Nandrolone decanoate increases the volume but not the length of the proximal and distal convoluted tubules of the mouse kidney

Anabolic androgenic steroids are widely used by athletes for increasing their muscle mass. These drugs are also used by some patients with chronic renal disease. But the effect of these drugs on the renal structure has received less attention. To investigate which parts of the kidney are affected by these drugs, mice kidneys were studied stereologically after injection of nandrolone decanoate (ND), an anabolic androgenic steroid. The treated group received nandrolone decanoate intraperitoneally (solved in olive oil) in doses of 3mg/kg of body weight and administered in one, two and three doses, respectively, in the first, second and third week of treatment. The mice in the control group received an olive oil solution. One week after the last injection, the mice were anaesthetized and their kidney removed. The analysis of data revealed that the weight of kidney was increased approximately 30% (p < or = 0.006) and its volume increased approximately 25% (p < or = 0.02) in ND treated mice in comparison with the control group. The volume of the cortex increased in ND treated animals approximately 44% (p < or = 0.006). Proximal convoluted tubules (PCT) and distal convoluted tubules (DCT) volume increased approximately 25% (p < or = 0.02) and approximately 68% (p < or = 0.02) in ND treated mice. The volume of glomeruli, other ducts, connective tissues, vessels and the length of PCT, DCT, collecting and Henle's ducts and vessels did not show significant differences. CONCLUSION: ND can increase the volume of the renal cortex and its two main parts, i.e. PCT and DCT in mice.     

Tandem diazonium salt electroreduction and click chemistry as a novel, efficient route for grafting macromolecules to gold surface

Bis-alkynylated oligoethyleneglycol (OEG) and a monopropargyl-functionalized perfluorinated ethylene glycol (FEG) were clicked to azide-functionalized gold surface (Au–N₃) at room temperature via the well known 1,3 cycloaddition click chemical reaction. The Au–N₃ substrate was obtained by nucleophilic attack of NaN₃ on gold substrates modified by the electrochemical reduction of the , ⁺N₂–C₆H₄–CH₂Br diazonium salt. This electrochemical process yields aryl layer-modified gold of the type Au–C₆H₄–CH₂Br (hereafter Au–Br). The untreated and modified gold plates were examined by XPS, PMIRRAS and contact angle measurements. XPS brought evidence for electrografting aryl layers by the detection of Br3d; azide functionalization by the increase of the N/Br atomic ratio; and click reaction of OEG with Au–N₃ by the increase of O/N ratio. In addition, the perfluorinated plate (Au-FEG) exhibited F1s and characteristic C1s peaks from -(CF₂)₇- chain and terminal CF₃. Infra red spectroscopy (PMIRRAS) evidenced (i) grafting N₃ to Au–Br; (ii) characteristic stretching bands, from ethylene glycol units, C–O–C (1100–1300 cm⁻¹); CF₂ (1000–1100 cm⁻¹) and CF₃ (1100–1350 cm⁻¹) from FEG grafts; and (iii) suppression of alkynyl bands from OEG and FEG after surface click chemistry. More importantly, PMIRRAS results support an important bridging of the bispropargyl oligoethylene glycol at the gold surface. Water drop contact angles were found to be 48.7° and 83.0° for Au-OEG and Au-FEG, respectively, therefore highlighting the control over the hydrophilic/hydrophobic character of the clicked substrate.This work shows that clicking macromolecules to grafted, diazonium salt-derived aryl layers is a novel, simple and valuable approach for designing robust, functional surface organic coatings.     

The first suberate lanthanum(III) complex without uncoordinated water

catena‐Poly­[[aqua­lanthanum(III)]‐μ‐(8‐carboxy­octanoato)‐μ‐octanedioato], [La(C₈H₁₂O₄)(C₈H₁₃O₄)(H₂O)]_n, is, to our knowledge, the first reported rare‐earth complex containing a flexible long‐chain ligand that crystallizes without water of crystallization. The layered polymeric structure is built from infinite chains of one‐edge‐sharing LaO₈(H₂O) polyhedra, connected through the carbon backbone chains of the ligands. The two chemically different ligands act in the same coordination modes, exhibiting chelating bonds and μ‐1,1‐bridging monodentate linkage, and adopting the same extended conformation. In the relatively limited hydrogen‐bonding network, a very strong hydrogen bond between the deprotonated and protonated ligand ends stabilizes the framework.     

Brönsted Acidic Ionic Liquid as an Efficient Catalyst for Acetylation of Alcohols and Phenols

A novel Brönsted acidic room temperature ionic liquid (1‐H‐3‐methyl‐imidazolium bisulfate) is found to catalyze efficiently the acetylation of a wide rang of alcohols as well as phenols with acetic anhydride in good to excellent yields at 50°C under solvent‐free conditions. Products are easily isolated by extraction with ether and the protocol is mild and green, compared to the existing method based on toxic solvents.     

Proteomic strategies for the identification of proteinaceous binders in paintings

The identification of proteinaceous components in paintings remains a challenging task for several reasons. In addition to the minute amount of sample available, complex and variable chemical composition of the paints themselves, possible simultaneous presence of several binders and contaminants, and degradation of the original materials due to aging and pollution are complicating factors. We proposed proteomic strategies for the identification of proteins in binders of paintings that can be adapted to overcome the requirements and difficulties presented by specific samples. In particular, we worked on (1) the development of a minimally invasive method based on the direct tryptic cleavage of the sample without protein extraction; (2) the use of microwave to enhance the enzymatic digestion yield, followed by the analysis of the peptide mixtures by nanoLC-MS/MS with electrospray ionization (ESI). Moreover, as an additional tool to tackle the problem of contaminating proteins, we exploited the possibility of generating an exclusion list of the mass signals that in a first run had been fragmented and that the mass spectrometer had to ignore for fragmentation in a subsequent run. The methods, tested on model samples, allowed the identification of milk proteins in a sample from paintings attributed to Cimabue and Giotto, thirteenth-century Italian masters, decorating the vaults of the upper church in the Basilica of St. Francis in Assisi, Italy.     

An improved electrochemical method for the synthesis of some benzofuran derivatives

Electrochemical oxidation of catechol and some 3-substituted catechols (1a--c) has been studied in the presence of 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3) in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the quinones derived from catechols (1a--c) participate in a Michael addition reaction with 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3) with consumption of only two electrons per molecule of (1a--c) to from the corresponding benzoforans (10a--c). The electrochemical synthesis of benzofurans has been successfully performed at a carbon rod electrode and in an undivided cell with high yields and purity.     

QCD Ghost Dark Energy in RS II Braneworld with Bulk-Brane Interaction

We investigate the QCD ghost model of dark energy in the framework of RS II braneworld. We assume there is an energy flow between the brane and bulk, and hence the continuity equation for the ghost dark energy is violated, while it is still preserved for the dark matter on the brane. We find that with the brane-bulk interaction, the equation of state parameter of ghost dark energy on the brane, can cross the phantom line w _D =?1 at the present time, which confirms by some cosmological evidences. This result is in contrast to the standard cosmology where w _D of ghost dark energy never cross the phantom line and the universe enters a de Sitter phase at the late time.     

The Quantum and Klein-Gordon Oscillators in a Non-commutative Complex Space and the Thermodynamic Functions

In this work we study the quantum and Klein-Gordon oscillators in a non-commutative complex space. We show that a particle described by such oscillators behaves similarly as an electron with spin in a commutative space in an external uniform magnetic field. Therefore the wave-function $\psi (z,\bar{z} )$ takes values in C ⁴, spin up, spin down, particle, antiparticle, a result which is obtained by the Dirac theory. We obtain the energy levels by exact solutions. We also derive the thermodynamic functions associated to the partition function, and show that the non-commutativity effects are manifested in energy at the high temperature limit.     

Low-frequency variable charge solitary waves in a collisionless dusty plasma with a Cairns-Gurevich ion velocity distribution

In this paper, the problem of large amplitude dust acoustic (DA) solitons has been addressed in a charge varying dusty plasma with ions following a Cairns-Gurevich distribution. Based on the orbit motion limited approach, the correct Cairns-Gurevich ion charging current is presented for the first time. The expression relating the variable dust charge to the plasma potential is given in terms of the Lambert function and we take advantage of this transcendental function to, carefully, analyse DA solitons in a charge varying dusty plasma with trapped nonthermal ions. Our results show that the spatial patterns of the variable charge solitary wave are significantly changed due to the presence of ion population modelled by the Cairns-Gurevich distribution. An addition of a small concentration of trapped nonthermal ions makes the solitary structure less spiky, grows the net negative charge residing on the dust grain surface, and contributes to the electron depletion. Finally, our investigation is extended to highlight the effect of the grain dust charge variation. We have shown that under certain conditions, the impact of dust charge fluctuation may furnish an alternate physical mechanism rasing anomalous dissipation, which becomes more strong and may predominate over the dispersion as the nonthermal character of ions following the Cairns-Gurevich distribution increases.     

Combination of solid-phase extraction-hollow fiber for ultra-preconcentration of some triazole pesticides followed by gas chromatography-flame ionization detection

In this study, an extraction and preconcentration technique using solid-phase extraction (SPE) along with hollow fiber (HF) has been developed as an ultra-preconcentration technique for some triazole pesticides in aqueous samples. Triazole pesticides were employed as model compounds to assess the method and were monitored by gas chromatography-flame ionization detection (GC-FID). Initially, an aqueous solution of target analytes was passed through an RP-8 SPE cartridge and then the adsorbed analytes were eluted with μL amounts of toluene. The collected elute was slowly introduced into an HF that had one end blocked. This allowed precipitation inside the lumen and pores of the HF. Finally, the obtained HF was mounted on a home-made solid-phase microextraction syringe and entered into the GC injection port for thermal desorption-GC analysis. The effect of various experimental parameters including injection port temperature, desorption time, state of HF, washing solvent, elution solvent and its volume, sample volume, etc. were investigated for finding the optimum conditions. The calibration graphs were linear in the ranges of 2-1000 ng/mL (penconazole and hexaconazole), 5-1000 ng/mL (tebuconazole), 15-1000 ng/mL (triticonazole) and the detection limits (LODs) ranged from 0.6 to 4.5 ng/mL. The enhancement factors were in the range of 870-950. The relative standard deviations (RSD%) for five repeated experiments (C=250 ng/mL of each pesticide) varied from 4.5 to 8.7%. The relative recoveries obtained for analytes in grape juice samples, spiked with different levels of each pesticide, were in the range of 87-119%.