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Scenario statement: The lethal case of aortic and mitral valve endocarditis caused by Streptobacillus moniliformis.
Glucocorticoids (GCs) have been widely used in clinical treatment as anti-inflammatory, anti-shock and immunosuppressive medicines. However, the effect of excessive GCs on immune response and metabolism of kidney remains unclear. Here, we profiled the gene expression of kidney from mice with high-dose dexamethasone (DEX) treatment. A total of 1193 differentially expressed genes (DEGs) were screened in DEX treatment group compared with the saline group, including 715 down- regulated and 478 up-regulated. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses of these DEGs showed extracellular matrix (ECM)-receptor interaction, cell adhesion molecules signaling pathway were significantly enriched, and that the vast majority of DEGs were involved in monocarboxylic acid metabolism, leukocyte cell-cell adhesion and fatty acid metabolism. Gene set enrichment analysis (GSEA) revealed that DEGs were strongly associated with immune-response and cell adhesion gene sets, such as Fc γ R-mediated phagocytosis, leukocyte transendothelial migration, T-cell receptor signaling pathway, cell adhesion, ECM-receptor interaction and focal adhesion-associated pathways. KEGG pathway analysis of differentially expressed kinases (DEKs) showed T-cell receptor and forkhead box class O signaling pathway were enriched. Furthermore, we found multiple protein kinases expression were dysregulated greatly after dexamethasone treatment, including classical effector of GCs stimulation-serum and GC-regulated kinase. These protein kinases are involved in multiple signaling pathways in mice kidney, such as mitogen-activated protein kinase (MAPK) and phosphoinositide 3-kinase (PI3K)/Akt signaling pathway. We profiled the gene expression of the kidney from high-dose dexamethasone-treated mice and provided important information for further study the mechanism of side effects of GCs in clinical therapy.Several studies have reported differences in radiation toxicity between the sexes, but these differences have not been tested with respect to histopathology and genes. This animal study aimed to show an association between histopathological findings of radiation-induced lung toxicity and the genes ATM, SOD2, TGF-β1, XRCC1, XRCC3 and HHR2. In all, 120 animals were randomly divided into 2 control groups (male and female) and experimental groups comprising fifteen rats stratified by sex, radiotherapy (0 Gy vs. 10 Gy), and time to sacrifice (6, 12, and 24 weeks postirradiation). Histopathological evaluations for lung injury, namely, intra-alveolar edema, alveolar neutrophils, intra-alveolar erythrocytes, activated macrophages, intra-alveolar fibrosis, hyaline arteriosclerosis, and collapse were performed under a light microscope using a grid system; the evaluations were semi quantitatively scored. Then, the alveolar wall thickness was measured. Real-time quantitative reverse transcription PCR (RT-qPCR) was used to determine gene expression differences in ATM, TGF-β1, XRCC1, XRCC3, SOD2 and HHR2L among the groups. Histopathological data showed that radiation-induced acute, subacute, and chronic lung toxicity were worse in male rats. The expression levels of the evaluated genes were significantly higher in females than males in the control group, but this difference was lost over time after radiotherapy. Less toxicity in females may be attributable to the fact that the expression of the evaluated genes was higher in normal lung tissue in females than in males and the changes in gene expression patterns in the postradiotherapy period played a protective role in females. Additional data related to pulmonary function, lung weights, imaging, or outcomes are needed to support this data that is based on histopathology alone.Silicon plays a crucial part in developing high-performance energy storage materials, owing to a high specific capacity compared to carbon. Moreover, nanoscale silicon is beneficial for reducing the inherent disadvantage of large volume change during repeated lithiation/de-lithiation, while artificial synthesis methods usually involve complex procedures and high costs. On account of the abundant natural reserve and low cost, the manipulation of silicate minerals is a simple and economical approach to prepare silicon nanosheets. In this regard, this mini review introduces different classes of silicate minerals and summarizes some typical molten salt-assisted reduction methods and other valuable methods applied to prepare silicon nanosheets for energy storage. Finally, the challenges and perspectives in this field are also proposed.Two-dimensional (2D) magnets show promising applications in spintronic devices and appeal increasing attention. CrI2, a counterpart of CrI3, is a magnetic van der Waals crystal. However, the structure of CrI2 at the monolayer limit is not well studied. Here, based on the density functional theory, we revealed the relationship between different phases of CrI2 monolayer and proposed a novel and stable chain structure. The one-dimensional (1D) CrI2 chain is a ferromagnetic semiconductor with robust electronic properties against twisting and tensile strain. Interestingly, the CrI2 chain exhibits superelasticity with a failure strain as large as 39%. In addition, both the magnetic moments on Cr atoms and the exchange energy increase with an increase in the tensile strain. Our results push magnetic ordering from 2D to 1D, which shows possible application prospects in magnetoelectric and spintronic devices.This study reports an effective approach to improve dramatically the electrochemical performance of nanosized NaFePO4 with a maricite structure, which is commonly considered as electrochemically inactive due to the absence of structural channels for alkaline ion mobility. The approach is based on the complete oxidation under mild conditions (i.e. at low temperatures around 280 °C and traces of oxygen) of the nanosized maricite phase. It is prepared by the phosphate-formate precursor method and is additionally ball-milled with a carbon additive. The oxidation of Fe2+ proceeds at the nanoscale level within the maricite nanoparticles and causes a massive structural transformation of the maricite phase into a monoclinic NASICON phase Na3Fe2(PO4)3 with the preservation of the crystallinity. The oxidized maricite phase exhibits high specific capacities, cycling stability and rate capability when it is used as an electrode in both Na and Li half-cells. The effect of different sodium and lithium electrolytes on the storage performance is investigated as well. It is found that the highest specific capacity (of about 150 mA h g-1) is achieved in Li half-cells using the LiPF6 electrolyte, while in Na half-cells the electrolyte NaFSI/ECDMC achieves a specific capacity of around 100 mA h g-1. The rate capability is better in Na half-cells than that in Li half-cells. The mechanism of the reversible intercalation/deintercalation of Na+ and Li+ ions is studied by ex situ XRD and TEM analyses. The results show that the maricite is an electrochemically inactive phase, but through manipulation including oxidation or amorphization it becomes an active electrode material.The development of novel catalysts for C-H activation reactions with increased reactivity and improved selectivities has been attracting significant interest over the last two decades. More recently, promising results have been developed using tridentate pincer ligands, which form a stable C-M bond. Furthermore, based on mechanistic studies, the unique catalytic role of some metallacyclic intermediate species has been revealed. These experimental observations have subsequently translated into the rational design of advanced C-H activation catalysts in both Ru- and Ir-based systems. Recent breakthroughs in the field of C-H activation catalysed by metallacyclic intermediates are thus discussed.High internal phase Pickering emulsions (HIPPEs) stabilized by a food protein have attracted widespread attention. In this study, a novel cod protein-chitosan nanocomplex was prepared through electrostatic interactions and used as a particle emulsifier to stabilize the oil-water interface. The application of the cod protein-chitosan nanocomplex was demonstrated in the formation of stable HIPPEs with an internal phase as high as 84%. The influence of the system composition on the stability, microstructure and rheology of the HIPPEs was determined. The HIPPEs stabilized by the cod protein-chitosan nanocomplex formed a compact three-dimensional network structure, which gave the emulsion a higher storage modulus, viscoelasticity and good thixotropy. Interestingly, the chemical stability of astaxanthin was significantly improved by the developed HIPPEs. The bioavailability of astaxanthin in the HIPPEs stabilized by the nanocomplexes of 2.0% (w/w) cod protein and 0.1% (w/w) chitosan reached 49%. In summary, these results demonstrated that the food-grade cod protein-chitosan nanocomplex had potential in the development of HIPPEs, which could be used as carriers for hydrophobic bioactive compound delivery.Heteroanalogs of ascidian alkaloids have been synthesized, and for the first time 10 different types of saturated carbo- and heteroannulated pyridones have been obtained. A new method for the formation of decahydro[1,3]oxazolo[2,3-j]quinoline and octahydro-5H-cyclopenta[b][1,3]oxazolo[3,2-a]pyridine was proposed. The synthesis of these heterocycles is based on the three-component cyclization of trifluoroacetoacetic ester and cycloketones with 1,2- and 1,3-dinucleophiles. It was found that reactions with amino alcohols are distinguished by the possibility of isolating carbocyclopyridones of various degrees of saturation. The diastereomeric structure of the synthesized heterocycles has been studied, and the mechanism of their formation has been proposed. Antitumor, anti-influenza and analgesic agents have been found among the synthesized compounds.Magnetorheological fluids, especially those in high-power magnetorheological devices, inevitably work at high temperatures because of the wall slip, energized coils and frictions between particles. In order to prepare a magnetorheological fluid for high temperatures, this work investigates the properties of three main components (soft magnetic particles, surfactants and base carrier fluids) for a magnetorheological fluid at high temperatures. On this basis, a novel magnetorheological fluid for high temperatures is prepared. Its sedimentation stability, viscosity and shear yield stress are investigated at high temperatures. The results show that the novel magnetorheological fluid has acceptable sedimentation, suitable viscosity and stable shear yield stress at high temperatures. The novel magnetorheological fluid for high temperatures can be applied to most magnetorheological devices, especially high-power magnetorheological devices.Caryl-F bond activation has become an important and quickly developing method for construction of carbon-based materials. We report that alumina-mediated C-F bond activation (AmCFA) enables construction of PAHs with zigzag periphery. This method includes formal Csp3-H activation and opens an avenue for generation of carbon-based nanomagnets directly on technologically relevant surfaces.
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