MRI顺磁性造影剂增强及护理

目的 :进一步探讨 MRI增强前后的准备与护理方法。材料与方法 :共增强 833例 ,男 5 85例 ,女 2 4 8例。使用顺磁性造影剂 Gd- DTPA,按 0 .2 m L/kg体重给药。其中双倍量增强 110例 ,增强前认真履行告知义务和签署同意书。发生造影剂外漏者给予鲜马铃薯片外敷。结果 :增强效果达良好以上共 82 5例 ,占 99% ,未发生严重负反应。 3例造影剂外漏 ,鲜马铃薯片外敷后 3h痊愈。结论 :增强前充分细致的准备是保证增强效果的重要因素。认真履行告知义务和签置同意书 ,不仅尊重了病人的权利 ,也是依法行医 ,保证医疗安全的需要     

性传播疾病危险人群乙型肝炎和丙型肝炎病毒感染的血清流行病学调查

通过对４３１名卖淫妇女和１０９名正常妇女ＨＢＶ和ＨＣＶ感染的血清学指标的检测、性传播有关因素的调查，发现卖淫妇女ＨＢＶ和ＨＣＶ感染中的抗－Ｈｋｃ为４３．１５％，抗－ＨＢｓ为３６．８９％，ＨＢｓＡｇ为１０．４４％，抗－ＨＣＶ为９．５１％，明显高于正常妇女；有性传播疾病者ＨＢＶ和ＨＣＶ的各项感染指标也明显高于正常妇女。卖淫妇女的抗－ＨＣＶ感染率有随年龄增长而增高的趋势，与卖淫时限长、卖淫次数多有明显差别，这表明卖淫妇女中有较严重的ＨＢＶ和ＨＣＶ感染。     

血清白细胞介素－2受体的测定在脑血管性痴呆诊治中意义的探讨

目的 :检测脑血管性痴呆患者血清中可溶性白细胞介素 - 2 (s IL- 2 R)水平 ,评价 s IL- 2 R的测定在诊治脑血管性痴呆中的价值。方法 :采用双抗体夹心的 EL ISA法检测脑血管性痴呆患者血清中 s IL- 2 R的水平。结果 :脑血管性痴呆患者血清中的 s IL- 2 R水平较健康对照组显著增高 ,两组比较差异非常显著 (P <0 .0 1)。结论 :检测脑血管性痴呆患者血清中 s IL- 2 R水平 ,有助于了解患者的免疫功能变化及疗效观察     

骨髓间质干细胞移植对心肌再生的影响

目的研究移植骨髓间质干细胞(MSCs)对梗死区心肌和血管再生的影响.方法抽取香猪骨髓,体外分离MSCs,经5-氮胞苷 (5-aza)转化.结扎冠状动脉左前降支(LAD),经LAD和梗死区注射MSCs;对照组注射培养液.3周和6周后,行单光子发射型计算机断层(SPECT)心肌显像检查.结果SPECT显像,对照组心肌有明显的充盈缺损;实验组细胞移植3周后在梗死区内有岛状的灌注显像区,6周后这些区域相互之间以及与正常心肌之间发生融合.心肌灌注显像,实验组评分高于对照组(P<0.01).结论MSC移植可再生心肌组织和血管.经LAD注射结合多点局部注射的方法可使移植细胞均匀分布于整个心梗区,促进再生的心肌组织与宿主心肌组织之间产生融合.     

新银盐法测定化妆品中微量砷的研究

本文以硝酸——硝酸银——聚乙烯醇——乙醇为砷化氢吸收显色剂测定化妆品中的微量砷,操作简便快速,灵敏度高,重现性好。摩尔吸光系数为二乙氨基二硫代甲酸银法(DDC—Ag法)的5.7倍。     

核酸杂交反应中影响因素分析

以光敏生物素标记的R3 cDNA克隆为模型,采用正交设计的方法,对影响核酸杂交反应的主要因素:杂交反应温度,反应时间,探针浓度及甲酰胺浓度作了综合性分析。当探针浓度为800μg/L,甲酰胺浓度为10mol/L,50℃杂交反应6h,可获得最高灵敏度(10pg)。     

间接血凝试验诊断旋毛虫病

本文采用经Sephadex G-200层析后的旋毛虫幼虫抗原对实验感染旋毛虫大鼠和旋毛虫病人血清作间接血凝试验(IHA)。结果表明,20只大鼠感染后第16天全部出现阳性反应。9例旋毛虫病患者为阳性。本试验用于囊虫病、华枝睾吸虫病和健康人及正常大鼠均为阴性。检查本地区31只狗,阳性符合率为66.7％。     

Flow karyotypes and chromosomal DNA contents of genus Triticum species and rye (Secale cereale)

The flow cytometry and chromosome imaging method were jointly used for analyzing genome content and chromosomal DNA content of hexaploid wheat (AABBDD), hexaploid triticale (AABBRR), tetraploid wheat (AABB), and AA, BB, DD genome donors and RR genome rye. Their genome sizes were 34.4 pg, 40.9 pg, 26.2 pg, 12.1 pg, 13.7 pg, 10.5 pg, and 16.9 pg, respectively. The 2C nuclear DNA content of BB genome donor with 13.7 pg was the highest value among the other genome donors, AA or DD. The genome content of tetraploid wheat, unlike hexaploid wheat or hexaploid triticale, was larger than the sum of the genomes of AA and BB genome donors. The DNA content of each chromosome ranged from 1.22 pg in DD genome donor to 2.61 pg in rye. Each chromosome peak was divided into three to four groups. Only one chromosome was included in the highest chromosomal DNA peak in hexaploid wheat, tetraploid wheat, DD genome donor and rye but two chromosomes in AA, BB genome donors, and hexaploid triticale. Correlation between 2C nuclear DNA content and chromosome density volume was the highest value compared with the other chromosomal parameters of chromosome area, or chromosome length.     

Ventricular rate smoothing for atrial fibrillation: a quantitative comparison study.

AIMS: To quantitatively compare the ventricular rate-smoothing (VRS) effects of different ventricular pacing (VP) protocols for atrial fibrillation (AF). METHODS AND RESULTS: Using a recently developed open-source model that can simulate the ventricular response in AF and VP, the performance of fixed-rate pacing and four previously published VRS algorithms were assessed by the mean RR (mRR), the root mean square of successive RR differences (RMSSD), the percentage of ventricular senses (VS%), and the percentage of short RR intervals (sRR%). All pacing protocols cause rate-dependent reduction of RMSSD, VS%, and sRR% with or without shortening of mRR compared to spontaneous AF. Fixed-rate pacing was more sensitive to the intrinsic rate than the VRS algorithms. The performance was generally comparable between different VRS algorithms, although higher mRR and VS% can be achieved at the expense of larger RMSSD and sRR%. CONCLUSION: The effect of VP on ventricular rhythm in AF depends on both intrinsic rate and the aggressiveness of the pacing protocol. Adequate rate control is necessary for effective operation of the VRS algorithm. Choosing VRS algorithm should balance between the beneficial effects of rate regularization and the negative effects of increasing heart rate and percentage of VP.     

用SYBR Green I实时逆转录-聚合酶链反应定量检测人、小鼠精子中CatSper1 mRNA

目的:建立并优化SYBR GreenI实时RT-PCR体系,定量检测人、小鼠成熟精子中的CatSper1 mRNA。方法:用TRIzol分别提取人、小鼠成熟精子中的总RNA,逆转录后用SYBR GreenI实时PCR定量检测CatSper1 mRNA。SYBR GreenI实时PCR采用普通PCR试剂,加入SYBR GreenI染料,优化退火温度、Mg2+浓度及上、下游引物比例,并在PCR循环时采用四步法以消除引物二聚体的影响。优化完成后用不同浓度的精子cDNA为模板做标准曲线,以检测SYBR GreenI实时PCR的扩增效率。结果:定量检测CatSper1 mRNA的SYBR GreenI实时PCR体系适宜退火温度、Mg2+浓度及上、下游引物比例分别为63℃、3.0mmol/L和1∶1,四步法中采集荧光的温度为88℃。优化后用人和小鼠精子cDNA为模板做标准曲线分别为Y=-3.402log(X)+25.99和Y=-3.409log(X)+24.09,扩增效率分别为96.8%和96.5%,可定量检测人、小鼠成熟精子中的CatSper1 mRNA。结论:用普通的逆转录及PCR系统和试剂,建立了一种方便、廉价、可靠的SYBR GreenI实时荧光定量RT-PCR系统,可用于人、小鼠精子中CatSper1 mRNA定量检测。