Sub-chronic exposure to carbendazim induces biochemical and hematological alterations in male goats

The present investigation reports the effect of repeated (90 days) administration of carbendazim on the biochemical and hematological parameters in male goats. Carbendazim administered orally at a daily dose of 50 mg kg^?1 body weight for 90 consecutive days resulted in increased plasma concentration of aspartate aminotransferase (AST), alanine aminotransferase (ALT), lactate dehydrogenase (LDH), gamma-glutamyl transferase (GGT), creatinine and albumin, while alkaline phosphatase (ALP) and glucose levels were decreased. Decrease in total leukocyte (TLC) and neutrophil count and increase in lymphocyte count was observed in the treatment group. The findings of the present investigation indicate that sub-chronic exposure to carbendazim in male goats causes hepatic and slight kidney dysfunctions.     

Impacts of sublethal lead exposure on the hemato-immunological parameters in tilapia (Oreochromis mossambicus)

The effects of exposure of tilapia (Oreochromis mossambicus) to sublethal concentrations of lead on hematological and immunological parameters were investigated. The fish were semistatically exposed to low (L) (0.5 mg L^?1), medium (M) (2.5 mg L^?1), and high (H) (5 mg L^?1) lead concentrations for 14 days. At the end of the trial, red blood cell (RBC) count, hematocrit (Hct) ratio and hemoglobin levels showed significant decreases in M and H groups, while RBC was significantly increased in L group compared to control group. Lysozyme activity showed a decrease in all groups on day 14 compared to control. A decrease in myeloperoxidase activity was seen in M and H groups on day 7, and in all treatment groups on day 14. In conclusion, it was found that exposure of O. mossambicus to lead concentrations affected hematological and immunogical parameters adversely.     

Phytotoxicity assessment of phenanthrene and pyrene in soil using two barley genotypes

This study investigated the toxicity extent of phenanthrene and pyrene to two cultivars (CM-72 and Gairdner) of barley (Hordeum vulgare). Germination of barley seeds was evaluated in 69-d aged soil, separately spiked with phenanthrene at extractable concentrations of 0.95, 6.3, 59, and 300 mg kg^?1 (dry soil) and pyrene at 1.0, 9.0, 73, and 400 mg kg^?1 (dry soil). Although germination was not inhibited, significant (P < 0.05) reduction in root and shoot length occurred at concentrations of phenanthrene ≥6.3 mg kg^?1 and pyrene ≥9.0 mg kg^?1 after both 72 and 240 h. Fresh and dry biomass of both cultivars reduced with increasing concentrations of both polycyclic aromatic hydrocarbons (PAHs). Barley cultivar CM-72 was more sensitive than Gairdner, and it can be considered suitable for toxicity assessment of PAH-contaminated soils.     

Acute toxicity I: effect of profenofos and triazophos (organophosphates) and carbofuran and carbaryl (carbamates) to Labeo rohita

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.     

Organophosphorous compounds and oxidative stress: a review

Organophosphorous compounds (OP) have largely been used as pesticides globally. These chemicals induce oxidative stress as a possible mechanism of action, which has been a focus of toxicological research for the last decade. This review evaluated the presence of oxidative stress, balance between total antioxidant capacity, and oxygen free radicals associated with OP compound exposure. Oxidative stress induced by OP leads to disturbances in function of different organs and tissues. Evidence indicates that stimulation of free radical production, induction of lipid peroxidation, and disturbance of the total antioxidant capacity are mechanisms of toxicity induced by most OP. Thus, use of antioxidants may be beneficial in treatment of OP poisoning, which remains to be elucidated with further clinical trials.     

Toxic effect of microcystin-LR on blood vessel development

Abstract

The effect of microcystin-LR (MC-LR) at 50–1000?nmol/L on blood vessel development of zebrafish embryos has been explored. Upon exposure 72-h-post-fertilization (hpf), the hatching rate was significantly reduced and malformation and fatality rates were increased in a dose-dependent manner. MC-LR induced cell cycle arrest in the G0/G1-phase and damaged DNA structure in a dose-dependent manner. In human umbilical vein endothelial cells (HUVECs), MC-LR led to decreased activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) and increased lipid peroxidation. These findings indicated that MC-LR could cause oxidative DNA damage, which mediated cell cycle arrest and inhibited cell proliferation afterwards, and retarded the blood vessel development.     

Effect of dietary factors and environmental chemicals on intestinal drug metabolizing enzymes

The liver is the major site of metabolism of foreign chemicals, but contribution from intestinal biotransformation can influence the overall disposition of chemicals. The intestinal drug‐metabolizing enzymes are located in the endoplasmic reticulum and they possess biochemical properties similar to those of the hepatic system. In general, the rate of in vitro metabolism of drug substrates in intestines is lower than in the liver. There seem to be differences in regulation and induction of hepatic and intestinal drug‐metabolizing enzymes. The in vitro intestinal metabolism of foreign chemicals is affected by several factors including the nutritional status of the animal. Dietary components such as vitamins, lipids and vegetables can modify the activities of intestinal drug‐metabolizing enzymes. Phenobarbital or 3‐methyl‐cholanthrene (3‐MC) pre‐treatment induces the hepatic metabolism of a wide variety of drug substrates in a number of species, while the stimulation of intestinal enzymes is both substrate and species specific. Rabbit intestinal drug‐metabolizing enzymes seem to be resistant to induction by foreign chemicals.     

PFOS潜在替代品全氟丁基磺酸钾对不同营养水平水生生物的毒性

全氟丁基磺酸钾(PFBSK)作为全氟辛基磺酸(PFOS)潜在的替代品,极易溶于水,主要存在于水体中,因而其水生毒性的研究十分重要。采用OECD 201、OECD 202、OECD 203和OECD 211标准试验方法,研究了PFBSK对羊角月牙藻(Pseudokirchneriella subcapitata)、大型溞(Daphnia magna)和中国本土鱼种稀有鮈鲫(Gobiocypris rarus)的急性毒性效应以及对大型溞繁殖的影响。组合多终点急慢性水生生物毒性结果：PFBSK的急性毒性终点均大于100 mg·L^-1,大型溞繁殖试验的无观察效应浓度(NOEC)为571 mg·L^-1,最低可观察效应浓度(LOEC)为981 mg·L^-1。按GHS分类导则,PFBSK未表现出急性毒性和慢性毒性。与之相比,PFOS则对水生生物表现出毒性,黑头软口鲦(Pimephales promelas)为最敏感物种,其96 h-LC₅₀为4.7 mg·L^-1;大型溞繁殖试验的NOEC为12 mg·L^-1。按GHS分类导则,属于中等毒性物质。可见,PFBSK较PFOS水生毒性明显降低。     

三氯生对青海弧菌Q67和人乳腺癌细胞MCF-7的时间毒性

三氯生(triclosan,TCS)是一种广谱性抗菌剂,2005年欧盟水框架指令将TCS列为一种新型污染物。目前对TCS的研究局限于急性毒性实验,关于TCS毒性随时间的变化以及不同溶解状态下TCS的毒性差异的研究却鲜有报道。应用以96孔微板为暴露反应载体的微板毒性分析法,添加氢氧化钠(NaOH)或使用二甲亚砜(DMSO)作为助溶剂溶解TCS,分别测定其对青海弧菌Q67的相对发光抑制毒性(15min急性毒性和时间毒性)和对人乳腺癌细胞MCF-7在不同暴露时间(24、48和72h)内的细胞增殖抑制毒性。Q67的急性毒性实验结果表明,碱性条件下TCS的毒性(EC50=3.97(10-8mol.L-1)大于DMSO作为助溶剂时的毒性(EC50=1.68(10-4mol.L-1)。无论碱性条件还是DMSO助溶,TCS在不同暴露时间内对Q67的时间毒性没有明显差异。在不同暴露时间下MCF-7增殖抑制率实验中,DMSO作为助溶剂时,TCS的最高实验浓度为1.46(10-3mol.L-1,随着暴露时间的延长,抑制率在24、48和72h时分别为27.8%、44.2%和62.4%;碱性环境时TCS的最高实验浓度为1.39(10-6mol.L-1,随着暴露时间的延长,抑制率在24、48和72h时分别为20.2%、55.8%和73.9%。研究表明,在DMSO和NaOH作为助溶剂的条件下,TCS对MCF-7均存在时间毒性差异,并且NaOH碱性溶液中TCS对MCF-7的毒性远大于DMSO作为助溶剂时的毒性。     

Influence of some parameters on adsorption rate and toxicity of cadmium in activated sludge

The influence of pH, competitor ions (NaNO₃) and aerobic and anaerobic stabilization of activated sludge on the cadmium uptake by activated sludge solids was investigated. Above 0.08 mg L^‐1 cadmium in solution, biosorption was found to follow the Freundlich isotherm. Active cellular uptake of soluble cadmium does not appear to be a significant mechanism of the biosorption. In addition, the cadmium uptake is not completely reversible. The adsorption of cadmium by activated sludge seems to involve a physico‐chemical mechanism with especially weak electrostatic interactions with ion‐exchange reaction. The optimum adsorption pH was 7.5. Adsorption is influenced by sodium ion concentrations up to an equivalent conductivity of 10 000 μS cm^‐1. Aerobic and anaerobic stabilization of activated sludge increase systematically the initial adsorption capacities. Respirometric measurements were done to evaluate the inhibitive effects of cadmium on activated sludge. Monod's equation and the equation of non‐competitive inhibition were used to describe the toxicity related to cadmium uptake. These two equations appear to be complementary.