Procyanidins are potent inhibitors of LOX-1: a new player in the French Paradox

Lectin-like oxidized LDL receptor-1 (LOX-1) is an endothelial receptor for oxidized LDL (oxLDL) and plays multiple roles in the development of cardiovascular diseases. We screened more than 400 foodstuff extracts for identifying materials that inhibit oxLDL binding to LOX-1. Results showed that 52 extracts inhibited LOX-1 by more than 70% in cell-free assays. Subsequent cell-based assays revealed that a variety of foodstuffs known to be rich in procyanidins such as grape seed extracts and apple polyphenols, potently inhibited oxLDL uptake in Chinese hamster ovary (CHO) cells expressing LOX-1. Indeed, purified procyanidins significantly inhibited oxLDL binding to LOX-1 while other ingredients of apple polyphenols did not. Moreover, chronic administration of oligomeric procyanidins suppressed lipid accumulation in vascular wall in hypertensive rats fed with high fat diet. These results suggest that procyanidins are LOX-1 inhibitors and LOX-1 inhibition might be a possible underlying mechanism of the well-known vascular protective effects of red wine, the French Paradox.     

Optimization of cation structure of imidazolium-based ionic liquids as ionic solvents for rechargeable magnesium batteries

A series of imidazolium cation-based ionic liquids (ILs) have been synthesized and examined as ionic solvents for rechargeable magnesium batteries. The electrolyte solutions consist of these ILs dissolving methylmagnesium bromide with tetrahydrofuran (MeMgBr/THF). The chemical structure of imidazolium cation much influenced the ionic conductivity and the electrochemical window of the system. A reversible process of cathodic deposition and anodic dissolution of magnesium has been successfully achieved at room temperature. The highest value of anodic peak current for magnesium dissolution was obtained in an optimized-structure IL with allyl and methoxyethyl groups as the substituents.     

Preparation of polymethylsilsesquioxanes by the base‐catalyzed hydrolytic polycondensation of triisopropoxy(methyl)silane

Base‐catalyzed hydrolytic polycondensation of trialkoxymethylsilane was investigated to synthesize polymethylsilsesquioxanes (PMSs). The reaction of trimethoxy(methyl)silane and triethoxy(methyl)silane with tetramethylammonium hydroxide, tetrabutylammonium hydroxide, and also coline gave insoluble gels. Polymethylsilsesquioxane (PMS‐IP) was obtained by the reaction of triisopropoxy(methyl)silane (MTIPS) with tetrabutylammonium hydroxide as a catalyst. PMS‐IP was composed primarily of T² and T³ units. The percentage of T³ units and the molecular weight of PMS‐IP increased with increases in the molar ratios of catalyst and water to MTIPS and with the reaction time. PMS‐IP was soluble in organic solvents, except for methanol, and was separated by extraction with hexane and methanol into low‐ and high‐molecular‐weight fractions of M_w 2800–4000 and 7300–88,300, respectively. PMS‐IP coating films were prepared by dip coating on the organic, inorganic, and metal substrates, using the acetone–isopropyl alcohol solution of PMS‐IP. Since PMS‐IP solutions prepared with tetrabutylammonium hydroxide were hardly used because of the low content of hydroxy groups in the polymer, they showed low adhesion when compared with those solutions prepared with hydrochloric acid. The dielectric constant of the coating film prepared from the high‐molecular‐weight PMS‐IP was 2.6. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3623–3630, 2005     

Highly photoluminescent nanocrystals based on a gold(I) complex and their electrophoretic patterning

The fabrication of nanocrystals (NCs) composed of the cationic Au(I) complex was demonstrated by the reprecipitation method in which the colloidal solution of the NCs showed brilliant green phosphorescence with a quantum yield of 83% in n-hexane. Characterization of the prepared NCs was performed by transmission electron microscopy observation and elemental analysis with energy-dispersive X-ray spectroscopy. The obtained Au(I) NCs were particles of random shapes with a diameter of 200-400 nm. The selected-area electron diffraction and X-ray diffraction measurements showed the characteristic diffraction patterns attributable to the crystal structure of the bulk crystal of the Au(I) complex. A similar method was performed with a different counteranion, leading to a colloidal solution of the microcrystals (MCs) with brilliant yellow phosphorescence and a quantum yield of 26% in n-hexane. Luminescence patterning of the NCs and MCs was also achieved successfully by electrophoretic deposition onto an indium tin oxide (ITO)-coated glass substrate, resulting in characteristic luminescence patterns on the ITO substrates with relatively high photoluminescence quantum yields.     

Ultrasensitive CE for heavy metal ions using the variations in the chemical structures formed from new octadentate fluorescent probes and cationic polymers

Novel fluorescent probes have been developed for the ultratrace detection of heavy metal ions by capillary electrophoresis using laser-induced fluorescence detection. Based on a molecular design, the probes are composed of an octadentate chelating moiety, a macrocyclic DOTA (tetraazacyclododecanetetraacetic acid) and an acyclic DTPA (diethylenetriaminepentaacetic acid) frame, a spacer and a fluorophore (fluorescein). These were chosen on the basis of their ability to form kinetically inert and highly emissive complexes, and to prevent a quenching effect even with heavy and paramagnetic metal ions. Addition of a cationic polymer, polybrene, in the separation buffer provided high resolution and simultaneous detection of Ca(2+), Mg(2+), Cu(2+), Zn(2+), Ni(2+), Co(2+), Mn(2+), Cd(2+) and Pb(2+). The direct fluorescence detection of these metal ions with high sensitivity at lower ppt levels, typically 2-7 × 10(-11) M (potentially sub-ppt), was successfully achieved. While separation of anionic compounds using a counter cation ("Ion Association (IA)" mode) is typically controlled by the ion association equilibrium constants, K(ass), it was found that differences in the mobilities, μ(ep(IAC)), of the ion association complexes formed between the probe complexes and counter cations are the driving forces for separation in this new method. This suggests that each of the polybrene-probe complexes has different chemical structures among metal ions, which were able to be determined by CD spectra in this investigation. This novel separation mode was termed the "Ion Association Complex (IAC)" mode, distinct from the IA mode.     

Synthesis and crystal structure of disiloxane-1,3-diols and disiloxane-1,1,3,3-tetraol

1,3-Dimethyl- or 1,3-divinyl-1,3-di-t-butoxydisiloxane-1,3-diol and 1,3-diphenyldisiloxane-1,1,3,3-tetraol were synthesized by hydrolysis of the corresponding diisocyanatodisiloxanes and tetrachlorodisiloxane. The disiloxanediols were soluble in common organic solvents and thermally very stable, therefore, they could be sublimed without decomposition. X-ray crystallography showed that the disiloxane-1,3-diols in the crystal feature a 1.21 nm diameter columnar array with intermolecular hydrogen bonding. The disiloxane-1,1,3,3-tetraol, on the other hand, revealed molecules with a gauche- and anti-conformation depending on crystallization method which formed a columnar array and a sheet-like array, respectively. It was confirmed that these silanols can be potential building blocks for ladder oligosilsesquioxanes.     

On some slowly convergent series involving the Hurwitz zeta-function

We shall extract the essence of the Adamchik–Srivastava generating function method (Analysis (Munich) 18 (1998) 131) by proving the most far-reaching Ramanujan–Yoshimoto formula and by showing that some of the results stated in Srivastava and Choi (Series Associated with the Zeta and Related Functions, Kluwer Academic Publishers, Dordrecht, 2001) are simple consequences of the above-mentioned formula.     

Even subgraphs of bridgeless graphs and 2-factors of line graphs

By Petersen's theorem, a bridgeless cubic multigraph has a 2-factor. Fleischner generalised this result to bridgeless multigraphs of minimum degree at least three by showing that every such multigraph has a spanning even subgraph. Our main result is that every bridgeless simple graph with minimum degree at least three has a spanning even subgraph in which every component has at least four vertices. We deduce that if G is a simple bridgeless graph with n vertices and minimum degree at least three, then its line graph has a 2-factor with at most max{1,(3n-4)/10} components. This upper bound is best possible.