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The influence of travel time on perceived traveled distance varies by spatiotemporal scale. 旅行时间对感知旅行距离的影响因时空尺度而异。
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-07-02 DOI: 10.1007/s00221-024-06880-1
Cindy Jagorska, Martin Riemer

The influence of travel time on perceived traveled distance has often been studied, but the results are inconsistent regarding the relationship between the two magnitudes. We argue that this is due to differences in the lengths of investigated travel distances and hypothesize that the influence of travel time differs for rather short compared to rather long traveled distances. We tested this hypothesis in a virtual environment presented on a desktop as well as through a head-mounted display. Our results show that, for longer distances, more travel time leads to longer perceived distance, while we do not find an influence of travel time on shorter distances. The presentation through an HMD vs. desktop only influenced distance judgments in the short distance condition. These results are in line with the idea that the influence of travel time varies by the length of the traveled distance, and provide insights on the question of how distance perception in path integration studies is affected by travel time, thereby resolving inconsistencies reported in previous studies.

人们经常研究旅行时间对感知旅行距离的影响,但关于两者之间关系的研究结果并不一致。我们认为,这是由于所研究的旅行距离长度不同造成的,并假设旅行时间对较短旅行距离和较长的旅行距离的影响是不同的。我们在桌面和头戴式显示器上呈现的虚拟环境中测试了这一假设。结果表明,对于较长距离而言,旅行时间越长,感知距离就越长,而对于较短距离则没有发现旅行时间的影响。通过头戴式显示器和台式电脑显示的内容只影响短距离条件下的距离判断。这些结果与旅行时间的影响因旅行距离的长短而异的观点一致,并为路径整合研究中的距离感知如何受旅行时间影响的问题提供了见解,从而解决了以往研究中报告的不一致问题。
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引用次数: 0
Accumulated HIIT inhibits anxiety and depression, improves cognitive function, and memory-related proteins in the hippocampus of aged rats. 累积性 HIIT 可抑制焦虑和抑郁,改善认知功能和老年大鼠海马体中与记忆相关的蛋白质。
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-06-12 DOI: 10.1007/s00221-024-06869-w
Caíque Olegário Diniz E Magalhães, Ricardo Augusto Leoni De Sousa, Bruno Ferreira Mendes, Isabela Rocha Dias, Ramona Ramalho Souza Pereira, Gabriela Cruz Pereira, Kil Sun Lee, Marco Fabricio Dias Peixoto, Ricardo Cardoso Cassilhas

This study aimed to compare the effects of High-Intensity Interval Training (HIIT) performed in a single session(1xHIIT) versus three daily sessions (3xHIIT) on fitness level and behavior of aged rats. Eighteen-month-old Wistar rats were assigned to Untrained (UN), 1xHIIT, or 3xHIIT (n = 12/group). Both groups, 1xHIIT and 3xHIIT, performed 15 min of a treadmill running HIIT protocol during 8 weeks. 1xHIIT protocol consisted of a single daily session of 15 min, while the 3xHIIT performed three daily sessions of 5 min with a 4 h interval between the sessions. Morris Water Maze (MWM) task was used to evaluate spatial learning and memory. Splash test, Forced Swim test, and Elevated Plus Maze task (EPM) were used to evaluate anhedonic, depressive-like, and anxious behaviors, respectively. Rats were euthanized, and the hippocampus was harvested for western blot analyses (CaMKII and BDNF). Both HIIT protocols improved VO2max and spatial memory. Notably, only the 3xHIIT protocol attenuated anxious and depressive-like behaviors. Western blot analyses of the hippocampus revealed that both HIIT protocols increased BDNF levels. BDNF levels were higher in the 3xHIIT when compared with 1xHIIT group, and we observed increasement of the CamKII levels just in the 3x HIIT group. Therefore, this study provides evidence indicating that accumulated HIIT sessions is more effective than traditional daily HIIT sessions in improving fitness level, cognitive function, memory, inhibiting the development of mood disorders, and enhancing BDNF and CaMKII levels in the hippocampus of aged rats.

本研究旨在比较单次高强度间歇训练(HIIT)(1xHIIT)和每天三次高强度间歇训练(3xHIIT)对老年大鼠体能水平和行为的影响。18 个月大的 Wistar 大鼠被分配到未训练组(UN)、1xHIIT 或 3xHIIT 组(n = 12/组)。1xHIIT 和 3xHIIT 两组均在 8 周内进行 15 分钟的跑步机跑步 HIIT 训练。1xHIIT 每天进行一次,每次 15 分钟;3xHIIT 每天进行三次,每次 5 分钟,每次间隔 4 小时。莫里斯水迷宫(MWM)任务用于评估空间学习和记忆。泼水试验、强迫游泳试验和高架迷宫任务(EPM)分别用于评估失调行为、抑郁样行为和焦虑行为。对大鼠实施安乐死,并采集海马进行 Western 印迹分析(CaMKII 和 BDNF)。两种 HIIT 方案都提高了 VO2max 和空间记忆力。值得注意的是,只有 3xHIIT 方案减轻了焦虑和抑郁样行为。海马的 Western 印迹分析显示,两种 HIIT 方案都能提高 BDNF 水平。与 1xHIIT 组相比,3xHIIT 组的 BDNF 水平更高,而且我们还观察到 3xHIIT 组的 CamKII 水平也有所提高。因此,本研究提供的证据表明,累积 HIIT 训练比传统的每日 HIIT 训练更能有效改善老年大鼠的体能水平、认知功能、记忆力,抑制情绪障碍的发展,并提高海马中的 BDNF 和 CaMKII 水平。
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引用次数: 0
Perceptual decoupling in the sustained attention to response task is unlikely. 在持续注意反应任务中,知觉解耦的可能性不大。
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-07-03 DOI: 10.1007/s00221-024-06885-w
Aman Bedi, Paul N Russell, William S Helton

Researchers dispute the cause of errors in high Go, low No Go target detection tasks, like the Sustained Attention to Response Task (SART). Some researchers propose errors in the SART are due to perceptual decoupling, where a participant is unaware of stimulus identity. This lack of external awareness causes an erroneous response. Other researchers suggest the majority of the errors in the SART are instead due to response leniency, not perceptual decoupling. Response delays may enable a participant who is initially unaware of stimulus identity, perceptually decoupled, to become aware of stimulus identity, or perceptually recoupled. If, however, the stimulus presentation time is shortened to the minimum necessary for stimulus recognition and the stimulus is disrupted with a structured mask, then there should be no time to enable perception to recouple even with a response delay. From the perceptual decoupling perspective, there should be no impact of a response delay on performance in this case. Alternatively if response bias is critical, then even in this case a response delay may impact performance. In this study, we shortened stimulus presentation time and added a structured mask. We examined whether a response delay impacted performance in the SART and tasks where the SART's response format was reversed. We expected a response delay would only impact signal detection theory bias, c, in the SART, where response leniency is an issue. In the reverse formatted SART, since bias was not expected to be lenient, we expected no impact or minimal impact of a response delay on response bias. These predictions were verified. Response bias is more critical in understanding SART performance, than perceptual decoupling, which is rare if it occurs at all in the SART.

研究人员对高 Go 低 No Go 目标检测任务(如持续注意反应任务 (SART))中出现错误的原因存在争议。一些研究人员认为,SART 中的错误是由于知觉脱钩造成的,即受试者没有意识到刺激物的身份。这种外部意识的缺乏导致了错误的反应。其他研究人员则认为,SART 中的大部分错误是由于反应宽松造成的,而非知觉脱钩。反应延迟可能会使最初没有意识到刺激特征、知觉脱钩的被试意识到刺激特征或知觉再脱钩。但是,如果刺激呈现时间被缩短到识别刺激所需的最短时间,并且刺激被结构化掩码干扰,那么即使有反应延迟,也不应该有时间让知觉重新耦合。从知觉解耦的角度来看,在这种情况下,反应延迟对成绩应该没有影响。相反,如果反应偏差至关重要,那么即使在这种情况下,反应延迟也可能会影响成绩。在本研究中,我们缩短了刺激呈现时间,并添加了一个结构化掩码。我们考察了反应延迟是否会影响 SART 和 SART 反应形式相反的任务的成绩。我们预计反应延迟只会影响 SART 中的信号检测理论偏差 c,因为在 SART 中,反应宽松度是一个问题。而在反向格式的 SART 中,由于不存在宽松的偏差,我们预计反应延迟对反应偏差不会产生影响或影响极小。这些预测都得到了验证。与知觉脱钩相比,响应偏差对于理解 SART 的性能更为关键,而知觉脱钩即使在 SART 中出现,也是非常罕见的。
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引用次数: 0
Silencing CXCL16 alleviate neuroinflammation and M1 microglial polarization in mouse brain hemorrhage model and BV2 cell model through PI3K/AKT pathway. 沉默CXCL16可通过PI3K/AKT途径缓解小鼠脑出血模型和BV2细胞模型中的神经炎症和M1小胶质细胞极化。
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-06-19 DOI: 10.1007/s00221-024-06875-y
Lv Dingyi, Hu Libin, Piao Jifeng, Zhiquan Ding, Li Yulong, Wu Zhangyi, Yin Yunong, Wang Qinghua, Li Feng

Neuroinflammation and microglia polarization play pivotal roles in brain injury induced by intracerebral hemorrhage (ICH). Despite the well-established involvement of CXC motif chemokine ligand 16 (CXCL16) in regulating inflammatory responses across various diseases, its specific functions in the context of neuroinflammation and microglial polarization following ICH remain elusive. In this study, we investigated the impact of CXCL16 on neuroinflammation and microglia polarization using both mouse and cell models. Our findings revealed elevated CXCL16 expression in mice following ICH and in BV2 cells after lipopolysaccharide (LPS) stimulation. Specific silencing of CXCL16 using siRNA led to a reduction in the expression of neuroinflammatory factors, including IL-1β and IL-6, as well as decreased expression of the M1 microglia marker iNOS. Simultaneously, it enhanced the expression of anti-inflammatory factors such as IL-10 and the M2 microglia marker Arg-1. These results were consistent across both mouse and cell models. Intriguingly, co-administration of the PI3K-specific agonist 740 Y-P with siRNA in LPS-stimulated cells reversed the effects of siRNA. In conclusion, silencing CXCL16 can positively alleviate neuroinflammation and M1 microglial polarization in BV2 inflammation models and ICH mice. Furthermore, in BV2 cells, this beneficial effect is mediated through the PI3K/Akt pathway. Inhibition of CXCL16 could be a novel approach for treating and diagnosing cerebral hemorrhage.

神经炎症和小胶质细胞极化在脑内出血(ICH)诱发的脑损伤中起着关键作用。尽管 CXC motif 趋化因子配体 16(CXCL16)参与调节各种疾病的炎症反应已得到广泛证实,但它在 ICH 后神经炎症和小胶质细胞极化中的具体功能仍然难以捉摸。在本研究中,我们利用小鼠和细胞模型研究了 CXCL16 对神经炎症和小胶质细胞极化的影响。我们的研究结果表明,小鼠在 ICH 后以及 BV2 细胞在脂多糖(LPS)刺激后,CXCL16 表达升高。使用 siRNA 特异性沉默 CXCL16 可减少神经炎症因子(包括 IL-1β 和 IL-6)的表达,并降低 M1 小胶质细胞标志物 iNOS 的表达。同时,它提高了抗炎因子的表达,如 IL-10 和 M2 小胶质细胞标记 Arg-1。这些结果在小鼠和细胞模型中都是一致的。耐人寻味的是,在 LPS 刺激的细胞中,同时使用 PI3K 特异性激动剂 740 Y-P 和 siRNA 会逆转 siRNA 的作用。总之,沉默 CXCL16 能积极缓解 BV2 炎症模型和 ICH 小鼠的神经炎症和 M1 小胶质细胞极化。此外,在 BV2 细胞中,这种有益作用是通过 PI3K/Akt 通路介导的。抑制 CXCL16 可能是治疗和诊断脑出血的一种新方法。
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引用次数: 0
HDAC6 modulates the cognitive behavioral function and hippocampal tissue pathological changes of APP/PS1 transgenic mice through HSP90-HSF1 pathway. HDAC6通过HSP90-HSF1途径调节APP/PS1转基因小鼠的认知行为功能和海马组织病理变化
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-06-27 DOI: 10.1007/s00221-024-06858-z
Bingyi Wang, Siyu Liu, Kaimin Hao, YaruWang Wang, Zongjing Li, Yuanyuan Lou, Yuan Chang, Wenxiu Qi
<p><p>The aim of this study was to investigate histone deacetylase 6 (HDAC6) modifies the heat shock protein 90 (HSP90) and heat shock transcription factor 1 (HSF1) affect the levels of pathological markers such as Aβ oligomers (Aβo) and Tau phosphorylation (p-Tau) in APP/PS1 double transgenic mice hippocampal tissues or HT22 neurons as well as the changes in cognitive behavioral functions of mice. (1) APP/PS1 transgenic mice (6 months old, 25 ~ 30 g) were randomly assigned to 5 experimental groups, C57BL/6J mice (6 months old, 25 ~ 30 g) were used as 4 control groups, with 8 mice in each group. All mice underwent intracerebroventricular (i.c.v.) cannulation, and the experimental groups were administered with normal saline (APP + NS group), HDAC6 agonist tubastatin A hydrochloride (TSA) (APP + TSA group) or HDAC6 agonist theophylline (Theo) (APP + Theo group), HSP90 inhibitor Ganetespib (Gane) (APP + Gane group), or a combination of pre-injected Gane by TSA (APP + Gane + TSA group); the control group received i.c.v. injections of Gane (Gane group), TSA (TSA group), Theo (Theo group) or NS (NS group), respectively. (2) Mouse hippocampal neurons HT22 were randomly divided into a control group (Control) and an Aβ<sub>1-42</sub> intervention group (Aβ). Within the Aβ group, further divisions were made for knockdown HSP90 (Aβ + siHSP90 group), overexpression HSP90 (Aβ + OE-HSP90 group), knockdown HSF1(Aβ + siHSF1 group) and knockdown HSF1 followed by overexpression HSP90 (Aβ + siHSF1 + OE-HSP90 group), resulting in a total of 6 groups. Morris water maze test was used to evaluate the cognitive behavior of the mice. Western blot and immunohistochemistry or immunofluorescence were performed to detect the levels of HDAC6, HSP90, HSF1, Aβ<sub>1-42</sub>, Tau protein, and p-Tau in the hippocampal tissue or HT22 cells. qRT-PCR was used to measure the levels of hdac6, hsp90, and hsf1 mRNA in the hippocampus or nerve cells. (1) The levels of HDAC6, Aβ<sub>1-42</sub> and p-Tau were elevated, while HSP90 and HSF1 were decreased in the hippocampal tissue of APP/PS1 transgenic mice (all P < 0.01). Inhibiting HDAC6 upregulated the expressions of HSP90 and HSF1 in the hippocampal tissue of APP/PS1 mice, while decreasing the levels of Aβ<sub>1-42</sub> and p-Tau as well as improving the spatial cognitive behavior in mice (P < 0.05 or P < 0.01). The opposite effects were observed upon HDAC6 activation. However, inhibiting HSP90 reduced the expression of HSF1 (P < 0.01) and increased the levels of Aβ<sub>1-42</sub> and p-Tau (P < 0.05 or P < 0.01) but did not significantly affect the expression of HDAC6 (P > 0.05). No significant changes were observed in the aforementioned indicators in the 4 control groups (P > 0.05). (2) In the Aβ<sub>1-42</sub> intervention group, HDAC6 and Aβ<sub>1-42</sub>, p-Tau expression levels were elevated, while HSP90 and HSF1 expressions were all decreased, and cell viability was reduced (P < 0.05 or P < 0.01). Overexpression of HSP90 upreg
本研究旨在探讨组蛋白去乙酰化酶6(HDAC6)修饰热休克蛋白90(HSP90)和热休克转录因子1(HSF1)对APP/PS1双转基因小鼠海马组织或HT22神经元中Aβ寡聚体(Aβo)和Tau磷酸化(p-Tau)等病理标志物水平的影响以及小鼠认知行为功能的变化。(1)将APP/PS1转基因小鼠(6月龄,25~30 g)随机分为5个实验组,C57BL/6J小鼠(6月龄,25~30 g)为4个对照组,每组8只。所有小鼠均接受脑室内(i.c.v.插管,实验组分别注射生理盐水(APP + NS 组)、HDAC6 激动剂盐酸曲司他丁 A(TSA)(APP + TSA 组)或 HDAC6 激动剂茶碱(Theo)(APP + Theo 组)、HSP90 抑制剂加奈替斯匹(Gane)(APP + Gane 组)或预先注射 Gane 和 TSA 的组合(APP + Gane + TSA 组);对照组接受 i. c. v 注射 Gane(APP + Gane 组)。c.v.分别注射Gane(Gane组)、TSA(TSA组)、Theo(Theo组)或NS(NS组)。(2)将小鼠海马神经元 HT22 随机分为对照组(Control)和 Aβ1-42 干预组(Aβ)。在 Aβ 组中,又分为敲除 HSP90 组(Aβ + siHSP90 组)、过表达 HSP90 组(Aβ + OE-HSP90 组)、敲除 HSF1 组(Aβ + siHSF1 组)和敲除 HSF1 后过表达 HSP90 组(Aβ + siHSF1 + OE-HSP90 组),共 6 组。莫里斯水迷宫试验用于评估小鼠的认知行为。免疫印迹、免疫组化或免疫荧光检测海马组织或HT22细胞中HDAC6、HSP90、HSF1、Aβ1-42、Tau蛋白和p-Tau的水平;qRT-PCR检测海马或神经细胞中hdac6、hsp90和hsf1 mRNA的水平。(1)在APP/PS1转基因小鼠的海马组织中,HDAC6、Aβ1-42和p-Tau的水平升高,而HSP90和HSF1的水平降低(均为P 1-42和p-Tau),同时小鼠的空间认知行为也有所改善(P 1-42和p-Tau,P 0.05)。4 个对照组的上述指标均无明显变化(P > 0.05)。(2)Aβ1-42干预组中,HDAC6和Aβ1-42、p-Tau表达水平升高,HSP90和HSF1表达均下降,细胞活力降低(P 1-42和p-Tau,细胞活力升高(P 1-42和p-Tau,细胞活力降低(均P 0.05))。抑制HDAC6可以上调APP/PS1小鼠海马中HSP90和HSF1的表达,但降低Aβ1-42和p-Tau的水平,改善小鼠的认知行为功能;过表达HSP90可以增加海马神经元中HSF1的表达,但降低Aβ1-42和p-Tau的水平,增加细胞活性。提示HDAC6可能通过调节HSP90-HSF1通路影响AD转基因小鼠海马中Aβ寡聚体的形成和Tau蛋白磷酸化水平的变化,以及认知行为功能的改变。
{"title":"HDAC6 modulates the cognitive behavioral function and hippocampal tissue pathological changes of APP/PS1 transgenic mice through HSP90-HSF1 pathway.","authors":"Bingyi Wang, Siyu Liu, Kaimin Hao, YaruWang Wang, Zongjing Li, Yuanyuan Lou, Yuan Chang, Wenxiu Qi","doi":"10.1007/s00221-024-06858-z","DOIUrl":"10.1007/s00221-024-06858-z","url":null,"abstract":"&lt;p&gt;&lt;p&gt;The aim of this study was to investigate histone deacetylase 6 (HDAC6) modifies the heat shock protein 90 (HSP90) and heat shock transcription factor 1 (HSF1) affect the levels of pathological markers such as Aβ oligomers (Aβo) and Tau phosphorylation (p-Tau) in APP/PS1 double transgenic mice hippocampal tissues or HT22 neurons as well as the changes in cognitive behavioral functions of mice. (1) APP/PS1 transgenic mice (6 months old, 25 ~ 30 g) were randomly assigned to 5 experimental groups, C57BL/6J mice (6 months old, 25 ~ 30 g) were used as 4 control groups, with 8 mice in each group. All mice underwent intracerebroventricular (i.c.v.) cannulation, and the experimental groups were administered with normal saline (APP + NS group), HDAC6 agonist tubastatin A hydrochloride (TSA) (APP + TSA group) or HDAC6 agonist theophylline (Theo) (APP + Theo group), HSP90 inhibitor Ganetespib (Gane) (APP + Gane group), or a combination of pre-injected Gane by TSA (APP + Gane + TSA group); the control group received i.c.v. injections of Gane (Gane group), TSA (TSA group), Theo (Theo group) or NS (NS group), respectively. (2) Mouse hippocampal neurons HT22 were randomly divided into a control group (Control) and an Aβ&lt;sub&gt;1-42&lt;/sub&gt; intervention group (Aβ). Within the Aβ group, further divisions were made for knockdown HSP90 (Aβ + siHSP90 group), overexpression HSP90 (Aβ + OE-HSP90 group), knockdown HSF1(Aβ + siHSF1 group) and knockdown HSF1 followed by overexpression HSP90 (Aβ + siHSF1 + OE-HSP90 group), resulting in a total of 6 groups. Morris water maze test was used to evaluate the cognitive behavior of the mice. Western blot and immunohistochemistry or immunofluorescence were performed to detect the levels of HDAC6, HSP90, HSF1, Aβ&lt;sub&gt;1-42&lt;/sub&gt;, Tau protein, and p-Tau in the hippocampal tissue or HT22 cells. qRT-PCR was used to measure the levels of hdac6, hsp90, and hsf1 mRNA in the hippocampus or nerve cells. (1) The levels of HDAC6, Aβ&lt;sub&gt;1-42&lt;/sub&gt; and p-Tau were elevated, while HSP90 and HSF1 were decreased in the hippocampal tissue of APP/PS1 transgenic mice (all P &lt; 0.01). Inhibiting HDAC6 upregulated the expressions of HSP90 and HSF1 in the hippocampal tissue of APP/PS1 mice, while decreasing the levels of Aβ&lt;sub&gt;1-42&lt;/sub&gt; and p-Tau as well as improving the spatial cognitive behavior in mice (P &lt; 0.05 or P &lt; 0.01). The opposite effects were observed upon HDAC6 activation. However, inhibiting HSP90 reduced the expression of HSF1 (P &lt; 0.01) and increased the levels of Aβ&lt;sub&gt;1-42&lt;/sub&gt; and p-Tau (P &lt; 0.05 or P &lt; 0.01) but did not significantly affect the expression of HDAC6 (P &gt; 0.05). No significant changes were observed in the aforementioned indicators in the 4 control groups (P &gt; 0.05). (2) In the Aβ&lt;sub&gt;1-42&lt;/sub&gt; intervention group, HDAC6 and Aβ&lt;sub&gt;1-42&lt;/sub&gt;, p-Tau expression levels were elevated, while HSP90 and HSF1 expressions were all decreased, and cell viability was reduced (P &lt; 0.05 or P &lt; 0.01). Overexpression of HSP90 upreg","PeriodicalId":12268,"journal":{"name":"Experimental Brain Research","volume":" ","pages":"1983-1998"},"PeriodicalIF":1.7,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141456178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Electrocortical activity associated with movement-related fear: a methodological exploration of a threat-conditioning paradigm involving destabilising perturbations during quiet standing. 与运动相关恐惧有关的皮层电活动:对威胁条件范式的方法学探索,该范式涉及安静站立时的不稳定扰动。
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-06-19 DOI: 10.1007/s00221-024-06873-0
Adam Grinberg, Andrew Strong, Johan Strandberg, Jonas Selling, Dario G Liebermann, Martin Björklund, Charlotte K Häger

Musculoskeletal trauma often leads to lasting psychological impacts stemming from concerns of future injuries. Often referred to as kinesiophobia or re-injury anxiety, such concerns have been shown to hinder return to physical activity and are believed to increase the risk for secondary injuries. Screening for re-injury anxiety is currently restricted to subjective questionnaires, which are prone to self-report bias. We introduce a novel approach to objectively identify electrocortical activity associated with the threat of destabilising perturbations. We aimed to explore its feasibility among non-injured persons, with potential future implementation for screening of re-injury anxiety. Twenty-three participants stood blindfolded on a translational balance perturbation platform. Consecutive auditory stimuli were provided as low (neutral stimulus [CS-]) or high (conditioned stimulus [CS+]) tones. For the main experimental protocol (Protocol I), half of the high tones were followed by a perturbation in one of eight unpredictable directions. A separate validation protocol (Protocol II) requiring voluntary squatting without perturbations was performed with 12 participants. Event-related potentials (ERP) were computed from electroencephalography recordings and significant time-domain components were detected using an interval-wise testing procedure. High-amplitude early contingent negative variation (CNV) waves were significantly greater for CS+ compared with CS- trials in all channels for Protocol I (> 521-800ms), most prominently over frontal and central midline locations (P ≤ 0.001). For Protocol II, shorter frontal ERP components were observed (541-609ms). Our test paradigm revealed electrocortical activation possibly associated with movement-related fear. Exploring the discriminative validity of the paradigm among individuals with and without self-reported re-injury anxiety is warranted.

肌肉骨骼创伤通常会导致因担心未来受伤而产生的持久心理影响。这种担忧通常被称为运动恐惧症或再次受伤焦虑症,已被证明会阻碍恢复体育活动,并被认为会增加二次受伤的风险。目前,对再次受伤焦虑症的筛查仅限于主观问卷调查,这容易造成自我报告的偏差。我们引入了一种新方法来客观识别与不稳定干扰威胁相关的皮层电活动。我们的目的是在非受伤人员中探索这种方法的可行性,以便将来用于筛查再次受伤的焦虑症。23 名参与者蒙眼站在平移平衡扰动平台上。连续的听觉刺激为低音(中性刺激 [CS-])或高音(条件刺激 [CS+])。在主要实验方案(方案 I)中,一半的高音调之后是八个不可预测方向之一的扰动。另一个验证方案(方案 II)要求在没有干扰的情况下进行自愿下蹲,共有 12 名参与者参加。根据脑电图记录计算出事件相关电位(ERP),并使用间隔测试程序检测出重要的时域成分。在 "方案一 "的所有通道中,CS+试验的高振幅早期或然负变异(CNV)波明显高于CS-试验(> 521-800ms),前额和中线中部位置最为明显(P≤0.001)。在第二方案中,观察到的额叶ERP成分较短(541-609ms)。我们的测试范式揭示了可能与运动相关恐惧有关的皮层电激活。有必要在有和没有自我报告再受伤焦虑的个体中探索该范式的鉴别有效性。
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引用次数: 0
Visuo-spatial complexity potentiates the body-part effect in intransitive imitation of meaningless gestures. 视觉空间复杂性增强了无意义手势非传递性模仿中的身体部位效应。
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-06-06 DOI: 10.1007/s00221-024-06865-0
Mathieu Lesourd, Josselin Baumard, Maximilien Metaireau, Laurence Picard

Recent studies on the imitation of intransitive gestures suggest that the body part effect relies mainly upon the direct route of the dual-route model through a visuo-transformation mechanism. Here, we test the visuo-constructive hypothesis which posits that the visual complexity may directly potentiate the body part effect for meaningless gestures. We predicted that the difference between imitation of hand and finger gestures would increase with the visuo-spatial complexity of gestures. Second, we aimed to identify some of the visuo-spatial predictors of meaningless finger imitation skills. Thirty-eight participants underwent an imitation task containing three distinct set of gestures, that is, meaningful gestures, meaningless gestures with low visual complexity, and meaningless gestures with higher visual complexity than the first set of meaningless gestures. Our results were in general agreement with the visuo-constructive hypothesis, showing an increase in the difference between hand and finger gestures, but only for meaningless gestures with higher visuo-spatial complexity. Regression analyses confirm that imitation accuracy decreases with resource-demanding visuo-spatial factors. Taken together, our results suggest that the body part effect is highly dependent on the visuo-spatial characteristics of the gestures.

最近关于非传递性手势模仿的研究表明,身体部位效应主要依赖于双路模型中通过视觉转换机制的直接途径。在这里,我们检验了视觉构造假说,该假说认为视觉复杂性可能会直接增强无意义手势的身体部位效应。我们预测,手势和手指模仿之间的差异会随着手势的视觉空间复杂性而增加。其次,我们旨在确定无意义手指模仿技能的一些视觉空间预测因素。38 名参与者接受了包含三组不同手势的模仿任务,即有意义手势、视觉复杂度较低的无意义手势和视觉复杂度高于第一组无意义手势的无意义手势。我们的结果与视觉建构假说基本一致,显示手势和手指手势之间的差异增大,但仅针对视觉空间复杂度较高的无意义手势。回归分析证实,模仿的准确性会随着对资源要求较高的视觉空间因素而降低。综上所述,我们的研究结果表明,身体部位效应在很大程度上取决于手势的视觉空间特征。
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引用次数: 0
Sex differences in visuospatial cognition- a female advantage in jigsaw puzzle solving. 视觉空间认知的性别差异--女性在拼图解题中的优势。
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-05-20 DOI: 10.1007/s00221-024-06845-4
Daniela E Aguilar Ramirez, Jarrod Blinch, Kurt Robertson, Joseph Opdenaker, Claudia L R Gonzalez

Mentally visualizing objects, understanding relationships between two- or three- dimensional objects, and manipulating objects in space are some examples of visuospatial abilities. Numerous studies have shown that male participants outperform female participants in visuospatial tasks, particularly in mental rotation. One exception is solving jigsaw puzzles. Performance by seven- to eight-year-old girls was found to be superior to that of boys of the same age (Kocijan et al. 2017). No study, however, has confirmed this finding in an adult population, where sex differences are often detectable. Seventy-nine young adult participants were given four different jigsaw puzzles and the Shepard and Metzler mental rotation test (MRT) with two main goals: First, to investigate possible sex differences in jigsaw puzzle solving, and second, to explore a potential relationship between mental rotation and jigsaw puzzle solving. We hypothesized that female participants would outperform males in the jigsaw puzzles but males would outperform females in the MRT. The findings confirmed this hypothesis. Notably, the male performance in jigsaw puzzle solving was attributed to their sex and mediated by their higher MRT scores. These results yielded two key insights. First, they indicate a dissociation between these two visuospatial abilities, jigsaw puzzle solving and mental rotation; and second, female and male participants capitalize on their distinct cognitive strengths when solving visuospatial tasks.

在头脑中想象物体、理解二维或三维物体之间的关系以及在空间中操作物体都是视觉空间能力的一些例子。大量研究表明,男性参与者在视觉空间任务中的表现优于女性参与者,尤其是在心智旋转方面。拼图游戏是一个例外。研究发现,7 至 8 岁女孩的表现优于同龄男孩(Kocijan 等人,2017 年)。然而,没有任何研究在成年人群中证实了这一发现,而在成年人群中,性别差异往往是可以察觉的。我们给 79 名年轻的成年参与者提供了四种不同的拼图游戏以及 Shepard 和 Metzler 心理旋转测试(MRT),主要目的有两个:首先,研究拼图解题中可能存在的性别差异;其次,探索心理旋转与拼图解题之间的潜在关系。我们假设,女性参与者在拼图游戏中的成绩会优于男性,但男性在智力旋转测试中的成绩会优于女性。研究结果证实了这一假设。值得注意的是,男性在拼图游戏中的表现归因于他们的性别,并通过他们较高的 MRT 分数进行调解。这些结果产生了两个重要启示。首先,它们表明拼图解题和心智旋转这两种视觉空间能力之间存在差异;其次,女性和男性参与者在解决视觉空间任务时利用了各自不同的认知优势。
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引用次数: 0
Contribution of external reference frame to tactile localization. 外部参照系对触觉定位的贡献
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-06-25 DOI: 10.1007/s00221-024-06877-w
Shunsuke Otsuka, Han Gao, Koichi Hiraoka

The purpose of the present study was to elucidate whether an external reference frame contributes to tactile localization in blindfolded healthy humans. In a session, the right forearm was passively moved until the elbow finally reached to the target angle, and participants reached the left index finger to the right middle fingertip. The locus of the right middle fingertip indicated by the participants deviated in the direction of the elbow extension when vibration was provided to the biceps brachii muscle during the passive movement. This finding indicates that proprioception contributes to the identification of the spatial coordinate of the specific body part in an external reference frame. In another session, the tactile stimulus was provided to the dorsal of the right hand during the passive movement, and the participants reached the left index finger to the spatial locus at which the tactile stimulus was provided. Vibration to the biceps brachii muscle did not change the perceived locus of the tactile stimulus indicated by the left index finger. This finding indicates that an external reference frame does not contribute to tactile localization during the passive movement. Humans may estimate the spatial coordinate of the tactile stimulus based on the time between the movement onset and the time at which the tactile stimulus is provided.

本研究旨在阐明外部参照系是否有助于蒙眼健康人的触觉定位。在一次训练中,右前臂被动移动,直到肘部最终到达目标角度,参与者将左手食指伸向右手中指指尖。当被动运动过程中向肱二头肌提供振动时,参与者指示的右中指指尖位置偏离了肘部伸展的方向。这一发现表明,本体感觉有助于识别特定身体部位在外部参照系中的空间坐标。在另一个环节中,在被动运动过程中向右手背提供触觉刺激,参与者将左手食指伸向提供触觉刺激的空间位置。肱二头肌的振动并没有改变左手食指所指触觉刺激的感知位置。这一发现表明,在被动运动过程中,外部参照系不会对触觉定位产生影响。人类可以根据运动开始和触觉刺激提供之间的时间来估计触觉刺激的空间坐标。
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引用次数: 0
Frontal cortex neurometabolites and mobility in older adults: a preliminary study. 老年人额叶皮层神经代谢物与活动能力:一项初步研究。
IF 1.7 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 Epub Date: 2024-06-29 DOI: 10.1007/s00221-024-06881-0
Nikou Nikoumanesh, Colleen J Chase, Rajakumar Nagarajan, Katie Potter, Douglas N Martini

Background: The frontal cortex, relevant to global cognition and motor function, is recruited to compensate for mobility dysfunction in older adults. However, the in vivo neurophysiological (e.g., neurometabolites) underpinnings of the frontal cortex compensation for mobility dysfunction remain poorly understood. The purpose of this study was to investigate the relationships among frontal cortex neurophysiology, mobility, and cognition in healthy older adults.

Methods: Magnetic Resonance Spectroscopy (MRS) quantified N-acetylasparate (tNAA) and total choline (tCho) concentrations and ratios in the frontal cortex in 21 older adults. Four inertial sensors recorded the Timed Up & Go (TUG) test. Cognition was assessed using the Flanker Inhibitory Control and Attention Test which requires conflict resolution because of response interference from flanking distractors during incongruent trials. Congruent trials require no conflict resolution.

Results: tNAA concentration significantly related to the standing (p = 0.04) and sitting (p = 0.03) lean angles. tCho concentration (p = 0.04) and tCho ratio (p = 0.02) significantly related to TUG duration. tCho concentration significantly related to incongruent response time (p = 0.01). tCho ratio significantly related to both congruent (p = 0.009) and incongruent (p < 0.001) response times. Congruent (p = 0.02) and incongruent (p = 0.02) Flanker response times significantly related to TUG duration.

Conclusions: Altered levels of frontal cortex neurometabolites are associated with both mobility and cognitive abilities in healthy older adults. Identifying neurometabolites associated with frontal cortex compensation of mobility dysfunction could improve targeted therapies aimed at improving mobility in older adults.

背景:与整体认知和运动功能相关的额叶皮层被招募来补偿老年人的活动功能障碍。然而,人们对额叶皮层补偿行动功能障碍的体内神经生理学(如神经代谢物)基础仍然知之甚少。本研究旨在调查健康老年人额叶皮层神经生理学、活动能力和认知能力之间的关系:磁共振波谱(MRS)量化了 21 位老年人额叶皮层中 N-乙酰天冬氨酸(tNAA)和总胆碱(tCho)的浓度和比率。四个惯性传感器记录了定时上下楼(TUG)测试。该测试需要解决冲突,因为在不一致的试验中,反应会受到侧面干扰物的干扰。tCho浓度(p = 0.04)和tCho比率(p = 0.02)与TUG持续时间显著相关。tCho浓度与不一致反应时间显著相关(p = 0.01):额叶皮层神经代谢物水平的改变与健康老年人的活动能力和认知能力有关。确定与额叶皮层补偿活动功能障碍相关的神经代谢物可改进旨在改善老年人活动能力的靶向疗法。
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引用次数: 0
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Experimental Brain Research
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