Intergenerational Metabolomic Analysis of Mothers with a History of Gestational Diabetes Mellitus and Their Offspring

Shared metabolomic patterns at delivery have been suggested to underlie the mother-to-child transmission of adverse metabolic health. This study aimed to investigate whether mothers with gestational diabetes mellitus (GDM) and their offspring show similar metabolomic patterns several years postpartum. Targeted metabolomics (including 137 metabolites) was performed in plasma samples obtained during an oral glucose tolerance test from 48 mothers with GDM and their offspring at a cross-sectional study visit 8 years after delivery. Partial Pearson’s correlations between the area under the curve (AUC) of maternal and offspring metabolites were calculated, yielding so-called Gaussian graphical models. Spearman’s correlations were applied to investigate correlations of body mass index (BMI), Matsuda insulin sensitivity index (ISI-M), dietary intake, and physical activity between generations, and correlations of metabolite AUCs with lifestyle variables. This study revealed that BMI, ISI-M, and the AUC of six metabolites (carnitine, taurine, proline, SM(-OH) C14:1, creatinine, and PC ae C34:3) were significantly correlated between mothers and offspring several years postpartum. Intergenerational metabolite correlations were independent of shared BMI, ISI-M, age, sex, and all other metabolites. Furthermore, creatinine was correlated with physical activity in mothers. This study suggests that there is long-term metabolic programming in the offspring of mothers with GDM and informs us about targets that could be addressed by future intervention studies.     

Organic sulphur in the hard coal of the stratigraphic layers of the Upper Silesian coal basin

The paper presents the results of investigation of organic sulphur occurrence in the coal of Upper Silesian coal basin. Six hundred coal samples from 52 mines were tested. It has been found that the content of organic sulphur in the coal depends on the stratigraphic layer, coalification grade and geographic location in the Upper Silesia region. The highest mean content of organic sulphur has been found in the most recent (ca. 0.85%) and in the oldest (ca. 0.5%) strata. The lowest mean contents of organic sulphur have been found in the intermediate strata. In the case of the most recent coals, the content of organic sulphur decreases with increasing of coalification grade. When the carbon content (C^daf) exceeds 82%, the increase of coalification grade causes no further decrease of the mean content of organic sulphur. The share of organic sulphur in the total sulphur is lower in the case of more recent (<50%) and higher in the case of older coals (>50%).     

Crystallization of Polymer-Derived Silicon Carbonitride at 1873 K under Nitrogen Overpressure

The chemical stability of an amorphous silicon carbonitride ceramic, having the composition 0.57SiC·0.43Si₃N₄·0.49C is studied as a function of nitrogen overpressure at 1873 K. The ceramic suffers a weight loss at p _N2 < 3.5 bar (1 bar = 100 kPa), does not show a weight change from 3.5 to 11 bar, and gains weight above 11 bar. The structure of the ceramic changes with pressure: it is crystalline from 1 to 6 bar, amorphous at ∼10 bar, and is crystalline above ∼10 bar. The weight-loss transition, at 3.5 bar, is in excellent agreement with the prediction from thermodynamic analysis when the activities of carbon, SiC, and Si₃N₄ are set equal to those of the crystalline forms; this implies that the material crystallizes before decomposition. The amorphous to crystalline transition that occurs at ∼10 bar, and which is accompanied by weight gain, is likely to have taken place by a different mechanism. A nucleation and growth reaction with the atmospheric nitrogen is proposed as the likely mechanism. The supersaturation required to nucleate α-Si₃N₄ crystals is calculated to be 30 kJ/mol.     

Micellization Behavior of Long-Chain Substituted Alkylguanidinium Surfactants

Surface activity and micelle formation of alkylguanidinium chlorides containing 10, 12, 14 and 16 carbon atoms in the hydrophobic tail were studied by combining conductivity and surface tension measurements with isothermal titration calorimetry. The purity of the resulting surfactants, their temperatures of Cr→LC and LC→I transitions, as well as their propensity of forming birefringent phases, were assessed based on the results of ¹H and ¹³C NMR, differential scanning calorimetry (DSC), and polarizing microscopy studies. Whenever possible, the resulting values of Krafft temperature (T_K), critical micelle concentration (CMC), minimum surface tension above the CMC, chloride counter-ion binding to the micelle, and the standard enthalpy of micelle formation per mole of surfactant (Δ_micH°) were compared to those characterizing alkyltrimethylammonium chlorides or bromides with the same tail lengths. The value of T_K ranged between 292 and 314 K and increased strongly with the increase in the chain length of the hydrophobic tail. Micellization was described as both entropy and enthalpy-driven. Based on the direct calorimetry measurements, the general trends in the CMC with the temperature, hydrophobic tail length, and NaCl addition were found to be similar to those of other types of cationic surfactants. The particularly exothermic character of micellization was ascribed to the hydrogen-binding capacity of the guanidinium head-group.     

Differential Display of Investigative Behavior Permits Discrimination of Scent Signatures from Familiar and Unfamiliar Socially Dominant Female Marmoset Monkeys (Callithrix jacchus)

The hypothesis was tested that marmosets have differential displays of investigatory behavior towards circumgenital scent marks from socially dominant females based on degree of familiarity. In a series of two-choice behavioral discrimination bioassays, dominant males together with subordinate and dominant females were presented concurrently with scent secretions from familiar versus unfamiliar dominant females, and their investigative behaviors towards the scent were recorded. Test animals directed significantly different amounts of investigative behaviors towards familiar versus unfamiliar scents when the scent stimuli involved complete circumgenital scent marks, glandular secretion only, or urine only. When animals discriminated between the two scent samples, they did so by directing significantly increased amounts of behavior to scent from unfamiliar females. Chemical cues promoting differential displays of behavior to familiar versus unfamiliar scents appeared to be volatile in nature and were effective in the scent mark for at least one day following deposition. The reliable ability of marmosets to consistently discriminate between odors from familiar versus unfamiliar dominant females provides strong circumstantial evidence that individual female marmosets have distinct chemical signatures. The ability of marmosets to discriminate the odor from familiar versus unfamiliar dominant females may be important in the context of intergroup relations.     

Expression of RCAS1 Correlates with Urothelial Bladder Cancer Malignancy

RCAS1 is a protein that participates in regulation of the tumor microenvironment and its immune responses, all in order to evade the immune system. The aim of this study was to analyze RCAS1 expression in urothelial bladder cancer cells (and in fibroblasts and macrophages of the tumor stroma) and its relationship with the histological pattern of malignancy. Eighty-three postcystectomy patients were enrolled. We analyzed the histological maturity (grade), progress (pT stage), tissue invasion type (TIT), nonclassic differentiation number (NDN), and the ability to metastasize (pN). The expression of RCAS1 protein was analyzed by immunohistochemistry. Indicators of histological malignancy were observed solely in association with the RCAS1 expression in cells in the border parts (BPs) of the tumor. Histological malignancy of the tumor, indicated by the pT and pN, and metastasis-free survival time, correlated significantly with RCAS1 expression in tumor neoplastic cells, whereas malignancy determined by grade, TIT, and NDN correlated with RCAS1 expression in fibroblasts and macrophages in the tumor microenvironment. These findings suggest that the increased RCAS1 expression depends on its cellular source and that RCAS1 expression itself is a component of various signaling pathways. The immune escape occurs within the tumor BPs, where the increase in the RCAS1 expression occurs within tumor cells and stromal cells in its microenvironment. We conclude that the histological pattern of tumor malignancy, indicated by grade, TIT, NDN, pT, and pN is a morphological indicator of immune escape.     

Synthesis of Ternary Titanium Aluminum Carbides Using Self-Propagating High-Temperature Synthesis Technique

Different ternary carbide phases, namely Ti₃AlC₂, Ti₃AlC, and Ti₂AlC, were successfully synthesized in a self-sustaining regime. Direct reactions among elemental powders of titanium, aluminum, and carbon are strongly exothermic, and the resulting reaction products consist of binary carbides and they are partially molten. The use of TiAl, instead of elemental titanium and aluminum, significantly reduces the combustion temperature. As a result, ternary titanium aluminum carbide phases are formed. In addition, the combustion-synthesized products are not sintered and easy to deagglomerate. Reaction conditions and X-ray diffraction patterns of different ternary phases formed in a self-sustaining regime are presented.     

Nanoindentation of WC–Co hardmetals

WC–Co cemented carbide has been investigated using instrumented indentation with maximum applied loads from 0.1 to 10 mN. The hardness and indentation modulus of individual phases and the influence of crystallographic orientation of WC on the hardness and indentation modulus have been studied. The hardness of the Co binder was approximately 10 GPa and that of WC grains up to 50 GPa with relatively large scatter under the indentation load of 1 mN. Investigation of the role of crystallographic orientation of WC grains on hardness at 10 mN load revealed average values of H_ITbasal = 40.4 GPa (E_ITbasal = 674 GPa) and H_ITprismatic = 32.8 GPa (E_Itprismatic = 542 GPa), respectively. The scatter in the measured values at low indentation loads is caused by the effects of surface and sub-surface characteristics (residual stress, damaged region) and at higher loads by “mix-phase” volume below the indenter.     

The Role of Catalysis in Determining Men’s Quality of Life

Modern civilization, whose spectacular development took place in the second half of XX century as the result of scientific and information revolution has six characteristic features: (1) it is a mass civilization, (2) it is mobile, (3) it is global, (4) it is free of the spectre of famine, (5) it is built on informatics, (6) human lifespan is steadily prolonged. In order to achieve these goals it was necessary to invent thousands new materials and to find out methods of their fast and cheap production in large quantities. The unique possibility of the fast and selective production of the desired chemical molecules, required to obtain a material with defined properties, is offered by catalysis. Catalysis comprises technological processes of the largest scale, such as catalytic cracking of billions tons of crude oil per year and smallest scale enzymatic reactions with micrograms of product formed with 100% chemo-, regio- and stereoselectivity. With the rapidly growing earth’s population increasingly important becomes not only the production of materials needed in our modern society, but also the destruction of undesired by-products of its activities, making the application of catalysis to pollution control one of important tasks. The progress of catalysis, both science and technology, was in the last 50 years driven by the development in five fields: (1) new materials, particularly those based on the principle of molecular imprinting (use of templates), (2) application of new surface science techniques to identify active sites and surface reaction intermediates, (3) quantum chemical modeling of elementary steps of catalytic reactions, (4) design of new reactors, (5) development of computational catalysis, (6) development of new ways for carrying catalytic reactions, (7) biocatalysis using enzymes, modified by mutagenesis and recombination techniques to make them selective and active in conditions of the desired technological process. Application of molecular sieves, catalytic antibodies, metallocene catalysts, asymmetric catalysis, fuel cells, control of automotive exhaust are described and pending change of the paradigm of catalysis is discussed.     

Thermochemistry, lattice energetics and stability of hexahalogenohafnates

The enthalpies of thermal dissociation (Δ_dH) and formation (Δ_fH) found in the literature as well as the crystal lattice energies (E_c) of inorganic and organic hexahalogenohafnates (M^I₂(or M^{II)HfX2−₆}; M^I and M^II denote monovalent and divalent cations respectively and X denotes a halogen) are reviewed and discussed. The enthalpies of formation of the salts were evaluated using the above-mentioned Δ_dH values and known enthalpies of formation of products of decomposition. Combination of the enthalpies of formation of hexahalogenohafnates thus obtained or those of the literature with the literature values of the enthalpy of formation of cations and theoretically determined enthalpies of formation of HfX²⁻₆ (or electrostatic lattice energies of the salts) afforded lattice energies of the salts (or enthalpies of formation of gaseous HfX²⁻₆). Values of Δ_fH were also assessed taking theoretically obtained electrostatic lattice energies of the salts and enthalpies of formation of HfX²⁻₆ and literature or theoretically determined values of the enthalpy of formation of gaseous cations. The independent sets of crystal lattice energies and thermochemical radii for HfX²⁻₆ were obtained following the Kapustinskii—Yatsimirskii approach. Combination of the latter method with the thermochemical cycle afforded information on the influence of the dimensions of ions on the thermodynamic stability of hexahalogenohafnates with respect to dissociation and oxidation processes. The thermochemical quantities of experimental and theoretical origin correlate with each other reasonably well, thus increasing their reliability.