镉对大鼠肾皮质结合反应的影响

通过体内和体外试验分别研究了镉对肾皮质微粒体谷胱甘肽转移酶(GST)及游离肾近曲小管细胞中葡萄糖醛酸(GA)结合反应的影响.结果表明:(1)体外试验中,在10~(-7)—10~(-3)mol/L浓度范围内,镉可抑制肾皮质微粒休GST活力;(2)体内腹腔注射CdCl_2(2.4mg/kg,连续3天)后,大鼠肾皮质GST活力无明显改变;(3)按同样方式腹腔注射CdCl_2后,可降低游离肾近曲小管细胞中GA和7-羟基香豆素(7-HC)的结合反应;(4)体外试验中,低浓度镉(10~(-7)mol/L)可使肾皮质细胞中GA和7-HC的结合反应增强,而在10~(-6)—10~(-2)mol/L浓度范围内,镉可降低GA和7-HC的结合反应.     

Effects of phenanthrene on hepatic enzymatic activities in tilapia (Oreochromis niloticus♂×O. aureus♀)

The effects of phenanthrene (Phe) on hepatosomatic index (HSI) and hepatic enzymatic activities in hybrid tilapia (Oreochromis niloticus ♀× O.aureus ♂) were investigated via the static freshwater exposure at dosage of 50,100 or 400 μg/L for 4-14 d.Compared with the control group,HSI was significantly decreased (P<0.05) at 400 μg/L at day 14.Increased enzymatic activities (P<0.05) were observed for catalase (CAT),glutathione peroxidase μgPx) and superoxide dismutase (SOD) at either 100 or 400 μg/L at day 8 and 14,as well as for CAT at 50 μg/L at day 14,except for GPx at 400 μg/L at day 8.Ethoxyresorufin O-deethylase (EROD) activity was significantly increased (P<0.05) at all dosage at day 4 as well as at 50 μg/L at day 8,but significantly decreased at either 100 or 400 μg/L at day 14 (P<0.05).Glutathione-S-transferase μgST) activity was not affected.The results suggest that CAT,GPx,SOD and EROD,as well as HSI in tilapia may be used as the biomarkers or indexes for evaluating or monitoring the pollution of polycyclic aromatic hydrocarbons (PAHs) such as Phe.     

Effects of phenanthrene on hepatic enzymatic activities in tilapia (Oreochromis niloticus♂×O. aureus♀)

The effects of phenanthrene (Phe) on hepatosomatic index (HSI) and hepatic enzymatic activities in hybrid tilapia (Oreochromis niloticus O. aureus ) were investigated via the static freshwater exposure at dosage of 50, 100, and 400 g/L for 4–14 d. Compared with the control group, HSI was significantly decreased (P < 0.05) at 400 g/L at day 14. Increased enzymatic activities (P < 0.05) were observed for catalase (CAT), glutathione peroxidase (GPx) and superoxide dismutase (SOD) at either 100 or 400 g/L at day 8 and 14, as well as for CAT at 50 g/L at day 14, except for GPx at 400 g/L at day 8. Ethoxyresorufin O-deethylase (EROD) activity was significantly increased (P < 0.05) at all dosage at day 4 as well as at 50 g/L at day 8, but significantly decreased at either 100 or 400 g/L at day 14 (P < 0.05). Glutathione-S-transferase (GST) activity was not a ected. The results suggest that CAT, GPx, SOD and EROD, as well as HSI in tilapia may be used as the biomarkers or indexes for evaluating or monitoring the pollution of polycyclic aromatic hydrocarbons (PAHs) such as Phe.     

Differential response of multiple zebrafish hepatic F-box protein genes to 17α-ethinylestradiol treatment

Estrogens are accumulating in environment and their e ects on a variety of reproductive processes and tumorigenesis were reported by previous study, but the mechanism of estrogen promoting neoplasia was still not clear. F-box protein (FBP) is the component of E3 ubiquitin ligase which takes part in a variety of key biological processes. In this study, using mature male zebrafish, which are more sensitive to estrogen treatment, we examined influence of 17 -ethinylestradiol (EE2) exposure on the expression of a series of hepatic FBP genes, which take part in a variety of biological processes, including tumorigenesis. The influence of EE2 on the expression of hepatic mRNA concentrations of FBP genes were quantified based on the expression of the optimal internal control gene in male zebrafish after 7-day exposure to EE2, from a low-dose concentration (1 ng/L) to environmentally relevant concentrations (10, 100 ng/L). Our results showed that EE2 exposure reduced the expression of fbxl14a, fbxl14b, fbxo25 and -TRCP2b, but enchanced the expression of skp2. While the alterations in fbxl2, fbxw7, fbxo9, -TRCP2a, fbxl18 and fbxo45 mRNA levels were not observed after EE2 exposure. Thus, our results showed that the expression of hepatic FBP genes exhibited di erentially in male zebrafish exposed EE2. The changes of the expression level of FBP genes induced by EE2 may be an important clue to elucidate the correlations of estrogen and hepatic tumors.     

Chronic study of arsenic trioxide-induced hepatotoxicity in relation to arsenic liver accumulation in rats

This study measured activities of serum enzymes alkaline phosphatase, acid phosphatase, glutamic oxaloacetic transaminase (SGOT), and glutamic pyruvic transaminase (SGPT), markers of liver function in albino rats after continuous ingestion of arsenic trioxide (As₂0₃). For the study, treated animals were given AS₂O₃ (0.2 mg/100 g/day) orally for 180 days. After the completion of treatment, the blood was collected for the estimation of serum biochemical markers. The results obtained were compared with control group. Data showed a significant increase in SGOT and SGPT activity after 60 days of As₂0₃ administration. The level of alkaline phosphatase and acid phosphatase increased significantly after 90 and 120 days, respectively. Since the elevation of these serum enzymes is an indicator of hepatic damage, data indicate that As₂O₃ produces hepatotoxicity. When taken continuously, arsenic was also deposited in liver and blood and affected the enzymatic pathways. Total accumulated arsenic was determined by HG-AAS at 193.7 nm.     

Antibacterial and antimutagenic activitiy of extracts and essential oil from (Tunisian) Pistacia lentiscus

Aqueous and flavonoid-enriched extract as well as essential oil (EO) obtained from leaves of Pistacia lentiscus were assessed for antibacterial and antimutagenic activities. Antibacterial activity of different extracts and EO were evaluated against six bacterial strains. A marked inhibitory effect was observed against Salmonella typhimurium, whereas lower activity was observed against Staphylococcus aureus, Pseudomonas aeruginosa, and Salmonella enteritidis. EO showed significant inhibitory effects against Salmonella typhimurium, Salmonella enteritidis and Staphylococcus aureus. The antimutagenic activity of the different extracts against Aflatoxin B₁ (AFB₁) and sodium azide was demonstrated with the Salmonella typhymurium assay. The number of revertants per plate decreased significantly when the plant extracts were added to the assay system using Salmonella typhimurium TA100, TA98 and TA1535.     

Hydrolysis of di-n-butyl phthalate, butylbenzyl phthalate and di(2-ethylhexyl) phthalate in human liver microsomes

Diester phthalates are industrial chemicals used primarily as plasticizers to import flexibility to polyvinylchloride plastics. In this study, we examined the hydrolysis of di-n-butyl phthalate (DBP), butylbenzyl phthalate (BBzP) and di(2-ethylhexyl) phthalate (DEHP) in human liver microsomes. These diester phthalates were hydrolyzed to monoester phthalates (mono-n-butyl phthalate (MBP) from DBP, mono-n-butyl phthalate (MBP) and monobenzyl phthalate (MBzP) from BBzP, and mono(2-ethylhexyl) phthalate (MEHP)) by human liver microsomes. DBP, BBzP and DEHP hydrolysis showed sigmoidal kinetics in V-[S] plots, and the Hill coefficient (n) ranged 1.37-1.96. The S₅₀, V_max and CL_max values for DBP hydrolysis to MBP were 99.7 μM, 17.2 nmol min⁻¹ mg⁻¹ protein and 85.6 μL min⁻¹ mg⁻¹ protein, respectively. In BBzP hydrolysis, the values of S₅₀ (71.7 μM), V_max (13.0 nmol min⁻¹ mg⁻¹ protein) and CL_max (91.3 μL min⁻¹ mg⁻¹ protein) for MBzP formation were comparable to those of DBP hydrolysis. Although the S₅₀ value for MBP formation was comparable to that of MBzP formation, the V_max and CL_max values were markedly lower (<3%) than those for MBzP formation. The S₅₀, V_max and CL_max values for DEHP hydrolysis were 8.40 μM, 0.43 nmol min⁻¹ mg⁻¹ protein and 27.5 μL min⁻¹ mg⁻¹ protein, respectively. The S₅₀ value was about 10% of DBP and BBzP hydrolysis, and the V_max value was also markedly lower (<3%) than those for DBP hydrolysis and MBzP formation for BBzP hydrolysis. The ranking order of CL_max values for monoester phthalate formation in DBP, BBzP and DEHP hydrolysis was BBzP to MBzP ? DBP to MBP > DEHP to MEHP > BBzP to MBP. These findings suggest that the hydrolysis activities of diester phthalates by human liver microsomes depend on the chemical structure, and that the metabolism profile may relate to diester phthalate toxicities, such as hormone disruption and reproductive effects.     

Enzymatic and cellular level effects of nickel∗

The effects of Ni on hepatic enzymes of tilapia, viz. acid‐ and alkaline phosphatases, catalase and glucose‐6‐phosphatase, both under in vivo and in vitro conditions reflected the following tendencies. In vivo conditions indicated maximal increase in activity for acid phosphatase at 3.00 ppm, equivalent to 28.5%, followed by a slight decrease and increase thereafter. As for alkaline phosphatase, gradual increase in activity was observed with maximal activity at 9 ppm of Ni, equivalent to 16.8%. Catalase demonstrated similar tendencies with maximal activity at 9.0 ppm, equivalent to 101.2%. In the case of glucose‐6‐phosphatase, the tendency was the reverse with maximal inhibition at 9.00 ppm, i.e. 41.9%. In contrast to in vivo conditions, in vitro systems indicated that all investigated enzymes were inhibited in the region of 4–10% except for catalase which demonstrated a slight increase by 5–6% in activity between concentrations of 10–15 ppm of Ni but thereafter continuous inhibitory effects prevailed.

At cellular level, exposure of tilapia to a lethal dose of 9 ppm of Ni indicated not much of an adverse effect except for a slight depletion in fat and glycogen content. In the case of mitochondria, they were normal and a few large secondary lysosomes were observed. In relation to the cell membrane no dramatic change was detected.     

三唑醇杀菌剂在雄性丽斑麻蜥体内的对映选择性降解、蓄积和肝毒性研究

三唑醇(triadimenol, TN)是一种广泛使用的手性三唑类杀菌剂,它含有2个手性中心,4个手性对映体,包括对映体A(A1(R,S)和A2(S,R))以及对映体B(B1(R,R)和B2(S,S))。为了研究三唑醇在爬行动物体内的对映选择性行为和潜在的肝毒性,将雄性丽斑麻蜥分别一次经口暴露和28 d长期暴露于三唑醇(100 mg·kg~(-1) body weight),一次经口暴露结果显示,三唑醇进入大脑和肾中的浓度低于肝、性腺、皮肤和尾,B2(S,S)和B1(R,R)对映体具有相似的代谢速率。代谢过程中A1(R,S)的浓度明显高于A2(S,R),并且在暴露后12 h出现二次上升,这可能是A2(S,R)在体内手性转换为A1(R,S)导致。丽斑麻蜥长期(28 d)暴露于三唑醇后,性腺和肾中无明显蓄积现象,皮和尾中浓度显著高于其他组织,各个组织中三唑醇趋向于保持外消旋状态。三唑醇暴露后肝中主要的代谢基因cyp1a1c、yp3a4c、yp2b1和cyp2d3的表达量都出现明显上升,组织病理学分析进一步显示,三唑醇暴露后的肝组织出现组织空泡、血窦阻塞的症状,说明三唑醇对肝组织具有一定的毒性作用。上述结果为手性农药对爬行动物的生态毒理学评价提供了重要依据。