Early Season Hormonal and Biochemical Changes in Division I Field Hockey Players: Is Fitness Protective?

Walker, AJ, McFadden, BA, Sanders, DJ, Bozzini, BN, Conway, SP, and Arent, SM. Early season hormonal and biochemical changes in Division I field hockey players: is fitness protective? J Strength Cond Res 34(4): 975-981, 2020-The purpose was to evaluate changes in hormonal and biochemical markers as a result of the accumulated stress of the initial 4-week training block in field hockey players. Women's Division I field hockey players (N = 22; Mage = 19.7 ± 1.1 years) performed testing before the start of preseason (A1) that included body composition (%BF), vertical jump, and V[Combining Dot Above]O2max. Blood draws were conducted at A1 to assess creatine kinase (CK), iron (Fe), hemoglobin (HGB), hematocrit (HCT), percent saturation (%sat), total cortisol (TCORT), free cortisol (FCORT), interleukin-6 (IL-6), sex hormone-binding globulin (SHBG), prolactin (PRL), vitamin D (vitD), and thyroxine (T3). Blood draws were repeated 4 weeks later (A2). Athletes were monitored during this training block, which included 2 weeks of preseason and the first 2 weeks of the season, using heart rate monitors to determine energy expenditure (Kcal) and training load. There were significant disruptions in TCORT, FCORT, T3, CK, Fe, and SHBG (p < 0.05) from A1 to A2. V[Combining Dot Above]O2max accounted for 31% (p < 0.05) of the variance in TCORT and %BF accounting for an additional 20.1% (p < 0.05). V[Combining Dot Above]O2max accounted for 32.7% (p < 0.05) of the variance in FCORT. %BF accounted for 48.9% (p < 0.05) of the variance in T3. Kcal was positively correlated with V[Combining Dot Above]O2max (p < 0.05) and negatively correlated with %BF (p < 0.05). Athletes with higher V[Combining Dot Above]O2max and lower %BF may be capable of a higher work output and therefore more likely to experience increased physiological disruptions during intense training. The high-volume nature of preseason and differences in athlete fitness capabilities require coaches to manage players at an individual level to maintain athlete readiness.

Individual Observer Differences in the Use of Form and Motion to Perceive the Actor's Sex in Biological Motion Displays.

Recent research has shown that the perception of biological motion may be influenced by aspects of the observer's personality. In this study, we sought to determine how participant characteristics (including demographics, response inhibition, autism spectrum quotient, empathy, social anxiety, and motion imagery) might influence the use of form and motion to identify the actor's sex in biological motion displays. We varied the degree of form and motion in biological motion displays and correlated 76 young adult participants' performances for identifying the actor's sex in these varied conditions with their individual differences on variables of interest. Differences in the separate use of form and motion cues were predictive of participant performance generally, with use of form most predictive of performance. Female participants relied primarily on form information, while male participants relied primarily on motion information. Participants less able to visualize movement tended to be better at using form information in the biological motion task. Overall, our findings suggest that similar group level performances across participants in identifying the sex of the actor in a biological motion task may result from quite different individual processing.

Pleiotropic and novel phenotypes in the Drosophila gut caused by mutation of drop-dead.

Normal gut function is vital for animal survival, and deviations from such function can contribute to malnutrition, inflammation, increased susceptibility to pathogens, diabetes, neurodegenerative diseases, and cancer. In the fruit fly Drosophila melanogaster, mutation of the gene drop-dead (drd) results in defective gut function, as measured by enlargement of the crop and reduced food movement through the gut, and drd mutation also causes the unrelated phenotypes of neurodegeneration, early adult lethality and female sterility. In the current work, adult drd mutant flies are also shown to lack the peritrophic matrix (PM), an extracellular barrier that lines the lumen of the midgut and is found in many insects including flies, mosquitos and termites. The use of a drd-gal4 construct to drive a GFP reporter in late pupae and adults revealed drd expression in the anterior cardia, which is the site of PM synthesis in Drosophila. Moreover, the ability of drd knockdown or rescue with several gal4 drivers to recapitulate or rescue the gut phenotypes (lack of a PM, reduced defecation, and reduced adult survival 10-40 days post-eclosion) was correlated to the level of expression of each driver in the anterior cardia. Surprisingly, however, knocking down drd expression only in adult flies, which has previously been shown not to affect survival, eliminated the PM without reducing defecation rate. These results demonstrate that drd mutant flies have a novel phenotype, the absence of a PM, which is functionally separable from the previously described gut dysfunction observed in these flies. As the first mutant Drosophila strain reported to lack a PM, drd mutants will be a useful tool for studying the synthesis of this structure.

Molecular regulation of urea cycle function by the liver glucocorticoid receptor.

OBJECTIVE: One of the major side effects of glucocorticoid (GC) treatment is lean tissue wasting, indicating a prominent role in systemic amino acid metabolism. In order to uncover a novel aspect of GCs and their intracellular-receptor, the glucocorticoid receptor (GR), on metabolic control, we conducted amino acid and acylcarnitine profiling in human and mouse models of GC/GR gain- and loss-of-function. METHODS: Blood serum and tissue metabolite levels were determined in Human Addison's disease (AD) patients as well as in mouse models of systemic and liver-specific GR loss-of-function (AAV-miR-GR) with or without dexamethasone (DEX) treatments. Body composition and neuromuscular and metabolic function tests were conducted in vivo and ex vivo, the latter using precision cut liver slices. RESULTS: A serum metabolite signature of impaired urea cycle function (i.e. higher [ARG]:[ORN + CIT]) was observed in human (CTRL: 0.45 ± 0.03, AD: 1.29 ± 0.04; p < 0.001) and mouse (AAV-miR-NC: 0.97 ± 0.13, AAV-miR-GR: 2.20 ± 0.19; p < 0.001) GC/GR loss-of-function, with similar patterns also observed in liver. Serum urea levels were consistently affected by GC/GR gain- (∼+32%) and loss (∼-30%) -of-function. Combined liver-specific GR loss-of-function with DEX treatment revealed a tissue-autonomous role for the GR to coordinate an upregulation of liver urea production rate in vivo and ex vivo, and prevent hyperammonaemia and associated neuromuscular dysfunction in vivo. Liver mRNA expression profiling and GR-cistrome mining identified Arginase I (ARG1) a urea cycle gene targeted by the liver GR. CONCLUSIONS: The liver GR controls systemic and liver urea cycle function by transcriptional regulation of ARG1 expression.