胃复春片对慢性胃病患者窦D细胞的影响

目的：探讨胃复春片治疗慢性胃病患者前后生长抑素内分泌细胞(D细胞)数量变化。方法：用免疫组化酶链亲合素过氧化酶复合技术(SABC)对患者治疗前后胃粘膜组织的D细胞染色，观察治疗前后D细胞的形态和数量变化。结果：经胃复春片治疗后，患者胃窦粘膜D细胞阳性数及强阳性率均明显下降，有显著意义。结论：胃复春片对慢性胃病患者生长抑素D细胞有调整作用。     

玉郎伞提取物对大鼠自发性高血压的影响

目的：研究玉郎伞提取物(YLS)对自发性高血压大鼠(SHR)及正常大鼠血压(BP)的影响。方法：应用颈动脉插管测压法，连接MS2000多媒体生物信号记录系统测定静注YLS前及药后20s、30s、lmin、2min、5min时的收缩压(SP)、舒张压(DP)、平均动脉压(MP)。结果：YLS使SHR及正常大鼠血压明显降低(P＜0．01)，降压作用维持时间较短，给药后5min血压基本恢复正常；YLS对去甲肾上腺素(NA)和异丙肾上腺素（ISO)的作用无明显影响。结论：YLS对正常大鼠及SHR血压有明显的降低作用。     

弱呼吸敏感电极研究

应用物理学，化学和工艺等方法，分别处理５种国内外敏感器，以组成相应呼吸敏感电极，结果显示，各种电极的气－电转换性能有明显改善，其中以上海复旦片性能达到弱呼吸敏感电极要求。     

抑郁症患者的血糖、血脂水平及其与症状关系的对照研究

目的了解抑郁症患者糖脂代谢的情况及其与精神症状的关系。方法以HAMD17和HAMA评定92例近期未服用精神药物的抑郁症患者的精神症状,了解他们简易体质参数、测定其空腹血糖和血脂,并与60例健康者组成的对照组进行比较。结果抑郁症组的甘油三酯(TG)、空腹血糖(FBS)值显著高于对照组(P＜0．001),而高密度脂蛋白胆固醇(LDL—ch)、载脂蛋白A1(ApoA1)值显著低于对照组(P＜0．01)；血浆总胆固醇(TC)、高密度脂蛋白胆固醇(HDL—ch)和载脂蛋白B(ApoB)两组之间无显著性差异(P＞0．05)；相关分析发现,抑郁症患者的HAMA总分、精神性焦虑因子分以及躯体性焦虑因子分与TG水平呈正相关(P＜0．01或P＜0．05)。结论抑郁症患者存在一定的糖脂代谢异常,临床医师应该对抑郁症患者的血糖、血脂进行监测,以便早期发现,早期治疗。     

踝关节软组织撞击综合征临床研究

目的:总结与探讨踝关节软组织撞击综合征发生的相关因素、关节镜下表现和组织病理学特点。方法:自2000年11月至2005年4月,本所共收治21例踝关节撞击综合征患者,其中男性16例,女性5例,平均年龄24·7岁。运动员7例,非运动员14例。左踝9例,右踝12例。对所有患者均进行关节镜探查,镜下切除造成撞击的组织,同时对其进行病理检查。结果:21例患者中有20例发生于踝关节扭伤后,其中16例为内翻伤。单纯前外侧撞击9例,单纯前内侧撞击2例,单纯外侧撞击1例,前内和前外撞击同时存在9例。关节镜下发现撞击组织为滑膜组织的20例,下胫腓前韧带远侧束5例,纤维瘢痕组织4例,距腓前韧带组织3例,半月板样组织3例。合并关节软骨损伤16例。病理检查确认造成撞击的组织为慢性炎症性滑膜组织、韧带组织、肉芽组织。半月板样组织病理表现为慢性滑膜炎或致密结缔组织伴软骨化生,或慢性滑膜炎伴肉芽组织形成。结论:踝关节软组织撞击综合征多发生在创伤后,尤其内翻伤后较常见。部位以踝关节前外侧多见,内侧也可发生。撞击组织以滑膜组织最常见,其次为下胫腓前韧带远侧束增厚、纤维瘢痕组织和损伤的距腓前韧带组织。软组织撞击部位与软骨损伤部位符合程度不显著(χ~2=2·524,P=0·112)。     

糖尿病性心血管病变与血清微量元素铁、铬、锰水平的相关性研究

本文研究糖尿病并发心血管病变时血清脂类、脂类过氧化产物与微量元素水平的相关性,结果发现:血清微量元素铁(Fe)与总胆固醇(T—ch)水平呈负相关,与水溶性荧光物质(WSFS)呈正相关;血清微量元素锰(Mn)与极低密度脂蛋白—胆固醇(VLDL—ch)呈负相关,与丙二醛(MDA)呈正相关;微量元素铬(Cr)与高密度脂蛋白—胆固醇(HDL—ch)呈正相关。提示:微量元素Fe、Cr、Mn为糖尿病性心血管病变的易患元素。     

术前静脉造影对静脉管壁及其吻合效应的实验研究

以动物实验模拟行静脉造影后,肉眼观察,并以透射电镜和扫描电镜动态观察经灌注固定的局部静脉管壁和内皮细胞的改变,发现造影剂回流的静脉管壁在较长的时间内处于扩张状态,同时穿刺注射造影剂的部位出现较严重的淤血和血栓形成。内皮细胞连接有较广泛裂开、剥离及内皮下组织暴露。在受损严重的区域还可见有微血栓形成。造影1天后内皮细胞受损最为严重,至第3天基本恢复。血管吻合实验表明,术前3天静脉造影不影响直径为2.5mm静脉的吻合通畅率。     

The Influence of Intramammary Lipopolysaccharide Infusion on Serum Ca,P, Vitamin D,Cytokines and Cortisol Concentrations in Lactating Sows

Ten multiparous lactating sows were used to investigate whether intramammary infusion of lipopolysaccharides (LPS; Escherichia coli 0111:B4; 2.0 μg/kg of body weight) would affect the circulating concentrations of Ca, P, 25‐hydroxyvitamin D (25‐OHD), tumour necrosis factor‐α (TNF‐α), interleukin‐6 (IL‐6) and cortisol. The sows were randomly allotted to either control group (control) or LPS‐treated group with five individuals per group and were infused with either physiological saline solution or LPS solution. The rectal temperature and udder quarter appearance were recorded at 0 (just before infusion), 1, 3, 7, 12 or 24 h after infusion. Blood samples were taken at 0, 1, 3, 7, 12 or 24 h after infusion. Before infusion, the rectal temperatures of all sows were below 39.2°C. At 3 and 7 h after infusion, the sows in the LPS group had a rectal temperature over 39.4°C. At 24 h after infusion, the rectal temperatures returned to pre‐infusion levels. Serum Ca and P concentrations in the LPS group decreased (P < 0.05) after LPS infusion compared with the control group at 1 h after infusion. No significant differences (P > 0.05) in the concentrations of 25‐OHD were observed between groups control and LPS at any sampling time. Increased (P < 0.01) concentrations of serum TNF‐α, IL‐6 and cortisol were observed in the LPS group compared with the control group at 3 and 7 h after infusion respectively. In conclusion, the elevation of serum concentrations of TNF‐α, IL‐6 and cortisol and the alterations of circulating concentrations of Ca and P following LPS infusion indicate that the immune system has been activated and immune activation may affect macromineral homeostatic regulation, which might have important implications for metabolic health of lactating sows. Lowered serum Ca and P following immune activation also shows a causative mechanism whereby immune activation increases the risk of secondary disorders such as mastitis‐metritis‐agalactia syndrome. However, immune activation did not affect circulating concentrations of vitamin D metabolites.     

重组2型腺相关病毒-转化生长因子β3对实验性肝纤维化大鼠肝脏组织病理学和Ⅰ型胶原表达的影响

Objective To investgate the effects of TGF β 3 on rat hepatic fibrosis. Methods The TGF β 3 cDNA was cloned into rAAV2 vector. Rats were randomly divided into four groups: normal control group, model group, negative control group and TGF β 3 group. Hepatic fibrosis was induced by hypodermic injection of 40% CCI4. Recombinant AAV2-TGF β 3 viral particles were injected via the vena caudalis one week before CCh treatment. Rats were executed 8 weeks after CCI4 treatment, global histological change was observed after HE staining, the distribution of the collagen fibers was observed after masson staining, his-tochemistry was done to observe the expression of collagen Ⅰ; The positive area rate of the collagen fibers and the average optical rate of collagen Ⅰ were quantified. Results HE staining indicated that collagen fibers were reduced in the TGF β 3 group. Masson staining shown that the collagen fibers were distributed around the blood vessel, in the portal area and disse space. Compared to the model group (13.2%±2.2%) and negative control group (12.3%±1.5%), the collagen fibers in liver tissues of TGF β3 group (7.7% ± 1.5%) were significantly decreased (q = 9.456, P < 0.01; q = 8.217, P < 0.01). Histochemistry indicated that the collagen fibers of liver tissues of TGF 15 3 group (0.185±0.033) were significantly higher than those in the model group (0.252±0.042) and the negative control group (0.230±0.029), (q = 6.228, P < 0.01; q = 4.346, P < 0.01). Conclusion TGF β 3 alleviates the damage to hepatic cell and the level offibrosis in CCI4 treated rats and inhibits the expression of collagen Ⅰ.     

左旋肉毒碱对人成骨细胞增殖和凋亡的影响

目的观察左旋肉毒碱(L-carnitine,L-C)对人成骨细胞增殖和凋亡的作用。方法以3H掺入法(3H-TdR)测定左旋肉毒碱对人成骨细胞增殖的影响;以吖啶橙/溴化乙啶染色和细胞凋亡ELISA(酶联免疫吸附法)试剂盒测定左旋肉毒碱对人成骨细胞凋亡的影响;以免疫印记法检测左旋肉毒碱干预前后活化型Caspase-3、-9蛋白质表达水平的改变。结果10~100mmol/L左旋肉毒碱能促进人成骨细胞增殖。吖啶橙/溴乙啶染色法示100mmol/L左旋肉毒碱干预使人成骨细胞凋亡细胞明显减少。ELISA结果示10~100mmol/L左旋肉毒碱干预可显著抑制人成骨细胞凋亡。10~100mmol/L左旋肉毒碱干预可抑制无血清饥饿诱导的人成骨细胞caspase-3、9活化增加。结论左旋肉毒碱促进人成骨细胞增殖,并通过下调Caspase-3、-9的活化抑制人成骨细胞凋亡。