The pre-test subjects performed an incremental exercise on a treadmill (LT test), which consisted of 5-min stages with 30 s breaks between stages. The first stage was started at 1.0 m∙s−1, with increments of 0.5 m∙s−1 every 5 min. The criteria for ending testing were a blood lactate concentration over 4 mmol∙L−1 after each running speed or until volitional exhaustion [12 ,16 (link),37 (link)]. After four weeks of LIE, the same set-up was used for the post-test. HR and jogging/running speed at the 1.5, 2.0, and 4.0 mmol∙L−1 blood lactate concentration levels (La) were estimated using a mathematical model of the interpolation that has previously been explained in detail [16 (link),41 (link),42 (link),43 (link)]. Delta (∆) jogging/running speed and ∆HR at the 1.5, 2.0, and 4.0 mmol∙L−1 La between pre- and post-testing were calculated (S1.5, S2, S4, ∆S1.5, ∆S2, ∆S4 and HR1.5, HR2, HR4, ∆HR1.5, ∆HR2, ∆HR4). The HR of all subjects was recorded using HR telemetry (H10 sensor, Polar Electro, Finland). The mean value of HR over the last 30 s of each stage was determined for statistical analysis. Capillary blood sampling for lactate analysis was taken from the earlobe (0.2 µL) immediately after each 5-min stage. All blood lactate levels were determined by an enzymatic-amperometric method (Lactate Scout 4, EKF-diagnostics GmbH, Germany) [44 (link),45 (link)].
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