Oxide Loading Research Articles

Influence of Abdominal Obesity on the Relationship of Low-Density Lipoprotein Cholesterol with Atherosclerosis and Cardiovascular Risk in Rheumatoid Arthritis

Methods. Coronary artery calcium, number of coronary plaques, and extensive ( 5 plaques) or obstructive (>50% stenosis) disease was evaluated with computed tomography angiography in 150 patients at baseline and 101 patients 6.9±0.4 years later. Cardiovascular events were recorded. Oxidized LDL was measured with monoclonal antibody E06. Serum cholesterol loading capacity on macrophages was measured as intracellular cholesterol content with a fluorometric assay. Results. Abdominal obesity was not associated with per-patient number of coronary plaques or coronary artery calcium score at baseline. Low LDLc positively associated with number of plaques (b 2.13 [95% confidence interval 1.03 to 3.22]), likelihood of extensive or obstructive plaque (odds ratio 6.58, 95% confidence interval [1.63 to 26.46]), and log-transformed CAC (b 1.90 [0.89 to 2.91]) exclusively in nonobese patients (p-for-interaction <0.001, 0.061, and 0.001 respectively). Low LDLc associated with increased likelihood of >median oxidized LDL and higher ratio of cholesterol loading capacity to LDLc in nonobese patients (p-for-interaction 0.041 and 0.001 respectively). Abdominal obesity negatively associated with likelihood of plaque stenosis progression (odds ratio 0.19 [0.07 to 0.54]). Low LDLc associated with greater likelihood of per-segment plaque formation (OR 4.68 [2.26 to 9.66]) and increased stenotic severity (odds ratio 5.35 [1.62 to 17.67]) only in nonobese patients (p-for-interaction 0.002 and 0.040 respectively). Abdominal obesity was not linked to cardiovascular risk (Hazard Ratio 1.57, 95% confidence interval [0.66-3.73]). Low LDLc associated with higher cardiovascular risk in nonobese (Hazard Ratio 7.94 [1.52 to 41.36]) but not obese patients (p-for-interaction=0.017). Conclusion. Abdominal obesity was not linked to plaque progression or cardiovascular risk in RA. Only in nonobese patients, low LDLc associated with higher atherosclerosis burden, plaque progression and cardiovascular risk. This may reflect higher oxidation and macrophage cholesterol loading capacity of LDL when LDLc is <70mg/dl.

Tungsten oxide nanomaterial interactions below monolayer coverage

A tungsten oxide load at submonolayer coverage of alumina renders highly dispersed dimeric polytungstate (octahedral and distorted octahedral coordination) and isolated monotungstate (tetrahedral) species. The polytungstate/monotungstate proportion increases when approaching monolayer. Crystalline WO3 nanoparticles emerge at higher loads. All components display hexavalent oxidation; yet, tungsten‐ oxide (W–O–W) and tungsten‐ oxide‐ alumina (W–O–Al) interactions were discerned by X‐ ray photoelectron spectroscopy of the WOx/Al2O3 materials herein prepared with 1, 3, and 5 weight percentages. The 5 wt % sample displayed the highest intensity percentage of W–O–Al species correlated to the highest methanol conversion (45 %), ascribed to the appearance of the weak acidity disclosed by temperature‐ programmed desorption of ammonia.

Structural elucidation of Cr2O3-Al2O3 catalyst: Synthesis & characterization

The development of active, stable, and low-cost catalysts for efficient reactions is appealing but difficult. The objectives of this study are to synthesize Cr2O3-Al2O3 catalysts and analyze their physical properties using SEM, XRD, TGA-DTA, and FTIR. The impregnation method was used to create Cr2O3-Al2O3 catalysts with five different chromium oxide loadings (3wt%, 6wt%, 9wt%, 12wt%, and 15wt%). The physical properties of the catalysts were characterized using FTIR, SEM, BET, and TGA. The FTIR spectra and SEM images of the samples confirmed that Cr2O3 was successfully incorporated on Al2O3 support. TGA was used to evaluate the weight loss and thermal stability of the catalysts during the calcination process. The hydroxyl groups of alumina, as well as its water affinity, cause more mass loss when heated because water molecules are released. The addition of chromium oxide, on the other hand, alters thermal interactions, resulting in different mass loss behavior for chromium oxide alumina. The surface area changes seen by BET analysis gave insights into the structural flexibility of the catalyst across varied loading levels. The physical properties of synthesized catalysts demonstrated their ability to be utilized in a variety of catalytic reactions.

Bismuth ferrite based acetone gas sensor: evaluation of graphene oxide loading.

We report a BiFeO3/graphene oxide (BFO/GO) perovskite, synthesized using a CTAB-functionalized glycine combustion route, as a potential material for acetone gas sensing applications. The physicochemical properties of the developed perovskite were analysed using XRD, FE-SEM, TEM, HRTEM, EDAX and XPS. The gas sensing performance was analysed for various test gases, including ethanol, acetone, propanol, ammonia, nitric acid, hydrogen sulphide and trimethylamine at a concentration of 500 ppm. Among the test gases, the developed BFO showed the best selectivity towards acetone, with a response of 61% at an operating temperature of 250 °C. All the GO-loaded BFO samples showed an improved gas sensing performance compared with pristine BFO in terms of sensitivity, the response/recovery times, the transient response curves and the stability. The 1 wt% GO-loaded BiFeO3 sensor showed the highest sensitivity of 89% towards acetone (500 ppm) at an operating temperature of 250 °C. These results show that the developed perovskites have significant potential for use in acetone gas sensing applications.

The catalytic effect of calcium oxide and magnetite loading on magnetically supported calcium oxide-zeolite catalyst for biodiesel production from used cooking oil

This research focuses on developing a magnetically supported catalyst for efficient transesterification reaction of used cooking oil (UCO). The catalyst consists of calcium oxide (CaO) and ZSM-5 zeolite, which were synthesized using waste chicken eggshell and rice husk. Meanwhile, magnetite (Fe3O4) was used as a magnetic component. Various magnetic zeolite-supported CaO catalysts (CaZ/Fe) were prepared with different amounts of CaO (10, 30, 50, and 80 wt% of zeolite) and Fe3O4 (1:0.5, 1:1, 1:1.5 and 1:2 of CaO-zeolite:Fe3O4 ratio). The results identified the 50CaZ/0.5Fe catalyst as the most effective. The catalyst displayed a high surface area, strong basicity, and ideal morphology, thus contributing to a higher biodiesel yield of 91%. The recovery rate of the 50CaZ/0.5Fe catalyst was 88%, suggesting minimal loss and easy catalyst separation post-reaction using an external magnetic field. It also displayed superior stability, obtaining 85% biodiesel yield after 4 uses. The activation energy calculated in the kinetic study was 14.085 kJ/mol. Moreover, the properties of the synthesized biodiesel met the standards set by the ASTM D6751. Overall, the 50CaZ/0.5Fe catalyst with good magnetic behaviour and exhibits excellent catalytic activity suggested that this catalyst is promising for application in biodiesel production.

The architecture of redox microdomains: Cascading gradients and peroxiredoxins’ redox-oligomeric coupling integrate redox signaling and antioxidant protection

In the cytosol of human cells under low oxidative loads, hydrogen peroxide is confined to microdomains around its supply sites, due to its fast consumption by peroxiredoxins. So are the sulfenic and disulfide forms of the 2-Cys peroxiredoxins, according to a previous theoretical analysis [Travasso et al., Redox Biology 15 (2017) 297]. Here, an extended reaction-diffusion model that for the first time considers the differential properties of human peroxiredoxins 1 and 2 and the thioredoxin redox cycle predicts important new aspects of the dynamics of redox microdomains. The peroxiredoxin 1 sulfenates and disulfides are more localized than the corresponding peroxiredoxin 2 forms, due to the former peroxiredoxin's faster resolution step. The thioredoxin disulfides are also localized. As the H2O2 supply rate (vsup) approaches and then surpasses the maximal rate of the thioredoxin/thioredoxin reductase system (V), these concentration gradients become shallower, and then vanish. At low vsup the peroxiredoxin concentration determines the H2O2 concentrations and gradient length scale, but as vsup approaches V, the thioredoxin reductase activity gains influence. A differential mobility of peroxiredoxin disulfide dimers vs. reduced decamers enhances the redox polarity of the cytosol: as vsup approaches V, reduced decamers are preferentially retained far from H2O2 sources, attenuating the local H2O2 buildup. Substantial total protein concentration gradients of both peroxiredoxins emerge under these conditions, and the concentration of reduced peroxiredoxin 1 far from the H2O2 sources even increases with vsup. Altogether, the properties of 2-Cys peroxiredoxins and thioredoxin are such that localized H2O2 supply induces a redox and functional polarization between source-proximal regions (redox microdomains) that facilitate peroxiredoxin-mediated signaling and distal regions that maximize antioxidant protection.

REM Sleep Loss-Induced Elevated Noradrenaline Plays a Significant Role in Neurodegeneration: Synthesis of Findings to Propose a Possible Mechanism of Action from Molecule to Patho-Physiological Changes.

Wear and tear are natural processes for all living and non-living bodies. All living cells and organisms are metabolically active to generate energy for their routine needs, including for survival. In the process, the cells are exposed to oxidative load, metabolic waste, and bye-products. In an organ, the living non-neuronal cells divide and replenish the lost or damaged cells; however, as neuronal cells normally do not divide, they need special feature(s) for their protection, survival, and sustenance for normal functioning of the brain. The neurons grow and branch as axons and dendrites, which contribute to the formation of synapses with near and far neurons, the basic scaffold for complex brain functions. It is necessary that one or more basic and instinct physiological process(es) (functions) is likely to contribute to the protection of the neurons and maintenance of the synapses. It is known that rapid eye movement sleep (REMS), an autonomic instinct behavior, maintains brain functioning including learning and memory and its loss causes dysfunctions. In this review we correlate the role of REMS and its loss in synaptogenesis, memory consolidation, and neuronal degeneration. Further, as a mechanism of action, we will show that REMS maintains noradrenaline (NA) at a low level, which protects neurons from oxidative damage and maintains neuronal growth and synaptogenesis. However, upon REMS loss, the level of NA increases, which withdraws protection and causes apoptosis and loss of synapses and neurons. We propose that the latter possibly causes REMS loss associated neurodegenerative diseases and associated symptoms.

Structural Formation and Pore Control of Freeze-Cast Directional Graphene Aerogel (DGA).

Directional graphene aerogels (DGAs) are proposed as electrode materials to alleviate ionic and mass transport issues in organic redox flow batteries (ORFBs). DGAs with high pore directionality would provide low resistance channels for effective ionic charge and liquid electrolyte transport in these devices. DGAs' porous and directional characteristics can be controlled by the growth of ice crystals during freeze casting, which is influenced by the self-diffusivity of water, phase change driving forces, water-ice graphene interactions, and convection in the water-graphene media. It is found that mass transport-related properties of DGAs, including pore size and directionality, show a significant dependence on freezing temperature, graphene oxide (GO) loadings, and synthesis vessel diameter-to-height ratio (D/H). For the freezing temperature change from -20 to -115 °C, the average pore size progressively decreased from 120 to 20 μm, and the pore directionality transitioned from lamellar to ill-defined structures. When GO loadings were increased from 2 to 10 mg/mL at a fixed freezing temperature, pore size reduction was observed with less defined directionality. Furthermore, the pore directionality diminished with an increased width-to-height aspect ratio of DGA samples due to the buoyancy-driven convective circulation, which interfered with the directional ice/pore growth. Understanding the comprehensive effects of these mechanisms enables the controlled growth of ice crystals, leading to graphene aerogels with highly directional microstructures.

FexNiy/ SiO2-Al2O3 catalyzed hydrodeoxygenation of biorenewable platform molecules

A series of FexNiy/SA (SA = SiO2-Al2O3) catalysts were synthesized via solvothermal assisted deposition precipitation synthesis method and explored for low-temperature hydrodeoxygenation (HDO) reaction of methyl oleate into n-alkanes and vegetable oils. A comprehensive study on the effects of increasing iron oxide loading in catalyst samples, i.e., Fe1Ni1/SA, Fe3Ni1/SA, Fe5Ni1/SA and Fe7Ni1/SA, on the crystallographic, morphological, textual and surface chemical behavioural were investigated thoroughly using various spectroscopic techniques. The study disclosed excellent surface area, high acidic strength and reducibility of Fe1Ni1/SA catalyst due to the lowest Fe2+ or FeO species. In contrast, higher iron oxide loading leads to the accumulation of Fe2+ ions on the surface with reduced metal acid centres and diminished surface area. The catalytic conversion as well as C17-C18 selectivity in catalytic HDO was also scrutinised with particular reference to Fe2+/Fe3+ ion ratio. The obtained superior catalytic activity and C18 selectivity of Fe1Ni1/SA catalyst are due to the lowest Fe2+/Fe3+ ion ratio. However, the iron oxide loading increased the Fe2+/Fe3+ ion ratio, which ultimately decreased the catalytic activity. Thus, the role of Fe2+ species in the deactivation of catalyst was discussed in detail to establish conversion and selectivity control in the catalytic HDO pathway.

Competitive Mechanism between Interfacial Electric Field and Built‐In Electric Field for Silicon‐Based Tribovoltaic Effect

AbstractThe tribovoltaic effect raises an emerging semiconductor energy technology and silicon‐based tribovoltaic nanogenerator (Si‐TVNG) has aroused great attentions. However, the electrical output of Si‐TVNG is extremely unstable due to its complicated mechanism. Here, a competitive mechanism between the built‐in electric field (BEF) and the interfacial electric field (IEF) is proposed to determine the current direction and magnitude of the Si‐TVNG. The results indicate that the natural oxide layer, load pressure, and resistivity of Si significantly affect the IEF and BEF. The natural oxide layer can store surface charges by contact electrification, resulting in a IEF dominant carriers transport process. Conversely, lower resistivity and higher load pressure can reduce the contact resistance, thereby decreasing the surface charges caused by contact electrification and leading to a BEF dominant carrier transport process. This work contributes to deeper understandings of the tribovoltaic effect and further clarifies the theoretical mechanisms of carrier excitation and directional transport.

Hydrothermal synthesis of lanthanum oxide nanoparticles modified pumice: High lanthanum oxide loading ratio and efficiency phosphate removal

Efficient and less restrictive phosphorus pollution treatment methods are required to treat water eutrophication. Lanthanum oxide nanoparticles modified pumice (LOMP) with a high loading ratio was prepared by a simple hydrothermal synthesis method which adjusted the synthesis conditions. The XRD, SEM, and TEM results show that the lanthanum oxide nanoparticles have successfully modified on the surface of the pumice, forming a disordered hierarchical structure. The adsorption kinetics results showed that phosphate adsorption was more consistent with the pseudo-second-order model. The adsorption isotherm was more consistent with the Sips model, and the theoretical adsorption capacity was 82.77 mg P/L. The results of the effects of the initial pH and the coexisting anions indicate that LOMP has a good phosphate removal efficiency in a wide range of pH and a strong ability to resist the competition of anions. The superior phosphate adsorption performance can be ascribed to the ligand exchange, which also can be promote by hydrogen ions.

Catalytic upgrading of biomass pyrolysis vapors for selective production of phenolic monomers over metal oxide modified alumina catalysts

This study investigates the catalytic vapor phase upgrading of sawdust to produce improved biocrude enriched in phenolic monomers. Various mixed metal oxide catalysts (MgO, CuO, Bi2O3, NiO, ZnO supported on Al2O3) were screened to determine the product composition. Further, the effect of different process parameters such as temperature (350 – 600 °C), metal oxide loadings (0 – 20 wt%), catalyst to biomass ratios (1:1–1:6), sweeping gas flow rates (0 – 15 LPH) were studied in terms of biocrude composition. Under non-catalytic conditions, maximum biocrude yields (∼39%) were obtained at an optimum temperature of 550 °C. The biocrude composition varied significantly with the type of metal oxide in which MgO and CuO produced higher amounts of phenolics (∼58%). Increasing MgO loading (5–20 wt%) and higher catalyst to biomass ratios (1:1) resulted in enhanced hydrocarbon yields to ∼15%. Premixing of biomass and catalyst in a fixed bed arrangement resulted in enhanced hydrocarbons/aromatics with simultaneous reduction in the phenolic content.

Electrosorption of paraquat pesticide on activated carbon modified by aluminium oxide (Al2O3) with capacitive deionization

Composite electrode materials for removing paraquat from contaminated water were synthesized by loading aluminium oxide (Al2O3) onto activated carbon (AC) via co-precipitation method. The composite properties were investigated by X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and energy-dispersive X-ray spectroscopy. Capacitive deionization batch experiments compared the electrosorption of paraquat herbicide by the composite electrode and the pristine activated carbon. The performance of the composite electrodes showed that the removal efficiency and adsorption capacity depend on the aluminium oxide loading, applied potential, flow rate, and charging time. At 1.2 V, a flow rate of 15 mL/min, a charging time of 3 h and 20 mg/L PQ initial concentration, the composite electrode (AC/Al2O3-1:1) demonstrated a removal efficiency, electrosorption capacity, and energy consumption of 95.5 %, 1.27 mg/g, and 0.055 kWh/m3, respectively, compared to 62 %, 0.83 mg/g, and 0.11 kWh/m3 for the unmodified AC. The presences of other ions/pollutants were found to have negligible interference on PQ pesticide removal as the removal efficiency and electrosorption capacity of the AC/Al2O3-1:1 composite in both artificial (95.5 %, 1.27 mg/g) and natural water (87.5 % 1.17 mg/g). The study confirmed that composite electrode can reused several times, as there was no significant decrease in its regeneration efficiency even after multiple cycles.

Surface Activated Pyrolytic Carbon Black: A Dual Functional Sustainable Filler for Natural Rubber Composites.

The significant rise in end-of-life tires (ELTs) globally poses immediate environmental and human health risks. Therefore, to promote ELTs recycling and to reduce tire industry carbon emissions, herein we present a facile approach for fine-tuning the interfacial interactions between pyrolytic carbon black (P-CB) obtained from ELTs and natural rubber (NR) matrix using phosphonium-based ionic liquid (PIL). The reinforcing effect of PIL-activated P-CB was studied by replacing the furnace-grade carbon black (N330-CB) with varying PIL and P-CB loadings. Adding PIL improved the filler dispersion and the cross-linking kinetics with a substantially reduced zinc oxide (ZnO) loading. Considering the cross-linking and viscoelastic properties, it was concluded that the composite, P-CB/N330-CB-PIL (1.5)+ZnO (1) with half substitution of N330-CB with P-CB synergistically works with 1.5 phr PIL and 1 phr of ZnO resulting in improved dynamic-mechanical properties with a minimal loss tangent value at 60 °C (tanδ=0.0689) and improved glass transition temperature (Tg =-38 °C) compared to control composite. The significant drop (~29 % lower) in tanδ could reduce fuel consumption and related CO2 emissions. We envisage that this strategy opens an essential avenue for "Green Tire Technology" towards the substantial pollution abatement from ELTs and reduces the toxic ZnO.

170 Do you Have the Energy to Grind Feed Costs and Maximize Net Income in Demanding Economic Times?

Abstract Energy is not only the most expensive component of the diet, but also among the most complex. Energy impacts all aspects of the growth and metabolism of the pig. Therefore, when feed costs escalate, energy is a predictable though challenging target for increased attention. To achieve greatest success, a two-pronged approach is warranted. The first focuses on our understanding of the fundamentals of energy science and the second logically follows with applying this knowledge in practice. This presentation will address both the science and the application. Formulating energy in pig diets is a complicated process. For example, one can achieve equal dietary energy values with different proportions of protein, starch, fat and fiber. Each of these nutrients is used with a different level of efficiency by the pig, leading one to question whether equal performance should be expected just because ME or NE is the same. We will dig a bit more deeply into how energy values of ingredients are generated, what assumptions are made in this process and the limitations of these values in predicting pig performance. Beyond ME and NE, we will note that changing energy sources may also alter the microbiota, oxidative load, gut structure and function, and even the digestibility of dietary nutrients. This, in turn, can impact not only the performance of the pig, but also resistance to disease and susceptibility to environmental stress. We will also discuss why feed efficiency is sometimes highly correlated to dietary energy but in other cases, this relationship is quite weak; how can this be? On a positive note, the ME or NE of ingredients has been found to be highly correlated with certain dietary constituents. This infers that the prediction of the energy content of ingredients should be quite effective, and such predictions will improve the precision of diet formulation. Moving forward, it makes sense that wherever possible, energy response curves should be part of the toolkit available to swine nutritionists, but these curves should involve diverse diet composition, unlike the energy titration studies commonly used in our industry. When energy is the most expensive, and production margins are weakest, this is the very time to invest strategically in diet analysis to ensure that we are extracting every bit of energy we can from available ingredients. In other words, are we achieving our formulation targets? Because the topic of dietary energy is so large and complex, we will remind ourselves where we can have the greatest impact on net income by managing energy. In conclusion, energy drives feed costs and drives performance. As complex a topic as it is, we will be rewarded by understanding dietary energy more deeply, and applying that knowledge as effectively as possible in commercial practice.

Bisphenol S dysregulates thyroid hormone homeostasis; Testicular survival, redox and metabolic status: Ameliorative actions of melatonin

Bisphenol S (BPS) is an incipient threat for reproductive health augmenting societal burden of infertility worldwide. In the present study, we investigated the mechanism of BPS induced testicular dysfunctions and protective actions of melatonin in mice. BPS (150 mg/kg BW) treatment reduced serum T3/T4, testosterone and elevated insulin levels along with adverse effect on thyroid and testicular histoarchitecture. Further, BPS treatment compromised sperm quality, reduced mRNA expression of steroidogenic (StAR/CYP11A1) markers, elevated oxidative load and disrupts metabolic status. However, melatonin (5 mg/kg BW) administration to BPS treated mice showed improved hormonal/histological parameters, enhanced thyroid hormone (TR-α/Dio-2)/melatonin (MT-1) receptor expressions. Further, melatonin treatment modulated the expression of testicular survival/redox (SIRT1/PGC-1α/FOXO-1, Nrf2/HO-1, p-JAK2/p-STAT3), proliferative (PCNA) and metabolic (IR/pAKT/GLUT-1) markers. Furthermore, melatonin treatment enhanced testicular antioxidant status and reduced caspase-3 expression. In conclusion, our results showed that BPS induces endocrine/oxidative and metabolic anomalies while melatonin improved male reproductive health.

Highly efficient deborylative hydroxylation of boronic acids through a metal and base-free process using pectin as a reusable carbocatalyst: The positive effect of hydrogen-bond donating groups

Phenols are important organic compounds with a broad range of application in pharmaceuticals, polymers, and agrochemicals. A metal- and base-free pectin-catalyzed methodology has been introduced for the sustainable ipso-hydroxylation of aryl and heteroaryl boronic acids to phenols using 30% H2O2 as a benign oxidant. Pectin (Pec, galacturonic acid ≥74.0%) was chosen as an inexpensive and available polysaccharide with numerous extraction sources. Control experiments using high methoxy pectin (HM-Pec, 70-75% esterification) confirmed that the abundant carboxylic acid and hydroxyl groups on the Pec surface act as catalytically active sites to improve the oxidation process by adsorbing the substrates via hydrogen bonding. The use of H2O:EtOH (1:1 v/v) as a solvent system instead of H2O enhanced the reaction yield, substrate scope and separation of catalyst by improving the dissolution of less soluble arylboronic acids in water such as 1-naphthylboronic acid and 2-naphthylboronic acid and preventing the gel formation of Pec nanoparticles. The reaction endured a broad substrate scope for aryl and heteroaryl boronic acids with good to excellent yields (75-99%). Pec showed an excellent reusability up to 6 runs with negligible loss of activity which verified by FT-IR, XRD and FESEM of recycled catalyst. More importantly, as a metal- and base-free catalyst system, the present research gave a comparable result to previous homogeneous and heterogeneous catalyst systems in view of reaction time, yield, oxidant loading, and number of reusability cycles.

Experimental evidence of the neurotoxic effect of monosodium glutamate in adult female Sprague Dawley rats: The potential protective role of Zingiber officinale Rosc. rhizomes

Strategies to prevent the health abnormalities associated with the extensive use of MSG (monosodium glutamate) as a flavoring booster are badly needed. The current study was conducted to investigate oxidative stress, inflammation, and abnormal lipid profile as the main risk factors of neurotoxicity in MSG-exposed female albino rats. Besides, the effect of concurrent consumption of Zingiber officinale rhizomes powder was studied at low doses. Twenty rats (total) were split into 4 separate groups. The 1st group was a negative control group (without any treatment), while the others received 6 mg MSG/kg. The 2nd group was left untreated, whereas the 3rd and 4th groups were given a regular laboratory diet that included ginger rhizome powder supplements (GRP, 0.5 & 1%, respectively) for six weeks. In brain tissue homogenates, exposure to MSG caused a significant depletion of gamma-aminobutyric acid (GABA) and total protein levels, while triglycerides and cholesterol contents were significantly elevated. Moreover, a noteworthy upsurge in oxidative load and inflammation markers was also noticed associated with a marked reduction of antioxidant levels, which histopathological staining verified further. The rat diet formulated with GRP, with a dose-dependent effect, resulted in increased GABA and total protein contents and attenuated inflammation, oxidative stress, abnormal lipid profile, and marked histological changes in cerebral cortical neurons of MSG-administered animals. Therefore, this study reveals that GRP shields rats against the neurotoxicity that MSG causes. The anti-inflammatory as well as antioxidant, and lipid-normalizing properties of rhizomes of ginger may be accountable for their observed neuroprotective action.

Preparation and Catalytic Properties of Graphene Oxide/ Phosphotungstic Acid Composites

Background: Cellulose structures are in stable crystallineform. The hydrolysis of cellulose to small reducing sugars is difficult, but essential for its utilization Objective: To investigate the effect of graphene oxide (GO) loading on the catalytic performance of phosphotungstic acid (HPW) for the catalyzed hydrolysis of cellulose, with the purpose to get high yield of total reducing sugar (TRS). Methods: Graphene oxide/phosphotungstic acid (GO/HPW) composites were prepared using a liquid-phase composite method. The materials were applied to catalyze hydrolysis of microcrystalline cellulose in 1-butyl-3-methylimidazole chloride ionic liquid ([Bmim]Cl). The samples were characterized by Powder X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), Field emission scanning electron micrographs (FE-SEM), pyridine IR and acid-base chemical titration. Results: The Brønsted acidic sites were the main source of acidity in the composites and its concentration was determined to be 0.96 mmol/g. With the use of the GO/HPW composite as catalysts for cellulose hydrolysis, TRS yield of 90.5 % was obtained. Conclusion: GO/HPW composites retained the functional groups of both materials. It was the Brønsted acidic sites in the materials that effectively promoted the cellulose hydrolysis reaction. The structures of GO/HPW with the agglomeration of HPW scattered on GO had high accessibility of acidic sites and fast mass transfer of the reducing sugars to the outside of the catalysts in time to prevent their further conversion into by-products. TRS yield of 90.5 % was obtained from the hydrolysis of cellulose catalyzed by the GO/HPW (1:1.5) composites at 115 ℃ for 4 h using catalysts to cellulose 1:1 ratio.

Disorders of Endogenous and Exogenous Antioxidants in Neurological Diseases.

In diseases of the central nervous system, such as Alzheimer's disease (AD), Parkinson's disease (PD), stroke, amyotrophic lateral sclerosis (ALS), Huntington's disease (HD), and even epilepsy and migraine, oxidative stress load commonly surpasses endogenous antioxidative capacity. While oxidative processes have been robustly implicated in the pathogenesis of these diseases, the significance of particular antioxidants, both endogenous and especially exogenous, in maintaining redox homeostasis requires further research. Among endogenous antioxidants, enzymes such as catalase, superoxide dismutase, and glutathione peroxidase are central to disabling free radicals, thereby preventing oxidative damage to cellular lipids, proteins, and nucleic acids. Whether supplementation with endogenously occurring antioxidant compounds such as melatonin and glutathione carries any benefit, however, remains equivocal. Similarly, while the health benefits of certain exogenous antioxidants, including ascorbic acid (vitamin C), carotenoids, polyphenols, sulforaphanes, and anthocyanins are commonly touted, their clinical efficacy and effectiveness in particular neurological disease contexts need to be more robustly defined. Here, we review the current literature on the cellular mechanisms mitigating oxidative stress and comment on the possible benefit of the most common exogenous antioxidants in diseases such as AD, PD, ALS, HD, stroke, epilepsy, and migraine. We selected common neurological diseases of a basically neurodegenerative nature.