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Context: Croton cajucara Benth has been widely used in folk medicine, especially in the Amazonian region of Brazil, to treat several illnesses. Objectives: The objective of the study is to evaluate the stem bark hydroalcoholic extract (CC-EHA) of C. cajucara and their clerodane-type diterpene fractions (F1-7, F25-27, and F28) on promastigotes and axenic amastigotes of Leishmania amazonensis and trypomastigotes and epimastigotes of Trypanosoma cruzi. Materials and Methods: The extract was obtained in ethanol: water and the fractions with solvents of increasing polarity. The antiparasitic activities were assessed by 3,4,5-dimethylthiazol-2-yl-2,5-diphenyltetrazolium bromide method against promastigotes and axenic amastigotes from L. amazonensis in 24-h cultures and trypomastigotes and epimastigotes of T. cruzi in 72-h cultures. The experiments in triplicate were made in quadruplicate way in each time. The statistical tests used were t-Students and ANOVA. Results: Among those evaluated samples, the CC-EHA extract showed the higher antileishmanial activity of promastigote cultures (IC50 = 18.00 ± 0.01 μg/mL at 24 h). However, against axenic amastigotes, the polar fraction (F28), rich in diterpene transdehydrocrotonin (t-DCTN), showed the highest effect with an IC50 = 6.18 ± 0.02 μg/mL in culture of 24 h. In the T. cruzi assays, F28 also showed the greatest effect against trypomastigotes and epimastigotes, IC50 = 0.43 ± 0.02 μg/mL and 0.27 ± 0.02 μg/mL, respectively, at 72 h of culture. The results showed that the diterpene t-DCTN is the most important antiparasitic component in the hydroalcoholic extract obtained from C. cajucara, specifically against L. amazonensis and T. cruzi. Conclusion: Our results contribute to knowledge of these folk medicinal species as a promising antiparasitic phytotherapeutic alternative. [ABSTRACT FROM AUTHOR]

This paper aims at replying critical commentaries made by Leite, F. P., Aggio, G. O. e Angeli, E. (this Review, 2009) on two Author's theses. The first one states that, if public deficit is to be financed, then either interest rate applied is negative or government invests as if it where a profit-making business enterprise. Otherwise, public debt will mathematically follow an explosive trend. The second one says that if there is no debt and public deficit is paid with money issuing, then the monetary stock will tend to an equilibrium level. [ABSTRACT FROM AUTHOR]

Pleasant Mathematics. This paper suggests a reconsideration of the principle that public deficits should be financed by public debt. Two main reasons are offered. First, it is admitted that public debt is an economic variable whose time behaviour is better described by a first difference equation instead of an accounting identity. The convergence condition thus obtained requires either a nominal negative interest rate or that government bonds are used to raise tax income, hypotheses not theoretically granted. As a consequence, if primary surplus is not sufficient to match interests' payment, it will be observed an explosive trend in the public debt, the due interests and the money issuing. Therefore, it lacks support to the idea that public debt prevents inflation. Second, it is shown that financing public deficit through money issuing leads to a stable equilibrium money stock. The general conclusion is that, in order to simultaneously promote economic growth and inflation control, money issuing is preferable to public debt. [ABSTRACT FROM AUTHOR]

Synthesis and spectroscopic characterization of ten fluorinated thiosemicarbazones are reported. All synthesized compounds were evaluated for their anti- Trypanosoma cruzi activity, and the IC 50 values were obtained in the range of 5.64–29.19 μg mL −1 in 24 h of cultures. Among all assayed thiosemicarbazones the 2,3,4-trifluoro-substituted compound showed the higher activity with IC 50 = 5.64 μg mL −1 . QSAR studies involving electronic and hydrophobic parameters, as well as the 13 C NMR chemical shifts of iminic carbon indicated that the deshielding effect caused by the fluorine atoms and their hydrophobicity are significant features for the anti- T. cruzi activity. [ABSTRACT FROM AUTHOR]

A proper professional lighting design implies in a continuous search for the best compromise between both low power consumption and better lighting quality. This search converts this design into a hard to solve multi-objective optimization problem. Evolutionary algorithms are widely used to attack that type of hard optimization problems. However, professionals could not benefit from that kind of assistance since evolutionary algorithms have been unexplored by several commercial lighting design computer-aided softwares. This work proposes a system based on evolutionary algorithms which implement a computer-automated exterior lighting design both adequate to irregular shaped areas and able to respect lighting pole positioning constraints. The desired lighting design is constructed using a cluster of computers supported by a web client, turning this application into an efficient and easy tool to reduce project cycles, increase quality of results and decrease calculation times. This ELCAutoD-EA system consists in a proposal for a parallel multi-objective evolutionary algorithm to be executed in a cluster of computers with a Java remote client. User must choose lighting pole heights, allowed lamps and fixtures, as well as the simplified blue print of the area to be illuminated, marking the sub-areas with restrictions to pole positioning. The desired average illuminance must also be informed as well as the accepted tolerance. Based on user informed data, the developed application uses a dynamic representation of variable size as a chromosome and the cluster executes the evolutionary algorithm using the Island model paradigm. Achieved solutions comply with the illumination standards requirements and have a strong commitment to lighting quality and power consumption. In the present case study, the evolved design used 37.5% less power than the reference lighting design provided by a professional and at the same time ensured a 227.3% better global lighting uniformity. A better lighting quality is achieved because the proposed system solves multi-objective optimization problems by avoiding power wastes which are often unclear to a professional lighting engineer in charge of a given project. [ABSTRACT FROM AUTHOR]

Background: Leptospiral glycolipoprotein (GLP) is a potent and specific Na/K-ATPase inhibitor. Severe pulmonary form of leptospirosis is characterized by edema, inflammation and intra-alveolar hemorrhage having a dismal prognosis. Resolution of edema and inflammation determines the outcome of lung injury. Na/K-ATPase activity is responsible for edema clearance. This enzyme works as a cell receptor that triggers activation of mitogen-activated protein kinase (MAPK) intracellular signaling pathway. Therefore, injection of GLP into lungs induces injury by triggering inflammation. Methods: We injected GLP and ouabain, into mice lungs and compared their effects. Bronchoalveolar lavage fluid (BALF) was collected for cell and lipid body counting and measurement of protein and lipid mediators (PGE2 and LTB4). The levels of the IL-6, TNFα, IL-1B andMIP-1α were also quantified. Lung images illustrate the injury and whole-body plethysmography was performed to assay lung function. We used Toll-like receptor 4 (TLR4) knockout mice to evaluate leptospiral GLP-induced lung injury. Na/K-ATPase activity was determined in lung cells by nonradioactive rubidium incorporation. We analyzed MAPK p38 activation in lung and in epithelial and endothelial cells. Results: Leptospiral GLP and ouabain induced lung edema, cell migration and activation, production of lipid mediators and cytokines and hemorrhage. They induced lung function alterations and inhibited rubidium incorporation. Using TLR4 knockout mice, we showed that the GLP action was not dependent on TLR4 activation. GLP activated of p38 and enhanced cytokine production in cell cultures which was reversed by a selective p38 inhibitor. Conclusions: GLP and ouabain induced lung injury, as evidenced by increased lung inflammation and hemorrhage. To our knowledge, this is the first report showing GLP induces lung injury. GLP and ouabain are Na/K-ATPase targets, triggering intracellular signaling pathways. We showed p38 activation by GLP-induced lung injury, which was may be linked to Na/K-ATPase inhibition. Lung inflammation induced by GLP was not dependent on TLR4 activation. [ABSTRACT FROM AUTHOR]

In an effort to find effective and affordable ways to control of Aedes aegypti L. (Diptera: Culicidae), the larvicidal activities of 94 extracts from ten plant species belonging to eight families [ Guettarda grazielae and Spermacoce verticillata (Rubiaceae), Coccoloba mollis and Triplaris americana (Polygonaceae), Eschweilera ovata (Lecytidaceae), Merremia aegyptia (Convolvulaceae), Ouratea nitida (Ochnnaceae), Protium heptaphyllum (Burseraceae), Rourea doniana (Connaraceae), and Tovomita brevistaminea (Guttiferae)], widely found in the northeast of Brazil, were initially screened at 250 µg/mL. Nineteen of the 94 extracts from six plant species ( C. mollis, G. grazielae, M. aegyptia, R. doniana, S. verticillata, and T. americana) showed significant activity (>75% mortality) against the fourth instar larvae. Some of these extracts showed 100% mosquito larvae mortality, with LD50 values lower 200 µg/mL. When compared to synthetic insecticide Temephos (LD50 8.7 µg/mL), two of them, hexane (LD50 12.1 µg/mL) and ethyl acetate (LD50 51.6 µg/mL) extracts from stems of R. doniana and G. grazielae, respectively, were the most effective. The isolation and purification of these extracts are in progress and evaluation of these compounds will be needed to identify the active component. [ABSTRACT FROM AUTHOR]

Background: Leptospiral glycolipoprotein (GLP) is a potent and specific Na/K-ATPase inhibitor. Severe pulmonary form of leptospirosis is characterized by edema, inflammation and intra-alveolar hemorrhage having a dismal prognosis. Resolution of edema and inflammation determines the outcome of lung injury. Na/K-ATPase activity is responsible for edema clearance. This enzyme works as a cell receptor that triggers activation of mitogen-activated protein kinase (MAPK) intracellular signaling pathway. Therefore, injection of GLP into lungs induces injury by triggering inflammation.Methods: We injected GLP and ouabain, into mice lungs and compared their effects. Bronchoalveolar lavage fluid (BALF) was collected for cell and lipid body counting and measurement of protein and lipid mediators (PGE2 and LTB4). The levels of the IL-6, TNFα, IL-1B and MIP-1α were also quantified. Lung images illustrate the injury and whole-body plethysmography was performed to assay lung function. We used Toll-like receptor 4 (TLR4) knockout mice to evaluate leptospiral GLP-induced lung injury. Na/K-ATPase activity was determined in lung cells by nonradioactive rubidium incorporation. We analyzed MAPK p38 activation in lung and in epithelial and endothelial cells.Results: Leptospiral GLP and ouabain induced lung edema, cell migration and activation, production of lipid mediators and cytokines and hemorrhage. They induced lung function alterations and inhibited rubidium incorporation. Using TLR4 knockout mice, we showed that the GLP action was not dependent on TLR4 activation. GLP activated of p38 and enhanced cytokine production in cell cultures which was reversed by a selective p38 inhibitor.Conclusions: GLP and ouabain induced lung injury, as evidenced by increased lung inflammation and hemorrhage. To our knowledge, this is the first report showing GLP induces lung injury. GLP and ouabain are Na/K-ATPase targets, triggering intracellular signaling pathways. We showed p38 activation by GLP-induced lung injury, which was may be linked to Na/K-ATPase inhibition. Lung inflammation induced by GLP was not dependent on TLR4 activation. [ABSTRACT FROM AUTHOR]