心理社会因素在糖尿病发生过程中的作用及机理研究 Ⅳ.Ⅱ型糖尿病发生的危险因素分析

目的：分析影响人类Ⅱ型糖尿病发生的危险因素，比较心理社会因素及生物因素的影响程度。方法：对１３１名糖耐量低减和９１名糖耐量正常者平均追踪１８个月，对影响血糖变化和发生糖尿病的人群的社会心理因素及某些生理因素进行Ｌｏｇｉｓｔｉｃ回归分析和相关分析。结果：在对正常转糖耐量低减的回归分析中，年龄和体重指数的影响最大；但在正常和糖耐量低减转糖尿病的两个回归分析中，生活事件强度的贡献量均排在第１位。结论：心理社会因素在一定的生理条件下对糖尿病的发生起作用，其环节可能在糖耐量低减转糖尿病过程。     

腰椎体椎间盘的粘弹性性质实验研究

本文重点讨论人体湿润新鲜尸体腰椎体椎间盘的粘弹性性质，实验在不同应变率下测定它的变形规律，以及椎间盘的蠕变，松弛特性，加载与卸载的变化。     

人胰岛微血管和A细胞的微机三维重建

采用微机辅助三维重建的方法重建了人胰岛的微血管的A细胞，结果表明，所使用的软件重建速度快，图像速真，清晰度高，视觉效果好，可对重建物体进行多角度，多轴旋转，也可进行任何部位的切割，以便能进一步了解胰岛内各结构的详细情况，为进一步研究胰岛内微血管和细胞的立体位置关系提供方法学基础。     

示指血管神经的断面观测

用２７个成人示指作组织切片后，选取近侧、中间和远侧指横纹及相邻横纹１／２处的横断面切片，对指掌侧固有动脉、静脉和神经的位置、形态进行了观测。     

周围神经压迫症动物实验模型的制备

本文介绍大白鼠坐骨神经压迫症动物模型的制备和初步应用,以期为周围神经压迫综合症的深入研究提供一个较理想的动物实验模型。     

脂质体介导Neo R和Lac Z双标志基因共转导原代造血细胞及其表达的研究(英文)

在介导体内外基因转移方面,脂质体已显示出许多优于病毒载体的特征.然而,有关脂质体介导造血细胞基因转移的报道很少.本文描述了脂质体介导双标志基因(Neo~R和Lac Z)在体外共转移进入人及小鼠原代造血细胞的研究.基因转移的效率通过X-gal染色及观察集落的形成来评价.结果显示,在存在G418的体系中,转导细胞能够存活并形成集落,而未转导细胞则不能存活.同时,转导阳性细胞能够被X-gal染成蓝色.其蓝染阳性细胞率在人及小鼠造血细胞于G418选择前分别为13.33± 2.68%和16.28± 2.95%.经G418选择启分别达到46.06±3.47%及43.45±4.1%,显著高于筛选前(P<0.01).提示,利用脂质体这一简单、安全的转导策略在原代造血细胞可获得高效的基因转移及稳定的表达.同时,共转导双标志基因进入造血细胞可用作高集转导阳性细胞.这一结论对于临床进一步探讨造血重建的生物学特征、追踪白血病的复发机制以及利用造血细胞作为靶细胞进行基因治疗的研究提供了实验依据.     

近端联合远端收肌管阻滞在全膝关节置换术患者术后镇痛和早期功能康复中的应用

目的 探讨近端联合远端收肌管阻滞在全膝关节置换术患者术后镇痛和早期功能康复中的应用。方法 选取2019年1月至2020年12月在解放军总医院第六医学中心择期行单侧全膝关节置换术患者90例,按随机数字表法分为3组,每组30例。A组为对照组,于超声引导下行股神经联合腘窝上坐骨神经阻滞;B组为近端联合远端收肌管阻滞组,于超声引导下分别行收肌管近端和远端阻滞;C组为右美托咪定联合收肌管阻滞组,于超声引导下将罗哌卡因与右美托咪定混合液分别注射至收肌管近端和远端。比较3组患者术后6 h(T₁)、12 h(T₂)、24 h(T₃)和48 h(T₄)时静息VAS评分,术后T₃和T₄时运动VAS评分,48 h内羟考酮和氟比洛芬酯使用情况;以及术后24 h(T₃)、48 h(T₄)和72 h(T₅)膝关节活动范围(ROM)和股四头肌肌力;记录3组患者术后首次直腿抬高≥10 cm时间,术后首次下床活动时间,术后7...     

Duration of improved muscle glucose uptake after acute exercise in obese Zucker rats

Skeletal muscle is insulin resistant in the obese Zucker rat. Endurance training reduces muscle insulin resistance, but the effects of a single acute exercise session on muscle insulin resistance in the obese Zucker rat are unknown. Therefore, insulin responsiveness of muscle glucose uptake was measured in 15-week-old obese rats either 1, 48, or 72 hours after two hours of intermittent exercise (30:30 min; work:rest). Hindlimbs of sedentary lean (LS) and obese (OS) rats and exercised obese (OE) rats were perfused after a 10-hour fast under both basal (0 mU x ml(-1)) and maximal (20 mU x ml(-1)) insulin concentrations to measure net glucose uptake. Insulin responsiveness of net glucose uptake was significantly reduced in OS compared to LS (8.5 +/- 1.6 vs 15.3 +/- 2.0 micromol x g(-1) x h(-1), respectively). Compared to OS, insulin responsiveness of net glucose uptake was significantly increased by 56% and 80% at 1 hour and 48 hours after acute exercise. However, 72 hours after acute exercise, the increased insulin responsiveness of net glucose uptake was no longer evident. These results indicate that improved responsiveness of muscle glucose uptake persists for at least 48 hours after two hours of acute intermittent exercise in 15-week-old obese Zucker rats.     

Biotransformation of lovastatin--III. Effect of cimetidine and famotidine on in vitro metabolism of lovastatin by rat and human liver microsomes

The effects of the H2-receptor antagonists, cimetidine and famotidine, on the microsomal metabolism of [14C]lovastatin were investigated. Liver microsomes were prepared from control, phenobarbital- and 3-methylcholanthrene-pretreated rats and humans (male and female). Concentration-dependent inhibition of the metabolism of lovastatin (0.1 mM) was observed with cimetidine (0.1 to 1.0 mM). In contrast, famotidine at a similar concentration was a very weak inhibitor. The formation of 6'beta-hydroxy-lovastatin, the major microsomal metabolite of lovastatin, was similarly inhibited. The results suggest that in vivo metabolic interaction with concomitantly administered lovastatin is less likely with famotidine than with cimetidine. Phenobarbital pretreatment produced 58% stimulation in overall metabolism, whereas 3-methylcholanthrene pretreatment had no effect relative to control rats (5.4 nmol/mg protein/min). Liver microsomes from phenobarbital-pretreated rats produced 67% more of the 6'beta-hydroxy-lovastatin but 63-66% less of the 3'-hydroxy and 6'-exomethylene metabolites. Liver microsomes from 3-methylcholanthrene-treated rats also produced less 3"-hydroxy-lovastatin (49%) but similar quantities of the other two metabolites. 6'beta-Hydroxy-lovastatin was a major metabolite with human liver microsomes. Interestingly with these microsomes, hydroxylation at the 3'-position of the molecule was a negligible pathway and hydrolysis to the hydroxy acid form was not observed. The formation of 6'-exomethylene-lovastatin was also catalyzed by human liver microsomes (0.5 to 0.8 nmol/mg protein/min).     

经络轨迹的叩击、电阻、电流综合检测实验研究

<正> 应用多种方法对经络的循行路线进行了检测和显示,证明其行程与古典的经络路线基本一致,结果稳定,可重复。但是,显性感传的经络现象在人群中只占25％左右,而人群中大多数是属于隐性感传,应用生物物理学方法已观察到皮肤低电阻点(穴位)循