Isoflurane Protects Against Human Endothelial Cell Apoptosis by Inducing Sphingosine Kinase-1 via ERK MAPK

Endothelial dysfunction is a major clinical problem affecting virtually every patient requiring critical care. Volatile anesthetics are frequently used during the perioperative period and protect the heart and kidney against ischemia and reperfusion injury. We aimed to determine whether isoflurane, the most commonly used volatile anesthetic in the USA, protects against endothelial apoptosis and necrosis and the mechanisms involved in this protection. Human endothelial EA.hy926 cells were pretreated with isoflurane or carrier gas (95% room air + 5% CO(2)) then subjected to apoptosis with tumor necrosis factor-α or to necrosis with hydrogen peroxide. DNA laddering and in situ Terminal Deoxynucleotidyl Transferase Biotin-dUTP Nick-End Labeling (TUNEL) staining determined EA.hy926 cell apoptosis and percent LDH released determined necrosis. We also determined whether isoflurane modulates the expression and activity of sphingosine kinase-1 (SK1) and induces the phosphorylation of extracellular signal regulated kinase (ERK MAPK) as both enzymes are known to protect against cell death. Isoflurane pretreatment significantly decreased apoptosis in EA.hy926 cells as evidenced by reduced TUNEL staining and DNA laddering without affecting necrosis. Mechanistically, isoflurane induces the phosphorylation of ERK MAPK and increased SK1 expression and activity in EA.hy926 cells. Finally, selective blockade of SK1 (with SKI-II) or S1P(1) receptor (with W146) abolished the anti-apoptotic effects of isoflurane. Taken together, we demonstrate that isoflurane, in addition to its potent analgesic and anesthetic properties, protects against endothelial apoptosis most likely via SK1 and ERK MAPK activation. Our findings have significant clinical implication for protection of endothelial cells during the perioperative period and patients requiring critical care.     

Structural and thermoelectric properties of hydrothermal-processed Ag-doped Fe2O3

Fe_2-xAg_xO₃ (0?≤?x?≤?0.04) nanopowders with various Ag contents were synthesized at different hydrothermal reaction temperatures (150?°C and 180?°C). Their structural properties were fully investigated through an X-ray diffraction, a Fourier transform infrared spectroscopy, and an X-ray photoelectron spectroscopy. The hydrothermal reaction temperature, time, and Ag content remarkably affected the morphological characteristics and crystal structure of the synthesized powders. The Fe_2-xAg_xO₃ (0?≤?x?≤?0.04) powders synthesized at 150?°C for 6?h and the Fe_2-xAg_xO₃ (0.02?≤?x?≤?0.04) powders synthesized at 180?°C for 12?h formed the orthorhombic α-FeOOH phase with a rod-like morphology, whereas the Fe_2-xAg_xO₃ (0?≤?x?≤?0.01) powders synthesized at 180?°C for 12?h formed the rhombohedral α-Fe₂O₃ phase with a spherical-like morphology. The Fe_1.98Ag_0.02O₃ fabricated by utilizing Fe_1.98Ag_0.02O₃ powders synthesized at 180?°C showed the largest power factor (0.64?×10^?5 Wm^?1 K^?2) and dimensionless figure-of-merit (0.0036) at 800?°C.     

Single-walled carbon nanotube/silicone rubber composites for compliant electrodes

Single-walled carbon nanotube (SWCNT)/silicone rubber composites that can be used in fabricating compliant electrodes are prepared by spraying a mixed solution of ionic-liquid-based SWCNT gel and silicone rubber onto an elastic substrate. Subsequently, the composites are exposed to nitric acid vapor. Scanning electron microscopy and atomic force microscopy images of the composites show that the SWCNTs are finely dispersed in the polymer matrix due to the addition of the ionic liquid. Doping of the SWCNTs by nitric acid can significantly lower the sheet resistance (R_s) of the composites; samples with 4 wt% of SWCNT content exhibit the lowest R_s value (50 Ω sq^?1). This sheet resistance corresponds to a conductivity value of 63 S cm^?1. In addition, the composites retain a high conductivity after several tensile strains are applied. Stretching the composite sample to 300% of the original length increased the R_s value to 320 Ω sq^?1 (19 S cm^?1). Even after 20th stretch/release/stretch cycle, the conductivity remains constant at a value of 18 S cm^?1. These results provide a scalable route for preparing highly stretchable and conductive SWCNT composites with relatively low SWCNT concentrations.     

Simple and cost-effective reduction of graphite oxide by sulfuric acid

We report a simple, cost-effective, and environmentally benign process for reducing graphite oxide by treating solely with sulfuric acid. The suggested process consists of a two-step reduction of graphite oxide, first in aqueous sulfuric acid at room temperature and then in concentrated sulfuric acid with refluxing. X-ray diffractometry, X-ray photoelectron spectroscopy, Raman spectroscopy and thermogravimetric analysis demonstrated that the graphite oxide was reduced effectively and was comparable in composition to reduced graphite oxide prepared using previously described methods that rely on toxic and hazardous reducing agents, such as hydrazine, sodium borohydride, or hydrohalic acids.     

Preparation of activated graphene and effect of activation parameters on electrochemical capacitance

Activation parameters such as temperature and the amount of potassium hydroxide (KOH) were varied during the synthesis of activated microwave-exfoliated graphite oxide (a-MEGO) and the effects of these parameters on the specific surface area of a-MEGO and electrochemical capacitance of a-MEGO electrodes were investigated. At 800 °C and a KOH/MEGO mass ratio of 6.5, a maximum specific surface area of 3100 m²/g was obtained and a high specific capacitance of 172 F/g (at 1 A/g constant current and 3.5 V maximal voltage) was measured in a two-electrode cell with a-MEGO electrodes in an organic electrolyte.     

The production of a cellular graphene array by scanning probe lithography and its ability to store electrical charge

A graphene cellular array on an insulating SiO₂ layer was fabricated by scanning probe lithography. The graphene layer was oxidized by an electric field which was applied between the cantilever tip and Si substrate without any electrode directly connected to the graphene layer. When the bias voltage was applied on a cell of patterned graphene through the cantilever tip, charge was accumulated on the cell and preserved for a long time without decay. The accumulated charge and the surface potential were measured by an electrostatic force microscope. The charge retention was measured as a function of time, and the decay time constant was estimated to be ～70 min.     

The Aharonov-Bohm effect in graphene rings with metal mirrors

We measured the Aharonov-Bohm (AB) effect in graphene rings with superconducting-(Al) and normal-metal (Au) mirrors. The mirrors were deposited either on additional stubs connected to the rings in the transverse direction or on the ring bias lines. A significant enhancement of the visible phase coherence was observed in the latter case, in which we observed even the third harmonic of the AB oscillations. The superconductivity of the mirrors appears to be unimportant for the improved coherence in graphene. A large Fermi energy mismatch between graphene and the mirror material is sufficient for this effect. In addition, a transport gap was observed in our graphene structures at the gate voltage close to the Dirac point. The value of the gap can be reproduced by assuming the occurrence of Coulomb blockade effects in graphene.     

Anaerobic co‐digestion of food waste leachate and piggery wastewater for methane production: statistical optimization of key process parameters

BACKGROUND: Anaerobic co‐digestion of refractory liquid organic wastes is an alternative environmental management strategy with economic benefits arising out of biogas production. Laboratory‐scale experimental investigations were carried out on the anaerobic co‐digestion of two liquid organic wastes, food waste leachate (FWL) and piggery wastewater (PWW). Three important parameters affecting methane yield were chosen for this study, namely, mixing ratio, alkalinity and salinity, which were optimized using response surface methodology. RESULTS: The results were analyzed statistically and the optimum conditions identified as: mixing ratio (FWL: PWW) 33 (in terms of volatile solid, w/w) (2 on v/v), alkalinity 2850 mg CaCO₃ L^?1, and salinity 3.4 g NaCl L^?1. Under the optimum conditions, a cumulative methane yield (CMY) of 310 mL CH₄ g^?1 VS_added and VS reduction (VSR) of 54% were predicted. Mixing ratio and alkalinity showed the greatest individual and interactive effects on CMY and VSR (P < 0.05). A confirmation experiment under optimum conditions showed a CMY and VSR of 323 mL CH₄ g^?1 VS_added and 50%, respectively. This was only 1.04% and 1.1%, respectively, different from the predicted values. CONCLUSION: Anaerobic co‐digestion of FWL and PWW carried out under the optimum condition may be a feasible and efficient treatment option for methane production. Copyright © 2012 Society of Chemical Industry     

Electrochemical properties of lithium nickel oxide synthesized by the combustion method in an O2 stream

An appropriate mole ratio of urea/nitrate for preheating to synthesize LiNiO₂ was examined by varying the ratio from 1.2 to 9.6. The chemical equation of the combustion reaction was deduced from the XRD analysis result of the mixture after preheating. The XRD pattern of the LiNiO₂ sample calcined at 800 °C for 24 h, after preheating at the mole ratio of urea/nitrate of 3.6 at 400 °C, shows clear split of the 1 0 8 and 1 1 0 peaks, and the largest value of I₀₀₃/I₁₀₄. The sample calcined at 800 °C for 24 h has a relatively high first discharge capacity (164.2 mAh g^?1) and a good cycling performance. Derivative ?dx/|dV| vs. V curve of the LiNiO₂ sample at the voltage range of 2.7–4.4 V for the first cycle exhibits four peaks for charging and discharging, showing that this sample goes through four phase transitions.