Scorpion in Combination with Gypsum: Novel Antidiabetic Activities in Streptozotocin-Induced Diabetic Mice by Up-Regulating Pancreatic PPARγ and PDX-1 Expressions

The management of diabetes without any side effects remains a challenge in medicine. In this study, antidiabetic activity and the mechanism of action of scorpion combined with gypsum (SG) were investigated. Streptozotocin-induced diabetic mice were orally administrated with scorpion (200 mg kg−1 per day) in combination with gypsum (200 mg kg−1 per day) for 5 weeks. SG treatment resulted in decreased body weight, blood glucose and lipid levels, and increased serum and pancreatic insulin levels in diabetic mice. Furthermore, SG significantly increased the number and volume of beta cells in the Islets of Langerhans and promoted peroxisome proliferator-activated receptor gamma and pancreatic duodenal homeobox 1 expressions in pancreatic tissues. However, scorpion or gypsum alone had no significant effect in this animal model. Metformin showed a slight or moderate effect in this diabetic model, but this effect was weak compared with that of SG. Taken together, SG showed a new antidiabetic effect in streptozotocin-induced diabetic mice. This effect may possibly be involved in enhancing beta-cell regeneration and promoting insulin secretion by targeting PPARγ and PDX-1. Moreover, this new effect of SG offers a promising step toward the treatment of diabetic patients with beta-cell failure as a complementary and alternative medicine

A Mode-Sum Prescription for Vacuum Polarization in Even Dimensions

We present a mode-sum regularization prescription for computing the vacuum polarization of a scalar field in static spherically-symmetric black hole spacetimes in even dimensions. This is the first general and systematic approach to regularized vacuum polarization in higher even dimensions, building upon a previous scheme we developed for odd dimensions. Things are more complicated here since the even-dimensional propagator possesses logarithmic singularities which must be regularized. However, in spite of this complication, the regularization parameters can be computed in closed form in arbitrary even dimensions and for arbitrary metric function $f(r)$. As an explicit example of our method, we show plots for vacuum polarization of a massless scalar field in the Schwarzschild-Tangherlini spacetime for even $d=4,...,10$. However, the method presented applies straightforwardly to massive fields or to nonvacuum spacetimes.Comment: arXiv admin note: text overlap with arXiv:1609.0816

Metabonomics Combined with UPLC-MS Chemical Profile for Discovery of Antidepressant Ingredients of a Traditional Chinese Medicines Formula, Chaihu-Shu-Gan-San

This study proposed a new strategy for uncovering the active chemical constituents of a traditional Chinese medicines (TCMs) formula, Chaihu-Shu-Gan-San (CSGS). Metabonomics and chemical profile were integrated in combination with the multivariate statistical analysis (MVA) to discover the chemical constituents which contribute to the antidepressant effect of CSGS. Based upon the difference between CSGS and QZ (CSGS without Zhi-Qiao) extracts in the chemical profiles and the regulations of metabolic disturbances induced by CUMS, synephrine, naringin, hesperidin, and neohesperidin were recognized as the active constituents of CSGS from Zhi-qiao responsible for those missing regulations of CSGS when Zhi-Qiao was subtracted from the whole formula. They participated in the regulations of the deviated metabolites 2–4, 10–14, and 22–25, involved in metabolic pathways of ketone bodies synthesis, phenylalanine, tyrosine and tryptophan biosynthesis, valine, aspartate, glutamate metabolism, and glycolysis/gluconeogenesis. Furthermore, the assay of MAO-A activity confirmed the potential antidepressant effect of naringin and its active sites on the MAO-A was inferred by molecular docking study. The integration of metabonomics and chemical profile was proved to be a useful strategy for uncovering what the active chemical constituents in TCM formula are and how they make contributions for the efficacy of the formula

MiRNA-Directed Regulation of VEGF and Other Angiogenic Factors under Hypoxia

MicroRNAs (miRNAs) are a class of 20–24 nt non-coding RNAs that regulate gene expression primarily through post-transcriptional repression or mRNA degradation in a sequence-specific manner. The roles of miRNAs are just beginning to be understood, but the study of miRNA function has been limited by poor understanding of the general principles of gene regulation by miRNAs. Here we used CNE cells from a human nasopharyngeal carcinoma cell line as a cellular system to investigate miRNA-directed regulation of VEGF and other angiogenic factors under hypoxia, and to explore the principles of gene regulation by miRNAs. Through computational analysis, 96 miRNAs were predicted as putative regulators of VEGF. But when we analyzed the miRNA expression profile of CNE and four other VEGF-expressing cell lines, we found that only some of these miRNAs could be involved in VEGF regulation, and that VEGF may be regulated by different miRNAs that were differentially chosen from 96 putative regulatory miRNAs of VEGF in different cells. Some of these miRNAs also co-regulate other angiogenic factors (differential regulation and co-regulation principle). We also found that VEGF was regulated by multiple miRNAs using different combinations, including both coordinate and competitive interactions. The coordinate principle states that miRNAs with independent binding sites in a gene can produce coordinate action to increase the repressive effect of miRNAs on this gene. By contrast, the competitive principle states when multiple miRNAs compete with each other for a common binding site, or when a functional miRNA competes with a false positive miRNA for the same binding site, the repressive effects of miRNAs may be decreased. Through the competitive principle, false positive miRNAs, which cannot directly repress gene expression, can sometimes play a role in miRNA-mediated gene regulation. The competitive principle, differential regulation, multi-miRNA binding sites, and false positive miRNAs might be useful strategies in the avoidance of unwanted cross-action among genes targeted by miRNAs with multiple targets

Intestinal Absorption and First-Pass Metabolism of Polyphenol Compounds in Rat and Their Transport Dynamics in Caco-2 Cells

<div><h3>Background</h3><p>Polyphenols, a group of complex naturally occurring compounds, are widely distributed throughout the plant kingdom and are therefore readily consumed by humans. The relationship between their chemical structure and intestinal absorption, transport, and first-pass metabolism remains unresolved, however.</p> <h3>Methods</h3><p>Here, we investigated the intestinal absorption and first-pass metabolism of four polyphenol compounds, apigenin, resveratrol, emodin and chrysophanol, using the <em>in vitro</em> Caco-2 cell monolayer model system and <em>in situ</em> intestinal perfusion and <em>in vivo</em> pharmacokinetic studies in rats, so as to better understand the relationship between the chemical structure and biological fate of the dietary polyphenols.</p> <h3>Conclusion</h3><p>After oral administration, emodin and chrysophanol exhibited different absorptive and metabolic behaviours compared to apigenin and resveratrol. The differences in their chemical structures presumably resulted in differing affinities for drug-metabolizing enzymes, such as glucuronidase and sulphatase, and transporters, such as MRP2, SGLT1, and P-glycoprotein, which are found in intestinal epithelial cells.</p> </div

Study of the Protection of Aluminum Alloy Surfaces by a Graphene-Modified Fluorocarbon Anticorrosive Coating

Graphene-modified anticorrosion coatings have become a hot spot in the field of metal protection due to the large-scale promotion of aluminum alloys, which are prone to corrosion in marine and atmospheric environments. The protection of aluminum alloy surfaces by a graphene-modified anticorrosive coating was explored in this study by applying a graphene-modified anticorrosive coating to an aluminum alloy surface to test its resistance to corrosion. Dispersion-treated reduced graphene oxide (rGO) was used to modify the epoxy resin and fluorocarbon resin. It was found, by using a scanning electron microscopy (SEM) and the microstructure of the coating made by the Raman Spectroscopy Institute, that the addition of rGO could effectively improve the porosity of the epoxy primer, and the electrochemical workstation was able to resist the graphene-modified anticorrosive coating. The corrosion performance was quickly characterized, the polarization curve and the AC impedance curve were fitted, and it was found that the self-corrosion current density (Jcorr) of the graphene-modified anticorrosive coating was the smallest (1.190×10−7 A/cm2) when 0.6% of rGO was added; the impedance modulus (∣Z∣) was the largest (104), the capacitive reactance arc radius was the largest, and the coating resistance was the largest after fitting (15517 Ω). When 0.8% of rGO was added, the dispersion coefficient was large, and it had a good physical insulation performance. The main reason for the reduction of the corrosion resistance was that the agglomeration of rGO made the aluminum alloy matrix and the external corrosive environment form a highly conductive circuit, thereby accelerating the corrosion of the aluminum alloy matrix

Preparation of Graphene-Modified Anticorrosion Coating and Study on Its Corrosion Resistance Mechanism

When aluminum alloy is present in a Cl−-rich environment, the surface oxide film is easily damaged, resulting in faster dissolution of the substrate. The application of graphene-modified anticorrosion coating can effectively prevent the occurrence of corrosion. In this study, to explore the corrosion resistance of graphene-modified anticorrosion coating on the surface of aluminum alloy, we prepared graphene-modified anticorrosion coating on the surface of aluminum alloy and investigated the corrosion resistance mechanism. Epoxy resin primer and polyurethane top coat were modified by predispersed reduced graphene oxide (rGO). Scanning electron microscope (SEM) and Raman spectrum were used to investigate the microstructure of graphene-modified anticorrosion coating, and it was found that the addition of rGO could effectively improve the porosity defect of epoxy resin primer. Electrochemical workstation was used to quickly characterize the corrosion resistance of graphene-modified anticorrosion coating, and the change of the electrochemical curve during soaking in 3.5% NaCl was investigated every 5 hours. It was found that the application of rGO to modify the anticorrosion coating could improve the corrosion resistance of the anticorrosion coating, and as the soaking time increased, the corrosion resistance of graphene-modified anticorrosion coating changed regularly. The study results indicated that when the content of rGO was 0.4%, the porosity of epoxy coating decreased from 1.54% to 0.33%, the porosity dropped by an order of magnitude, and the self-corrosion voltage was relatively positive (-0.72434 V). The self-corrosion current density was the lowest (1.948×10−6 A/cm2), and at the low frequency, the impedance modulus was the highest (103). After the equivalent circuit fitting, the dispersion index was relatively high, the dispersion effect was relatively weak, and the corrosion resistance of the coating was improved. For graphene-modified anticorrosion coating, in the early stage of corrosion protection, the existence of pores and other defects in the coating might increase the dispersion effect, resulting in greatly decreased corrosion resistance of the coating. In the middle stage of corrosion protection, the pores in the coating would be completely filled by corrosive ions, resulting in a weakened dispersion effect. Therefore, the decrease in the corrosion resistance of the coating was slowed down and became stable