浅谈汽车氧传感器的检修

氧传感器是现代轿车上应甩广泛的传感器之一,对发动机的正常工作和尾气排放控制起着至关重要的作用.文章叙述氧传感器的工作原理,由氧传感器引发的故障实例,介绍检测与维修方法.     

工厂化水产养殖智能监控系统设计

提出了一种工厂化水产养殖中具有可溯源功能的智能监控系统.系统利用PROFIBUS-DP总线和工业以太网技术实现了数据的传输与共享,利用模糊控制与神经网络相结合的算法实现了对数据的处理分析,并得到控制信号,进行闭环控制,利用无线射频识别技术( RFID)实现了水产品质量的可溯源功能.结果表明,养殖环境各关键环境因子均满足控制精度,水产品的可溯源信息写入与读出均完整有效,完全达到了设计要求,能够满足工厂化水产养殖智能化的需要.     

Protective effect of BNDF on vascular endothelial cells with H2O2-induced oxidative injury

AIM: To study the protective effect of brain-derived neurotrophic factor (BDNF) on vascular endothelial cells with H₂O₂-induced oxidative injury. METHODS: Human umbilical vein endothelial cells (HUVECs) were cultured in vitro, and the oxidation injury model of HUVECs was established by treatment with H₂O₂. The oxidatively injured HUVECs were cultured with different concentrations (1, 10 and 100 μg/L) of BDNF. At the same time, the control group (no injury), PBS treatment after H₂O₂ injury group and TrkB inhibitor group (with 100 μg/L BDNF and 1: 1 000 TrkB inhibitor) were also set up. The viability of the HUVECs was detected by MTT assay. The levels of LDH, MDA, SOD and GSH were measured. The releases of NO, ET-1 and ICAM-1 were analyzed by ELISA. The changes of ROS production and cell apoptosis were evaluated by flow cytometry. The protein levels of TrkB, p-TrkB, cleaved caspase-3, Bcl-2 and Bax were determined by Western blot. RESULTS: Compared with uninjured control group, in H₂O₂ oxidative injury plus PBS treatment group, the viability of the cells was decreased significantly, the LDH and MDA levels were increased significantly and the activities of SOD and GSH were decreased significantly. The NO secretion was decreased, and the ET-1 and ICAM-1 concentrations were increased significantly. The ROS content and apoptotic rate were increased significantly. The protein levels of cleaved caspase-3 and Bax were increased but Bcl-2 protein expression was decreased significantly. Compared with PBS treatment group, in H₂O₂-injured HUVECs treated with different concentrations of BDNF, the cell viability was gradually increased, the LDH and MDA levels were decreased and the activities of SOD and GSH were increased gradually. The secretion of NO was increased but ET-1 and ICAM-1 were decreased gradually. The ROS content and apoptotic rate were decreased significantly. The TrkB and p-TrkB levels were significantly increased significantly, the protein expression of cleaved-caspase 3 and Bax was decreased gradually and the Bcl-2 protein expression increased gradually. The role of BDNF was inhibited by TrkB inhibitor. CONCLUSION: BDNF protects HUVECs from oxidative injury by binding with TrkB to activate the BDNF-TrkB signaling pathways.     

Sodium dichloroacetate improves radiosensitivity of U251 cells

AIM: To study the change of radiosensitivity of U251 cells after treated with sodium dichloroacetate (DCA) and further to explore the possible mechanism.METHODS: The U251 cells were divided into 4 groups: control group, DCA group, X-ray irradiation without DCA pretreatment (IR) group and X-ray irradiation with DCA pretreatment (DIR) group. MTT assay was applied to determine the cell viability. The intracellular reactive oxygen species (ROS) were detected by DHE fluorescence. The expression level of Bcl-2 was assessed by Western blot. The percentage of apoptosis of cells was determined by flow cytometry. RESULTS: No difference between control group and DCA group in cell viability (P>0.05) was observed. However, the cell viability of both IR group and DIR group was markedly reduced compared with control group (P<0.05). Furthermore, the viability of DIR group was significantly decreased compared with IR group (P<0.05). The percentage of ROS positive cells was obviously increased in DIR group compared with IR group (P<0.05). The expression level of Bcl-2 was sharply decreased in DIR group (P<0.05) and the percentage of apoptosis of cells was significantly elevated (P<0.05) in DIR group compared with IR group.CONCLUSION: The better antitumor effect was obtained by improving the radiosensitivity through pretreating the cells with DCA, and the possible mechanism was down-regulation of the Bcl-2 expression by developing the intracellular ROS.     

Allelochemical ethyl 2-methyl acetoacetate (EMA) induces oxidative damage and antioxidant responses in Phaeodactylum tricornutum

Ethyl 2-methyl acetoacetate (EMA) is a novel allelochemical exhibiting inhibitory effects on the growth of marine unicellular alga Phaeodactylum tricornutum (P. tricornutum). Oxidative damage and antioxidant responses in P. tricornutum were investigated to elucidate the mechanism involved in EMA inhibition on algal growth. The increase in reactive oxygen species (ROS) levels and malondialdehyde (MDA) contents following exposure to EMA suggested that alga was suffered from oxidative stress and severely damaged. The decrease in cell activity and cellular inclusions suggested that cell growth was greatly inhibited. The activities of the antioxidant enzymes including superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR), glutathione peroxide (GSH-PX) and glutathione S-transferase (GST) increased with the exposure concentration and decreased with the prolongation of exposure time. Cellular ascorbic acid (AsA) and reduced glutathione (GSH) systems were also involved in resisting oxidative stress of EMA by altering the composition of AsA and GSH pools. EMA exposure increased the contents of AsA, GSH, dehydroascorbate (DAsA) and glutathione (GSSG). However, the regeneration rate of AsA/DAsA did not change obviously between treatments and the control, while that of GSH/GSSG decreased significantly under 14 mmol/L EMA exposure on the 3rd day. These results showed that EMA-induced oxidative damage might be responsible for EMA inhibition on P. tricornutum growth and cellular antioxidant enzymes and non-enzymatic antioxidants were improved to counteract the oxidative stress.     

Hepatoprotective activity of angiotensin-converting enzyme (ACE) inhibitors, captopril and enalapril, against paraquat toxicity

Paraquat is a highly toxic herbicide that is used in most countries without restriction. The cytotoxic action of paraquat is mediated by reactive radicals that are products of its metabolic reduction in cells. It has already been hypothesized that some angiotensin-converting enzyme inhibitors (e.g., captopril and enalapril) could show antioxidant and radical scavenging activity through their structural thiol groups, increasing antioxidant enzymes production or nitric oxide synthesis. In this study the hepatoprotective effect of captopril and enalapril against paraquat induced oxidative stress cytotoxicity was evaluated in isolated rat hepatocyte. Subtoxic concentrations of captopril (0.2 mM) and enalapril (0.2 mM) significantly (p < 0.05) protected the hepatocytes against paraquat (2 mM) induced oxidative stress cytotoxicity markers including: cell lysis, reactive oxygen species (ROS) generation, lipid peroxidation, glutathione depletion, mitochondrial membrane potential decrease, lysosomal membrane oxidative damage and cellular proteolysis. Moreover, we showed that non-thiol enalapril acts as well as thiol containing captopril at inhibiting oxidative stress cytotoxicity markers. Finally, our results support the hypothesis that it is the increase in nitric oxide synthesis and not the presence of the thiol group that accounts for the antioxidant activity of ACE inhibitors.     

溶氧因素对冬虫夏草摇瓶培养的影响

对冬虫夏草菌丝体摇瓶培养中影响溶氧的主要因素进行分析。通过测定不同摇床转速、装液量、封口方式下摇瓶培养后的菌丝得率,并对其进行单因素分析,选择单因素较优水平,然后进行3因素正交试验。结果表明,最适宜溶氧条件为摇床转速140r/min、装液量50%、封口采用无菌培养容器封口膜;各因素影响培养的显著性依次为摇床转速、装液量、封口方式;不同摇床转速下对有效成分含量测定显示,摇床转速对虫草多糖及虫草酸含量影响不显著。     

果蔬采后高O2处理研究进展

综述了高O2处理对果蔬采后呼吸强度、乙烯释放量、色泽、品质、褐变及病原微生物的影响,分析了高O2处理在果蔬保鲜中的可行性与应用前景.     

低浓度Na2CO3胁迫下星星草幼苗保护酶活性与活性氧之间的关系

对低浓度(0.2%)Na2CO3胁迫和无胁迫正常生长的星星草幼苗的相对电导率、可溶性蛋白质含量、SOD活性、POD活性、CAT活性、MDA含量、H2O2含量和产生O2-·速率的研究结果表明,星星草幼苗各保护酶、活性氧及相对电导率之间存在一定的变化关系,这种变化关系在0.2% Na2CO3胁迫和无胁迫正常生长的星星草幼苗间存在差异.在一定程度上揭示了抗盐碱植物在正常生长情况下与碱胁迫下的活性氧(H2O2和O2-·)代谢可能存在不同的调节机制.     

热处理降低哈密瓜果实活性氧代谢减轻冷害

为探讨热处理能否激发哈密瓜果实抗冷性,减轻冷害。该文以"西州密25号"哈密瓜为原料,在已有研究的基础上,将哈密瓜在55℃热水中浸泡3 min,以室温(22±2)℃清水浸泡3 min为对照,待其表面水分完全晾干以后,放置于3~5℃机械冷库中贮藏,测定贮藏期间哈密瓜品质及生理指标。结果表明,与对照相比,热处理诱导哈密瓜果肉过氧化氢H_2O_2和超氧阴离子O_2~-含量短暂增加,但明显减少贮藏中后期(14~35 d)H_2O_2,O_2~-的积累(P0.05),提高活性氧清除酶过氧化物酶和超氧化物歧化酶的活性(P0.05),抑制细胞膜相对渗透率和丙二醛含量上升,降低贮藏后期的冷害发生率(P0.05),缓解果实可溶性固形物和抗坏血酸含量下降(P0.05),保持果实较好的品质。热处理主要通过诱导活性氧信号分子,提高活性氧清除酶活性、减少膜脂过氧化作用,从而减轻果实的冷害。研究结果为哈密瓜采后贮藏技术提供理论参考。