普通额镜下鼻内激光泪囊鼻腔造孔术治疗慢性泪囊炎

报告在普通额镜下以YAG激光经鼻腔行泪囊鼻腔造孔术，治疗慢性泪囊炎患者37例（45眼），经3～24个月的随访观察，泪道阻塞均解除，有效率为95．6％，治愈率为88．9％。本手术具有损伤小，操作简便，快捷，术后反应轻，并发症少等优点。并对手术方法及影响疗效的因素进行了探讨。     

中药“二黄”滴耳剂治疗急慢性化脓性中耳炎的临床观察(附1000例分析)

本文总结了“二黄”滴耳剂治疗急慢性中耳炎1000例，结果表明总有效率为89％，尤其对急性化脓性中耳炎效果更为明显，与其它抗生素相比具有很多优点。抗菌谱广，对革兰氏阳性菌及革兰氏阴性菌、病毒都有一定作用，低浓度抑菌，高浓度杀菌，不易产生抗药性及过敏反应，对第八对脑神经无毒性，价格低廉应用方便优于任何一种抗生素。     

声门上型喉癌临床N_0病理转移的观察

目的：为探讨喉癌颈淋巴结转移的规律，选择手术方法。方法：采用１１０例临床Ｎ０声门上型喉癌的１６４侧颈廓清术标本淋巴结连续切片方法观察。结果：发现颈淋巴结转移率为３５．５％（３９／１００）。提出临床Ｎ０病理转移的特点：１）转移淋巴结大小大多数介于０．５～１．５之间占８４．２％。２）转移淋巴结大多数为早期侵入期和生长发展期占８６．０％。３）转移淋巴结绝大多数为单发型占７４．４％。４）各个Ｔ分期均有转移淋巴结。结论：在颈淋巴结处理上，我们支持尽可能同期行选择性颈廓清术的观点     

HPLC法测定黄芪炮制品中黄芪甲甙含量

建立了测定黄芪甲甙的ＨＰＬＣ法，采用Ｃ_１８柱，流动相为乙腈水（１∶２．３），检测波长为２０３ｎｍ。用此法对黄芪６种炮制品中黄芪甲甙的含量进行了对比研究。     

ODC反义寡核苷酸对K562细胞生长抑制作用

鸟氨酸脱羧酶(ornithine decarboxylase,ODC)是催化多胺生物合成的限速酶.过去的研究表明多胺在维持肿瘤恶性表型中起着重要作用.用ODC不可逆抑制剂抑制多胺生物合成不仅能抑制肿瘤细胞的增殖而且还诱导细胞分化.近年我们采用反义技术,以ODC反义RNA转染肿瘤细胞,通过对ODC表达的封闭,成功地使其恶性表型得到了逆转.提示抑制肿瘤细胞的多胺合成可能是抗癌的有效途径.本文用ODC反义寡核苷酸控制肿瘤细胞的多胺生物合成,观察了其对K562细胞生长特性的影响,以期为ODC反义寡核苷酸在肿瘤临床的应用提供实验依据.     

Antivirus effect of polysaccharides of brewer yeast in vitro]

The antivirus effect of polysaccharides of brewer yeast from yeast mud on 13 kinds of viruses including DNA and RNA virus along with their mechanisms were studied. The result showed that this effect was remarkable on the infections with poliovirus III, adenovirus III, ECHO6 virus, enterovirus 71, vesicular stomatitis virus, herpesvirus I, II, coxsackie A16 virus and coxsackie B3 virus. The polysaccharides of brewer yeast could also inhibit the development of cytopathic effect(CPE) and protect cultural cells from being infected with the above viruses.     

EB病毒VCA-IgA抗体水平与鼻咽癌病人远期疗效关系

目的：分析ＥＢ病毒血清学ＶＣＡ－ＩｇＡ抗体与鼻咽癌病人远期疗效关系，为临床治疗提供参考依据。方法：１９８５年本院病理确诊的５２２例鼻咽癌病人，按治疗前、后ＶＣＡ－ＩｇＡ抗体滴度分为三组：低滴度组（１：５～１：２０）、中滴度组（１：４０～１：８０）和高滴度组（１：１６０以上），随访１０年，比较生存率的异同。结果：治疗前鼻咽癌病人高滴度组１０年生存率低于低滴度组（Ｐ＜０．０５），但和中滴度组差别无显著性（Ｐ＞０．０５）。治疗后三组病人１０年生存率比较，高、中滴度二组差别无显著性（Ｐ＞０．０５），但低于低滴度组。结论：ＥＢ病毒ＶＣＡ－ＩｇＡ抗体水平可以作为估计预后的重要参考依据，与远期疗效有密切关系。     

云南玉溪地区甲型副伤寒沙门菌的耐药性变迁

目的了解本地区甲型副伤寒沙门菌对几种临床常用药物的耐药现状,重点讨论培氟沙星的耐药性变迁。方法就本院1999年1月至2004年8月从患者临床标本中分离的2335株甲型副伤寒沙门菌,对几种临床常用抗菌药物的药敏试验结果作动态分析。结果甲型副伤寒沙门菌对培氟沙星的耐药率已由1999年的0上升到2004年的98.1%(P<0.01),MIC90≥4mg·L-1;头孢噻肟、头孢他啶、头孢西丁、亚胺培南、呋喃妥因以及复方磺胺甲口恶唑的耐药率均相对较低,MIC90分别为≤4、8、4、4、32和10mg·L-1。结论甲型副伤寒沙门菌对培氟沙星的耐药率上升迅速;临床需加强对氟喹诺酮类药物的合理使用。     

不同来源的N-乙酰神经氨酸裂合酶的特性及在大肠埃希菌中的表达

综述了N-乙酰神经氨酸裂合酶的特性、应用及反应机理，对不同来源的N-乙酰神经氨酸裂合酶进行了比较。简要阐述N-乙酰神经氨酸裂合酶在大肠埃希菌中的克隆表达及其纯化。     

Intracerebral transportation and cellular localisation of insulin-like growth factor-1 following central administration to rats with hypoxic-ischemic brain injury

Insulin-like growth factor-1 (IGF-1) has been shown to be neuroprotective when administered centrally following hypoxic-ischemic (HI) brain injury. However, the cerebral distribution and site of action of IGF-1 after intracerebroventricular (i.c.v.) administration are not known. A unilateral HI brain injury was induced in adult rats by a modified Levine method. Either 3H-IGF-1 alone, or in combination with unlabelled IGF-1, was administered into the lateral ventricle 2 h after injury. The activity of 3H-IGF-1 signal in the potentially injured cortex was compared between two treatment groups using image analysis. The regional distribution and cellular localisation of 3H-IGF-1 were examined autoradiographically in potentially injured hemispheres at 0.5 and 6 h after administration. Tritiated IGF-1 was detected predominantly in the pia mater, perivascular spaces and subcortical white matter tracts 0.5 h after administration and decreased by 6 h (p<0.05). The signals associated with the perivascular spaces and pia mater were not blocked by unlabelled IGF-1, suggesting non-saturable binding in these brain areas. IGF-1 signal was co-localised with IGF binding protein (IGFBP)-2 immunostaining in the white matter tracts where the signal was blocked by unlabelled IGF-1, suggesting competitive association. IGF-1 signal associated with neurons and glia was maximal in the cerebral cortex and less in the CA1-2 subregion of the hippocampus which were blocked by unlabelled IGF-1 (p<0.05). The signals from cortical neurons did not decrease 6 h after administration, suggesting specific and persistent binding to these cells. Our results indicate that centrally administered IGF-1 can be translocated to neurons and glia via the perivascular circulation and the ependymal cell-white matter tract pathways.