1,392 research outputs found

    A Validation Study of a Noninvasive Lactate Threshold Device

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    International Journal of Exercise Science 12(2): 221-232, 2019. The lactate threshold is considered a key marker of endurance exercise performance and identification of this threshold is important in writing an exercise training program. Unfortunately, assessment of the lactate threshold has traditionally required venous or capillary blood samples and a specialized meter to assess blood lactate concentrations. Recently, a consumer grade, non-invasive device was developed to determine muscle oxygenation and estimate the lactate threshold. Purpose: The aim of this study was to assess the validity of a noninvasive lactate threshold device (NID) to determine lactate threshold heart rate (LTHR). Methods: Twenty-one recreational athletes (14 females, 39 ± 7 years, 29.1 ± 5.2% fat, 37.8 ± 6.0 ml·kg-1·min-1; 7 males, 42 ± 9 years, 16.8 ± 2.2% fat, 45.9 ± 6.4 ml·kg-1·min-1) completed a personalized graded exercise test on a treadmill. All participants wore the NID and blood lactate samples were taken at the end of 3-minute stages. LTHR was then calculated using two traditional methods (4 mmol/L and \u3e1 mmol/L increase) and compared against the same heart rate values calculated by the NID. Results: No significant differences (p = .87) were found in LTHR between the NID and the traditional lactate methods (NID: 167 ± 9 bpm, 4 mmol/L: 167 ± 12 bpm, \u3e1 mmol/L: 167 ± 12 bpm). Conclusions: This study provides preliminary support for the validity of the NID for estimation of LTHR

    Comparison of Post-Activation Potentiating Stimuli on Jump and Sprint Performance

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    Post-activation potentiation (PAP) is a phenomenon characterized by improved muscle performance based on the previous contractile activity of the muscle. The purpose of this study was to determine the effect of different potentiating stimuli on jump and sprint performance in 13 resistance trained, college-aged men and women. After determining back squat 1 repetition max, subjects returned for testing on separate days to complete one of four interventions (dynamic resistance, weighted plyometric, isometric, or control) in a randomized order. A standardized warmup was performed, followed by a baseline countermovement jump (CMJ) and 20m sprint. Following warm-up and baseline measurements, subjects performed one of the four experimental conditions. CMJ and 20m sprint measurements were completed again at 20-seconds, 4, 8, 12, 16, and 20-minutes. Results revealed significantly faster 0-20m sprint times (p \u3c .05) at the 4, 8, 12, 16, and 20-minute time points compared to baseline and 20-second time points. Significantly faster 0-20m sprint times (p \u3c .05) were also shown for the squat intervention compared to control at 4-minutes, the plyometric and squat intervention compared to control at 8-minutes, the isometric intervention compared to control at 12 and 16- minutes, and the isometric intervention compared to the squat at 20-minutes. These findings indicate that while all PAP stimuli utilized can be effective at improving sprint performance, specific optimal time points may exist

    Attempting to Acutely Manipulate Ground Contact Time Imbalances Impairs Running Economy

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    Running economy (RE) is a key performance determinant. Biomechanical markers have been linked to RE, including ground contact time (GCT), cadence, and vertical oscillation (VO). Recently, we showed a strong relationship between GCT imbalances and RE. Because these markers can be tracked real-time with consumer-wearable devices, runners now have access to instant feedback concerning their mechanics. PURPOSE: Determine if attempting to correct GCT imbalances real-time alters mechanics and RE. METHODS: 7 recreational runners (38 ± 15 years, 24.7 ± 2.8 kg/m2, 5 male) completed 2, 10-minute running trials (9.65 km/hr) on separate days. For both trials, subjects ran with a heart rate (HR) monitor/watch that measured GCT, GCT imbalances, cadence, and VO. For the control (CT) trial, subjects were not permitted to receive feedback from the watch. During the feedback (FB) trial, the watch was set to display GCT imbalances, and subjects were prompted every 20-30 seconds to monitor/attempt to correct any imbalances. Both trials were preceded by a dynamic warmup and 5-minute jog. For the FB trial warmup, subjects were acclimated to the watch and allowed to experiment with manipulating their GCT imbalances. VO2 was monitored continuously throughout each 10-minute trial, and average values from 6 to 9 minutes were determined for each trial. Average values for all running biomechanical variables were calculated from 0.5 minutes to 9.5 minutes. Comparisons between trials were made with a dependent sample t-test. RESULTS: The FB trial elicited a significantly higher (p = .011) working VO2 (35.5 ± 1.6 ml/kg/min) compared to the CT trial (33.4 ± 1.8 ml/kg/min). There were no other significant differences between trials for the other measured variables. Average values for each variable by trial were as follows: RER (CT: .91 ± .04; FB: .92 ± .05), HR (CT: 159 ± 26 bpm; FB: 163 ± 24 bpm), GCT % difference (CT: 1.69 ± .67%; FB: 1.70 ± 1.70%), GCT absolute difference (CT: 9 ± 3 ms; FB: 8 ± 7 ms), GCT (CT: 272 ± 26 ms; FB: 268 ± 31 ms), Cadence (CT: 165 ± 9 steps/min; FB: 167 ± 9 steps/min); VO (CT: 9.3 ± 2.0 cm; FB: 9.2 ± 1.9 cm), VO ratio (CT: 9.5 ± 1.6 cm/m; FB: 9.5 ± 1.6 cm/m). CONCLUSIONS: Acutely attempting to correct GCT imbalances did not result in improved mechanics and actually impaired RE. Altering mechanics based on real-time feedback from consumer-wearable devices may impair performance in the short term. Given that GCT imbalances have been linked to impaired RE, future research should determine how to better correct these imbalances rather than attempting to acutely manipulate them

    A biophysical model of cell adhesion mediated by immunoadhesin drugs and antibodies

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    A promising direction in drug development is to exploit the ability of natural killer cells to kill antibody-labeled target cells. Monoclonal antibodies and drugs designed to elicit this effect typically bind cell-surface epitopes that are overexpressed on target cells but also present on other cells. Thus it is important to understand adhesion of cells by antibodies and similar molecules. We present an equilibrium model of such adhesion, incorporating heterogeneity in target cell epitope density and epitope immobility. We compare with experiments on the adhesion of Jurkat T cells to bilayers containing the relevant natural killer cell receptor, with adhesion mediated by the drug alefacept. We show that a model in which all target cell epitopes are mobile and available is inconsistent with the data, suggesting that more complex mechanisms are at work. We hypothesize that the immobile epitope fraction may change with cell adhesion, and we find that such a model is more consistent with the data. We also quantitatively describe the parameter space in which binding occurs. Our results point toward mechanisms relating epitope immobility to cell adhesion and offer insight into the activity of an important class of drugs.Comment: 13 pages, 5 figure

    Ground Contact Time Imbalances Strongly Related to Impaired Running Economy

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    Running economy (RE) is defined as the oxygen consumption (VO2) or caloric unit cost required to move at a specific velocity and is an important performance marker. Ground contact time (GCT) has been associated with RE; however, it has not been established how GCT imbalances between feet impact RE. Purpose: Determine the relationship between cadence, GCT, and GCT imbalances and RE. Methods: 11 NCAA Division I distance runners (7 male) completed a graded exercise test on a treadmill to determine lactate threshold (LT) and VO2max. Body composition was also assessed via DEXA. Subjects ran with a heart rate monitor capable of measuring cadence, GCT, and GCT balance between feet. VO2 and respiratory exchange ratio were recorded over the last minute of the 5-minute stages. RE expressed as caloric unit cost (kcal·kg-1· km-1) was calculated for the stage determined to be just below the LT (prior to \u3e 4mmol/L) and was correlated with cadence, GCT, and GCT imbalance by Pearson correlations. Results: Pearson correlations between RE and the running dynamics measures were as follows: cadence (r = -.444, p = .171), GCT (r = .492, p = .125), GCT Imbalance (r = .808, p \u3c .005). An independent t-test revealed greater (p = .023) leg lean mass imbalances in runners with larger GCT imbalances compared to runners with smaller GCT imbalances. Conclusion: GCT imbalances are strongly related to impaired RE. Future research should determine how to improve GCT imbalances and if doing so improves RE

    Evolutionary relationships in Panicoid grasses based on plastome phylogenomics (Panicoideae; Poaceae)

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    Background: Panicoideae are the second largest subfamily in Poaceae (grass family), with 212 genera and approximately 3316 species. Previous studies have begun to reveal relationships within the subfamily, but largely lack resolution and/or robust support for certain tribal and subtribal groups. This study aims to resolve these relationships, as well as characterize a putative mitochondrial insert in one linage. Results: 35 newly sequenced Panicoideae plastomes were combined in a phylogenomic study with 37 other species: 15 Panicoideae and 22 from outgroups. A robust Panicoideae topology largely congruent with previous studies was obtained, but with some incongruences with previously reported subtribal relationships. A mitochondrial DNA (mtDNA) to plastid DNA (ptDNA) transfer was discovered in the Paspalum lineage. Conclusions: The phylogenomic analysis returned a topology that largely supports previous studies. Five previously recognized subtribes appear on the topology to be non-monophyletic. Additionally, evidence for mtDNA to ptDNA transfer was identified in both Paspalum fimbriatum and P. dilatatum, and suggests a single rare event that took place in a common progenitor. Finally, the framework from this study can guide larger whole plastome sampling to discern the relationships in Cyperochloeae, Steyermarkochloeae, Gynerieae, and other incertae sedis taxa that are weakly supported or unresolved.Fil: Burke, Sean V.. Northern Illinois University; Estados UnidosFil: Wysocki, William P.. Northern Illinois University; Estados UnidosFil: Zuloaga, Fernando Omar. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Botánica Darwinion. Academia Nacional de Ciencias Exactas, Físicas y Naturales. Instituto de Botánica Darwinion; ArgentinaFil: Craine, Joseph M.. Jonah Ventures; Estados UnidosFil: Pires, J. Chris. University of Missouri; Estados UnidosFil: Edger, Patrick P.. Michigan State University; Estados UnidosFil: Mayfield Jones, Dustin. Donald Danforth Plant Science Center; Estados UnidosFil: Clark, Lynn G.. Iowa State University; Estados UnidosFil: Kelchner, Scot A.. University of Idaho; Estados UnidosFil: Duvall, Melvin R.. Northern Illinois University; Estados Unido

    Trends in marine survival of Atlantic salmon populations in eastern Canada

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    Declines in wild Atlantic salmon (Salmo salar) abundance throughout the north Atlantic are primarily attributed to decreases in survival at sea. However, comparing trends in marine survival among populations is challenging as data on both migrating smolts and returning adults are sparse and models are difficult to parameterize due to their varied life histories. We fit a hierarchical Bayesian maturity schedule model to data from seven populations in eastern Canada to estimate numbers of out-migrating smolts, survival in the first and second year at sea, and the proportion returning after 1 year. Trends in survival at sea were not consistent among populations; we observe positive, negative, and no correlations in these, suggesting that large-scale patterns of changes in marine survival are not necessarily representative for individual populations. Variation in return abundances was mostly explained by marine survival in the first winter at sea in all but one population. However, variation in the other components were not negligible and their relative importance differed among populations. If salmon populations do not respond in a uniform manner to changing environmental conditions throughout their range, future research initiatives should explore why.publishedVersio

    Resolving deep relationships of PACMAD grasses: a phylogenomic approach

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    Background Plastome sequences for 18 species of the PACMAD grasses (subfamilies Panicoideae, Aristidoideae, Chloridoideae, Micrairoideae, Arundinoideae, Danthonioideae) were analyzed phylogenomically. Next generation sequencing methods were used to provide complete plastome sequences for 12 species. Sanger sequencing was performed to determine the plastome of one species, Hakonechloa macra, to provide a reference for annotation. These analyses were conducted to resolve deep subfamilial relationships within the clade. Divergence estimates were assessed to determine potential factors that led to the rapid radiation of this lineage and its dominance of warmer open habitats. Results New plastomes were completely sequenced and characterized for 13 PACMAD species. An autapomorphic ~1140 bp deletion was found in Hakonechloa macra putatively pseudogenizing rpl14 and eliminating rpl16 from this plastome. Phylogenomic analyses support Panicoideae as the sister group to the ACMAD clade. Complete plastome sequences provide greater support at deep nodes within the PACMAD clade. The initial diversification of PACMAD subfamilies was estimated to occur at 32.4 mya. Conclusions Phylogenomic analyses of complete plastomes provides resolution for deep relationships of PACMAD grasses. The divergence estimate of 32.4 mya at the crown node of the PACMAD clade coincides with the Eocene-Oligocene Transition (EOT). The Eocene was a period of global cooling and drying, which led to forest fragmentation and the expansion of open habitats now dominated by these grasses. Understanding how these grasses are related and determining a cause for their rapid radiation allows for future predictions of grassland distribution in the face of a changing global climate.This work was supported in part by the Plant Molecular Biology Center, the Department of Biological Sciences at Northern Illinois University and the National Science Foundation under Grant Numbers DEB-1120750 to LGC, DEB-1120856 to SAK and DEB-1120761 to MRD.This article is made openly accessible in part by an award from the Northern Illinois University Libraries’ Open Access Publishing Fund
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