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The experiment was conducted to study the effects of the addition of encapsulated and nonencapsulated compound acidifiers in a diet based on maize-soyabean meal-extruded soyabean on gastrointestinal pH, growth performance, villus height and crypt depth of jejunum, intestinal digestive enzymes activities, microbial population and intestinal mucosal secretory immunoglobulin A in weaning piglets. Sixty-four 28-day-old, crossbred piglets (Landrace×Large White), weighing an average of 7.00 ± 0.10 kg, were randomly assigned to four treatments with four replicates and four piglets (2 male and 2 female) per pen, according to single-factor design principle. The feeding trial lasted 35 days. The results showed that encapsulated compound acidifiers significantly reduced the gastrointestinal pH (P<0.01), and improved the average daily gain and the feed conversion ratio (P<0.05), but they had no significant effect on the average daily feed intake. In addition, encapsulated compound acidifiers significantly increased the ratio between the villus height and crypt depth of jejunum (P<0.01), and stimulated the sucrase activity and lactase activity (P<0.05) as well; during the later weaning period, encapsulated compound acidifiers significantly increased the counts of Lactobacillus and decreased the counts of Escherichia coli in the caecum and the colon (P<0.01); it was also noted that there was an insignificant tendency of lower secretion of intestinal mucosal secretory IgA (P>0.05). These results indicate that the encapsulated compound acidifiers improve the intestinal morphology and function by reducing the gastrointestinal pH, so as to enhance the intestinal adaptation and immunity, and consequently improve the growth performance of weaning piglets.
We studied the relationship between hydrogen peroxide (H2O2) and MEK1/2 in jasmonic acid (JA) signaling in regulating the redox states of ascorbate (AsA) and glutathione (GSH). JA increased H2O2 production, MEK1/ 2 phosphorylation, the transcription levels and activities of AsA and GSH metabolic enzymes (APX, GR, DHAR, MDHAR, GalLDH and γ-ECS), AsA and GSH contents, and the redox states of AsA and GSH (ratios of AsA/DHA and GSH/GSSG). Above increases were inhibited by applications of H2O2 synthesis inhibitor DPI and scavenger DMTU. However, applications of MEK1/2 inhibitors PD98059 and U0126 had no significant effect on JA-induced H2O2 production. Treatments with exogenous H2O2 also increased MEK1/2 phosphorylation, the transcription levels and activities of AsA and GSH metabolic enzymes, AsA and GSH contents, and the redox states of AsA and GSH. Above increases except the transcription level and activity of γ-ECS were all suppressed by pretreatments with PD98059 and U0126. Our results suggested that Jainduced H2O2 could trigger MEK1/2 phosphorylation and activation leading to the upregulation of AsA and GSH metabolic enzymes.
Whereas strong antioxidant properties of spermine have been reported mostly in in vitro studies, there is lack of the in vivo studies on spermine influence conducted on mammals. The main objective of this study was to investigate the effects of different doses of spermine and the period of its supplementation on the liver and spleen antioxidant capacity in weaned rats. Male Sprague-Dawley rats at the age of 19 days received intragastrically spermine at the dose of 0.2 or 0.4 μmol · g-1 body weight for 3 or 7 days, respectively. Control rats received saline in analogical way. It was found that liver anti-superoxide anion (ASA) capacity, catalase (CAT) activity, glutathione (GSH) content and total antioxidant capacity (T-AOC) were increased in group supplemented with higher dose of spermine after 3 days, and anti-hydroxy radical (AHR) capacity was increased when treatment lasted for 7 days. In the spleen the higher spermine dose supplementation increased ASA capacity and total superoxide dismutase (T-SOD) activity (after 3 and 7 days), AHR capacity (after 7 days) and T-AOC (after 3 days) in comparison to the corresponding control groups (P < 0.05). Only in the spleen the lower spermine dose reduced lipid peroxidation level and increased CAT activity and GSH content regardless treatment duration (P < 0.05). The obtained results suggest that spermine supplementation can improve the antioxidant properties of the liver and spleen of weaned rats in a dose-, time- and tissue-dependent manner.
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