Oxidative stress and genotoxicity of 1-methyl-3-octylimidazolium chloride on loach (Misgurnus anguillicaudatus)

This study was a preliminary step to evaluate the acute toxicity of 1-methyl-3-octylimidazolium chloride ([C₈mim]Cl) on loach (Misgurnus anguillicaudatus) by determining the effects on hepatic antioxidant enzyme activities and by the comet assay. The results showed that [C₈mim]Cl had acute toxicity at concentrations above 20 mg L^?1, inducing oxidative stress and genotoxicity on fish liver cells. In respect to enzyme activities, [C₈mim]Cl induced changes in the activities of superoxide dismutase, catalase, and glutathione content the livers of fish exposed at 20–80 mg L^?1. [C₈mim]Cl at the same exposure level caused a remarkable increase in malondialdehyde level. The comet assay indicated that [C₈mim]Cl at 20–80 mg L^?1 induced genotoxicity in liver cells. With increased exposure concentration and time, the two comet parameters trailing rate and tail moment were significantly increased, with significant differences (P < 0.05) observed between control group and each treatment group. The present study shows that ionic liquids can be a threat to the health of aquatic organism when accidentally released to aquatic ecosystems.     

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.     

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。     

草甘膦与镉复合胁迫对玉米幼苗抗氧化酶活性及光合作用的影响

为了探讨草甘膦(PMG)与重金属镉(Cd)复合胁迫对作物(玉米幼苗)生长的影响作用机制。通过温室盆栽试验,分别进行了不同浓度的PMG单一处理(浓度分别设计为0、1.25、2.5、5、10、20 mg·kg~(-1))和不同浓度的PMG(浓度分别为0、1.25、2.5、5、10、20 mg·kg~(-1))与浓度5 mg·kg~(-1)Cd2+的复合处理。采用分光光度法和连续激发式荧光仪分别对玉米幼苗抗氧化酶(过氧化物酶POD、过氧化氢酶CAT、超氧化物歧化酶SOD)、丙二醛(MDA)、叶绿素含量、荧光动力学曲线及相关参数进行了测定。结果表明,单一和复合胁迫分别在PMG浓度为1.25~5 mg·kg~(-1)、1.25~2.5 mg·kg~(-1)时,玉米幼苗通过增大抗氧化酶(SOD、POD、CAT)活性,清除积累过多的活性氧自由基,提高叶绿素含量的合成,加大光合作用速率,促进玉米幼苗的生长;单一和复合胁迫分别在PMG浓度为5~20 mg·kg~(-1)、2.5~20 mg·kg~(-1)时,由于玉米幼苗积累了过多的膜脂过氧化物,导致抗氧化系统损坏,阻碍叶绿素含量的合成,同时也损害了PSII的功能(MO、φPO、ΨO、φEO、φDO、ABS/RC、TRO/RC、ETO/RC、DIO/RC、PIABS),导致玉米幼苗光合作用受到抑制,阻碍幼苗的生长。研究表明,草甘膦单一胁迫和与重金属镉复合胁迫,对玉米幼苗酶活性及光合作用的影响,均随处理浓度的升高表现为双阶段性,低浓度促进,高浓度抑制;与同浓度的PMG单一处理相比,Cd2+的存在,加大了PMG单独存在时的损害作用,使得玉米幼苗对PMG胁迫的敏感浓度点从5 mg·kg~(-1)降低到2.5 mg·kg~(-1)。     

体育场馆内PM_(2.5)暴露对运动大鼠行为学及相关无氧代谢酶活性的影响

通过非暴露式气管滴注法建立损伤模型,按照低、中、高3种剂量细颗粒物(PM_(2.5))进行染毒,以研究不同浓度PM_(2.5)对运动大鼠行为学及部分无氧代谢酶活性的影响。实验选取32只雄性Wistar SPF(specific pathogen free,SPF)大鼠随机分为运动对照组(EC)、高剂量运动组(30 mg·kg~(-1))(HPE)、中剂量运动组(15 mg·kg~(-1))(MPE)、低剂量运动组(7.5 mg·kg~(-1))(LPE),利用卒中指数和神经病学症状评分对大鼠的行为学进行评价,通过酶联免疫法(ELISA)测定大鼠血清、肺泡灌洗液(BALF)以及股四头肌组织中己糖激酶(HK)、丙酮酸激酶(PK)、磷酸果糖激酶(PFK-1)的活性。结果表明,与EC相比,3个剂量暴露组中,卒中指数和神经病学症状评分差异均有统计学意义;LPE、MPE、HPE组各组织中HK、PK、PFK-1活性均下降,差异有统计学意义(P0.05或P0.01)。综上所述,急性PM_(2.5)暴露可对大鼠行为学产生不利的影响,使大鼠部分组织的无氧代谢酶酶活性降低,影响机体的运动能力。     

Monitoring of soil biochemical quality parameters under greenhouse spinach cultivation through animal waste recycling

Under the intensive agricultural system, direct application of animal slurries to soils can provide a sustainable disposal of these wastes by inducing positive changes in soil quality and fertility. However, how animal wastes quantitatively affect the key nutrients (C, N, P and S) transforming soil enzymes is not clearly known. A greenhouse spinach cultivation study demonstrated that pig slurry, either in raw (RS) or processed (aerobically aged) (PS) form, significantly (p?β-glucosidase (23–39%), urease (59–103%), nitrate reductase (73–103%) and dehydrogenase (27–72%)) and microbial growth in soil as compared to the unamended control. However, it did not significantly (p?>?.05) alter the aryl sulphatase enzyme activity. Slurry applications also significantly improved the macro (N, P and K) and micronutrients (Cu, Mn, Zn and Fe) uptake by spinach plant and hence the yield (2.9–3.38 times higher than control). Similarly, compared to chemical fertilisers the application of pig slurries improved soil biological and biochemical parameters as well as plant nutrients uptake. This study demonstrated the closing of global energy and nutrient cycles through land application of animal wastes without compromising the crop yield.     

Influence of glucose feeding on the ligninolytic enzyme production of the white-rot fungus Phanerochaete chrysosporium

The present work studied the influence of glucose feeding on the ligninolytic enzyme production of Phanerochaete chrysosporium in a nitrogen-limited (C/N ratio is 56/8.8 mmol/L) medium. Several sets of shaking flask experiments were conducted. The results showed that 2 g/L glucose feeding on the first day of the culture (24 h after the inoculation) simulated both fungal biomass growth and enzyme production. The manganese peroxidase (MnP) activity was 2.5 times greater than that produced in cultures without glucose feeding. Furthermore, the glucose feeding mode in fed-batch culture was also investigated. Compared to cultures with glucose feeding every 48 h, cultures with glucose feeding of 1.5 g/L (final concentration) every 24 h produced more enzymes. The peak and total yield of MnP activity were 2.7 and 3 times greater compared to the contrast culture, respectively, and the enzyme was kept stable for 4 days with an activity of over 200 U/L. Translated from Acta Scientise Circumstantiae, 2007, 27(3): 363–368 [译自: 环境科学学报]