活血化瘀法治疗慢性胃炎68例临床研究

我们从2001年以来，采用活血化瘀法治疗慢性胃炎，经多年的临床研究观察，获得显著疗效。现总结如下。     

新时期医院的职业道德建设

现代社会市场竞争日趋激烈，对从业人员职业观念、职业态度、职业技能、职业纪律和职业作风的要求越来越高。加强卫生行业职业道德建设是落实“三个代表”重要思想的具体要求，又是社会主义精神文明建设的重要内容，更是纠正行业不正之风的治本之策。全面贯彻“以德治国”的方略，努力形成与社会主义市场经济发展相适应的医学职业道德观念业已成为医院管理的一项重要任务。     

雄性大白鼠球海绵体肌和坐骨海绵体肌的运动神经元—HRP法研究

本实验用HRP注射于大白鼠的一侧球海绵体肌和坐骨海绵体肌后,在脊髓腰骶段的不同平面可观察到支配该两肌的运动神经元胞体出现标记并具有一定的局部定位关系。支配球海绵体肌的运动神经元主要位于L_5～S_1的背内侧群,而支配坐骨海绵体肌的运动神经元主要位于背外侧群和腹侧群。本文认为大白鼠腰骶段前角背内侧群和背外侧群同腹外侧群细胞一样,同属于Onuf's核的同源神经细胞。本文还观察了大白鼠腰骶段脊髓前柱细胞的配布。     

乌蛇败毒胶囊对接触性皮炎小鼠血清IL-2、TNF-α的影响

目的探讨乌蛇败毒胶囊治疗湿疹的机理。方法采用变应性接触性皮炎小鼠模型,分为模型组,对照组及大、中、小剂量组和空白组,观察各组治疗前后血清IL-2、TNF-α的变化。结果中药组能明显降低模型小鼠血清中IL-2、TNF-α的含量(P<0.01),降低诱发后鼠耳的肿胀度,减少真皮内单一核及多形核白细胞数目(P<0.01)。结论乌蛇败毒胶囊治疗湿疹的部分机理是抑制小鼠Ⅳ型变态反应、降低血清IL-2,TNF-α含量,减轻炎症损伤。     

胸腹水中唾液酸含量在鉴别良恶性疾病上的价值

本文测定恶性、炎性和肝硬化3组胸腹水中的总唾液酸(TotalSialic Acid TSA)和脂质结合唾液酸(Lipid-bound Sialic Acid LSA)含量,结果表明恶性组和炎性组的 TSA 和 LSA 明显高于肝硬化组,但恶性组和炎性组的 TSA 和 LSA 则无明显差异。恶性、炎性和肝硬化组的 TSA 值分别为499.52±183.98mg/L、508.68±208.79mg/L 和117.71±70.46mg/L;LSA则分别为146.28±103.62mg/L、115.26±72.13mg/L 和58.90±35.46mg/L。以肝硬化组的 TSA+2SD 作为恶性组和肝硬化组的鉴别值,其敏感性为88%,特异性为90.47%,有效性为89.13%。LSA 则无鉴别价值。     

大骨节病儿童手部X线征与年龄的关系

本文分析了2800例4～13岁大骨节病儿童掌指骨X线病变与年龄的关系,结果表明手部掌指骨干骺端X线征随年龄增加而趋于下降,骨端、骨骺、腕骨X线征的类型与检出率则随年龄而呈上升趋势,反映出大骨节病关节病变的范围有随年龄增长而扩大和增重的趋势。     

视网膜下液对培养的人视网膜色素上皮细胞、神经胶质细胞及成纤维细胞生长的刺激作用

目的:研究视网膜下液(subrefinal fluid,SRF)对增殖性玻璃体视网膜病变(proliferativeVitreoretinopathy，PVR)的多种细胞增殖的影响. 方法；采用直接细胞计数和_³H-TdR掺入率测定DNA合成两种方法观察28例孔源性视网膜脱离患者SRF对培养的人视网膜色索上皮(retinal pigment epithelium，RPE)细胞，视网膜神经胶质(retinal glia，RG)细胞及成纤维细胞(flbroblast，FB)生长刺激作用． 结果：所有标本均具有刺激RPE细胞、RG细胞及FB增殖和DNA合成能力，增殖率范围分别在基线上52.5%～233.3%、36.4%～177.8%、55.4%~277.8%之间．SRF促细胞增殖串在三种细胞间比较无显著差异。 结论：SRF具有促多种细胞增殖的能力，推测SRF中含有促细胞增殖的活性物质。 （中华眼底病杂志，1996，12：233-235）     

Evolution of North American PVYNTN Strain Tu 660 from Local PVYN by Mutation rather than Recombination

A North American (NA) isolate of tobacco veinal necrotic strain of Potato virus Y (PVY^N) (N-Jg) and a NA isolate of potato tuber necrotic strain of Potato virus Y (PVY^NTN) (Tu 660) were tested for their phenotypes by inoculation to potato plants of three potato cultivars. Upon inoculation with Tu 660, tubers of the cultivars Norchip and Ranger Russet developed potato tuber necrotic ringspot disease (PTNRD) but not the tubers of Russet Burbank. N-Jg failed to induce PTNRD in the tested cultivars. The genomic RNAs of both strains were completely sequenced and analysed. High homology (98% and 99% identity on nucleotide and polyprotein, respectively) was found between Tu 660 and N-Jg. When polyproteins were compared with other isolates, high identity was observed between Tu 660 and an European (Eu) PVY^N-605 (98%) and with an Eu-PVY^NTN-H (96%). However, when individual mature proteins were compared, much lower identities (86.5–94%) were found between Tu 660 and PVY^NTN-H compared to 98–99.5% between Tu 660 and PVY^N-605 in the P3, 6K1 and CI regions. Further sequence analysis indicated that the PVY^NTN-H is a hybrid molecule of the genomic RNA recombination of PVY^O and Eu-PVY^N as shown by Glais et al. (Arch Virol 147, 363–378), whereas NA-PVY^NTN Tu 660 is free of recombination points. Phylogenetic analysis confirmed this observation, and suggested that, in light of high homology, the Tu 660 might have evolved from NA-PVY^N by mutations rather than the genome recombinations. The non-recombinant nature of NA-PVY^NTN Tu 660 strongly suggests that the recombinant structure of genome is not a necessary prerequisite for the PTNRD phenotype.     

Distinct expression and localization of serine protease HtrA1 in human endometrium and first-trimester placenta.

Mammalian embryos cannot survive without the placenta. Development of the human placenta requires trophoblast proliferation, differentiation, and invasion as well as highly coordinated modulation of the maternal uterus. HtrA1 is a member of the recently identified mammalian HtrA (high temperature requirement factor A) serine protease family with a high level of expression in the placenta. In this study, we examined whether HtrA1 expression (mRNA and protein) is associated with placental development in the human. HtrA1 is up-regulated in both endometrial glands and decidual cells during endometrial preparation for embryo implantation and during first-trimester pregnancy at placentation. HtrA1 expression was also detected in certain trophoblast subtypes during early pregnancy. The villous syncytiotrophoblast and cytotrophoblast showed the strongest expression while the interstitial extravillous trophoblast showed the lowest or no expression of HtrA1. The distinct distribution of HtrA1 at the maternal-trophoblast interface suggests that HtrA1 may play a role in placental development.