The Impact of Duodenal Mucosal Vulnerability in the Development of Epigastric Pain Syndrome in Functional Dyspepsia

An unidentified cause of functional dyspepsia (FD) is closely associated with medication resistance. Acid suppression is a traditional and preferential method for the treatment of FD, but the efficacy of this treatment varies between epigastric pain syndrome (EPS) and postprandial syndrome (PDS): it is efficient in the former but not much in the latter. Transepithelial electrical resistance (TEER), a surrogate of mucosal barrier function, was measured under pH 3 and pH 5 acidic conditions using duodenal biopsy specimens obtained from the patients with EPS and PDS and asymptomatic healthy controls. The infiltration of inflammatory cells to the duodenal mucosa was accessed by immunohistochemical analysis. The duodenal mucosal TEER in EPS patients was decreased by exposure to the acidic solution compared to that of the controls and the PDS patients. The decrease in TEER of the EPS patients was observed even under pH 5 weak acidic condition and was correlated to degree of the epigastric pain. Moreover, the duodenal mucosa of EPS patients presented an increase in mast cells and plasma cells that expressed Ig-E. Duodenal mucosal vulnerability to acid is likely to develop EPS.     

Metal‐chloride‐anion‐containing polymers with expanded π‐conjugation systems derived from through‐space interactions in the piperazinium ring

Reactions of N‐(2,4‐dinitrophenyl)pyridinium chloride (salt(Cl)) with H⁺MCl₄^?1 (M ≡ Fe and Bi) resulted in an anion exchange between Cl^? and MCl₄^? to yield Zincke salts with metal chloride anions, namely salt(Fe) and salt(Bi), respectively. Reactions of the Zincke salts with piperazine resulted in ring‐opening of the pyridinium ring, yielding ionic polymers with 5‐piperazinium‐2,4‐dienylideneammonium metal chloride units, namely polymer(Fe) and polymer(Bi). The corresponding model compounds were synthesized via reactions using salt(Bi) or salt(Cl) as starting materials. The UV–visible spectra of the polymers had absorption maxima at longer wavelengths than those of the model compounds. This indicated that the π‐conjugation system is expanded along the polymer main chain. Superconducting quantum interference device measurements indicated that polymer(Fe) was paramagnetic. Cyclic voltammetry analysis suggested that the polymers underwent electrochemical oxidation. © 2019 Society of Chemical Industry     

Seismic analysis of nuclear power plants by using three-dimensional finite element models: a review

ABSTRACT

Seismic design of nuclear power plants (NPPs) is important for ensuring their integrity during earthquakes. Seismic analysis has been conducted using lumped mass beam models (LMBMs) for the design of plants in Japan, whereas three-dimensional (3D) finite element models (FEMs) have been used for novel plants outside Japan. The purposes of this study are to organize issues related to the development and application of 3D FEMs for seismic analysis of Japanese NPPs and to indicate future study directions. To organize these issues, the authors systematically investigated: (1) international guides and standards related to seismic analysis and (2) 3D FEMs of novel NPPs outside Japan. By considering other studies on the issues, the authors suggest directions for future studies. Resolving the issues will contribute to application of 3D FEMs for seismic analysis in the design of Japanese NPPs.     

Agglomeration of magnesium oxide particles formed by the decomposition of magnesium hydroxide

Agglomeration of magnesium oxide (MgO) particles was studied by decomposing magnesium hydroxide (Mg(OH)₂). The properties of agglomerates varied according to the decomposition temperature region: (i) below 650° C, (ii) 650° C to 850° C, (iii) 850° C to 1050° C, and (iv) 1050° C to 1200°C. In region (i), the original Mg(OH)₂ frameworks or pseudomorphs remained in the powder and showed agglomeration. The strength of agglomerates containing the pesudomorphs was about 50 MPa; the primary particles in pseudomorphs are bonded chemically by the interaction of MgO and residual water. In region (ii) the pseudomorphs began to show some fragmentation: the bonding strength of these pseudomorphs reduced rapidly. In region (iii), both crystallite and primary particles were grown by the sintering; this growth may be due to an increase in contact area based on the collapse of pseudomorphs. The primary particles whose necks were grown by the sintering could be easily pulled apart by grinding. In region (iv) pore growth due to the rearrangement of primary particles caused the suppression of both densification rate and crystal growth of MgO.     

Kinetic Study of the Scavenging Reaction of the Aroxyl Radical by Eight Kinds of Vegetable Oils in Solution

A detailed kinetic study was performed for the reaction of the aroxyl radical (ArO?) with eight vegetable oils 1–8, which contain different concentrations of α‐, β‐, γ‐, and δ‐tocopherols and ‐tocotrienols (‐Tocs and ‐Toc‐3s). The second‐order rate constants (k_s) and aroxyl radical absorption capacity (ARAC) values for the reaction of ArO? with vegetable oils 1–8 (rice bran 1, perilla 2, rapeseed 3, safflower 4, grape seed 5, sesame 6, extra virgin olive 7, and olive oils 8) were measured in ethanol/chloroform/D₂O (50:50:1, v/v/v) solution at 25 °C using stopped‐flow spectrophotometry. The k_s value (16.1 × 10^?3 L g^?1 s^?1) of rice bran oil 1 with the highest activity was 8.0 times larger than that (2.02 × 10^?3) of olive oil 8 with the lowest activity. The concentrations (in mg 100 g^?1) of α‐, β‐, γ‐, and δ‐Tocs and ‐Toc‐3s contained in the vegetable oils 1–8 were determined using high performance liquid chromatography‐mass spectrometry/mass spectrometry (HPLC‐MS/MS). From these results, it was clarified that the ArO?‐scavenging rates (k_s) (i.e., the relative ARAC value) obtained for the vegetable oils 1–8 may be well explained as the sum of the product of the rate constant () and the concentration ([AOH‐i]/10⁵) of AOH‐i (Tocs and Toc‐3s) included in vegetable oils. The results suggest that the ARAC assay method might be used in the evaluation of antioxidant activity of general food extracts.     

Plasma Phosphatidylethanolamine and Triacylglycerol Fatty Acid Concentrations are Altered in Major Depressive Disorder Patients with Seasonal Pattern

Disturbances in peripheral and brain lipid metabolism, including the omega-3 fatty acid docosahexaenoic acid (DHA), have been reported in major depressive disorder (MDD). However, these changes have yet to be confirmed in MDD with seasonal pattern (MDD-s), a subtype of recurrent MDD. The present exploratory study quantified plasma plasmalogen and diacyl-phospholipid species, and fatty acids within total phospholipids, cholesteryl esters, triacylglycerols and free fatty acids in non-medicated MDD-s participants (n = 9) during euthymia in summer or fall, and during depression in winter in order to screen for potential high sensitivity lipid biomarkers. Triacylglycerol alpha-linolenic acid concentration was significantly decreased, and myristoleic acid concentration was significantly increased, during winter depression compared to summer-fall euthymia. 1-stearyl-2-docosahexaenoyl-sn-glycero-3-phosphoethanolamine, a diacyl-phospholipid containing stearic acid and DHA, was significantly decreased in winter depression. Concentrations of cholesteryl ester oleic acid and several polyunsaturated fatty acids between summer/fall and winter increased in proportion to the increase in depressive symptoms. The observed changes in lipid metabolic pathways in winter-type MDD-s offer new promise for lipid biomarker development.     

Characterization of bimetallic surface structures of highly active Rh-Sn/SiO2 catalysts for NO-H2 reaction by EXAFS

Rh-Sn/SiO₂ catalysts prepared by the reaction of (CH₃)₄Sn with Rh metal particles supported on SiO₂ have remarkably high activities for NO-H₂ reaction and NO dissociation. The bimetallic surface structure of Rh-Sn/SiO₂ composed of an isolated Rh atom surrounded by six Sn atoms, is presented by Rh K-edge and Sn K-edge EXAFS, FT-IR, TEM and CO adsorption.     

In situ XAFS analysis of Pd–Pt catalysts during hydrotreatment of model oil

Supported Pd–Pt catalysts are efficient for hydrodesulfurization (HDS) and hydrodearomatization (HDA) reactions of diesel fuel and their activity varied with the kinds of supports. Concerning HDA, alumina supported catalysts showed four times higher TOF (turn over frequency) than silica supported one. In order to elucidate the difference in activity, the structural analysis of the active phase was performed. After reduction pretreatment, relatively uniform and large metallic alloy Pd–Pt particles were formed on SiO₂, whereas, Pd and Pt atoms formed rather segregated particles on Al₂O₃. Subsequent X-ray absorption of fine structure (XAFS) analysis under HDS conditions showed no contribution of sulfur for SiO₂ supported catalyst, whereas, formation of sulfided metal species was observed in XAFS spectra for the Al₂O₃ supported catalyst. It is suggested that on Pd–Pt/SiO₂, thin sulfide layer on the metal cluster surface blocked the active sites and lowered the HDA activity. Presence of partially sulfided phase originated from rather segregated structure like Pd–Pt/Al₂O₃ is thought to be requisite for high HDA activity.     

A discontinuous exponential stabilization law for an underactuated X4-AUV

In this paper, stabilization of a class of second-order nonholonomic systems for an underactuated X4-AUV is investigated. We present a model of the underactuated X4-AUV with six degrees of freedom (DOF) and four control inputs. Then, the system is written in a control-affine form by applying a partial linearization technique, and a dynamic controller based on Astolfi’s discontinuous control is derived to stabilize all states of the system to the desired equilibrium point exponentially. The present approach does not necessitate the conversion of the system model into a “chained form”, and thus does not rely on any special transformation techniques to obtain a canonical form. A simulation is conducted to demonstrate the effectiveness of the proposed controller.     

Identifying shocks in regionally integrated East Asian economies with structural VAR and block exogeneity

In this paper we use a structural VAR model with block exogeneity to investigate if external shocks originating from the USA played a dominant role in influencing the macroeconomic fluctuations in East Asia during the period 1978-2007. The empirical results show a dynamic effect of external shocks, implying that, even though regional integration appears to be deepening and accelerating, especially after the recent global financial crisis, the influence of US shocks on real output fluctuations in the East Asian region is still very strong. The effects of Chinese shocks show an increasing trend over time, but the impacts are still small and not comparable with those of US shocks. The world oil price shock has become increasingly important in influencing the stability of real output growth in the region. The results from variance decomposition and impulse response analysis confirm the findings. Even though Japanese firms have established production networks in East Asia through trade and investment, and China has also grown rapidly and become a key regional country, the results suggest that US influence in the region is still asymmetric and strong. Therefore, it is difficult to conclude that shocks to the East Asian economies have become more regionally oriented.