BackgroundDexmedetomidine (Dex) was reported to exhibit anti-inflammatory effect in the nervous system. However, the mechanism by which Dex exhibits anti-inflammation effects on LPS-stimulated BV2 microglia cells remains unclear. Thus, this study aimed to investigate the role of Dex in LPS-stimulated BV2 cells.MethodsThe BV2 cells were stimulated by lipopolysaccharides (LPS). BV2 cells were infected with short-hairpin RNAs targeting NF-κB (NF-κB-shRNAs) and NF-κB overexpression lentivirus, respectively. In addition, miR-340 mimics or miR-340 inhibitor was transfected into BV2 cells, respectively. Meanwhile, the dual-luciferase reporter system assay was used to explore the interaction of miR-340 and NF-κB in BV2 cells. CCK-8 was used to detect the viability of BV2 cells. In addition, Western blotting was used to detect the level of NF-κB in LPS-stimulated BV2 cells. The levels of TNF-α, IL-6, IL-1β, IL-2, IL-12, IL-10 and MCP-1 in LPS-stimulated BV2 cells were measured with ELISA.ResultsThe level of miR-340 was significantly upregulated in Dex-treated BV2 cells. Meanwhile, the level of NF-κB was significantly increased in BV2 cells following infection with lenti-NF-κB, which was markedly reversed by Dex. LPS markedly increased the expression of NF-κB and proinflammatory cytokines in BV2 cells, which were reversed in the presence of Dex. Moreover, miR-340 mimics enhanced the anti-inflammatory effects of Dex in LPS-stimulated BV2 cells via inhibiting NF-κB and proinflammatory cytokines. Furthermore, Dex obviously inhibited LPS-induced phagocytosis in BV2 cells.ConclusionTaken together, our results suggested that Dex might exert anti-inflammatory effects in LPS-stimulated BV2 cells via upregulation of miR-340. Therefore, Dex might serve as a potential agent for the treatment of neuroinflammation.

In this work, we prepared large-area, three-dimensional interconnected graphene oxide (GNO) intercalated by self-doped polyaniline nanofibers (SPAN, a copolymer of aniline and m-aminobenzenesulfonic acid) through a simple adsorption and intercalation route via sonication of the mixed dispersions of both components. The strong p-p* stacking between the backbones of SPAN and the GNO basal planes, and the electrostatic repulsion between the negatively charged SPAN and graphene oxide sheets yield a unique free-standing, three-dimensional interconnected nanostructure. The nanocomposite possesses a large specific surface area and maintains a homogenous and stable dispersion with SPAN, which endows it with a high conductivity and good electrocatalytic activity. Because the negative charge and specific structure of the nanocomposite can prompt the adsorption of positively charged guanine and adenine via strong p-p* interactions or electrostatic adsorption, the hybrid was adopted as an excellent sensing platform for highly sensitive determination of guanine and adenine. The electrocatalytic platform exhibited some advantages, such as high sensitivity, good reproducibility and long-term stability.

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Polyethylene (PE) samples were surface fluorinated by the F2/N2 mixture for 30, 60, 120 or 240 min to investigate the influence of the fluorinated layer characteristics on space charge accumulation. After polarization at 50 kV mm−1 dc electrical field and 40 °C for 240 min, the charge amounts of the samples fluorinated for the different times, normalized to the charge amount of the original sample, are 1.17, 0.51, 0.49 and 0.22, respectively, showing significant suppression of the charge accumulation by the longer treatments, especially for the 240 min treatment. Infrared analyses and SEM cross-section images of the fluorinated samples indicate the increases in degree of fluorination and thicknesses of the fluorinated layer with the treatment time, and the fluorinated layer thicknesses were determined to be 0.39, 0.45, 0.65 and 0.80 µm. Surface energy calculations show that the polar component increased from 2.9 to 14.7 mJ m−2 after the 30 min treatment, and subsequently decreased to 11.8, 11.5 and 9.5 mJ m−2 for the longer treatments of 60, 120 and 240 min. This suggests a similar change in surface layer permittivity with the treatment time. The fluorinations led to the shift of thermally stimulated discharge current peak from 156 °C of the original sample to 145, 142, 144 and 149 °C of the fluorinated samples, and thus reduced the trap depth of the surface layer. But, the longer treatments of 60, 120 and 240 min significantly improved the barrier properties of the surface layer to the diffusion of the chemical species from the semi-conductive electrode to the PE by the decrease in free volume of the surface layer. The chemical species diffused into the sample surface layer reduced the depth of surface traps. The decrease in free volume is more important in suppressing the charge accumulation than the increase in surface layer permittivity and the change in surface trap, because it would reduce the charge transport in the surface layer and the charge direct injection at both electrodes.