Whereas a variety of pre-exercise activities have been incorporated as part of a "warm-up" prior to work, combat, and athletic activities for millennia, the inclusion of static stretching (SS) within a warm-up has lost favour in the last 25 years. Research emphasised the possibility of SSinduced impairments in subsequent performance following prolonged stretching without proper dynamic warm-up activities. Proposed mechanisms underlying stretch-induced deficits include both neural (i.e. decreased voluntary activation, persistent inward current effects on motoneurone excitability) and morphological (i.e. changes in the force-length relationship, decreased Ca 2+ sensitivity, alterations in parallel elastic component) factors. Psychological influences such as a mental energy deficit and nocebo effects could also adversely affect performance. However, significant practical limitations exist within published studies, e.g. long stretching durations, stretching exercises with little task specificity, lack of warm-up before/after stretching, testing performed immediately after stretch completion, and risk of investigator and participant bias.Recent research indicates that appropriate durations of static stretching performed within a full warm-up (i.e. aerobic activities before and task-specific dynamic stretching and intense physical activities after SS) have trivial effects on subsequent performance with some evidence of improved force output at longer muscle lengths. For conditions in which muscular force production is compromised by stretching, knowledge of the underlying mechanisms would aid development of mitigation strategies. However, these mechanisms are yet to be perfectly defined. More information is needed to better understand both the warm-up components and mechanisms that contribute to performance enhancements or impairments when SS is incorporated within a pre-activity warm-up.

Isolated injury to the long head of biceps femoris is the most common type of acute hamstring strain injury (HSI). However, the precise hamstring injury mechanism (i.e., sprint-type) is still not well understood, and research is inconclusive as to which phase in the running cycle HSI risk is the greatest. Since detailed information relating to hamstring muscle function during sprint running cannot be obtained in vivo in humans, the findings of studies investigating HSI mechanisms are based on modeling that requires assumptions to be made based on extrapolations from anatomical and biomechanical investigations. As it is extremely difficult to account for all aspects of muscle-tendon tissues that influence function during high-intensity running actions, much of this complexity is not included in these models. Furthermore, the majority of analyses do not consider the influence of prior activity or muscular fatigue on kinematics, kinetics and muscle activation during sprinting. Yet, it has been shown that fatigue can lead to alterations in neuromuscular coordination patterns that could potentially increase injury risk. The present critical review will evaluate the current evidence on hamstring injury mechanism(s) during high-intensity running and discuss the interactions between fatigue and hamstring muscle activation and function.

Vaile, J.M., N.D. Gill, and A.J. Blazevich. The effect of contrast water therapy on symptoms of delayed onset muscle soreness. J. Strength Cond. Res. 21 (2): 697-702. 2007.-This study examined the effect of contrast water therapy (CWT) on the physiological and functional symptoms of delayed onset muscle soreness (DOMS) following DOMS-inducing leg press exercise. Thirteen recreational athletes performed 2 experimental trials separated by 6 weeks in a randomized crossover design. On each occasion, subjects performed a DOMS-inducing leg press protocol consisting of 5 ϫ 10 eccentric contractions (180 seconds recovery between sets) at 140% of 1 repetition maximum (1RM). This was followed by a 15-minute recovery period incorporating either CWT or no intervention, passive recovery (PAS). Creatine kinase concentration (CK), perceived pain, thigh volume, isometric squat strength, and weighted jump squat performance were measured prior to the eccentric exercise, immediately post recovery, and 24, 48, and 72 hours post recovery. Isometric force production was not reduced below baseline measures throughout the 72-hour data collection period following CWT (ഠ4-10%). However, following PAS, isometric force production (mean Ϯ SD) was 14.8 Ϯ 11.4% below baseline immediately post recovery (p Ͻ 0.05), 20.8 Ϯ 15.6% 24 hours post recovery (p Ͻ 0.05), and 22.5 Ϯ 12.3% 48 hours post recovery (p Ͻ 0.05). Peak power produced during the jump squat was significantly reduced (p Ͻ 0.05) following both PAS (20.9 Ϯ 13.4%) and CWT (12.8 Ϯ 8.0%), with the mean reduction in power for PAS being marginally (not significantly) greater than for CWT (effect size ϭ 0.76). Thigh volume measured immediately following CWT was significantly less than PAS. No significant differences in the changes in CK were found; in addition, there were no significant (p Ͼ 0.01) differences in perceived pain between treatments. Contrast water therapy was associated with a smaller reduction, and faster restoration, of strength and power measured by isometric force and jump squat production following DOMS-inducing leg press exercise when compared to PAS. Therefore, CWT seems to be effective in reducing and improving the recovery of functional deficiencies that result from DOMS, as opposed to passive recovery.

Dunn, EC, Humberstone, CE, Franchini, E, Iredale, KF, and Blazevich, AJ. Relationships between punch impact force and upper- and lower-body muscular strength and power in highly trained amateur boxers. J Strength Cond Res 36(4): 1019–1025, 2022—This study examined the relationship between upper- and lower-body strength and power characteristics and punch performance in 28 highly trained male amateur boxers. Punch performance was assessed with a custom-built punch integrator using a 3-minute maximal effort punch test that contained straight- and bent-arm punches from the lead and rear hands. Peak punch force and force-time variables including impulse and rate of force development (RFD; calculated to various points) were assessed. Force, power, and RFD of the upper and lower body were assessed with countermovement bench throw, isometric bench push, countermovement jump (CMJ), and isometric midthigh pull (IMTP) tests. Correlation and regression analyses revealed significant (p < 0.05) relationships between peak punch force and forces measured in CMJ and IMTP tests. In addition, peak punch force was moderately and significantly correlated to body mass, but RFD in the lower body was not. Moreover, no meaningful relationships between punch performance characteristics and any upper-body strength or power parameter were identified. The results of this study show that lower-body strength but not RFD had a moderate to strong positive and significant correlation to peak punch force production. Although upper-body strength and power are expected to be important in boxing, they did not discriminate between boxers who punched with higher or lower peak force nor were they correlated to peak punch force. Training that improves lower-body strength without increasing total body mass (to maintain weight category) may positively influence punch capacity in highly trained amateur boxers.

Prolonged (≥60 s) passive muscle stretching acutely reduces maximal force production at least partly through a suppression of efferent neural drive. The origin of this neural suppression has not been determined, however some evidence suggests that reductions in the amplitude of persistent inward currents (PICs) in the motoneurons may be important. The aim of the present study was to determine whether acute passive (static) muscle stretching affects PIC strength in gastrocnemius medialis (GM) and soleus (SOL) motor units. We calculated the difference in instantaneous discharge rates at recruitment and derecruitment (ΔF) for pairs of motor units in GM and SOL during triangular isometric plantar flexor contractions (20% maximum) both before and immediately after a 5-min control period and immediately after five 1-min passive plantar flexor stretches. After stretching there was a significant reduction in SOL ΔF (−25.6%; 95%CI=−45.1 to −9.1 %, p=0.002) but not GM ΔF. These data suggest passive muscle stretching can reduce the intrinsic excitability, via PICs, of SOL motor units. These findings (1) suggest that PIC strength might be reduced after passive stretching, (2) are consistent with previously-established post-stretch decreases in SOL but not GM EMG amplitudes during contraction, and (3) indicate that reductions in PIC strength could underpin the stretch-induced force loss.

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Temporal biomechanical and physiological responses to physical activity vary between individual hamstrings components as well as between exercises, suggesting that hamstring muscles operate differently, and over different lengths, between tasks. Nevertheless, the force-length properties of these muscles have not been thoroughly investigated. The present review examines the factors influencing the hamstrings’ force-length properties and relates them to in vivo function. A search in four databases was performed for studies that examined relations between muscle length and force, torque, activation, or moment arm of hamstring muscles. Evidence was collated in relation to force-length relationships at a sarcomere/fiber level and then moment arm-length, activation-length, and torque-joint angle relations. Five forward simulation models were also used to predict force-length and torque-length relations of hamstring muscles. The results show that, due to architectural differences alone, semitendinosus (ST) produces less peak force and has a flatter active (contractile) fiber force-length relation than both biceps femoris long head (BFlh) and semimembranosus (SM), however BFlh and SM contribute greater forces through much of the hip and knee joint ranges of motion. The hamstrings’ maximum moment arms are greater at the hip than knee, so the muscles tend to act more as force producers at the hip but generate greater joint rotation and angular velocity at the knee for a given muscle shortening length and speed. However, SM moment arm is longer than SM and BFlh, partially alleviating its reduced force capacity but also reducing its otherwise substantial excursion potential. The current evidence, bound by the limitations of electromyography techniques, suggests that joint angle-dependent activation variations have minimal impact on force-length or torque-angle relations. During daily activities such as walking or sitting down, the hamstrings appear to operate on the ascending limbs of their force-length relations while knee flexion exercises performed with hip angles 45–90° promote more optimal force generation. Exercises requiring hip flexion at 45–120° and knee extension 45–0° (e.g. sprint running) may therefore evoke greater muscle forces and, speculatively, provide a more optimum adaptive stimulus. Finally, increases in resistance to stretch during hip flexion beyond 45° result mainly from SM and BFlh muscles.