The sustainability of VO2max: effect of decreasing the workload.

The study examined the maintenance of VO(2max) using VO(2max) as the controlling variable instead of power. Therefore, ten subjects performed three exhaustive cycling exercise bouts: (1) an incremental test to determine VO(2max) and the minimal power at VO(2max) (PVO(max)), (2) a constant-power test at PVO(max) and (3) a variable-power test (VPT) during which power was varied to control VO(2) at VO(2max). Stroke volume (SV) was measured by impedance in each test and the stroke volume reserve was calculated as the difference between the maximal and the average 5-s SV.

NMR metabolomics for assessment of exercise effects with mouse biofluids.

Exercise modulates the metabolome in urine or blood as demonstrated previously for humans and animal models. Using nuclear magnetic resonance (NMR) metabolomics, the present study compares the metabolic consequences of an exhaustive exercise at peak velocity (Vp) and at critical velocity (Vc) on mice. Since small-volume samples (blood and urine) were collected, dilution was necessary to acquire NMR spectra.

Cardiac output and performance during a marathon race in middle-aged recreational runners.

Purpose: Despite the increasing popularity of marathon running, there are no data on the responses of stroke volume (SV) and cardiac output (CO) to exercise in this context. We sought to establish whether marathon performance is associated with the ability to sustain high fractional use of maximal SV and CO (i.e, cardiac endurance) and/or CO, per meter (i.

A new incremental test for VO₂max accurate measurement by increasing VO₂max plateau duration, allowing the investigation of its limiting factors.

The purpose of this study was to (1) validate a new exercise protocol for accurate measurement of VO(2max) by obtention of a VO(2max) plateau for all subjects fit and unfit (2) test the hypothesis that VO(2max) plateau duration is not correlated with VO(2max) and (3) verify that limiting factors of VO(2max) plateau duration are different from those of VO(2max) amplitude. Therefore, 14 subjects performed two incremental cycling tests: (1) a classical incremental test (CIT) to determine VO(2max), the power at VO(2max) (PVO(2max)) and at the lactate threshold (PLT) (2) a new incremental test (NIT) in which the power was decreased just after the subject reached VO(2max). During both protocols, heart rate, stroke volume, cardiac output, the arterio-venous difference and the oxygen blood saturation were recorded.