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41.
The acetylcholine release enhancer linopirdine induces Fos in neocortex of aged rats 总被引:1,自引:0,他引:1
Centrally acting cholinergic agents induce the immediate early gene c-fos in the rat brain resulting in transient increases of Fos protein, most notably in the cerebral cortex. In this study we have monitored by Fos immunohistochemistry the effect of the acetylcholine release enhancer linopirdine (DUP996) on the immediate early gene c-fos in brains of 3 months and 30 months old rats. In young rats linopirdine had only a marginal effect on Fos expression. In contrast, in aged rats linopirdine caused widespread expression of Fos throughout neocortex. In somatosensory cortex, the induction of the c-fos gene by linopirdine was nearly completely blocked by atropine and scopolamine and strongly attenuated by the NMDA receptor blockers CPP and MK-801. The results suggest that the age-related decline in acetylcholine release in rodents can be partially compensated for by administration of linopirdine. 相似文献
42.
IL-13对大鼠急性肾缺血再灌注时IL-1β表达的影响 总被引:2,自引:0,他引:2
目的:观察IL-13对急性肾缺血再灌注时IL-1β表达的影响。方法:Wistar雄性大鼠57只,随机分为8组:正常组(normal);假手术组(sham);缺血组:(I)缺血再灌注组(I/R);治疗对照组-1(C-1);治疗对照组-2(C-2);治疗组-1(T-1)和治疗组-2(T-2)。阻断大鼠双侧肾脏血流45min再灌注24h建立急性肾缺血再灌注模型;治疗组分别于阻断血流前、后分别从双侧肾动脉开口注射入1.5μg/50gbw鼠重组白细胞介素13(rmIL-13);检测各组大鼠IL-1β血清水平和肾脏表达,以及肾功能和肾脏病理。结果:(1)治疗组肾脏IL-1β基因(TtoC:P<0.01)和蛋白表达(T-1toC-1:P<0.01;T-2toC-2:P<0.05)明显减少,血清IL-1β水平明显下降;(2)肾功能障碍和肾组织病理变化明显减轻,肾小管损害评分减少(C-1toT-1:45.20±8.64to21.05±8.82,P<0.01;C-2toT-2:42.25±11.15to23.25±7.31,P<0.01);(3)血清IL-1β水平与BUN、Cr成正相关(r=0.708,P<0.01;r=0.770,P<0.01)。结论:IL-13能有效地抑制大鼠急性肾缺血再灌注损伤IL-1β的表达。 相似文献
43.
目的:揭示人类绒毛膜促性腺激素(hCG)是否通过改变细胞因子的生成而影响滋养细胞的侵袭性。方法:以永生化的滋养细胞系JEG-3为研究对象,采用逆转录多聚酶链反应(RT-PCR)方法观察了hCG对JEG-3细胞与细胞侵袭力调节有关的多种因素因子表达的影响,结果:JEG-3细胞表达HGF,IGF-II,VEGF和TGF-β3,且VEGF的表达以VEGF121和VEGF165为主,而不表达IGF,TGF-1β,TGF-β2,IL-β1,25U/mL hCG处理50h可显著降低JEG-3细胞中HGF的表达,同时强烈诱导VEGF121和VEGF165的表达,而其它基因的表达未发生明显变化,结论:HGF对滋养细胞的侵入起促进作用,而VEGF则具有抑制效应,说明,高浓度的hCG可能通过两种细胞因子的自分泌机制对滋养细胞的侵入起抑制作用。 相似文献
44.
散发性急性戊型肝炎血清抗体动态变化和肝脏超微… 总被引:1,自引:0,他引:1
为探讨散发性戊型肝为血清抗体动态变化,应用酶联免疫法(EIA)检测了7例急性戊型肝炎抗戊型肝炎病毒(HEV)IgG和IgM抗体、并对1例2进行了肝超微结构病理检测,结果表明,发病10天至45天内抗HEV-IgG和IgM滴度最高,发病第40天仍有肝细胞肿胀,胞浆空化和线粒体固缩等病理变化。患者轿清抗-HEVIgM滴度在45天后逐渐下降,2个月内全中消失,抗-HEVIgM滴度在45天后逐渐下降,2个月 相似文献
45.
Inflammatory cytokine response to Vibrio vulnificus elicited by peripheral blood mononuclear cells from chronic alcohol users is associated with biomarkers of cellular oxidative stress
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Vibrio vulnificus is the leading cause of death in the United States associated with the consumption of raw seafood, particularly oysters. In epidemiological studies, primary septicemia and inflammation-mediated septic shock caused by V. vulnificus is strongly associated with liver disease, often in the context of chronic alcohol abuse. The present study was undertaken to determine whether clinical biomarkers of liver function or cellular oxidative stress are associated with peripheral blood mononuclear cell inflammatory cytokine responses to V. vulnificus. Levels of interleukin-1 beta (IL-1 beta), IL-6, IL-8, and tumor necrosis factor alpha elicited in response to V. vulnificus and measured in cell supernatants were not associated with the liver biomarkers aspartate aminotransferase (AST) or alanine aminotransferase (ALT) or the AST/ALT ratio. In contrast, reduced glutathione (GSH) levels were associated with the release of all four cytokines (IL-1 beta [R(2) = 0.382; P = 0.006], IL-6 [R(2) = 0.393; P = 0.005], IL-8 [R(2) = 0.487; P = 0.001], and TNF-alpha [R(2) = 0.292; P = 0.021]). Those individuals with below-normal GSH levels produced significantly less proinflammatory cytokines in response to V. vulnificus. We hypothesize that persons with markers for cellular oxidative stress have increased susceptibility to V. vulnificus septicemia. 相似文献
46.
肝素酶和碱性成纤维细胞生长因子与非小细胞肺癌转移和预后的关系 总被引:6,自引:0,他引:6
目的 探讨肝素酶(heparanase)和碱性成纤维细胞生长因子(bFGF)在人非小细胞肺癌(NSCLC)组织中表达的临床意义及其与肺癌转移和预后的关系。方法 采用免疫组织化学、原位杂交和Western blot方法,检测115例人NSCLC石蜡切片和45例新鲜肺癌及对应癌旁正常组织中肝素酶和bFGF的表达情况。采用χ^2检验、t检验、生存曲线和Cox比例风险回归等方法分析肝素酶和bFGF分别表达及共表达的意义。结果 免疫组织化学染色证实肝素酶(91/115)和bFGF(89/115)主要表达在癌细胞质和(或)细胞膜中,在正常肺泡上皮和支气管上皮中则呈阴性表达。Western blot也证实肝素酶在肺癌中的表达明显增高(P=0.041)。统计分析结果显示:肝素酶和bFGF的表达具有明显的一致性(P:0.0001),二者单独表达和共表达均与肺癌的分期、血管侵袭、淋巴结转移、微血管密度和预后有关,其中,二者共表达时与分期和微血管密度的相关性更显著;另外,bFGF还与肺癌的分化程度有关。多因素分析结果显示,肺癌的分化程度、血管浸润、淋巴结转移和bFGF的表达可以作为判断肺癌预后的危险因素,但肝素酶不是影响预后的独立因素。结论 肝素酶和bFGF均与肺癌的转移、血管生成和预后密切相关。 相似文献
47.
Zhan Y Brown LE Deliyannis G Seah S Wijburg OL Price J Strugnell RA O'Connell PJ Lew AM 《Immunologic research》2004,30(1):1-14
The most common models of CD4 T-cell deficiency are mice exogenously injected with anti-CD4 antibody (Ab), CD4 knockout (CD4−/−) and major histocompatibility complex (MHC) class II knockout (class II−/−) mice. We recently described the anti-CD4 Ab transgenic mouse (GK) as an improved CD4 cell-deficient model. This review compares
this new GK mouse model with the widely available class II−/− and CD4−/− mice, when exposed to complex antigens (foreign grafts and during bacterial or viral infection). We highlight here the cytometric
and functional differences (including Ab isotype, viral or bacterial clearance, and graft survival) among these CD4 cell-deficient
models. For example, whereas grafts are generally rejected in class II−/− and CD4−/− mice as quickly as in wild-type mice, they survive longer in GK mice. Also, CD4−/− mice produce IgG against both simple model and complex antigens, but class II−/− and GK mice produce small amounts of IgG2a against complex antigens but not simple model antigens. These differences harbinger
the caveats in the use of these various mice. 相似文献
48.
Differential expression of p53 gene family members p63 and p73 in head and neck squamous tumorigenesis 总被引:39,自引:0,他引:39
p73 and p63 are recently cloned genes that share considerable structural and functional homologies with the p53 tumor suppressor gene. These genes, unlike p53, express multiple mRNA isoforms with variable biologic functions, and their suppressor nature has yet to be confirmed. To determine the interrelationship between these genes in the tumorigenesis of head and neck squamous carcinoma (HNSC), we performed immunohistochemical analyses of their protein products and compared the data with clinicopathologic parameters in 38 patients. In histologically normal epithelium, p53 and p73 showed similar basal and/or parabasal expression, but that of p53 was weaker and discontinuous. p63 staining was noted in more suprabasal cellular layers and was stronger. In dysplasias, all three markers manifested variable but gradual increase in extent and intensity of cellular expression with histologic progression. In carcinomas, p63 was the most frequently expressed (94.7%), followed by p73 (68.4%) and p53 (52.6%). Significant statistical correlation was noted only between p63 and p73 expressions (P =.04). Although no statistical correlation was found between p53 and p63 or p73, p53-negative tumors overexpressed either p63 or p73. p73 expression was associated with distant metastasis and perineural/vascular invasion. Our study indicates that (1) p63 and p73 expression may represent an early event in HNSC tumorigenesis, (2) the lack of correlation between p73 or p63 and p53 expression suggests an independent and/or compensatory functional role, (3) p73 expression may play a part in HNSC progression, and (4) p73 and p63 may function as oncogenes in the development of these tumors. 相似文献
49.
Recurrent genetic alterations in 26 colorectal carcinomas and 21 adenomas from Chinese patients 总被引:5,自引:0,他引:5
He QJ Zeng WF Sham JS Xie D Yang XW Lin HL Zhan WH Lin F Zeng SD Nie D Ma LF Li CJ Lu S Guan XY 《Cancer Genetics and Cytogenetics》2003,144(2):112-118
Colorectal cancer (CRC) is one of the most common malignancies worldwide. The incidence of CRC in the Chinese population has increased dramatically during the last two decades; however, nonrandom chromosomal alterations in Chinese patients have not been described. In the present study, comparative genomic hybridization (CGH) was applied to detect recurrent chromosome alterations in 26 primary colorectal carcinomas and 21 colorectal adenomas from Chinese patients. In CRC, several recurrent chromosomal changes were found, including gains of 8q (14/26 cases, 54%), 20q (54%), 3q (50%), 13q (50%), 5p (46%), 7p (42%), 7q (42%), and 12p (38%) and losses of 18q (65%) and 17p (42%). From comparison with previous CGH studies, the frequent gains of 3q and 12p might be distinctive occurrences in Chinese patients. The distribution of frequently found chromosomal alterations in different locations was studied. The gain of 20q was more frequently found in colon cancer (P<0.01) and the gain of 12p was more frequently found in rectal cancer. Chromosomal alterations were found in 19/21 of adenomas; the most frequent chromosomal alteration was the loss of 18q (9/21 cases, 43%). These recurrent alterations provide several starting points for the isolation of candidate oncogenes and tumor suppressor genes. 相似文献
50.
构建7q32区域鼻咽癌和正常鼻咽上皮细胞部分基因的表达图谱 总被引:7,自引:2,他引:7
目的构建7q32区域鼻咽癌细胞和组织及原代培养人正常鼻咽上皮细胞的部分基因表达图谱。方法通过差异RT-PCR和Northern杂交的方法检测定位于7q32区域的20个EST在鼻咽癌细胞和鼻咽癌组织及原代培养人正常鼻咽上皮细胞mRNA的表达水平。结果8个EST在鼻咽癌细胞HNE1和原代培养人正常鼻咽上皮细胞中表达量较一致,7个EST在两种细胞中均无表达,3个EST(W72688、H19830、AA130630)在鼻咽癌细胞株中表达上调,而2个EST(AA070437、H90882)在原代培养人鼻咽上皮细胞中表达上调。在13例鼻咽癌活检组织中30.7%(4/13)的AA070437表达下调,77%(10/13)的W72688和77%(10/13)的H19830表达上升。结论构建了7q32区域鼻咽癌细胞和组织及原代培养人正常鼻咽上皮细胞部分基因表达图谱,并初步认为A070437的表达下调和W72688、H19830的过表达与鼻咽癌的发生有关。 相似文献