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[Preclinical Development Process and Prospects of Real-time Fluorescence Quantitative Polymerase Chain Reaction Detection Kits]. 实时荧光定量聚合酶链反应检测试剂盒的临床前研究进展与展望
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960508
Chuan Wang, Shaohe Li, Shirong Zhang

In recent years, real-time fluorescence quantitative polymerase chain reaction (qPCR) technology has become an essential tool for molecular diagnosis, pathogen detection, and gene expression analysis, thanks to its high sensitivity, speed, and real-time quantification capabilities. In 2022, the global market size of nucleic acid testing-related products and services, including instruments, reagents, consumables, and after-sales service support, reached 7.3 billion US dollars, with PCR-based technologies accounting for 66.7% of the market share and exhibiting a consistent growth trend. Although qPCR technology has been widely applied across multiple fields, the preclinical development of diagnostic kits-a process that includes primer design and reaction system optimization-still faces such issues as unclear procedures, non-standardized methods, and inconsistent evaluation criteria. Herein, we reviewed the guidelines, key resources, and standardized processes of qPCR assay reagent development, aiming to provide theoretical support for improving the efficiency and quality control of assay reagent development, and to discuss future directions for the optimizing and improving qPCR technology in the context of artificial intelligence.

近年来,实时荧光定量聚合酶链反应(qPCR)技术因其灵敏度高、速度快、实时定量能力强,已成为分子诊断、病原体检测、基因表达分析等领域的重要工具。2022年,全球核酸检测相关产品和服务(包括仪器、试剂、耗材和售后服务支持)的市场规模达到73亿美元,其中基于pcr的技术占市场份额的66.7%,并呈现持续增长趋势。尽管qPCR技术已广泛应用于多个领域,但诊断试剂盒的临床前开发——包括引物设计和反应系统优化的过程——仍然面临着程序不明确、方法不标准化、评价标准不一致等问题。本文综述了qPCR检测试剂开发的指南、关键资源和标准化流程,旨在为提高检测试剂开发的效率和质量控制提供理论支持,并探讨人工智能背景下qPCR技术优化和改进的未来方向。
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引用次数: 0
[Cheng's Juanbi Decoction Inhibits Rheumatoid Arthritis Pathology by Blocking the WTAP-Wnt7b-Wnt/β-Catenin Signaling Axis]. [程氏蠲痹汤通过阻断WTAP-Wnt7b-Wnt/β-Catenin信号轴抑制类风湿关节炎病理]。
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960106
Yajie Wu, Wenbo Xu, Meiling Yuan, Xinyue Zhou, Yikang Cai, Huibo Cao, Qiangjun Duan, Tongxiang Tao, Chenggui Miao
<p><strong>Objective: </strong>Cheng's Juanbi Decoction (CSJBD) is a classic traditional Chinese medicine formula for treating rheumatoid arthritis (RA), exhibiting significant clinical efficacy, but the underlying mechanisms remain unclear. We investigated whether CSJBD inhibited RA pathology by blocking the WTAP-Wnt7b-Wnt/β-catenin signaling axis using a collagen-induced arthritis (CIA) mouse model and fibroblast-like synoviocytes (FLSs) derived from RA patients (RA FLSs) and examined the underlying mechanisms.</p><p><strong>Methods: </strong>We conducted <i>in vivo</i> experiments. Male C57BL/6 mice weighing 17 to 20 g were used to establish the CIA model. The mice were assigned to 6 groups, including the normal group, the model (CIA) group, the model + CSJBD-L (8.1 g/kg) group, the model + CSJBD-M (16.2 g/kg) group, the model + CSJBD-H (32.4 g/kg) group, and the model + leflunomide (LEF) (0.05 mg/10 g) group, with 10 mice in each group. CSJBD was administered twice daily via gastric gavage, while LEF was administered once daily via gastric gavage, for a duration of 28 days. We also conducted <i>in vitro</i> experiments. RA FLSs were assigned to 4 groups, including the RA FLSs + CSJBDS-L group receiving 10% CSJBDS-containing serum, the RA FLSs + CSJBDS-M group receiving 15% CSJBDS-containing serum, the RA FLSs + CSJBDS-H group receiving 20% CSJBDS-containing serum, and the RA FLSs + NC group (negative control). To study whether WTAP regulated Wnt7b, RA FLSs were divided into the RA FLSs group, the RA FLSs + si-<i>WTAP</i>#3 group, the RA FLSs + si-<i>WTAP</i>#3 + Wnt7b-OE group, and the RA FLSs + si-<i>WTAP</i>#3 + Wnt7b-NC group. To study the underlying mechanism by which CSJBT affected RA FLSs, RA FLSs were divided into the RA FLSs group, the RA FLSs + CSJBDS-M group, the RA FLSs+CSJBDS-M + Wnt7b-OE group, and the RA FLSs+CSJBDS-M + NC group. We used ultra-high performance liquid chromatography (UPLC) to identify and quantify key monomer compounds from CSJBD as quality criteria for CSJBD preparation. Bioinformatics, CCK-8, RT-qPCR, Western blot, immunofluorescence, and related methods were employed to assess the therapeutic efficacy and underlying mechanisms of CSJBD in treating RA.</p><p><strong>Results: </strong>According to the UPLC analysis, ferulic acid, osthole, mulberroside A, notopterol, and gentiopicroside were identified as quality control standards for the preparation of CSJBD formula. CSJBD improved RA pathology in CIA mice, reduced the levels of interleukin (IL)-6, IL-1β, IL-8, and tumor necrosis factor-α (TNF-α) in their serum, and decreased the expression of RA pathological genes <i>MMP3</i> and fibronectin, with the difference between groups being statistically significant. Bioinformatics analysis suggested that CSJBD might inhibit RA pathology by suppressing the Wnt/β-catenin signaling pathway through Wnt7b. Experimental results showed that the expression of WTAP and Wnt7b was significantly increased in RA. After knocking do
目的:程氏蠲痹汤是治疗类风湿关节炎(RA)的经典中药方剂,临床疗效显著,但作用机制尚不清楚。我们使用胶原诱导关节炎(CIA)小鼠模型和源自RA患者的成纤维细胞样滑膜细胞(FLSs)研究CSJBD是否通过阻断WTAP-Wnt7b-Wnt/β-catenin信号轴来抑制RA病理,并研究其潜在机制。方法:采用活体实验。选用体重17 ~ 20 g的雄性C57BL/6小鼠建立CIA模型。将小鼠分为正常组、模型(CIA)组、模型+ CSJBD-L (8.1 g/kg)组、模型+ CSJBD-M (16.2 g/kg)组、模型+ CSJBD-H (32.4 g/kg)组、模型+来氟米特(0.05 mg/10 g)组6组,每组10只。CSJBD每天2次灌胃给药,LEF每天1次灌胃给药,连续28 d。我们还进行了体外实验。将RA FLSs分为4组,RA FLSs + CSJBDS-L组(含csjbds血清10%)、RA FLSs + CSJBDS-M组(含csjbds血清15%)、RA FLSs + CSJBDS-H组(含csjbds血清20%)、RA FLSs + NC组(阴性对照)。为了研究WTAP是否调控Wnt7b,我们将RA FLSs分为RA FLSs组、RA FLSs + si-WTAP#3组、RA FLSs + si-WTAP#3 + Wnt7b- oe组和RA FLSs + si-WTAP#3 + Wnt7b- nc组。为研究CSJBT对RA FLSs的影响机制,将RA FLSs分为RA FLSs组、RA FLSs+CSJBDS-M组、RA FLSs+CSJBDS-M + Wnt7b-OE组和RA FLSs+CSJBDS-M + NC组。采用超高效液相色谱法(UPLC)对CSJBD中的关键单体化合物进行鉴定和定量,作为CSJBD制剂的质量标准。采用生物信息学、CCK-8、RT-qPCR、Western blot、免疫荧光等方法评价CSJBD治疗RA的疗效及机制。结果:通过UPLC分析,确定阿魏酸、蛇床子素、桑葚苷A、诺托特罗、龙胆苦苷为CSJBD制剂的质量控制标准。CSJBD改善CIA小鼠RA病理,降低血清白细胞介素(IL)-6、IL-1β、IL-8、肿瘤坏死因子-α (TNF-α)水平,降低RA病理基因MMP3、纤连蛋白表达,组间差异有统计学意义。生物信息学分析提示CSJBD可能通过Wnt7b抑制Wnt/β-catenin信号通路,从而抑制RA病理。实验结果显示,WTAP和Wnt7b在RA中的表达显著升高。敲除WTAP后,Wnt7b的表达显著降低,Wnt/β-catenin信号通路也受到抑制,组间差异有统计学意义(P < 0.05),证实WTAP通过Wnt7b调控该通路。经实验验证,CSJBD显著抑制Wnt/β-catenin信号通路,抑制RA FLSs的增殖。Wnt7b过表达逆转了CSJBD对Wnt/β-catenin信号通路和RA FLSs增殖的抑制作用,表明Wnt7b是CSJBD的直接靶点。结论:CSJBD通过阻断WTAP-Wnt7b-Wnt/β-catenin信号轴抑制RA病理,Wnt7b被确定为CSJBD的直接治疗靶点。
{"title":"[Cheng's Juanbi Decoction Inhibits Rheumatoid Arthritis Pathology by Blocking the WTAP-Wnt7b-Wnt/β-Catenin Signaling Axis].","authors":"Yajie Wu, Wenbo Xu, Meiling Yuan, Xinyue Zhou, Yikang Cai, Huibo Cao, Qiangjun Duan, Tongxiang Tao, Chenggui Miao","doi":"10.12182/20250960106","DOIUrl":"10.12182/20250960106","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;Cheng's Juanbi Decoction (CSJBD) is a classic traditional Chinese medicine formula for treating rheumatoid arthritis (RA), exhibiting significant clinical efficacy, but the underlying mechanisms remain unclear. We investigated whether CSJBD inhibited RA pathology by blocking the WTAP-Wnt7b-Wnt/β-catenin signaling axis using a collagen-induced arthritis (CIA) mouse model and fibroblast-like synoviocytes (FLSs) derived from RA patients (RA FLSs) and examined the underlying mechanisms.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;We conducted &lt;i&gt;in vivo&lt;/i&gt; experiments. Male C57BL/6 mice weighing 17 to 20 g were used to establish the CIA model. The mice were assigned to 6 groups, including the normal group, the model (CIA) group, the model + CSJBD-L (8.1 g/kg) group, the model + CSJBD-M (16.2 g/kg) group, the model + CSJBD-H (32.4 g/kg) group, and the model + leflunomide (LEF) (0.05 mg/10 g) group, with 10 mice in each group. CSJBD was administered twice daily via gastric gavage, while LEF was administered once daily via gastric gavage, for a duration of 28 days. We also conducted &lt;i&gt;in vitro&lt;/i&gt; experiments. RA FLSs were assigned to 4 groups, including the RA FLSs + CSJBDS-L group receiving 10% CSJBDS-containing serum, the RA FLSs + CSJBDS-M group receiving 15% CSJBDS-containing serum, the RA FLSs + CSJBDS-H group receiving 20% CSJBDS-containing serum, and the RA FLSs + NC group (negative control). To study whether WTAP regulated Wnt7b, RA FLSs were divided into the RA FLSs group, the RA FLSs + si-&lt;i&gt;WTAP&lt;/i&gt;#3 group, the RA FLSs + si-&lt;i&gt;WTAP&lt;/i&gt;#3 + Wnt7b-OE group, and the RA FLSs + si-&lt;i&gt;WTAP&lt;/i&gt;#3 + Wnt7b-NC group. To study the underlying mechanism by which CSJBT affected RA FLSs, RA FLSs were divided into the RA FLSs group, the RA FLSs + CSJBDS-M group, the RA FLSs+CSJBDS-M + Wnt7b-OE group, and the RA FLSs+CSJBDS-M + NC group. We used ultra-high performance liquid chromatography (UPLC) to identify and quantify key monomer compounds from CSJBD as quality criteria for CSJBD preparation. Bioinformatics, CCK-8, RT-qPCR, Western blot, immunofluorescence, and related methods were employed to assess the therapeutic efficacy and underlying mechanisms of CSJBD in treating RA.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;According to the UPLC analysis, ferulic acid, osthole, mulberroside A, notopterol, and gentiopicroside were identified as quality control standards for the preparation of CSJBD formula. CSJBD improved RA pathology in CIA mice, reduced the levels of interleukin (IL)-6, IL-1β, IL-8, and tumor necrosis factor-α (TNF-α) in their serum, and decreased the expression of RA pathological genes &lt;i&gt;MMP3&lt;/i&gt; and fibronectin, with the difference between groups being statistically significant. Bioinformatics analysis suggested that CSJBD might inhibit RA pathology by suppressing the Wnt/β-catenin signaling pathway through Wnt7b. Experimental results showed that the expression of WTAP and Wnt7b was significantly increased in RA. After knocking do","PeriodicalId":39321,"journal":{"name":"四川大学学报(医学版)","volume":"56 5","pages":"1260-1272"},"PeriodicalIF":0.0,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12712374/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145805999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Mother-to-Child Transmission of Chikungunya Virus and Its Impact on the Neonatal Nervous System]. [基孔肯雅病毒母婴传播及其对新生儿神经系统的影响]
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960201
Keren Luo, Jun Tang

Chikungunya fever is an infectious disease caused by the Chikungunya virus (CHIKV), an arbovirus. In recent years, large-scale outbreaks of Chikungunya fever have occurred in many parts of the world, posing a serious challenge to public health. Perinatal infection of CHIKV and its impact on neonates have attracted growing attention. This article aims to introduce the mechanisms and the influencing factors of mother-to-child transmission of CHIKV and to explore its impact on the nervous system in neonates. According to reported findings, CHIKV can cross the placental barrier, causing infection in the fetus, and can cross the blood-brain barrier, leading to various neurological diseases in neonates, such as microcephaly and encephalitis. In addition, factors influencing mother-to-child transmission include the maternal viral load and the stage of pregnancy at the time of infection. Through a review of current scholarly works, this article provides ideas and a theoretical basis for the prevention and control of mother-to-child transmission of CHIKV and for research into the mechanisms underlying CHIKV-induced brain injury in neonates.

基孔肯雅热是一种由基孔肯雅病毒(CHIKV)引起的传染病,这是一种虫媒病毒。近年来,基孔肯雅热在世界许多地方大规模暴发,对公共卫生构成严重挑战。围生期感染及其对新生儿的影响日益引起人们的关注。本文旨在介绍CHIKV母婴传播的机制及影响因素,探讨其对新生儿神经系统的影响。据报道发现,CHIKV可穿过胎盘屏障,引起胎儿感染,并可穿过血脑屏障,导致新生儿出现小头畸形、脑炎等多种神经系统疾病。此外,影响母婴传播的因素包括母亲的病毒载量和感染时的怀孕阶段。本文通过对国内外相关研究的综述,为预防和控制CHIKV母婴传播以及研究CHIKV致新生儿脑损伤的机制提供思路和理论依据。
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引用次数: 0
[Effects of Multiple Lifestyle Factors on Cardiovascular Biological Aging and Their Relative Contributions]. 多种生活方式因素对心血管生物衰老的影响及其相关贡献
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960608
Jiajie Cai, Ning Zhang, Yi Xiang, Hongmei Zhang, Xiong Xiao

Objective: To investigate the association between healthy lifestyle factors and cardiovascular biological aging, as well as the relative contributions of different lifestyle factors.

Methods: Based on the clinical biochemical data and anthropometric data from the baseline survey of the UK Biobank (UKB), the Klemera-Doubal method (KDM) was used to establish cardiovascular biological age (CBA), and CBA acceleration was calculated accordingly. Multiple linear regression models were used to estimate the associations between healthy lifestyle factors and CBA acceleration. Then, the Quantile g-computation (QGC) was applied to evaluate the relative contributions of different lifestyle factors to CBA acceleration, with further analyses conducted separately for male and female populations. Additionally, stratified analyses were performed based on age, sex, body mass index (BMI), racial background, and family history of cardiovascular diseases to examine population heterogeneity.

Results: A total of 251478 participants were included in the study. Both the overall healthy lifestyle score and each of the 7 lifestyle factors were negatively associated with CBA acceleration (overall lifestyle score: β = -0.75, 95% CI: -0.77 to -0.73). Regarding the relative contributions of different lifestyle factors, alcohol consumption and diet accounted for the highest proportions (25.8% and 25.7%, respectively). However, there were differences by sex-alcohol consumption contributed the most in men (29.5%), followed by diet (23.0%), while in women, diet contributed the most (34.5%) and alcohol consumption accounted for a relatively low proportion (5.5%). Stratified analyses suggested that sex, BMI, and race might be potential effect modifiers.

Conclusion: Lifestyle factors, as modifiable behaviors, can slow the rate of cardiovascular biological aging. Among these factors, alcohol consumption and diet may represent effective targets for intervention.

目的:探讨健康生活方式因素与心血管生物衰老的关系,以及不同生活方式因素的相对贡献。方法:基于英国生物银行(UKB)基线调查的临床生化数据和人体测量数据,采用klemera - double法(KDM)建立心血管生物年龄(CBA),并计算CBA加速。采用多元线性回归模型估计健康生活方式因素与CBA加速之间的关系。然后,应用分位数g计算(QGC)评估不同生活方式因素对CBA加速的相对贡献,并分别对男性和女性人群进行进一步分析。此外,根据年龄、性别、体重指数(BMI)、种族背景和心血管疾病家族史进行分层分析,以检查人群异质性。结果:共纳入251478名受试者。总体健康生活方式评分和7种生活方式因素均与CBA加速呈负相关(总体生活方式评分:β = -0.75, 95% CI: -0.77 ~ -0.73)。在不同生活方式因素的相对贡献方面,饮酒和饮食所占比例最高(分别为25.8%和25.7%)。然而,性别之间存在差异,男性中饮酒贡献最大(29.5%),其次是饮食(23.0%),而女性中,饮食贡献最大(34.5%),饮酒占相对较低的比例(5.5%)。分层分析表明,性别、体重指数和种族可能是潜在的影响因素。结论:生活方式因素作为可改变的行为,可以减缓心血管生物老化的速度。在这些因素中,饮酒和饮食可能是干预的有效目标。
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引用次数: 0
[Advances in Novel Disinfection Technologies for Biofilm-Associated Nosocomial Infections]. [生物膜相关医院感染消毒新技术进展]。
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960203
Donghui Ke, Xingyan Tan, Kun Chen, Xu Xue, Ni An, Kerui Ye, Xiaorui Zhang, Yuqing Li, Jumei Zeng

The elimination of biofilms is a crucial step in controlling hospital-acquired infections. Once biofilms colonize luminal instruments, it is difficult to remove them using traditional disinfection methods. Conventional disinfection approaches now face a series of challenges, including microbial resistance, corrosiveness, cytotoxicity, residual disinfection byproducts, and environmental pollution. Therefore, developing novel disinfection technologies specifically targeting biofilm removal is vitally important. New disinfection technologies, such as slightly acidic electrolyzed water, plasma technology, surface modification techniques, nanomaterial-based disinfection, bacteriophage disinfection, and enzymatic disinfection, are constantly emerging. These technologies exhibit excellent performance against biofilms by leveraging the synergistic effects of multiple mechanisms, including the reactive oxygen species (ROS) burst, photocatalytic oxidation, physical disruption, and biological targeting. This review summarizes the characteristics, underlying mechanisms, and potential application scenarios of these novel disinfection technologies, with a particular focus on their effects against biofilms formed by common pathogenic bacteria on surfaces in hospital settings. It aims to provide a reference basis for the practical application and translation of these disinfection technologies and the development of new disinfection strategies.

消除生物膜是控制医院获得性感染的关键一步。一旦生物膜在腔内仪器上定植,很难用传统的消毒方法去除它们。传统的消毒方法现在面临着一系列挑战,包括微生物耐药性、腐蚀性、细胞毒性、残留消毒副产物和环境污染。因此,开发专门针对生物膜去除的新型消毒技术至关重要。微酸性电解水、等离子体技术、表面修饰技术、纳米材料消毒、噬菌体消毒、酶法消毒等新型消毒技术不断涌现。这些技术通过利用多种机制的协同作用,包括活性氧(ROS)爆发、光催化氧化、物理破坏和生物靶向,对生物膜表现出优异的性能。本文综述了这些新型消毒技术的特点、潜在机制和潜在应用前景,重点介绍了它们对医院环境中常见致病菌在表面形成的生物膜的影响。旨在为这些消毒技术的实际应用和转化以及新的消毒策略的开发提供参考依据。
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引用次数: 0
[Dynamic Effects of High-Altitude Exposure on Sleep and Mood States and the Underlying Neural Mechanisms]. [高原暴露对睡眠和情绪状态的动态影响及其潜在的神经机制]。
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960507
Wanlin He, Hailong Li, Jinli Meng, Li Feng, Zan Zhou, Yonghong Huang, Kejin Xiang, Hengyan Li, Xiaomei Li, Yuanyuan He, Xiaoyan Luo, Lu Che, Xiaoqi Huang
<p><strong>Objective: </strong>To analyze changes in sleep, mood state, and brain function in healthy populations living in near-sea-level environments before and after exposure to high-altitude environment, and to explore the correlations between regional brain functional changes and variations in sleep and mood states.</p><p><strong>Methods: </strong>A total of 45 healthy volunteers were enrolled. The participants came from regions of near-sea-level altitudes and were exposed to the high-altitude environment for a short period of time. The Pittsburgh Sleep Quality Index (PSQI), Zung Self-Rating Depression Scale (SDS), Patient Health Questionnaire-9 (PHQ-9), Zung Self-Rating Anxiety Scale (SAS), and Generalized Anxiety Disorder-7 (GAD-7) were administered to assess sleep quality as well as depressive and anxiety symptoms at 4 time points-prior to high-altitude exposure, immediately after exposure, one month after returning to low-altitude regions, and three months after returning to low-altitude regions. Resting-state functional magnetic resonance imaging (rs-fMRI) data were collected before and after high-altitude exposure, and regional brain functional parameters, including the amplitude of low-frequency fluctuations (ALFF) and functional connectivity strength, were analyzed. Statistical analyses were performed, including a linear mixed-effects model to evaluate longitudinal changes in scale scores, paired-sample <i>t</i>-tests to compare brain function differences before and after exposure, and Pearson correlation analyses to examine the relationship between brain functional changes and alterations in sleep and mood states.</p><p><strong>Results: </strong>Compared with the pre-exposure findings, the participants exhibited significantly increased PSQI scores (8.89 ± 4.41 vs. 5.08 ± 2.69, <i>P</i> < 0.05) and PHQ-9 scores (3.60 ± 4.19 vs.1.54 ± 2.30, <i>P</i> < 0.05) immediately after high-altitude exposure. One month after returning to the low-altitude environment, both sleep and depression scores decreased relative to the findings immediately after exposure (PSQI: 3.88 ± 2.13 vs. 8.89 ± 4.41, <i>P</i> < 0.05; PHQ-9: 1.50 ± 2.25 vs. 3.60 ± 4.19, <i>P</i> < 0.05) and showed no statistically significant difference compared with the pre-exposure findings (<i>P</i> > 0.05). Three months after returning to near-sea-level environment, sleep, depression, and anxiety scores were all reduced compared with the findings immediately after exposure (PSQI: 3.76 ± 2.31 vs. 8.89 ± 4.41, <i>P</i> < 0.05; PHQ-9: 1.24 ± 2.13 vs. 3.60 ± 4.19, <i>P</i> < 0.05; SAS: 23.84 ± 5.93 vs. 27.93 ± 7.05, <i>P</i> < 0.05), also showing no significant difference compared with the pre-exposure levels (<i>P</i> > 0.05). Brain function analysis revealed that, relative to the pre-exposure levels, ALFF in the bilateral superior temporal gyrus, insula, and dorsolateral prefrontal cortex (DLPFC) increased after high-altitude exposure (<i>P</i> < 0.05), and that functional connectiv
目的:分析生活在近海平面环境中的健康人群暴露于高海拔环境前后的睡眠、情绪状态和脑功能变化,探讨脑区域功能变化与睡眠和情绪状态变化的相关性。方法:选取45名健康志愿者。参与者来自海拔接近海平面的地区,并在短时间内暴露在高海拔环境中。采用匹兹堡睡眠质量指数(PSQI)、Zung抑郁自评量表(SDS)、患者健康问卷-9 (PHQ-9)、Zung焦虑自评量表(SAS)和广泛性焦虑障碍-7 (GAD-7)在高海拔暴露前、暴露后、返回低海拔地区1个月和返回低海拔地区3个月4个时间点评估睡眠质量以及抑郁和焦虑症状。采集高海拔暴露前后静息状态功能磁共振成像(rs-fMRI)数据,分析区域脑功能参数,包括低频波动幅度(ALFF)和功能连接强度。进行了统计分析,包括线性混合效应模型来评估量表得分的纵向变化,配对样本t检验来比较暴露前后的脑功能差异,Pearson相关分析来检查脑功能变化与睡眠和情绪状态改变之间的关系。结果:与暴露前相比,暴露后受试者PSQI得分(8.89±4.41比5.08±2.69,P < 0.05)和PHQ-9得分(3.60±4.19比1.54±2.30,P < 0.05)显著提高。返回低海拔环境1个月后,睡眠和抑郁评分均较暴露后立即下降(PSQI: 3.88±2.13比8.89±4.41,P < 0.05; PHQ-9: 1.50±2.25比3.60±4.19,P < 0.05),与暴露前比较差异无统计学意义(P < 0.05)。返回近海平面环境3个月后,睡眠、抑郁、焦虑得分均较暴露后立即下降(PSQI: 3.76±2.31比8.89±4.41,P < 0.05; PHQ-9: 1.24±2.13比3.60±4.19,P < 0.05; SAS: 23.84±5.93比27.93±7.05,P < 0.05),与暴露前比较差异无统计学意义(P < 0.05)。脑功能分析显示,与暴露前相比,高海拔暴露后,双侧颞上回、脑岛和背外侧前额叶皮层(DLPFC)的ALFF增加(P < 0.05), DLPFC的功能连接强度也增加(P < 0.05)。此外,DLPFC功能连接强度的变化与睡眠和情绪评分的变化呈正相关(P < 0.05)。结论:高海拔暴露对近海平面地区人群的睡眠、情绪状态和脑功能有显著影响,尤其是DLPFC与睡眠和情绪状态的变化密切相关。本研究结果为高海拔地区健康管理和干预策略提供了理论依据。
{"title":"[Dynamic Effects of High-Altitude Exposure on Sleep and Mood States and the Underlying Neural Mechanisms].","authors":"Wanlin He, Hailong Li, Jinli Meng, Li Feng, Zan Zhou, Yonghong Huang, Kejin Xiang, Hengyan Li, Xiaomei Li, Yuanyuan He, Xiaoyan Luo, Lu Che, Xiaoqi Huang","doi":"10.12182/20250960507","DOIUrl":"10.12182/20250960507","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To analyze changes in sleep, mood state, and brain function in healthy populations living in near-sea-level environments before and after exposure to high-altitude environment, and to explore the correlations between regional brain functional changes and variations in sleep and mood states.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A total of 45 healthy volunteers were enrolled. The participants came from regions of near-sea-level altitudes and were exposed to the high-altitude environment for a short period of time. The Pittsburgh Sleep Quality Index (PSQI), Zung Self-Rating Depression Scale (SDS), Patient Health Questionnaire-9 (PHQ-9), Zung Self-Rating Anxiety Scale (SAS), and Generalized Anxiety Disorder-7 (GAD-7) were administered to assess sleep quality as well as depressive and anxiety symptoms at 4 time points-prior to high-altitude exposure, immediately after exposure, one month after returning to low-altitude regions, and three months after returning to low-altitude regions. Resting-state functional magnetic resonance imaging (rs-fMRI) data were collected before and after high-altitude exposure, and regional brain functional parameters, including the amplitude of low-frequency fluctuations (ALFF) and functional connectivity strength, were analyzed. Statistical analyses were performed, including a linear mixed-effects model to evaluate longitudinal changes in scale scores, paired-sample &lt;i&gt;t&lt;/i&gt;-tests to compare brain function differences before and after exposure, and Pearson correlation analyses to examine the relationship between brain functional changes and alterations in sleep and mood states.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Compared with the pre-exposure findings, the participants exhibited significantly increased PSQI scores (8.89 ± 4.41 vs. 5.08 ± 2.69, &lt;i&gt;P&lt;/i&gt; &lt; 0.05) and PHQ-9 scores (3.60 ± 4.19 vs.1.54 ± 2.30, &lt;i&gt;P&lt;/i&gt; &lt; 0.05) immediately after high-altitude exposure. One month after returning to the low-altitude environment, both sleep and depression scores decreased relative to the findings immediately after exposure (PSQI: 3.88 ± 2.13 vs. 8.89 ± 4.41, &lt;i&gt;P&lt;/i&gt; &lt; 0.05; PHQ-9: 1.50 ± 2.25 vs. 3.60 ± 4.19, &lt;i&gt;P&lt;/i&gt; &lt; 0.05) and showed no statistically significant difference compared with the pre-exposure findings (&lt;i&gt;P&lt;/i&gt; &gt; 0.05). Three months after returning to near-sea-level environment, sleep, depression, and anxiety scores were all reduced compared with the findings immediately after exposure (PSQI: 3.76 ± 2.31 vs. 8.89 ± 4.41, &lt;i&gt;P&lt;/i&gt; &lt; 0.05; PHQ-9: 1.24 ± 2.13 vs. 3.60 ± 4.19, &lt;i&gt;P&lt;/i&gt; &lt; 0.05; SAS: 23.84 ± 5.93 vs. 27.93 ± 7.05, &lt;i&gt;P&lt;/i&gt; &lt; 0.05), also showing no significant difference compared with the pre-exposure levels (&lt;i&gt;P&lt;/i&gt; &gt; 0.05). Brain function analysis revealed that, relative to the pre-exposure levels, ALFF in the bilateral superior temporal gyrus, insula, and dorsolateral prefrontal cortex (DLPFC) increased after high-altitude exposure (&lt;i&gt;P&lt;/i&gt; &lt; 0.05), and that functional connectiv","PeriodicalId":39321,"journal":{"name":"四川大学学报(医学版)","volume":"56 5","pages":"1313-1319"},"PeriodicalIF":0.0,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12709070/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145783165","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Central Nervous System Infection After Neuroendoscopic and Microscopic Combined Hematoma Removal: Risk Factors and Construction of a Nomogram Prediction Model]. [神经内窥镜和显微镜联合血肿清除后中枢神经系统感染:危险因素和Nomogram预测模型的构建]。
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960607
Dan Liang, Kun Zhou, Bo Shu

Objective: To analyze the risk factors associated with central nervous system (CNS) infection in patients after neuroendoscopic hematoma removal combined with and microscopic hematoma removal, and to construct and validate a nomogram prediction model.

Methods: A total of 460 patients who underwent neuroendoscopic hematoma removal combined with microscopic hematoma removal at our hospital between January 2021 and December 2024 were retrospectively enrolled. The patients were assigned to a modeling cohort (n = 322) and a validation cohort (n = 138) in a 7∶3 ratio. Furthermore, the modeling cohort was divided into an infection group (n = 68) and a non-infected group (n = 254) according to whether CNS infection occurred. The independent predictors of central nervous system infection were identified by logistic regression analysis, and a nomogram prediction model was constructed accordingly.

Results: The overall incidence of CNS infection in the 460 patients was 20.65% (95/460). According to the logistic regression analysis, the independent risk factors for CNS infection in patients after neuroendoscopic and microscopic combined hematoma removal included a history of diabetes mellitus (odds ratio [OR] = 3.431, 95% CI: 1.300-9.057), the Glasgow Coma Scale (GCS) score (OR = 0.574, 95% CI: 0.462-0.711), cerebrospinal fluid leakage (OR = 4.492, 95% CI: 1.430-14.116), operation duration (OR = 1.011, 95% CI: 1.004-1.019), duration of drainage tube placement (OR = 5.452, 95% CI: 2.423-12.268) and albumin (ALB) level (OR = 0.778, 95% CI: 0.720-0.840) (P < 0.05). Based on these risk factors, a nomogram prediction model was constructed, and the area under the receiver operating characteristic curve (AUC) of the predicted events in the modeling cohort and the validation cohort was 0.928 (95% CI: 0.895-0.960) and 0.918 (95% CI: 0.885-0.951), respectively. The calibration curve fitted well with the ideal curve (Hosmer-Lemeshow test, P > 0.05), and the decision curve analysis demonstrated significant net benefit.

Conclusion: The nomogram model based on history of diabetes mellitus, GCS score, cerebrospinal fluid leakage, operation duration, duration of drainage tube placement, and ALB level demonstrates high predictive performance for CNS infection after neuroendoscopy-assisted microscopic hematoma removal.

目的:分析神经内镜下血肿切除联合显微镜下血肿切除后患者中枢神经系统(CNS)感染的相关危险因素,构建并验证nomogram预测模型。方法:回顾性分析我院于2021年1月至2024年12月行神经内镜下血肿清除联合显微镜下血肿清除术的460例患者。将患者按7∶3的比例分为建模队列(n = 322)和验证队列(n = 138)。根据是否发生中枢神经系统感染,将建模队列分为感染组(n = 68)和未感染组(n = 254)。通过logistic回归分析,确定了中枢神经系统感染的独立预测因素,并建立了相应的nomogram预测模型。结果:460例患者中中枢神经系统感染的总发生率为20.65%(95/460)。根据logistic回归分析,神经内镜与显微镜联合血肿清除术后患者发生中枢神经系统感染的独立危险因素包括糖尿病史(比值比[OR] = 3.431, 95% CI: 1.300 ~ 9.057)、格拉斯哥昏迷量表(GCS)评分(OR = 0.574, 95% CI: 0.462 ~ 0.711)、脑脊液漏(OR = 4.492, 95% CI: 1.430 ~ 14.116)、手术时间(OR = 1.011, 95% CI:1.004 ~ 1.019)、置管时间(OR = 5.452, 95% CI: 2.423 ~ 12.268)、白蛋白(ALB)水平(OR = 0.778, 95% CI: 0.720 ~ 0.840) (P < 0.05)。基于这些危险因素构建nomogram预测模型,模型队列和验证队列预测事件的受试者工作特征曲线下面积(AUC)分别为0.928 (95% CI: 0.895-0.960)和0.918 (95% CI: 0.885-0.951)。校正曲线与理想曲线拟合良好(Hosmer-Lemeshow检验,P > 0.05),决策曲线分析显示净效益显著。结论:基于糖尿病病史、GCS评分、脑脊液漏、手术时间、置管时间、ALB水平的nomogram模型对神经内窥镜辅助下血肿清除术后CNS感染具有较高的预测价值。
{"title":"[Central Nervous System Infection After Neuroendoscopic and Microscopic Combined Hematoma Removal: Risk Factors and Construction of a Nomogram Prediction Model].","authors":"Dan Liang, Kun Zhou, Bo Shu","doi":"10.12182/20250960607","DOIUrl":"10.12182/20250960607","url":null,"abstract":"<p><strong>Objective: </strong>To analyze the risk factors associated with central nervous system (CNS) infection in patients after neuroendoscopic hematoma removal combined with and microscopic hematoma removal, and to construct and validate a nomogram prediction model.</p><p><strong>Methods: </strong>A total of 460 patients who underwent neuroendoscopic hematoma removal combined with microscopic hematoma removal at our hospital between January 2021 and December 2024 were retrospectively enrolled. The patients were assigned to a modeling cohort (<i>n</i> = 322) and a validation cohort (<i>n</i> = 138) in a 7∶3 ratio. Furthermore, the modeling cohort was divided into an infection group (<i>n</i> = 68) and a non-infected group (<i>n</i> = 254) according to whether CNS infection occurred. The independent predictors of central nervous system infection were identified by logistic regression analysis, and a nomogram prediction model was constructed accordingly.</p><p><strong>Results: </strong>The overall incidence of CNS infection in the 460 patients was 20.65% (95/460). According to the logistic regression analysis, the independent risk factors for CNS infection in patients after neuroendoscopic and microscopic combined hematoma removal included a history of diabetes mellitus (odds ratio [OR] = 3.431, 95% CI: 1.300-9.057), the Glasgow Coma Scale (GCS) score (OR = 0.574, 95% CI: 0.462-0.711), cerebrospinal fluid leakage (OR = 4.492, 95% CI: 1.430-14.116), operation duration (OR = 1.011, 95% CI: 1.004-1.019), duration of drainage tube placement (OR = 5.452, 95% CI: 2.423-12.268) and albumin (ALB) level (OR = 0.778, 95% CI: 0.720-0.840) (<i>P</i> < 0.05). Based on these risk factors, a nomogram prediction model was constructed, and the area under the receiver operating characteristic curve (AUC) of the predicted events in the modeling cohort and the validation cohort was 0.928 (95% CI: 0.895-0.960) and 0.918 (95% CI: 0.885-0.951), respectively. The calibration curve fitted well with the ideal curve (Hosmer-Lemeshow test, <i>P</i> > 0.05), and the decision curve analysis demonstrated significant net benefit.</p><p><strong>Conclusion: </strong>The nomogram model based on history of diabetes mellitus, GCS score, cerebrospinal fluid leakage, operation duration, duration of drainage tube placement, and ALB level demonstrates high predictive performance for CNS infection after neuroendoscopy-assisted microscopic hematoma removal.</p>","PeriodicalId":39321,"journal":{"name":"四川大学学报(医学版)","volume":"56 5","pages":"1296-1304"},"PeriodicalIF":0.0,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12709062/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145783197","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Determination of 18 Perfluorinated Compounds in Tea Leaves by a Quick, Easy, Cheap, Effective, Rugged, and Safe Method Combined With Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry]. [快速、简便、廉价、有效、可靠、安全的超高效液相色谱-串联质谱法测定茶叶中18种全氟化合物]。
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960603
Weiyang Sun, Yujing Chuai, Xiaotao Zhou, Tianai Zhang, Li Yong, Lin Ren, Xinyue Luo, Xiaoli Zou
<p><strong>Objective: </strong>To establish an analytical method for the simultaneous determination of 18 perfluoroalkyl compounds (PFCs) in tea leaves using a quick, easy, cheap, effective, rugged, and safe (QuEChERS) method for sample pretreatment combined with ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).</p><p><strong>Methods: </strong>The target analytes-18 PFCs-included 13 carboxylic acid PFCs (perfluorobutanoic acid [PFBA], perfluoropentanoic acid [PFPeA], perfluorohexanoic acid [PFHxA], perfluoroheptanoic acid [PFHpA], perfluorooctanoic acid [PFOA], perfluorononanoic acid [PFNA], perfluorodecanoic acid [PFDA], perfluoroundecanoic acid [PFUdA], perfluorododecanoic acid [PFTrDA], perfluorotridecanoic acid [PFTeDA], perfluorotetradecanoic acid [PFHxDA], perfluorohexadecanoic acid [PFHpS], and perfluorooctadecanoic acid [PFODA]) and 5 sulfonic acid PFCs (perfluorobutanesulfonic acid [PFBS], perfluorohexanesulfonic acid [PFHxS], perfluoroheptanesulfonic acid [PFHpS], perfluorooctanesulfonic acid [PFOS], and perfluorodecanesulfonic acid [PFDS]). The QuEChERS pretreatment parameters were systematically optimized using the response surface methodology. The tea leave samples were extracted with an 80% acetonitrile solution and subsequently purified by adding a mixed absorbent consisting of 20 mg N-propyl-ethylenediamine (PSA), 210 mg graphitized carbon black GCB), and 60 mg octadecylsilane (C<sub>18</sub>). The supernatant was concentrated by nitrogen blowing and subsequently re-dissolved in 50% methanol-2 mmol/L ammonium acetate solution. The re-dissolved solution was injected into the UHPLC-MS/MS for analysis. The target analytes were separated on an ACQUITY UPLC BEH C<sub>18</sub> column (2.1 mm × 50 mm, 1.7 µm). The mobile phases consisted of methanol (phase A) and 2 mmol/L aqueous ammonium acetate (phase B), with a gradient elution procedure. The total running time was 18 min. The mass spectrometry analysis was conducted using an electrospray ionization source in negative ionization mode and multi-reaction monitoring (MRM), with quantification performed using the internal standard curve method. The greenness of the analytical method was assessed using Analytical GREEnness calculator (AGREE) and the Analytical Eco-Scale method (AES).</p><p><strong>Results: </strong>Under the optimized conditions, the limits of detection (LODs) and limits of quantification (LOQs) of the method were 0.0057-1.23 ng/g and 0.019-4.09 ng/g, respectively. The average recoveries of most target compounds were 71.1%-117.9%, with relative standard deviations (RSDs) below 15%. The AGREE index of the method was 0.49, and the AES score was 76. At least one PFC was detected in each of the 132 tea leave samples, and the detection rate of carboxylic acid PFC was higher than that of sulfonic acid PFC. The highest detection rates were observed for PFBA at 97.74%, PFHpA at 93.23%, and PFOA at 92.24%. In contrast, PFHpS, PFUdA, PFDoA, PFHxDA, and P
目的:建立快速、简便、廉价、有效、坚固、安全的QuEChERS样品前处理联合超高效液相色谱-串联质谱(UPLC-MS/MS)同时测定茶叶中18种全氟烷基化合物(PFCs)的分析方法。方法:目标分析物-18种全氟碳化物-包括13种羧酸型全氟碳化物(全氟丁酸[PFBA]、全氟戊酸[PFPeA]、全氟己酸[PFHxA]、全氟庚酸[PFHpA]、全氟辛酸[PFOA]、全氟壬酸[PFNA]、全氟癸酸[PFDA]、全氟癸酸[PFUdA]、全氟十二烷酸[PFTrDA]、全氟三十一烷酸[PFTeDA]、全氟十四烷酸[PFHxDA]、全氟十六烷酸[PFHpS]、以及全氟十二烷酸[PFODA])和5种磺酸全氟碳化合物(全氟丁烷磺酸[PFBS]、全氟己磺酸[PFHxS]、全氟庚烷磺酸[PFHpS]、全氟辛烷磺酸[PFOS]和全氟十烷磺酸[PFDS])。采用响应面法对QuEChERS预处理参数进行了系统优化。用80%乙腈溶液提取茶叶样品,然后加入由20 mg n -丙基-乙二胺(PSA)、210 mg石墨化炭黑(GCB)和60 mg十八烷基硅烷(C18)组成的混合吸附剂进行纯化。上清液经吹氮浓缩后再溶解于50%甲醇-2 mmol/L乙酸铵溶液中。再溶液注入UHPLC-MS/MS进行分析。目标分析物在ACQUITY UPLC BEH C18色谱柱(2.1 mm × 50 mm, 1.7µm)上分离。流动相为甲醇(A相)和2 mmol/L醋酸铵(B相),采用梯度洗脱法。总运行时间为18分钟。质谱分析采用负电离模式电喷雾电离源和多反应监测(MRM),定量采用内标曲线法。采用分析绿色度计算器(AGREE)和分析生态尺度法(AES)对分析方法的绿色度进行评价。结果:在优化条件下,方法的检出限和定量限分别为0.0057 ~ 1.23 ng/g和0.019 ~ 4.09 ng/g。多数目标化合物的平均加样回收率为71.1% ~ 117.9%,相对标准偏差(rsd)在15%以下。该方法的AGREE指数为0.49,AES评分为76。132份茶叶样品中至少检出1种PFC,羧酸PFC检出率高于磺酸PFC,其中PFBA检出率最高,为97.74%,PFHpA检出率最高,为93.23%,PFOA检出率最高,为92.24%。而PFHpS、PFUdA、PFDoA、PFHxDA、PFODA均未检出。结论:该方法简便、快速、灵敏,适用于茶叶中全氟化合物的分析。该方法绿色度高,对操作者和环境的影响最小。市场上销售的茶叶中普遍存在PFC污染,需要加强监测和监管。
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引用次数: 0
[Advances in Nanozyme-Aptamer Systems for the Detection of Foodborne Pathogens]. [纳米酶-适体系统检测食源性病原体的进展]。
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960204
Hao Liang, Shiyu Jia, Zhou Zhan, Yujiao Cai, Xiangheng Niu

Food safety problems caused by foodborne pathogenic bacteria pose a serious threat to public health, creating an urgent need to develop testing methods and techniques with excellent performance and are simple to use and of affordable cost. Traditional testing methods, such as isolation and culture, morphological observation, biochemical identification, and serological tests, have many limitations, including complex procedures, reliance on specialized technical equipment and personnel, and long turnaround time, rendering them inadequate for meeting current and future testing demands. Therefore, it is particularly important to develop simple, rapid, and highly sensitive methods for analyzing pathogenic bacteria. The fusion of nucleic acid aptamers and nanozymes brings new ideas for the rapid testing of pathogenic bacteria. On one hand, aptamers offer specific recognition capability for target bacteria and can be combined with various nucleic acid signal amplification techniques. On the other hand, the enzyme-like catalytic activity and signal amplification effect of many nanomaterials provide a basis for highly sensitive testing. This review highlights the application potential of nanozyme‒aptamer coupling systems in the field of microbial analysis by briefly summarizing the latest research progress in the use of nanozymes combined with aptamers for the detection of foodborne pathogenic bacteria. First of all, two main approaches to conjugating nanozymes with aptamers are introduced. Then, the testing mechanisms and typical applications of nanozyme‒aptamer coupling systems for foodborne pathogenic bacteria are discussed. Finally, future development trends and existing challenges are disucssed from four perspectives, including specificity, high sensitivity, high throughput, and intelligent detection. This review aims to provide a useful reference for the fusion of nanozymes and aptamers and for the development of on-site rapid testing techniques for foodborne pathogens, and to encourage broader academic interest to further advance this promising research field.

食源性致病菌引起的食品安全问题对公众健康构成严重威胁,迫切需要开发性能优良、使用简单、成本合理的检测方法和技术。传统的检测方法,如分离培养、形态学观察、生化鉴定和血清学检测,存在许多局限性,包括程序复杂、依赖专门的技术设备和人员、周转时间长,无法满足当前和未来的检测需求。因此,开发简单、快速、高灵敏度的病原菌分析方法显得尤为重要。核酸适体与纳米酶的融合为病原菌的快速检测带来了新的思路。一方面,适体对目标细菌具有特定的识别能力,可与多种核酸信号扩增技术相结合;另一方面,许多纳米材料的酶样催化活性和信号放大效应为高灵敏度测试提供了基础。本文简要综述了纳米酶-适体偶联系统在食源性致病菌检测中的最新研究进展,重点介绍了纳米酶-适体偶联系统在微生物分析领域的应用潜力。首先,介绍了纳米酶与适配体结合的两种主要方法。然后,讨论了纳米酶-适体偶联系统对食源性致病菌的检测机理和典型应用。最后,从特异性、高灵敏度、高通量和智能检测四个方面探讨了未来的发展趋势和存在的挑战。本文旨在为纳米酶与适体的融合及食源性病原体现场快速检测技术的发展提供有益的参考,并鼓励更广泛的学术兴趣,进一步推进这一前景广阔的研究领域。
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引用次数: 0
[Research Progress on the Mechanisms of Visual Cortical Plasticity]. [视觉皮层可塑性机制研究进展]。
Q3 Medicine Pub Date : 2025-09-20 DOI: 10.12182/20250960107
Yinmiao Dong, Longqian Liu

A growing body of evidence indicates that the visual cortex retains a considerable degree of plasticity well into adulthood, suggesting that the visual acuity and binocular visual function of adult amblyopic patients can be improved even beyond the critical period of visual development. Currently, as novel treatment options for amblyopia, pharmacological and non-invasive methods that can enhance the plasticity of the visual cortex have not yet been widely applied in clinical practice. Therefore, it is of critical importance to investigate the underlying mechanisms of visual cortex plasticity to pave the way for the development of new therapeutic strategies for amblyopia. This paper reviews current research progress on mechanisms contributing to changes in visual cortical plasticity, including the regulation of the balance between excitatory and inhibitory neural activities, extracellular matrix remodeling, inhibitory factors associated with plasticity, and neurotrophic factors. With the continued advancement of various neuroimaging technologies, future research should aim to elucidate the precise mechanisms that control the initiation and closure of the critical period, and to clarify how the various factors involved in the regulation of visual cortical plasticity act jointly across different cell types and signaling pathways. Such investigations will provide new approaches and strategies for the treatment of amblyopia.

越来越多的证据表明,视觉皮层在成年后仍保持相当程度的可塑性,这表明成人弱视患者的视力和双眼视觉功能即使在视力发育的关键时期之后也可以得到改善。目前,增强视皮层可塑性的药物和非侵入性方法作为治疗弱视的新选择尚未广泛应用于临床。因此,研究视觉皮层可塑性的潜在机制,为开发新的弱视治疗策略铺平道路至关重要。本文综述了视觉皮层可塑性变化机制的研究进展,包括兴奋性和抑制性神经活动的平衡调节、细胞外基质重塑、可塑性相关的抑制因子和神经营养因子。随着各种神经影像学技术的不断进步,未来的研究应致力于阐明控制关键期启动和关闭的确切机制,并阐明参与视觉皮质可塑性调节的各种因素如何在不同的细胞类型和信号通路中共同作用。这些研究将为弱视的治疗提供新的途径和策略。
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引用次数: 0
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四川大学学报(医学版)
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