Exosomes from miRNA‐126‐modified endothelial progenitor cells alleviate brain injury and promote functional recovery after stroke

AimsWe previously showed that the protective effects of endothelial progenitor cells (EPCs)‐released exosomes (EPC‐EXs) on endothelium in diabetes. However, whether EPC‐EXs are protective in diabetic ischemic stroke is unknown. Here, we investigated the effects of EPC‐EXs on diabetic stroke mice and tested whether miR‐126 enriched EPC‐EXs (EPC‐EXs^miR126) have enhanced efficacy.MethodsThe db/db mice subjected to ischemic stroke were intravenously administrated with EPC‐EXs 2 hours after ischemic stroke. The infarct volume, cerebral microvascular density (MVD), cerebral blood flow (CBF), neurological function, angiogenesis and neurogenesis, and levels of cleaved caspase‐3, miR‐126, and VEGFR2 were measured on day 2 and 14.ResultsWe found that (a) injected EPC‐EXs merged with brain endothelial cells, neurons, astrocytes, and microglia in the peri‐infarct area; (b) EPC‐EXs^miR126 were more effective than EPC‐EXs in decreasing infarct size and increasing CBF and MVD, and in promoting angiogenesis and neurogenesis as well as neurological functional recovery; (c) These effects were accompanied with downregulated cleaved caspase‐3 on day 2 and vascular endothelial growth factor receptor 2 (VEGFR2) upregulation till day 14.ConclusionOur results indicate that enrichment of miR126 enhanced the therapeutic efficacy of EPC‐EXs on diabetic ischemic stroke by attenuating acute injury and promoting neurological function recovery.     

瘀祛补肾法治疗前列腺增生症46例

我院在1998年6月～2004年6月采用瘀祛补肾法治疗前列腺增生症46例,现总结如下.     

多形性低度恶性腺癌的组织病理学与免疫组化研究

目的：研究多形性低度恶性腺癌（PLGA）的组织病理学和免疫组织化学特点，并与腺样囊性癌（ACC）进行比较。方法；采用组织病理学与免疫组织化学方法，对8例PLGA与10例ACC进行分析。结果；PLAC的特点是组织学上具有细胞形态的一致性与组织结构的多形性；免疫级化染色呈阳性或部分阳性反应，与ACC没有明显差异。结论：光镜下组织结构的多形性是鉴别PLGA与ACC的重要指征；免疫组化对二者的区分意义不大；均起源于闰管储备细胞是导致二者相似性的根本原因。     

论提高专科临床护理课程教学质量的重要环节

针对现阶段专科层次临床护理课程教学存在的问题，主要从把好教师关、备课关、课堂教学关和临床见习关4个方面进行质量控制，以增强教师教学责任感，激发学生学习兴趣，促进教学质量的提高。     

Identification of cultured male epidermal allografts by detecting Y chromosome DNA fragments in female burn victims

ltiswellknownthattheskinofextensivelyburnedcasesthemselvesisinsufficienttoprovidecoverageforwounds.Thoughallogeneicskincancoverthewoundstemporari1y,itwillberejectedwithin2-3weeks.Thiscanthreatenthepatient'slifeifthereisnoenoughautogenousskintoreplacetherejectedoneontime.GreenetalL1]reportedthattheburnwoundsofpatientswithextensiveburnscouldbetreatedbytransplantingepidermalautograftsafterautologousepidermalcellsmulti-plyforthousandsoftimesinvltrowithinashortperiodoftime-Butittakesatleast2-3weeks…     

王焕禄老中医治疗哮喘发作期的用药经验

王焕禄老中医在长期的临床实践中，总结出治疗哮喘病的一些用药体会，兹介绍如下，以飨读者。     

应用VIDAS免疫分析系统检测血清抗伯氏包柔螺旋体抗体

莱姆病（Ｌｙｍｅｄｉｓｅａｓｅ）是最近十年来才被认识的一种蜱媒传染流行病，Ｌｙｍｅ病的血清学诊断方法有间接荧光免疫法（ＩＦＡ），酶免疫试验（）ＥＩＡ），免疫印迹法（ＷＢ），梅里埃生物公司（Ｂｉｏｍｅｒｉｅｕｘ）推出ＶＩＤＡＳ免疫诊断系统能够自动定性和半定量地检查Ｌｙｍｅ病的抗伯氏包柔螺旋体抗（抗ＢＢ抗体）。本方法结合了酶和荧光免疫两种方法。硷性磷酸酶标记二抗的底物是４ｍｅｔｈｙｌｕｍｂｅｌｌｉｆｅ     

格尔木地区蠓类生态习性调查研究

目的:调查了解青海省格尔木地区蠓类的活动规律,为防治提供科学依据。方法:网捕法。结果:调 查发现蠓科4属28种,即吸血蠓2属22种,非吸血蠓2属6种;其中细蠓属14种,库蠓属8种,毛蠓属5种和铗 蠓属1种。观察阐述了当地蠓类的一日活动规律与季节消长。     

血小板活化因子、癌胚抗原、糖类抗原724在结直肠癌中的表达及与临床病理特征的关系

目的:探讨血小板活化因子(PAF)、癌胚抗原(CEA)、糖类抗原724(CA-724)在结直肠癌(CRC)患者术前血清中的阳性表达率及与临床病理特征的关系、发病的独立危险因素。方法:选取2019年12月至2021年10月于包头医学院第一附属医院就诊的CRC患者75例为CRC组,另选取同时期在本院体检的健康志愿者75例为对照组。采用酶联免疫吸附(ELISA)法分别检测CRC患者术前及对照组的晨空腹外周静脉血PAF含量;回顾性分析上述入组患者术前血清CEA、CA-724含量,进行统计分析。结果:(1)CRC组PAF、CEA、CA-724单独检测和联合检测的阳性率分别为25.33%、42.67%、30.67%、74.67%,均高于对照组,且联合检测的阳性率均高于单独检测指标的阳性率,组间差异均具有统计学意义(P<0.05);(2)单因素方差分析结果显示,血清CEA表达水平的影响因素为患者的淋巴结转移(P<0.05);血清CA-724表达水平的影响因素为患者的年龄(P<0.05);(3)二元Logistic回归分析结果显示,PAF表达在临床病理特征之间的差异无统计学意义(P&...     

Animal models in the investigation of anorexia

Anorexia nervosa (AN) is an eating disorder of unknown origin that most commonly occurs in women and usually has its onset in adolescence. Patients with AN invariably have a disturbed body image and an intense fear of weight gain. There is currently no definitive treatment for this disease, which carries a 20% mortality over 20 years. Development of an appropriate animal model of AN has been difficult, as the etiology of this eating disorder likely involves a complex interaction between genetic, environmental, social, and cultural factors. In this review, we focus on several possible rodent models of AN. In our laboratory, we have developed and studied three different mouse models of AN based on clinical profiles of the disease; separation stress, activity, and diet restriction (DR). In addition, we discuss the spontaneous mouse mutation anx/anx and several mouse gene knockout models, which have resulted in an anorexic phenotype. We highlight what has been learned from each of these models and possibilities for future models. It is hoped that a combination of the study of such models, together with genetic and clinical studies in patients, will lead to more rational and successful prevention/treatment of this tragic, and often fatal, disease.