countermeasure

对策
  • 文章类型: Journal Article
    血流限制(BFR)已被确定为缓解太空飞行中生理失调的潜在对策。指南建议相对于肢体闭塞压力(LOP)规定止血带压力;然而,尚不清楚身体倾斜或重力降低类似物是否会影响LOP。我们检查了仰卧卧床和体重悬吊(BWS)在6°头向下倾斜(HDT)时腿部和手臂的LOP,水平(0°),和9.5°抬头倾斜(HUT)位置。27名成年人(年龄,26±5年;身高,1.75±0.08m;体质量,73±12kg)在卧床期间完成所有倾斜。一个子组(n=15)在BWS期间额外完成了倾斜。在每个位置,在休息5分钟后,再休息5分钟后,使用Delfi个性化止血带系统在腿和手臂中测量LOP两次。在卧床和BWS中,腿部LOP从6°HDT到9.5°HUT显着增加了9-15mmHg(Cohen\sd=0.7-1.0)。在水平姿势和9.5°HUT姿势的BWS期间,腿部LOP相对于卧床期间的相同角度显着提高了8mmHg(Cohen'sd=0.6)。手臂LOP在身体倾斜和类似物之间保持不变。在所有条件下,在初始和随后的5分钟休息期后进行的LOP测量的组内相关系数介于0.91-0.95(腿)和0.83-0.96(臂)之间。建议在应用血管闭塞之前在相同的身体倾斜/设置中测量LOP,以最大程度地减少实际止血带压力与规定止血带压力之间的差异。
    Blood flow restriction (BFR) has been identified as a potential countermeasure to mitigate physiological deconditioning during spaceflight. Guidelines recommend that tourniquet pressure be prescribed relative to limb occlusion pressure (LOP); however, it is unclear whether body tilting or reduced gravity analogues influence LOP. We examined LOP at the leg and arm during supine bedrest and bodyweight suspension (BWS) at 6° head-down tilt (HDT), horizontal (0°), and 9.5° head-up tilt (HUT) positions. Twenty-seven adults (age, 26 ± 5 years; height, 1.75 ± 0.08 m; body mass, 73 ± 12 kg) completed all tilts during bedrest. A subgroup (n = 15) additionally completed the tilts during BWS. In each position, LOP was measured twice in the leg and arm using the Delfi Personalized Tourniquet System after 5 min of rest and again after a further 5 min. The LOP at the leg increased significantly from 6° HDT to 9.5° HUT in bedrest and BWS by 9-15 mmHg (Cohen\'s d = 0.7-1.0). Leg LOP was significantly higher during BWS at horizontal and 9.5° HUT postures relative to the same angles during bedrest by 8 mmHg (Cohen\'s d = 0.6). Arm LOP remained unchanged between body tilts and analogues. Intraclass correlation coefficients for LOP measurements taken after an initial and subsequent 5 min rest period in all conditions ranged between 0.91-0.95 (leg) and 0.83-0.96 (arm). It is advised that LOP be measured before the application of a vascular occlusion in the same body tilt/setting to which it is applied to minimize discrepancies between the actual and prescribed tourniquet pressure.
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  • 文章类型: Editorial
    暂无摘要。
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  • 文章类型: Journal Article
    近地轨道(LEO)以外的任务将使宇航员暴露于太阳能粒子(SEP)和银河宇宙射线(GCR)形式的电离辐射(IR),包括高原子序数和能量(HZE)核。胃肠道(GI)系统被证明是高度放射敏感性的,即使是相对低剂量的IR暴露也能够诱导粘膜损伤并破坏上皮屏障功能。IR也是结肠直肠癌(CRC)的既定风险因素,有几项研究使用肿瘤倾向的APC小鼠模型检查了SEP/GCR暴露的长期GI影响。对野生型小鼠模型中建模的空间辐射暴露的急性短期影响的研究更为有限,并且对于更好地定义带电粒子诱发的胃肠道病理和测试新型医学对策(MCM)以促进宇航员安全是必要的。
    在这项研究中,我们进行了地面研究,其中雄性和雌性C57BL/6J小鼠暴露于γ射线,50MeV质子,或在NASA太空辐射实验室(NSRL)的1GeV/nFe-56离子,在辐照后的前24小时测量组织学和免疫组织化学终点,以定义立即的SEP/GCR-GI诱导的改变。
    我们的数据表明,与匹配的γ射线对照不同,急性暴露于质子和铁离子会破坏肠道功能并引起粘膜损伤,血管充血,上皮屏障破坏,粘膜相关淋巴组织明显增大。我们还测量了DNA双链断裂(DSB)修复的动力学使用γ-H2AX特异性抗体和凋亡通过TUNEL标记,注意仅在带电粒子辐照的样品中,由γ-H2AX标记的核外细胞质DNA的诱导和消失。我们表明,通过IV注射递送的姜黄素负载纳米脂蛋白颗粒(cNLP)进行18小时预处理可减少DSB相关的病灶水平和凋亡,并恢复隐窝绒毛长度。
    这些数据提高了我们对暴露于建模空间辐射后胃肠道生理变化的理解,并证明了有希望的空间辐射MCM的有效性。
    UNASSIGNED: Missions beyond low Earth orbit (LEO) will expose astronauts to ionizing radiation (IR) in the form of solar energetic particles (SEP) and galactic cosmic rays (GCR) including high atomic number and energy (HZE) nuclei. The gastrointestinal (GI) system is documented to be highly radiosensitive with even relatively low dose IR exposures capable of inducing mucosal lesions and disrupting epithelial barrier function. IR is also an established risk factor for colorectal cancer (CRC) with several studies examining long-term GI effects of SEP/GCR exposure using tumor-prone APC mouse models. Studies of acute short-term effects of modeled space radiation exposures in wildtype mouse models are more limited and necessary to better define charged particle-induced GI pathologies and test novel medical countermeasures (MCMs) to promote astronaut safety.
    UNASSIGNED: In this study, we performed ground-based studies where male and female C57BL/6J mice were exposed to γ-rays, 50 MeV protons, or 1 GeV/n Fe-56 ions at the NASA Space Radiation Laboratory (NSRL) with histology and immunohistochemistry endpoints measured in the first 24 h post-irradiation to define immediate SEP/GCR-induced GI alterations.
    UNASSIGNED: Our data show that unlike matched γ-ray controls, acute exposures to protons and iron ions disrupts intestinal function and induces mucosal lesions, vascular congestion, epithelial barrier breakdown, and marked enlargement of mucosa-associated lymphoid tissue. We also measured kinetics of DNA double-strand break (DSB) repair using gamma-H2AX- specific antibodies and apoptosis via TUNEL labeling, noting the induction and disappearance of extranuclear cytoplasmic DNA marked by gamma-H2AX only in the charged particle-irradiated samples. We show that 18 h pre-treatment with curcumin-loaded nanolipoprotein particles (cNLPs) delivered via IV injection reduces DSB-associated foci levels and apoptosis and restore crypt villi lengths.
    UNASSIGNED: These data improve our understanding of physiological alterations in the GI tract immediately following exposures to modeled space radiations and demonstrates effectiveness of a promising space radiation MCM.
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  • 文章类型: Journal Article
    克里米亚-刚果出血热(CCHF),由CCHF病毒引起,是一种可以导致一系列疾病结果的蜱传疾病,从无症状感染到致命的病毒性出血热;这种疾病已经在超过30个国家被描述。我们进行了文献综述,以提供病毒学的概述,发病机制,和临床医生的CCHF病理学。病毒生命周期和分子相互作用是复杂的,没有充分描述。尽管发病机制和免疫生物学尚未完全了解,很明显,多个过程有助于病毒进入,复制,和病理损伤。有限的尸检报告描述了多器官受累并伴有外渗和出血。对CCHF病毒发病机制和免疫学的深入了解将改善患者护理并加快CCHF医学对策的发展。
    Crimean-Congo hemorrhagic fever (CCHF), caused by CCHF virus, is a tickborne disease that can cause a range of illness outcomes, from asymptomatic infection to fatal viral hemorrhagic fever; the disease has been described in >30 countries. We conducted a literature review to provide an overview of the virology, pathogenesis, and pathology of CCHF for clinicians. The virus life cycle and molecular interactions are complex and not fully described. Although pathogenesis and immunobiology are not yet fully understood, it is clear that multiple processes contribute to viral entry, replication, and pathological damage. Limited autopsy reports describe multiorgan involvement with extravasation and hemorrhages. Advanced understanding of CCHF virus pathogenesis and immunology will improve patient care and accelerate the development of medical countermeasures for CCHF.
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  • 文章类型: Journal Article
    克里米亚-刚果出血热(CCHF)是一种从无症状到致命的蜱传感染,已在30多个国家进行了描述。早期识别和隔离疑似或确诊的CCHF患者,并采取适当的预防和控制措施,对于防止人与人之间的传播至关重要。这里,我们提供了流行病学的概述,临床特征,以及CCHF的预防和控制。鉴于其广泛的地理分布,CCHF构成了持续的公共卫生威胁,有可能传播到新的地区,遗传变异倾向,以及严重和致命疾病的可能性,除了有限的预防和治疗医学对策。高度怀疑,全面的旅行和流行病学史,和临床评估对于及时诊断至关重要。感染控制措施可以有效降低传播风险,但需要正确和一致的应用。
    Crimean-Congo hemorrhagic fever (CCHF) is a tickborne infection that can range from asymptomatic to fatal and has been described in >30 countries. Early identification and isolation of patients with suspected or confirmed CCHF and the use of appropriate prevention and control measures are essential for preventing human-to-human transmission. Here, we provide an overview of the epidemiology, clinical features, and prevention and control of CCHF. CCHF poses a continued public health threat given its wide geographic distribution, potential to spread to new regions, propensity for genetic variability, and potential for severe and fatal illness, in addition to the limited medical countermeasures for prophylaxis and treatment. A high index of suspicion, comprehensive travel and epidemiologic history, and clinical evaluation are essential for prompt diagnosis. Infection control measures can be effective in reducing the risk for transmission but require correct and consistent application.
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  • 文章类型: English Abstract
    The goal of achieving elimination of schistosomiasis across all endemic counties in China by 2030 was proposed in the Outline of the Healthy China 2030 Plan. On June 16, 2023, the Action Plan to Accelerate the Elimination of Schistosomiasis in China (2023-2030) was jointly issued by National Disease Control and Prevention Administration and other 10 ministries, which deployed the targets and key tasks of the national schistosomiasis elimination programme in China. This article describes the progress of the national schistosomiasis control programme, analyzes the opportunities to eliminate schistosomiasis, and proposes targeted recommendations to tackle the challenges of schistosomiasis elimination, so as to accelerate the process towards schistosomiasis elimination and facilitate the building of a healthy China.
    [摘要] 《“健康中国2030”规划纲要》提出了2030年我国所有血 吸虫病流行县达到消除标准的目标。2023年6月16日, 国家疾病 预防控制局等11部门联合印发了《加快实现消除血吸虫病目标行 动方案 (2023—2030年) 》, 对我国血吸虫病消除工作目标和重点 任务进行了明确部署。本文就我国血吸虫病防治工作进展、实现 消除血吸虫病目标的机遇进行了剖析, 并就面临的挑战提出针对 性的建议, 以推动全国血吸虫病消除进程、助力健康中国建设。.
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  • 文章类型: Journal Article
    目的:各种组织中线粒体功能的改变是太空飞行引起的物理调节的关键决定因素。与组织活检相比,血细胞生物能量学有望成为一种系统性和更容易获得的生物标志物,在头下倾斜卧床休息(HDTBR)期间进行了评估,建立的地面模拟,用于航天引起的人类生理变化。更具体地说,本研究探讨了HDTBR和运动对策对外周血单个核细胞(PBMC)线粒体呼吸的影响。
    方法:我们对24名健康参与者进行了严格的30天HDTBR方案。对照组(n=12)仅接受HDTBR,而对策组(n=12)进行常规仰卧位自行车运动,然后在运动后进行静脉闭塞大腿袖带6小时。我们在卧床休息前14天评估了常规血液参数,通过高分辨率呼吸测定PBMC的呼吸能力,在卧床休息前2天和第30天的柠檬酸合酶活性。我们通过流式细胞术确认了PBMC组成。
    结果:对策组PBMC最大氧化磷酸化能力(OXPHOS)的变化增加了11%,而对照组下降了10%(p=0.04)。OXPHOS的限制仅在对照组中增加,而其他呼吸状态不受任何干预的影响。相关分析显示白细胞之间呈正相关,淋巴细胞,两组中都有PBMC生物能量学的嗜碱性粒细胞。
    结论:这项研究表明,有规律的运动对策对PBMC线粒体功能有积极影响,证实了血细胞生物能学在人类太空飞行中的潜在应用。
    Altered mitochondrial function across various tissues is a key determinant of spaceflight-induced physical deconditioning. In comparison to tissue biopsies, blood cell bioenergetics holds promise as a systemic and more readily accessible biomarker, which was evaluated during head-down tilt bed rest (HDTBR), an established ground-based analog for spaceflight-induced physiological changes in humans. More specifically, this study explored the effects of HDTBR and an exercise countermeasure on mitochondrial respiration in peripheral blood mononuclear cells (PBMCs).
    We subjected 24 healthy participants to a strict 30-day HDTBR protocol. The control group (n = 12) underwent HDTBR only, while the countermeasure group (n = 12) engaged in regular supine cycling exercise followed by veno-occlusive thigh cuffs post-exercise for 6 h. We assessed routine blood parameters 14 days before bed rest, the respiratory capacity of PBMCs via high-resolution respirometry, and citrate synthase activity 2 days before and at day 30 of bed rest. We confirmed PBMC composition by flow cytometry.
    The change of the PBMC maximal oxidative phosphorylation capacity (OXPHOS) amounted to an 11% increase in the countermeasure group, while it decreased by 10% in the control group (p = 0.04). The limitation of OXPHOS increased in control only while other respiratory states were not affected by either intervention. Correlation analysis revealed positive associations between white blood cells, lymphocytes, and basophils with PBMC bioenergetics in both groups.
    This study reveals that a regular exercise countermeasure has a positive impact on PBMC mitochondrial function, confirming the potential application of blood cell bioenergetics for human spaceflight.
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  • 文章类型: Journal Article
    驾驶员疲劳是所有致命事故中约10-30%的原因。与疲劳相关的碰撞的预防依赖于驾驶员疲劳的可靠检测和有效对策的应用。一种潜在的对策是施用香料,因为气味会对人类产生警示作用。这里的目的是研究是否可以将掺入三叉神经成分的香料用作驾驶员疲劳的车内对策。香水在驾驶模拟器中对21名健康但睡眠不足的参与者进行了测试。每个参与者执行了两次单调的驾驶任务,一次含有含有三叉神经成分的活性香料,一次含有嗅觉香料,交叉单盲设计。三叉神经/嗅觉香味的顺序是随机的,并对参与者不知情。两种香料(三叉神经/嗅觉)在参与者入睡时(定义为眼睛闭合>3s)或在参与者未入睡约45分钟后施用。在驾驶过程中每5分钟使用Karolinska嗜睡量表(KSS)评估自我报告的嗜睡。记录每个驱动器的速度和横向位置的变化以及线交叉频率以测量驱动性能。收集心率测量值(ECG)和眨眼(EOG)以研究香气的潜在唤醒作用并跟踪困倦的客观迹象。平均眨眼持续时间,这被用作睡意的客观衡量标准,显著下降,香水曝光后,越线的频率也是如此,但是三叉神经刺激的香气和纯嗅觉香气之间没有统计学上的显着差异。结果与其他常用疲劳对策的效果一致,喜欢大声播放音乐。这些对策可以在短时间内恢复警觉性和驾驶性能。这是否足以支持驾驶性能,直到驾驶员可以在实际交通中安全停车仍然是未来研究的主题。
    Driver fatigue is a contributing factor in about 10-30% of all fatal crashes. Prevention of fatigue-related crashes relies on robust detection of driver fatigue and application of effective countermeasures. A potential countermeasure is fragrance administration since odors can have alerting effects on humans. The aim here was to investigate if a fragrance incorporating trigeminal components could be used as an in-vehicle countermeasure for driver fatigue. The fragrance was tested in a driving simulator with 21 healthy but sleep-deprived participants. Each participant performed a monotonous driving task twice, once with active fragrance containing a trigeminal component and once with olfactory fragrance, in a cross-over single-blind design. The order of trigeminal/olfactory fragrance was randomized and blinded to the participants. Both fragrances (trigeminal/olfactory) were administered either when the participant fell asleep (defined as eye closure > 3 s) or after approximately 45 min if the participant did not fall asleep. Self-reported sleepiness was assessed using the Karolinska Sleepiness Scale (KSS) every 5 min during driving. Variability in speed and lateral position and line crossing frequency were logged for each drive to measure driving performance. Heart rate measurements (ECG) and eye blinks (EOG) were collected to investigate potential arousing effects of the fragrance and to track objective signs of sleepiness. Mean blink duration, which was used as an objective measure of sleepiness, decreased significantly, after fragrance exposure, as did the frequency of line crossings, but there were no statistically significant differences between the fragrance with trigeminal stimulus and the pure olfactory fragrance. The results are in line with the effects found for other commonly used fatigue countermeasures, like playing loud music. These countermeasures can restore alertness and driving performance for a short while. Whether this is sufficient to support driving performance until the driver can make a safe stop in real traffic remains a topic for future studies.
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  • 文章类型: Journal Article
    UNASSIGNED: Long-duration space missions will be a real challenge for maintaining astronauts\' adaptability. Research on transcutaneous vagus nerve stimulation (taVNS) is expanding rapidly, and its modalities constitute a major research challenge. A growing number of reviews stress the need to validate biomarkers for monitoring effects to enhance our understanding of the processes by which taVNS acts. Heart rate variability (HRV) appears to be a relevant candidate that informs on the autonomic nervous system (ANS). This is a promising technique to minimize the pathogenic effects of such large-scale missions and thus might be a relevant countermeasure. This study aimed to investigate the impact of taVNS on cognitive, psychological, and physiological functioning, including ANS functioning, and the benefits of increasing the number of taVNS sessions.
    UNASSIGNED: A total of 44 healthy participants were randomly assigned to one of the two cross-over protocols: a single session protocol (one taVNS and one sham simulation) or a repeated session protocol (three taVNS and three sham simulations). Cognitive, psychological, and physiological measures were performed before (pre) and after (post) each intervention. Sleep monitoring was only recorded before the first and after the last intervention in each protocol. For the repeated session protocol only, participants were allocated to two groups according to their parasympathetic activation gain during the three interventions: high parasympathetic delta (HPd) and low parasympathetic delta (LPd).
    UNASSIGNED: Participants in the repeated session protocol increased their HRV, cognitive performance, and sleep efficiency. In particular, taVNS induced higher parasympathetic activation and cardiac flexibility compared to the sham simulation in the repeated session protocol. Nevertheless, the perception of stress may indicate a nocebo effect of the repeated session. The HPd profile had higher interoceptive awareness, HRV highlighted by non-linear measures, and cognitive performance, but presented a decrease in some indicators of sleep efficiency compared to the LPd profile.
    UNASSIGNED: taVNS seems to induce positive health outcomes, especially when the stimulation is repeated three times per week. Our findings highlight the benefits of parasympathetic activation during taVNS on psychophysiological and cognitive functioning. Further research is needed to validate these results on a large sample, using longitudinal measures over several months. This intervention appears promising as a countermeasure to extreme missions and occupations.
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  • 文章类型: Journal Article
    神经毒素对人类健康和安全构成重大威胁,因为它们破坏和损害神经系统。它们的强大和结构多样性给制定有效对策带来了挑战。在这项研究中,引入了一种独特的纳米颗粒设计,结合了双重仿生机制,以增强神经毒素的解毒功效。使用蛇毒毒素(STX),最致命的神经毒素之一,和它的天然结合蛋白萨克斯蛋白(Sxph)作为模型系统,成功开发了人类神经元膜涂层和Sxph负载的金属有机框架(MOF)纳米海绵(称为“Neuron-MOF/Sxph-NS”)。由此产生的Neuron-MOF/Sxph-NS具有仿生设计,不仅可以通过神经元膜涂层模仿宿主神经元进行基于功能的解毒,而且还通过将Sxph蛋白封装在纳米颗粒核心中来模拟毒素抗性生物体。全面的体外试验,包括细胞渗透肿胀,钙通量,和细胞毒性测定,证明神经元-MOF/Sxph-NS的解毒功效得到改善。此外,在STX中毒的小鼠模型中,神经元-MOF/Sxph-NS的应用在治疗和预防方案中均显示出显着的生存益处,没有任何明显的急性毒性。总的来说,神经元-MOF/Sxph-NS的发展代表了神经毒素解毒的重要进展,为治疗由神经毒素引起的损伤和疾病提供了有希望的潜力,并解决了目前神经毒素对策的局限性。
    Neurotoxins present a substantial threat to human health and security as they disrupt and damage the nervous system. Their potent and structurally diverse nature poses challenges in developing effective countermeasures. In this study, a unique nanoparticle design that combines dual-biomimicry mechanisms to enhance the detoxification efficacy of neurotoxins is introduced. Using saxitoxin (STX), one of the deadliest neurotoxins, and its natural binding protein saxiphilin (Sxph) as a model system, human neuronal membrane-coated and Sxph-loaded metal-organic framework (MOF) nanosponges (denoted \"Neuron-MOF/Sxph-NS\") are successfully developed. The resulting Neuron-MOF/Sxph-NS exhibit a biomimetic design that not only emulates host neurons for function-based detoxification through the neuronal membrane coating, but also mimics toxin-resistant organisms by encapsulating the Sxph protein within the nanoparticle core. The comprehensive in vitro assays, including cell osmotic swelling, calcium flux, and cytotoxicity assays, demonstrate the improved detoxification efficacy of Neuron-MOF/Sxph-NS. Furthermore, in mouse models of STX intoxication, the application of Neuron-MOF/Sxph-NS shows significant survival benefits in both therapeutic and prophylactic regimens, without any apparent acute toxicity. Overall, the development of Neuron-MOF/Sxph-NS represents an important advancement in neurotoxin detoxification, offering promising potential for treating injuries and diseases caused by neurotoxins and addressing the current limitations in neurotoxin countermeasures.
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