Effect of “Re Du Qing” on the activation,proliferation and membrane fluidity of lymphocytes

Summary Effects of Chinese Medicinal Preparation “Re Du Qing” (RDQ) on the activation, proliferation and membrane fluidity of T lymphocytes from human peripheral blood Were studied by means of³H-TdR incorporation and DPH fluorescence polarization. The results showed that “RDQ” can:1) significantly inhibit the activation of T lymphocytes; 2) restrain the proliferation of activated T lymphoblasts in the presence of exogenous interleukin-2 (IL-2); and 3) increase the membrane fluidity of T lymphocytes and antagonize the decreased fluidity of lymphocyte membrane mediated by Con A or PHA. The functional abnormalities of T lymphocytes in some autoimmune diseases such as arthritis and the usefulness of RDQ in the treatment of these diseases were also discussed.     

氟康唑食管给药与静脉给药的药代动力学对比研究

目的:进行氟康唑食管给药与静脉给药的药代动力学研究。方法:采用HPLC法测定14名受试者静脉及食管给予氟康唑后经时血浓度,比较药代动力学参数及药物生物利用度变化。结果:两种给药途径,氟康唑主要药代动力学参数Cmax为(13.31±1.38)和(10.93±0.73)μg/ml,Tmax为(1.04±0.19)和(1.74±0.73)h,T1/2为(40.77±7.13)和(40.05±4.90)h,AUC为(271.09±30.48)和(261.93±32.60)μg/ml·h。食管给药生物利用度为(95.93±6.49)%,两种给药途径的生物利用度无统计学差异(P>0.05)。结论:食管给药是一种安全有效的给药方法。     

梗阻性黄疸引起肾脏病理学及超微病理学改变的实验与临床研究

作者对梗阻性黄疸（梗黄）大鼠及６例临床梗黄病人的肾脏组织进行了光镜和电镜观察。目的是描述肾脏损害的病理和超微病理改变，并试图从病理改变来探讨肾脏损害的可能病因及肾脏功能的改变。观察发现主要病变为肾小球萎缩，鲍曼氏囊间隙扩大，肾小球毛细血管基膜明显增厚，其三层结构消失，内有大量胆色素颗粒沉积，血管内皮窗孔明显减少，足突融合；近曲小管上皮细胞变性、坏死，胞质内有大量胆色素颗粒沉积，小管腔内可见脱落的坏死细胞、胆泥、胆栓及蛋白管型，微绒毛紊乱、稀疏、脱落，线粒体高度水肿，内质网扩张，脂滴、溶酶体明显增多。据此，我们认为：（１）梗黄可引起明显肾脏损害，其病变同时累及肾小球和肾小管，但以近曲小管病变为重；（２）胆汁成分于肾脏内的沉积在梗黄引起肾脏损害的发病中起一定作用；（３）梗黄可导致肾脏功能改变。     

左旋布比卡因蛛网膜下腔阻滞的进展

左旋布比卡因是一种新型的长效酰胺类局麻药,为麻醉中常用局麻药物布比卡因的左旋体.左旋布比卡因中枢神经系统和心脏毒性明显低于布比卡因,且具有儿乎与布比卡因相同的麻醉效能.长效局麻药用于蛛网膜下腔的安全性长期以来一直是麻醉学家关注的问题,近年来国内外已有很多学者对左旋布比卡因蛛网膜下腔的应用进行了大量研究.现就左旋布比卡因蛛网膜下腔阴滞的安全性、可行性和临床应用等方面的进展作一综述.     

Pharmacokinetics of intravenously administered sodium dichloroacetate in rabbits

ＰｈａｒｍａｃｏｋｉｎｅｔｉｃｓｏｆｉｎｔｒａｖｅｎｏｕｓｌｙａｄｍｉｎｉｓｔｅｒｅｄｓｏｄｉｕｍｄｉｃｈｌｏｒｏａｃｅｔａｔｅｉｎｒａｂｂｉｔｓＧｕＢｉｎ（顾斌）；ＳｏｎｇＬｉｎｇ（宋岭）；ＪｉａｎｇＹｏｎｇｐｅｉ（蒋永培）；ＷｅｎＡｉｄｏｎｇ（文...     

伽玛刀治疗垂体大腺瘤临床分析(附30例报告)

目的 研究伽玛刀治疗垂体大腺瘤的效果及影响疗效的因素。方法 30例垂体大腺瘤病人用1．0T磁共振定位，Gamma-plan计划系统规划，等剂量曲线45％～60％(平均49．7％)，周边剂量12～35Gy(平均22.9Gy)，中心剂量24～70Gy(平均45．4Gy)．Leksell伽玛刀实施放射外科治疗。分析治疗后垂体大腺瘤病例，总结其疗效和影响疗效的因素。结果 随访12～60个月，平均28个月，肿瘤完全消失6例(20％)，肿瘤缩小19例(63．3％)，无变化5例(16．7％)；19／20(95．5％)功能性垂体腺瘤内分泌症状改善，临床症状好转，1例过早绝经(年龄36岁)；5／10(50％)无功能性垂体腺瘤体积缩小．症状改善。结论 伽玛刀对于垂体大腺瘤仍是一种有效的治疗方法，其疗神与腺瘤的举类型、体积、照射剂量、剂量体剂、MRI信号特征密切相姜。     

局麻下深龋充填对成人牙科畏惧症的影响

目的　探讨局麻下深龋充填对成人牙科畏惧症的影响。方法　采用Corah’s牙科畏惧症评分法 ,筛选出 10 0例需深龋充填的DF成人患者 ,分为实验组与对照组。实验组在局麻下行深龋充填术 ,对照组则为常规的牙科治疗。结果　实验组DF程度明显降低 ,与治疗前以及对照组比较都有显著性差异 (P <0 .0 1)。牙科治疗过程中两组脉搏的变化有显著性差异 (P <0 .0 1)。结论　局麻下行深龋充填术 ,对成人牙科畏惧症有治疗作用     

非同位素PCR方法检测脆性X 综合征FMR-1基因CGG重复序列数目

目的 建立一种可靠、简便的非同位素PCR方法检测脆性X综合征的突变基因。方法 采用生物素标记的CGG寡核苷酸探针，检测通过PCR扩增的FMR-1基因中CGG三核苷酸重复序列数目。从而判断所检样品中FMR—1基因是否正常。结果 该法可检测出正常人及携带者的CGG重复拷贝数。结论 该方法可以简便、安全、可靠地检测FMR—1基因中(CGG)n重复拷贝数，从而确定为正常人或携带者，可作为临床上筛查脆性X综合征的首选方法。     

山东产四种菟丝子免疫增强作用的比较研究

目的 比较山东产四种菟丝子对小鼠免疫功能、抗疲劳、耐缺氧等方面的作用。方法 选用昆明种小鼠，用山东产四种菟丝子的水、醇提取物灌胃，观察小鼠腹腔巨噬细胞吞噬功能、免疫器官重量的变化、游泳实验和耐缺氧等指标。结果 山东产四种菟丝子均可增加小鼠吞噬百分率，使幼龄小鼠的胸腺和脾脏增重，并可显著延长小鼠的游泳及缺氧存活时间。其中以菟丝子和南方菟丝子的作用较好，水提取物的作用优于醇提取物。结论 山东产四种菟丝子具有增强机体免疫功能、抗疲劳、耐缺氧作用。菟丝子中的多糖是其提高机体免疫力，增强体质的有效物质之一。     

In vitro differentiation of human adipose-derived adult stromal cells into neuron-like cells in hippocampal astrocyte conditioned medium

BACKGROUND: At present, researches on differentiating from human adipose-derived adult stromal cells (hADASC) to neuron-like cells are focus on inducing by artificial-synthetic compound solution; however, hippocampal astrocyte conditioned medium (HCAM) can induce in vitro differentiation from hADASC to neuron-like cells is still unclear. OBJECTIVE: To observe whether HCAM can induce in vitro differentiation from hADASC to neuron-like cells. DESIGN: Randomized control study. SETTING: Department of Neurology, Taixing People's Hospital; Central Laboratory, North China Coal Medical College. MATERIALS: Donor of adipose tissue was donated by female volunteers suffering from caesarean section in the department of obstetrics & gynecology in our hospital and aged 20－35 years. Adipose tissue was collected from subcutaneous tissue of abdomen during the operation. In addition, 8 male newborn Wistar rats within 24 hours with average body mass of 20 g were provided by Animal Institute of Chinese Academy of Medical Sciences. Rabbit-anti-human Nestin polyclonal antibody, rabbit-anti-human glial fibriliary acidic protein (GFAP) polyclonal antibody, rabbit-anti-human neuro-specific enolase polyclonal antibody and mouse-anti-human microtubal associated protein 2 (MAP-2) polyclonal antibody were provided by Wuhan Boster Company. METHODS: The experiment was carried out in the Central Laboratory of North China Coal Medical College from October 2004 to June 2005. hADASC was cultured with HCAM and its growth and morphological changes were observed under inverted phase contrast microscope. Immunocytochemistry, immunofluorescence and Western blotting were used to evaluate the expressions of Nestin, which was a specific sign of nerve precursor, neuro-specific enolase and MAP-2, which was a specific sign of nerve cell, and GFAP, which was a specific sign of neuroglial cells. MAIN OUTCOME MEASURES: Nestin, which was a specific sign of nerve precursor, neuro-specific enolase and MAP-2, which was a specific sign of nerve cell, and GFAP, which was a specific sign of neuroglial cells. RESULTS: On the 3rd day of culture, partial hADASC started deformation from slender shuttle-shape cells to neuron-like cells. It suggested that cells stretched out apophysis, which were mainly double-pole or multiple-pole cells. Five days later, immunohistochemical detection suggested that expression of Nestin (10.5±0.037) was found out in cells; meanwhile, expressions of GFAP (38.4±0.052) and neuro-specific enolase (NSE) (15.7±0.023) were also found out in cells; however, expression of MAP-2 was not observed. Western blot indicated that, 5 days after effect of HCAM, Nestin was found out in hADASC; meanwhile, expressions of GFAP and neuro-specific enolase were also found out; however, expression of MAP-2 was not observed. CONCLUSION: HCAM can induce the differentiation from hADASC to neuron-like cells in vitro.