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AbstractThis study aims to explore the mechanisms of the inhibitory effect of kaempferol on the invasion and metastasis of gastric cancer (GC) cells through network pharmacology prediction and experimental verification. It identifies core targets via PPI network analysis and finds that kaempferol binds to these targets well. In vitro experiments showed that kaempferol could inhibit the proliferation, colony formation, migration and invasion of GC cells. Western blotting indicated kaempferol may reduce AKT and GSK3β phosphorylation, leading to lower expression of invasion-related genes SRC, MMP9, CXCR4, KDR, and MMP2. Overall, kaempferol may prevent migration and invasion of GC cells via the AKT/GSK3β signaling pathway. [ABSTRACT FROM AUTHOR]

Carbon paper is one of the most commonly used materials for the gas diffusion layer of proton exchange membrane fuel cell, and its performance is the premise to ensure the stable operation of the cell. In order to improve the structure and properties of carbon paper and make it better meet the performance requirements of fuel cell, this study was conducted to press different amounts of graphite plates in the carbonization process to control the applied pressure and analyze the microstructure evolution and mechanism of carbon paper under different pressure. In addition, the effects of applied pressure on the in-plane resistivity, pore size distribution, surface roughness and mechanical properties of carbon paper were also studied. The results show that applying pressure helps to restrain the cracking of resin carbon, reduce the generation of cracks and improve graphitization degree of carbon paper to a certain extent. Furthermore, with the increase of applied pressure, the surface roughness of carbon paper is reduced gradually, while the average and maximum apertures also decrease. When the applied pressure reaches 3600 Pa, compared with the samples without pressure, the in-plane resistivity of carbon paper decreases from 17.15 mΩ·cm to 12.79 mΩ·cm, the tensile strength and flexural strength are improved by 150% and 82.9% respectively.

Due to its large specific surface area, excellent penetration resistance and a large number of functional groups distributed on the surface, graphene oxide(GO) has become a research hotspot in the fields of anticorrosion, permeation separation and coating mechanical properties. The research progress of GO application on metal surface in recent years was reviewed. On the basis of domestic and foreign literature, the research progress of GO applied on metal surface for anticorrosion, permeation separation, mechanical properties of coating and other aspects was described, and the mechanism was summarized and analyzed. The anticorrosion mechanism is mainly the physical barrier effect of GO and its chemical inertness to the electroactive medium. The mechanism of osmotic separation is mainly the multi-layer pore structure and functional groups of GO. The main mechanism of mechanical properties of the coating is the good compatibility between GO and coating and the formation of chemical bond between surface functional groups and metal matrix. It was pointed out that there is still a lack of GO composite preparation technology that meets the requirements of environmental protection, low cost and large-scale industrialization, the technological parameters involved, the design of composite phase system and other aspects still need further study. It was also proposed to be applied to metal anticorrosion, oil-water separation and mechanical properties of coating, so as to solve the key problems such as corrosion resistance of metal surface, oil-water permeability and separation performance, bonding force between coating and metal substrate.

Accumulated evidence has shown that microRNAs (miRNAs) are closely related to the pathogenesis and progression of senile cataracts. Here we investigate the effect of miR-29a-3p in cataractogenesis and determined the potential molecular mechanism involved. In this study, we constructed a selenite cataract model in rats and obtained the miRNAs related to cataracts by whole transcriptome sequencing. To investigate the effect and mechanism of miR-29a-3p on cataracts, we performed several in vivo and in vitro experiments, including CCK8 assay, flow cytometry, luciferase reporter assay, Edu assay, and western blot analysis. Sequencing data showed downregulation of miR-29a-3p in rats with selenite cataracts. Down-regulation of miR-29a-3p could promote lens epithelial cells (SRA01/04) proliferation and inhibit cell apoptosis, and miR-29a-3p silence could inhibit the development of cataracts. Additionally, CAND1 was a direct target gene for miR-29a-3p. These data demonstrate that miR-29a-3p inhibits apoptosis of lens epithelial cells by regulating CAND1, which may be a potential target for senile cataracts. [ABSTRACT FROM AUTHOR]

Alkaloids and lignans in Zanthoxylum armatum display important biological activities, but the quanitification method of alkaloids has not been reported. In this study, an effective extraction method was developed through an orthogonal design, and ten compounds in roots, stems, branches and leaves of Zanthoxylum armatum were simultaneously quantified by ultra-fast liquid chromatography-tandem quadrupole mass spectrometry (UFLC-MS/MS). The roots, stems, branches and leaves of Z. armatum were ultrasonically extracted with methanol (solvent-to-sample ratio 100 : 1, v/w) for 10 min. An UFLC-MS/MS method was developed with a gradient UFLC mobile phase and triple quadruple tandem mass spectrometry with electrospray ionization in the positive ion mode. The method was validated for linearity, precision, repeatability and accuracy. The limits of detection and quantification were within 0.01-7.5 and 0.04-30 ng/mL, respectively. The root samples collected from Tian'e County were abundant in N-methylanhydrotetrahydroberberrubine A, escholidine perchlorate and pinoresinol monomethyl ether, eudesminthe., Author(s): Yi-ran Wang [sup.1], Shi-ying Mai [sup.1], Yong-hui Li [sup.1], Hai-long Li [sup.1], Tao Guo [sup.3], An Jia [sup.2], Jun-qing Zhang [sup.1] [sup.2] Author Affiliations: (1) grid.443397.e, 0000 0004 0368 [...]

Background: A sight-threatening, cataract is a common degenerative disease of the ocular lens. This study aimed to explore the regulatory mechanism of age-related cataract (ARC) formation and progression. Methods: Cataracts in Sprague Dawley rats were induced by adopting the method that injected selenite subcutaneously in the nape. We performed high-throughput RNA sequencing technology to identify the mRNA and microRNA(miRNA) expression profiles of the capsular membrane of the lens from Na2SeO3-induced and saline-injected Sprague Dawley rats. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were carried out to forecast the regulatory and functional role of mRNAs in cataracts by DAVID and Metascape. The protein–protein interaction(PPI) network of differentially expressed mRNA(DEmRNAs) was built via the STRING. Target miRNAs of hub genes were predicted by miRBD and TargetScan. Furthermore, differentially expressed miRNA(DEmiRNAs) were selected as hub genes' targets, validated by quantitative real-time polymerase chain reaction(qRT-PCR), and a DEmiRNA-DEmRNA regulatory network was constructed via Cytoscape. Result: In total, 329 DEmRNAs including 40 upregulated and 289 downregulated genes were identified. Forty seven DEmiRNAs including 29 upregulated and 18 downregulated miRNAs were detected. The DEmRNAs are involved in lens development, visual perception, and aging-related biological processes. A protein–protein interaction network including 274 node genes was constructed to explore the interactions of DEmRNAs. Furthermore, a DEmiRNA-DEmRNA regulatory network related to cataracts was constructed, including 8 hub DEmRNAs, and 8 key DEmiRNAs which were confirmed by qRT-PCR analysis. Conclusion: We identified several differentially expressed genes and established a miRNA-mRNA-regulated network in a Na2SeO3-induced Sprague Dawley rat cataract model. These results may provide novel insights into the clinical treatment of cataracts, and the hub DEmRNAs and key DEmiRNAs could be potential therapeutic targets for ARC. [ABSTRACT FROM AUTHOR]