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Bisphenol A (BPA) is an industrial toxicant that can potentially damage the liver. Tangeretin (TGN) is a natural flavonoid that displays various pharmacological activities. This experiment was carried out to evaluate the protective effects of TGN against BPA-induced hepatic impairment in the male albino rat. Twenty-four male albino rats were equally divided into four different groups: control, BPA (100mg/kg), BPA+ TGN (100mg/kg+50mg/kg) and TGN (50mg/kg). BPA exposure significantly decreased the activities of catalase (CAT), superoxidase dismutase (SOD), peroxidase (POD), glutathione reductase (GSR), glutathione S-transferase (GST), and glutathione (GSH) content while substantially increasing the thiobarbituric acid reactive substances (TBARS) and hydrogen peroxide (H2O2) levels. A substantial increase in the levels of alanine aminotransferase (ALT), alkaline phosphatase (ALP), aspartate aminotransferase (AST) was also observed in BPA treated rats. Moreover, BPA significantly increased the inflammatory markers, including tumor necrosis factor-α (TNF-α), nuclear factor kappa-B (NF-κB), Interleukin-6 (IL-6), Interleukin-1β (IL-1β)levels, cyclooxygenase-2 (COX-2) activity, and histopathological damages. However, co-treatment with TGN efficiently minimized the BPA-induced biochemical, inflammatory, and histopathological impairments in rat liver. The present study shows that TNG has significant potential to avert BPA-induced liver damage to its antioxidant and anti-inflammatory properties.

Carbon tetrachloride (CCl4) is a Potential nephrotoxin that causes severe and prolonged chemical toxicity. Investigations have been accomplished on numerous species of genus Artemisia, but the plant Artemisia brevifolia has hardly been used in this respect. The present study was considered to ascertain the effects of “Artemisia brevifolia plant extract” against CCl4 prompted nephrotoxicity in male albino rats. Forty-eight male albino rats were allocated into eight groups containing 6 rats in each. Group I was the control group. Group II was given dimethyl sulfoxide (DMSO) (1 ml/kg) orally. Group III was treated with dissolved CCl4 in olive oil (1 ml/kg). Group IV was given CCl4 + Silymarine. Group V and VI were administered with Artemisia brevifolia extract (150 and 300 mg/kg respectively) + CCl4. Group VII and VIII were provided with only 150 and 300 mg/kg extract of Artemisia brevifolia respectively. Results displayed that CCl4 administration significantly (p

Diabetes mellitus and hyperglycemia can lead to other health complications. The pathogenesis of diabetes mellitus can affect numerous tissues in the eye structure and cataracts are one of the major causes of visual impairment in diabetes mellitus patients. In this study, we aim to investigate the ability of D-limonene to inhibit aldose reductase hypoglycemic activity in lens organ culture and its anti-glycating properties in STZ-induced cataracts of rats with diabetes. D-limonene repressed aldose reductase in-vitro with IC50 ranges of ~13.9 ± 0.31 µg/mL in an uncompetitive manner. This compound also prevented hyperglycemic induced increases in aldose reductase activity, accumulation of sorbitol, altered crystalline proteins (α, β and γ), and opacification of the rat lens in ex-vivo lens organ culture. Supplementation of D-limonene in STZ-induced diabetic rats restored these changes and delayed the progression of cataracts. This study demonstrates that D-limonene is a pharmaceutically active component that inhibits rat-lens aldose reductase. Therefore, this study showed that D-limonene prevents advanced glycation end product formation contributing to the integrity of α-crystallin chaperone activity and delays cataract development. It has been concluded, D-limonene has a role in inhibiting aldose reductase activity and advanced glycation end products formation in vivo, and in delaying the development of diabetic cataracts. Further studies of D-limonene are needed to assess other complications in DM as they may provide additional evidence for establishing D-limonene as a potential pharmacological target therapy for diabetes mellitus complications. Keywords: D-limonene, Aldose reductase, α-Crystalline, Advanced glycation, End products, Cataracts

Bioengineered green approaches of metal nanomaterials plays an extensive role against current environmental affairs and clinical pathogens. In the current exploration, biomolecule loaded silver nanoparticles (AgNPs) were engineered by microwave irradiation mode using the leaf extracts of Ludwigia octovalvis and characterized by Ultraviolet–visible spectroscopy (UV), Fourier transform infrared spectroscopy (FTIR), Field emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX) and X-ray diffraction (XRD) analysis. FTIR revealed feasible biomolecules available in capping and bioreduction of AgNPs. XRD result clearly pinpoints the crystallinity of the synthesized AgNPs. FESEM analysis taped that AgNPs were found to be polyhedrons in nature with average size 28–50 nm. The antimicrobial properties of AgNPs was investigated against different bacterial pathogens (Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumoniae, Proteus vulgaris and Staphylococcus epidermidis). A potential anti-biofilm activity of phytocompounds loaded AgNPs against P. aeruginosa and S. epidermidis were recorded. As well, the enhanced decolouration action of AgNPs were detected against deadly pollutant dyes Alizarin red, Congo red, Methylene blue and Rhodamine b. The outcome undoubtedly indicated that the AgNPs may be considered as an successful nano based therapeutic drug for various diseases caused by pathogens and vigorous catalytic agent against toxic dyes.

The study is to scrutinize andrographolides with Indoleamine 2,3-dioxygenase (IDO) inhibitory potential, its molecular mechanism against streptozotocin (STZ) diabetic retinopathy (DR) in Wistar rats. Oxidative stress markers such as Kynurenine metabolites, retinal histopathological changes have been studied. Further, IDO gene expression and docking studies have been performed. Andrographolide treated rats have been reducing the level of thiobarbituric acid reactive substances and protein carbonyls Kynurenine metabolites with an improvement in the level of GSH and expression of IDO as revealed by morphological changes in inner and outer nuclear layer of the retina. The current results of this study have been generated information about an activity of the andrographolide in the essential pocket of IDO. Our results explain, involving IDO and andrographolide would constitute an attempt to identify natural products with therapeutic value and further studies in this direction would be of immense significance in the administration of diabetes and its related problems. Keywords: Diabetes, Andrographolide, Oxidative stress, Metabolites, GSH

The issue of male sexual dysfunction arises due to numerous complications linked with sperm motility, imbalance of antioxidant enzymes and hormonal levels. Carbon tetrachloride (CCl4) is widely used as a standard toxin to induce chemical injury and toxicity. A lot of research has been performed on many species of the genus Nepeta in vitro and in vivo but the plant Nepeta paulsenii have been rarely used in this aspect. The current research was designed to explore the impacts of methanolic extract of the Nepeta paulsenii plant on CCl4 induced testicular impairment in male albino rats. Forty-eight rats were distributed equally into 8 groups; Control, Vehicle control, CCl4 treated (1 ml/kg), CCl4 + Silymarine treated, CCl4 + Nepeta paulsenii (200 mg/kg) treated, CCl4 + Nepeta paulsenii (400 mg/kg), Nepeta paulsenii (200 mg/kg) and Nepeta paulsenii (400 mg/kg) treated. Blood and testicles were obtained and analyzed. To check antioxidant enzymes, hormonal concentrations, daily sperm production (DSP), protein content and histopathology various analyses were performed. CCl4 exposure resulted in adverse morphological changes and significant (p

The study was implemented to actuate the qualitative and quantitative phyto constituents of Iresine herbstii extracts and its antiviral efficacy against avian ND virus. Among four tested solvents, the ethanolic extract of Iresine herbstii revealed the presence of highest quantity of all tested phytochemicals while petroleum ether extract showed the least. Folin-Ciocalteu method assessed the range of TPC extended from 81.01 ± 0.67 to 126.35 ± 0.45 µg GAE/mg. Acetonic extract showed the highest amount among all extracts and petroleum ether possessed the lower quantity. TFC ranged from 54.37 ± 0.45 to 88.12 ± 0.26 µg QE/mg followed by colorimetric method. From all extract ethanolic extract showed highest quantity and petroleum ether revealed the lower. HPLC analysis of ethanolic extract of I. herbstii confesses the presence six bioactive components by using the HP5-MS column. To check the antiviral potential of plants, different prepared treatments of plant extract and live virus were inoculated at 9 days old SPF embryonated chicken eggs. Results exposed that all plant extracts produce antiviral activity against NDV in ovo according to their potential and phytochemical profile. The highest survival rate was observed in the ethanolic extract at 400 µg/mL and acetonic extract at 300 µg/mL as it controls the NDV activity completely, evidence of absence of embryo death and HA titre. Dichloromethane and petroleum ether could not inhibit the virus completely. 600 µg/mL concentration was proved as toxic in all extracts except petroleum ether extract which showed a dose dependent pattern. Keywords: Iresine herbstii, Phytochemicals, Antiviral activity, In ovo, Newcastle disease virus

Extensive application of pesticide in agricultural field affects the enzymatic activity of non-target animals, including fishes. In this study, the impact of sublethal concentration of fenvalerate on marker enzymes of freshwater Zebra fish was evaluated. Pesticide-induced stress can specifically affect non target fishes, through elevated level of reactive oxygen species which is responsible for biochemical, cell metabolism and physiological activities. The oxidative stress mediated by fenvalerate at sub lethal concentrations after 28 days of exposure of Zebra fish. Following 28 days of exposure of pesticide, catalase, superoxide dismutase, aspartate amino transferases, alanine amino transferase, alkaline phosphatase and acid phosphatase were assessed. Results revealed reduction of superoxide dismutase activity after 28 days of exposure in sub lethal concentration of fenvalerate in liver and gills. In liver, catalase activity was found to be less in fenvalerate exposed fish than control fish. In liver, increase of 75.75% aspartate amino transferase and 38% increase in alanine amino transferase in gills. SGPT activity was relatively higher than SGOT suggests more contribution of phyruvalate than oxaloacetate formation. Fenvalerate induced changes in acid phosphatase and alkaline phosphatase activity in the liver and gills of Zebra fish after four weeks of exposure. Fenvalerate induced expression of various stress proteins in gill, liver, followed by muscle. Some proteins lost its intensity due to fenvalerate toxicity. Result revealed that enzyme assays and SDS-PAGE analysis for protein subunits determination is relevant tool to monitor stress in freshwater ecosystem. The findings suggest that in monitoring fenvalerate toxicity programme, enzyme activities can be potent diagnostic tool for fenvalerate induced toxicity. Keywords: Pyrethroid, Fenvalerate, Fish, Toxicity, Metabolic enzymes, Stress

The aim of this study was to determine the level of contamination and genotoxic impact through micronucleus assay and histopathology in Wallago attu and Cirrhinus mrigala procured from the polluted site of the River Chenab at industrial and sewage waste disposal. The water sample was found viciously contaminated with heavy metals i.e. Ni, Cr, Mn, Co, Pb, Hg, Zn, Sn, Cu while all other physio-chemical variables crossed the suggested limits of WHO. The heavy metals load induced histopathological alterations were correlated to environmental degradation and the productivity of this biological system. W. attu and C. mrigala harvested from contaminated sites of the river indicated higher intensity of DNA damage through micronucleus induction and nuclear abnormalities with 5.46 ± 0.17, 1.23 ± 0.08 and 4.2 ± 0.11, 0.4 ± 0.04‰ respectively. Muscle sections of W. attu and C. mrigala harvested from the polluted section of river demonstrated the necrosis, degeneration of muscle fibers, intra-fibular edema and release of the blood into the tissues due to the bursting of blocked of the blood vessels. Dermal layers showed degeneration of the collagen bundles those were found loose or collapsed in some regions. Photomicrography also revealed vacuolar degeneration in muscle tissues and atrophy of muscle bundles. Intra fibular edema and splitting of muscle fibers were also seen along with bioaccumulation of toxicants. W. attu showed maximum incidence of alterations with highest histopathological alteration index related to environmental degradation. Control fish samples showed normal muscle tissues with normal equally spaced muscle bundles and myotomes. Keywords: Pollution, Xenobiotics, Fish, Micronucleus, Histopathology

Cisplatin (CP) is an active cytotoxic agent, which has been verified to be effective in multiple cancer regimen. In this study, potential antioxidant effects of casticin (CAS) were assessed against CP generated oxidative stress in rat liver. “Twenty-four male Sprague Dawley rats were divided into four experimental groups. Group-1 (control group) received only normal saline”. Group-2 was intraperitoneally injected with CP (10 mg/kg). Group-3 was orally provided by CAS (50 mg/kg) along with CP (10 mg/kg) injection at first day. Group-4 group was orally administered with CAS (50 mg/kg) throughout the experiment. The rats of group-1 indicated “increase in serum levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP), while a significant decrease in the activities of catalase (CAT), superoxide dismutase (SOD) and peroxidase (POD)” was noticed, which revealed that CP generated oxidative stress in rat liver. Moreover, administration of CP increased the hydrogen peroxide (H2O2) concentration and level of “thiobarbituric acid reactive substances (TBARS)”, while reducing the % DNA head and head length in liver cell nuclei. CP disturbs the lobular structure of the liver and increased the sinusoidal dilation in rat liver. However, co-treatment with CAS successfully mitigated the CP generated DNA disruption, biochemical and pathological changes in rat liver. These findings revealed that an effective antioxidant, CAS, alleviated the CP generated hepatotoxicity and oxidative stress in rats. Keywords: Cisplatin, Oxidative stress, DNA damage, Liver damage, Antioxidant, Casticin

Cisplatin (CP) is one of the most effective chemotherapeutic drugs used to treat different tumors. Vitexin (VIT) is a natural flavonoid having various pharmacological activities along with its curative effects. The present research was planned to evaluate the therapeutic potential of VIT on cisplatin-induced renal damage in male albino rats. Twenty-four male albino rats were divided into four equal groups. These groups were treated with CP (10 mg/kg injection on the first day of trial) administered group, cotreated (CP; 10 mg/kg + VIT; 10 mg/kg) and only VIT (10 mg/kg orally till the end of the trial) treated group and a control. CP administration significantly decreased the activities of catalase (CAT), superoxide dismutase (SOD), peroxidase (POD), glutathione S-transferase (GST), glutathione (GSH), and glutathione reductase (GSR). The levels of thiobarbituric acid reactive substances (TBARS) and hydrogen peroxide (H2O2) were increased. CP-treatment significantly increased the levels of urea, creatinine, kidney injury molecule-1 (KIM-1), and neutrophil gelatinase-associated lipocalin (NGAL) while considerably reducing the creatinine clearance. The results demonstrated that CP significantly increased the inflammation markers, including tumor necrosis factor-α (TNF-α), nuclear factor kappa B (NF-κB), Interleukin-1β (IL-1β), Interleukin-6 (IL-6) levels and cyclooxygenase-2 (COX-2) activities and histopathological damages. However, co-treatment with VIT efficiently minimized the CP-induced biochemical, inflammatory, and histopathological impairments in rat kidneys. The study's outcomes indicated the significant curative efficacy of VIT to overcome CP-induced nephrotoxicity in male albino rats.

The present research was planned to analyze the toxic effects of thimerosal on rat liver. Mercury and mercury compounds are universally known toxicants for animals and humans. Thimerosal is widely used in the vaccines as a preservative which contains 49.6% mercury. Twenty-four adult male albino rats were distributed into four groups (n=6). The first group was considered as a control group. While, second, third and fourth groups were intoxicated with 0.5, 10 and 50 µg/kg thimerosal (i.m.) respectively. After 30 days, rats were slaughtered to analyze the liver tissues. The results of the experiment exposed that thimerosal instigated significant (p

Polypropylene microplastics are the primary pollutant in aquatic ecosystems and their toxicity assessment study remains limited. The proposed study focuses on acute exposure of polypropylene microplastic in Daphnia similis, which alters the biochemical parameter due to the accumulation of microplastics in the digestive tract. Moreover, the commercially available polypropylene bags have been converted into microplastic using xylene. FTIR results showed the absence of xylene residue in prepared microplastics particles and it was spherical shaped, size range (FE-SEM) from 11.86µm – 44.62µm. The outcome of the impact reveals that acute exposure to polypropylene microplastic in D. similis leads to immobilization. Further, the biochemical results showed that ingestion of microplastics increases reactive oxygen species (ROS) production. This leads to an increase in the antioxidant enzymes of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione-S-transferase (GST) and a non-antioxidant enzyme of reduced glutathione (GSH) and also oxidative stress effects in lipid (lipid peroxidation - LPO), protein (Carbonyl protein - CP) gradually increases due to production of free radicals in D. similis. In addition, the neurotransmitter enzyme acetylcholinesterase (AChE) level diminished. These results reflect that accumulation of polypropylene microplastic should exacerbate harmful pollutants on filter-feeding organisms.

Cisplatin (CP) is a commonly used, powerful antineoplastic drug, having numerous side effects. Casticin (CAS) is considered as a free radical scavenger and a potent antioxidant. The present research was planned to assess the curative potential of CAS on CP persuaded renal injury in male albino rats. Twenty four male albino rats were distributed into four equal groups. Group-1 was considered as a control group. Animals of Group-2 were injected with 5mg/kg of CP intraperitoneally. Group-3 was co-treated with CAS (50mg/kg) orally and injection of CP (5mg/kg). Group-4 was treated with CAS (50mg/kg) orally throughout the experiment. CP administration substantially reduced the activities of catalase (CAT), superoxide dismutase (SOD), peroxidase (POD), glutathione S-transferase (GST), glutathione reductase (GSR), glutathione (GSH) content while increased thiobarbituric acid reactive substances (TBARS), and hydrogen peroxide (H2O2) levels. Urea, urinary creatinine, urobilinogen, urinary proteins, kidney injury molecule-1 (KIM-1), and neutrophil gelatinase-associated lipocalin (NGAL) levels were substantially increased. In contrast, albumin and creatinine clearance was significantly reduced in CP treated group. The results demonstrated that CP significantly increased the inflammation indicators including nuclear factor kappa-B (NF-κB), tumor necrosis factor-α (TNF-α), Interleukin-1β (IL-1β), Interleukin-6 (IL-6) levels and cyclooxygenase-2 (COX-2) activity and histopathological damages. However, the administration of CAS displayed a palliative effect against CP-generated renal toxicity and recovered all parameters by bringing them to a normal level. These results revealed that the CAS is an effective compound having the curative potential to counter the CP-induced renal damage. Resumo A cisplatina (CP) é uma droga antineoplásica poderosa, comumente usada, com vários efeitos colaterais. Casticin (CAS) é considerado um eliminador de radicais livres e um potente antioxidante. A presente pesquisa foi planejada para avaliar o potencial curativo da CAS em lesão renal induzida por PC em ratos albinos machos. Vinte e quatro ratos albinos machos foram distribuídos em quatro grupos iguais. O Grupo 1 foi considerado grupo controle. Os animais do Grupo 2 foram injetados com 5 mg / kg de PB por via intraperitoneal. O Grupo 3 foi cotratado com CAS (50 mg / kg) por via oral e injeção de CP (5 mg / kg). O Grupo 4 foi tratado com CAS (50 mg / kg) por via oral durante todo o experimento. A administração de CP reduziu substancialmente as atividades de catalase (CAT), superóxido dismutase (SOD), peroxidase (POD), glutationa S-transferase (GST), glutationa redutase (GSR), glutationa (GSH), enquanto aumentou as substâncias reativas ao ácido tiobarbitúrico (TBARS) e níveis de peróxido de hidrogênio (H2O2). Os níveis de ureia, creatinina urinária, urobilinogênio, proteínas urinárias, molécula 1 de lesão renal (KIM-1) e lipocalina associada à gelatinase de neutrófilos (NGAL) aumentaram substancialmente. Em contraste, a albumina e a depuração da creatinina foram significativamente reduzidas no grupo tratado com PC. Os resultados demonstraram que a CP aumentou significativamente os indicadores de inflamação, incluindo fator nuclear kappa-B (NF-κB), fator de necrose tumoral-α (TNF-α), interleucina-1β (IL-1β), interleucina-6 (IL-6) níveis e atividade da ciclooxigenase-2 (COX-2) e danos histopatológicos. No entanto, a administração de CAS apresentou um efeito paliativo contra a toxicidade renal gerada por CP e recuperou todos os parâmetros, trazendo-os a um nível normal. Estes resultados revelaram que o CAS é um composto eficaz com potencial curativo para combater o dano renal induzido por CP.

Highlights A novel hierarchical structure constructed by encapsulating cobalt sulfide nanowires within nitrogen-doped porous branched carbon nanotubes (NBNTs) is designed for lithium-ion batteries.The unique hierarchical Co9S8@NBNT electrode displayed a reversible specific capacity of 1310 mAh g−1 at a current density of 0.1 A g−1. Electronic supplementary material The online version of this article (10.1007/s40820-019-0259-z) contains supplementary material, which is available to authorized users., Lithium-ion batteries (LIBs) are considered new generation of large-scale energy-storage devices. However, LIBs suffer from a lack of desirable anode materials with excellent specific capacity and cycling stability. In this work, we design a novel hierarchical structure constructed by encapsulating cobalt sulfide nanowires within nitrogen-doped porous branched carbon nanotubes (NBNTs) for LIBs. The unique hierarchical Co9S8@NBNT electrode displayed a reversible specific capacity of 1310 mAh g−1 at a current density of 0.1 A g−1, and was able to maintain a stable reversible discharge capacity of 1109 mAh g−1 at a current density of 0.5 A g−1 with coulombic efficiency reaching almost 100% for 200 cycles. The excellent rate and cycling capabilities can be ascribed to the hierarchical porosity of the one-dimensional Co9S8@NBNT internetworks, the incorporation of nitrogen doping, and the carbon nanotube confinement of the active cobalt sulfide nanowires offering a proximate electron pathway for the isolated nanoparticles and shielding of the cobalt sulfide nanowires from pulverization over long cycling periods. Electronic supplementary material The online version of this article (10.1007/s40820-019-0259-z) contains supplementary material, which is available to authorized users.

Introduction: Nanoparticles (NPs) have become very important owing to their various uses. In this research, an environmentally friendly biological technique was used to synthesize silver nanoparticles with Coriandrum sativum L. The objective of this research to use the source for the fabrication of silver NPs from C. sativum L., and to check the activity of the fabricated silver NPs was determined versus a couple of gram negative and a couple of gram positive bacteria in the presence of antibiotic viz. gentamicin to judge their impact. Methodology: A silver nitrate solution, which served as the reducing and capping agent, was mingled with coriander leaf extract. The solution’s temperature and pH were maintained at 75 °C and 8.6, respectively. The observed mean particle size (z-average) and polydispersity index were 390.2 nm and 0.452, respectively. The synthesized Ag NPs were characterized using different techniques, including scanning electron microscopy (SEM), X-ray diffraction, and Fourier transmission infrared (FTIR) analysis. The globular shape of the silver nanoparticles was depicted in SEM illustrations. Results: XRD data revealed the mean size of the particles was 11.9 nm. The FTIR analysis showed the existence of various functional groups, including CO and OH. When their antibacterial ability was tested, it was found that the fabricated Ag NPs inhibited Bacillus subtilis, Pasteurella multocida, Enterobacter aerogenes, and Staphylococcus aureus, with a greater effect against B. subtilis and P. multocida compared to E. aerogenes and S. aureus. Conclusion: It has been concluded small silver NPs benefited from a higher surface area ratio, as shown by the results of experiments where smaller particles had a better bactericidal proficiency than large silver-based NPs. Silver-based NPs infiltrate bacterial cells, as well as interfere with their exterior membrane. Silver ions also have the potential to interact with bacterial DNA, inhibiting the reproductive system of the cell. Keywords: Silver nanoparticles, Coriander leaf extract, Antimicrobial activity

This study was conducted to assess the effect of heavy metals (Cd, Hg, Cu, Mn, Zn, Pb, Cr, and Sn) on the fatty acid profiles of Catla catla, Labeo rohita, and Cirrhinus mrigala collected from two polluted sites in the Chenab River and Jhelum River (non-polluted site). The heavy-metal levels were determined using atomic absorption spectrophotometry. The results showed that the levels of Cd, Hg, Cu, Mn, Zn, Pb, Cr, and Sn in the river water exceeded the permissible limits recommended by various international agencies. Some important fatty acids were not detected in the muscle samples of the fish species collected from the highly polluted site (HPS). Caprylic acid (C8:0) and lauric acid (C12:0) were undetectable in Catla catla and Cirrhinus mrigala. Palmitoleic acid and eicosapentaenoic acid were present in Catla catla alone, and they were not found in Labeo rohita and Cirrhinus mrigala harvested from a less polluted site (LPS). More saturated fatty acids and less fatty acids were detected in the muscle samples of Catla catla, Labeo rohita, and Cirrhinus mrigala collected from HPS than in those collected from LPS. The untreated discharge of domestic and industrial waste probably causes a reduction in the fatty acids in the biomass of microalgae and zoobenthos and, ultimately, adversely affects the upper links of the food chain in the river.

Carbon dioxide gas is the key element of the carbon cycle and a major source for photosynthesis, but for the past 150 years, the atmospheric CO2 has been increased drastically from 250 to 418 ppm due to the extreme utilization of fossil fuels. This accelerated release of CO2 acts as a major source for climatic change due to the greenhouse gas effect resulting in global warming and melting of polar ice caps, alteration in biogeochemical cycles, altered rainfall, ocean acidification, eutrophication of lakes, imbalance in the ecological communities and extinction of some species, effects on soil fertility, changes in the metabolism and at the molecular level. Reduce, reuse and recycle strategy can be applied to control elevated CO2 levels by preventing deforestation, using renewable energy as an alternative for fossil fuels and reusing the atmospheric CO2. Carbon capture and storage (CCS), Carbon capture and utilization (CCU) are the two technologies adapted to capture the atmospheric CO2, utilize it, and focus on permanent storage in the geological sites. Captured CO2 is used to produce many value added products such as polymers, biofuels, reactants etc. Plants and microorganisms act as a natural CO2 filter. Several biomolecules such as carbohydrates, proteins, and lipids are produced due to the biological carbon fixation process using photosynthesis. Six different photosynthetic pathways and some non-photosynthetic pathways to fix atmospheric CO2 have been reported in diverse species of plants and microbes such as bacteria, fungi, yeast, algae etc. Algae are the most potent microbe in CO2 utilization and biological carbon fixation compared to other microbes and used widely on a large industrial scale for biofuel production. Algal biofuel production using captured CO2 is the best productive method to recycle and reduce atmospheric CO2.

Copper nanoparticles were synthesized using Manilkara zapota leaf extract. The synthesis of the nanoparticle was primarily visualized when the colour of the reaction mixture turned into reddish-brown. Biosynthesized nanoparticles were characterized by UV–vis, FT-IR, XRD, SEM and EDX. The UV spectra showed maximum absorption at 584 nm. FT-IR studies showed stretching frequency at 592.76 cm−1, which is the fingerprint region for Cu-O bond. The crystallinity of the synthesized copper nanoparticles (Mz–Cu NPs) was revealed through XRD analysis. The synthesized Mz–Cu NPs were spherical with an average size of 18.9–42.5 nm and it was shown by SEM analysis. EDX analysis displayed that the nano sample contains 58 % of copper. The antimicrobial property of the synthesized nanoparticles was evaluated against fungal plant pathogens Rhizoctonia solani (MTCC 12232), Sclerotium oryzae (MTCC 12230) and bacterial species, namely Bacillus subtilis (ATCC 23857), Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 25923), Vibrio harveyi (ATCC 35084), Vibrio parahaemolyticus (ATCC 33845). In in-vitro haemolytic assay, the particle showed 5.73, 3.34, 0.5 % hemolysis at 100, 50, 25 μg/mL concentration respectively. In the antiproliferative assay, the IC50 values of MCF7 and Vero cells were found to be 53.89 and 883.69 μg/μl. The particle degraded Methyl violet, Malachite green and Coomassie brilliant blue by 92.2, 94.9 and 78.8 %, within 50, 40 and 60 min, respectively, through its photocatalytic activity.

Thimerosal is an organomercurial compound, which is used in the preparation of intramuscular immunoglobulin, antivenoms, tattoo inks, skin test antigens, nasal products, ophthalmic drops, and vaccines as a preservative. In most of animal species and humans, the kidney is one of the main sites for mercurial compounds deposition and target organs for toxicity. So, the current research was intended to assess the thimerosal induced nephrotoxicity in male rats. Twenty-four adult male albino rats were categorized into four groups. The first group was a control group. Rats of Group-II, Group-III, and Group-IV were administered with 0.5µg/kg, 10µg/kg, and 50µg/kg of thimerosal once a day, respectively. Thimerosal administration significantly decreased the activities of catalase (CAT), superoxide dismutase (SOD), peroxidase (POD), glutathione reductase (GR), glutathione (GSH), and protein content while increased the thiobarbituric acid reactive substances (TBARS) and hydrogen peroxide (H2O2) levels dose-dependently. Blood urea nitrogen (BUN), creatinine, urobilinogen, urinary proteins, kidney injury molecule-1 (KIM-1), and neutrophil gelatinase-associated lipocalin (NGAL) levels were substantially increased. In contrast, urinary albumin and creatinine clearance was reduced dose-dependently in thimerosal treated groups. The results demonstrated that thimerosal significantly increased the inflammation indicators including nuclear factor kappaB (NF-κB), tumor necrosis factor-α (TNF-α), Interleukin-1β (IL-1β), Interleukin-6 (IL-6) levels and cyclooxygenase-2 (COX-2) activities, DNA and histopathological damages dose-dependently. So, the present findings ascertained that thimerosal exerted nephrotoxicity in male albino rats. Resumo O timerosal é um composto organomercurial, utilizado na preparação de imunoglobulina intramuscular, antivenenos, tintas de tatuagem, antígenos de teste cutâneo, produtos nasais, gotas oftálmicas e vacinas como conservante. Na maioria das espécies animais e nos humanos, o rim é um dos principais locais de deposição de compostos de mercúrio e órgãos-alvo de toxicidade. Assim, a presente pesquisa teve como objetivo avaliar a nefrotoxicidade induzida pelo timerosal em ratos machos. Vinte e quatro ratos albinos machos adultos foram categorizados em quatro grupos. O primeiro grupo era um grupo de controle. Ratos do Grupo II, Grupo III e Grupo IV receberam 0,5µg / kg, 10µg / kg e 50µg / kg de timerosal uma vez ao dia, respectivamente. A administração de timerosal diminuiu significativamente as atividades de catalase (CAT), superóxido dismutase (SOD), peroxidase (POD), glutationa redutase (GR), glutationa (GSH) e conteúdo de proteína, enquanto aumentou as substâncias reativas ao ácido tiobarbitúrico (TBARS) e peróxido de hidrogênio (H2O2) níveis dependentes da dose. Os níveis de nitrogênio ureico no sangue (BUN), creatinina, urobilinogênio, proteínas urinárias, molécula de lesão renal-1 (KIM-1) e lipocalina associada à gelatinase de neutrófilos (NGAL) aumentaram substancialmente. Em contraste, a albumina urinária e a depuração da creatinina foram reduzidas de forma dependente da dose nos grupos tratados com timerosal. Os resultados demonstraram que o timerosal aumentou significativamente os indicadores de inflamação, incluindo fator nuclear kappaB (NF-κB), fator de necrose tumoral-α (TNF-α), interleucina-1β (IL-1β), níveis de interleucina-6 (IL-6) e atividades da ciclooxigenase-2 (COX-2), DNA e danos histopatológicos dependentes da dose. Portanto, os presentes achados verificaram que o timerosal exerceu nefrotoxicidade em ratos albinos machos.

This research aimed to evaluate the curative impact of nobiletin (NOB) on paraquat (PQ) induced mitochondrial impairment in rats' hepatic tissues. Twenty-four male rats were divided into control, PQ, PQ + NOB, and NOB treated groups. The alanine aminotransferase levels, aspartate aminotransferase, and alkaline phosphatase were increased in the experimental animals after exposure with PQ. A significant decrease in the level of catalase, glutathione peroxidase, superoxide dismutase, glutathione, thiobarbituric acid reactive substances, and reactive oxygen species were recorded in rats exposed to PQ. The mitochondrial TCA cycle enzyme activities, including isocitrate-dehydrogenase, succinate-dehydrogenase, alpha-ketoglutarate dehydrogenase, and malate-dehydrogenase, were reduced in PQ exposed rats. The activities of mitochondrial enzymes including NADH dehydrogenase, coenzyme Q-cytochrome reductase, succinic-coenzyme Q and cytochrome c-oxidase were significantly decreased after the PQ-exposure. PQ administration also reduced the mitochondrial membrane potential. However, the administration of mitochondria with NOB can decrease the toxic effect of the PQ in isolated mitochondria. NOB treatment potentially reduced the damaging effects of the PQ in the mitochondria isolated from hepatic tissues. Thus, the current study revealed that the NOB could attenuate PQ-induced mitochondrial damage in rats' hepatic tissues.

The cyto-nephrotoxicity in fishes induced by dyes is a global issue. Fluorescein dye has a wide range of applications in industry and biological laboratories. In vivo experiment was planned to assess the sublethal effects of Fluorescein dye, Eosin Y, and Eosin B in Labeo rohita. This freshwater fish was exposed to increasing concentrations (0.0011, 0.0023, and 0.0047 mg/L) of both dyes in the aquarium for definite time intervals. A dye-free trial was set as a control. Fish was anesthetized and dissected by cutting on the ventral side to remove a kidney. Cyto-nephrotoxicity was detected through histopathology. The fish's significant mortality was observed when exposed to 0.0023 mg/L (LC50) and 0.0047 mg/L concentration of Eosin Y dye. These trial groups showed many kidney tissues alterations such as glomerular, tubular epithelial cell's degeneration, a reduced lumen of tubules, vacuolation, absence of bowmen's space, necrosis, glomerulonephritis with increased per tubular space, shrinking of the glomerulus, congestion, clogging, and degeneration of tubules. Eosin B showed less mortality and tissue damage, including glomerular contraction and increased space between glomerulus and capsule. ANOVA showed a highly significant reduction in weight gain of fish at different treatments levels of Eosin Y, but less or none in the case of Eosin B. Increase in fish weight was found to be 66.3 ± 0.38 g when exposed to Eosin Y at 0.0047 mg/L, but it was 69.05 ± 0.63 g when exposed to Eosin B while it was almost identical 69.2 ± 0.23 g for both dye-free trial groups. The pair-wise comparison showed that exposure of the Eosin Y at treatment level 0.0047 mg/L was found to be highly toxic for the kidneys of Labeo rohita. Although both classes of dye are cytotoxic at small concentrations, Eosin Y is acute cyto-nephrotoxic and was found to be involved in growth retardation. To prevent society from fatal consequences, usage of dyes having acute toxicity must be banned or switched to alternates having no effects.

Recent trends in anticancer therapy is to use therapeutic agents which not only kill the cancer cell, but are less toxic to surrounding normal cells/tissue. One approach is to cut the nutrient supply to growing tumor cells, by blocking the formation of new blood vessels around the tumor. As the phytochemicals and botanical crude extracts have proven their efficacy as natural antiangiogenic agents with minimum toxicities, there is need to explore varieties of medicinal plants for novel antiangiogenic compounds.Rumex vesicarius L. (Humeidh), is an annual herbal plant with proven medicinal values. The antiangiogenic potential, and developmental toxicity of humeidh in experimental animal models has never been studied before. The crude extracts were prepared from the roots, stems, leaves and flowers of Rumex vesicarius L. in methanol, chloroform, ethyl acetate and n-hexane. The developmental toxicity screening in zebrafish embryos, has revealed that Rumex vesicarius was not toxic to zebrafish embryos. The chloroform stem extract showed significant level of antiangiogenic activity in zebrafish angiogenic assay on a dose dependent manner. Thirty five (35) bioactive compounds were identified by gas chromatography mass spectrophotometry (GC–MS) analysis in the stem extract of Rumex vesicarius. Propanoic acid, 2-[(trimethylsilyl)oxy]-, trimethylsilyl ester, Butane, 1,2,3-tris(trimethylsiloxy), and Butanedioic acid, bis(trimethylsilyl) ester were identified as major compound present in the stem of R. vasicarius.The anticancer activity of roots, stem, leaves and flowers crude extract was evaluated in human breast cancer (MCF7), human colon carcinoma (Lovo, and Caco-2), human hepatocellular carcinoma (HepG2) cell lines. Most of the crude extracts did not show significant level of cytotoxicity in tested cancer cells line, except, chloroform extract of stem which exhibited strong anticancer activity in all tested cancer cells with IC50 values in micro molar range.Based on these results, it is recommended that formulation prepared from R. vesicarius can further be tested in clinical trials in order to explore its therapeutic potential as an effective and safe natural anticancer product. Keywords: Rumex vasicarius L., Angiogenesis, Phytochemical screening, Developmental toxicity, Zebrafish embryos

This research work was carried out to determine the effects of water contamination on the fatty acid (FA) profile of periphyton, zoobenthos, two Chinese carps and a common carp (Hypophthalmichthys molitrix, Ctenopharygodon idella and Cyprinus carpio), captured from highly polluted (HP), less polluted (LP), and non-polluted (NP) sites of the Indus river. We found that the concentration of heavy metals in the river water from the polluted locations exceeded the permissible limits suggested by the World Health Organization (WHO) and the US Environmental Protection Agency (EPA). Fatty acid profiles in periphyton, zoobenthos, H. molitrix, C. idella, and C. carpio in the food web of river ecosystems with different pollution levels were assessed. Lauric acid and arachidic acids were not detected in the biomass of periphyton and zoobenthos from HP and LP sites compared to NP sites. Alpha-linolenic acid (ALA), eicosadienoic acid and docosapentaenoic acid were not recorded in the biomass samples of periphyton and zoobenthos in both HP and LP sites. Caprylic acid, lauric acid, and arachidic acid were not found in H. molitrix, C. idella, and C. carpio captured from HP. In this study, 6 and 9 omega series FAs were identified in the muscle samples of H. molitrix, C. idella and C. carpio captured from HP and LP sites compared to NP sites, respectively. Less polyunsaturated fatty acids were observed in the muscle samples of H. molitrix, C. idella, and C. carpio collected from HP than from LP. The heavy metals showed significant negative correlations with the total FAs in periphyton, zoobenthos, and fish samples.

Specimens of Heteropneustes fossilis were treated with various levels of malathion and its 96 h LC50 value was determined. The effects of sub-lethal concentrations of insecticide on hematological and biochemical profile of Heteropneustes fossilis were also registered. The 96 h LC50 value obtained was 8.81 mg/l. Exposure of sub-lethal doses (0.44, 0.88 and 1.76 mg/l which are 5, 10 and 20% of the LC50) of malathion to Heteropneustes fossilis for 3 weeks demonstrated that the toxicant had a detrimental effect on the blood profile of fish. Blood cell (Erythrocyte and leucocytes) counts (from 1.66 to 1.44 cell × 106 × mm3 and 37.93 to 30.24 cell × 103 × mm3; respectively), haemoglobin (Hb) level (from 6.21 to 3.54 g/dl) and haematocrit (Ht) estimates (from 34.26 to 30.52%) were reduced in the fishes exposed to malathion. Elevated level (from 46.25 to 92.45 mg/100 ml) of glucose and decreased quantity (29.95 to 24.25 g/dl) of protein in plasma was registered. Glycogen content in muscle and liver was also decreased. The activity of enzymes glutamic-oxaloacetic transaminase (GOT) and glutamic-pyruvic transaminase (GPT) were high in the fish treated with pesticide. The possible causes for variations in the different parameters were identified and discussed.

In the present study, TiO2 nanoparticles (NPs) were green-synthesized for first time using the extracts of Azadirachta indica twigs, Ficus benghalensis and Syzygium aromaticum. The green-synthesized G-TiO2 NPs were widely characterized by UV-Vis spectroscopy, XRD, FTIR, DRS-UV, HR-TEM, EDX and Zeta potential. The shapes of the G-TiO2 NPs are crystalline and tetragonal. The antibacterial and antibiofilm activities of G-TiO2 NPs were tested against bacteria (Streptococcus mutans and Citrobacter freundii) and fungi (Candida albicans). Both the bacterial and fungal biofilms were inhibited at 100 μg mL−1. Furthermore, the mosquito larvicidal activity was evaluated against the Zika virus vector Aedes aegypti. The mortality of A. aegypti was 98% at 75 μg mL−1 of G-TiO2 NPs. The LC50 and LC90 values were 12.2 and 61.21 μg mL-1, respectively. Additionally, the photocatalytic activity of G-TiO2 NPs was determined by the degradation of organic dye (methylene blue) and the pharmaceutical drug (paracetamol). The photocatalytic degradation efficacy of G-TiO2 NPs was greater against paracetamol (88%) compared to the methylene blue (70%).

Warfarin sodium (WFS) is a widely used oral anticoagulant drug but has a narrow therapeutic window. Since traditional detection methods applied for therapeutic drug monitoring suffer some shortcomings, including difficulty in obtaining timely reports, high costs and tedious operation, it is necessary to develop a detection system for the rapid monitoring of WFS in biological samples. Here we report a novel electrochemical sensor, which was facilely fabricated by coupling nanoporous gold leaf (NPGL) with molecularly imprinted polymer (MIP) to afford ultrasensitive and selective determination of WFS. The morphological characterization via scanning electron microscopy proved the successful modification of the sensor by NPGL followed with MIP layer modification. The influencing parameters including the type of monomer, pH and molar ratio of template to monomer were optimized during electro-polymerization. Using Fe(CN)63−/4− as a probe acting as an electrical indicator, a linear relationship of the current response versus the concentration of WFS was obtained in the range from 1.0 × 10−10 to 8.0 × 10−8 M under the optimal experimental conditions, with a detection limit of 4.1 × 10−11 M (S/N = 3). In addition, the as-prepared sensor exhibited specific detection of WFS over its structural analogues and interferents, and the established electrochemical approach was validated using the standard method – high performance liquid chromatography. Eventually, rapid and accurate determination of WFS in human blood was carried out after easy sample pretreatment.

A novel contaminant was isolated from Madin Darby Bovine Kidney (MDBK) cells. The organism was unable to grow on standard microbiological media by conventional techniques, but grew well in Dulbecco's Modified Eagle's Medium (DMEM) containing high glucose concentration. The organism formed a white biofilm on the bottom without any signs of turbidity. Upon genome sequence analysis of 16 S rDNA, the contaminant was identified as Sphingomonas sp. Shah, a member of the group α-Proteobacteria. Neutral red dye uptake method confirmed clear cytotoxic potential of the bacterium on A-549 cells. The organism was capable of invading and infecting different mammalian cell lines: MDBK, ZZ-R, 293-T, A549, and HeLa cells. Infected cells showed a variety of cytopathic effects including vacuolation at perinuclear area, cytoplasmic granulation and membrane blebbing. Microscopic analysis of the infected cells revealed the presence of cytoplasmic vacuoles harboring motile organisms. Apparently local serum preparations seem to be the source of this contamination, which is imperceptibly passed on from one culture passage to the other and ultimately leading to serious cytopathic manifestations. J. Cell. Biochem. 116: 934–942, 2015. © 2015 Wiley Periodicals, Inc.

The levels of dichlorodiphenyltrichloroethane (DDT), dichlorodiphenyldichloroethylene (DDE), endosulfan, endosulfan sulfate, carbofuran, and cartap were determined in muscles of Cyprinus Carpio sampled from 10 different sites of River Ravi between Shahdara to Balloki Headworks to assess level of contamination of these pesticides by GC-ECD (gas chromatograph equipped with electron capture detector) method. All fish samples were found contaminated with different concentrations of DDT, DDE, endosulfan, and carbofuran. DDT and DDE concentrations were higher than maximum residue limits (MRL) in food standards, while endosulfan sulfate and cartap were not detected. These findings indicate that pesticide concentrations in fish muscles decreased in the order: DDT > DDE > carbofuran > endosulfan. Furthermore, the sampling sites after Degh fall and beyond Hudiara Nulla Fall river sampling sites were more polluted. It is proposed that constant monitoring programs are needed to assess potential exposure risks.

Antioxidant enzyme activities of fish (Oreochromis niloticus) were determined in order to assess the status of pollution in the Wadi Namar (WN), near Riyadh, Saudi Arabia. Activities of four antioxidant enzymes as superoxide dismutase (SOD), catalase (CAT), glutathione S-transferase (GST), and concentrations of glutathione (GSH) and oxidant malondialdehyde (MDA) were selected as bioindicators. Fish (n = 14) were sampled in the month of April 2013 from WN and a control site (CS). SOD activity was increased by 37.9%, 47%, and 29% in kidney, liver, and heart, respectively, while a significant decrease (36.4%) was observed in gills of O. niloticus from WN as compared to fish from CS. CAT activity was reduced by 51%, 55%, 47%, and 35% in kidney, liver, heart, and gills of O. niloticus from WN. The GST activities in kidney, liver, and heart of O. niloticus from WN were elevated by 34%, 48%, and 32%, respectively. However, significant fall (49%) in gills of fish was noted from WN compared to fish from CS. GSH le...

A study was conducted to determine the effects of long-term exposure to carbofuran on erythrocyte and liver acetylcholinesterase (AChE) activity in Cyprinus carpio, and assess which tissue was more sensitive to pesticide exposure examining this enzyme. Fish were allowed to accilimatize in toxicant-free water for 24 days after 60-day exposure. AChE activity was determined with a spectrophotometer using acetylthiocholine iodide as a substrate in erythrocytes and liver. Enzymic activity of erythrocytes and liver decreased over time. A higher degree of enzyme inhibition was observed in erythrocyte compared to liver. The degree of enzyme inhibition was positively correlated with exposure time. When exposed fish were transferred to clean water, recovery was greater in erythrocytes than liver. Erythrocyte AChE activity recovered after 18 days, while it required 21 days in liver. The findings of this study indicate that erythrocyte AChE is more sensitive to carbofuran than liver. The greater sensitivity of erythr...

Profenofos and trizaophos (organophosphates) carbofuran and carbaryl (carbamates) are among the major toxicants polluting freshwater bodies, as well as exerting a significant effect on the health of fish. In this study, the 96 h LC50 of the most commonly used organophosphates and carbamates was determined in one of the indigenous fish species, Labeo rohita fingerlings. Pesticides were applied to fingerlings that had been grown under optimized standard conditions under a maintained static bioassay system. Probit analysis was used for the determination of LC50 values, which were ascertained as 6.64, 0.32, 1.4, and 8.24 mg/L for triazophos, profenofos, carbofuran, and carbaryl, respectively. Acute toxic stress was noted with fish exhibiting behavioral toxicity including suffocation, lying on the bottom, erratic swimming, lethargy and downward movements, and gulping prior to mortality.

A highly sensitive and multiple microRNA (miRNA) detection method by combining three-dimensional (3D) DNA tetrahedron-structured probes (TSPs) to increase the probe reactivity and accessibility with duplex-specific nuclease (DSN) for signal amplification for sensitive miRNA detection was proposed. Briefly, 3D DNA TSPs labeled with different fluorescent dyes for specific target miRNA recognition were modified on a gold nanoparticle (GNP) surface to increase the reactivity and accessibility. Upon hybridization with a specific target, the TSPs immobilized on the GNP surface hybridized with the corresponding target miRNA to form DNA-RNA heteroduplexes, and the DSN can recognize the formed DNA-RNA heteroduplexes to hydrolyze the DNA in the heteroduplexes to produce a specific fluorescent signal corresponding to a specific miRNA, while the released target miRNA strands can initiate another cycle, resulting in a significant signal amplification for sensitive miRNA detection. Different targets can produce different fluorescent signals, leading to the development of a sensitive detection for multiple miRNAs in a homogeneous solution. Under optimized conditions, the proposed assay can simultaneously detect three different miRNAs in a homogeneous solution with a logarithmic linear range spanning 5 magnitudes (10

Organophosphates and carbamates are major agrochemicals that strongly affect different neuroenzymes and the growth of various fish species. Here, we study the effect of sublethal concentrations of profenofos and carbofuran on the activity of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) and the associated health risk in fish. Labeo rohita fingerlings were exposed to three sublethal concentrations of profenofos and carbofuran. The minimum cholinesterase activities in the brain, gills, muscle, kidney, liver, and blood were after exposure to profenofos (0.06 mg/L). The minimum AChE and BuChE activities in the brain, gills, muscle, kidney, liver, and blood were after exposure to carbofuran (0.28 and 0.198 mg/L). Exposure to both types of pesticides affected the functions of these organs, including metabolism and neurotransmission, to various extents at different exposure concentrations. These findings suggest that they are required to be properly monitored in the environment, to reduce their toxic effects on nontarget organisms.

A novel electrochemical sensor has been facilely fabricated by applying composite elements consisting of nitrogen and sulfur co-doped activated graphene (N,S-AGR) and molecularly imprinted polymer (MIP). N,S-AGR was synthesized by one-pot pyrogenation of a mixture of thiourea, KOH and graphene oxide, which was introduced to improve electron transfer capability and surface area of the electrode, while the electro-polymerized MIP layer afforded simultaneous recognition and quantification of cyclophosphamide (CPA) by utilizing Fe(CN)63-/4- as probe to indicate electrical signals. Under the optimal conditions, a calibration curve of current shift versus concentration of CPA was got in the range of 8×10-12-8×10-7molL-1, and the developed sensor gave a remarkably low detection limit (LOD) of 3.4×10-12mol L-1 (S/N=3). Moreover, the as-prepared sensor illustrated other good merits like stability and selectivity, and played a role in real-time therapeutic drug monitoring after CPA administration in rabbit.

The present study was conducted to determine the effect of sodium cyanide on oxidative metabolism, alterations in the activities of lactate dehydrogenase (LDH) and succinate dehydrogenase (SDH), behavior, respiratory rate and metabolites (lactic and pyruvic acid) of the fingerling of Clarias gariepinus. The fingerlings were exposed to a sublethal concentration (0.75 mgL-1) of sodium cyanide. Fish showed a gradual decrease in respiratory rate, increase in LDH and decrease in SDH levels, and lactic acid followed a similar trend with pyruvate in an eight-day trial. The changes in the levels of these enzyme activities may be as a result of impaired oxidative metabolism and cellular damage, which had effect on the release of these enzymes. Elevation in the level of lactic acid and decrease in pyruvic acid was due to shift from aerobic to anaerobic metabolism which resulted to a severe drop in the respiratory rate of the fish. It may be as a result of blockage of electron transfer from cytochrome-c oxidase to molecular oxygen which might lead to cellular hypoxia even in the presence of normal oxygenation of hemoglobin. Thus, inhibition of oxidative metabolism by sodium cyanide in C. garipenus was reconfirmed. Behavioral changes caused by sodium cyanide exposure in the fish were probably due to the combination of lactate acidosis with cytotoxic hypoxia, which might depress the central nervous system.Key words: Succinate dehydrogenase (SDH), lactate dehydrogenase (LDH), lactic acid, pyruvate, behavior, enzymes.

A simple electrochemical sensor has been developed for highly sensitive detection of octopamine and tyramine by electrodepositing reduced graphene oxide (ERGO) nanosheets onto the surface of a glassy carbon electrode (GCE). The electrocatalytic oxidation of octopamine and tyramine is individually investigated at the surface of the ERGO modified glassy carbon electrode (ERGO/GCE) by using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Several essential factors including the deposition cycle of reduced graphene oxide nanosheets and the pH of the running buffer were investigated in order to determine the optimum conditions. Furthermore, the sensor was applied to the quantification of octopamine and tyramine by DPV in the concentration ranges from 0.5 to 40 μM and 0.1 to 25 μM, respectively. In addition, the limits of detection of octopamine and tyramine were calculated to be 0.1 μM and 0.03 μM (S/N = 3), respectively. The sensor showed good reproducibility, selectivity and stability. Finally, the sensor successfully detected octopamine and tyramine in commercially available beer with satisfactory recovery ranges which were 98.5%–104.7% and 102.2%–103.1%, respectively. These results indicate the ERGO/GCE based sensor is suitable for the detection of octopamine and tyramine.

Background: Pesticides widely used for agricultural purposes are carbamates, organophosphates as well as organochlorines. Among these pesticides, organochlorine compounds have been extensively used to control disease vectors as well as agricultural pests. The objective of this experiment was to study the chronic effect of a commercial formulation of profenofos on acetylcholinesterase (AChE) and butylcholinesterase (BuChE) activity in various tissues in Catla catla, Labeo rohita and Cirrhinus mrigala fingerlings was investigated. Materials and Methods: Healthy fingerlings of Catla catla, Labeo rohita and Cirrhinus mrigala with an average body length 90±6 mm and 30.00±2.00 g body weight were collected from the fish seed hatchery and brought to the laboratory. Fishes were maintained in 70 litter glass aquaria (27 ± 1oC, 2.70–2.80 ms and 8.85–9.40 pH). The fingerlings of Catla catla, Labeo rohita and Cirrhinus mrigala were exposed to the 3 sub lethal concentrations of profenofos (0.038, 0.019, 0.012; 0.06, 0.03, 0.02 and 0.041, 0.020 and 0.013 mg/L) for 8 weeks. The control experiments were also performed with the addition of carrier solvent alone. Acetylcholinesterase and butyrylcholinesterase level were estimated according to the methodology of Ellman et al. (1961) and Kuster (2005). Total soluble proteins were determined by the Bradford (1976) standard method to assess enzymatic activity of the protein. Results: The least activity of AChE was recorded in muscle samples of Catla catla (1.07±0.040 μmoles/min/g of protein), exposed to the highest concentration of profenofos. BuChE activity was also reduced against various concentrations of profenofos. The AChE and BuChE activity was significantly inhibited even when exposed to a minimum concentration of this insecticide. Profenofos exposure affected the functioning of brain, blood, gills, muscle, kidneys and liver. We concluded that profenofos caused more inhibition in the liver for AChE and BuChE compared to other tissues. Conclusion: It has been concluded that profenofos is very highly toxic to the C. catla, L. rohita and C. mrigala fingerlings, but further studies are required to assign a certain level of toxicity to the said pesticide. Considering the high toxicity of profenofos, it is suggested to handle the profenofos carefully using all the precautionary measures in order to minimize the harmful effects on non-target organisms.

The measurement of sulfide, especially hydrogen sulfide, has held the attention of the analytical community due to its unique physiological and pathophysiological roles in biological systems. Electrochemical detection offers a rapid, highly sensitive, affordable, simple, and real-time technique to measure hydrogen sulfide concentration, which has been a well-documented and reliable method. This review details up-to-date research on the electrochemical detection of hydrogen sulfide (ion selective electrodes, polarographic hydrogen sulfide sensors, etc.) in biological samples for potential therapeutic use.

Two different weight groups of farmed Labeo rohita were collected from fish hatchery, Satiana Road Faisalabad, Pakistan. Pesticide residues were determined by high-performance liquid chromatography (HPLC). HPLC analysis showed that seven pesticide residues (α-endosulfan, DDE, parathion methyl, isoproturon, atrazine, carbofuran, and deltamethrin) were detected in L. rohita in weight group W 1.Six pesticide residues (α-endosulfan, parathion methyl, isoproturon, atrazine, carbaryl, and carbofuran) were found in L. rohita weight group W 2. The overall comparison between two weight groups of L. rohita showed that maximal concentration of pesticide residues were observed in underweight group W 2 compared to W 1 weight group.

Current study investigated the fermentative production of cell mass and crude protein using an axenic culture of the thermotolerant strain of Chlorella vulgaris grown mixotrophically in an illuminated 10-l glass bioreactor. The process was then upscaled to 1,000-l bioreactor. The organism supported maximum specific growth rate, crude protein volumetric productivity, and specific productivity of 1.2 day−1, 2.26 g l−1 day−1, and 0.76 g g−1 day−1, respectively, with urea as nitrogen source. Gibbs free energy, enthalpy, and entropy values for its formation were 74.3, 56. 2 kJ mol−1, and −59.1 J mol−1 K−1, respectively, in both reactors and corresponded to those of thermotolerant organisms. Algal biomass grown in 10-l bioreactor contained 0.52 ± 0.03, 12.6 ± 2.0, 60.0 ± 4.5, 0.4 ± 0.02, 4.5 ± 0.2, 12 ± 0.5, and 3.81 ± 0.5% carotenoids, carbohydrates, crude protein, DNA, RNA, lipids, and total chlorophyll, respectively. Dry biomass supported good growth of fish larvae comparable with that on commercial diet.

The aim of this work was to investigate and compare the antiproliferative, antioxidant and antibacterial activities of Rosmarinus officinalis essential oil, native to Pakistan. The essential oil content from the leaves of R. officinalis was 0.93 g 100g-1. The GC and GC-MS analysis revealed that the major components determined in R. officinalis essential oil were 1,8-cineol (38.5%), camphor (17.1%), α-pinene (12.3%), limonene (6.23%), camphene (6.00%) and linalool (5.70%). The antiproliferative activity was tested against two cancer (MCF-7 and LNCaP) and one fibroblast cell line (NIH-3T3) using the MTT assay, while, the antioxidant activity was evaluated by the reduction of 2, 2-diphenyl-1-picryl hydrazyl (DPPH) and measuring percent inhibition of peroxidation in linoleic acid system. The disc diffusion and modified resazurin microtitre-plate assays were used to evaluate the inhibition zones (IZ) and minimum inhibitory concentration (MIC) of R. officinalis essential oil, respectively. It is concluded from the results that Rosmarinus officinalis essential oil exhibited antiproliferative, antioxidant and antibacterial activities.

Maternal oxidative stress during pregnancy may impair fetal growth and help in the development of diseases in adulthood. The aim of current study was to assess total oxidation status (TOS), related parameters and their relationship to DNA damage (%) and homocysteine level in normal pregnant women in low-income participants. In a cross-sectional study healthy women were grouped as normal, while age matched nulliparous and singleton pregnancies were included for first, second and third trimester groups. TOS (P < 0.01), melanodialdehyde (MDA) (P < 0.001), aspartate aminotransferase (AST) (P < 0.01), triiodothyronine (T3) (P < 0.01), thyroxine (T4) (P < 0.01), and homocysteine (P < 0.001), in pregnant women were significantly higher as compared to normal healthy women. While serum total proteins (P < 0.01), albumin (P < 0.01) and total antioxidant status (TAS) (P < 0.001) decreased significantly as compared to normal healthy women. Women in third trimester showed a significantly high level of body temperature (P < 0.01), triglyceride (P < 0.01), LDL-cholesterol (P < 0.05), AST (P < 0.01), T3 (P < 0.01), homocysteine (P < 0.001), TOS (P < 0.01) and MDA (P < 0.001) but a lower concentration of serum proteins, albumin and TAS at the end of the pregnancy. Pearson correlation indicated a positive relationship of homocysteine with triglycerides (P < 0.027), TOS (P < 0.01), MDA (P < 0.035) and had a negative relationship with total protein (P < 0.026). DNA damage was strongly related with T3 (P < 0.008), TOS (P < 0.02), MDA (P < 0.037) and MBI (P < 0.048) profiles of pregnant women. These changes were considered normal for pregnant women having optimum blood pressure and normal child birth. Hormonal influences and hemodilution may contribute towards the observed changes in this study.

Chitin based polyurethane bio-nanocomposites (PUBNC) were prepared by emulsion polymerization. A mixture of polymer and bentonite clay enriched in montmorillonite (MMT) was formed in emulsion polymerization, in which MMT dispersed differently depending on interaction of MMT with polymer chains. Cation exchange capacity (CEC) of bentonite clay enriched in montmorillonite was found 74 meq/100 g. The existence of the intercalated clay by PU in the hybrid was confirmed using optical microscope (OM) technique. Optical microscope (OM) photographs verified the well dispersed ordered intercalated assembles layers of bentonite in PU matrix.

Shape memory polyurethanes (SMPUs) were prepared from polycaprolactone diol 4000 (PCL 4000), 4,4′-diphenylmethane diisocyanate (MDI), 1,4-butanediol (BDO), chitin, dimethylol propionic acid (DMPA), and triethylamine (TEA). The synthesized samples were irradiated for 50, 100, and 200 h in an UV exposure unit. The effects of chitin and DMPA contents in the polyurethane (PU) formulation on surface properties of the UV-irradiated PU samples were investigated by contact angle measurements, surface free energy and water absorption (%), total work of water adhesion to polymer and equilibrium degree of swelling. Results of the aforementioned surface techniques revealed that the UV-irradiated PU samples were affected by varying the UV exposure period. The interactions of the PU films with solvents on the surface were clearly related to the contents of DMPA and chitin in the final polyurethane formulation and UV-irradiation time.

A study of the levels of six pesticide residues (endosulfan, carbofuran, cypermethrin, profenofos, triazophos, and deltamethrin) was conducted to determine possible environmental and health risks in surface waters, sediment, and fish Catla catla. Samples were analyzed by gas chromatography with an electron capture detector. The total concentration of pesticides in water, sediment, and fish ranged from 0.005 to 3.17 μg/l, 0.61 to 23.06 ng/g dry weight, and 0.35 to 19.15 μg/g lipid-normalized units, respectively. According to the concentrations and detection frequencies, endosulfan and profenofos were the most dominant pesticides recorded in fish tissue and sediment samples. Profenofos and cypermethrin, meanwhile, were the most abundant pesticides recorded in water samples at these sites. Cypermethrin and triazophos were not detected in the sediment samples. The concentration of endosulfan, carbofuran, and deltamethrin were higher than the permissible limits for fish set by international agencies and pose a potential ecological risk to the aquatic ecosystem and a consequent hazard to human health.

The collagen of skin, scales and fins of Catla catla and Cirrhinus mrigala were isolated and characterised. Nine fishes of each fish species of three weight groups were collected from a commercial fish farm. Collagen characterisation using SDS-PAGE revealed the molecular weights (kDa) of the C. catla skin, scales, and fins which ranged from 120 to 210, 70 to 201, and 68 to 137 kDa, respectively. The size of the collagen of C. mrigala skin, scales and fins ranged from 114 to 201, 77 to 210, and 70 to 147 kDa, respectively. Glycine and alanine were the most abundant amino acid, whereas tryptophan was totally absent in all selected tissues. Thus, significant variation exists in type of collagen and amino acid profile within the weight groups of the two fish species. The imino acid (proline and hydroxyproline) contents estimated in C. catla and C. mrigala skin (161–165 and 160–168), scales (155–159 and 152–161) and fins (162–171 and (152–155) residues/1,000 residues, respectively. The proximate analysis was also performed for skin, scales and fins. The maximum protein content of the skin was determined as 26.10 % and 22.90 % in the C. catla and C. mrigala, respectively, from the W3 weight group. The scales of the W3 weight group exhibited maximum protein contents of 25.90 and 21.77 % for C. catla and C. mrigala, respectively. The maximum protein contents (19.04 % and 18.12 %) were recorded for C. catla and C. mrigala, respectively in the fins.

The present study investigated the presence and potent source of pesticides and specific pesticide bearing effluent release points on the River Ravi, between the Shahdara and Balloki Headworks. Pakistan has banned the use of organochlorine and nitrogen containing pesticides, yet no attention has been paid to the continuous monitoring and assessment of these banned pesticides to make sure that they are not being used in practice. Levels of selected organochlorine and nitrogen containing pesticide residues were assessed in water collected from 18 sampling sites on the River Ravi and its tributaries using a gas chromatograph equipped with an electron capture detector (GC-ECD). All water samples were found to be contaminated with varying concentrations of pesticide residues. However, levels of pesticides were below the tolerance limits suggested in national and international standards. Pesticide concentrations in the water of river sites ranged from 0.034 to 0.045 microg/L for DDT, 0.033 to 0.046 microg/L for DDE, 0.108 to 0.123 microg/L for endosulfan and 0.028 to 0.040 microg/L for carbofuran. In tributaries, pesticide concentrations ranged from 0.0468 to 0.0685 microg/L for DDT, 0.0390 to 0.0637 microg/L for DDE, 0.111 to 0.147 microg/L for endosulfan and 0.0396 to 0.0631 microg/L for carbofuran. The results show pesticide concentrations in river water in the order: endosulfan > DDE > DDT > carbofuran. Pesticide concentrations in tributary waters decreased in the order: endosulfan > DDT> DDE > carbofuran. After Degh Fall and After Hudiara Nulla Fall river sampling sites were severely contaminated while, among the tributaries, Degh Fall and Hudiara Drain were severely contaminated with DDT, DDE, endosulfan and carbofuran. Constant monitoring programs should to be initiated to reform the present situation.