA damage was observed at the highest dose in the 50 µg/kg/d treated group, but sperm motility was not reduced.     

Ecotoxicological assessment of sediment from Texcalac River and agricultural soil of riverside area,in Tlaxcala,Mexico

This study assesses the potential risk of Texcalac River and riparian area. The p,p′ DDT and ∑DDTs levels in agricultural soils (3.9–208.0?µg/kg) and in surface sediments (0.6–137?µg/kg) surpassing the guidelines for protection of aquatic life (75% > TEC). The ∑PCBs concentration oscillated from 135 to 93941?µg/kg; the half of sediments exceeded the international guidelines (PEL, PEC), as well as two soils (SQGE?=?500?µg/kg). The TEQ concentration of four PCB-DL varied between 0.1 and 24.9?µg TEQ/kg, chiefly affected by PCB 169. Five sediments were lethal for E. foetida, two resulted to be cytotoxic and the 58% produced genotoxicity higher than negative control (A?=?0.28?±?0.05; DICA?=?72.5?±?16.9 au). Likewise, 31.6% of samples increased the micronuclei frequency in V. faba in comparison with negative control. The analytical data and the bioassays results suggest a significant and immediate risk to exposed biota of this region, highlighting a specific area in Texcalac River and other one in Sambrano Ravine. It is necessity assess the dispersion of pollutants and perform biomonitoring studies that display the exposure levels in biota with the goal to characterise the ecotoxicological risk.     

Effects of bisphenol A on Gammarus fossarum and Lumbriculus variegatus in artificial indoor streams

The impact of bisphenol A (BPA) on Gammarus fossarum and Lumbriculus variegatus was studied in four artificial indoor streams (0, 5, 50 and 500?µg?L^?1 BPA, nominal) over 103 days in a pulse–dose exposure scenario (weekly BPA application). For G. fossarum populations at day 103, the proportions of juveniles and of breeding females from the highest BPA treatment were in tendency reduced. For individually exposed gammarid pairs an EC₁₀ of 17?µg?L^?1 BPA (nominal) for the proportion of reproductive females in the fourth brood was determined. During the first three broods, the largest brood size occurred at the highest BPA concentration, whereas in the fourth brood it decreased concentration-dependently (fourth brood EC₁₀?=?5?µg?L^?1 BPA, nominal). Effects on L. variegatus were a reduced population growth (103?d-EC₁₀ of 2?µg?L^?1 BPA, nominal) and an increase in dry weight and the number of segments in large, complete worms.     

Effects to perfluorooctane sulfonate (PFOS) on the mollusk Unio ravoisieri under laboratory exposure

To understand acute toxicity and oxidative stress of perfluorinated compounds in the freshwater ecosystems, we exposed freshwater mussels (Unio ravoisieri) to perfluorooctane sulfonate (PFOS), over a range of concentrations from 10 to 100?mg/L, in a laboratory experiment. Lethal concentration (LC50) was of about 65.9?mg/L after 96?h of exposure. The oxidative stress was assessed in gill and digestive gland of the freshwater mussels after 7 days of exposure to different nominal PFOS concentrations (C1=?2?mg/L, C2?=?6?mg/L and C3=?10?mg/L). C1 and C2 increased significantly (p?<?.05) the superoxide dismutase activity in both tissues compared, while the highest C3 decreased the enzyme activity. This implements an unfavourable response that highlights the excess of reactive oxygen species produced after contamination. The Catalase activity was also increased by about 40.05% and 66.63%, respectively, in gill and digestive gland after exposure to C3. The Malondialdehyde (MDA) level was increased in both gill and digestive gland in a concentration-dependent pattern. In contrast, the contamination of U. ravoisieri by PFOS did not affect the acetylcholinesterase activity in both organs (p?>?.005). These results provided information on potential biomarkers that could be effectively applied for the monitoring of freshwater ecosystem using indicator species such as U. ravoisieri.     

Role of the necrosis factor-κB pathway in dibutyl phthalate mediated effects on human glioma cells

Abstract

The human glioma cell line U251 was incubated for 12?h and 24?h in medium containing dibutyl phthalate at concentrations of 25?µmol/L and 100?µmol/L. Decreased cell viability and increased oxidative stress show the cytotoxicity of dibutyl phthalate. Nuclear factor-κB and nuclear factor-κB pathway-related proteins were altered, which could be attenuated by vitamin E at 20?µmol/L. Thus, dibutyl phthalate induces cytotoxicity through activation of nuclear factor-κB and vitamin E exerts neuroprotection against dibutyl phthalate-mediated cytotoxicity in vitro.     

Protective role of epigallocatechin 3-gallate against lead-induced toxicity in human neuroblastoma cells

Lead (Pb) is a heavy metal, known to induce oxidative stress and produce damage to the antioxidant defence system ultimately leading to cell death. Antioxidants such as epigallocatechin 3-gallate (EGCG), a green tea polyphenol, was shown to play a protective role during Pb-exposure. In this study, human SH-SY5Y neuroblastoma cells were exposed to different concentrations (0.01–10?µM) of Pb for 48?h to determine effects on the viability of cells. It was observed that IC₅₀ was at 5?µM and at this concentration the cells exhibited a significant increase in caspase-3 activity, an indicator of apoptosis at least by 10-fold and the decrease of 59.4% in glutathione (GSH) content. The total cellular prostaglandin-E₂ (PGE₂) level was found to be elevated at least 10-fold upon Pb exposure. However, the effects of Pb on cells pre-incubated with 50?µM EGCG followed by 5?µM Pb showed 40% inhibition in cell viability, 17.3% decrease in caspase-3 activity, 23% increase in GSH content, and 11.4% fall in PGE₂ levels when compared with cells exposed to Pb only. Data suggest that EGCG exerted a significant protection to cell viability in preventing cell death and elevation in levels of GSH in cells exposed to Pb. However, EGCG did not elicit any significant effect on release of PGE₂ indicating the nature of EGCG as an effective anti-apoptotic, antioxidant, and anti-inflammatory agent.     

Evaluation of environmental stress by comet assay on freshwater snail Lymnea luteola L. exposed to titanium dioxide nanoparticles

The use of aquatic organisms to monitor for contamination is well-established. Therefore, this study was designed to assess the adverse effects of titanium dioxide nanoparticles (TiO₂NP) in freshwater snail Lymnea luteola L. (L. luteola). For TiO₂NPs ecotoxicity tests, snails were exposed for seven days. A dose and time-response relationship was observed for TiO₂NP-induced genotoxicity. Induction of oxidative stress in digestive gland was observed by a decrease in glutathione and gluthathions-S-transferase levels accompanied by elevated malondialdehyde levels at TiO₂NP (9 and 28 µg/mL). Superoxide dismutase activities were markedly reduced at TiO₂NP (9 and 28 µg/mL) at days 1 and 3, but not at day 7. Catalase activities were decreased at days 1 and 3 but increased at higher concentration of TiO₂NP at day 7. DNA fragmentation occurring in L. luteola due to ecotoxic impact TiO₂NP was further substantiated by alkaline single-cell gel electrophoresis assay and expressed in terms of percent tail DNA and olive tail moment. The results indicate that the interaction of these TiO₂NP with snail influences the toxicity, which is mediated by oxidative stress in a dose- and time-dependent manner. The measurement of DNA integrity in L. luteola thus provides an early warning signal of contamination of the aquatic ecosystem by TiO₂NP. Data suggest the freshwater snail L. luteola is a potential biomonitor organism.     

Morpho-histological and enzymatic alterations in earthworms Drawida willsi and Lampito mauritii exposed to urea,phosphogypsum and paper mill sludge

The effects of varying concentrations of urea, phosphogypsum and paper mill sludge (PMS) on the morphology, histology, tissue protein content, lipid peroxidation (LPX), activities of lactate dehydrogenase (LDH), acetylcholinesterase (AChE) and catalase in earthworms Drawida willsi and Lampito mauritii have been studied over an exposure period of 24?hr. Integumentary lesions, clitellar swelling and loss of pigmentations were found to be major morpho-pathological changes in the worms. Histology indicated cuticular damage, ruptured epithelium and muscle fibres with accumulation of cellular debris. Lowest tissue protein content (57.02?±?4.02?mg/g tissue) and highest LPX (0.113?±?0.04, 0.137?±?0.08?nmol/mg protein) were noticed in D. willsi at a high concentration of PMS, whereas highest tissue protein content was observed in L. mauritii (115.32?±?7.18?mg/g tissue) with the same treatment. In both the species, LDH activity was minimum at a high concentration of urea (0.172?±?0.02; 0.247?±?0.08?U/mg protein). AChE activity was highest (0.099?±?0.002?U/mg protein) at a high concentration of PMS in D. willsi, whereas catalase activity was the maximum (0.338?±?0.02?U/mg protein) at high concentrations of PMS in L. mauritii. The study indicated that morpho-histological and enzymatic alterations in these earthworms exposed to agrochemicals could be useful biomarkers to evaluate soil toxicity.     

Determination of cytotoxic,genotoxic, and oxidative damage from deltamethrin on primary hepatocyte culture of Lake Van fish,Alburnus tarichi

ABSTRACT

Deltamethrin is a widely used pyrethroits worldwide. Although the chemical is used to combat insects, it has effects on other non-target organisms. Deltamethrin is extensively used in agriculture, animal husbandry, and domestic areas in the Lake Van basin. The aim of this study was to determine the cytotoxic, genotoxic, and oxidative damage from deltamethrin on the primary hepatocyte culture of Lake Van fish (Alburnus tarichi). In this study, the toxic effects of different concentrations (0.01, 0.1, 1, and 10?µM) of deltamethrin in the primary hepatocyte culture of Lake Van fish were investigated via liver enzymes aspartase aminotransferase (AST) and alanine aminotransferase (ALT), and the total antioxidant status (TAS), total oxidant status (TOS), lipid peroxidation (MDA), and DNA damage (8-OHdG).

Deltamethrin caused an increase in the AST and ALT levels dependent on the dosage and time. The TAS and TOS levels increased at the end of 24?h and there was no difference at the end of 48?h. Deltamethrin did not affect the MDA level, but increased the 8-OHdG (P?<?0.05). In conclusion, it can be said that high doses of deltamethrin (1 and 10?µM) have a toxic effect on the primary hepatocyte culture of Lake Van fish.     

Susceptibility of the freshwater pulmonate snail Lymnea luteola L. to copper oxide nanoparticle

Copper oxide nanoparticles (CuONP) are among the most widely used engineered nanoparticles and thus likely to permate the environment predominantly in sediments. The present study was designed to examine the adverse effects of CuONP in freshwater snail Lymnea luteola L. (L. luteola) exposed for 5 days. Induction of oxidative stress in digestive gland was evidenced by a decrease in reduced glutathione (GSH) levels, and activities of glutathione peroxidase (GPx) and glutathione-S-transferase (GST) whereas lipid peroxidation levels were increased at CuONP 7 or 21 µg/L. Superoxide dismutase activity was numerically higher at lower concentration of CuONP at 1 day but significantly decreased at 5 days. Catalase activity was reduced at 2 days but elevated at lower concentration of CuONP at 5 days. DNA impairment was noted in L. luteola based upon comet assay findings and expressed in terms of % tail DNA and olive tail moment. Results indicate that interaction of CuONP with snail produces toxicity, which is mediated by oxidative stress.     

In vitro and in vivo inhibition of Ca2+-Mg2+-ATPase activity by cadmium in post larvae of Penaeus monodon

Ca²⁺-Mg²⁺-ATPase is a membrane-bound enzyme and is responsible for regulating cytosolic free calcium. In vitro and in vivo effects of cadmium were studied on Ca²⁺-Mg²⁺-ATPase activity in plasma membrane/mitochondrial fraction of Penaeus monodon post larvae. In vitro studies revealed a concentration-dependent decrease in enzyme activity with an IC₅₀ value of 11.02?µM. In vivo experiments were conducted by exposing the post larvae to 1/10th (0.12?ppm) and 1/5th (0.24?ppm) of LC₅₀ values of cadmium for 30 days. Both ATPase activity and metal accumulation were estimated in post larvae exposed to 0.12 and 0.24?ppm of cadmium at different intervals of 24?h, 48?h, 96?h, 10 days and 30 days. ATPase activity showed a gradual decrease in post larvae on exposure to both the sub-lethal concentrations with respect to their controls and the decrease was significant (p?相似文献   

邻苯二甲酸二乙基己酯对蚕豆根尖微核及幼苗超氧化物歧化酶的影响

为了初步探讨邻苯二甲酸二乙基己酯(Di-(2-ethylhexyl)phthalate,DEHP)对植物的毒害作用,采用不同浓度的DEHP溶液对蚕豆根部进行处理(终含量0、0.2、2、20、200mg·kg-(1细沙)),检测根尖微核率和对幼苗茎、叶SOD活性的影响.结果表明:对蚕豆根尖进行短期(6h)处理后,各DEHP处理组微核率随DEHP含量的升高呈显著上升趋势(与对照比较,p<0.05或p<0.01).处理7d后,随DEHP含量的升高(0～20mg·kg-(1细沙)),蚕豆幼苗茎、叶SOD活性均呈逐渐升高趋势;DEHP含量在20～200mg·kg-(1细沙)时,SOD活性均略有下降.以上结果表明DEHP对蚕豆种子具有遗传毒性,且能够对蚕豆幼苗产生氧化损伤.