Oxidative stress mediated cytotoxicity of TiO2 nano anatase in liver and kidney of Wistar rat

This study examined the adverse effects of TiO₂ nanoparticle (nano-TiO₂) on the kidney and liver of Wistar rats. Changes of serum biochemical parameters and pathological lesions indicated that liver and kidney were significantly affected in animals treated with 50?mg?kg^?1 of nano-TiO₂. The inverse relationship between the level of reactive oxygen species and the activities of superoxide dismutase, catalase, and glutathione peroxidase indicates that nano-TiO₂ induces oxidative stress. A significant increase in the apoptosis of liver and kidney in a dose-dependent manner was also observed. The ultrastructural observations confirmed the internalization of nano-TiO₂ and their direct involvement in the mitochondria-mediated cytotoxicity. Data indicated that nano-TiO₂ induce oxidative stress which produces genotoxicity such as oxidative DNA damage, micronuclei (MN) induction, and cell apoptosis in liver and kidney.     

Toxicological impact of anilofos on some physiological processes of a rice field cyanobacterium Anabaena torulosa

This study deals with the toxicological impact of the herbicide anilofos on photosynthesis, respiration, nitrogen assimilation, and antioxidant system in a diazotrophic rice field cyanobacterium Anabaena torulosa. Treatment of anilofos (1.25, 2.5, and 5?mg?L^?1) affected growth, photosynthetic pigments, photosynthesis, and respiration of the cyanobacterium. Although all the photosynthetic pigments were affected, a maximum effect of the herbicide was observed on phycocyanin (51% reduction) followed by the carotenoids. The effect of the herbicide on photosynthetic pigments resulted in 57% decrease in photosynthetic O₂ evolution. Studies on the photochemical activity demonstrated that both photosystems (PS I and PS II) were affected by the herbicide. Decrease in the photosynthesis rate resulted in decreased nitrogen assimilation, as revealed by reduced nitrate (20%) and ammonium (26%) uptake and decreased activities of nitrogenase (63% decrease) and glutamine synthetase (22% decrease). This ultimately resulted in the reduced growth of the organism. Activities of superoxide dismutase, catalase, and peroxidase in the presence of anilofos increased by 1.8–3.5 times over control cultures. Proline content increased by 1.6 times, while the content of ascorbate decreased slightly. These results indicate that the organism was able to tolerate the herbicide stress by activating oxidative stress defense mechanism.     

Effects of arsenic on reactive oxygen species and antioxidant defense system in tomato plants

In this study, the generation of reactive oxygen species, the induction of oxidative stress, and the response of the antioxidative system in hydroponically grown tomato plants as the cause of arsenic-induced phytotoxicity are investigated. Reduction in plant growth was measured in terms of dry weight and length of roots and shoots, the latter accumulating more arsenic than the roots. The treatment resulted in increased formation of superoxide anion (O₂^.?), H₂O₂, and thiobarbituric acid reactive substances, which indicate augmented lipid peroxidation. Superoxide dismutase, catalase (CAT), and ascorbate peroxidase activities were increased in arsenic-treated tomato plants while CAT activity was insignificantly increased.     

Model reactions of chromium compounds with mammalian and bacterial cells†

Chromate uptake, reduction, cytotoxicity and mutagenicity were studied with human red blood cells, Chinese hamster ovary (CHO) cells and/or Salmonella typhimurium mutant cells. All cell types rapidly took up chromates whereas chromium(III) salts were excluded under the experimental conditions. Red blood cells reduced and accumulated chromium from chromate. At concentrations above 0.1 mM, chromate inactivated the red cell chromate carrier. Chromate above 0.01 mM inhibited CHO cell proliferation irrespective of the cations present. Chromate and two chromium(III) complexes were mutagenic with Salmonella mutants in the Ames’ assay. A model for chromate metabolism and genotoxicity is proposed.     

The cytotoxicity of nici2 for mammalian cells in culture†

The effects of NiCl₂ were studied in two human cell lines, HeLa and diploid embryonic fibroblasts as well as in V79 Chinese hamster cells and in L‐A mouse fibroblasts. NiCl₂ produces a dose‐dependent depression of proliferation, mitotic rate, and viability, accompanied by an increasing release of lactic dehydrogenase and stimulation of lactic acid production. The plating efficiency is reduced, as are DNA and protein synthesis and, to a lesser degree, RNA synthesis.

The cytotoxicity of NiCl₂ is comparable in degree to those of PbCl₂ and MnCl₂, but is weaker than those of HgCl₂ and CdCl₂. However, the different sensitivities of different cell lines must also be considered.

NiCl₂ effects are more severe in serum‐free medium than in medium containing serum or serum albumin indicating that serum constituents, notably albumin, bind the metal effectively and inhibit cellular uptake; this confirms earlier reports on the serum binding and slow uptake of NiCl₂.

Synchronized cells are most sensitive in the Gl and early S phases of the cell cycle. In the Painter test the depression of DNA synthesis persists following cessation of exposure to NiCI₂. These findings contribute an explanation for the known genotoxic effects of nickel.     

Electron microscopy documenting the cellular metabolic fate of Zn IONS∗

In vertebrates and invertebrates Zn exist as complexed compounds with metallothioneins. However, its cellular level effects and metabolic fates are scantly documented. In the elucidation of this fact, EM results on hepatic cellular alterations in fish under lethal dose exposure at 4.0 ppm over a week is illustrated.

A large number of lysosomes in hepatic cells prevailed on exposure to Zn in its sulfate form. Evidently, due to metal compound stress and cellular damage lysosomal activity is augmented. The lysosomes harboured digestible material, presumably the aforementioned substrates. Contrary to it, fat droplets prevailed while glycogen depletion is noticeable. Unlike the effects of Hg, the nuclei were normal with granular chromatin and prominent nucleoli. However, the mitochondria contained some small intramitochondrial bodies. Similar to the effects of Hg, the cell membrane remained intact.

In vivo enzymatic studies indicated augmentation in catalase, acid‐ and alkaline‐phosphatases, while glucose‐6‐phosphatase is inhibited. However, only alkaline‐ and glucose‐6‐phosphatases are inhibited under in vitro conditions.

Thus, it is evident that Zn enhances cellular bioenergetic requirements culminating in glycogen depletion owing to stress, concomitantly envisaging inhibition of oxidative phosphorylation in the electron transport system.     

膜生物反应器中EPS的提取方法

以一体式膜生物反应器(MBR)中的活性污泥为对象,以蛋白质、多糖和核酸的提取量作为污泥中附着性胞外聚合物(B-EPS)提取总量的衡量指标,研究了加热法、超声法、NaOH+甲醛法、高速离心法、蒸汽法、硫酸法等6种不同方法对B-EPS提取的最优条件;并在最优提取条件下对B-EPS提取总量进行比较分析,确定最佳B-EPS提取方法。结果表明:超声提取法、高速离心提取法、蒸汽提取法、硫酸提取法对B-EPS的提取总量较低;NaOH+甲醛法对B-EPS的提取总量虽然较高,但易导致测定出现误差,且抽滤时有结晶,影响操作;加热法对B-EPS提取效果较好,对细胞破坏程度小,且操作过程简单。因此,确定加热法为B-EPS的最佳提取方法。     

Behaviour of pendimethalin and oxyfluorfen in peanut field soil: effects on soil biological and biochemical activities

A field experiment was conducted to study the dissipation kinetics of herbicides pendimethalin and oxyfluorfen in black soil of peanut field at half recommended rate (HRE), recommended rate and double recommended rate as well as to assess their effects on soil microbial parameters and enzymatic activities. In addition, their role in the transformations and availability of some plant nutrients like nitrogen transformation (through ammonification and nitrification processes) and availability of phosphorous were also studied. Incorporation of these herbicides was found to stimulate the activity of soil microbial biomass carbon, fluorescein diacetate hydrolysing activity, alkaline phosphatase and ammonification rates, while dehydrogenase activity, acid phosphatase, nitrification rate and available phosphorous was adversely affected. However, urease remains almost unchanged except for little stimulation at later stages. Dissipation of pendimethalin and oxy?uorfen followed first-order reaction kinetics with half-life (T_1/2) of 13.7–20.1 and 21.5–27.4 days, respectively. Residues of both herbicides persisted up to 60 days in the soil at all the doses except 45 days for pendimethalin at HRE.     

大气高CO2浓度对油菜氮素同化累积与植株生长的影响

为了指导高CO2浓度条件下甘蓝型油菜Brassica napus L.合理施氮、创建油菜高产高效以及进一步探明油菜氮代谢的调节机制提供理论依据,本研究采用微区试验,研究2个油菜品种（沪油15-33号和742-2）在2个CO2浓度水平（自然CO2摩尔分数400μmol·mol-1和高CO2摩尔分数（800±20）μmol·mol-1）和2个氮素水平（施氮与不施氮）条件下,氮素同化酶（NR和GS）活性和可溶性蛋白含量的变化,以及油菜地上部干物质量和氮素累积量的响应。试验结果表明,高CO2浓度会提高NR和GS活性;在氮素处理的影响方面,NR活性的变化与油菜的品种和生育时期不同有关：在高CO2浓度条件下,品种A在各时期的施氮处理的酶活性高于不施氮处理;品种B只在抽薹期的施氮处理低于不施氮处理,其他时期则升高;对于GS酶活性,在自然CO2浓度条件下施氮会提高GS酶活性,高CO2浓度条件下施氮则降低其活性（苗期除外）。CO2浓度升高会降低叶片中可溶性蛋白含量（盛花期除外）;在正常CO2浓度下,增施氮肥会提高叶片中可溶性蛋白含量,而在高CO2浓度下,增施氮肥会降低叶片中可溶性蛋白含量。CO2浓度升高和增施氮肥都会提高油菜地上部干物质量与氮素累积量,油菜干物质量与氮素累积量总体上与上述测定指标呈极显著相关。     

废水处理系统中生物聚集体胞外多聚物研究进展

胞外多聚物(Extracellular polymeric substances,EPS)是废水生物处理系统中生物聚集体(包括絮体污泥、生物膜、颗粒污泥等)的重要组成部分,直接包裹于微生物细胞壁外,其理化性质及所处的特殊位置决定了它在生物聚集体中的重要作用.综述了EPS对废水生物处理系统污泥沉降性能、脱水性以及膜生物反应器膜污染影响的相关研究,分析认为EPS组成与结构特性改变污泥表面电位、疏水性等,进而影响污泥沉降与脱水性能、膜污染程度;以好氧颗粒污泥为典型的生物聚集体代表,总结了EPS组分含量与分布对颗粒污泥的形成与结构稳定性的影响,并在EPS提取方法标准化、现代理化技术与分子生物学技术综合分析等方面进行了展望,进一步的研究有望揭示生物絮凝体形成过程EPS的产生与调控机制.