1962名男性新兵人格诊断问卷(PDQ-4~+)结果分析

目的了解部队新兵人格倾向特征。方法采用人格诊断问卷(PDQ-4+)对某部队1 962名男性新兵进行抽样调查,并与大学生样本进行比较。结果 (1)除表演型、反社会型分量表外,新兵其他各分量表及总量表得分均显著低于大学生(P<0.05);新兵人格倾向亚型的阳性检出率在7.25%~36.07%。(2)低年龄组新兵在偏执型、分裂型、自恋型、边缘型、反社会型、依赖型分量表及总量表的得分均高于高年龄组新兵(P<0.05);父母关系和睦的新兵各个人格倾向亚型(除强迫型外)得分均显著低于父母关系不和睦新兵的得分(P<0.05);农村与城市新兵的偏执型、分裂型、表演型、自恋型、边缘型、反社会型和被动攻击型分量表得分,差异有统计学意义(P<0.05),且城市新兵人格障碍得分更高(P<0.05);除分裂样型、自恋型、强迫型分量表外,独生子女新兵其他分量表及总量得分均高于非独生子女新兵(P<0.05)。结论新兵的人格倾向问题好于大学生样本,低龄、父母关系不和睦、居住在城市和独生子女新兵有更多的人格倾向问题。     

骨盆前环皮下内固定支架与微创经皮钢板内固定治疗骨盆前环骨折的疗效比较

目的 比较前环皮下内固定支架（INFIX）和微创经皮钢板内固定（MIPPO）治疗骨盆前环骨折的疗效。方法 回顾性分析2016年7月至2020年5月我院收治且符合标准的48例不稳定型骨盆骨折病人的临床资料,其中INFIX组22例,MIPPO组26例。INFIX组,男15例,女7例,年龄为（36.89±11.12）岁（21~58岁）。MIPPO组,男17例,女9例,年龄为（43.70±17.66）岁（21~71岁）。比较两组手术时间、术中出血量、骨折复位质量（Matta标准）、骨折愈合时间、骨折术后功能恢复情况（Majeed评分系统）,并记录并发症。结果 两组均获得随访,随访时间为5~17个月,平均为13个月。INFIX组手术时间[（75.41±15.25） min]低于MIPPO组[（85.62±17.92） min],差异无统计学意义（t=-5.154,P=0.101）;INFIX组术中出血量[（30.27±7.67） mL]明显低于MIPPO组[（111.15±24.30） mL],差异有统计学意义（t=-14.971,P=0.006）;两组负重时间[（16.00±2.06）周vs.（15.94±2.32）周]、Majeed评分[（81.90±7.73）分vs.（83.44±3.54）分]、骨折复位优良率[81.8% vs.84.6%]比较,差异均无统计学意义（P均＞0.05）,但MIPPO组能够达到更好的解剖复位。INFIX组1例病人出现股外侧皮神经损伤,两组病人未出现内固定失败情况。结论 治疗骨盆前环骨折,INFIX具有出血少、手术创伤小等优点,钢板能够达到更好的解剖复位,两组具有相似的术后功能恢复情况。可根据术者经验和病人具体情况选择适宜的固定方式。     

脂质体介导Bcl-2反义寡核苷酸对胆管癌细胞株QBC939的作用

目的：观察Bcl-2反义硫代磷酸寡脱氧核苷酸（ASODN）对人胆管癌QBC939细胞的作用及对Bcl-2蛋白表达的影响。方法：脂质体LipofectamineTM2000介导Bcl-2 ASODN转染QBC939细胞,应用台盼篮拒染实验检测细胞存活率、克隆形成实验检测克隆形成率、Western blot检测Bcl-2蛋白表达。结果：Bcl-2 ASODN转染后Bcl-2蛋白免疫印迹条带光密度显著低于对照组（P<0.01）;台盼篮拒染实验和克隆形成实验均显示Bcl-2 ASODN可以部分抑制QBC939细胞增殖,经ASODN作用,细胞的存活率和克隆形成率均显著低于对照组（P<0.05）。结论：Bcl-2 ASODN通过封闭人胆管癌QBC939细胞bcl-2基因表达抑制人胆管癌QBC939细胞的增殖。     

Clonal evolution in B-lineage acute lymphoblastic leukemia by contemporaneous VH-VH gene replacements and VH-DJH gene rearrangements

B-cell acute lymphoblastic leukemia (B-ALL), more frequently than any other B-lineage neoplasm, exhibits oligoclonal Ig heavy chain (IgH) gene rearrangement in 15% to 43% of all cases studied. To study the molecular processes that promote multiple IgH rearrangements, a comprehensive sequence analysis of a B-ALL case was performed in which seven clonal IgH gene rearrangements were identified. The genetic profiles suggested that a single leukemic progenitor clone evolved into several subclones through dual processes of variable (VH) to preexisting diversity-joining (DJH) gene segment rearrangement and VH to VH gene replacement. Predominant IgH-V usage and the uniquely rearranged clonotype-specific VHDJH region gene sequences were identified using a novel DNA-based gene amplification strategy. Polymerase chain reaction (PCR) was directed by an IgH-J generic primer and a complement of family-specific IgH-V primers that defined the major B-cell IgH-V gene usage. Clonality of rearranged VHDJH bands was substantiated by high resolution denaturant gel electrophoretic analysis. Sequence patterns of the amplified VHDJH fragments segregated into two groups defined by common DJH sequences. Partial N region homology at the VHD junction as well as shared DJH sequences firmly established VH to VHDJH gene replacement as a mechanism generating clonal evolution in one group. In the second subset, oligoclonality was propagated by independent VH gene rearrangements to a common DJH precursor. The contributions of all clonal Ig-VHDJH repertoires for each group was approximately 50% and reflected a symmetric distribution of leukemic subclones generated by either process. Thus, oligoclonal rearrangements evolved by two independent, yet seemingly contemporaneous molecular genetic mechanisms. All seven clones displayed nonfunctional Ig-VHDJH recombinations. These observations may have relevance to the recombinatorial opportunities available during normal B-cell maturation.     

海南虎刺枝叶中化学成分及其抗类风湿性关节炎活性研究

目的 研究茜草科虎刺属植物海南虎刺Damnacanthus hainanensis枝叶中的化学成分及其抗类风湿性关节炎活性。方法 综合运用硅胶柱色谱、反相硅胶柱色谱、Sephadex LH-20凝胶柱色谱以及制备型HPLC等色谱技术进行系统分离和纯化,根据分离得到化合物的理化性质及其波谱数据,并通过与文献中报道的波谱数据进行比对,鉴定化合物的结构;采用MTS法通过对分离得到化合物的体外抑制滑膜细胞增殖的活性进行测试以评价其抗类风湿性关节炎活性。结果 从海南虎刺枝叶的甲醇提取物中分离得到了18个化合物,分别鉴定为naucleidinal（1）、1,2,3,4-tetrahydronorharman-1-one（2）、19-O-methyl-3,14-dihydroangustoline（3）、latifoliamide B（4）、latifoliamide D（5）、bacilsubteramide A（6）、vinmajine I（7）、naucleofficine D（8）、1-甲氧甲酰-β-咔巴啉（9）、naphthisoxazol A（10）、1,6-dihydroxy-2-methyl-9,10-anthraquinone（11）、rubiadin-1-methyl ether（12）、1,3,6-trihydroxy-2-methoxymethyl-9,10-anthraquinone（13）、3,6-dihydroxy-2-hydroxymethyl-9,10-anthra quinone（14）、7-羟基色原酮（15）、5,7-二羟基色原酮（16）、6,4''-dihydroxy-3''-methoxyaurone（17）和farnisin（18）。抗类风湿性关节炎活性评价结果表明,化合物11～14、17和18对滑膜成纤维MH7A细胞增殖抑制活性的半数抑制浓度（median inhibition concentration,IC₅₀）值为（8.93±0.09）～（152.58±0.32）μmol/L。结论 所有化合物均为首次从虎刺属植物中分离得到。化合物11～14、17和18表现出了较为显著的抗类风湿性关节炎活性。     

Alosetron versus traditional pharmacotherapy in clinical practice: effects on resource use,health-related quality of life,safety and symptom improvement in women with severe diarrhea-predominant irritable bowel syndrome

Objective: Severe diarrhea-predominant irritable bowel syndrome (IBS-D) is associated with decreased health-related quality of life (HRQOL) and increased health care costs. Treatment recommendations for IBS-D often start with traditional pharmacotherapy (TP), with escalation to alosetron, rifaximin or eluxadoline if there is no success. There has been no previous head-to-head clinical trial comparing IBS-D treatment outcome for alosetron versus TP. This study, GSK protocol S3B30020, evaluated resource use, work productivity, health-related quality of life and global symptom response in women with IBS-D who were treated with alosetron or TP.

Methods: A total of 1956 patients who met criteria for severe IBS-D were randomized to treatment with alosetron 1?mg twice daily (BID) or only TP for up to 24 weeks. Work productivity and resource use were evaluated by standard questionnaires, HRQOL by the IBSQOL instrument and IBS symptoms by the Global Improvement Scale (GIS).

Results: Compared to only TP, alosetron-treated patients reported: (1) fewer clinic/office visits for any health problem (p?=?.0181) or for IBS-D (p?=?.0004); (2) reduced use of over-the-counter medications for IBS-D (p < .0001); (3) fewer days of lost work productivity (p < .0001); (4) decreased restriction of social and outdoor activities (p < .0001); and (5) greater global improvement in IBS-D symptoms (p < .0001). Alosetron treatment improved HRQOL scores for all domains (p < .0001). Incidence of adverse events during alosetron use was not remarkable and was similar to that previously reported.

Conclusions: Alosetron 1?mg BID significantly reduced health care utilization and lost productivity, and significantly improved global IBS symptoms, HRQOL, and participation in outdoor and social activities compared with treatment response to TP.     

关节镜下内减压术治疗膝关节半月板囊肿的应用

目的：分析探讨关节镜下减压术治疗膝关节半月板囊肿的临床效果。方法选取该院2012年12月—2013年12月收治的膝关节半月板囊肿患者72例,采用膝关节镜下内减压术及半月板部分或全部切除或缝合治疗,术后指导患者进行膝关节功能锻炼。对所有患者进行随访,术前术后均进行膝关节Lysholm 功能评分,对比观察疗效。结果术前Lysholm 功能评分为（58.6±9.2）分,明显高于术后评分（93.3±4.6）分,术前术后评分对比t=18.167,P<0.05,差异有统计学意义。结论关节镜下减压术及切除或缝合半月板治疗膝关节半月板囊肿具有非常好的疗效,创伤较小,术后患者的膝关节功能恢复情况良好,可以显著提高患者的生活质量,对膝关节稳定性及生理功能干扰较小,值得临床大力推广。     

The Mood Stabilizer Lithium Potentiates the Antidepressant-Like Effects and Ameliorates Oxidative Stress Induced by Acute Ketamine in a Mouse Model of Stress

Background:

Evidence suggests that mammalian target of rapamycin activation mediates ketamine’s rapid but transient antidepressant effects and that glycogen synthase kinase-3β inhibits this pathway. However, ketamine has associated psychotomimetic effects and a high risk of abuse. The mood stabilizer lithium is a glycogen synthase kinase-3 inhibitor with strong antisuicidal properties. Here, we used a mouse stress model to investigate whether adjunct lithium treatment would potentiate ketamine’s antidepressant-like effects.

Methods:

Mice received chronic restraint stress and long-term pre- or postketamine lithium treatment in drinking water. The effects of lithium on ketamine-induced antidepressant-like effects, activation of the mammalian target of rapamycin/brain-derived neurotrophic factor signaling pathways, oxidative stress, and dendritic spine density in the brain of mice were investigated.

Results:

Subtherapeutic (600mg/L) lithium-pretreated mice exhibited an antidepressant-like response to an ineffective ketamine (2.5mg/kg, intraperitoneally) challenge in the forced swim test. Both the antidepressant-like effects and restoration of dendritic spine density in the medial prefrontal cortex of stressed mice induced by a single ketamine (50mg/kg) injection were sustained by postketamine treatment with 1200mg/L of lithium for at least 2 weeks. These benefits of lithium treatments were associated with activation of the mammalian target of rapamycin/brain-derived neurotrophic factor signaling pathways in the prefrontal cortex. Acute ketamine (50mg/kg) injection also significantly increased lipid peroxidation, catalase activity, and oxidized glutathione levels in stressed mice. Notably, these oxidative stress markers were completely abolished by pretreatment with 1200mg/L of lithium.

Conclusions:

Our results suggest a novel therapeutic strategy and justify the use of lithium in patients who benefit from ketamine.