Neuroscience
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Long-term potentiation (LTP) is a widely studied phenomenon since the underlying molecular mechanisms are widely believed to be critical for learning and memory and their dysregulation has been implicated in many brain disorders affecting cognitive functions. Central to the induction of LTP, in most pathways that have been studied in the mammalian CNS, is the N-methyl-D-aspartate receptor (NMDAR). Philippe Ascher discovered that the NMDAR is subject to a rapid, highly voltage-dependent block by Mg2+. ⋯ It explains how this unusual molecular mechanism underlies the Hebbian nature of synaptic plasticity and the hallmark features of NMDAR-LTP (input specificity, cooperativity and associativity). Then the role of the Mg2+ block of NMDARs is discussed in the context of memory and dementia. In particular, the idea that alterations in the voltage-dependent block of the NMDAR is a component of cognitive decline during normal ageing and neurodegenerative disorders, such as Alzheimer's disease, is discussed.
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Dual-task paradigms, which involve performing cognitive and motor tasks simultaneously, are commonly used to study how attentional resources are allocated and managed under varying task demands. This study aimed to investigate cognitive-motor interferences (CMI) under different levels of cognitive and motor task difficulty without instruction on task prioritization. 17 healthy young adults performed an auditory oddball task with increasing cognitive and motor (walking vs. sitting) difficulty. Cognitive and motor performances, along with P3 (P3a and P3b) brainwave components, were analysed. ⋯ Our study suggests managing attentional resources to balance cognitive and motor tasks rather than linearly increasing task complexity. Viewing dual tasks as a new, integrated task is proposed, supported by previous neural network integration studies. Thus, understanding how the brain organizes tasks in response to constraints is crucial for comprehending complex task execution.
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The neuroinflammatory response promotes secondary brain injury after traumatic brain injury (TBI). Triggering receptor expressed on myeloid cells 1 (TREM1) is a key regulator of inflammation. However, the role of TREM1 in TBI is poorly studied. ⋯ Moreover, after TREM1 was inhibited, the secretion of the proinflammatory factors TNF-α and IL-1β was significantly reduced, while the secretion of the anti-inflammatory factors IL-4 and IL-10 was significantly increased. Additionally, inhibition of TREM1 by LP17 significantly reduced neuronal apoptosis and ameliorated nerve dysfunction in TBI model rats. In conclusion, our findings suggest that TREM1 enhances neuroinflammation and promotes neuronal apoptosis after TBI, and these effects may be partly mediated via the ERK/cPLA2 signalling pathway.
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Fechner's law proposes a logarithmic relationship between the physical intensity and perceived magnitude of a stimulus. The principle of logarithmic magnitude representation has been extensively utilized in various theoretical frameworks. Although the neural correlates of Weber's law have been considered as possible evidence for Fechner's law, there is still a lack of direct evidence for a logarithmic representation in the central nervous system. ⋯ Behavioral results showed that a Bayesian model, which assumes a logarithmic representation of spatiotemporal information, was better at predicting production times than a model relying on a linear representation. The EEG results revealed that P2 and P3b amplitudes increased linearly with the logarithmic transformation of spatiotemporal information, and these event-related potentials were localized in the parietal cortex. Our study provides direct evidence supporting logarithmic magnitude representation in the central nervous system.
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Meta Analysis
Mendelian randomization in Alzheimer's disease and mild cognitive impairment: Hippocampal volume associations.
This study investigates the association between cognitive dysfunction and hippocampal volumes in Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI) using Mendelian randomization. A meta-analysis of 503 healthy controls, 562 MCI patients, and 389 CE patients revealed significant reductions in hippocampal and subregion volumes in MCI and AD compared to controls. While various subregions showed volume reductions, no causal relationship between hippocampal volume and AD was established through Mendelian randomization analysis. In conclusion, significant volume reductions were observed in MCI and AD patients, highlighting the complexity of the relationship between hippocampal volume and cognitive impairment.