Genotoxicity assessment of acute exposure of chlorpyrifos to freshwater fish Channa punctatus (Bloch) using micronucleus assay and alkaline single-cell gel electrophoresis

Chlorpyrifos (O,O-diethyl O-3,5,6-trichloro-2-pyridylphosphorothioate) is one of the organophosphate pesticides widely used in agricultural practices throughout world and irreversible inhibitor of cholinesterase in all animal species. Limited efforts have been made to study acute genotoxic effects of chlorpyrifos (CPF) in different tissues of fish using genotoxic biomarkers. Therefore, the present investigation was aimed to study the induction of DNA damage by CPF in freshwater teleost fish Channapunctatus using micronucleus assay (MN assay) and alkaline single-cell gel electrophoresis (comet assay). The value of LC(50) - 96 h of CPF was determined as 811.98 microgl(-1) for C. punctatus, in a semi-static system and on the basis of LC(50) value three acute concentrations viz., 203, 406 and 609 microgl(-1) were determined. The fishes were exposed to the different concentrations of CPF for 96 h and samplings were done at regular intervals for assessment of the MN frequencies and DNA damage. In general, significant effects (P<0.01) from both concentrations and time of exposure were observed in exposed fishes. It was found that the micronucleus induction was highest on 96 h at all concentrations in the peripheral blood. Similar trend was observed for the DNA damage measured in terms of the percentage of tail DNA in the lymphocyte and gill cells. This study explored the combined use of micronucleus assay and comet assay for in vivo laboratory studies using fresh water fish for screening the genotoxic potential of xenobiotics.     

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.     

Nickel oxide nanoparticles exert cytotoxicity via oxidative stress and induce apoptotic response in human liver cells (HepG2)

Increasing use of nickel oxide nanoparticles (NiO NPs) necessitates an improved understanding of their potential impact on human health. Previously, toxic effects of NiO NPs have been investigated, mainly on airway cells. However, information on effect of NiO NPs on human liver cells is largely lacking. In this study, we investigated the reactive oxygen species (ROS) mediated cytotoxicity and induction of apoptotic response in human liver cells (HepG2) due to NiO NPs exposure. Prepared NiO NPs were crystalline and spherical shaped with an average diameter of 44 nm. NiO NPs induced cytotoxicity (cell death) and ROS generation in HepG2 cells in dose-dependent manner. Further, ROS scavenger vitamin C reduced cell death drastically caused by NiO NPs exposure indicating that oxidative stress plays an important role in NiO NPs toxicity. Micronuclei induction, chromatin condensation and DNA damage in HepG2 cells treated with NiO NPs suggest that NiO NPs induced cell death via apoptotic pathway. Quantitative real-time PCR analysis showed that following the exposure of HepG2 cells to NiO NPs, the expression level of mRNA of apoptotic genes (bax and caspase-3) were up-regulated whereas the expression level of anti-apoptotic gene bcl-2 was down-regulated. Moreover, activity of caspase-3 enzyme was also higher in NiO NPs treated cells. To the best of our knowledge this is the first report demonstrating that NiO NPs caused cytotoxicity via ROS and induced apoptosis in HepG2 cells, which is likely to be mediated through bax/bcl-2 pathway. This work warrants careful assessment of Ni NPs before their commercial and industrial applications.     

Role of ROS generation in acute genotoxicity of azoxystrobin fungicide on freshwater snail Lymnaea luteola L

Environmental Science and Pollution Research - Azoxystrobin (AZ) is an aryloxy pyrimidine fungicide extensively applied in the agriculture field all over the world. There is a little information...     

Potential histopathological and molecular changes in rat vas deferens inhaled by Boswellia papyrifera and Boswellia carterii

Boswellia papyrifera and Boswellia carterii released from smoke contaminate indoor environment and consequently adversely affect humans as evidenced by respiratory disturbances. The aim of this study was to determine the effects of these plants on pathological and biochemical changes in vas deferens of albino rats. Animals were administered 4 g/kg body weight B. papyrifera and B. carterii daily for 120 days along with controls. Significant changes were observed in epithelial cell types and some cells showed signs of degeneration. The ultrastructural studies revealed marked changes in cytoplasmic organelles. Microvilli were missing and lysosomes were found in the cytoplasm. In addition, all treated groups plasma fructose and other biochemical parameters were decreased indicating reduced energy necessary for motility and contractility of spermatozoa. Many spermatozoa were disorganized and agglomerated. Data suggest that smoke from these plants adversely affects vas deferens.     

Detection of oxidative stress and DNA damage in freshwater snail <Emphasis Type="Italic">Lymnea leuteola</Emphasis> exposed to profenofos

Extensive production and use of organophosphate pesticide in agriculture, has risen concerned about its ecotoxicity and risk assessment of insecticides, which are more important. Therefore, the present investigation was aimed to study the induction of oxidative stress and DNA damage by organophosphate insecticide profenofos (PFF) in freshwater snail Lymnea luteola (L. luteola). The median lethal value (96 h LC₅₀) of PFF was estimated as 1.26 mg/L for L. luteola in a semi-static system and on the basis of LC₅₀ value three concentrations viz., 0.126 (1/10 of LC₅₀, Sublethal I), 0.63 (1/2 of LC₅₀, Sublethal II) and 0.84 mg/L (2/3 of LC₅₀, Sublethal III) were determined. Snails were exposed to above-mentioned concentrations of PFF along with solvent control (acetone) and negative control for 96 h. The haemolymph was collected at 24 and 96 h of after treatment. In heamolymph of PFF exposed snail, lipid peroxide, glutathione reduced glutathione S transferase and superoxide dismutase activities at the tested concentrations significantly differ from those in the control. The genotoxicity induced in hemocytes of treated snails was measured by alkaline single cell gel electrophoresis assay. The data of this experiment demonstrated significantly enhancement of oxidative stress and DNA damage in the treated snails as compared to controls. Also, we observed statistically significant correlations of ROS with DNA damage (% tail DNA) (R² = 0.9708) for 24 h and DNA damage (R2 = 0.9665) for 96 h.

Results of the current experiment can be useful in risk evaluation of PFF among aquatic organisms. The study confirmed the use of comet assay for in vivo laboratory experiments using freshwater snail for selecting the toxic potential of industrial chemicals and environmental contaminants.

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The ameliorative effects of ceftriaxone and vitamin E against cisplatin-induced nephrotoxicity

Environmental Science and Pollution Research - Nephrotoxicity is a common adverse effect of treatment with cisplatin (CDDP). This study was performed to evaluate the antioxidant and...     

Size and temperature-dependent variations in intermolt duration and size increment at molt of Northern Shrimp, Pandalus borealis

Growth of Pandalus borealis post-larval stages was measured in relation to size and temperature. Growth characteristics, including intermolt period (IP), molt increment (MI) in size and mass, and tissue allocation in juvenile, male, and female shrimp, were evaluated at 2, 5, and 8°C, the temperature range where this species is generally found in the Northwest Atlantic. Significant variations in growth were associated with temperature and shrimp size. IP (days) increased significantly with shrimp size and was inversely related to temperature. Size (cephalothorax length in mm) and temperature effects were best described by IP = 10^{(0.67 log(CL) − 0.06 T − 1.34)}. The pronounced effect of temperature on IP while MI_S changed little indicated that the main influence of temperature on growth rate of P. borealis was through IP. Specific growth rate (SGR_S) decreased rapidly with size to near zero values in females. Overall, juveniles were much more sensitive to temperature variations than adults, suggesting that temperatures encountered during the juvenile stage will largely influence the growth trajectory of the population.     

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.     

UVR-induced toxicity of sludge and polycyclic aromatic hydrocarbons on seed germination and seedling growth of Triticum aestivum L.

The depletion of the ozone layer and enhancement of solar radiation may exert an adverse influence on the ecosystem. Phototoxicity of sludge and polycyclic aromatic hydrocarbons (PAHs) under ultraviolet radiation (UVR) to seedling was studied. Seeds of wheat (Triticum aestivum) were planted in sludge and PAHs (anthracene (An), benzo(a)pyrene (BaP) and pyrene (Py)) with and without UVR. Toxicity of sludge increased in the presence of UVR in wheat. UVB radiation was found to be more hazardous than UVA radiation. Results demonstrated that An, BaP and Py induced phototoxicity at various concentrations (1–10?µg/mL) under UVA (1.5?mW/cm²) or UVB (1.08?J/cm²) exposure. The pattern of phototoxicity was An?>?Py?>?BaP to shoot length, root length, and fresh weight; chlorophyll, protein content, enzyme activity of catalase and α-amylase were reduced while the activity of superoxide dismutase and starch was enhanced. Reduction in seedling growth and biochemical parameters may be related to less photosynthesis, less nutritional uptake, and distortion of root cap. Thus, the synergistic effect may be due to alterations in photosynthesis, phytohormones, or nutritional uptake.