Strenuous exercise triggers deleterious effects on the intestinal epithelium, but their mechanisms are still uncertain. Here, we investigated whether a prolonged training and an additional exhaustive training protocol alter intestinal permeability and the putative effect of alanyl-glutamine (AG) pretreatment in this condition. Rats were allocated into 5 different groups: 1) sedentary; 2 and 3) trained (50 min per day, 5 days per week for 12 weeks) with or without 6 weeks oral (1.5 g/kg) AG supplementation; 4 and 5) trained and subjected to an additional exhaustive test protocol with or without oral AG supplementation. Venous blood samples were collected to determine gasometrical indices at the end of the 12-week protocol or after exhaustive test. Lactate and glucose levels were determined before, during, and after the exhaustive test. Ileum tissue collected after all experimental procedures was used for gene expression analysis of Zonula occludens 1 (ZO-1), occludin, claudin-2, and oligopeptide transporter 1 (PepT-1). Intestinal permeability was assessed by urinary lactulose/mannitol test collected after the 12-week protocol or the exhaustive test. The exhaustive test decreased pH and base excess and increased pCO2. Training sessions delayed exhaustion time and reduced the changes in blood glucose and lactate levels. Trained rats exhibited upregulation of PEPT-1, ZO-1, and occludin mRNA, which were partially protected by AG. Exhaustive exercise induced intestinal paracellular leakage associated with the upregulation of claudin-2, a phenomenon protected by AG treatment. Thus, AG partially prevented intestinal training adaptations but also blocked paracellular leakage during exhaustive exercise involving claudin-2 and occludin gene expression.

Bredemeyera floribunda roots are popularly used to treat snakebites in the semiarid region of Northeast Brazil, and previous studies indicate the anti-ophidian actions of triterpenoid saponins found in its roots. To assess B. floribunda root extract (BFRE) activity against the effects of Bothrops jararacussu venom (BjuV), antiphospholipasic, antiproteolytic, antihemorrhagic, antinecrotic, and anti-edematogenic activities were investigated in mice. Phytochemical analysis revealed the presence of saponins, flavonoids, and sugars, with rutin and saccharose being the major constituents of BFRE. Acute toxicity was determined and BFRE was nontoxic to mice. Phospholipase A2 and proteolytic activities induced by BjuV were inhibited in vitro by BFRE at all concentrations tested herein. BFRE (150 mg/kg) inhibited paw edema induced by BjuV (50 µg/animal), reducing total edema calculated by area under the curve, but carrageenan-induced paw edema was unchanged. Hemorrhagic and necrotizing actions of BjuV (50 µg/animal) were considerably decreased by BFRE treatment. Thus, BFRE blocked the toxic actions of B. jararacussu venom despite having no anti-inflammatory activity, which points to a direct inhibition of venom’s toxins, as demonstrated in the in vitro assays. The larger amounts of rutin found in BFRE may play a role in this inhibition, since 3′,4′-OH flavonoids are known inhibitors of phospholipases A2.

Epithelial cell migration is an essential response to enteric pathogens such as enteropathogenic Escherichia coli (EPEC). This study aimed to investigate the effects of EPEC infection on intestinal epithelial cell migration in vitro, as well as the involvement of type III secretion system (T3SS) and Rho GTPases. Crypt intestinal epithelial cells (IEC-6) were infected with EPEC strains (E2348/69, ΔescF, and the LDI001 strain isolated from a malnourished Brazilian child) and commensal E. coli HS. Wound migration and cell death assays were performed at different time-points. Transcription and expression of Rho GTPases were evaluated using real-time PCR and western blotting. Overall, EPEC E2348/69 reduced migration and increased apoptosis and necrosis levels compared to EPEC LDI001 and E. coli HS strains. Moreover, EPEC LDI001 impaired cell migration at a higher level than E. coli HS and increased necrosis after 24 hours compared to the control group. The different profiles of virulence genes between the two wild-type EPEC strains, characterized by the absence of espL and nleE genes in the LDI001, might explain the phenotypic results, playing significant roles on cell migration impairment and cell death-related events. Moreover, the type III secretion system is determinant for the inhibition of intestinal epithelial cell migration by EPEC 2348/69, as its deletion prevented the effect. Active Rac1 concentrations were increased in E2348/69 and LDI001-infected cells, while the T3SS-deficient strain did not demonstrate this activation. This study contributes with valuable insight to characterize the mechanisms involved in the impairment of intestinal cell migration induced by EPEC.

The decomposition of hydrogen peroxide was studied on Pd catalysts between 293 K and 313 K. The apparent activation energy value was calculated for all the catalysts and it varied between 27 and 55 kJ/mol. For all the catalysts tested, treatment with hydrogen resulted in a significant increase in the reaction rate, as well as a decrease in the apparent activation energy for the reaction. All the reactions were well represented by a first order rate law with respect to H2O2. The effect of the treatment with H2O2 was studied in successive reactions without catalyst exchange. A small deactivation was observed in the 5.0% Pd/AC and 0.5% Pd/AC catalysts after four H2O2 decomposition reactions.

Cinco vacas holandesas pluríparas, com cânulas no rúmen e no duodeno, foram distribuídas em delineamento de quadrado latino 5 x 5. As vacas foram submetidas a cinco rações experimentais contendo 40% de cana-de-açúcar, 60% de concentrado e cerca de 30% de amido. As rações diferiram quanto ao processamento ou à fonte principal do amido utilizado: milho grosseiramente moído, milho finamente moído, milho floculado a 310g/l, milho floculado a 360g/l ou raspa de mandioca. Não houve diferença (P>0,05) no consumo de matéria seca entre os tratamentos. A digestibilidade ruminal do amido foi maior na ração que continha raspa de mandioca. As digestibilidades ruminal da fibra em detergente neutro e da fibra em detergente ácido não diferiram entre os tratamentos. Os dados médios de pH ruminal se mantiveram acima de 6,0, exceto às 2 e às 4h após a alimentação com a dieta que continha raspa de mandioca. Não houve efeito significativo dos tratamentos sobre a concentração de ácidos graxos voláteis totais. O processo de floculação promoveu aumento da digestibilidade do amido do milho, em relação à moagem de forma grosseira. A digestibilidade ruminal do amido presente na raspa de mandioca foi maior do que a do milho, independentemente da forma de processamento utilizada.

Five multiparous lactating Holsteins cows, cannulated in the rumen and proximal duodenum, were used in a 5 x 5 latin square. Cows were fed a 40:60 forage: concentrate diet (40% fresh sugar cane and 60% concentrate). Diets were formulated to have 30% of starch and treatments were starch sources and ration processing forms: cracked corn, finely ground corn, flaked corn at 310g/l, flaked corn at 360g/l, or cassava scrapings. No difference (P>0.05) was observed among treatments for dry matter intake. Starch ruminal digestibility was higher for cassava scrapings treatment. NDF and ADF digestibility were similar among treatments. Average values of ruminal pH were above 6, except at 2 and 4h after feeding the cassava diet. There was no effect of treatment on concentrations of total volatile fatty acids. The flocculation process increased corn starch digestibility. Ruminal degradability of the cassava scrapings starch was higher than corn, without effect of processing form.