Intra-abdominal pressure (IAP) is closely related to breathing behavior during lifting. Abdominal muscles contribute to both IAP development and respiratory function. The purpose of this study was to examine whether spontaneous breath volume and IAP altered with increased isometric lifting effort, and to compare the effect of different abdominal muscle strengths on these parameters. Maximal IAP during the Valsalva maneuver (maxIAP) and maximal isometric trunk flexor strength were measured in 10 highly trained judo athletes (trained) and 11 healthy men (controls). They performed isometric lifting with 0 (rest), 30, 45, 60, 75, 90, and 100% of maximal lifting effort (MLE). Natural inspiratory and expiratory volumes were calculated from air-flow data immediately before and after the start of lifting. IAP, measured using an intra-rectal pressure transducer during lifting, was normalized by maxIAP (%maxIAP). Trained athletes had higher maxIAP and stronger trunk flexor muscles than controls. A significant main effect of lifting effort was found on %maxIAP and respiratory volume. An interaction (lifting effort by group) was found only for %maxIAP. No significant group main effect or interaction was found for respiratory volume. Inspiratory volume increased significantly from tidal volume to above 60 and 45% of MLE in trained athletes and controls, respectively. Expiratory volume decreased significantly from tidal volume at above 30% of MLE in both the groups. These results suggest that spontaneous breath volume and IAP development are coupled with increased lifting effort, and strong abdominal muscles can modify IAP development and inspiratory behavior during lifting.
The kynurenine (Kyn) pathway plays crucial roles in several inflammation-induced disorders such as depression. In this study, we measured Kyn and other related molecules in the blood plasma, brain, and urine of male C57BL/6J mice (B6) fed non-purified (MF) and semi-purified (AIN-93G and AIN-93M) standard rodent diets. Mice fed MF had increased plasma Kyn levels compared with those on AIN93-based diets, as well as decreased hippocampal Kyn levels compared with those fed AIN-93G. Previous studies showed that branched chain amino acids (BCAAs) suppress peripheral blood Kyn transportation to the brain, but plasma BCAA levels were not significantly different between the diet groups in our study. Urine metabolome analysis revealed that feed ingredients affected the excretion of many metabolites, and MF-fed mice had elevated excretion of kynurenic and quinolinic acids, pivotal metabolites in the Kyn pathway. Collectively, the level of critical metabolites in the Kyn pathway in the central and peripheral tissues was strongly affected by feed ingredients. Therefore, feed selection is a critical factor to ensure the reproducibility of experimental data in studies involving rodent models.
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