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The in vitro gas production, the kinetics of fermentation, and the apparent degradability of dry matter (DM) of the legume Albizia lebbekoides (albizia), incubated alone or with polyethylene glycol (PEG-6000), zeolite or both, were determined in a completely randomized design with four repetitions per treatment. The gas production was compared at 6, 12, 24, and 48 h of incubation. The in vitro kinetics of fermentation was estimated according to the exponential model Y=D* (1-Exp (-C*(Hora-L)), and the apparent degradability at 48 h of incubation, by gravimetry. The in vitro gas production differed at 12 (P < 0.01), 24, and 48 h (P < 0.001) between the treatments with PEG (albizia with PEG and albizia with PEG and zeolite). The performance was different for those not including PEG (albizia alone and albizia with zeolite). The increase in the gas production with PEG was of 385 % at 4 h of incubation, and at 6 h, it was more moderate (213 %). It was reduced as the in vitro fermentation advanced up to 48 h, being of 146 %. The kinetics of fermentation of the legume showed that the treatments with zeolite increased slightly the rate of gas production (C). The treatments in which the tannins were inactivated with PEG decreased the lag phase (L) and increased the potential of gas production. It is concluded that zeolite did not affect the rumen degradability of albizia in in vitro conditions, whereas the use of PEG improved the gas production and the fermentation potential of the legume. Besides, it reduced the lag phase of the in vitro fermentation. [ABSTRACT FROM AUTHOR]

En un diseño completamente aleatorizado, con cuatro repeticiones por tratamiento, se determinó la producción de gas in vitro, la cinética de fermentación y la degradabilidad aparente de la materia seca (MS) de la leguminosa Albizia lebbekoides (albizia), incubada sola o con polietilenglicol (PEG-6000), zeolita o ambos compuestos. La producción de gas se comparó a las 6, 12, 24 y 48 h de incubación. Se estimó la cinética de fermentación in vitro, según el modelo exponencial Y= D*(1-Exp (-C*(Hora-L)) y la degradabilidad aparente a las 48 h de incubación, por gravimetría. La producción de gas in vitro difirió a las 12 (P < 0.01), 24 y 48 h (P < 0.001) entre los tratamientos con PEG (albizia con PEG y albizia con PEG y zeolita). No fue así para los que no incluyeron PEG (albizia sola y albizia con zeolita). El incremento de la producción de gas con PEG fue de 385 % a las 4 h de incubación y a las 6 h fue más moderado (213 %). Se redujo a medida que avanzó la fermentación in vitro hasta las 48 h, en que fue de 146 %. La cinética de fermentación de la leguminosa mostró que los tratamientos con zeolita incrementaron ligeramente la velocidad de producción de gas (C). Los tratamientos en que se inactivaban los taninos con PEG disminuyeron la fase Lag (L) e incrementaron el potencial de producción de gas. Se concluye que la zeolita no influyó en la degradabilidad ruminal de albizia en condiciones in vitro, mientras que el empleo del PEG mejoró la producción de gas y el potencial de fermentación de la leguminosa. Además, redujo la fase Lag de la fermentación in vitro. [ABSTRACT FROM AUTHOR]

Acridones are a class of compounds that have attracted attention in recent years for their wide range of biological properties, including selective inhibition of diverse human pathogenic viruses. The wide spectrum of antiviral activity includes DNA and RNA viruses, such as herpes simplex virus, cytomegalovirus, adenovirus, hepatitis C virus, dengue virus, and Junin virus, among others, indicative of the involvement of cellular factors as potential targets of acridone derivatives. At the present, their precise mode of action is not clearly determined, although the predominant action seems to be centered on the synthesis of nucleic acids. Regarding this point, inhibitory activity against cellular and viral enzymes and the ability to intercalate into nucleic acid molecules was demonstrated for some acridone compounds. Then, the possibility of a multiple effect on different targets renewed interest in these agents for virus chemotherapy allowing a potent inhibitory effectiveness associated to less feasibility of generating antiviral resistance. This review summarizes the current knowledge regarding the methods of synthesis, the antiviral properties of acridone derivatives, their mechanism of action, and structural characteristics related to antiviral activity as well as the perspectives of this class of compounds for clinical application against human viral infections.

Twenty-three healthy mixed-breed male adult dogs were examined using serial magnetic resonance (MR) renograms. The images were obtained using a dynamic gradient-echo, fast SPGR, T1-weighted sequence and low doses of gadolinium chelates (0.025 mmol/kg). Time-intensity curves were obtained to assess typical urinary excretion parameters, namely, time to vascular peak (TVP), time to vascular drop (TVD), time to glomerular peak (TGP), parenchymal phase length (PPL), gradient of parenchymal phase (GPP) and pattern of excretory segment. The mean TVP, TVD, TGP and PPL were 31.6±11.8, 43.4±11.2, 154.0±36.2 and 115.2±37.7s, respectively. The GPP was 24.1±8.6% of signal intensity per min. The excretory segment was concave in all cases, and at the end of the examination, 87.1% of kidneys had shown a reduction in signal intensity of 50%. This MR nephrography protocol can provide adequate time-intensity curve parameters for the urinary system of dogs, offers excellent anatomical detail, and represents an alternative to radionuclide nephrography., (Copyright © 2010 Elsevier Ltd. All rights reserved.)

The promyelocytic leukemia protein (PML) forms nuclear bodies (NB) that can be redistributed by virus infection. In particular, lymphocytic choriomeningitis virus (LCMV) influences disruption of PML NB through the interaction of PML with the arenaviral Z protein. In a previous report, we have shown that the disulfide compound NSC20625 has antiviral and virucidal properties against arenaviruses, inducing unfolding and oligomerization of Z without affecting cellular RING-containing proteins such as the PML. Here, we further studied the effect of the zinc-finger-reactive disulfide NSC20625 on PML-Z interaction. In HepG2 cells infected with LCMV or transiently transfected with Z protein constructs, treatment with NSC20625 restored PML distribution from a diffuse-cytoplasmic pattern to punctate, discrete NB which appeared identical to NB found in control, uninfected cells. Similar results were obtained in cells transfected with a construct expressing a Z mutant in zinc-binding site 2 of the RING domain, confirming that this Z-PML interaction requires the integrity of only one zinc-binding site. Altogether, these results show that the compound NSC20625 suppressed Z-mediated PML NB disruption and may be used as a tool for designing novel antiviral strategies against arenavirus infection., (Copyright 2010 Elsevier Inc. All rights reserved.)

Glutamatergic N-methyl-d-aspartate NMDA receptors (NMDAR) are considered to play a key role in ischemia-induced damage. Long-term (hours) changes in their expression upon ischemia have been shown. Here we report short-term changes in the mRNA levels of the major hippocampal NMDAR subunits (NR1, NR2A and NR2B), as well as c-fos, in an ex vivo ischemia model using hippocampal slices. This effect can be observed also in a calcium free incubation solution. Striking early decreases in the NMDAR subunit mRNA levels were observed after 30 min of oxygen and glucose deprivation (OGD) as well as a partial recovery when the tissues were returned to the balanced salt solution (reperfusion-like period) for 3 h. Since OGD-induced damage has been reported to be a consequence of the increase in OGD-related glutamate release, we also analyzed NMDAR mRNA levels following increased glutamate levels in hippocampal sections in which no significant effects on NMDAR subunit mRNA levels were detected. Furthermore, we describe that the presence of MK-801 (a selective NMDAR antagonist), CNQX (a selective AMPA/kainate receptor antagonist) or their combined action in the incubation solution is able to induce a significant decrease in NMDAR expression but in these conditions the OGD does not induce further decreases in mRNA levels. We suggest that the mechanisms triggered during OGD to downregulate mRNA levels of NMDAR subunits could be the same than those induced by glutamate receptor antagonists.

The zinc finger proteins have fascinated many research groups because of their modular assembly, broad range of biological functions and more recently because they are attractive targets for antiviral therapy. The zinc finger domain is a very stable structural element whose hallmark is the coordination of a zinc ion by several amino acid residues, usually cysteines and histidines. These structural motifs are associated with protein-nucleic acid recognition as well as protein-protein interactions. The biological function of the zinc finger proteins is strongly dependent on the zinc ion, which assure integrity and stability. Thus, the disruption of critical zinc finger viral proteins represents a fundamentally new approach to inhibit viral replication in the absence of mutations leading to drug resistance phenotypes. This review summarizes the drug design and potential therapeutic applications of viral zinc fingers disrupting agents for the control of viral diseases.

Several disulfide-based compounds, including intermolecular aromatic disulfides of the type Ph-S-S-Ph and dithianes with the sulfur atoms tethered in a ring structure, have shown effective inhibitory activity against the arenaviruses Junin (JUNV), agent of Argentine hemorrhagic fever, and Tacaribe (TCRV). These compounds showed a strong virucidal effect with inactivating concentration 50% (IC(50)) values in the range 0.6-5.0 microM, and also were effective to reduce virus yields from infected cells. The mode of inactivating action of two active compounds, the aromatic bis disulfide NSC20625 and the dithiane NSC624152, was further studied. Both compounds were able to inactivate arenaviruses after a few minutes of direct contact with virions, in a concentration- and time-dependent manner. The ability of drug-treated virus to perform several steps of the replication cycle was analyzed. The killed virus particles were found to bind and enter to Vero cells with the same efficacy as infectious native virions, but the ability of inactivated virions to synthesize viral proteins in Vero cells was abolished. Thus, treatment of JUNV and TCRV with these compounds destroyed virion infectivity, generating particles which entered the host cell but were unable to complete the viral biosynthetic processes.

A pulsed Nd:YAG laser operating on the fourth (266 nm) and second (532 nm) harmonics has been used to generate plasmas on the target surface in air at atmospheric pressure. The influence of wavelength on quantitative analysis of 4 minor elements in stainless steel samples (Si, Ti, Nb and Mo) was investigated. Stainless steel samples with different elemental concentrations were prepared and analyzed by laser-induced plasma spectrometry (LIPS). The effect of laser wavelength on analytical figures of merit (calibration curves, correlation coefficients, linear dynamic ranges, analytical precision, and accuracy values) was found to be negligible when internal standardization (an Fe line) and time-resolved laser-induced plasma are employed. For both wavelengths, the calibration curves presented a good linearity and an acceptable linear dynamic range in the concentration interval investigated. For the four elements studied, limits of detection lower than 150 microg g(-1) were achieved. To evaluate the influence of wavelength on precision and accuracy, a set of fifteen high-alloyed steel samples from different stages of steelmaking process have been analyzed. Finally, the long-term stability of the analytical measurements for Mo with 532 nm wavelength has been discussed. RSD values were lower than 5.3% for the elements studied.

To study the functional involvement of cellular membrane properties on arenavirus infection, saturated fatty acids of variable chain length (C10-C18) were evaluated for their inhibitory activity against the multiplication of Junin virus (JUNV). The most active inhibitor was lauric acid (C12), which reduced virus yields of several attenuated and pathogenic strains of JUNV in a dose dependent manner, without affecting cell viability. Fatty acids with shorter or longer chain length had a reduced or negligible anti-JUNV activity. Lauric acid did not inactivate virion infectivity neither interacted with the cell to induce a state refractory to virus infection. From mechanistic studies, it can be concluded that lauric acid inhibited a late maturation stage in the replicative cycle of JUNV. Viral protein synthesis was not affected by the compound, but the expression of glycoproteins in the plasma membrane was diminished. A direct correlation between the inhibition of JUNV production and the stimulation of triacylglycerol cell content was demonstrated, and both lauric-acid induced effects were dependent on the continued presence of the fatty acid. Thus, the decreased insertion of viral glycoproteins into the plasma membrane, apparently due to the increased incorporation of triacylglycerols, seems to cause an inhibition of JUNV maturation and release.

Fifteen antiretroviral Zn-finger active compounds with diverse chemical structures, including azoic compounds, hydrazide derivatives, disulphide-based reagents and others were screened in vitro against Junin virus (JUNV), the aetiological agent of Argentine haemorrhagic fever, by a virus yield inhibition assay in Vero cells. Cytotoxicity was evaluated simultaneously by the MTT method. Of the compounds, three were totally inactive as antivirals, nine presented moderate anti JUNV-activity and three were truly active with EC50 (effective concentration 50%) values in the range 6.5-9.3 microM and with selectivity indices greater than 10. The most active inhibitors, named NSC20625, 3-7 and 2-71, demonstrated a broad range of action against arenaviruses, including several attenuated and pathogenic strains of JUNV as well as the antigenically related Tacaribe virus (TACV) and Pichinde virus (PICV). The direct treatment of JUNV and TACV virions with the compounds showed two types of behaviour: the aromatic disulphide NSC20625 was a very potent virucidal agent, whereas the other two compounds exhibited moderate or negligible virus-inactivating properties.