Cationic colloidal gold (CCG) and scrapie-infected mouse brain samples embedded in Lowicryl K4M were used for ultrastructural localization of negatively charged microdomains (anionic sites) in the cerebral microvasculature. The distribution of anionic sites on both fronts (luminal and abluminal) of endothelial cells and in the basement membrane (BM) in the majority of micro-blood vessels (MBVs) located outside the plaque area and in the remaining cerebral cortex was similar to that which has been previously observed in non-infected animals. Some MBVs (especially capillaries), however, located inside the plaque areas and surrounded directly by amyloid fibers contained attenuated endothelium, the luminal surface of which showed a segmental lack or diminution of anionic sites. In these vessels the BM was frequently infiltrated and replaced by the amyloid fibers. In some vessels located mainly in the areas of the neuropil vacuolization deposits of homogenous material causing the thickening of the BM were noted. These changes were accompanied by irregular labeling of the BM with gold particles. At the sites of bifurcation of some MBVs, predominantly in the area of the venular estuary at the mouth of capillary (at capillary-venular connections), a discontinuity in the distribution of anionic sites was noted. The observed disturbances in the distribution of anionic sites can be associated with a previously noted increased permeability of some MBVs in the brains of scrapie-infected mice.
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January 2025
Advanced Materials Institute of Nano Convergence Engineering (BK21 FOUR), Dept. of Nano Convergence Engineering, Jeonbuk National University, Jeonju, Jeonbuk, 54896, Republic of Korea.
Developing cost-effective, highly efficient, and durable bifunctional electrocatalysts for water electrolysis remains a significant challenge. Nickel-based materials have shown promise as catalysts, but their efficiency in alkaline electrolytes is still lacking. Fascinatingly, Mott-Schottky catalysts can fine-tune electron density at interfaces, boosting intermediate adsorption and facilitating desorption to reduce the energy barrier.
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January 2025
Department of Physics, Dongguk University, Seoul, 04620, Republic of Korea.
The hydrogen spillover phenomenon provides an expeditious reaction pathway via hydrogen transfer from a strong H adsorption site to a weak H adsorption site, enabling a cost-efficient hydrogen evolution reaction (HER) analogous to platinum with moderate H adsorption energy. Here, a high-entropy oxychalcogenide (HEOC) comprising Co, Ni, Mo, W, O, Se, and Te is prepared by a two-step electrochemical deposition for hydrogen spillover-enhanced HER in acidic and alkaline water electrolysis. The anodic-cathodic reversal current enables the co-deposition of cations and aliovalent anions, facilitating a glass structure with multiple active sites for hydrogen spillover.
View Article and Find Full Text PDFAdv Mater
January 2025
Department of Mechanical Engineering, City University of Hong Kong, Hong Kong, China.
Transition metal oxide electrocatalysts (TMOEs) are poised to revive grid-scale all-vanadium redox flow batteries (VRFBs) due to their low-cost and unique electronic properties, while often inescapably harboring surface vacancies. The role of local vacancy-induced physicochemical properties on vanadium-redox electrochemistry (VRE), encompassing kinetics, and stability, remains profoundly unveiled. Herein, for the first time, it is revealed that vacancies induce atomic-scale polarization in TMOEs and elucidate its mechanism in VRE.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Anion-exchange membrane fuel cell (AEMFC) is a cost-effective hydrogen-to-electricity conversion technology under a zero-emission scenario. However, the sluggish kinetics of the anodic hydrogen oxidation reaction (HOR) impedes the commercial implementation of AEMFCs. Here, we develop a Pd single-atom-embedded NiN catalyst (Pd/NiN) with unconventional PdNi trimer sites to drive efficient and durable HOR in alkaline media.
View Article and Find Full Text PDFNat Commun
January 2025
DST Unit of Nanoscience (DST UNS) and Thematic Unit of Excellence (TUE), Department of Chemistry, Indian Institute of Technology, Madras, Chennai, 600036, India.
We report the synthesis of [Ag(o-CBT)] abbreviated as Ag, a stable 8e⁻ anionic cluster with a unique Ag@Ag@Ag core-shell structure, where o-CBT is ortho-carborane-1-thiol. By substituting Ag atoms with Au and/or Cu at specific sites we created isostructural clusters [AuAg(o-CBT)] (AuAg), [AgCu(o-CBT)] (AgCu) and [AuAgCu(o-CBT)] (AuAgCu). These substitutions make systematic modulation of their structural and electronic properties.
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