Effect and Mechanism of Armillaria mellea 07-22 Fermentation on the Degradation of Zearalenone

This study used Armillaria mellea 07-22 as the experimental strain to degrade zearalenone (ZEN) by fungal biological fermentation. The degradation effects of Armillaria mellea on ZEN were studied, including the degradation effects of different concentrations of ZEN by the strain and the effects of different culture time, culture temperature, initial pH value and inoculation amount on the degradation of ZEN by the strain. Then the degradation mechanism was explored, the degradation effects of mycelium, fermentation supernatant and cell contents on ZEN were analyzed, and the effects of different fermentation time, pH values, and metal ions on degradation of ZEN by fermentation supernatant were studied, and the correlation between degradation effect and laccase production activity of the strain was illustrated. The results showed that Armillaria mellea 07-22 had a good degradation effect on ZEN. When the ZEN concentration was 5 μg/mL, the optimal degradation conditions were culture time of 8 days, culture temperature of 27 ℃, initial pH of 7.0, and inoculation amount of 10%. At this time, the degradation rate of ZEN was 78.72%. The degradation rates of ZEN by mycelium, fermentation supernatant and cell contents were 47.42%, 37.05% and 13.08% respectively. The extracellular enzymes secreted by Am-07-22 were the main way to degrade ZEN, and the mycelium cells also had a certain adsorption effect on ZEN. In addition, the correlation between the degradation rate of ZEN by fermentation supernatant and laccase activity was 0.973, and Cu2+ had the best promoting effect on the degradation of ZEN by fermentation supernatant

Targeted Lipidomics and Inflammation Response to Six Weeks of Sprint Interval Training in Male Adolescents

Lipids play an important role in coordinating and regulating metabolic and inflammatory processes. Sprint interval training (SIT) is widely used to improve sports performance and health outcomes, but the current understanding of SIT-induced lipid metabolism and the corresponding systemic inflammatory status modification remains controversial and limited, especially in male adolescents. To answer these questions, twelve untrained male adolescents were recruited and underwent 6 weeks of SIT. The pre- and post-training testing included analyses of peak oxygen consumption (VO2peak), biometric data (weight and body composition), serum biochemical parameters (fasting blood glucose, total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triacylglycerol, testosterone, and cortisol), inflammatory markers, and targeted lipidomics. After the 6-week SIT, the serum C-reactive protein (CRP), interleukin (IL)-1β, IL-2, IL-4, IL-10, tumor necrosis factor (TNF)-α, and transforming growth factor (TGF)-β significantly decreased (p p p 1.2 or <1/1.2). The correlation analysis revealed that the changes in the inflammatory markers were closely correlated with the changes in some of the lipids, such as LPC, HexCer, and FFA. In conclusion, the 6-week SIT induced significant changes in the inflammatory markers and circulating lipid composition, offering health benefits to the population

Targeted lipidomics and inflammation response to six weeks of sprint interval training in male adolescents

Lipids play an important role in coordinating and regulating metabolic and inflammatoryprocesses. Sprint interval training (SIT) is widely used to improve sports performance and healthoutcomes, but the current understanding of SIT-induced lipid metabolism and the correspondingsystemic inflammatory status modification remains controversial and limited, especially in maleadolescents. To answer these questions, twelve untrained male adolescents were recruited andunderwent 6 weeks of SIT. The pre- and post-training testing included analyses of peak oxygenconsumption (VO2peak), biometric data (weight and body composition), serum biochemical pa-rameters (fasting blood glucose, total cholesterol, high-density lipoprotein cholesterol, low-densitylipoprotein cholesterol, triacylglycerol, testosterone, and cortisol), inflammatory markers, and tar-geted lipidomics. After the 6-week SIT, the serum C-reactive protein (CRP), interleukin (IL)-1β, IL-2,IL-4, IL-10, tumor necrosis factor (TNF)-α, and transforming growth factor (TGF)-β significantlydecreased (p &lt; 0.05), whereas IL-6 and IL-10/TNF-α significantly increased (p &lt; 0.05). In addition,the targeted lipidomics revealed changes in 296 lipids, of which 33 changed significantly (p &lt; 0.05,fold change &gt; 1.2 or &lt;1/1.2). The correlation analysis revealed that the changes in the inflammatorymarkers were closely correlated with the changes in some of the lipids, such as LPC, HexCer, andFFA. In conclusion, the 6-week SIT induced significant changes in the inflammatory markers andcirculating lipid composition, offering health benefits to the population