Theoretical study of polymerization of pyrrole

The polymerization process of pyrrole has been theoretically studied using the semiempirical molecular orbital (MO) method. As a model for the polymerization, particularly representing the initial-stage reaction near the anode of the electropolymerization system, the dimerization of pyrrole is examined by the process of coupling of two cationic monomer radicals in two specifically different ways, i.e., via the σ-radical or via the π-radical. Furthermore, some related calculations are undertaken in connection with the reactions between cationic monomer and dimer radicals, and between a neutral monomer and a cationic monomer radical.     

How to improve mechanical properties of polylactic acid with bamboo fibers

Bamboo fibers (BF) were mixed in polylactic acid (PLA) to improve its mechanical properties: impact strength and heat resistance. Three different types of BF were extracted from raw bamboo by either sodium hydroxide (NaOH) treatment or steam explosion in conjunction with mechanical processing. They were designated as “short fiber bundle,” “alkali-treated filament” and “steam-exploded filament,” respectively. Composite samples were fabricated by injection molding using PLA/BF pellets prepared by a twin-screw extruding machine. Among them, the highest bending strength was obtained when steam-exploded filaments were put into PLA matrix. Impact strength of PLA was not greatly improved by addition of short fiber bundles as well as both filaments. In order to improve the impact strength of PLA/BF composites, PLA composite samples were alternatively fabricated by hot pressing using medium length bamboo fiber bundles (MFB) to avoid the decrease in fiber length at fabrication. Impact strength of PLA/MFB composite significantly increased, in which long fiber bundles were pulled out from the matrix. The addition of BF improves thermal properties and heat resistance of PLA/BF composites due to the constraint of deformation of PLA in conjunction with crystallinity promoted by anneal (at 110 °C for 5 h).     

Stress evolution of sol-gel-derived silica coatings during heating: The effects of the chain length of alcohols as solvents

The effects of the solvent on in-plane stress evolution were studied on sol-gel-derived silica gel coatings during heating. Si(OC₂H₅)₄-H₂O-HNO₃-ROH (ROH = CH₃OH, C₂H₅OH, n-C₃H₇OH, and n-C₄H₉OH) solutions were prepared where the mole ratio Si(OC₂H₅)₄:H₂O:HNO₃ = 1:8:0.01 and the volume ratio Si(OC₂H₅)₄:ROH = 1:1.1. Silica gel films were deposited by spin coating on Si (100) wafers 4 in. in diameter, and heated at 5 °C/min up to 500 °C, where in situ stress measurement was conducted by measuring the substrate curvature. The stress was tensile and increased with increasing temperature. The stress was found to be identical below 200 °C between the films prepared with different alcohols while the stress above 200 °C was larger in the order, n-C₄H₉OH < n-C₃H₇OH ≈ C₂H₅OH < CH₃OH, namely in the order of the boiling points of the solvents.     

Cilostazol Attenuates AngII-Induced Cardiac Fibrosis in apoE Deficient Mice

Cardiac fibrosis is characterized by the net accumulation of extracellular matrix in the myocardium and is an integral component of most pathological cardiac conditions. Cilostazol, a selective inhibitor of phosphodiesterase type III with anti-platelet, anti-mitogenic, and vasodilating properties, is widely used to treat the ischemic symptoms of peripheral vascular disease. Here, we investigated whether cilostazol has a protective effect against Angiotensin II (AngII)-induced cardiac fibrosis. Male apolipoprotein E-deficient mice were fed either a normal diet or a diet containing cilostazol (0.1% wt/wt). After 1 week of diet consumption, the mice were infused with saline or AngII (1000 ng kg⁻¹ min⁻¹) for 28 days. AngII infusion increased heart/body weight ratio (p < 0.05), perivascular fibrosis (p < 0.05), and interstitial cardiac fibrosis (p < 0.0001), but were significantly attenuated by cilostazol treatment (p < 0.05, respectively). Cilostazol also reduced AngII-induced increases in fibrotic and inflammatory gene expression (p < 0.05, respectively). Furthermore, cilostazol attenuated both protein and mRNA abundance of osteopontin induced by AngII in vivo. In cultured human cardiac myocytes, cilostazol reduced mRNA expression of AngII-induced osteopontin in dose-dependent manner. This reduction was mimicked by forskolin treatment but was cancelled by co-treatment of H-89. Cilostazol attenuates AngII-induced cardiac fibrosis in mice through activation of the cAMP–PKA pathway.     

Possible Action of Olaparib for Preventing Invasion of Oral Squamous Cell Carcinoma In Vitro and In Vivo

Despite recent advances in treatment, the prognosis of oral cancer remains poor, and prevention of recurrence and metastasis is critical. Olaparib is a PARP1 inhibitor that blocks polyADP-ribosylation, which is involved in the epithelial–mesenchymal transition (EMT) characteristic of tumor recurrence. We explored the potential of olaparib in inhibiting cancer invasion in oral carcinoma using three oral cancer cell lines, HSC-2, Ca9-22, and SAS. Olaparib treatment markedly reduced their proliferation, migration, invasion, and adhesion. Furthermore, qRT-PCR revealed that olaparib inhibited the mRNA expression of markers associated with tumorigenesis and EMT, notably Ki67, Vimentin, β-catenin, MMP2, MMP9, p53, and integrin α2 and β1, while E-Cadherin was upregulated. In vivo analysis of tumor xenografts generated by injection of HSC-2 cells into the masseter muscles of mice demonstrated significant inhibition of tumorigenesis and bone invasion by olaparib compared with the control. This was associated with reduced expression of proteins involved in osteoclastogenesis, RANK and RANKL. Moreover, SNAIL and PARP1 were downregulated, while E-cadherin was increased, indicating the effect of olaparib on proteins associated with EMT in this model. Taken together, these findings confirm the effects of olaparib on EMT and bone invasion in oral carcinoma and suggest a new therapeutic strategy for this disease.     

日本的河流水管理

对日本的河流、河流水权和河流水源开发管理进行了介绍。日本的河流众多，但流程短、水流急，主要由地方政府通过完善的水权制度进行管理。水权通过申请获得，根据不同情况收取水权费。河流水源由水资源机构按计划开发，建设和运营资金通过多渠道筹集。     

Mesoscale variability of vertical profiles of environmental radionuclides (40K, 226Ra, 210Pb and 137Cs) in temperate forest soils in Germany

Vertical profiles of environmental radionuclides (40K, 226Ra, 210Pb and 137Cs) were investigated in several temperate forest soils in Germany to estimate heterogeneity of the soil horizon of interest. Absolute values of the activity concentrations of these nuclides varied to a large extent depending on the properties of individual forests as well as local geology. Several trends were generally observed independent of the location: (1) Activity concentrations of 40K increased with increasing soil density reflecting that most potassium is contained in mineral components of the soil. The variations in the 40K activity with depth may relate to biological activities in subsoil, such as root uptake of the nutrients. (2) Profiles of 226Ra with depth could be an indicator for evaluating soil heterogeneity within a horizon of interest. They are also useful to estimate anthropogenic 210Pb (210Pbexc) derived from the atmosphere via dry fallout or wet deposition. In several forests, there appeared surface enrichment of 210Pb down to a depth of approximately 10 cm, in which the 210Pb would have come from the atmosphere by combustion of fossil fuels. (3) Depth profiles of 137Cs were roughly divided into three types in which (a) the activity concentration decreased exponentially with soil depth, (b) small amounts of 137Cs existed only in the upper-most layer of the soil (0-5 cm) and (c) 137Cs disappeared at certain depths and appeared again at deeper portions of the soil. Consequences of bioturbation could be deduced from variability in vertical profiles of the environmental radionuclides. It is probable that a site showing an exponential decrease of the 137Cs activity with depth and also having a surface enrichment of 210Pb is not significantly influenced by bioturbation.     

Alpha-substituted phosphonate analogues of lysophosphatidic acid (LPA) selectively inhibit production and action of LPA

Isoform-selective agonists and antagonists of the lysophosphatidic acid (LPA) G-protein-coupled receptors (GPCRs) have important potential applications in cell biology and therapy. LPA GPCRs regulate cancer cell proliferation, invasion, angiogenesis, and biochemical resistance to chemotherapy- and radiotherapy-induced apoptosis. LPA and its analogues are also feedback inhibitors of the enzyme lysophospholipase D (lysoPLD, also known as autotaxin), a central regulator of invasion and metastasis. For cancer therapy, the ideal therapeutic profile would be a metabolically stabilized pan-LPA receptor antagonist that also inhibits lysoPLD. Herein we describe the synthesis of a series of novel alpha-substituted methylene phosphonate analogues of LPA. Each of these analogues contains a hydrolysis-resistant phosphonate mimic of the labile monophosphate of natural LPA. The pharmacological properties of these phosphono-LPA analogues were characterized in terms of LPA receptor subtype-specific agonist and antagonist activity using Ca(2+) mobilization assays in RH7777 and CHO cells expressing the individual LPA GPCRs. In particular, the methylene phosphonate LPA analogue is a selective LPA(2) agonist, whereas the corresponding alpha-hydroxymethylene phosphonate is a selective LPA(3) agonist. Most importantly, the alpha-bromomethylene and alpha-chloromethylene phosphonates show pan-LPA receptor subtype antagonist activity. The alpha-bromomethylene phosphonates are the first reported antagonists for the LPA(4) GPCR. Each of the alpha-substituted methylene phosphonates inhibits lysoPLD, with the unsubstituted methylene phosphonate showing the most potent inhibition. Finally, unlike many LPA analogues, none of these compounds activate the intracellular LPA receptor PPARgamma.