Leucine supplementation does not affect protein turnover and impairs the beneficial effects of endurance training on glucose homeostasis in healthy mice

Endurance exercise training as well as leucine supplementation modulates glucose homeostasis and protein turnover in mammals. Here, we analyze whether leucine supplementation alters the effects of endurance exercise on these parameters in healthy mice. Mice were distributed into sedentary (C) and exercise (T) groups. The exercise group performed a 12-week swimming protocol. Half of the C and T mice, designated as the CL and TL groups, were supplemented with leucine (1.5 % dissolved in the drinking water) throughout the experiment. As well known, endurance exercise training reduced body weight and the retroperitoneal fat pad, increased soleus mass, increased VO_2max, decreased muscle proteolysis, and ameliorated peripheral insulin sensitivity. Leucine supplementation had no effect on any of these parameters and worsened glucose tolerance in both CL and TL mice. In the soleus muscle of the T group, AS-160^Thr-642 (AKT substrate of 160 kDa) and AMPK^Thr-172 (AMP-Activated Protein Kinase) phosphorylation was increased by exercise in both basal and insulin-stimulated conditions, but it was reduced in TL mice with insulin stimulation compared with the T group. Akt phosphorylation was not affected by exercise but was lower in the CL group compared with the other groups. Leucine supplementation increased mTOR phosphorylation at basal conditions, whereas exercise reduced it in the presence of insulin, despite no alterations in protein synthesis. In trained groups, the total FoxO3a protein content and the mRNA for the specific isoforms E2 and E3 ligases were reduced. In conclusion, leucine supplementation did not potentiate the effects of endurance training on protein turnover, and it also reduced its positive effects on glucose homeostasis.     

Wheat Resistance to Spot Blotch Potentiated by Silicon

Spot blotch, caused by the fungus Bipolaris sorokiniana, is one of the most important diseases on wheat. The effects of silicon (Si) on this wheat disease were studied. Plants of wheat cultivars BR‐18 and BRS‐208 were grown in plastic pots containing Si‐deficient soil amended with either calcium silicate (+Si) or calcium carbonate (?Si). The content of Si in leaf tissue was significantly increased by 90.5% for the +Si treatment. There was no significant difference between Si treatments for calcium content, so variations in Si accounted for differences in the level of resistance to spot blotch. The incubation period was significantly increased by 40% for the +Si treatment. The area under spot blotch progress curve, number of lesions per cm² of leaf area, and real disease severity significantly decreased by 62, 36 and 43.5% in +Si treatment. There was no significant effect of Si on lesion size. The role played by total soluble phenolics in the increased resistance to spot blotch of plants from both cultivars supplied with Si was not clear. Plants from cultivar BR‐18 supplied with Si showed the highest values for concentration of lignin‐thioglycolic acid derivatives during the most advanced stages of fungus infection. Chitinase activity was high at the most advanced stages of fungus infection on leaves from both cultivars supplied with Si and may have had an effect on fungus growth based on the reduction of the components of resistance evaluated. Peroxidase activity was found to be high only at 96 h after inoculation of both cultivars supplied with Si. Polyphenoloxidase activity had no apparent effect on resistance regardless of Si treatments. Results revealed that supplying Si to wheat plants can increase resistance against spot blotch.     

Effect of genistein and coenzyme Q10 in oxidative damage and mitochondrial membrane potential in an attenuated type II mucopolysaccharidosis cellular model

Mucopolysaccharidosis type II (MPS II) is an inborn error of the metabolism resulting from several possible mutations in the gene coding for iduronate-2-sulfatase (IDS), which leads to a great clinical heterogeneity presented by these patients. Many studies demonstrate the involvement of oxidative stress in the pathogenesis of inborn errors of metabolism, and mitochondrial dysfunction and oxidative stress can be related since most of reactive oxygen species come from mitochondria. Cellular models have been used to study different diseases and are useful in biochemical research to investigate them in a new promising way. The aim of this study is to develop a heterozygous cellular model for MPS II and analyze parameters of oxidative stress and mitochondrial dysfunction and investigate the in vitro effect of genistein and coenzyme Q10 on these parameters for a better understanding of the pathophysiology of this disease. The HP18 cells (heterozygous c.261_266del6/c.259_261del3) showed almost null results in the activity of the IDS enzyme and presented accumulation of glycosaminoglycans (GAGs), allowing the characterization of this knockout cellular model by MPS II gene editing. An increase in the production of reactive species was demonstrated (p < .05 compared with WT vehicle group) and genistein at concentrations of 25 and 50 µm decreased in vitro its production (p < .05 compared with HP18 vehicle group), but there was no effect of coenzyme Q10 in this parameter. There was a tendency for lysosomal pH change in HP18 cells in comparison to WT group and none of the antioxidants tested demonstrated any effect on this parameter. There was no increase in the activity of the antioxidant enzymes superoxide dismutase and catalase and oxidative damage to DNA in HP18 cells in comparison to WT group and neither genistein nor coenzyme q10 had any effect on these parameters. Regarding mitochondrial membrane potential, genistein induced mitochondrial depolarization in both concentrations tested (p < .05 compared with HP18 vehicle group and compared with WT vehicle group) and incubation with coenzyme Q10 demonstrated no effect on this parameter. In conclusion, it is hypothesized that our cellular model could be compared with a milder MPS II phenotype, given that the accumulation of GAGs in lysosomes is not as expressive as another cellular model for MPS II presented in the literature. Therefore, it is reasonable to expect that there is no mitochondrial depolarization and no DNA damage, since there is less lysosomal impairment, as well as less redox imbalance.     

Behavioral models of hydrothermal regulation in anurans: A field study in the Atlantic Forest,Brazil

Anurans rely on different microhabitats and microclimates for hydro-thermoregulation, which is an important physiological property for locomotor performance, body temperature, water flux, and pathogen defense. We ask whether microhabitat scouting is related to physiological states, specifically if microhabitat choice benefits the production of behavioral fever (e.g., increasing body temperature by selecting warmer places) or sickness behavior (e.g., inactivity and anorexia). We investigated how thermoregulatory behaviors affect hydro-thermoregulation in anurans, using agar models as a sampling unit, simulating four behaviors related to behavioral fever and sickness behavior. We compared the models' hydro-thermal balance in two different environments (wet and transitional forests). We showed that the wet forest was warmer and more stable than transitional forest and the agar models in the wet forest were warmer. Still, the four behavioral simulations exhibited similar average temperatures during the five-day study period in both forests. However, the apathetic behavior models had the lowest daily temperatures. The percentage hydration across models was higher in the wet forest, and daily variation in water loss for each behavioral simulation was higher in the transitional forest. Nevertheless, when limiting the analysis to the warmest times (1000–1600 h), apathetic behavior models lost less water than the others in both forests. We showed that different forests provide microclimatic variation for understory anurans, but different thermoregulatory behaviors may lead to similar body temperatures. Therefore, the Atlantic Forest offers different microclimates and thermoregulation options for anurans, as some species could develop behavioral fever while others demonstrate sickness behavior. Abstract in Portuguese is available with online material.     

Habitat use,abundance, and persistence of Neotropical migrant birds in a habitat matrix in northeast Belize

ABSTRACT To ensure adequate protection of nonbreeding habitats used by Neotropical migratory landbirds, we must first address questions about habitat use and quality. On the Yucatan peninsula, migrants use many habitats, several of which remain unstudied, and methodological differences preclude interhabitat comparisons based on studies to date. We used distance sampling along line transects in six habitats in northeast Belize to examine use of previously unstudied habitats (e.g., salt marsh) by Neotropical migrants and to permit comparison across habitats. We calculated unadjusted and adjusted (for detectability) density estimates for individual migrant species and for all species combined to generate hypotheses about habitat quality based on the assumption that density and quality are positively correlated. Adjusted density estimates for all migrants were highest in black mangrove habitat (1799 ± 110 ind/km²), intermediate in three forest types and milpa (range 598–802 ind/km²), and lowest in salt marsh (207 ± 32.3 ind/km²). By combining density estimates with habitat availability in our study region, we estimated that evergreen forest and black mangrove supported 70% and 9% of the region's migrant population, respectively. At the species level, five of the 10 most common species had habitat preferences (>50% detections in one habitat). Given the diversity of habitat preferences among species and apparent seasonal movements, our results indicate that Neotropical migrants in northeast Belize are dependent on a matrix of interconnected habitats.     

Effects of freezing on bone histological morphology

Allograft bone has been widely used for reconstruction of different portions of the skeleton. The fragment of bone harvested must be kept under low temperatures. The cryopreservation also contributes to decrease the antigenic potential of the tissue. Although this technique is considered safe, there is little information about the morphological modifications that the medullary and cortical portions of bone suffer after freezing. Hence, the aim of this study was to investigate the morphology of bone tissue after freezing under different temperatures and periods. Twelve rabbits were used to analyze the effects of two temperatures, −20°C and −70°C, during four periods of time: 30, 60, 90, 120 days. Tissues were analyzed by HE, picro-sirius stains and also by Feulgen’s reaction, through qualitative and morphometric ways, considering the area occupied by cells and nuclei, medullary and cortical portions, as well as by collagen expression at cortical. The differences among the treatments were analyzed by Tukey′s test, at 5% significance level. Bone freezing increased cellular and nuclear areas at cancellous bone and diminished nuclear area at the cortical bone. Cortical bone collagen suffered denaturation proportionally to temperature decrease and to freezing duration. These alterations compromised the morphology of tissues after 90 or 120 days of freezing at the temperature of −70°C. Cells necrosed during freezing, contributing to reduce bone antigenicity.