Phenotypic profiling of mGlu7 knockout mice reveals new implications for neurodevelopmental disorders

Neurodevelopmental disorders are characterized by deficits in communication, cognition, attention, social behavior and/or motor control. Previous studies have pointed to the involvement of genes that regulate synaptic structure and function in the pathogenesis of these disorders. One such gene, GRM7, encodes the metabotropic glutamate receptor 7 (mGlu₇), a G protein‐coupled receptor that regulates presynaptic neurotransmitter release. Mutations and polymorphisms in GRM7 have been associated with neurodevelopmental disorders in clinical populations; however, limited preclinical studies have evaluated mGlu₇ in the context of this specific disease class. Here, we show that the absence of mGlu₇ in mice is sufficient to alter phenotypes within the domains of social behavior, associative learning, motor function, epilepsy and sleep. Moreover, Grm7 knockout mice exhibit an attenuated response to amphetamine. These findings provide rationale for further investigation of mGlu₇ as a potential therapeutic target for neurodevelopmental disorders such as idiopathic autism, attention deficit hyperactivity disorder and Rett syndrome.     

Antiphospholipid antibody‐activated NETs exacerbate trophoblast and endothelial cell injury in obstetric antiphospholipid syndrome

Despite the widespread use of antiplatelets and anticoagulants, women with antiphospholipid syndrome (APS) may face pregnancy complications associated with placental dysplasia. Neutrophil extracellular traps (NETs) are involved in the pathogenesis of many autoimmune diseases, including vascular APS; however, their role in obstetric APS is unclear. Herein, we investigated the role of NETs by quantifying cell‐free DNA and NET marker levels. Live‐cell imaging was used to visualize NET formation, and MAPK signalling pathway proteins were analysed. Cell migration, invasion and tube formation assays were performed to observe the effects of NETs on trophoblasts and human umbilical vein endothelial cells (HUVECs). The concentrations of cell‐free DNA and NETs in sera of pregnant patients with APS were elevated compared with that of healthy controls (HCs) matched to gestational week. APS neutrophils were predisposed to spontaneous NET release and IgG purified from the patients (APS‐IgG) induced neutrophils from HCs to release NETs. Additionally, APS‐IgG NET induction was abolished with inhibitors of reactive oxygen species, AKT, p38 MAPK and ERK1/2. Moreover, NETs were detrimental to trophoblasts and HUVECs. In summary, APS‐IgG‐induced NET formation deserves further investigation as a potential novel therapeutic target in obstetrical APS.     

High‐throughput analysis of vocalizations reveals sex‐specific changes in Fmr1 mutant pups

There have been several reports that individuals with Fragile X syndrome (FXS) and animal models of FXS have communication deficits. The present study utilized two different call classification taxonomies to examine the sex‐specificity of ultrasonic vocalization (USV) production on postnatal day (PD8) in the FVB strain of Fmr1 knockout (KO) mice. One classification protocol requires the investigator to score each call by hand, while the other protocol uses an automated algorithm. Results using the hand‐scoring protocol indicated that male Fmr1 KO mice exhibited longer calls (P = .03) than wild types on PD8. Male KOs also produced fewer complex, composite, downward, short and two‐syllable call‐types, as well as more frequency steps and chevron call‐types. Female heterozygotes exhibited no significant changes in acoustic or temporal aspects of calls, yet showed significant changes in call‐type production proportions across two different classification taxonomies (P < .001). They exhibited increased production of harmonic and frequency steps calls, as well as fewer chevron, downward and short calls. According to the second high‐throughput analysis, female heterozygotes produced significantly fewer single‐type and more multiple‐type syllables, unlike male KOs that showed no changes in these aspects of syllable production. Finally, we correlated both scoring methods and found a high level of correlation between the two methods. These results contribute further knowledge of sex differences in USV calling behavior for Fmr1 heterozygote and KO mice and provide a foundation for the use of high‐throughput analysis of neonatal USVs.     

新型冠状病毒的动物源性和传染源控制

根据现有的数据,新型冠状病毒(2019 novel coronavirus,2019-nCoV)比严重急性呼吸综合征冠状病毒(severe acute respiratory syndrome coronavirus,SARS-CoV)的传染性强、传播速度快、疫情规模大、病死率低。其传染性、传播速度和疫情规模似乎具有甲型流感病毒(influenza A virus)的特点。尽管2019-nCoV来源于何种动物尚无定论,但它与SARS-CoV同属冠状病毒,具有共同之处。如果流行过后 2019-nCoV没能在人群中持续传播和存在(如同SARS-CoV一样),则控制野生动物传染源乃重中之重;如果2019-nCoV获得了能在人群中持续传播的能力,预防控制策略将与SARS-CoV明显不同,疫苗便成为至关重要的手段。     

严重急性呼吸综合征冠状病毒2型 IgM / IgG、病毒核酸和白细胞介素6的联合检测在2019冠状病毒病诊断和治疗中的价值

探讨严重急性呼吸综合征冠状病毒2型(severe acute respiratory syndrome coronavirus 2,SARS-CoV-2)免疫球蛋白M(Immunoglobulin M,IgM)/免疫球蛋白G(Immunoglobulin G,IgG)、病毒核酸和白细胞介素6(interleukin 6, IL-6)的联合检测在2019冠状病毒病(coronavirus disease 2019, COVID-19)诊断和治疗中的临床价值。本研究按照《新型冠状病毒肺炎诊疗方案(试行第七版)》的标准收集了93例确诊病例(51例危重型、18例重型,15例轻型和9例普通型)和20例疑似病例(核酸检测阴性但临床症状和CT检测结果均符合标准)。选取110例儿科、妇科、肿瘤、血液和消化等疾病患者并排除COVID-19作为对照组。采用全自动化学发光免疫分析技术和电化学发光技术检测所有研究对象血清中SARS-CoV-2 IgM/IgG和IL-6。用实时荧光定量反转录聚合酶链反应对病例组和对照组的咽拭子进行SARS-CoV-2核酸检测。结果发现,血清IgM、IgG和IL-6在疑似病例中的阳性率分别为85%、75%和0%,在确诊病例中的阳性率分别为98.9%、95.7%和75.2%(其中危重型分别为100%、100%和100%,重型分别为94.4%、100%和97.9%,轻型分别为100%、93.3%和5%、普通型分别为100%、66.7%和0%)。IL-6和 SARS-CoV-2 IgM/IgG表达水平的改变与患者疾病的严重程度存在一定的关联性,差异有统计学意义(χ²＝273.51,χ²＝149.37;P＜0.05)。血清IL-6和SARS-CoV-2 IgM/IgG的联合检测可作为诊断和治疗COVID-19的监测指标,也可作为SARS-CoV-2核酸检测假阴性的有效互补。     

268份人类免疫缺陷病毒抗体待确定样本的检测结果分析

为了提高实验室人类免疫缺陷病毒(human immunodeficiency virus,HIV)抗体检测能力及对免疫蛋白印迹(Western blot,WB)实验结果的判断能力,对送检至北京市东城区艾滋病确证实验室的268份HIV抗体待确定样本进行确证实验及结果分析。按照试剂说明书和实验室标准作业程序(Standard Operation Procedure,SOP)操作对送检的全部样本进行WB确证实验;了解HIV筛查实验结果与确证实验结果的相关性,并分析不同送检机构、送检人群样本的检测结果差异以及不同试剂、不同检测方法的结果差异。结果显示在筛查出抗体待确定的268份样本中,确证阳性170份,阳性率63.43%;确证阴性51份,阴性率19.03%;不确定结果47份,占筛查有反应的17.54%。确证阳性病例来自监管场所、自愿咨询检测门诊(Voluntary Counseling and Test,VCT)和医疗机构,不同送检单位及不同人群的阳性样本率有显著统计学意义(P<0.01)。WB确证阳性样本带型以全条带和次全条带为主,且所有确证阳性标本均来自双试剂阳性样本。不同检测方法阳性样本率的差异有显著统计学意义(P<0.01),其中化学发光法的样本阳性率占46.27%,酶联免疫吸附实验(ELISA)占88.29%,胶体硒法占43.48%。本研究结果提示,对潜在HIV感染者,应扩大检测面,加强医疗机构检测,并提供一种以上方法的多次检测,以减少漏检的风险。     

合并慢性气道疾病的ARDS临床特征及预后影响因素研究

目的:探讨急性呼吸窘迫综合征(ARDS)合并慢性气道疾病患者的临床特征及影响预后的因素。方法:167例ARDS患者根据并发症发生情况分为对照组(单纯性ARDS组,A组,n=39)及观察组(ARDS合并慢性气道疾,B组,n=49,C组,n=41,D组,n=38),比较各组患者一般情况、临床特征、生化指标、治疗方式及预后状况,通过logistic回归分析ARDS合并慢性气道疾病患者预后的影响因素。结果:观察组(B、C、D组)年龄、中性粒细胞、IL-6、IL-8、TNF-α、白蛋白、pro-BNP、乳酸、氧合指数、住院时间、住院费用与对照组(A组)比较差异有统计学意义,P0.05;128例ARDS合并慢性气道疾病患者中死亡76例,好转52例,病死率59.38%;单因素分析结果显示,观察组(B、C、D组)患者中临床结局好转患者与死亡患者比较,白细胞、淋巴细胞、CRP、TNF-α、IL-8、降钙素、肌酐、pro-BNP、氧合指数、住院费用、机械通气时间、抗生素数量差异有统计学意义,P0.05;通过多因素logistic回归分析发现肌酐是影响ARDS合并慢性气道疾病的潜在危险因素,氧合指数为保护因素,P0.05。结论:ARDS合并慢性气道疾病的能量代谢紊乱程度可能较单纯ARDS加重,且两者炎性特征不同。肌酐、氧合指数是影响ARDS合并慢性气道疾病的重要影响因素。     

定坤丹对多囊卵巢综合征患者性激素水平、胰岛素抵抗及妊娠情况的影响

目的:探讨定坤丹对多囊卵巢综合征患者性激素水平、胰岛素抵抗及妊娠情况的的影响。方法:选择2016年5月至2018年5月我院收治的210例多囊卵巢综合征患者,根据随机化原则将其分为两组,每组105例。对照组患者接受达英-35与二甲双胍治疗,研究组在对照组的基础上口服定坤丹治疗。连续治疗3个月后,比较两组治疗前后的性激素水平及胰岛各相关指标的变化。治疗结束后随访1年,比较两组的排卵及妊娠情况。结果:与治疗前相比,两组治疗后的血清睾酮(Testosterone,T)、黄体生成素(Luteinizing hormone,LH)及LH/FSH均明显降低,且研究组以上指标均显著低于对照组(P<0.05)。两组治疗前后的卵泡刺激素(Follicle-stimulating hormone,FSH)水平比较无统计学差异(P>0.05)。与治疗前相比,两组治疗后的空腹胰岛素(Fasting insulin,FINS)、餐后2 h胰岛素(Postprandial 2 hours insulin,2hPINS)及β细胞胰岛素分泌功能(Homeostasis model assessment ofβcell,HOMA-β)均明显升高,胰岛素敏感指数(Homeostasis model assessment-Insulin sensitivity index,HOMA-IS)明显降低,且研究组以上指标较对照组改善更明显(P<0.05)。研究组排卵及成功妊娠率均显著高于对照组(P<0.05)。结论:定坤丹有助于改善多囊卵巢综合征患者性激素水平及胰岛素抵抗,提高排卵及妊娠率。     

55岁以下急性冠状动脉综合征的影响因素分析

目的:探究55岁以下急性冠状动脉综合征(Acute coronary syndrome,ACS)患者的影响因素。方法:选择2010年3月至2013年3月于我院就诊的180例55岁以下ACS患者为研究对象,按照其性别将其区分为男性组(101例)和女性组(79例)。收集和比较两组患者一般临床资料,血清血红蛋白(Hemoglobin,HGB)、甘油三酯(Triglyceride,TG)、胆固醇(Cholesterol,TC)、低密度脂蛋白胆固醇(Low density lipoprotein cholesterol,LDL-C)、高密度脂蛋白胆固醇(High density lipoprotein cholesterol,HDL-C)、血尿酸水平。对两组患者进行5年随访,对比两组患者心血管不良事件(Major adverse cardiovas-cular events,MACE)的发生率、死亡率及再发病率。结果:(1)女性组平均发病年龄高于男性组,女性组伴发高血压、糖尿病、脑卒中比率高于男性组,男性组吸烟史比率高于女性组(P<0.05),两组BMI、心血管病家族史对比差异无统计学意义(P>0.05);(2)女性组TC、TG、LDL-C、HDL-C水平均高于男性组(P<0.05),女性组血尿酸水平低于男性组(P<0.05);(3)对比5年预后,男性组MACE发生率为9.90%(10/101),女性组MACE发生率为11.39%(9/79),男性组死亡率为1.98%(2/101),女性组为1.27%(1/79),再发病率男性组为5.94%(6/101),女性组为6.33%(5/79),两组上述指标对比差异均无统计学意义(P>0.05)。结论:女性ACS患者发病年龄高于男性患者,糖尿病、高血压等病对女性患者影响更为明显,而吸烟则对男性影响更大,女性ACS患者血脂、血尿酸等指标异常程度甚于男性患者,但女性与男性患者远期预后相当。     

尺神经原位松解术与尺神经皮下前置术治疗肘管综合征近期疗效比较的回顾性研究

目的:比较尺神经原位松解术与尺神经皮下前置术治疗肘管综合征(CuTS)近期疗效。方法:本研究为回顾性研究,选取2016年7月～2017年7月期间我院二部收治的60例CuTS患者,根据手术方式的不同分为A组(n=32,尺神经原位松解术)和B组(n=28,尺神经皮下前置术),比较两组患者优良率、并发症、围术期指标、感觉运动功能(肌力、小指指端两点辨别觉、神经传导速度)以及DASH上肢功能障碍(DASH)评分。结果:B组术后12个月的优良率为92.86%(26/28),高于A组的68.75%(22/32)(P0.05)。两组术后并发症总发生率比较差异无统计学意义(P0.05)。两组术后12个月肌力、神经传导速度升高,且B组高于A组(P0.05),两组术后12个月小指指端两点辨别觉降低,且B组低于A组(P0.05)。两组术后3个月、术后6个月、术后12个月DASH评分呈下降趋势,且B组低于A组(P0.05)。B组手术切口长度、手术时间长于A组(P0.05),两组术后住院时间比较差异无统计学意义(P0.05)。结论:与尺神经原位松解术相比,尺神经皮下前置术治疗CuTS患者,虽然手术切口长度、手术时间相对较长,但其优良率更高,同时可有效恢复患者感觉运动功能及减轻其上肢功能障碍,且不增加并发症发生率,具有一定的临床应用价值。