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OP-SM03 Sports Medicine 3<br />

DISCUSSION: The results <strong>of</strong> this study showed that vigorous but relatively short late-night exercise performed 2-2.5 hours before bed time<br />

affects cardiac autonomic control especially during the first hours <strong>of</strong> sleep. However, objective and subjective sleep quality may be even<br />

enhanced after exercise compared to control condition. We conclude that this kind <strong>of</strong> exercise procedure has minor effects on the essential<br />

recovery process during sleep.<br />

ROLE OF STRENGTH TRAINING IN ENDURANCE RUNNERS DURING PREPARATORY, MAXIMAL VERSUS EXPLOSIVE,<br />

AND REDUCED STRENGTH TRAINING PERIODS.<br />

TAIPALE, R.S., GITONGA, D., WALKER, S., NUMMELA, A., VESTERINEN, V., MIKKOLA, J., HÄKKINEN, K.<br />

UNIVERSITY OF JYVÄSKYLÄ, KIHU-RESEARCH INSTITUTE FOR OLYMPIC SPORTS<br />

Strength (STR) and endurance (END) training produce divergent adaptations and are <strong>of</strong>ten performed concurrently. An interference effect<br />

(1) between STR and END training is <strong>of</strong>ten related to high intensity/volume and long duration <strong>of</strong> training, but it is possible for concurrent<br />

training to lead to increased STR and END performances even in endurance athletes (2). A reduction in training stimulus leads to a reversal<br />

in adaptations as demonstrated by decreased activation and STR <strong>of</strong> detrained muscles (3).<br />

Twenty-eight male recreational END runners (mean±SD, age 35.4±6.8yrs, height 180±5.3cm, body mass 79.3±7.5kg) were divided into<br />

three STR training groups: maximal (M=11), explosive (E=10) and circuit training (C=7). Within these groups, subjects completed 6 weeks <strong>of</strong><br />

common preparatory STR training (PRE) and then a specific 8-week STR training intervention (STI) followed by 14 weeks <strong>of</strong> intentionally<br />

reduced strength training and increased endurance training (RST). STR training (including at least two exercises for leg extensors) occurred<br />

on average 1.3±.02, 1.5±.03 and 0.5±.03 times per week in each training period, respectively, while END training volume (running<br />

km) increased progressively throughout the study. Concentric leg press strength (1RM), jumping power (CMJ), muscle activation (EMG <strong>of</strong> VL<br />

+ VM) and END performance (vVO2, VO2MAX, running economy (RE)) were measured prior to PRE (-6), at 0, 4 and 8 weeks <strong>of</strong> STI and<br />

after RST (+14).<br />

During PRE and STI, 1RM improved significantly in all groups peaking at 4 (7.7, 3.2 and 6.4% in M, E and C from -6, respectively), while<br />

significant gains in CMJ peaked at 8. Gains in 1RM were accompanied by increased EMG <strong>of</strong> VL+VM in M and E (p=0.027 and 0.002) but<br />

not in C. VO2max increased only in M from -6 to 8 (4.3%), vVO2 improved significantly in all groups from -6 to 8 and RE in E improved<br />

significantly by 2.4%. Following RST, progressive decreases were observed in 1RM, CMJ and EMG which were significant in 1RM and EMG<br />

<strong>of</strong> M (p=0.002 and 0.038). However, significant increases in vVO2 <strong>of</strong> M and E (4.7 and 2.4%), RE <strong>of</strong> M (7.7%) as well as some gains (n.s.) in<br />

VO2max continued in M and E.<br />

Both M and E STR training performed concurrently with high volume END training led to increases in 1RM, CMJ and EMG but strength<br />

development plateaued indicating some interference over a prolonged period. Nevertheless, these neuromuscular improvements were<br />

accompanied by progressive gains in VO2max, vVO2 and RE. RST resulted in decreases in 1RM, CMJ and EMG; however, vVO2 and RE<br />

continued to improve in M and E. Adaptations to ST were maintained to some extent, since 1RM, CMJ and EMG did not fall below starting<br />

values. Thus, improved neuromuscular performance and increased preparedness for an increase in running volume due to STR enabled<br />

subjects to improve END performance.<br />

1. Hickson RC Eur J Appl Physiol. 45: 255-263, 1980.<br />

2. Mikkola J et al. J Strength Cond Res. 21:613-620, 2007.<br />

3. Häkkinen K Crit Rev Phys Rehab Med. 6:161-198, 1994.<br />

10:15 - 11:45<br />

Oral presentations<br />

OP-SM03 Sports Medicine 3<br />

EFFECT OF NSAID ON HUMAN SKELETAL MUSCLE SATELLITE CELLS FOLLOWING ECCENTRIC EXERCISE<br />

MIKKELSEN, U.R., MACKEY, A.L., HELMARK, I.C., SKOVGAARD, D., KJÆR, M., LANGBERG, H.L.<br />

INSTITUTE OF SPORTS MEDICINE COPENHAGEN, BISPEBJERG HOSPITAL, DK-2400 COPENHAGEN NV, DENMARK<br />

Introduction: Satellite cells – the stem cells <strong>of</strong> skeletal muscle – are essential for skeletal muscle adaptation to exercise and for muscle<br />

regeneration. They contribute to hypertrophy by providing new myonuclei and assist in repair <strong>of</strong> damaged muscle fibre segments. Nonsteroidal<br />

anti-inflammatory drugs (NSAIDs) are widely consumed by athletes when faced with injuries and by rheumatic patients, but the<br />

influence <strong>of</strong> these drugs on muscle satellite cells and adaptation is not fully understood. Following a 36 km run the observed increase in<br />

satellite cell number (27%) was blunted by ingestion <strong>of</strong> NSAIDs (Mackey et al., 2007) pointing towards a negative influence <strong>of</strong> NSAIDs on<br />

satellite cell proliferation in vivo in humans. The aim <strong>of</strong> the present study was to investigate the effect <strong>of</strong> local NSAID infusion on satellite<br />

cells in vivo in human muscle.<br />

Materials/Methods: Eight healthy male subjects (unaccustomed to leg resistance exercise) performed 200 maximal eccentric contractions<br />

with each leg. NSAID (Indomethacin) was infused via a microdialysis catheter into one leg (NSAID leg) before, during and for 5 hrs after<br />

exercise, the other leg being working control (unblocked leg). Biopsies were sampled from m.vastus lateralis before and 8 days post<br />

exercise. Satellite cells were analyzed by immunohistochemistry using antibodies against the transcription factor Pax7, and neural cell<br />

adhesion molecule (NCAM). Cell proliferation was analyzed using an antibody against the cell cycle marker Ki67.<br />

Results: The number <strong>of</strong> Pax7+ cells per my<strong>of</strong>ibre was increased by 75 % on day 8 post exercise in the unblocked leg (mean 0.13, SE 0.03)<br />

compared with pre exercise (mean 0.08, SE 0.02, P=0.03), while levels were unchanged in the NSAID leg (mean 0.06, SE 0.01, P=1.0). On<br />

day 8 post exercise the number <strong>of</strong> Pax7+ cells (per my<strong>of</strong>ibre) tended to be lower (P=0.06) in the NSAID leg compared to the unblocked<br />

leg.<br />

Very few proliferating (Ki67+) cells were found with no effect <strong>of</strong> NSAID, on average only one Ki67+ cell was found per 100 my<strong>of</strong>ibres on<br />

day 8 post exercise.<br />

Conclusion: The results indicate that NSAIDs may negatively affect satellite cells and muscle adaptation following eccentric exercise. This<br />

is clinically relevant given the widespread consumption <strong>of</strong> NSAIDs among athletes and rheumatic patients.<br />

526 14 TH<br />

ANNUAL CONGRESS OF THE EUROPEAN COLLEGE OF SPORT SCIENCE

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