Interaction of alcohol and kola nut on brain sodium pump activity in Wistar rats

The effect of interaction of alcohol and kola nut on sodium pump activity was studied in Wistar rats. Thirty Wistar rats were divided into six groups of five rats per group. Control received a placebo (4 mL of distilled water). Groups 2–6 were treated for a period of 21 days with 10% (v/v) alcohol, 50 mg caffeine/kg, 50 mg kola nut/kg, or a combination of 10% (v/v) alcohol + 50 mg kola nut/kg, or 10% (v/v) alcohol + 50 mg caffeine/kg, respectively. One day after the final exposure, brains were harvested and several biochemical parameters examined including activities of total ATPase, ouabain-insensitive ATPase, ouabain sensitive ATPase (Na⁺–K⁺-ATPase) and levels of nonenzymatic breakdown of ATP and inorganic phosphate (P_i) released. Results showed that the essential enzyme of the brain responsible for neuronal function, Na⁺–K⁺-ATPase, was inhibited by alcohol–kola nut co-administration relative to control, resulting in a decreased ATP production, ion transport and action potential, leading to loss of neuronal activities.     

In vitro cytotoxicity of multi-wall carbon nanotubes on human cell lines

The aim of this study was to evaluate the in vitro toxicity of two multi-wall carbon nanotubes on four different cell lines: human alveolar epithelial (A549) cells, hepatocytes (Hep 3B cells), human embryonic kidney cells, and intestinal (P407 cells) cells. The adverse effects of carbon nanoparticles were analyzed after 24 h incubation with different cell lines using the trypan blue dye exclusion method. Incubation of carbon nanotubes with different cells produced a concentration-dependent inhibition of growth of the cells. The TC₅₀ or IC₅₀ values (toxic concentration 50, i.e., concentration of particles inducing 50% cell mortality) of two nanoparticles were (1) found to be in the range 23.5–30.5 µg mL^?1, and (2) less than that of quartz (known toxic agent, 28.8–66.9 µg mL^?1), indicating the greater cytotoxic effect of carbon nanoparticles than quartz particles.     

Mutagenicity of polyaromatic hydrocarbons by chemical models for cytochrome P450 in Ames assay

DNA damage is an important step in carcinogenesis. The Ames assay is a short-term screening of carcinogens that induce DNA damage. Most carcinogens require enzymatic activation through oxidation by cytochrome P450 (CYP450) in the presence of S9 mix. A combination of iron (Fe)(III) porphyrin and an oxidant is also able to oxidize compounds as an alternative metabolic pathway to CYP450. Previously it was reported that a chemical model containing a water-soluble 5,10,15,20-tetrakis(1-methylpyridinium4-yl)porphyrinatoiron(III) chloride (4-MPy) and tert-butyl hydroperoxide (t-BuOOH) activated aromatic amines and amides. In this study, a chemical model composed of an Fe porphyrin, water-insoluble 5,10,15,20-tetrakis(pentafluorophenyl)porphyrinatoiron(III) chloride (F₅P) or water-soluble 4-MPy was optimized with an oxidant – t-BuOOH, magnesium monoperoxyphthalate (MPPT), or iodosylbenzene (PhIO). Subsequently the mutagenicity of benzo[a]pyrene (B[a]P) and chrysene in Salmonella typhimurium TA strains was compared. B[a]P was activated by a combination of F₅P or 4-MPy plus MPPT or PhIO in S. typhimurium TA1538. The B[a]P-induced mutagenicity with F₅P plus oxidant was higher than 4-MPy plus oxidant. Mutagenicity of chrysene, a tetracyclic aromatic hydrocarbon, was not detected in the presence of F₅P/PhIO in S. typhimurium TA98, but was activated in the presence of F₅P/MPPT. The F₅P/MPPT activated other polyaromatic hydrocarbons (PAH) in the S. typhimurium TA98 assay including dibenz[a,c]anthracene, dibenz[a,h]anthracene, 3-methylcholanthrene, and benzo[a]anthracene. The results indicated that the F₅P/MPPT was the most efficient model for detecting PAH-induced mutagenicity in the Ames assay.     

Assessment of potentially toxic elements in Swiss chard and sediments of Akaki River,Ethiopia

For the determination of 15 potentially toxic elements (V, Cr, Fe, Mn, Co, Ni, Cu, Zn, As, Se, Ag, Cd, Sn, Hg, and Pb) in plant and sediment samples of the Akaki River, Ethiopia, inductively coupled plasma–mass spectrometry, inductively coupled plasma–optical emission spectrometry, and a RA-915+ mercury analyzer were applied. Sediment and plant samples were mineralized using a closed-vessel microwave-assisted digestion system. The elemental concentrations varied considerably in plant and sediment samples. The minimum concentration was observed for known toxic elements (As, Hg, and Cd) while the highest concentration was observed for the elements of relatively low toxicity Zn, Mn, and Fe. The concentration of Cr, Fe, Pb, Zn, and As in Swiss chard surpassed the maximum permissible levels at specific sites. At some of the sites, the sediment quality guidelines are surpassed for Cu, Zn, and Pb.     

Biochemical and histological alterations induced by a formulation of dicofol in the embryonic liver of Gallus domesticus

In the present investigation, hepatotoxic effect of a commercially available insecticide formulation of dicofol (Colonel–S® 18.5% emulsified concentrate) was studied in the developing chick embryo. Fertilized eggs of Gallus domesticus were immersed in three different dose concentrations, i.e. 250, 500, and 1000 mg L^?1 of Colonel–S on “0” and fourth days of incubation for 60 min at 37 °C and incubated till embryonic day 16. Severe histopathological cellular lesions, such as extensive cell degeneration and necrosis with enlarged blood sinusoids, cytoplasmic vacuolization, and leucocyte infiltrations with congestion or dilation of central vein, appeared in dose-depended manner. Dicofol treatment also caused significant decrease in the levels of total protein, glycogen, and glutathione content and an increase in alkaline phosphatase activity of embryonic liver, whereas glutamic pyruvic transaminase activity showed mixed response.     

Determination of cobalt by air-assisted liquid–liquid microextraction

Abstract

A rapid and selective technique for extraction, preconcentration and determination of trace amounts of cobalt in water and pharmaceutical samples by air-assisted liquid–liquid microextraction combined with flame atomic absorption spectrometry is proposed. 1-Nitroso-2-naphthol is used as a complexing agent and 1-octanol as an extraction solvent. Parameters relevant for analytical effectivity, i.e. pH of sample solution, concentration of complexing agent, volume of extraction solvent, and number of extraction cycles are optimized using a Box–Behnken design. At optimum conditions, a dynamic linear range of 5–600?µg L^?1 is obtained, with a limit of detection of 1.2?µg L^?1. The method is used for determination of Co(II) in environmental water and pharmaceutical samples.     

铬污染土壤超低频复电阻率频散特性

在超低频段(2-5~26Hz)内,研究了铬污染土壤复电阻率在不同含水率、铬含量和孔隙率下的幅值及相位频散特性. 结果显示,铬污染土壤复电阻率的幅值随频率的增大呈单调递减趋势,但相位随频率的变化曲线呈平放的S形. 含水率、铬含量和孔隙率的变化均会引起土壤复电阻率的幅值和相位大小的改变,而相位峰值的位置只对含水率及孔隙率的变化较为敏感,与铬含量变化的关系不大. 含水率从0.08增至0.24时可导致相位峰值的位置产生约8Hz的右移;而当w(Cr6+)从0.5g/kg增至4.0g/kg时,相位峰值的位置基本不发生变化. 表明铬含量和含水率的增大均会引起电阻率减小的异常现象,若单纯地使用电阻率很难区分引起这2种异常现象的原因,但结合土壤复电阻率频散特性特别是相位峰值的位置可以进行有效判别,进而可判定铬污染场地的铬含量分布.      

Phosphorous cycling and biogeochemistry in a Venezuelan-flooded savanna

In 1970, a programme of land recuperation started in Venezuelan savannas, strongly affected by the seasonality of precipitation; therefore, a network of dykes has been built to alleviate the floods and retain water throughout the dry period. Under the dyked system, the environment has been altered, allowing a change in the herbaceous vegetation towards aquatic species and an increase in primary production. It is assumed that a considerable quantity of nutrients is lost from the ecosystem through the floodgates, a situation that could be worsened with the climate change. This contribution describes the atmospheric input and total output in stream run-off of phosphorous (P) in a flooded savanna. Internal pools of the biogeochemical cycle of P associated with terrestrial compartments are described. In the flooded savanna, a large amount of P is immobilised (29.6?kg?ha^?1) in their above ground biomass by grasses, and in soil microbial biomass. The P budget was nearly balanced, as measured losses were cancelled out by the inputs in rainfall. Soils act as a sink, retaining P coming either from precipitation or from desorption/mineralisation processes. That interruption can be maximised, and losses of P and other nutrients can be minimised with an adequate management of the floodgate.     

Natural and Anthropogenic Effects On Phytoplankton Primary Productivity in Mangroves

Abstract

Spatial and temporal variations and the factors influencing primary production have been studied in three different mangrove waters (Pichavaram, Ennore Creek and Adyar Estuary) of South India characterised by different anthropogenic impacts. the gross primary productivity in the unpolluted Pichavaram mangrove was 113 g Cm^?2yr^?1 exhibiting natural variability with the environmental forcing factors. Human activities have elevated primary productivity in the Ennore Creek mangrove (157g Cm^?2yr^?1) primarily through the direct discharge of fertilizer effluents. By contrast, a combination of domestic and industrial effluent discharges into the Adyar Estuary mangrove has considerably reduced phytoplankton primary productivity 83g Cm^?2yr^?1 the Redfield N: P ratio varies from 0.96 N: 1P at Ennore Creek, 1.75N: 1P at Adyar Estuary to 15.2 N: 1P at Pichavaram mangroves. This suggests that the Pichavaram mangroves represent a well equilibrated ecosystem with N: P ratio close to steady-state values in contrast to the anthropogenically altered mangrove ecosystems studied. Results show a significant temporal variability in nutrient concentration in the three mangrove areas. Distinct differences in nutrient concentrations between the dry and the wet seasons have been observed.