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1.
为了观察糖皮质激素对哮喘患者白细胞介素(IL)-5mRNA表达与嗜酸性粒细胞激活作用的影响,本研究用逆转录(RT)-聚合酶链反应(PCR)法半定量分析了哮喘患者用糖皮质激素治疗前后外周血单个核细胞(PBMC)中IL-5mRNA表达水平的变化,检测了血清嗜酸细胞阳离子蛋白(ECP)浓度、一秒钟用力呼气容积(FEV1)下降20%时的乙酰甲胆碱(MCH)激发浓度(MCH-PC20值)和基础FEV1占用力肺活量比值(FEV1%)等指标。结果发现,糖皮质激素不仅能改善哮喘患者的气道高反应性和通气功能,而且还可抑制PBMC中IL-5mRNA的表达和降低血清ECP浓度(P<0.05);血清ECP浓度下降幅度或MCH-PC20值改善幅度与IL-5mRNA表达水平下降幅度之间均呈显著正相关(r分别为0.5426和0.4857,P值<0.05)。提示糖皮质激素可能是通过抑制IL-5基因的转录,从而抑制后者对嗜酸性粒细胞的活化,而发挥其抗气道炎症反应和降低气道高反应性的作用。  相似文献   

2.
支气管哮喘患者痰白细胞介素16的测定及其意义   总被引:11,自引:1,他引:10  
目的探讨白细胞介素16(IL16)在支气管哮喘发病机制中的作用。方法收集12例过敏性哮喘患者、8例非过敏性哮喘患者、10例过敏性体质患者和10名正常对照者的痰液,以酶联免疫吸附测定法测定痰中IL16的含量,并以免疫染色技术检测CD+4细胞和活化嗜酸细胞(EG2细胞)数。结果哮喘患者无论是过敏性还是非过敏性,痰液中IL16水平与过敏体质但无哮喘的患者和正常组比较,差异有显著性(P<0.01)。急性发作期哮喘患者经治疗后IL16水平能达缓解期水平。此外,痰液中CD+4细胞和IL16水平比较呈显著正相关(r=0.76,P<0.01),痰液中EG2细胞数与IL16水平呈显著正相关(r=0.61,P<0.01)。结论IL16参与了哮喘的发病过程,其机制可能是通过募集CD+4T细胞从而在CD+4T细胞所介导的哮喘气道嗜酸细胞炎症反应中发挥作用。  相似文献   

3.
探讨哮喘和慢性阻塞性疾病患者吸入糖皮质激素治疗后痰液中细菌因子和嗜酸细胞阳离子蛋白浓度及糖皮质激素对其影响。方法采用荧光酶联免疫法检测糖皮质激素治疗前后痰液中白细胞介素(IL)-5、IL-8、ECP浓度及嗜酸细胞和嗜中性粒细胞计数。  相似文献   

4.
为研究口服糖皮质激素泼尼松对哮喘患者体内CD4T淋巴细胞,嗜酸细胞活化的影响,用酶联免疫法对治疗前后哮喘患者血清白细胞介素-5,嗜酸细胞阳离子帽白浓度进行了检测。结果表明,口服泼泥松治疗1周后,血清IL-5,ECP浓度降低,提示糖皮质激素可能通过抑制CD4T淋巴细胞活化,减少细胞因子的释放而对哮喘发挥抗炎作用。  相似文献   

5.
为了观察糖皮质激素对哮喘患者白细胞介素(IL)-5mRNA表达与嗜酸性粒细胞激活作用的影响,本研究用逆转录(RT)-聚合酶链反应(PCR)法半定量分析了哮喘患者用糖皮质激素治疗前后外周血单个核细胞(PBMC)中IL-5mRNA表达水平的变化,检测了血清嗜酸细胞阳离子蛋白(ECP)浓度、一秒钟用力呼气容积(EFV1)下降20%时的乙酰甲胆碱(MCH)激发浓度(MCH-PC20值)和基础FEV1占用力  相似文献   

6.
嗜酸细胞凋亡在激素抵抗型哮喘中的意义   总被引:4,自引:1,他引:4  
目的 观察激素抵抗型(SR)哮喘是否存在嗜酸细胞(EOS)凋亡功能的异常及促炎症细胞因子白细胞介素5(IL-5)和粒-巨细胞集落刺激因子(GM-CSF)的调节作用。方法 分离SR(15例)、激素敏感型(SS,30例)两组哮喘患外周血单个核细胞(PBMCS)及EOS,体外培养后测定:(F1)PBMCS在糖皮质激素处理前、后和细胞因子的能力;(2)自发的或糖皮质激素诱导的或用PBMCS培养上液处理后  相似文献   

7.
哮喘气道炎症粘附机制的实验研究   总被引:9,自引:0,他引:9  
目的评价细胞间粘附分子1(ICAM1)、P选择素在哮喘气道炎症粘附机制中的作用,进一步阐明哮喘的发病机理。方法用酶联免疫吸附试验、肺组织免疫组化检查和呼吸生理学方法系统观察正常组和哮喘组豚鼠各项指标。结果(1)哮喘组豚鼠肺潮气量、动态肺顺应性(Cdyn)和肺气道阻力与对照组比较差异有显著性(P<0.01及P<0.05)。(2)哮喘组豚鼠血浆和肺泡灌洗液(BALF)可溶性ICAM1(sICAM1)、可溶性P选择素、血清和BALF嗜酸粒细胞阳离子蛋白(ECP)与对照组比较,差异有显著性(P<0.01);BALF中白细胞介素8(IL8)与对照组比较差异也有显著性(P<0.01)。(3)哮喘组豚鼠肺组织(气道上皮和血管内皮)ICAM1和IL8表达与对照组比较,差异有显著性(P<0.01)。结论ICAM1、P选择素、IL8、ECP参与介导了哮喘气道炎症的粘附过程  相似文献   

8.
哮喘患者吸入人重组白细胞介素(IL)5,观察其外周血嗜酸细胞(Eos)数及嗜酸细胞阳离子蛋白(ECP)浓度的变化,旨在探讨IL5在哮喘发病机制中的作用。一、对象与方法18例无吸烟史的轻、中度哮喘缓解期志愿者,男5例,女3例,年龄19~58岁,实...  相似文献   

9.
氨茶碱体外诱导人嗜酸细胞凋亡的研究   总被引:4,自引:1,他引:3  
嗜酸细胞(EOS)是支气管哮喘的关键效应细胞,EOS浸润增加是其显著的病理特征。近年来研究表明,氨茶碱不仅具有支气管扩张作用,还有免疫调节和抗炎作用。我们观察了氨茶碱对白细胞介素5(IL5)、粒细胞巨噬细胞集落刺激因子(GMCSF)和IL3介导的体外EOS存活和凋亡的影响,以进一步阐明氨茶碱的作用机制。材料与方法 (1)主要材料:人重组IL3、IL5、GMCSF由美国GeneticsInstitute(GI)MegO′Donell教授惠赠。Percoll分离液购自瑞典Pharmac…  相似文献   

10.
为研究吸入皮质激素倍氯米松对哮喘患者体内嗜酸粒细胞、T-淋巴细胞功能状态的影响,对治疗前后哮喘患者血清嗜酸性阳离子蛋白(ECP)、可溶性白细胞介素-2(sIL-2R)浓度及患者乙酰甲胆碱气道反应性进行检测。结果表明,吸入皮质激素6周后,血清ECP、sIL-2R浓度降低,肺功能改善,乙酰甲胆碱-PC20(FEV1下降20%时的乙酰甲胆碱激发浓度)值增高。提示:糖皮质激素能抑制嗜酸性粒细胞、T-淋巴细  相似文献   

11.
目的 分析肺结核史患者妊娠时间和肺结核复发间相关性.方法 选取我院收治的有肺结核史的妊娠妇女576例作为研究对象,对其妊娠前肺结核治疗、治愈后妊娠时间、妊娠后复发肺结核等进行分析,总结有肺结核史育龄女性的妊娠时间和肺结核复发之间的关系.结果 肺结核治愈后不同时间段妊娠者的结核复发率比较,差异具有显著性(P<0.05),停药后间隔时间越久妊娠,肺结核复发的几率越小.结论 加强孕期痰菌检查,及早发现复发肺结核,提高母婴安全.  相似文献   

12.
骨关节结核是危害人们健康的严重感染性疾病,近95%由他处结核病继发而来.罹患骨关节结核疾病后几乎均将致残,严重影响人们的健康、工作和生活.建国以来在党和国家的关心和支持下,骨关节结核的诊治水平取得了长足进步.时至今日,由于多种原因,学科发展和被重视程度受到一定的制约,同整个医疗行业的发展不相适应.回顾过去,展望未来,我们需要重新审视骨关节结核的诊治方法,努力推进骨关节结核诊疗技术的科学发展.  相似文献   

13.
AIM To study the effect of phosphorylation ofMAPK and Stat3 and the expression of c-fos andc-jun proteins on hepatocellular carcinogenesisand their clinical significance.METHODS SP immunohistochemistry was usedto detect the expression of p42/44~(MAPK), p-Stat3,c-fos and c-jun proteins in 55 hepatocellularcarcinomas (HCC) and their surrounding livertissues.RESULTS The positive rates and expressionlevels of p42/44~(MAPK), p-Stat3, c-fos and c-junproteins in HCCs were significantly higher thanthose in pericarcinomatous liver tissues (PCLT).A positive correlation was observed between theexpression of p42/44~(MAPK) and c-fos proteins, andbetween p-Stat3 and c-jun, but there was nosignificant correlation between P42/44~(MAPK) and p-Stat3 in HCCs and their surrounding livertissues.CONCLUSION The abnormalities of Ras/Raf/MAPK and JAKs/ Stat3 cascade reaction maycontribute to malignant transformation ofhepatocytes. Hepatocytes which are positive forp42/ 44~(MAPK), c-fos or c-jun proteins may bepotential malignant pre-cancerous cells.Activation of MAPK and Stat3 proteins may be anearly event in hepatocellular carcinogenesis.  相似文献   

14.
15.
AIM To study the effect of phosphorylation ofMAPK and Stat3 and the expression of c-fos andc-jun proteins on hepatocellular carcinogenesisand their clinical significance.METHODS SP immunohistochemistry was usedto detect the expression of p42/44MAPK, p-Stat3,c-fos and c-jun proteins in 55 hepatocellularcarcinomas (HCC) and their surrounding livertissues.RESULTS The positive rates and expressionlevels of p42/44MAPK, p-Stat3, c-fos and c-junproteins in HCCs were significantly higher thanthose in pericarcinomatous liver tissues (PCLT).A positive correlation was observed between theexpression of p42/44MAPK and c-fos proteins, andbetween p-Stat3 and c-jun, but there was nosignificant correlation between p42/44MAPK and p-Stat3 in HCCs and their surrounding livertissues.CONCLUSION The abnormalities of Ras/Rat/MAPK and JAKs/ Stat3 cascade reaction maycontribute to malignant transformation ofhepatocytes. Hepatocytes which are positive forp42/ 44MAPK, c-fos or c-jun proteins may bepotential malignant pre-cancerous cells.Activation of MAPK and Stat3 proteins may be anearly event in hepatocellular carcinogenesis.  相似文献   

16.
The Enterovirus (EV) and Parechovirus genera of the picornavirus family include many important human pathogens, including poliovirus, rhinovirus, EV-A71, EV-D68, and human parechoviruses (HPeV). They cause a wide variety of diseases, ranging from a simple common cold to life-threatening diseases such as encephalitis and myocarditis. At the moment, no antiviral therapy is available against these viruses and it is not feasible to develop vaccines against all EVs and HPeVs due to the great number of serotypes. Therefore, a lot of effort is being invested in the development of antiviral drugs. Both viral proteins and host proteins essential for virus replication can be used as targets for virus inhibitors. As such, a good understanding of the complex process of virus replication is pivotal in the design of antiviral strategies goes hand in hand with a good understanding of the complex process of virus replication. In this review, we will give an overview of the current state of knowledge of EV and HPeV replication and how this can be inhibited by small-molecule inhibitors.  相似文献   

17.
Non-invasive techniques to monitor stress hormones in small animals like mice offer several advantages and are highly demanded in laboratory as well as in field research. Since knowledge about the species-specific metabolism and excretion of glucocorticoids is essential to develop such a technique, we conducted radiometabolism studies in mice (Mus musculus f. domesticus, strain C57BL/6J). Each mouse was injected intraperitoneally with 740 kBq of 3H-labelled corticosterone and all voided urine and fecal samples were collected for five days. In a first experiment 16 animals (eight of each sex) received the injection at 9 a.m., while eight mice (four of each sex) were injected at 9 p.m. in a second experiment. In both experiments radioactive metabolites were recovered predominantly in the feces, although males excreted significantly higher proportions via the feces (about 73%) than females (about 53%). Peak radioactivity in the urine was detected within about 2h after injection, while in the feces peak concentrations were observed later (depending on the time of injection: about 10h postinjection in experiment 1 and about 4h postinjection in experiment 2, thus proving an effect of the time of day). The number and relative abundance of fecal [3H]corticosterone metabolites was determined by high performance liquid chromatography (HPLC). The HPLC separations revealed that corticosterone was extensively metabolized mainly to more polar substances. Regarding the types of metabolites formed, significant differences were found between males and females, but not between the experiments. Additionally, the immunoreactivity of these metabolites was assessed by screening the HPLC fractions with four enzyme immunoassays (EIA). However, only a newly established EIA for 5alpha-pregnane-3beta,11beta,21-triol-20-one (measuring corticosterone metabolites with a 5alpha-3beta,11beta-diol structure) detected several peaks of radioactive metabolites with high intensity in both sexes, while the other EIAs showed only minor immunoreactivity. Thus, our study for the first time provides substantial information about metabolism and excretion of corticosterone in urine and feces of mice and is the first demonstrating a significant impact of the animals' sex and the time of day. Based on these data it should be possible to monitor adrenocortical activity non-invasively in this species by measuring fecal corticosterone metabolites with the newly developed EIA. Since mice are extensively used in research world-wide, this could open new perspectives in various fields from ecology to behavioral endocrinology.  相似文献   

18.
目的:通过分析心电图(Electrocardiogram,ECG)和心电向量图(Vectorcardiogram,VCG)的改变与冠脉造影(CAG)结果进行对比,探讨ECG、VCG在冠状动脉病变中的诊断价值。方法: 选择2008年1月~2009年12月临床拟诊断为冠心病患者108例,行常规ECG、VCG检查,并于1周内进行CAG,对检查结果依据各自的诊断标准进行判定,以CAG为标准诊断法,利用四格表法,计算相关评价真实性的指标并进行比较。结果: ①VCG检测的灵敏度、特异度、准确度显著高于ECG(P<0.05,P<0.01)。②ECG、VCG阳性率与冠脉病变支数组间比较:在单支病变、双支病变中,VCG阳性率明显高于ECG(P<0.05),左主干或三支病变无统计学意义;组内比较:ECG组左主干或三支病变组较单支病变、双支病变阳性率高(P<0.05,P<0.01);VCG组左主干或三支病变组较单支病变阳性率高(P<0.05);与双支病变阳性率比较无统计学意义;③ECG、VCG阳性率与冠脉病变程度组间比较:冠脉病变狭窄50%~69%的VCG阳性率明显高于ECG (P<0.05),其他两组阳性率比较无统计学意义;组内比较:ECG组冠脉病变狭窄≥90%较50%~69%、70%~89%的阳性率高(P<0.05,P<0.01); VCG组狭窄≥90%较50%~69%阳性率高(P<0.01),其他无统计学意义。结论: VCG对冠心病检测价值显著高于ECG。  相似文献   

19.
Here we report the structural characterization of the product formed from the reaction between hydroethidine (HE) and superoxide (O(2)(.-)). By using mass spectral and NMR techniques, the chemical structure of this product was determined as 2-hydroxyethidium (2-OH-E(+)). By using an authentic standard, we developed an HPLC approach to detect and quantitate the reaction product of HE and O(2)(.-) formed in bovine aortic endothelial cells after treatment with menadione or antimycin A to induce intracellular reactive oxygen species. Concomitantly, we used a spin trap, 5-tert-butoxycarbonyl-5-methyl-1-pyrroline N-oxide (BMPO), to detect and identify the structure of reactive oxygen species formed. BMPO trapped the O(2)(.-) that formed extracellularly and was detected as the BMPO-OH adduct during use of the EPR technique. BMPO, being cell-permeable, inhibited the intracellular formation of 2-OH-E(+). However, the intracellular BMPO spin adduct was not detected. The definitive characterization of the reaction product of O(2)(.-) with HE described here forms the basis of an unambiguous assay for intracellular detection and quantitation of O(2)(.-). Analysis of the fluorescence characteristics of ethidium (E(+)) and 2-OH-E(+) strongly suggests that the currently available fluorescence methodology is not suitable for quantitating intracellular O(2)(.-). We conclude that the HPLC/fluorescence assay using HE as a probe is more suitable [corrected] for detecting intracellular O(2)(.-).  相似文献   

20.
荣宝和氯硝柳胺灭螺效果比较及成本分析   总被引:2,自引:0,他引:2  
目的 评价新型灭螺药物荣宝杀灭钉螺的效果,探讨其推广应用价值.方法 按目前推荐的荣宝灭螺剂量,喷洒法为30 g/m2,浸杀法为50 g/m3;氯硝柳胺喷洒法和浸杀法分别采用2 g/m2和2 g/m3杀螺剂量,分别在室内和现场进行灭螺试验,观察两种药物的灭螺效果并初步分析评估其成本.结果 在现场气温22~30℃条件下,荣宝50 g/m3浸杀3、5、7 d后,螺袋内钉螺校正死亡率均达到100.0%,与氯硝柳胺2 g/m3灭螺效果相似;荣宝30 g/m2剂量喷洒3、5、7、15 d后,钉螺校正死亡率分别为54.5%、58.0%、69.0%、79.1%,氯硝柳胺喷洒组钉螺校正死亡率分别为61.0%、69.4%、76.7%、77.9%.在室温18℃条件下,荣宝以30 g/m2喷洒3、5、7、15 d后,钉螺校正死亡率分别为72.9%、87.2%、91.5%、76.1%;而相应2 g/m2氯硝柳胺喷洒后的钉螺校正死亡率分别为81.3%、95.7%、97.9%、80.4%.同样完成1000 m2的喷洒灭螺任务,荣宝所需灭螺药物和人力资费成本比氯硝柳胺多支出0.114元/m2;完成72 m3的浸杀灭螺任务,荣宝所需灭螺药物和人力资费成本比氯硝柳胺多支出0.127元/m3.50 g/m3荣宝浸杀灭螺剂量,对成鱼(>250 g)的活力不会造成影响,但对鱼类幼苗仍具较强毒性.结论 荣宝与氯硝柳胺灭螺效果相似,由于其成本较高,氯硝柳胺仍然是目前首选灭螺药物,但荣宝的鱼类毒性低,可作为氯硝柳胺之外有益的补充灭螺药物.  相似文献   

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