Maximal aerobic capacity (VO) and running economy (RE) are markers of running performance. A valid evaluation of RE may occur through allometric scaling of body mass (alloVO; ml kg min), energy cost (EC; kcal kg km), or percent of VO (%VO). Little is known about physiological changes that occur in competitive runners over a marathon training cycle. The VDOT score, incorporating VO and RE, enables comparison of race performances under different temperature conditions. This study's purpose was to determine whether VO and measures of RE change with marathon training, and to evaluate the relationship between these variables and VDOT. Eight runners (age 34±2 years; marathon <3:00 males, <3:30 females; five females) completed treadmill marathon-intensity-effort (MIE) and VO tests at 10 and 1-2 weeks pre-marathon. Body composition (%BF) was determined using hydrostatic weighing. Paired t-tests were used to compare pre- and post-training values. The alpha level for significance was set at 0.05. Body fat decreased from 18.7±1.5% to 16.7±1.6%, VO increased from 51.6±2.4 to 63.9±1.1 ml kg min, and %VO during the MIE decreased from 82.1±2.0 to 72.3±3.2% (p < 0.05 for all). VDOT was significantly associated with alloVO (r = -0.779, p = 0.039) but not with VO (r = 0.071, p = 0.867). Experienced competitive runners may increase VO and decrease %BF after a marathon-specific training cycle. The decrease in %VO in a MIE is likely due to a higher VO, as other measures of RE did not change significantly. In this cohort, alloVO was negatively correlated with race performance.
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http://dx.doi.org/10.14198/jhse.2020.151.08 | DOI Listing |
Eur J Appl Physiol
January 2025
Department of Medicine, University of Udine, P. le Kolbe 4 - 33100, Udine, Italy.
Purpose: The aim of this study was to investigate the influence of prolonged aerobic exercise on cardiac, muscular and renal inflammatory markers in a group of trained obese men.
Methods: Seventeen men (aged 40 ± 6 years; body mass index [BMI] 31.3 ± 2.
Cells
December 2024
Workgroup Endocrinology of Farm Animals, Research Institute for Farm Animal Biology (FBN), 18196 Dummerstorf, Germany.
Metabolic flexibility describes the capability to switch between oxidative fuels depending on their availability during diet or exercise. In a previous study, we demonstrated that in response to training, marathon (DUhTP) mice, paternally selected for high treadmill performance, are metabolically more flexible than unselected control (DUC) mice. Since exercise-associated metabolic flexibility can be assessed by indirect calorimetry or partially by circulating lactate concentrations, we investigated these parameters in DUhTP and DUC mice.
View Article and Find Full Text PDFBMC Cardiovasc Disord
January 2025
Department of Ultrasonography, Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Background: Long-term endurance training is associated with structural, functional, and biochemical markers of cardiac dysfunction in highly trained athletes. Many studies have focused on structural changes in the right ventricle (RV) and few have examined functional adaptation of the right ventricle. This meta-analysis aims to compare the changes in right ventricular systolic function between endurance athletes and controls before and after exercise using speckle tracking echocardiography (STE).
View Article and Find Full Text PDFSci Rep
January 2025
Department of Physical Education, States University of Pará, Pará, Brazil.
It is well known that elite athletes of specific ethnicities and/or nationalities dominate certain sports disciplines (e.g., East Africans in marathon running).
View Article and Find Full Text PDFAlzheimers Dement (N Y)
November 2024
Department of Psychiatry, Harvard Medical School Massachusetts General Hospital Boston Massachusetts USA.
Objective: Physical activity (PA) has been linked to reduced Alzheimer's disease (AD) risk. However, less is known about its effects in the AD preclinical stage. We aimed to investigate whether greater PA was associated with lower plasma biomarkers of AD pathology, neural injury, reactive astrocytes, and better cognition in individuals with autosomal-dominant AD due to the presenilin-1 E280A mutation who are virtually guaranteed to develop dementia.
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