Anatomical aspects and phytochemical potential of Caryocar villosum (Aubl.) Pers. (pequiá)/ Aspectos anatômicos e potencial fitoquímico de Caryocar villosum (Aubl.) Pers. (pequiá)

The knowledge of anatomical and phytochemical structures of many species has drawn the attention of researchers in several areas, because these species are characterized by the production of chemical compounds, mainly fixed and essential oils, which are of great industrial interest. The “pequiá” tree is a majestic tree from primary forest and represents huge economic potential. This work aimed to study the anatomical aspects, extraction and characterization of the fixed oil present in the fruit and the seed of Caryocar villosum. There were used fifty fruits of pequiá collected from the municipality of Tartarugalzinho (Amapá). The identification of species was made by comparison with exsiccates available in the Amapá Herbarium – HAMAB. For anatomical and phytochemical analyses, conventional methodology was used. The result in the macerate of the mesocarp corresponds to a yellow mass impregnated by lipids; in the endocarp there were registered trichomes which secret these lipids, forming an arc in all its extension. In the solvent-based phytochemical analyses of the mass of pericarp, mesocarp and fixed oil seed, favorable and satisfactory oil yields were obtained. The analyses of the acidity, saponification, ester and peroxide indexes are parameters that are related to the quality of the oil, therefore, the values obtained meet the Anvisa/2015 Resolution. It is thus concluded that the fixed oil obtained from the mesocarp/seed of C. villosum is indicated for alimentary purposes, with potential to reduce total cholesterol and LDL cholesterol, as well as in cosmetic industry. Therefore, anatomical analyses help phytochemical studies (CNPq/IEPA)

Efficiency of light-emitting diode and halogen units in reducing residual monomers

In this in-vitro study, we aimed to compare the residual monomers in composites beneath brackets bonded to enamel, using a light-emitting diode (LED) or a halogen unit, and to compare the residual monomers in the central to the peripheral areas of the composite

Effects of temperature on caffeine and carbon nanotubes co-exposure in Ruditapes philippinarum

In the marine environment, organisms are exposed to a high and increasing number of different con- taminants that can interact among them. In addition, abiotic factors can change the dynamics between contaminants and organisms, thus increasing or even decreasing the toxic effect of a particular com- pound. In this study, the effects of caffeine (CAF) and functionalized multi-walled carbon nanotubes (f- MWCNTs) induced in the clam Ruditapes philippinarum were evaluated, acting alone and in combination (MIX), under two temperature levels (18 and 21 C). To assess the impact of such compounds, their interaction and the possible influence of temperature, biochemical and histopathological markers were investigated. The effects of f-MWCNTs and caffeine appear to be clearly negative at the control tem- perature, with lower protein content in contaminated clams and a significant decrease in their meta- bolism when both pollutants were acting in combination. Also, at control temperature, clams exposed to pollutants showed increased antioxidant capacity, especially when caffeine was acting alone, although cellular damages were still observed at CAF and f-MWCNTs treatments. Increased biotransformation capacity at 18 C and MIX treatment may explain lower caffeine concentration observed. At increased temperature differences among treatments were not so evident as at 18 C, with a similar biological pattern among contaminated and control clams. Higher caffeine accumulation at MIX treatment under warming conditions may result from clams’ inefficient biotransformation capacity when exposed to increased temperatures

The PYRIN Domain-only Protein POP1 Inhibits Inflammasome Assembly and Ameliorates Inflammatory Disease

SummaryIn response to infections and tissue damage, ASC-containing inflammasome protein complexes are assembled that promote caspase-1 activation, IL-1β and IL-18 processing and release, pyroptosis, and the release of ASC particles. However, excessive or persistent activation of the inflammasome causes inflammatory diseases. Therefore, a well-balanced inflammasome response is crucial for the maintenance of homeostasis. We show that the PYD-only protein POP1 inhibited ASC-dependent inflammasome assembly by preventing inflammasome nucleation, and consequently interfered with caspase-1 activation, IL-1β and IL-18 release, pyroptosis, and the release of ASC particles. There is no mouse ortholog for POP1, but transgenic expression of human POP1 in monocytes, macrophages, and dendritic cells protected mice from systemic inflammation triggered by molecular PAMPs, inflammasome component NLRP3 mutation, and ASC danger particles. POP1 expression was regulated by TLR and IL-1R signaling, and we propose that POP1 provides a regulatory feedback loop that shuts down excessive inflammatory responses and thereby prevents systemic inflammation

Luminous Red Galaxies in Simulations: Cosmic Chronometers?

There have been a number of attempts to measure the expansion rate of the universe at high redshift using Luminous Red Galaxies (LRGs) as "chronometers". The method generally assumes that stars in LRGs are all formed at the same time. In this paper, we quantify the uncertainties on the measurement of H(z) which arise when one considers more realistic, extended star formation histories. In selecting galaxies from the Millennium Simulation for this study, we show that using rest-frame criteria significantly improves the homogeneity of the sample and that H(z) can be recovered to within 3% at z~0.42 even when extended star formation histories are considered. We demonstrate explicitly that using Single Stellar Populations to age-date galaxies from the semi-analytical simulations provides insufficient accuracy for this experiment but accurate ages are obtainable if the complex star formation histories extracted from the simulation are used. We note, however, that problems with SSP-fitting might be overestimated since the semi-analytical models tend to over predict the late-time star-formation in LRGs. Finally, we optimize an observational program to carry out this experiment.Comment: 11 pages, 10 figures. Accepted to MNRAS

An Intracellular Arrangement of Histoplasma capsulatum Yeast-Aggregates Generates Nuclear Damage to the Cultured Murine Alveolar Macrophages

Histoplasma capsulatum is responsible for a human systemic mycosis that primarily affects lung tissue. Macrophages are the major effector cells in humans that respond to the fungus, and the development of respiratory disease depends on the ability of Histoplasma yeast cells to survive and replicate within alveolar macrophages. Therefore, the interaction between macrophages and H. capsulatum is a decisive step in the yeast dissemination into host tissues. Although the role played by components of cell-mediated immunity in the host's defense system and the mechanisms used by the pathogen to evade the host immune response are well understood, knowledge regarding the effects induced by H. capsulatum in host cells at the nuclear level is limited. According to the present findings, H. capsulatum yeast cells display a unique architectural arrangement during the intracellular infection of cultured murine alveolar macrophages, characterized as a formation of aggregates that seem to surround the host cell nucleus, resembling a crown. This extranuclear organization of yeast-aggregates generates damage on the nucleus of the host cell, producing DNA fragmentation and inducing apoptosis, even though the yeast cells are not located inside the nucleus and do not trigger changes in nuclear proteins. The current study highlights a singular intracellular arrangement of H. capsulatum yeast near to the nucleus of infected murine alveolar macrophages that may contribute to the yeast’s persistence under intracellular conditions, since this fungal pathogen may display different strategies to prevent elimination by the host's phagocytic mechanisms

A Search for the Most Massive Galaxies. II. Structure, Environment and Formation

We study a sample of 43 early-type galaxies, selected from the SDSS because they appeared to have velocity dispersion > 350 km/s. High-resolution photometry in the SDSS i passband using HRC-ACS on board the HST shows that just less than half of the sample is made up of superpositions of two or three galaxies, so the reported velocity dispersion is incorrect. The other half of the sample is made up of single objects with genuinely large velocity dispersions. None of these objects has sigma larger than 426 +- 30 km/s. These objects define rather different relations than the bulk of the early-type galaxy population: for their luminosities, they are the smallest, most massive and densest galaxies in the Universe. Although the slopes of the scaling relations they define are rather different from those of the bulk of the population, they lie approximately parallel to those of the bulk "at fixed sigma". These objects appear to be of two distinct types: the less luminous (M_r>-23) objects are rather flattened and extremely dense for their luminosities -- their properties suggest some amount of rotational support and merger histories with abnormally large amounts of gaseous dissipation. The more luminous objects (M_r<-23) tend to be round and to lie in or at the centers of clusters. Their properties are consistent with the hypothesis that they are BCGs. Models in which BCGs form from predominantly radial mergers having little angular momentum predict that they should be prolate. If viewed along the major axis, such objects would appear to have abnormally large sigma for their sizes, and to be abnormally round for their luminosities. This is true of the objects in our sample once we account for the fact that the most luminous galaxies (M_r<-23.5), and BCGs, become slightly less round with increasing luminosity.Comment: 21 pages, 19 figures, accepted for publication in MNRA

Efficiency of the fluorescent antibody and indirect hemagglutination (IHR) tests for the diagnosis of the canine visceral leishmaniasis

Dogs are the main reservoir of Leishmania donovani however, better standardization of serological tests for the diagnosis of canine Calaazar still has to be done. Thus, in this paper the fluorescent antibody (FA) and indirect hemagglutination (IHA) tests for this diagnostic purpose were standardized and evaluated in 42 sera from animals with clinical and parasitological diagnosis of Calaazar and 60 sera from healthy dogs. The stipulated cut-offs for FR and IHA tests were, respectively, 20 and 40. The indices of sensibility, specificity, efficiency, positive and negative predictive values for FA tests were as follow: 0.952, 1.000, 0.983, 1.000 and 0.968 and, for the IHA test: 0.857, 1.000, 0.941, 1.000 and 0.909. It was concluded that both FA and IHA tests are efficient for the diagnosis of canine leishmaniasis.A sorologia da leishmaniose visceral em cães não teve, ainda, um estudo de padronização, embora esta espécie animal constitua importante reservatório de Leishmania donovani. Este trabalho teve como objetivo verificar a eficiência das reações de. imunofluorescência indireta (RIFI) e de hemaglutinação passiva (RHP) para o diagnóstico do calazar canino. Assim, 42 soros de cães com calazar comprovado clinica e parasitologicamente e 60 soros de cães clinicamente sadios foram testados. Analisou-se a distribuição de títulos e a eficiência dos testes para os diferentes níveis de limiar de reatividade. Para a eficiência máxima dos testes, o limiar de reatividade foi de 20 e 40 respectivamente para RIFI e RHP. Desta forma, a sensibilidade, a especificidade, a concordância ou a eficiência diagnóstica, o valor preditivo positivo e o valor preditivo negativo foram de 0,952, 1,000, 0,983, 1,000 e 0,968 para RIFI e 0,857, 1,000, 0,941, 1,000 e 0,909 para RHP. Concluiu-se que tanto a RIFI quanto a RHP são eficientes para estabelecer o diagnóstico sorológico da leishmaniose canina

Lipid compartments and lipid metabolism as therapeutic targets against coronavirus

Lipids perform a series of cellular functions, establishing cell and organelles’ boundaries, organizing signaling platforms, and creating compartments where specific reactions occur. Moreover, lipids store energy and act as secondary messengers whose distribution is tightly regulated. Disruption of lipid metabolism is associated with many diseases, including those caused by viruses. In this scenario, lipids can favor virus replication and are not solely used as pathogens’ energy source. In contrast, cells can counteract viruses using lipids as weapons. In this review, we discuss the available data on how coronaviruses profit from cellular lipid compartments and why targeting lipid metabolism may be a powerful strategy to fight these cellular parasites. We also provide a formidable collection of data on the pharmacological approaches targeting lipid metabolism to impair and treat coronavirus infection

Three- dimensional assessment of craniofacial asymmetry in children with transverse maxillary deficiency after rapid maxillary expansion: A prospective study

ObjectiveThe aim of this study was to evaluate craniofacial asymmetry in children with transverse maxillary deficiency, with or without functional unilateral posterior crossbite (UPC), before and after rapid maxillary expansion (RME).Setting and sample populationA sample of 51 children with cone beam computed tomography scans obtained before RME (T1) and a year after RME (T2).Material and methodsThis prospective study consisted of 2 groups: 25 children with functional UPC (6.77 ± 1.5 years) and 26 children without UPC (7.41 ± 1.31 years). Linear and angular measurements were obtained from zygomatic, maxilla, glenoid fossa and mandible, using original and mirrored 3D overlapped models. All right and left side comparisons in both groups and intergroups asymmetries were compared using MANOVA and t test for independent samples, respectively, statistically significant at P < .05.ResultsThe UPC group showed no side differences, but mandibular horizontal rotation at T1, and this asymmetry was improved in T2. The non- UPC group showed at baseline significant lateral asymmetry in orbitale, position of palatine foramen, respectively, in average 2.95 mm and 1.16 mm, and 0.49 mm of average asymmetry in condylar height. The glenoid fossa was symmetric in both groups at T1 and T2.ConclusionsChildren with transverse maxillary deficiency showed slight morphological asymmetry, located in the mandible position in cases of UPC, and in the orbital and maxillary regions in cases without UPC. One year after RME, patients improved their craniofacial asymmetry, with significant changes in the mandible and correction of the mandibular rotation in patients who presented UPC.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/156195/2/ocr12370_am.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/156195/1/ocr12370.pd