Effects of long-term in vitro exposure to phosphodiesterase type-3 inhibitors on follicle and oocyte development

Germinal vesicle (GV)-stage oocytes retrieved from antral follicles undergo nuclear maturation in vitro, which typically occurs prior to cytoplasmic maturation. Short-term culture with meiotic inhibitors has been applied to arrest oocytes at the GV stage aiming to synchronize nuclear and ooplasmic maturity. However, the results obtained are still far from the in vivo situation. In order to acquire competence, immature oocytes may require meiotic arrest in vitro for a more extended period. The phosphodiesterase type 3-inhibitor (PDE3-I) is a potent meiotic arrester. The effects of a prolonged culture with PDE3-I on oocyte quality prior to and after reversal from the inhibition are not known. This study tested the impact of long-term in vitro exposure of two PDE3-Is, org9935 and cilostamide, on oocytes using a mouse follicle culture model. The results showed that PDE3-I (maximum of 10 microM) during a 12-day culture of follicle-enclosed oocytes did not alter somatic cell proliferation, differentiation or follicle survival. In addition, the steroid production profile was not significantly modified by a 12-day exposure to PDE3-I. The recombinant human chorionic gonadotrophin/recombinant human epidermal growth factor stimulus induced a characteristic normal progesterone peak of luteinization and normal mucification of the cumulus cells, while the enclosed oocyte remained blocked at the GV stage. In vitro maturation of denuded or cumulus-enclosed oocytes derived from org9935- or cilostamide-exposed follicles progressed through meiosis and formed morphologically normal meiotic spindles with chromosomes properly aligned at the equator. In conclusion, long-term culture with PDE3-I was harmless to somatic cell function, differentiation, oocyte growth and maturation. Our results suggested that PDE3-I can be applied when extended oocyte culture is required to improve ooplasmic maturation.     

Metallization and Ar‐O plasma effects on dental enamel roughness evaluated with SEM and MeX™ for 3D reconstruction

The MeX? software is a useful tool for tridimensional data collection for surface evaluation and could be relevant to evaluate the same specimen in different phases of the study, assuming repeated measures of dental enamel roughness. The aim of this study was to evaluate the influence of sample metallization for dental enamel roughness analysis with 3D images reconstructed using MeX? software from Scanning Electron Microscopy (SEM) images. The influence of 74.98% (%mol/mol) argon?oxygen plasma for carbon layer removal on surface roughness of the metallized specimen was also evaluated. Dental enamel specimens were prepared for SEM analysis with and without carbon metallization using conventional or environmental modes. Argon?oxygen plasma for carbon layer removal was used and surface roughness was re‐evaluated. Roughness obtained by SEM and MeX? reconstructed images, with or without metallization, did not differ. No significant alteration on surface roughness after carbon layer removal using plasma was found. SEM baseline evaluation using conventional mode without sample preparation and in environmental mode were not comparable. Roughness of enamel 3D images reconstructed with MeX? software from SEM images, with or without metallization was similar. The 74.98% (%mol/mol) argon?oxygen plasma removed the carbon layer with no effect on enamel roughness.     

Hancornia speciosa latex for biomedical applications: physical and chemical properties,biocompatibility assessment and angiogenic activity

The latex obtained from Hancornia speciosa is used in folk medicine for treatment of several diseases, such as acne, warts, diabetes, gastritis and inflammation. In this work, we describe the biocompatibility assessment and angiogenic properties of H. speciosa latex and its potential application in medicine. The physical–chemical characterization was carried out following different methodologies (CHN elemental analyses; thermogravimetric analyses and Fourier transform infrared spectroscopy). The biocompatibility was evaluated through cytotoxicity and genotoxicity tests in fibroblast mouse cells and the angiogenic properties were evaluated using the chick chorioallantoic membrane (CAM) assay model. The physical–chemical results showed that the structure of Hancornia speciosa latex biomembrane is very similar to that of Hevea brasiliensis (commercially available product). Moreover, the cytotoxicity and genotoxicity assays showed that H. speciosa latex is biocompatible with life systems and can be a good biomaterial for medical applications. The CAM test showed the efficient ability of H. speciosa latex in neovascularization of tissues. The histological analysis was in accordance with the results obtained in the CAM assay. Our data indicate that the latex obtained from H. speciosa and eluted in water showed significant angiogenic activity without any cytotoxic or genotoxic effects on life systems. The same did not occur with H. speciosa latex stabilized with ammonia. Addition of ammonia does not have significant effects on the structure of biomembranes, but showed a smaller cell survival and a significant genotoxicity effect. This study contributes to the understanding of the potentialities of H. speciosa latex as a source of new phytomedicines.     

Isogeometric analysis of the isothermal Navier–Stokes–Korteweg equations

This paper is devoted to the numerical simulation of the Navier–Stokes–Korteweg equations, a phase-field model for water/water-vapor two-phase flows. We develop a numerical formulation based on isogeometric analysis that permits straightforward treatment of the higher-order partial–differential operator that represents capillarity. We introduce a new refinement methodology that desensitizes the numerical solution to the computational mesh and achieves mesh invariant solutions. Finally, we present several numerical examples in two and three dimensions that illustrate the effectiveness and robustness of our approach.     

In vitro and in vivo inhibition of Daphnia magna acetylcholinesterase by surfactant agents: possible implications for contamination biomonitoring

This study was designed to investigate the effect of two surfactants, dodecyl benzyl sulfonate (DBS), sodium dodecyl sulfate (SDS), and of a domestic detergent (Y) on the AChE activity of the crustacean cladoceran Daphnia magna. All the chemicals significantly inhibit the activity of the enzyme, both in vitro and in vivo conditions. In vitro lowest observed effect concentration (LOEC) values ranged from 12.5 to 100 mg/l and correspondent IC50 (50% inhibition concentration) values ranged from 6.6 to 58.5 mg/l. In vivo LOEC values ranged from 2 to 11.9 mg/l, while EC50 (50% effect concentration) values ranged from 11.4 to 56.7 mg/l. AChE inhibition by environmental contaminants such as surfactants, detergents and metals may lead to false diagnostics and even wrong conclusions in biomonitoring studies based on the use of AChE as a specific biomarker for organophosphorous and carbamate compounds.     

Selection of a powder for ceramic injection moulding

Ceramic suspensions were prepared from six alumina powders using the same high molecular weight organic vehicle. 18 mm diameter cylinders were compression moulded from four of these suspensions which were suitable for ceramic injection moulding. The organic vehicle in each cylinder was removed by thermal degradation according to the same temperature ramp. The defects present in the cylinders after removal of the organic vehicle are discussed in terms of the powder characteristics. Criteria for the selection of ceramic powders that could be used together with a high molecular weight organic vehicle for this shape-forming method, are deduced from the results obtained.     

Aromatization of heptanes,ethylcyclopentane, and cycloheptane over “nonacidic” platinum-alumina catalyst. Comparison of the mechanisms of aromatization over chromia-alumina and over platinum-alumina catalysts

n-Heptane, 2- and 3-methylhexane, ethylcyclopentane, and cycloheptane were passed in the presence of hydrogen at 500 °C over “nonacidic” platinum-alumina catalyst containing 3% by weight of platinum. The conversion ranged between 12 and 26%, depending on the interval of time the product was removed for analysis. In the case of cycloheptane, however, the conversion amounted to 98% during the first 30 min on stream and with time, during the approximate period between 2 and 3 h, it decreased to 69%. The products from the reaction contained besides toluene, also hydrocarbons resulting from a skeletal isomerization and dehydrocyclization of the original hydrocarbons, and to a smaller extent from a bond shift process, and a repetitive 1,5-ring closure followed by hydrogenolysis. Using 1,1-dimethylcyclohexane as a model compound, it was shown that the skeletal isomerization accompanying the aromatization of the seven-carbon hydrocarbons does not proceed through cationic intermediates. A survey of the literature relating to the mechanism of aromatization of hydrocarbon over “nonacidic” chromia-alumina and platinum-alumina catalysts is presented, and the differences between the two mechanisms are discussed.