双歧三联活菌胶囊联合美沙拉嗪对 溃疡性结肠炎患者肠道微生态影响

目的探讨双歧三联活菌胶囊联合美沙拉嗪肠溶片对溃疡性结肠炎(ulcerative colitis,UC)患者肠道微生态的影响。方法选取2015年1月至2017年4月我院内科门诊治疗的活动期轻中度UC患者78例,随机分为观察组和对照组。两组均给予口服美沙拉嗪肠溶片1.0 g/次,4次/d。观察组在此基础上加以双歧三联活菌胶囊420 mg/次,3次/d,口服,两组均连用8周。比较两组治疗前后肠道菌群中乳杆菌、双歧杆菌、大肠埃希菌数量的变化和双歧杆菌(B)与大肠埃希菌(E)的比值变化,并评估两组治疗后临床效果。结果治疗前两组乳杆菌、双歧杆菌与大肠埃希菌及B/E比值比较,差异无统计学意义(P0.05)。治疗8周后,两组双歧杆菌、乳杆菌数量及B/E比值明显上升(P0.01),大肠埃希菌数量下降(P0.05),但观察组变化幅度更大(P0.05),且总有效率较对照组更高(χ2=4.13,P0.05)。结论双歧三联活菌胶囊联合美沙拉嗪肠溶片可治疗UC,能调节肠道菌群紊乱,重建肠道微生态平衡。     

散居型西藏飞蝗九个地理种群形态特征的数量分析

为阐明西藏飞蝗Locusta migratoria tibetensis Chen散居型地理种群数量性状的地理变异,将散居型西藏飞蝗9个地理种群雌、雄个体的前翅长度(E)、后足股节长度(F)、头宽(C)、前翅长度与后足股节长度比值(E/F)、后足股节长度与头宽比值(F/C)5项形态特征参数进行系统聚类分析和主成分分析....     

毛蕊花苷对递增负荷运动小鼠骨骼肌损伤的保护作用

本研究采用小鼠跑台训练模型,应用免疫共沉淀等方法,研究毛蕊花苷对递增负荷运动小鼠骨骼肌损伤的保护作用及对谷胱甘肽的影响。90只小鼠随机分为:正常对照组(A)、正常+毛蕊花苷组(B)、单纯运动组(C)、运动+毛蕊花苷低剂量组(D)、运动+毛蕊花苷中剂量组(E)、运动+毛蕊花苷高剂量组(F).结果表明:与C组比较,D、E、F组小鼠骨骼肌损伤程度依次减轻,F组小鼠骨骼肌形态基本正常。F组小鼠血浆CK水平、骨骼肌组织GSSG含量分别低于C、D、E组;但CK水平高于A、B组,均P0.01;GSSG含量与A、B组比较,差异无显著性,P0.05。F组小鼠骨骼肌组织GSH含量、GSH/GSSG比值、GCL和GR酶活性、RyR1复合物中GSH表达水平分别高于C、D、E组,但低于A、B组,均P0.01。研究结果提示毛蕊花苷能降低递增负荷运动小鼠血浆CK的活性,保护运动鼠骨骼肌的形态;其机理与其提高运动鼠骨骼肌组织GSH含量和GCL、GR酶的活性,降低GSSG/GSH比值;提高RyR1复合物中GSH表达水平有关。     

吉林东部天然林林下光质分布特征

天然林林下光质对乔木幼苗以及灌草的组成与更新具有重要的生态学意义。但目前对于林下光质的研究仍然有限。以吉林东部地区天然林为例,通过调查乔木数据和林下光质数据,基于移动窗口法分析不同空间尺度森林冠层结构与林下光质的关系。结果表明：不同林型下红光光子通量密度(R)与蓝光光子通量密度(B)存在差异。其中沙松-千金榆-花楷槭混交林林下蓝光光子通量密度最小,而沙松-紫椴-臭冷杉混交林和长白落叶松纯林林下最大。随着尺度的增大,天然林乔木胸高断面积与R/PFD(红光/光子通量密度比值)和B/PFD(蓝光/光子通量密度比值)的比值呈显著正相关(P<0.05)。并且随着尺度的增加,相关系数总体逐渐增大,在35m处达到峰值。在此基础上在南向、东向和西向各延伸10m时呈现显著正相关(P<0.05)。在该尺度下分析优势树种对林下R/PFD和B/PFD比值的影响时发现：R/PFD与B/PFD比值随着针叶林胸高断面积的增加而增加。相对于阔叶林来说,多数林型针叶林下的冠层结构与林下R/PFD和B/PFD比值之间显著正相关(P<0.05)。在不同树种下,乔木冠层结构对R/PFD和B/PFD比值的影响...     

肱动脉内皮依赖性舒张功能鉴别左室舒张功能假性正常化的价值

目的:研究冠心病患者左室舒张功能假性正常化与肱动脉内皮依赖性舒张功能的关系。方法:将75例行选择性冠状动脉造影的患者按冠状动脉病变程度分为单/双支病变组和三支病变组两组,选取48例健康志愿者作为对照组。检测左室舒张功能指标二尖瓣口血流频谱E峰、A峰、E/A比值,同时观察休息时肱动脉反应性充血后内径变化率。结果:单/双支病变组(第一组)E峰、E/A比值下降,肱动脉反应性充血后内径变化率低于正常对照组(P<0.05);三支病变组(第二组)E峰、E/A值无明显改变,肱动脉反应性充血后内径变化率明显低于对照组(P<0.01)。结论:肱动脉内皮依赖性舒张功能可作为鉴别冠心病左室舒张功能假性正常的指标。     

妊娠期高血压患者血清热休克蛋白70水平与心功能及免疫球蛋白的关系研究

目的:探究妊娠期高血压患者血清热休克蛋白70(HSP70)水平与心功能及免疫球蛋白的关系。方法:选择2017年4月至2018年4月在陕西省人民医院诊治的200例妊娠期高血压患者作为妊娠期高血压组,同时选择同期在我院进行孕检的200名健康孕妇作为对照组。采用酶联免疫吸附法检测血清HSP70水平,采用全自动生化分析仪检测免疫球蛋白G(Ig G)、免疫球蛋白M(Ig M)、免疫球蛋白A(Ig A)、免疫球蛋白D(Ig D)和免疫球蛋白E(Ig E)水平,采用多普勒超声心动图监测两组的左心室后壁厚度(LVPWT)、左心室舒张末期内径(LVEDD)和室间隔厚度(IVST)、左心室收缩末期内径(LVESD)、左心室射血分数(LVEF)和每搏指数(SVI),计算左心室质量(LVM)、二尖瓣舒张早期血流速度峰值与二尖瓣环侧壁舒张早期运动峰速度的比值(E/Em)、舒张早期与舒张晚期血流速度峰值的比值(E/A)。采用spearman相关性分析血清HSP70水平与血清免疫球蛋白水平及心功能指标的相关性。结果:与对照组相比,妊娠期高血压组的血清HSP70水平明显升高,而Ig G和Ig M水平明显下降,并且LVESD、LVEF、E/A也明显下降(P0.05)。血清HSP70水平与Ig G、Ig M、LVESD、LVEF、E/A均呈负相关性(P0.05)。结论:妊娠期高血压患者的血清HSP70水平明显升高,并且血清HSP70水平与妊娠期高血压患者免疫功能和心功能下降存在相关性,在妊娠期高血压患者的诊断和治疗中具有一定临床价值。     

珠子参地上部分氨基酸测定及营养评价

对珠子参茎、叶、花的氨基酸组成与含量进行测定和营养评价分析。结果表明,珠子参茎、叶、花中均含有17种常见氨基酸,氨基酸总量分别为3.73%,14.80%和8.72%;珠子参的茎中必需氨基酸与总氨基酸的比值(E/T)为0.39,必需氨基酸与非必需氨基酸的比值(E/N)为0.64,叶中E/T为0.41,E/N为0.71,花中E/T为0.39,E/N为0.63,氨基酸配比较为合理;珠子参茎、叶、花中蛋氨酸+胱氨酸均为第一限制氨基酸;珠子参茎、叶、花中均含有γ-氨基丁酸,含量分别为0.12%,0.26%和0.16%,叶片中γ-氨基丁酸的含量最高。     

悉生小鼠体内大肠杆菌和青春型双歧杆菌对艰难梭菌的拮抗作用

本文应用悉生小鼠做模型,研究了大肠杆菌(E.coli)和青春型双歧杆菌(Bifidobacterium adolescentis)对艰难梭菌(Clostridium diffi-cile)的拮抗作用。E.coli和B.adolescentis预先接种无菌SSB小鼠,再用C.difficile攻击。结果表明,E.coli和E.coli B.adolescentis对小鼠均有保护作用,保护平分别为87.5%(7/8)和100%(8/8)。B.adolescentis定值后数量达10~(10.28)CFU/g,且对E.coli数量和小鼠本身无影响。E.coli和B.adolescentis联合比E.coli单独抑制C.difficile在肠道中繁殖的作用更强(0.02>P>0.01),但对其毒素产生和粘附力的作用无明显差异。C.difficile攻击后的1～14天,小鼠粪便中C.difficile菌数在10~4至10~8CFU/g内变化,细胞毒素为10~3CFU/g,A毒素滴度为10~2/g,B.adolescentis也一度下降10~2CFU/g。接种C.difficile后,小鼠虽无明显的腹泻症状,但组织学仍可观察到肠粘膜有充血和分泌增加等轻度损害。扫描电镜和普通光镜均发现E.coli单独或与B.adolescentis共同吸附在肠粘膜微绒毛表面,未见有C.difficile吸附。     

珠子参地上部分氨基酸测定及营养评价

对珠子参茎、叶、花的氨基酸组成与含量进行测定和营养评价分析.结果表明,珠子参茎、叶、花中均含有17种常见氨基酸,氨基酸总量分别为3.73％,14.80％和8.72％;珠子参的茎中必需氨基酸与总氨基酸的比值(E/T)为0.39,必需氨基酸与非必需氨基酸的比值(E/N)为0.64,叶中E/T为0.41,E/N为o.71,花中E/T为0.39,E/N为0.63,氨基酸配比较为合理;珠子参茎、叶、花中蛋氨酸+胱氨酸均为第一限制氨基酸;珠子参茎、叶、花中均含有γ-氨基丁酸,含量分别为0.12％,0.26％和0.16％,叶片中γ-氨基丁酸的含量最高.     

食管鳞癌患者血清血管内皮生长因子与内皮抑素表达及其与临床病理特征的关系

目的:探讨食管鳞癌患者血清中血管内皮生长因子(VEGF)和内皮抑素(Endostatin)的表达及其与食管鳞癌临床病理特征和预后的关系。方法:采用ELISA法检测126例食管鳞癌患者和14例正常健康人血清VEGF及Endostatin表达水平。结果:126例食管鳞癌患者血清中VEGF(20.68±3.09)ug/L水平和Endostatin水平(4.96±1.72)ug/mL均显著高于正常健康人(3.82±6.28)μg/L和(1.60±0.37)μg/L(P<0.05),V/E比值也非常显著高于正常人。食管鳞癌患者血清中VEGF、endostatin水平以及V/E比值与其分化程度、P-TNM分期、病变长度、淋巴结转移状态等显著相关(P<0.01),与其年龄、性别、肿瘤部位、浸润深度等无明显关系(P>0.05)。食管鳞癌患者血清中VEGF与Endostatin表达呈非常显著正相关(r=0.594,P<0.01)。结论:食管鳞癌患者血清中VEGF、Endostatin水平升高,与食管鳞癌的恶性程度及肿瘤负荷密切相关,其两者的比值(V/E)对食管鳞癌患者预后、生物学行为评估具有重要意义。     

肠益生治疗小儿腹泻及便秘临床疗效及B／E值变化的观察与评价

本文应用双歧杆菌发酵乳型制剂治疗小儿急性腹泻４８例和便秘３５例,并比较了腹泻患儿治疗前后双歧杆菌与大肠杆菌的比值变化。结果表明：肠益生对腹泻有很好的疗效,并促进肠道菌群的恢复,治疗前后Ｂ／Ｅ值得显著性差异。     

Activation induced differential regulation of stem cell antigen-1 (Ly-6A/E) expression in murine B cells

Expression of stem cell antigen-1 (Ly-6A/E) is developmentally regulated in murine B cells. However, little is known about its modulation during B cell activation. We report here the differential regulation of Ly-6A/E expression in response to diverse activation signals in mature B cells. Stimulation of resting B cells through the antigen receptor (BCR) inhibited, Ly-6A/E surface expression in dose dependent manner. Activation induced downregulation of Ly-6A/E is specific to BCR mediated signaling events as stimulation of B cells with anti-CD40, lipopolysaccharide or interferon-γ induced upregulation of Ly-6A/E surface expression. The activation induced differential modulation of Ly-6A/E expression is mediated at the mRNA levels. A role for BCR signaling in inhibition of Ly-6A/E expression was further confirmed using STAT-1^−/− B cells, which expressed constitutive, but not inducible Ly-6A/E. The BCR induced inhibition of Ly-6A/E RNA and surface expression was mimicked by ionomycin, but not phorbol myristate acetate, indicating a role for calcium but not protein kinase C dependent signaling events. Inhibition of calcineurin reversed the BCR or ionomycin inhibited Ly-6A/E expression. Interestingly, in vitro differentiation analysis of Ly-6A/E⁺ and Ly-6A/E⁻ splenic B cells revealed the Ly-6A/E⁺ cells to be the major source of antibody production, suggesting a potential role for Ly-6A/E in B cell differentiation. These studies provide the first evidence for activation induced differential modulation and differentiation of Ly-6A/E⁺ B cells.     

Nucleophosmin/B23 is a target of CDK2/cyclin E in centrosome duplication

In animal cells, duplication of centrosomes and DNA is coordinated. Since CDK2/cyclin E triggers initiation of both events, activation of CDK2/cyclin E is thought to link these two events. We identified nucleophosmin (NPM/B23) as a substrate of CDK2/cyclin E in centrosome duplication. NPM/B23 associates specifically with unduplicated centrosomes, and NPM/B23 dissociates from centrosomes by CDK2/cyclin E-mediated phosphorylation. An anti-NPM/B23 antibody, which blocks this phosphorylation, suppresses the initiation of centrosome duplication in vivo. Moreover, expression of a nonphosphorylatable mutant NPM/ B23 in cells effectively blocks centrosome duplication. Thus, NPM/B23 is a target of CDK2/cyclin E in the initiation of centrosome duplication.     

Cross-linkage of Ly-6A/E induces Ca2+ translocation in the absence of phosphatidylinositol turnover and mediates proliferation of normal murine B lymphocytes

Ly-6A/E is a phosphatidylinositol (PI)-linked membrane protein whose expression is induced or upregulated on normal murine T and B cells by IFN-gamma. Cross-linkage of Ly-6A/E expressed on normal murine T cells stimulates Ca2+ translocation, and in the presence of a protein kinase C (PKC) activator, lymphokine secretion, and cellular proliferation. Utilizing an anti-Ly-6A/E mAb, we studied the effect of cross-linking Ly-6A/E on IFN-gamma-treated resting B cells, for Ca2+ translocation, PI turnover, and cellular proliferation. Since these events are known to be stimulated by cross-linkage of B cell membrane (m)Ig, we compared the changes mediated through these respective membrane proteins. We show that cross-linkage of B cell Ly-6A/E stimulates a large, rapid, and sustained increase in the concentration of intracellular free calcium ([Ca2+]i) comparable in magnitude, though somewhat delayed, relative to that observed after cross-linking of mIg. Cross-linkage of B cell Ly-6A/E does not, however, stimulate detectable PI turnover, in contrast to PI turnover induced by ligation of mIg. Both the Ly-6A/E- and mIg-mediated increase in [Ca2+]i occur through mobilization of internal Ca2+ stores as well as entry of Ca2+ into the cell from the extracellular compartment. Ly-6A/E-mediated Ca2+ translocation appears to be under the regulation of PKC in that short term pretreatment of B cells with the PKC activator, PMA, inhibits the Ly-6A/E- as well as the mIg-mediated increase in [Ca2+]i, whereas prolonged exposure to PMA, under conditions that lead to depletion of PKC, results in an augmentation in Ca2+ translocation after ligation of either Ly-6A/E or mIg. Co-capping studies indicate that Ly-6A/E and mIg cap independently in the B cell membrane, thus suggesting that the Ly-6A/E-induced effects on Ca2+ translocation are not mediated through simultaneous modulation of mIg. Anti-Ly6A/E, by itself, does not stimulate an increase in [3H]thymidine incorporation by IFN-gamma-treated resting B cells, but induces a striking increase in the presence of PMA. By contrast, anti-Ig by itself stimulates significant increases in [3H]thymidine incorporation that is inhibited by PMA. Thus, Ly-6A/E is a potent mediator of B cell activation that may use a signal transduction system in quiescent B cells that is distinct from that of the Ag receptor.     

Functional regulation of FEZ1 by the U-box-type ubiquitin ligase E4B contributes to neuritogenesis

E4B (also known as UFD2a) is a mammalian homolog of Saccharomyces cerevisiae Ufd2, which was originally described as a ubiquitin chain assembly factor (E4). E4B is a U-box-type ubiquitin-protein isopeptide ligase (E3) and likely functions as either an E3 or an E4. With a yeast two-hybrid screen, we have now identified FEZ1 (fasciculation and elongation protein zeta 1) as a protein that interacts with E4B. FEZ1 is implicated in neuritogenesis when phosphorylated by protein kinase Czeta (PKCzeta). Interaction between E4B and FEZ1 in mammalian cells was enhanced by coexpression of constitutively active PKCzeta. E4B mediated the polyubiquitylation of FEZ1 but did not affect its intracellular stability, suggesting that such modification of FEZ1 is not a signal for its proteolysis. Polyubiquitylation of FEZ1 by E4B required Lys(27) of ubiquitin. Expression of a dominant-negative mutant of E4B in rat pheochromocytoma PC12 cells resulted in inhibition of neurite extension induced either by nerve growth factor or by coexpression of FEZ1 and constitutively active PKCzeta. These findings indicate that E4B serves as a ubiquitin ligase for FEZ1 and thereby regulates its function but not its degradation.     

Regulation of B lymphocyte responses to IL-4 and IFN-gamma by activation through Ly-6A/E molecules

The Ly-6 family of cell surface molecules has previously been shown to participate in T cell activation. We show that Ly-6A/E proteins also modulated the response of normal B lymphocytes in three separate in vitro assays. First, unfractionated or small resting B cells proliferated when cultured with IFN-gamma, IL-4, and an anti-Ly-6A/E mAb. Second, this anti-Ly-6A/E mAb restored B cell proliferation responses that were inhibited when coculturing the B cells in IFN-gamma, IL-4, and anti-IgM. Third, anti-Ly-6A/E specifically up-regulated the cell surface expression of its own Ag, and this response was dependent upon co-stimulation with IFN-gamma. Mixing of T and B cells in culture suggested that T cells did not contribute substantially to the B cell proliferative response. Moreover, up-regulation of Ly-6A/E was observed for one B cell lymphoma, WEHI-231. Therefore, it appeared that modulation of B cell function by anti-Ly-6A/E was due to a direct effect of the mAb binding to the B cells. Taken together, these data suggest Ly-6A/E proteins are functional on B cells and may play a regulatory role in B cell activation.