Acteoside and isoacteoside alleviate renal dysfunction and inflammation in lipopolysaccharide-induced acute kidney injuries through inhibition of NF-κB signaling pathway.

Acute kidney injury (AKI) is a sudden loss of renal function with a high mortality rate and inflammation is thought to be the underlying cause. The phenylpropanoid components acteoside (ACT) and isoacteoside (ISO), which were isolated from Cistanche deserticola Y.C.Ma, have been reported to have preventive effects against kidney disorders. This study aimed to investigate the anti-inflammatory properties and protective mechanisms of ACT and ISO. In this investigation, kidney function was assessed using a semi-automatic biochemical analyzer, histopathology was examined using Hematoxylin-Eosin staining and immunohistochemistry, and the concentration of inflammatory cytokines was assessed using an enzyme-linked immunosorbent assay (ELISA) test. In addition, using Western blot and q-PCR, the expression of proteins and genes connected to the NF-κB signaling pathway in mice with lipopolysaccharide (LPS)-induced AKI was found. The findings showed that under AKI intervention in LPS group, ACT group and ISO group, the expression of Rela (Rela gene is responsible for the expression of NFκB p65 protein) and Tlr4 mRNA was considerably elevated (P<0.01), which led to a significant improvement in the expression of MyD88, TLR4, Iκ-Bɑ and NF-κB p65 protein (P<0.001). The levels of Alb, Crea and BUN (P<0.001) increased along with the release of downstream inflammatory factors such as IL-1ß, IL-6, Cys-C, SOD1 and TNF-α (P<0.001). More importantly, the study showed that ISO had a more favorable impact on LPS-induced AKI mice than ACT. In conclusion, by inhibiting NF-κB signaling pathway, ACT and ISO could relieve renal failure and inflammation in AKI, offering a fresh possibility for the therapeutic management of the condition.

Degradation of urea-formaldehyde resin residues by a hydrothermal oxidation method into recyclable small molecular organics.

Urea-formaldehyde (UF) resin residues and the related product wastes as organic hazardous wastes are difficult to be biodegraded or recycled. In this research, a hydrothermal oxidation method using hydrogen peroxide (H2O2) solution has been developed for the degradation and recycling of UF resin residues. The effects of solution concentration, temperature, and time on the degradation efficiency and products of UF resin residues were studied. Under optimal conditions, i.e., 140 °C and 5 wt% H2O2 solution, over 75% of UF resin residues was degraded after 3 h. The degradation efficiency is much higher than that of the traditional hydrothermal treatment or acid hydrolysis method. In addition, results from Fourier transform infrared spectroscopy (FTIR), gas chromatography-mass spectroscopy (GC-MS), nuclear magnetic resonance spectroscopy (NMR), and X-ray diffraction (XRD) confirmed that H2O2 solution degrades UF resin residues to low molecular compounds, such as alcohols, methylal, and amides. This research provides a novel and high-efficient hydrothermal oxidization process for the degradation of UF resin residues, which might be a promising environmentally friendly and low-cost method for the disposal and recycling of industrial UF resin residues.

Tuning the bandgap of exfoliated InSe nanosheets by quantum confinement.

Strong quantization effects and tuneable near-infrared photoluminescence emission are reported in mechanically exfoliated crystals of γ-rhombohedral semiconducting InSe. The optical properties of InSe nanosheets differ qualitatively from those reported recently for exfoliated transition metal dichalcogenides and indicate a crossover from a direct to an indirect band gap semiconductor when the InSe flake thickness is reduced to a few nanometers.