This study examined the effects of acute hypoxia on maximal and explosive torque and fatigability in knee extensors of skiers. Twenty-two elite male alpine skiers performed 35 maximal, repeated isokinetic knee extensions at 180°s-1 (total exercise duration 61.25 s) in normoxia (NOR, FiO2 0.21) and normobaric hypoxia (HYP, FiO2 0.13) in a randomized, single-blind design. Peak torque and rate of torque development (RTD) from 0 to 100 ms and associated Vastus Lateralis peak EMG activity and rate of EMG rise (RER) were determined for each contraction. Relative changes in deoxyhemoglobin concentration of the VL muscle were monitored by near-infrared spectroscopy. Peak torque and peak EMG activity did not differ between conditions and decreased similarly with fatigue (p < 0.001), with peak torque decreasing continuously but EMG activity decreasing significantly after 30 contractions only. Compared to NOR, RTD, and RER values were lower in HYP during the first 12 and 9 contractions, respectively (both p < 0.05). Deoxyhemoglobin concentration during the last five contractions was higher in HYP than NOR (p = 0.050) but the delta between maximal and minimal deoxyhemoglobin for each contraction was similar in HYP and NOR suggesting a similar muscle O2 utilization. Post-exercise heart rate (138 ± 24 bpm) and blood lactate concentration (5.8 ± 3.1 mmol.l-1) did not differ between conditions. Arterial oxygen saturation was significantly lower (84 ± 4 vs. 98 ± 1%, p < 0.001) and ratings of perceived exertion higher (6 ± 1 vs. 5 ± 1, p < 0.001) in HYP than NOR. In summary, hypoxia limits RTD via a decrease in neural drive in elite alpine skiers undertaking maximal repeated isokinetic knee extensions, but the effect of hypoxic exposure is negated as fatigue develops. Isokinetic testing protocols for elite alpine skiers should incorporate RTD and RER measurements as they display a higher sensitivity than peak torque and EMG activity.
Purpose To determine whether isokinetic muscle recovery following ACLR using a hamstring tendon (HT) would be equivalent (non-inferior) in knees that had high-grade pivot-shift and adjuvant modified Lemaire procedure versus knees that had minimal pivot-shift and no adjuvant modified Lemaire procedure. Methods We evaluated 96 consecutive patients that underwent primary ACLR. Nine were excluded because of contralateral knee injury, and of the remaining 87, ACLR was performed stand-alone in 52 (Reference group), and with a Lemaire procedure in 35 (Lemaire group) who had high-grade pivot-shift, age < 18, or genu recurvatum > 20°. At 6 months, isokinetic tests were performed at 240°/s and 90°/s to calculate strength deficits of hamstrings (H) and quadriceps (Q). At 8 months, patients were evaluated using IKDC, Lysholm, and Tegner scores. Results Compared to the Reference group, the Lemaire group were younger (23.0 ± 2.5 vs 34.2 ± 10.5, p = 0.021) with a greater proportion of males (80% vs 56%, p < 0.001). The Lemaire group had no complications, but the Reference group had one graft failure and one cyclops syndrome. Strength deficits at 240°/s and at 90°/s were similar in both groups, but mixed H/Q ratios were lower for the Lemaire group (1.02 ± 0.19 vs 1.14 ± 0.24, p = 0.011). IKDC and Lysholm scores were similar in both groups, but Tegner scores were higher in the Lemaire group (median, 6.5 vs 6.0, p = 0.024). Conclusions ACLR with a modified Lemaire procedure for knees with rotational instability grants equivalent isokinetic muscle recovery as stand-alone ACLR in knees with no rotational instability. For ACL-deficient knees with high-grade pivot-shift, a Lemaire procedure restores rotational stability without compromising isokinetic muscle recovery. Study design Level III, comparative study.
Although the benefits of physical exercise to preserve bone quality are now widely recognized, the intimate mechanisms leading to the underlying cell responses still require further investigations. Interval training running, for instance, appears as a generator of impacts on the skeleton, and particularly on the progenitor cells located in the bone marrow. Therefore, if this kind of stimulus initiates bone cell proliferation and differentiation, the activation of a devoted signaling pathway by mechano-transduction seems likely. This study aimed at investigating the effects of an interval running program on the appearance of the zinc finger protein FHL2 in bone cells and their anatomical location. Twelve 5-week-old male Wistar rats were randomly allocated to one of the following groups (n = 6 per group): sedentary control (SED) or high-intensity interval running (EX, 8 consecutive weeks). FHL2 identification in bone cells was performed by immuno-histochemistry on serial sections of radii. We hypothesized that impacts generated by running could activate, in vivo, a specific signaling pathway, through an integrin-mediated mechano-transductive process, leading to the synthesis of FHL2 in bone marrow cells. Our data demonstrated the systematic appearance of FHL2 (% labeled cells: 7.5%, p < 0.001) in bone marrow obtained from EX rats, whereas no FHL2 was revealed in SED rats. These results suggest that the mechanical impacts generated during high-intensity interval running activate a signaling pathway involving nuclear FHL2, such as that also observed with dexamethasone administration. Consequently, interval running could be proposed as a non-pharmacological strategy to contribute to bone marrow cell osteogenic differentiation.
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