Genetic Fingerprint of Immunosuppression Following Half-marathon Running in Microarray Study

ABSTRACT Introduction: An acute bout of exhaustive exercise such as marathon or half-marathon running can interfere with immunity, reflected by transient immunosuppression and inflammation like reaction following the event. To gain more insights into these mechanisms, the capacity of whole blood cultures in profiling gene expression in response to endotoxin (LPS) was studied in athletes before, 30min after, 3h after and 24h after a half-marathon run. Methods: Four well trained men and 4 well trained women participated and gene expression patterns were assessed in LPS-stimulated (1h) and unstimulated whole blood using Affymetrix GeneChip microarrays. Results: exercise significantly altered several genes in LPS-stimualted and unstimulated blood cultures of male and female athletes. A row of genes with prominent anti-inflammatory function were strongly up-regulated in unstimulated cultures in both sexes (ARG-1, SOCS3, DUSP-1, BMX, GOS2, CD177, and GJB6). In the same cultures a row of highly inflammatory and apoptotic genes were down-regulated (Granzymes A-M-B-K-H, PRF1, SPON2, Granulysin, KLRF1, PLEKHF1). Some of these genes which were significantly up-or down-regulated in unstimulated cultures were also strongly regulated in LPS-stimulated cultures (GJB6, ARG-1, ORM2, KLRF1, TRA@///TRD@, Granzymes, SPON2). In addition, there were some strongly regulated genes which could only be detected in LPS-stimulated cultures but not in unstimulated cultures. Among these, TNIP3, PLAU, HIVEP1, and SLED were up-regulated and IFN-β, IFN-γ, L-12B, CXCL4. CXCL10 and TRAF1 were significantly down-regulated. Conclusion: there is a row of genes which are strongly regulated through exercise but can only be detected in (endotoxin) stimulated cultures. This is direct evidence showing that the response to pathogens is strongly down-regulated following prolonged exhaustive exercise through different ways

Comparison of Habitual and Maximal Gait Speed and their Impact on Sarcopenia Quantification in German Nursing Home Residents.

OBJECTIVES Sarcopenia is characterized by loss of muscle strength and muscle mass. The EWGSOP2 specifications include physical functioning determination for quantification of the sarcopenia severity. However, there is a lack in the use of habitual and maximal gait speed and their influence on sarcopenia quantification. We hypothesize differences in sarcopenia quantification using habitual and maximal gait speed. METHODS Sixty-six residents from five nursing homes were examined. Habitual and maximal gait speed were measured by 4-meter-walking-Test. McNemar-Test and χ2-test were used to identify quantification differences. Effect sizes of both gait speeds were calculated with Spearman's rank-correlation-coefficient. RESULTS Significant difference was identified for twenty-two residents in physical functioning classification by McNemar-Test (p<.001). χ2-Test identified a significant frequency distribution for sarcopenia categories between both gait speeds (χ2 (df2)=11.215, p=.004; Cramer's V=.412). Significant correlations (p<.05) were only shown for maximal gait speed in variables falls in the last three months (|rs|=.326), Barthel-Index (|rs|=.415), and SARC-F (|rs|=.335). CONCLUSIONS The use of habitual and maximal gait speed has a significant impact on sarcopenia quantification in nursing home residents. An adapted standardization in the EWGSOP2 specifications should follow

Medium Chain Acylcarnitines Dominate the Metabolite Pattern in Humans under Moderate Intensity Exercise and Support Lipid Oxidation

Background: Exercise is an extreme physiological challenge for skeletal muscle energy metabolism and has notable health benefits. We aimed to identify and characterize metabolites, which are components of the regulatory network mediating the beneficial metabolic adaptation to exercise