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1.
目的研究细胞因子IL-1α影响单核细胞(MNC)与体外培养的牛脑微血管内皮细胞(BCMEC)粘附、迁移的动力学过程及药物的保护作用。方法利用培养在胶原层上的内皮细胞单层,对粘附于内皮细胞单层上的MNC及胶原层中的MNC计数,计算MNC粘附率及迁移率。结果IL-1α(500kU·L-1)可促进MNC与BCMEC的粘附与迁移,其促粘附与迁移作用具明显的时效关系。IL-1α促进粘附达最大效应时间为2h,粘附率达37.3%,较对照提高62.6%。IL-1α促迁移作用2h达到坪值,迁移率为17.4%,较对照提高141.7%。药物欧芹素乙(imperatorin,IMP)、已酮可可碱(pentoxifyline,PTX)对IL-1α引起的MNC与BCMEC的粘附与迁移有抑制作用,且呈剂量依赖性。在浓度为1、10及100μmol·L-1时,其粘附抑制率分别为37.7%、42.0%、66.0%和38.3%、64.2%、87.0%;迁移抑制率分别为32.8%、66.4%、70.7%和38.8%、55.2%、74.1%。结论IMP与PTX呈剂量依赖性抑制MNC与IL-1α诱导的BCMEC的粘附及迁移。  相似文献   

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目的研究细胞因子IL-1α影响单核细胞(MNC)与体外培养的牛脑微血管内皮细胞(BCMEC)粘附、迁移的动力学过程及药物的保护作用。方法利用培养在胶原层上的内皮细胞单层,对粘附于内皮细胞单层上的MNC及胶原层中的MNC计数,计算MNC粘附率及迁移率。结果IL-1α(500kU·L-1)可促进MNC与BCMEC的粘附与迁移,其促粘附与迁移作用具明显的时效关系。IL-1α促进粘附达最大效应时间为2h,粘附率达37.3%,较对照提高62.6%。IL-1α促迁移作用2h达到坪值,迁移率为17.4%,较对照提高141.7%。药物欧芹素乙(imperatorin,IMP)、已酮可可碱(pentoxifyline,PTX)对IL-1α引起的MNC与BCMEC的粘附与迁移有抑制作用,且呈剂量依赖性。在浓度为1、10及100μmol·L-1时,其粘附抑制率分别为37.7%、42.0%、66.0%和38.3%、64.2%、87.0%;迁移抑制率分别为32.8%、66.4%、70.7%和38.8%、55.2%、74.1%。结论IMP与PTX呈剂量依赖性抑制MNC与IL-1α诱导的BCMEC的粘附及迁移。  相似文献   

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目的:研究缺氧/再给氧(H/R)对中性粒细胞(Neu)和单核细胞(Mon)与诱导的培养牛脑微血管细胞粘附作用的影响.方法:牛脑微血管内皮细胞(CMEC)和平滑肌细胞(CMSMC)经H/R处理或经TNFα和IL1α刺激,Mon和Neu与CMEC和CMSMC粘附的细胞数目用流式细胞仪测定.结果:CMEC先缺氧2h再经复氧与TNFα(2μg·L-1)作用2h,Mon和Neu与CMEC的粘附率分别提高到350%±09%和360%±06%(TNFα处理组分别是289%±11%和288%±13%).CMSMC也按上述处理,Mon和Neu的粘附率分别显著提高为499%±04%和439%±14%(TNFα处理组分别为340%±19%和340%±13%).CMEC和CMSMC经IL1α刺激,可得到类似结果.结论:H/R提高Mon和Neu与TNFα和IL1α诱导的CMEC和CMSMC的粘附作用.  相似文献   

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研究细胞因子IL-1α影响单核细胞与体外培养的牛脑微血管内皮细胞粘 ,迁移的动力学过程及药物的保护作用。方法 利用培养在胶原层上的内皮细胞单层,对粘附于内皮细胞单层上的MNC及胶原层中的MNC计数,计算MNC粘附率及迁移率。结果 IL-1α可促进MNC与BCMEC的粘附与迁移,其促粘附与迁移作用具明显的时效关系。  相似文献   

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研究TNF介导的BCMEC释放PDGF及药物对BCMSMC增殖的保护作用.方法:体外培养BCMEC和BCMSMC,用结晶紫染色法观察TNF引起的BCMEC释放PDGF继而促进BCMSMC增殖作用.结果:TNF不能促进无血清培养的BCMSMC增殖,但TNF(5-20μg·L-1)剂量依赖地促进BCMEC释放PDGF.TNF(20μg·L-1)促进BCMSMC增殖的百分率为34±4%.药物Imperatorin,isoimperatorin和PMDP不影响TNF引起BCMEC释放PDGF,但能剂量依赖地(1-100μmol·L-1)抑制PDGF促BCMSMC增殖的作用.结论:TNF促进BCMEC释放PDGF继而引起BCMSMC的增殖.药物能抑制PDGF引起的BCMSMC增殖.  相似文献   

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目的:研究缺氧/再给氧(H/R)对中性粒细胞(Neu)和单核细胞(Mon)与诱导的培养牛脑微血管细胞粘附作用的影响。方法:牛脑微血管内皮细胞(CMFC)和平滑肌细胞(CMSMC)经H/R处理或经TNF-α和IL-1α刺激,Mon和Neu与CMEC和CMSMC粘附的细胞数目用流式细胞仪测定,结果:CMEC先缺氧2h再经复氧与TNF-α(2μg.L^-1)作用2h,Mon和Neu与CMEC的粘附率分别  相似文献   

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目的··:观察烟碱对牛脑微血管内皮细胞(BCMEC)表达E-选择素的影响。方法··:离体培养新生牛脑微血管内皮细胞;血细胞计数仪测定BCMEC粘附大鼠血单核细胞(MN)的数目;应用ELISA法检测BCMEC表达E-选择素的量。结果··:高浓度烟碱(10-5mol·L-1)单独作用于BCMEC2h后,使BCMEC对MN的粘附率从12.9%±s0.4%增至15.7%±s0.6%,且BCMEC也可表达少量的E-选择素;而当烟碱与BCMEC作用2h后,再经白细胞介素1β(IL-1β)诱导4h,烟碱可浓度依赖性(10-7mol·L-1-10-5mol·L-1)地增强IL-1β的诱导作用,增加BCMEC对MN的粘附率以及E-选择素的表达量;抗E-选择素单克隆(AEmAb)能显著阻断IL-1β诱导BCMEC后对MN的粘附率。结论··:烟碱增强IL-1β诱导的脑微血管内皮细胞表达E-选择素的作用。  相似文献   

8.
探讨丹参酮ⅡA磺酸钠(Tan)对培养人脐静脉内皮细胞(HUVEC)和人血小板表达粘附分子的影响.方法:用流动血细胞计数仪测定肿瘤坏死因子(TNFα)诱导人脐静脉内皮细胞ICAM1和凝血酶诱导人血小板P选择素的表达.结果:HUVEC经TNFα处理后,明显增加细胞表面ICAM1的表达,增加HL60细胞粘附到内皮细胞表面达加入细胞总数的30%±6%(对照组为46%±07%).在TNFα处理前,用Tan(25-200μmol·L-1)与HUVEC共孵育,则Tan剂量依赖性地抑制TNFα的作用.Tan(25-200μmol·L-1)与人血小板孵育后,可剂量依赖性地抑制凝血酶诱导人血小板表面Pselectin的表达.结论:Tan可抑制内皮细胞和血小板表达粘附分子.  相似文献   

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目的:研究佛波醇酯(PMA)地大鼠脑微血管内皮细胞(RBMEC)表达细胞间粘附分子-1(ICAM-1)及PKC抑制剂H7与已酮可可碱(PTX)的抑制作用。方法:采用ELISA方法测定培养RBMEC表达ICAM-1。结果:PMA在10-100.L^-1范围内剂量依赖性地诱导RBMEC表达ICAM-1;在4-16h范围内时间依赖性诱导RBMEC表达ICAM-1。H7和PTX分别在5-50μmol.L^  相似文献   

10.
目的:研究氧化型低密度脂蛋白(oxLDL)对单核细胞与血管内皮细胞粘附作用.方法:用超速离心方法分离健康人血浆低密度脂蛋白,以10μmol·L-1CuSO4氧化.观察oxLDL对人外周血单核细胞(MC)与小牛主动脉血管内皮细胞(BAEC)粘附作用的影响.结果:oxLDL能以时间和剂量依赖性方式促进MC与BAEC粘附作用.放线菌酮D和staurosporine(Sta)能取消这种促进作用,但硫酸葡聚糖对此作用无影响.PMA和6μmol·L-1溶血性磷酯酰胆硷也显著增强MC与BAEC的粘附作用,且此增敏作用也可被Sta取消.结论:oxLDL能通过激活蛋白激酶C促进MC与BAEC的粘附作用.  相似文献   

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Clinical and in vitro investigations were carried out to test the efficacy of gut lavage, hemodialysis, and hemoperfusion in the treatment of poisoning with paraquat or diquat. In a patient suffering from diquat intoxication 130 times more diquat was removed by gut lavage 30 h after ingestion than was removed by complete aspiration of the gastric contents.Determination of in vitro clearances for paraquat and diquat by hemodialysis showed that, at serum concentrations of 1–2 ppm, such as are frequently encountered in poisoning in man, toxicologically relevant quantities of herbicide cannot be removed from the body. At a concentration of 20 ppm, on the other hand, hemodialysis proved to be effective, the clearance being 70 ml/min at a blood flow rate of 100 ml/min. The efficacy of hemoperfusion with coated activated charcoal was on the whole better. Especially at concentrations around 1–2 ppm, the clearance values for hemoperfusion were some 5–7 times higher than those for hemodialysis.In a patient suffering from paraquat poisoning, both hemodialysis as well as hemoperfusion were carried out. The in vitro results could be confirmed: At serum concentrations of paraquat less than 1 ppm no clearance could be obtained by hemodialysis while by hemoperfusion with activated charcoal quite high clearance values were measured and the serum level dropped down to zero.
Zusammenfassung Klinische Untersuchungen und Laboratoriumsversuche wurden durchgeführt, um die Wirksamkeit von Darmspülung, Hämodialyse und Hämoperfusion bei Paraquat- und Deiquat-Vergiftungen zu prüfen.Bei einem Patienten wurde 30 Std nach Deiquat-Aufnahme durch Darmspülung 130mal mehr Deiquat entfernt als durch vollständige Aspiration des Mageninhaltes. In vitro-Versuche ergaben, daß bei Blutserumkonzentrationen von 1–2 ppm, die bei Vergiftungen oft gemessen werden, durch Hämodialyse keine toxikologisch relevanten Paraquat- oder Deiquat-Mengen entfernt werden können. Dagegen erwies sich die Hämodialyse bei 20 ppm und einer Blutumlaufgeschwindigkeit von 100 ml/min mit einer Clearance von 70 ml/min als wirksam. Die Hämoperfusion mit beschicheter Aktivkohle war in diesen Versuchen aber eindeutig überlegen, denn insbesondere bei Konzentrationen um 1–2 ppm waren die Clearance-Werte 5–7mal höher als bei der Hämodialyse.Die in vitro-Ergebnisse wurden bei einem Patienten mit einer Paraquat-Vergiftung bestätigt: Bei Konzentrationen unter 1 ppm war die Hämodialyse wirkungslos, während durch Hämoperfusion relativ hohe Clearance-Werte erreicht wurden, so daß der Serumspiegel rasch unter die Nachweisgrenze abfiel.
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This study describes a new approach for organophosphorous (OP) antidotal treatment by encapsulating an OP hydrolyzing enzyme, OPA anhydrolase (OPAA), within sterically stabilized liposomes. The recombinant OPAA enzyme was derived from Alteromonas strain JD6. It has broad substrate specificity to a wide range of OP compounds: DFP and the nerve agents, soman and sarin. Liposomes encapsulating OPAA (SL)* were made by mechanical dispersion method. Hydrolysis of DFP by (SL)* was measured by following an increase of fluoride ion concentration using a fluoride ion selective electrode. OPAA entrapped in the carrier liposomes rapidly hydrolyze DFP, with the rate of DFP hydrolysis directly proportional to the amount of (SL)* added to the solution. Liposomal carriers containing no enzyme did not hydrolyze DFP. The reaction was linear and the rate of hydrolysis was first order in the substrate. This enzyme carrier system serves as a biodegradable protective environment for the recombinant OP-metabolizing enzyme, OPAA, resulting in prolongation of enzymatic concentration in the body. These studies suggest that the protection of OP intoxication can be strikingly enhanced by adding OPAA encapsulated within (SL)* to pralidoxime and atropine.  相似文献   

16.
In order to find out the values of the steroid resources for the future use. the compositions and contents of steroidal sapogenins from 13 domestic plants have been investigated. As a result,Dioscorea nipponica, D. quinqueloba andSmilax china were found to have large amount of diosgenin. And pennogenin inTrillium kamtschaticum andParis verticillata, yuccagenin inAllium fistulosum, hecogenin inAgave americana and neochlorogenin inSolanum nigum were appeared to be major steroidal sapogenins.  相似文献   

17.
We report herein the condensation of 4,7-dichloroquinoline (1) with tryptamine (2) and D-tryptophan methyl ester (3) . Hydrolysis of the methyl ester adduct (5) yielded the free acid (6) . The compounds were evaluated in vitro for activity against four different species of Leishmania promastigote forms and for cytotoxic activity against Kb and Vero cells. Compound (5) showed good activity against the Leishmania species tested, while all three compounds displayed moderate activity in both Kb and Vero cells.  相似文献   

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Abstract

The uptake of metals from food and water sources by insects is thought to be additive. For a given metal, the proportions taken up from water and food will depend both on the bioavailable concentration of the metal associated with each source and the mechanism and rate by which the metal enters the insect. Attempts to correlate insect trace metal concentrations with the trophic level of insects should be made with a knowledge of the feeding relationships of the individual taxa concerned. Pathways for the uptake of essential metals, such as copper and zinc, exist at the cellular level, and other nonessential metals, such as cadmium, also appear to enter via these routes. Within cells, trace metals can be bound to proteins or stored in granules. The internal distribution of metals among body tissues is very heterogeneous, and distribution patterns tend to be both metal and taxon specific. Trace metals associated with insects can be both bound on the surface of their chitinous exoskeleton and incorporated into body tissues. The quantities of trace meals accumulated by an individual reflect the net balance between the rate of metal influx from both dissolved and particulate sources and the rate of metal efflux from the organism. The toxicity of metals has been demonstrated at all levels of biological organization: cell, tissue, individual, population, and community. Much of the literature pertaining to the toxic effects of metals on aquatic insects is based on laboratory observations and, as such, it is difficult to extrapolate the data to insects in nature. The few experimental studies in nature suggest that trace metal contaminants can affect both the distribution and the abundance of aquatic insects. Insects have a largely unexploited potential as biomonitors of metal contamination in nature. A better understanding of the physico-chemical and biological mechanisms mediating trace metal bioavailability and exchange will facilitate the development of general predictive models relating trace metal concentrations in insects to those in their environment. Such models will facilitate the use of insects as contaminant biomonitors.  相似文献   

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