Contamination of the River Ganga and its toxic implication in the blood parameters of the major carp Labeo rohita (Ham)

A field study was conducted to examine different physicochemical properties of water and various haematological and biochemical parametres of the fish Labeo rohita collected from the Ganga River (National river of India) at Varanasi district, India. The water was found to be greatly contaminated with a number of dissolved metals (Fe, Cr, Zn, Cu, Mn, Ni and Pb) whose concentrations were above the safe limits suggested by Bureau of Indian Standard (BIS 1991) for drinking water (Fe, 1,353.33 %; Cr, 456 %; Mn, 553.33 %; Ni, 4,490 % and Pb, 1,410 %). The metal accumulation in the fish blood was very high (Fe, 2,408 %; Cr, 956.57 %; Zn, 464.90 %; Cu, 310.57 %; Mn, 1,115.48 %) in comparison to the control fish maintained under strict quality control. Lower values of the various haematological parameters (total erythrocytes count, haemoglobin, haematocrit, mean corpuscular volume and O₂-carrying capacity) in the river fish in comparison to the control indicate toxic manifestation exerted by the contaminated river water on the fish. The higher level of total leucocytes count further illustrates stressed condition of the river fish. The toxic impact of the Ganga water is also expressed in the fish by the presence of higher levels of cholesterol, glucose, elevated activities of the enzymes aspartate amino transferase and alanine amino transferase, and lowered protein concentration.     

Indoor exposure to respirable particulate matter and particulate-phase PAHs in rural homes in North India

In order to evaluate the exposure of the northern India rural population to polyaromatic hydrocarbon (PAH) inhalation, indoor pollution was assessed by collecting and analyzing the respirable particulate matter PM_2.5 and PM₁₀ in several homes of the village Bhithauli near Lucknow, UP. The home selection was determined by a survey. Given the nature of biomass used for cooking, homes were divided into two groups, one using all kinds of biomass and the second type using plant materials only. Indoor mean concentrations of PM_2.5 and associated PAHs during cooking ranged from 1.19 ± 0.29 to 2.38 ± 0.35 and 6.21 ± 1.54 to 12.43 ± 1.15 μg/m³, respectively. Similarly, PM₁₀ and total PAHs were in the range of 3.95 ± 1.21 to 8.81 ± 0.78 and 7.75 ± 1.42 to 15.77 ± 1.05 μg/m³, respectively. The pollutant levels during cooking were significantly higher compared to the noncooking period. The study confirmed that indoor pollution depends on the kind of biomass fuel used for cooking.     

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.     

Toxic responses in primary rat hepatocytes exposed with occupational dust collected from work environment of bone-based industrial unit

In this in vitro study we investigated the toxic responses in hepatocytes treated with occupational dust to which workers are exposed in bone-based industrial units. The present study investigated the toxicity mechanism of bone-based occupational dust, from a particular industrial unit, on isolated rat hepatocytes. The hepatocytes were isolated by collagenase perfusion method and cell viability was determined by trypan blue exclusion and MTT [3-(4,5-dimethyl thiazol-2-yl)-2,5-diphenyl tetrazolium bromide] assay treated with occupational dust at 0.1-1.0 mgmL(-1), for 120 min. The cell viability decreased significantly in a concentration-dependent manner. Dust induced significant membrane damage measured by lactate dehydrogenase (LDH) and glutathione (GSH) release in culture media for 30-, 60- and 120 min treatment duration. The toxicity was found to be correlated with the induction of lipid peroxidation (LPO). In addition, nitric oxide (NO), and hydrogen peroxide (H(2)O(2)) generation by occupational dusts were also found to be time- and concentration-dependent. Over all the present study provides initial evidences for the toxic potential of occupational dust generated in bone-based industries and, therefore, the dust exposure to workers in unorganized industrial units should be controlled.     

Assessment of the potential threat of nickel(II) oxide nanoparticles to fish Heteropneustes fossilis associated with the changes in haematological,biochemical and enzymological parameters

Environmental Science and Pollution Research - The present study has been conducted to evaluate the potential threat of NiO nanoparticles (NiO NPs) on an edible fish Heteropneustes fossilis. Fishes...     

Industrial hygiene and toxicity studies in unorganized bone-based industrial units

A large variety of ornamental and decorative items are manufactured from bone waste by various unorganized sectors in India. An initial survey indicated that workers were exposed at various phases of final product. The subjects (12 industrial units) were tested for total suspended particulate matter (TSPM), particulate matter <10  $\upmu $ m (PM₁₀), and particulate matter <2.5  $\upmu $ m (PM_2.5). Prevalent levels of TSPM ranged between 2.90 and 5.89 mg m^???3. Respirable fractions of occupational dust as PM₁₀ and PM_2.5 were found in the range of 0.30?C2.08 and 0.26?C0.50 mg m^???3, respectively. Cytotoxicity study was conducted using hemolysis as a sensitive marker. In an in vitro study, rat RBCs were exposed to the concentration of 25?C1,000  $\upmu $ g/ml for 15?C120 min. A considerable variation was observed in the hemolytic activity of samples collected from different areas. At 500  $\upmu $ g/ml concentration, the hemolytic activity (12 h) was found to be in the range of 18?C25%. Due to limitation in sample mass of respirable fractions, only one concentration (100  $\upmu $ g/ml/2 h) was used for comparative study on hemolysis of RBCs caused by PM₁₀ and PM_2.5. Interestingly, the hemolytic activity was more at PM_2.5 than PM₁₀ and TSPM. These results suggest that the respirable particles are capable of reaching deep into the respiratory system. The finding is significant notably when there are no standards available in occupationally exposed populations. This is the first such study. Data could be of importance to policy makers and regulators.     

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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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.     

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.