纳米氧化铜(CuO NPs)对紫花苜蓿幼苗根系活性氧(ROS)、抗氧化酶活性和根系活力的影响

根系通常是植物直接受到外界环境物质(如重金属离子和纳米金属氧化物)毒害的主要器官。本研究以紫花苜蓿的幼苗为实验材料,探讨了CuO NPs胁迫对紫花苜蓿幼苗根系的活性氧(ROS)积累、抗氧化酶活性和根系活力的影响。研究结果表明:(1)不同浓度的CuO NPs对紫花苜蓿幼苗根系H_2O_2和O-2·含量具有显著影响。随CuO NPs浓度增大,紫花苜蓿幼苗根系中H_2O_2和O-2·整体上呈现先增大后减少的趋势,除了0.00125 mol·L~(-1)CuO NPs浓度下紫花苜蓿幼苗根系中H_2O_2含量比对照减少外,其他浓度下的H_2O_2和O-2·的含量都比对照有所增加,并且H_2O_2和O-2·的含量都是在0.0125 mol·L~(-1)CuO NPs浓度下达到最大值。(2)不同浓度的CuO NPs对紫花苜蓿幼苗根系抗氧化酶活性具有显著影响。随CuO NPs浓度增大,紫花苜蓿幼苗根系中SOD、POD、APX和CAT酶的活性都呈现先增大后减少的趋势,其中,SOD和POD、APX、CAT酶的活性分别是在0.00625、0.0125、0.0625 mol·L~(-1)CuO NPs处理下达到最大,表明这些抗氧化酶在清除根系中的活性氧方面表现出较强的协同性和补偿性。(3)不同浓度的CuO NPs对紫花苜蓿幼苗根系活力具有显著的影响。随着CuO NPs浓度的增加,紫花苜蓿幼苗根系活力逐步升高,这是一种生物适应性应激响应的体现。     

孕酮诱导非洲爪蟾卵母细胞生发泡破裂(GVBD)实验方法的优化及干扰物质筛查

非洲爪蟾卵母细胞生发泡破裂(GVBD)是生物学上研究卵细胞成熟过程及其机制的良好模型。由于GVBD受激素的调控,曾有研究将孕酮诱导的非洲爪蟾GVBD试验用于内分泌干扰物的筛查。通过预注射人体绒毛膜促性腺激素(HCG)提高非洲爪蟾卵母细胞对孕酮的敏感性、缩小个体差异,缩短试验时间等优化GVBD试验方法;并选用甲氧氯作为阳性参照物对优化的方法进行验证,最后用此方法研究了米非司酮、来曲唑、咪鲜胺3种化学物质对孕酮诱导GVBD的影响。结果发现,甲氧氯对GVBD的发生具有明显抑制作用,随着剂量的增加抑制作用增强,显示优化方法的可靠性。米非司酮作为孕酮受体拮抗剂,没有表现出抑制GVBD的效应,证明孕酮诱导爪蟾GVBD并非完全由孕酮受体(PR)介导。同时,来曲唑和咪鲜胺对孕酮诱导爪蟾GVBD没有影响,显示此两种物质在孕酮诱导GVBD过程中不具有内分泌干扰作用。     

Relationships between octan‐1‐ol/water partition coefficients,aqueous activity coefficients and reversed phase HPLC capacity factors of alkylbenzenes,chlorobenzenes, chloronaphthalenes and chlorobiphenyls

Linear relationships between logarithms of octan‐1‐ol/water partition coefficients (K_d,oct), aqueous activity coefficients (y_aq) and extrapolated RP HPLC capacity factors (k‘_w) are found for four types of aromatic hydrocarbons (alkylbenzenes and poly‐chlorinated benzenes, ‐naphthalenes and ‐biphenyls).

Both log K,_d,oct and logk‘_w increase with the increasing number of chlorine or methyl‐ene substituents. These increases of log K,_d,oct and log k‘_w are proportional and almost independent of the parent compound. In addition, these increases are linear to increases of logy_aq. The slopes of logk‘_w‐logy_aq and log K,_d,oct‐logv_aq relationships deviate significantly from 1.0. This suggests that the activity coefficients of the test compounds in both octan‐1‐ol and in the stationary phase of the RP column increase after substitution of aromatic compounds with methylene or chlorine.     

洱海表层沉积物碱性磷酸酶活性时空变化

研究了2010—2011年洱海表层沉积物中碱性磷酸酶活性的时空变化,并探讨了沉积物及水体理化因子对碱性磷酸酶活性的影响.结果表明:①洱海表层沉积物中碱性磷酸酶活性为45.63～144.67μmol/(g·h),空间分布总体呈北部＞南部＞中部,受外源污染物输入影响较大的区域,其沉积物中w(TN)、w(TP)较高,碱性磷酸酶活性也较高;②洱海表层沉积物中碱性磷酸酶活性呈明显的季节性变化特征,秋季(11月)<冬季(2月)<春季(5月)<夏季(8月),并且西部沿岸区域的季节性变化差异显著;③碱性磷酸酶活性与沉积物中w(OM)、w(TN)、w(OP)、w(TP)、m(C)/m(N)及水体ρ(OP)、ρ(TN)和ρ(COD_Mn)呈显著正相关. 沉积物及水体的理化因子是影响其碱性磷酸酶活性的重要内因,而外源污染物输入则是重要外因.      

Antifungal activity of volatile metabolites emitted by mycelial cultures of saprophytic fungi

The antifungal activity of molecular identified Chilean saprobiontic fungi, Trichoderma viride, Schizophyllum commune and Trametes versicolor, on the fungal plant pathogens Botrytis cinerea and Fusarium oxysporum, and the saprotrophic mould Mucor miehei was investigated using two types of inhibition bioassay: (1) bi-compartmented Petri dishes and (2) two Erlenmeyer flasks connected by their upper parts. The chemical composition of volatile organic compounds (VOCs) released by saprobiontic fungi was also investigated using headspace solid-phase microextraction (SPME) and gas chromatography/mass spectrometry (GC-MS) analysis. Of the saprobiontic fungi evaluated, one isolate of S. commune showed the highest inhibitory activity against B. cinerea and M. miehei, 86.0±5.4 and 99.5±0.5% respectively. The volatile profiles of fungal isolates were shown to contain a different class of compounds. The major components in the headspace of mycelial cultures were 6-pentyl-α -pyrone (T. viride), ethanol and β -bisabolol (S. commune), and a sesquiterpene alcohol (Tr. versicolor). This is the first study reported on the release of VOCs by Chilean native fungi and their antifungal activity wrt. plant pathogenic fungi.     

Studies on the water extracts of medicinal plants grown in copper mining areas and their antioxidant effects

High copper (Cu) accumulation in medicinal plants might favor lipid peroxidation and hence affect antioxidant responses. This effect was studied by determining antioxidant activities in the water extracts of medicinal plants from Cu mining impact site and compared with control samples. Antioxidant activities of the extracted medicinal plants were assayed by measuring (1) total phenolic and flavonoid contents, (2) diphenyl-1-picrylhydrazyl (DPPH)^? free radical scavenging activity, and (3) inhibition capacities of lipid peroxidation. The total phenolic as well as total flavonoid contents of the mining impact samples and control samples are not significantly different. However, inhibition of lipid peroxidation capacities was significantly less (12–60%) for mining impact samples as reflected by the IC₅₀ values. These anomalies were attributed to high concentrations of Cu (2–4-fold higher) in mining impact samples as measured by inductively coupled plasma mass spectrometry. A positive correlation was observed between Cu levels and IC₅₀ values for the inhibition of lipid peroxidation for mining impact samples.     

Nerve conduction studies in sprayers occupationally exposed to mixture of pesticides in a mango plantation at Lucknow,North India

In this study, nerve conduction, organochlorine (OC) pesticide residues in blood and cholinesterase activity levels of pesticide sprayers employed in mango plantations at Lucknow, North India, were determined. Fifty-two sprayers from mango plantations who regularly spray mixture of pesticides like organophosphates (OP), OCs, and carbamates were considered as exposed group. Eighteen subjects with similar socio-economic status of exposed group, who do not handle pesticides, were selected as controls. Questionnaire-based interviews related to personal and occupational histories of the study subjects were carried out. Sprayers did not use any personal protective equipment during pesticide handling. The blood-pesticide analyses of sprayers show higher mean values of hexachlorohexane (HCH), γ-HCH, δ-HCH, total HCH, op-DDT compared with the controls. Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) activites were significantly reduced among sprayers. Risk of motor nerve conduction deficits was observed in sprayers with low AChE activity. Negative correlation of motor and sensory nerve conduction deficits was observed with the duration of exposure and age among sprayers. The study demonstrated that the prolonged exposure to mixture of pesticides, ergonomic factors, decline in cholinesterase activity may lead to nerve conduction dysfunction. The findings suggest the need for controlled use of pesticides in the plantation and indicated the need for training and implementation of hygiene practices like proper usage of personal protective equipments.     

Design,synthesis, antinociceptive,and anti-inflammatory properties of thiazolopyrimidine derivatives

Ten 2-(substituted benzylidene)-7-(4-chlorophenyl)-5-(furan-2-yl)-2H-thiazolo[3,2-a]pyrimidin-3(7H)-one derivatives were synthesized and evaluated. A series of heterocyclic, 2-(substituted benzylidene)-7-(4-chlorophenyl)-5-(furan-2-yl)-2H-thiazolo[3,2-a]pyrimidin-3(7H)-one were synthesized by reaction of 7-(4-chloro phenyl)-5-(furan-2-yl)-2H-thiazolo[3,2-a]pyrimidin-3(7H)-one with appropriately substituted aldehydes in the presence of anhydrous sodium acetate and glacial acetic acid. The antinociceptive activity was evaluated by tail-flick technique, anti-inflammatory activity was evaluated by carrageenan-induced paw edema test and their ulcerogenicity index was determined. The para-substituted methyl, hydroxy, fluoro, chloro, bromo, and nitro derivatives showed significant antinociceptive and anti-inflammatory activities. The detailed synthesis, spectroscopic data, and pharmacological screening of the synthesized compounds were reported.     

Hepatoprotective activity of 1-(4-(Dimethylamino)Benzylidene)-5-(2-Oxoindolin-3-ylidene) Thiocarbohydrazone in rats

The aim of the present study was to evaluate the hepatoprotective activity of 1-(4-(dimethylamino)benzylidene)-5-(2-oxoindolin-3-ylidene) thiocarbohydrazone, a novel isatin derivative against carbon tetrachloride (CCl₄)-induced hepatotoxicity in rats. Hepatic damage was induced by administration of CCl₄ (1 ml/kg, b.w., p.o.) in combination with liquid paraffin (1:1) as a single dose. The hepatotoxic rats were treated with test compound at doses of 50 or 100 mg/kg for three days and liver damage biomarkers, including activities of serum glutamate pyruvate transaminase (SGPT), serum glutamate oxaloacetate transaminase (SGOT), serum alkaline phosphatase (ALP), and levels of total serum bilirubin (TB) measured in blood samples. Results demonstrated that treatment with test compound at doses of 50 or 100 mg/kg to hepatotoxic rats produced a significant dose-dependent reduction of elevated SGOT, SGPT, ALP activities and TB levels indicating a hepatoprotective effect that was confirmed by histopathological examination of liver tissues. The study results confirmed the hepatoprotective activity of 1-(4-(dimethylamino)benzylidene)-5-(2-oxoindolin-3-ylidene) thiocarbohydrazone in rats.     

Synthesis and in vitro biological evaluation of 3, 4-annelated coumarin-pyrimido-pyrimidine systems

3,4-Annelated coumarin-pyrimido-pyrimidine systems (7-imino-8-mercapto-7H-5-oxa-7a,9,12-triaza-benzo[a]anthracen-6-one 2 and 8-hydroxy-7-imino-10-methyl-7H-5-oxa-7a,9,12-triaza-benzo[a]anthracen-6-one 3) were synthesized by the action of 4-amino-2-mercapto-pyrimidine, 2-amino-4-hydroxy-6-methylpyrimidine, respectively, on 4-chlorocoumarin-3-carbonitrile 1. The synthesized compounds were examined for in vitro antibacterial activity against 4 bacterial cultures: Staphylococcus aureus, Streptococcus pneumonia, Escherichia coli, and Aeromonas Salmonicida. The antibacterial activity of synthesized compounds 2 and 3 was compared to antibacterial activity of novobiocin as a standard drug.