油溶纳米蜂胶液联合两种根充糊剂对感染根管常见菌的体外抑菌性研究

目的探讨蜂胶类根充糊剂对感染根管常见菌的体外抑菌作用。方法选择感染根管的6种常见菌为实验菌种,琼脂扩散法观察蜂胶类根充糊剂的抗微生物作用;建立体外根管粪肠球菌感染模型,评价蜂胶类根充糊剂在离体牙根管内的抗粪肠球菌作用。结果蜂胶类根充糊剂对实验的各种细菌均具有抑菌作用,除油溶纳米蜂胶氢氧化钙甘油糊剂对粪肠球菌和具核梭杆菌的抑菌作用小于对照组外,其他实验组与对照组相比均增强了(P0.05或P0.01)或并未减弱(P0.05)原始糊剂的抑菌效果,糊剂中水溶蜂胶加入后短期内的抑菌作用优于油溶纳米蜂胶。结论蜂胶类根充糊剂对感染根管常见菌具有良好的抑菌效果,将其用作根管充填的材料具有一定的应用前景。     

高频电对感染根管消毒作用的初步实验研究

目的:初步验证高频电对感染根管是否具有较理想的消毒作用,并且与氢氧化钙药尖的消毒作用进行初步比较分析。方法:本实验制作10只家兔40颗门齿的感染根管动物模型,其中20颗用高频电消毒为实验组。20颗用氢氧化钙药尖消毒为对照组,消毒前后分别作需氧菌和厌氧菌培养并比较其消毒效果。结果:消毒前实验组和对照组各20个根管的需氧及厌氧菌培养全部阳性。实验组消毒后需氧菌3个阳性根管、厌氧菌2个阳性根管,消毒前后对需氧和厌氧菌杀灭作用的差异均具有极显著性(P<0.005)。对照组消毒后需氧菌13个阳性根管消毒作用的差异有显著性(P<0.05)。对照组消毒后厌氧菌11个阳性根管消毒作用的差异有极显著性(P<0.005)。实验组和对照组分别对需氧和厌氧2个菌种之间消毒作用的差异均无显著性(P>0.05)。实验组和对照组对需氧菌的消毒作用和对厌氧菌的消毒作用的组间差异均具有极显著性(P<0.005)。结论:高频电对感染根管内容物的消毒作用优于氢氧化钙药尖,具有临床应用的可行性。值得进一步研究。     

高频电对感染根管消毒作用的初步实验研究

目的：初步验证高频电对感染根管是否具有较理想的消毒作用,并且与氢氧化钙药尖的消毒作用进行初步比较分析.方法：本实验制作10只家兔40颗门齿的感染根管动物模型,其中20颗用高频电消毒为实验组.20颗用氢氧化钙药尖消毒为对照组,消毒前后分别作需氧菌和厌氧菌培养并比较其消毒效果.结果：消毒前实验组和对照组各20个根管的需氧及厌氧菌培养全部阳性.实验组消毒后需氧菌3个阳性根管、厌氧菌2个阳性根管,消毒前后对需氧和厌氧菌杀灭作用的差异均具有极显著性 （P〈0.005）.对照组消毒后需氧菌13个阳性根管消毒作用的差异有显著性（P〈0.05）.对照组消毒后厌氧菌11个阳性根管消毒作用的差异有极显著性（P〈0.005）.实验组和对照组分别对需氧和厌氧2个菌种之间消毒作用的差异均无显著性（P〉0.05）.实验组和对照组对需氧菌的消毒作用和对厌氧菌的消毒作用的组间差异均具有极显著性（P〈0.005）.结论：高频电对感染根管内容物的消毒作用优于氢氧化钙药尖,具有临床应用的可行性.值得进一步研究.     

次氯酸钠和洗必泰作为牙根管消毒冲洗液对根管内的感染物质的影响

摘要 目的：探究次氯酸钠和洗必泰作为牙根管消毒冲洗液的对根管内感染物质的影响。方法：选取76例接受根管治疗的患者根据随机数字表法分为观察组和对照组2组,其中对照组患者采用次氯酸钠治疗,观察组患者则采用次氯酸钠和洗必泰联合治疗。对比分析两组患者根管内细菌菌落计数、根管内感染物质、治疗效果、远期有效率和不良反应发生率。结果：根管消毒冲洗后观察组根管内细菌菌落计数和根管内感染物质显著低于对照组,差异具有统计学意义（P<0.05）;观察组患者治疗总有效率和不良反应的发生率分别为100.00%和13.16%,对照组患者治疗总有效率和不良反应的发生率分别为88.00%和65.79%,差异具有统计学意义（P<0.05）。另外,观察组患者第3个月、第6个月和1年后的治疗有效率均大于对照组。结论：次氯酸钠和洗必泰作为牙根管消毒冲洗液能够有效的减少根管内的感染物质的数量,提高治疗有效率,降低不良反应的发生率,值得临床推广使用。     

奥硝唑用于感染根管消毒的细菌学研究

目的　观察和探讨新型抗厌氧菌药物奥硝唑消毒感染根管的抗菌效果。方法　选择感染根管患牙98颗,常规根管预备后,随机分为试验组(奥硝唑组)和对照组(甲醛甲酚组)各4 9颗。分别在根管预备前、预备后及封药后进行根管内细菌标本采样、培养、分离与鉴定,测定根管内细菌变化及检出情况,并观察封药后临床症状和体征的变化。结果　2组封药后,根管内细菌数量及检出率均较封药前明显降低( P<0 .0 5 ) ,根管内细菌数量及检出率比较,差异无显著性( P>0 .0 5 ) ,奥硝唑的近期临床疗效优于甲醛甲酚。结论　奥硝唑是一种较安全、有效的根管消毒药物     

两种根管冲洗液对狗牙根管内细菌抗菌作用的实验研究

目的观察2%洗必泰溶液和3%双氧水2种根管冲洗液对狗牙根管内粪肠球菌、溶血链球菌、微小消化链球菌、中间普氏菌及具核酸杆菌的影响,为临床根管治疗提供参考。方法选择成年健康杂种狗3只,共有24个实验牙,48个实验牙根。于狗牙根管内接种粪肠球菌、溶血链球菌、微小消化链球菌、中间普氏菌及具核酸杆菌。对狗牙完成根管治疗。于治疗后12个月拍摄根尖X线片,并记录牙齿和根尖周组织的临床表现。将患牙随机分为3组,每组7颗患牙,去除根管内充填物并进行根管预备,实验一组用2%洗必泰溶液冲洗根管,实验二组用3%双氧水冲洗根管,对照组用0.9%NaC l溶液冲洗根管。分别在根管预备前及根管预备冲洗后对根管内细菌取样,培养,鉴定并记录细菌菌落数量,测定根管内细菌变化情况。结果根管预备冲洗后3组根管内的细菌量均较根管预备前显著下降（P〈0.05）。2%洗必泰溶液和3%双氧水2种根管冲洗液的杀菌效果明显好于0.9%NaC l溶液（P〈0.05）,2%洗必泰溶液明显好于3%双氧水（P〈0.05）。结论2%洗必泰溶液是有效的根管冲洗药物,可明显减少狗牙根管内粪肠球菌、溶血链球菌、微小消化链球菌、中间普氏菌及具核酸杆菌的数量,但不能完全清除根管内的细菌。     

两种皮肤消毒剂控制导管相关感染发生率的比较

目的探讨降低导管相关感染发生率的有效皮肤消毒剂。方法将我院ICU中心静脉置管的210例患者随机分为A组105例和B组105例,每48－72h对中心静脉置管处周围皮肤进行消毒,A组给予2％氯己定消毒皮肤;B组给予10％碘酊消毒皮肤,酒精脱碘。观察比较两组感染发生率。结果A组的感染发生率较B组低,差异有显著性（P〈0．01）。结论使用氯己定消毒皮肤能明显降低导管相关感染发生率。     

根管治疗失败病例根管内细菌对根尖周组织致病力的实验研究

目的观察根管治疗失败病例根管内分离的主要微生物对狗牙根尖周组织的影响。方法选择成年健康杂种狗5只,共有40个实验牙,80个实验牙根。实验一组于狗牙根管内接种溶血链球菌、微小消化链球菌、产黑色素类杆菌及具核梭杆菌;实验二组于狗牙根管内接种粪肠球菌及上述4种细菌;对照组不接种细菌。对狗牙完成根管治疗。分别于治疗后3、6、12个月拍摄根尖X线片,并记录牙齿和根尖周组织的临床表现;根管治疗后12个月处死动物,制备根尖周组织病理标本,观察根尖周骨组织破坏情况;动物处死前,根管内进行微生物的取样、培养和鉴定。结果实验组可见狗牙槽骨尖周骨质吸收,牙周膜纤维排列受到破坏,实验二组对根尖周破坏重于实验一组,对照组根尖周骨组织无破坏。结论从根管治疗失败病例根管内分离的主要微生物粪肠球菌、溶血链球菌、微小消化链球菌、产黑色素类杆菌及具核梭杆菌对狗牙根尖周组织有明显的破坏作用。     

超声波对感染根管消毒作用的实验研究

目的:通过与氢氧化钙药尖消毒作用的比较,验证超声波对感染根管的消毒作用并判断其消毒作用的临床应用价值。方法:10只3月龄的小型健康实验家兔随机分成二组后,制备成感染根管动物模型。对模型进行术前细菌培养后,分别做超声根管内消毒和氢氧化钙药尖消毒,术后细菌培养。结果:超声波和氢氧化钙对需氧菌和厌氧菌的杀灭作用无菌种之间的差别;但杀菌效果存在显著差异。实验发现超声波消毒的特点是:第一,无抗菌谱的差异。第二,无热效应,根管壁表面升温不明显。第三,作用无方向性,对任何角度方向上的有机物均能使其失活。第四,越是细小根管作用越强。这些正是根管消毒所要求的特殊条件。结论:1)超声波对感染根管的消毒作用明显优于氢氧化钙药尖。2)超声波对感染根管的消毒作用无抗菌谱的差异。3)超声波对感染根管具有较可靠的消毒作用,作为一种根管消毒手段值得进一步研究。     

Vitapex糊剂与氢氧化钙糊剂根尖诱导术治疗年轻恒牙根管感染患儿的疗效比较研究

摘要 目的：对比Vitapex糊剂与氢氧化钙糊剂根尖诱导术治疗年轻恒牙根管感染患儿的临床疗效。方法：选择2016年1月至2018年1月于我院进行诊治的年轻恒牙根管感染的120例患儿为研究对象,随机将其分为研究组（n=68）和对照组（n=52）,研究组接受Vitapex糊剂进行根尖诱导术治疗,对照组接受氢氧化钙糊剂进行根尖诱导术治疗,评价两组治疗前和治疗后1个月根管治疗期间疼痛（EIP）程度、牙根尖孔直径、根尖闭合时间和检测龈沟液白细胞介素（IL）-1β、IL-8和肿瘤坏死因子（TNF）-α水平,分别于治疗后1个月、6个月、1 年和2 年对临床疗效进行评估。结果：治疗后1个月研究组EIP程度0级、Ⅰ级、Ⅱ级和Ⅲ级的改善程度均明显优于对照组（P＜0.05）。治疗后1个月研究组龈沟液中IL-1 β、IL-8、TNF-α水平以及根尖孔直径、根尖闭合时间均明显低于对照组（P＜0.05）。治疗后6个月、1年和2年研究组的有效率为97.06%（66/68）、97.06%（66/68）和95.59%（65/68）,均明显高于对照组的82.69%（43/52）、80.77%（42/52）和76.92%（40/52）（P＜0.05）。结论：年轻恒牙根管感染患儿采用Vitapex糊剂进行根尖诱导术治疗的临床疗效优于氢氧化钙糊剂根尖诱导术,其可缓解患儿疼痛程度,降低龈沟液中IL-1 β、IL-8和TNF-α水平,促进根尖闭合,缩短根尖闭合时间。     

Protein Bodies in the Pine Megagametophyte in vitro Culture: Ultrastructural, Histochemical and Electrophoretic Observations

The megagametophytes of the European black pine (Pinus nigra Arn.) were cultured on modified MS medium. After 10 d, protein bodies showed well-marked degradation on freeze-etched replicas and in preparations observed by scanning electron microscopy. After 20 d of cultivation, the megagametophyte cells were completely empty. Proteins secreted into the agar medium were determined by electrophoresis and 15 different proteins, in the range of 6.5 to 71 kDa, were identified.     

花烛叶色嵌合体不同生长阶段叶色性状的保持特征

对20个花烛叶色嵌合体株系在不同生长阶段的叶色性状保持特征进行观察,并通过计算机程序辅助分析发现:离体培养阶段,植株嵌合叶片总数占总叶片数的比率及平均单株非绿色部分占总叶面积的比率均为最高,分别为81%和50.1%,两项数值分别高于温室生长阶段新生嵌合叶数占新生叶片总数的比率(46.2%)及新生叶片非绿色部分占新生叶片总面积的比率(23.0%);移栽后,叶片非绿色部分比率超过50%的9个株系中有7个不能正常生长而死亡,所剩13个株系的新生叶片嵌合叶数减少,非绿色部分面积比率缩小,叶片趋向转为绿色;施用营养液后,5个株系的新叶非绿色部分面积比率回升。这些现象表明:营养条件充分有利于嵌合株系花叶性状的保持;嵌合株系中非绿色部分面积大于50%的株系生活力弱,不宜过早移栽;在茎尖分生组织形成叶原基的过程中,可能存在正常细胞与突变细胞的竞争,其结果是一方取代另一方或二者达到动态平衡。     

用喷雾质谱法分析2种红曲霉所产橙色素的组成

分析了红色红曲霉（Monascus ruber）和烟色红曲霉（Monascus fuliginosus）发酵米粉所产橙色素的喷雾质谱图,发现烟色红曲霉所产橙色素与文献报道的相同;而红色红曲霉所产色素与文献报道不同,其主要组分是分子量分别为340．3和312.3的2种物质。     

Experimental approach to follow the spatiotemporal wood degradation in fungal microcosms

To investigate the spatiotemporal growth dynamics in fungal microcosms and to follow the spatial degradation effects of fungal lignocellulose fermentation, a new and flexible experimental setup was developed and tested. White and brown rot fungi were cultivated under solid-state conditions in beech wood-filled silicon tubes for 5 weeks. After inoculation of wood material at one end of the tube, the culture vessels were aerated and moistured by flushing air through alkaline and aqueous solutions. After incubation, the silicon tubes were harvested and segmented to follow different growth and degradation parameters. This new approach holds great potential since it allows the use of different growth substrates, variable aeration or moisturization conditions and is therefore a useful tool for diverse degradation studies, e.g. respiration/mineralization studies involving flow meters or carbon dioxide sensors or for molecular biological approaches.     

Changes in the placenta and in the rat embryo caused by the demethylating agent 5-azacytidine

DNA methylation is an important mechanism for regulation of gene expression during vertebrate development. 5-azacytidine is used as an experimental tool for demethylation. In this work, a single dose of 5-azacytidine (5 mg/kg body weight) was administered to rats at different stages of development. After 5-azacytidine administration on the first or third day of pregnancy, no changes were detected. After administration on the fourth day of pregnancy or later, a reduction in growth was observed. After treatment on day five and on any other day till day eleven of pregnancy, no living fetuses were found. Of those treated on day twelve, 24% of fetuses survived, but forelimb and hindlimb malformations were present. Administered on day thirteen, 5-azacytidine did not interfere with survival, but malformations were still present. From day fourteen on, 5-azacytidine caused no gross external malformations. Placentas were also influenced by 5-azacytidine. They were significantly smaller and histological evaluation showed the labyrinthine part to be severely reduced. In contrast, trophoblast giant cells were more abundant than in controls.     

The spatial distribution of bacteria in Grana-cheese during ripening

The microbial composition and its spatial distribution of Grana Trentino, a hard Parmesan-like cheese, was determined, from vat milk to cheese. After cutting along the vertical axis of the cheese wheels, three layers were sampled diagonally across the cheese: under the cheese rind, an intermediate section and the cheese core. After two different ripening periods (9 and 18 months), the cheese samples were analysed using traditional culture dependent and culture independent methods. Milk samples were dominated by mesophilic and psychrophilic bacterial counts. Thermophilic bacteria (Lactobacillus helveticus) were found in high amounts in cooked whey and natural whey starter cultures. After 9 months of ripening, lactic acid bacteria (LAB) counts were higher than those after 18 months. Furthermore, the LAB numbers in the cheese core was lower than those under the rind or in the intermediate section. The main LAB species isolated from milk (Lactococcus lactis, Pediococcus pentosaceus, Streptococcus uberis and Lactococcus garvieae) were not found in the corresponding cheeses. Some differences were observed in the species composition among the three cheese sections. Microbiota under the rind and in the intermediate section was similar and dominated by Lactobacillus paracasei and Lactobacillus rhamnosus. The core, after 18 months of ripening, was characterized by a total absence of LAB. In each sample, all LAB were genotypically grouped and the different biotypes were subjected to several technological tests indicating that some non-starter LAB (NSLAB) displayed technological features that are favorable for the production of Grana Trentino cheese.     

A simple technique for supporting single cells in electron microscopic immunocytochemistry and embedding.

Cell suspensions of rat anterior pituitaries were filtered with a polycarbonate filter (pore size 3 micron) and fixed on the filter. After fixation the cells were adherent to the filter and immunocytochemical staining could be accomplished by simply dipping the filter into the different incubation media. The cells could be dehydrated and embedded in Epon 812 on the filter. After polymerization the embedded filter was sawn into small blocks and the cell layer was sectioned tangentially on an ultramicrotome. This method also seems to be applicable to other histochemical studies on single cells.     

No correlation between binding of glucocorticosteroids to specific cytoplasmic proteins in vivo and enzyme induction in the rat liver.

Time- and dose-dependence of the formation of the different cytoplasmic hormone-protein complexes were studied in the rat liver after administration in vivo of [3H]cortisol or [3H]dexamethasone and compared with the stimulation of RNA polymerase B and induction of tyrosine aminotransferase and tryptophan oxygenase. No correlation could be found between formation in vivo of any of the five cytoplasmic hormone-protein complexes found and stimulation of RNA polymerase B activity or enzyme induction. After administration of [3H]cortisol, different metabolites of cortisol could be demonstrated in the isolated hormone-protein complexes. No time- or dose-dependence of the metabolite patterns could be observed after application of hormone doses that were in the range of the biologically active doses. After administration of [3H]dexamethasone, the same hormone-protein complexes were observed, which contained, however, the injected steroid instead of metabolites. These results seem to indicate that the cytoplasmic binding components present in the rat liver are enzymes involved in the metabolism of the glucocorticosteroids and that dexamethasone binds to these enzymes as a substrate analogue.     

Integrated State of Oncornavirus DNA in Normal Chicken Cells and in Cells Transformed by Avian Myeloblastosis Virus

The covalent linkage of oncornavirus-specific DNA to chicken DNA was investigated in normal chicken embryo fibroblasts (CEF) and in virus-producing leukemic cells transformed by avian myeloblastosis virus (AMV). The virus-specific sequences present in cellular DNA fractionated by different methods were detected by DNA-RNA hybridization by using 70S AMV RNA as a probe. In CEF and in leukemic cells, the viral DNA appeared to be present only in the nucleus. After cesium chloride-ethidium bromide density equilibrium sedimentation, the viral DNA was present as linear, double-stranded molecules not separable from linear chicken DNA. After extraction by the Hirt procedure, the viral DNA precipitated with the high-molecular-weight DNA. After alkaline sucrose velocity sedimentation, the viral DNA cosedimented with the high-molecular-weight cellular DNA. The results indicate that in both types of cells studied, the oncornavirus-specific DNA sequences were linked by alkali stable bonds to nuclear cellular DNA of high molecular weight and did not appear to be present in free form of any size.     

Changes in protein metabolism in brain neurons during the withdrawal syndrome in chronically alcoholized rats (histo-autoradiographic and interferometric research)

The incorporation of 3H-leucine into the neuronal proteins and cytochemistry of nuclear and cytoplasmic protein levels in pyramidal neurons in layer III, V of the sensomotor cortex and hippocampus of the brain were studied in rats which were exposed to chronic ethanol consumption at different stages of "the abolish syndrome". There were significant heterogeneous changes of the neuronal protein metabolism at all studied structures in the experimental group as compared to control group. It was shown that after abolishment of ethanol consumption the neuronal protein synthesis decreased and content of protein increased in the nucleus and cytoplasm of neurons. After 12 h there was elevated synthetic activity of protein system and tendency to reduction of content of protein in the nucleus. After 24 h reduction of synthetic activity and tendency to normalization of the content of the neuronal protein were found. The functional importance of the results obtained is discussed.