仿SOD催化剂的合成及其清除氧自由基作用

合成了一种钢配合物[Cu_2(C_(34)H_(32)N_(10)(Br)_3)Br·2H_2O作为仿Cu·Zn-SOD催化剂,用核黄素-蛋氨酸光照法等证实它有清除的作用;ESR等证实它还有清除,OH的作用;大鼠心脏缺血再灌注实验表明此铜配合物能降低活性氧自由基(和·OH)对心肌的损伤程度,对再灌注损伤心肌有保护作用。     

胃癌患者胃液可溶性白细胞介素-2受体初步研究

应用双抗体夹心ELISA法对87例消化道疾病患者胃液可溶性白细胞介素-2受体(sIL-2R)水平进行测定。结果表明,胃癌患者胃液sIL-2R水平明显高于慢性浅表性胃炎及十二指肠溃疡患者(P相似文献   

三种皮片匀浆上清蛋白的免疫生化分析

利用紫外吸收光谱、PAGE 垂直板 SDS—PAGE 及快速染色盘状 PAGE 酯酶电泳技术,对人、豚鼠的三种不同皮片的匀浆上清液蛋白成份含量及酯酶同工酶进行了比较分析,旨在为临床上应用新生皮片储皮移植提供理论依据。结果表明,豚鼠皮及人皮皮片匀浆上清液中的蛋白含量、光谱分析、PAGE、SDS-PAGE 及酯酶同工酶电泳,均是新生皮组的变化显著低于其它两组,而-196℃处理组与成年新鲜皮片组存在着较小差别,因此上述免疫生化学指标的判定结果为:新生皮<(差于)-196℃处理成年皮<(差于)新鲜成年皮。     

Lewis Histo-Blood Group System and Associated Secretory Phenotypes

This review summarises present knowledge of the chemistry, immunology, genetics and clinical significance of antibodies in the Lewis and secretor histoblood group systems. Although red cell serology has laid the foundations for these systems, more recent advances have been made by studying Lewis and related glycoconjugates with monoclonal antibodies, determining structures by mass spectrometry and NMR spectroscopy, identifying enzymes and their specificities, and identifying the genes by molecular biology. The expression of Lewis system antigens is dependent on Lewis and secretor loci. Fucosyltransferases coded by genes at these loci compete and interact with each other and with other transferases to determine an individual's Lewis and secretor phenotype. Exocrine epithelial cells, mostly of endodermal origin, synthesise the Lewis antigens which, as plasma glycolipids, are secondarily acquired by cells of the peripheral circulation. Phenotyping red cells is often regarded as a simple way of determining the Lewis and sometimes the secretor status of an individual; however, the red cell phenotype is influenced by many factors and may not necessarily reflect someone's Lewis and secretor genotypes. Two main red cell Lewis groups are usually found, Lewis negative and Lewis positive. In Lewis-negative individuals, the secretor genotype does not affect the Lewis phenotype, but in Lewis-positive individuals, the non-secretor genotype generates the Le(a+b–) phenotype, the secretor genotype causes the Le(a–b+) phenotype, and the partial secretor genotype gives rise to the Le(a+b+) phenotype.     

无张力疝修补术后顽固性疼痛原因和对策

目的 探讨无张力疝修补术后的顽固性疼痛病因及预防治疗。方法 将同期无张力疝修补术与传统的腹股沟疝修补方法进行比较。结果 无张力疝修补术后的顽固性疼痛率为9．02％(12／133)，传统的腹股沟疝修补方法疼痛率为8．61％(18／209)。无张力疝修补与传统的腹股沟疝修补相比，术后顽固性疼痛的发生率差异无显著性(P＞0．05)。结论 无张力疝修补并不一定减少传统的腹股沟疝修补术后顽固性疼痛，手术规范操作是预防的关键，治疗应先保守治疗，无效再考虑手术治疗。     

扩散法被动式甲醛个体监测器（Ⅱ型）的研制

介绍了一种基于气体分子扩散原理的被动式甲醛个体采样器，它是在Ⅰ型采样器的基础上完成的。采用甘油（２０％）／偏重亚硫酸钠（０．２５％）浸渍的定量滤纸（φ４２ｍｍ）作为吸收层，空气中甲醛扩散到吸收层上，形成稳定的化合物。采样一定时间后，取出吸收层，洗脱后，用ＡＨＭＴ化学比色法测定所采集到的甲醛。这种采样器的平均采样速率为８３ｍｌ／ｍｉｎ，标准偏差为７．２ｍｌ／ｍｉｎ，与有动力吸收管采样的方法相比较，总不确定度小于±２５％。     

病理性损伤因素对肾小管上皮细胞表型转化的影响

目的 :观察低血清、高糖、高蛋白刺激下肾小管上皮细胞向间叶性细胞的表型转化 ,探讨损伤的肾小管上皮细胞在肾小管间质纤维化中的作用。方法 :以体外培养的人近端肾小管上皮细胞为对象 ,分别用含低血清(0 .2mol·L-1小牛血清 )、高葡萄糖 (4.5 g·L-1)、高白蛋白 (15 g·L-1)的培养液培养 7d ,透射电镜检测细胞形态变化 ;免疫组化和Westernblot检测细胞表型改变 ,包括CK、Vimentin、α SMA、Ⅰ和Ⅲ型胶原 ,原位杂交检测Ⅰ型胶原mRNA表达 ,同时检测细胞TGFβ1蛋白表达。 结果 :低血清、高糖、高蛋白直接刺激下 ,肾小管上皮细胞出现明显形态学改变 ,包括细胞变为长梭形 ;透射电镜下细胞内线粒体明显减少 ,粗面内质网明显增加 ,并出现actin样微丝。免疫组化染色和Westernblot显示CK表达明显减弱 ,Vimentin、Ⅰ、Ⅲ型胶原、α SMA和TGFβ1表达增强。原位杂交显示Ⅰ型胶原mRNA表达增强。结论 :低血清、高糖、高蛋白可直接引起人近端肾小管上皮细胞TGFβ1表达增加 ,并发生向间叶性细胞的表型转化     

Adenoid cystic carcinoma: DNA as a prognostic indicator

A retrospective study was performed on 20 patients with adenoid cystic carcinomas of major salivary glands to see if DNA. patterns correlated with their prognoses. Fourteen tumors were found to be DNA. diploid; 6 were DNA aneuploid. Histologically, all DNA-aneu-ploid tumors had solid components, compared with only 5 of the DNA-diploid tumors. All of the DNA-aneuploid tumors recurred, in contrast to only 2 of the DNA-diploid tumors; the difference was highly significant (P<0.001). All of the patients with no recurrences had DNA-diploid tumors. In our study, DNA measurements of adenoid cystic carcinomas gave statistically significant information about prognosis and correlated to histological grading. We propose that evaluation of DNA content may be performed before planning the treatment of adenoid cystic carcinomas.