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[Moxibustion on back plate epidermis involving bloodstream stasis: the randomized manipulated trial].
Some amino acids (AAs) have been proven to suppress fat mass and improve insulin sensitivity. However, the impact of important essential AAs, threonine, lysine, and methionine, on obesity has not been clarified. In the present study, after an 8 week period of obesity induction, mice were grouped to receive either a high-fat diet (HFD) or HFD supplemented with lysine, threonine, or methionine (3% in drinking water) for another 10 weeks. The results showed that dietary supplementation with threonine significantly decreased body weight, epididymal and perirenal fat pad weights, serum concentrations of glucose, triacylglycerols, total cholesterol, and LDL-cholesterol compared to the HFD group. HOMA-IR and serum leptin and adiponectin were improved by threonine supplementation. In epididymal adipose tissue, threonine treatment significantly down-regulated the expression levels of lipogenesis and up-regulated expressions of lipolysis compared to the HFD group. Threonine addition stimulated the expression of UCP-1 and related genes in brown adipose tissue. However, lysine or methionine supplementation showed little effect on body weight, WAT weight, serum lipid profiles, and lipid-metabolism-related gene expressions of HFD-fed mice. These findings suggest that threonine inhibited fat mass and improved lipid metabolism of already obese mice, providing a potential agent in treating obesity.Single crystals of synthetic nickel sulfate monohydrate, α-NiSO4·H2O (space-group symmetry C2/c at ambient conditions), were subject to high-pressure behavior investigations in a diamond-anvil cell up to 10.8 GPa. By means of subtle spectral changes in Raman spectra recorded at 298 K on isothermal compression, two discontinuities were identified at 2.47(1) and 6.5(5) GPa. Both transitions turn out to be apparently second order in character, as deduced from the continuous evolution of unit-cell volumes determined from single-crystal X-ray diffraction. The first structural transition from α- to β-NiSO4·H2O is an obvious ferroelastic C2/c-P1̅ transition. It is purely displacive from a structural point of view, accompanied by symmetry changes in the hydrogen-bonding scheme. The second β- to γ-NiSO4·H2O transition, further splitting the O2 (hydrogen bridge acceptor) position and violating the P1̅ space-group symmetry, is also evident from the splitting of individual bands in the Raman spectra. It can be attributed to symmetry reduction through local violation of local centrosymmetry. Lattice elasticities were obtained by fitting second-order Birch-Murnaghan equations of state to the p-V data points yielding the following zero-pressure bulk moduli values K0 = 63.4 ± 1.0 GPa for α-NiSO4·H2O, K0 = 61.3 ± 1.9 GPa for β-NiSO4·H2O, and K0 = 68.8 ± 2.5 GPa for γ-NiSO4·H2O.Poly(ADP-ribose) polymerase-1 (PARP-1) is an abundant and ubiquitous nuclear enzyme that catalyzes the transfer of ADP-ribose from donor NAD+ molecules to specific amino acids on substrate proteins. The catalytic activity of PARP-1 has long been known to be allosterically stimulated by the free ends of DNA, such as those found at double-strand breaks in the genome. A number of studies have also shown that the catalytic activity of PARP-1 can also be stimulated by various types of RNA. A recent study by Nakamoto et al., however, has contradicted these results, concluding that the apparent stimulatory activity of the RNAs was due to contaminating DNA in the RNA preparations used in the biochemical assays. Here we show using a carefully controlled set of biochemical assays that DNA-free, in vitro-transcribed, PARP-1-interacting snoRNAs can stimulate PARP-1 catalytic activity. We confirmed the activation of PARP-1 by snoRNAs using a chemically synthesized snoRNA, as well as CRISPR/Cas9-mediated knockout of snoRNAs in cells. Finally, we provide a set of considerations and experimental conditions for the careful evaluation of RNA-stimulated PARP-1 catalytic activity that will help researchers avoid artifacts.We introduce a highly efficient photoligation system, affording a pro-fluorescent Diels-Alder product that, on demand, converts into an intensively fluorescent naphthalene via E1 elimination in the presence of catalytic amounts of acid. The Diels-Alder reaction of the photocaged diene (o-quinodimethane ether or thioether) with electron-deficient alkynes is induced by UV or visible light. In contrast to previously reported ligation techniques directly leading to fluorescent products, the fluorescence is turned on after the photoligation. Thus, the light absorption of the fluorophore does not undermine the photoligation via competitive absorption, and as a result, photobleaching or side reactions of the fluorophore are not observed. Critically, the gated generation of a fluorescent product allows for fluorometric determination of the conversion. We employ a simple synthesis strategy for heterobifunctional electron-deficient alkynes allowing for facile functionalization of payload molecules.Considering their superior electrochemical performances, extensive studies have been carried out on composite nanomaterials based on porous carbon nanofibers. However, the introduction of inorganic components into a porous structure is complex and has a low yield. In this study, we propose a simple synthesis of cobalt-oxide-incorporated multichannel carbon nanofibers (P-Co-MCNFs) as electrode materials for electrochemical applications. click here The cobalt oxide component is directly formed in the carbon structure by a simple oxygen plasma exposure of the phase-separated polymer nanofibers. P-Co-MCNF displays high specific capacitance (815 F g-1 at 2.0 A g-1), rate capability (821 F g-1 at 1 A g-1 and 786 F g-1 at 20 A g-1), and cycle stability (92.1% for 5000 cycles) as a supercapacitor electrode. Moreover, excellent sensitivity (down to 1 nM) and selectivity to the glucose molecule is demonstrated for nonenzyme sensor applications.Electrospray deposition (ESD) is a spray coating process that utilizes a high voltage to atomize a flowing solution into charged microdroplets. These self-repulsive droplets evaporate as they travel to a target substrate, depositing the solution solids. Our previous research investigated the conditions necessary to minimize charge dissipation and deposit a thickness-limited film that grows in area over time through self-limiting electrospray deposition. Such sprays possess the ability to conformally coat complex three-dimensional (3D) objects without changing the location of the spray needle or orientation of the object. This makes them ideally suited for the postprocessing of materials fabricated through additive manufacturing (AM), opening a paradigm of independent bulk and surface functionality. Having demonstrated 3D coating with film thickness in the range of 1-50 μm on a variety of conductive objects, in this study, we employed model substrates to quantitatively study the technique's limits with regard to geometry and scale.
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