Micro/Nano-Structuring of Medical Stainless Steel using Femtosecond Laser Pulses

AbstractThe medical stainless steel (SUS 304) surface is irradiated by femtosecond laser pulses with linear or circular polarization to form nanostructure-covered conical microstructures. The mean spacing of the conical microstructures and the type of the nanostructure can be controlled by the laser-processing parameters. The liquid test (water and normal-saline solution) demonstrates that the process provides a fast single-step structuring method to generate hydrophobic-enhanced metal parts. The biocompatibility test demonstrated that the femtosecond laser micro/nano- structuring surfaces have excellent biocompatibility properties compared to an untreated surface

The effect of bending loads on the dynamic behaviors of a rolling guide

Dynamic behaviors of ball-type contact surfaces under unbalanced bending loads are studied using point-to-point analysis, three-dimensional finite element simulation based on the Hertz Contact Theory, and a modal test. Results derived from these models are very similar but the Finite Element Model provides the best results since it allows for more elements of study, such as the steel ball, carriage, rail etc. In the study, results also show that frequencies vary slightly, but there is an obvious change in shapes. Therefore, the contact stiffness in simulations must be properly selected with the conclusion that different external loadings may affect the dynamic characteristics of such structures significantly

Ginkgo biloba extract attenuates oxLDL-induced oxidative functional damages in endothelial cells

Ou HC, Lee WJ, Lee IT, Chiu TH, Tsai KL, Lin CY, Sheu WH. Ginkgo biloba extract attenuates oxLDL-induced oxidative functional damages in endothelial cells. J Appl Physiol 106: 1674-1685, 2009. First published February 19, 2009; doi:10.1152/japplphysiol.91415.2008.-Atherosclerosis is a chronic inflammatory process with increased oxidative stress in vascular endothelium. Ginkgo biloba extract (GbE), extracted from Ginkgo biloba leaves, has commonly been used as a therapeutic agent for cardiovascular and neurological disorders. The aim of this study was to investigate how GbE protects vascular endothelial cells against the proatherosclerotic stressor oxidized low-density lipoprotein (oxLDL) in vitro. Human umbilical vein endothelial cells (HUVECs) were incubated with GbE (12.5-100 mu g/ml) for 2 h and then incubated with oxLDL (150 mu g/ml) for an additional 24 h. Subsequently, reactive oxygen species (ROS) generation, antioxidant enzyme activities, adhesion to monocytes, cell morphology, viability, and several apoptotic indexes were assessed. Our data show that ROS generation is an upstream signal in oxLDL-treated HUVECs. Cu,Zn-SOD, but not Mn-SOD, was inactivated by oxLDL. In addition, oxLDL diminished expression of endothelial NO synthase and enhanced expression of adhesion molecules (ICAM, VCAM, and E-selectin) and the adherence of monocytic THP-1 cells to HUVECs. Furthermore, oxLDL increased intracellular calcium, disturbed the balance of Bcl-2 family proteins, destabilized mitochondrial membrane potential, and triggered subsequent cytochrome c release into the cytosol and activation of caspase-3. These detrimental effects were ameliorated dose dependently by GbE (P < 0.05). Results from this study may provide insight into a possible molecular mechanism underlying GbE suppression of the oxLDL-mediated vascular endothelial dysfunction

Glial activation involvement in neuronal death by Japanese encephalitis virus infection

Japanese encephalitis is characterized by profound neuronal destruction/dysfunction and concomitant microgliosis/astrogliosis. Although substantial activation of glia is observed in Japanese encephalitis virus (JEV)-induced Japanese encephalitis, the inflammatory responses and consequences of astrocytes and microglial activation after JEV infection are not fully understood. In this study, infection of cultured neurons/glia with JEV caused neuronal death and glial activation, as evidenced by morphological transformation, increased cell proliferation and elevated tumour necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, IL-6 and RANTES (regulated upon activation, normal T-cell expressed and secreted) production. Replication-competent JEV caused all glial responses and neurotoxicity. However, replication-incompetent JEV lost these abilities, except for the ability to change microglial morphology. The bystander damage caused by activated glia also contributed to JEV-associated neurotoxicity. Microglia underwent morphological changes, increased cell proliferation and elevated TNF-alpha, IL-1 beta, IL-6 and RANTES expression in response to JEV infection. In contrast, IL-6 and RANTES expression, but no apparent morphological changes, proliferation or TNF-alpha/IL-1 beta expression, was demonstrated in JEV-infected astrocytes. Supernatants of JEV-infected microglia, but not JEV-infected astrocytes, induced glial activation and triggered neuronal death. Antibody neutralization studies revealed that TNF-alpha and IL-1 beta, but not RANTES or IL-6, released by activated microglia appeared to play roles in JEV-associated neurotoxicity. In conclusion, following JEV infection, neuronal death was accompanied by concomitant microgliosis and astrogliosis, and neurotoxic mediators released by JEV-activated microglia, rather than by JEV-activated astrocytes, had the ability to amplify the microglial response and cause neuronal death

Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

Type 2 diabetes (T2D) affects Latinos at twice the rate seen in populations of European descent. We recently identified a risk haplotype spanning SLC16A11 that explains ∼20% of the increased T2D prevalence in Mexico. Here, through genetic fine-mapping, we define a set of tightly linked variants likely to contain the causal allele(s). We show that variants on the T2D-associated haplotype have two distinct effects: (1) decreasing SLC16A11 expression in liver and (2) disrupting a key interaction with basigin, thereby reducing cell-surface localization. Both independent mechanisms reduce SLC16A11 function and suggest SLC16A11 is the causal gene at this locus. To gain insight into how SLC16A11 disruption impacts T2D risk, we demonstrate that SLC16A11 is a proton-coupled monocarboxylate transporter and that genetic perturbation of SLC16A11 induces changes in fatty acid and lipid metabolism that are associated with increased T2D risk. Our findings suggest that increasing SLC16A11 function could be therapeutically beneficial for T2D. Video Abstract [Figure presented] Keywords: type 2 diabetes (T2D); genetics; disease mechanism; SLC16A11; MCT11; solute carrier (SLC); monocarboxylates; fatty acid metabolism; lipid metabolism; precision medicin

Quantitative temporal viromics: an approach to investigate host-pathogen interaction

A systematic quantitative analysis of temporal changes in host and viral proteins throughout the course of a productive infection could provide dynamic insights into virus-host interaction. We developed a proteomic technique called “quantitative temporal viromics” (QTV), which employs multiplexed tandem-mass-tag-based mass spectrometry. Human cytomegalovirus (HCMV) is not only an important pathogen but a paradigm of viral immune evasion. QTV detailed how HCMV orchestrates the expression of >8,000 cellular proteins, including 1,200 cell-surface proteins to manipulate signaling pathways and counterintrinsic, innate, and adaptive immune defenses. QTV predicted natural killer and T cell ligands, as well as 29 viral proteins present at the cell surface, potential therapeutic targets. Temporal profiles of >80% of HCMV canonical genes and 14 noncanonical HCMV open reading frames were defined. QTV is a powerful method that can yield important insights into viral infection and is applicable to any virus with a robust in vitro model

INVESTIGATION OF CHEMICAL QUALITY OF SUGARCANE (SACCHARUM OFFICINARUM L.) WINE DURING FERMENTATION BY SACCHAROMYCES CEREVISIAE

The purpose of this study was to examine the changes in the contents of sugar ethanol, organic acids, volatile compounds, pH and acidity in sugarcane wine during fermentation using Saccharomyces cerevisiae and the consumer preference test was also conducted to investigate the optimal fermentation. According to the results, the maximal population of S. cerevisiae reached to 8.12 log cfu/mL at the sixth day of :fermentation. The maximum ethanol content, 15.16%, was obtained at the ninth day, while the sucrose and glucose concentrations were almost exhausted at the SOW time. As for organic acids, citric acid was detected as the most abundant one at the second day of fermentation, followed by lactic and succinic acids. The volatile compounds were analyzed by SPME/GC-MS, and the concentrations of alcohols, esters and acids were all highest in sugarcane wine at the sixth day of fermentation. The results' have demonstrated that sugarcane wine fermentation with S. cerevisiae at the sixth day is enough to reach the highest aroma quality as indicated by the highest ester/alcohols in the wine and the most abundant amount of aroma-related compounds. The overall preference of consumer test also supports the above result with the sugarcane wine fermented at day 6 having highest scores

INVESTIGATION OF FERMENTING CONDITIONS FOR SUGARCANE (SACCHARUM OFFICINARUM L.) WINE USING RESPONSE SURFACE METHODOLOGY

The purpose of this study was to investigate the effects of alcoholic fermenting conditions such as sugar content, fermentation temperature and pH on the sensory quality and ethanol content of sugarcane wine (SCW) by response surface methodology. The results from contour plots showed that the maximum ethanol content was around 11% with the initial sugar content at 25.0 degrees Brix, and fermentation at 26.3C and pH 5.5. The results of consumer tests showed that under the fermentation condition with sugar content at 24 degrees Brix or below and higher temperature favored the color acceptance of SCW. While the sugar content above 24 degrees Brix, the lower temperature favored the aroma, flavor and overall preference. Statistical analysis with the central composite rotatable design showed that the total soluble solids of SCW was significantly (P < 0.05) correlated with sugar content, pH and fermentation temperature. The sugar content and fermentation temperature significantly (P < 0.05) affected the ethanol content and aroma of SCW, while the pH significantly (P < 0.05) affected the flavor and overall preference. Based on the results of total soluble solids, ethanol contents, consumer tests and confirmative experiments, it was determined that the sugar content at 24-26 degrees Brix, pH at 5.5 and fermentation temperature at 24-27C were the optimal fermentation conditions for SCW

Inhibition of nitric oxide production by quercetin in endotoxin/cytokine-stimulated microglia

Aims: Flavonoids possess several biological and pharmacological activities. Quercetin, a naturally occurring flavonoid, has been shown to down-regulate inflammatory responses and provide neuroprotection. However, the mechanisms underlying the anti-inflammatory properties of quercetin are poorly understood. In the present study, we investigated the modulatory effect of quercetin against neuroinflammation. Main methods: We herein describe a potential regulatory mechanism by which quercetin suppresses nitric oxide (NO) production by lipopolysaccharide (LPS)/interferon-gamma (IFN-gamma)-stimulated BV-2 microglial cells. The underlying regulatory cascades were approached by biochemical and pharmacological strategies. Key findings: Quercetin produced an inhibitory effect on inducible nitric oxide synthase (iNOS) expression and NO production. Biochemical studies revealed that the anti-inflammatory effect of quercetin was accompanied by the down-regulation of extracellular signal-regulated kinase, c-Jun N-terminal kinase, p38, Akt, Src, Janus kinase-1, Tyk2, signal transducer and activator of transcription-1, and NF-kappa B. In addition, quercetin scavenged free radicals and produced inhibitory effects on serine/threonine and tyrosine phosphatase activities. Intriguingly, the accumulation of lipid rafts, which is the critical step for signaling, was disrupted by quercetin. Significance: The data indicate that the anti-inflammatory action of quercetin may be attributable to its raft disrupting and anti-oxidant effects. These distinct mechanisms work in synergy to down-regulate iNOS expression and NO production. (C) 2010 Elsevier Inc. All rights reserved