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Background: Cerebral small vessel disease exacerbates cognitive decline, yet the structural-functional coupling mechanisms in vascular cognitive impairment (VCI) remain unclear.
Methods: This study included 121 participants, with 68 individuals with VCI and 53 healthy controls. Participants underwent neuropsychological assessments and multimodal imaging. We compared white matter integrity, structural network topology, and functional network topology between groups, exploring the relationship between structure-function coupling and cognitive function. Family-wise error (FWE) correction was applied to account for multiple comparisons.
Results: VCI participants showed reduced fractional anisotropy and increased mean and radial diffusivity in white matter. Structural network analysis revealed lower global and local efficiency, reduced small-world properties, and increased characteristic path length. Nodal properties, particularly in key regions of the default mode and visual networks, were significantly altered in VCI participants. While no significant differences were observed in functional network topology, VCI participants exhibited enhanced structure-function coupling in critical nodes of the default mode and visual networks. This enhancement correlated with memory function and information processing speed in the temporal calcarine, insula, occipital, and lingual regions.
Conclusions: The study identifies disrupted brain networks and enhanced compensatory mechanisms in VCI, offering insights into neuroplasticity in VCI and contributing to dementia prevention strategies.
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http://dx.doi.org/10.1111/cns.70205 | DOI Listing |
PLoS Pathog
September 2025
Department of Microbiology, Biochemistry, and Molecular Genetics, New Jersey Medical School, Rutgers Biomedical and Health Sciences, Newark, New Jersey, United States of America.
Ethanolamine signaling through the transmembrane quorum-sensing receptor CqsR influences Vibrio cholerae niche recognition and host colonization. In this study, we present a comprehensive structure-function analysis of CqsR. Specifically, we have determined X-ray crystal structures of the CqsR periplasmic domain bound to the signaling agonist ethanolamine and its analogs, serinol and L-alaninol, as well as the ligand-free (apo) form of CqsR.
View Article and Find Full Text PDFCoord Chem Rev
February 2025
Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo náměstí 2, 166 10, Praha 6, Czech Republic.
The broad class of O-activating coupled-binuclear copper (CBC) metalloenzymes contain a unique [CuO] catalytic core. This core is responsible for catalyzing challenging biochemical transformations, particularly the regioselective monooxygenations/oxidations of substituted phenols. Despite almost four decades of intense experimental and theoretical research, the factors governing the diverse reactivity of CBC enzymes had remained only partially understood.
View Article and Find Full Text PDFWe investigate the spatiotemporal organization of resting-state brain activity in individuals with and without major depressive disorder (MDD), identifying stable and recurring whole-brain functional co-activation patterns that serve as attractor-like configurations. A particularly prominent brain state, marked by suppressed default mode and frontoparietal networks and heightened salience system engagement, occurring more frequently and with shorter dwell times in MDD and correlating with greater anhedonia severity. Transition dynamics further reveal that MDD participants exhibit reduced transitions between visual-attentional and limbic-default mode systems, which is associated with higher overall depression symptoms, suggestive of affective and cognitive rigidity.
View Article and Find Full Text PDFACS Appl Energy Mater
August 2025
Materials, Chemistry, and Computational Sciences, National Renewable Energy Laboratory, Golden, Colorado 80401, United States.
Affordable, long-lasting energy storage has become critical to support increased electricity demand in recent years. Cobalt-free, lithium- and manganese-rich lithium nickel manganese oxide (LMR-NM) cathodes stand to reduce cost and supply-chain concerns associated with traditional cobalt-containing cathodes for lithium-ion batteries by leveraging more earth-abundant materials; however, they have shown issues with long-term cycling stability. Here, we investigate lithium difluoro-(oxalate)-borate (LiDFOB), tris-(trimethylsilyl) phosphite (TMSPi), and vinylene carbonate (VC) electrolyte additives for their ability to improve cycling performance of LMR-NM (0.
View Article and Find Full Text PDFInorg Chem
September 2025
Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
Proton-coupled electron transfer (PCET) is an important mechanism that defines the reactivity of H atom equivalents at reducible metal oxide (MO) surfaces. To better understand structure-function properties that dictate the thermochemistry and kinetics of PCET at MO surfaces, our group has employed polyoxovanadate-alkoxide (POV-alkoxide) complexes as molecular models of extended materials. In this work, we investigate the influence of anionic dopants on PCET reactivity in POV-alkoxides.
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