Experimental Physiology

IntroductionHealthy, resting skeletal muscle primarily oxidizes lipid, but insulin resistant muscle oxidizes carbohydrate and shows metabolic inflexibility during hyperinsulinemia. It is unclear whether fuel selection and metabolic flexibility are dependent on insulin sensitivity in skeletal muscle performing mild exercise. Research Design and MethodsSedentary volunteers underwent a cycle exercise protocol using stepwise increments in power output (15, 30, and 45 watts) and indirect calorimetry to estimate fuel oxidation in working muscle. Euglycemic clamps, indirect calorimetry and muscle biopsies were used to measure insulin sensitivity and acetylation and content of Adenine Nucleotide Translocase 1 (ANT1), which might be involved in fuel selection via acetylation of lysine 23, which was quantified using mass spectrometry. ResultsMild exercise produced predicted rates of oxygen consumption (11-12 ml O2/min), with low and stable blood lactate, allowing use of indirect calorimetry to calculate a respiratory exchange ratio in working muscle (RERm). ANT1 acetylation varied from 0.6 to 21% (10.3 {+/-} 1.2%). Exercising muscle mainly oxidized carbohydrate (45 {+/-} 9, 62 {+/-} 6, and 70 {+/-} 5% of total at 15, 30, and 45watts). Multiple linear regression showed that RERm rose with increasing power output (P < 0.001) and was lower with greater protein content of ANT1 (P < 0.001). Insulin-stimulated glucose disposal, ANT acetylation, and VO2peak were not predictors of RERm. ConclusionsMildly exercising muscle in sedentary people prefers to oxidize carbohydrate independent of insulin sensitivity but depending on ANT1 protein content. The ability to oxidize lipid may be regulated by higher ANT1 content due to either higher mitochondrial abundance or greater ANT content per mitochondrial mass.

Cellular viscoelastic modulus in skeletal muscle tissue responds dynamically to chronic stressors, such as age and exercise. Passive tissue mechanics may also be sensitive to acute stimuli such as mechanical loading and/or activation-induced muscle fatigue. These insights are largely derived from preclinical studies of age and acute muscle activation. Therefore, we sought to understand the relative responsiveness of muscle cellular passive mechanics to chronic (resistance training) and acute (muscle fatigue) stressors in healthy young males and females categorized as "resistance trained" or "untrained". We measured passive mechanics to test the hypothesis that Youngs Modulus and stress would be greater in fibers from trained versus untrained participants and both would be reduced following fatigue. We further assessed the translation of these findings to composite tissue in a sub-set of volunteers where muscle tissue bundles, containing both fibers and extracellular matrix, were analyzed in addition to single fibers. We report a main effect of training such that cellular passive mechanical measures were increased in single fibers from trained versus untrained participants. We likewise report reductions in passive mechanical measures following fatiguing exercise. Surprisingly, both training and acute fatigue only impacted muscle fiber passive measures in males, whereas females showed a more variable response across conditions. Last, we provide preliminary evidence supporting the translation of per-individual cellular differences to the tissue level. Together, these data suggest males respond more dynamically to acute and chronic stressors of muscle tissue mechanics, potentially linking cellular response and sex-dependent differences in musculotendinous injury risk. New and noteworthyWe report that passive stress and modulus in single muscle fibers was higher in resistance trained healthy adults and fatiguing exercise reduced passive stress and modulus. In each case, dynamic responsiveness of muscle fibers to chronic and acute stressors was observed consistently in males, whereas responses in females varied considerably. We provide further evidence that cellular mechanisms may contribute to multicellular muscle tissue samples, suggesting these findings have relevance to in vivo tissue mechanics.

The rate of initial acceleration during the first steps of a maximal-effort (sprint) run often determines success or failure in prey capture and predator evasion, and is a vital factor of success in many modern sports. However, accelerative events are commonly performed after having already run considerable distances, and the associated fatigue should impair muscle force production and thus reduce acceleration rate. Despite this, the effects of running-induced fatigue on our ability to accelerate as well as the running technique used to achieve it has been incompletely studied. We recorded 3-D kinematics and ground reaction forces during the first three steps of the acceleration phase from a standing start before and after performing a high-speed, multi-directional, fatiguing run-walk protocol in well-trained running athletes who were habituated to accelerative sprinting. We found that the athletes were able to maintain their rate of initial acceleration despite changing running technique, which was associated with use of a more upright posture, longer ground contact time, increased vertical ground reaction impulse, decreased hip flexion and extension velocities, and a shift in peak joint moments, power, and positive work from the hip to the knee joint; no changes were detected in ankle joint function. Thus, a compensatory increase in knee joint function alleviated the reduction in hip flexor-extensor capacity. These acute adaptations may indicate that the hip extensors (gluteal and hamstring muscle groups) were more susceptible to fatigue than the ankle and knee musculature, and may thus be a primary target for interventions promoting fatigue resistance.

Skeletal muscle hypertrophy results from the integrated regulation of anabolic and proteolytic processes in response to mechanical loading. Although increases in resistance training (RT) volume are used to increase mechanical stress, it remains uncertain whether large and abrupt volume progressions could exceed muscle adaptive capacity by disrupting the balance between anabolic and catabolic signaling. The present study investigated whether a large increase in weekly RT volume (+120%) leads to impaired hypertrophic outcomes and intracellular regulatory responses compared with a modest increase (+20%). Twenty-five resistance-trained men and women (18-35 years old) completed an 8-week randomized, single-blind, within-subject unilateral intervention. Each participant trained both legs twice weekly, with one leg assigned to the large (VOL120) and the contralateral leg to the modest (VOL20) weekly volume progressions relative to habitual training volume. Vastus lateralis muscle cross-sectional area (mCSA) was assessed by ultrasonography before and after training. Muscle biopsies were obtained at baseline, post-intervention, and 24 h after the last session to quantify muscle fiber cross-sectional area (fCSA), satellite cell myonuclear content, and anabolic/catabolic signaling markers. Both protocols induced increases in mCSA over time (p<0.001), with no protocol vs. time interaction. No significant effects were observed for fCSA nor satellite cell number or myonuclear content. Additionally, molecular responses related to translational regulation and protein degradation were largely similar between protocols. Collectively, these data indicate that a large, abrupt increase in weekly set volume does not impair hypertrophic adaptations or meaningfully alter the anabolic-catabolic signaling profile in resistance-trained individuals.

We investigated the effects of performing a period of resistance training (RT) on the performance and molecular adaptations to a subsequent period of endurance training (ET). Twenty-five young adults were divided into RT+ET (n=13), which underwent seven weeks of RT followed by seven weeks of ET, and ET-only (n=12), which performed seven weeks of ET. Body composition, endurance performance, and muscle biopsies were collected before RT (T1, baseline for RT+ET), before ET (T2, post RT for RT+ET and baseline for ET), and after ET (T3). Immunohistochemistry was performed to determine fiber cross-sectional area (fCSA), myonuclear content, myonuclear domain size, satellite cell number, and mitochondrial content. Western blots were used to quantify markers of mitochondrial remodeling. Citrate synthase activity and markers of ribosome content were also investigated. Resistance training improved body composition and strength, increased vastus lateralis thickness, mixed and type II fCSA, myonuclear number, markers of ribosome content, and satellite cell content (p<0.050). In response to ET, both groups similarly decreased body fat percentage and improved endurance performance (e.g., VO2max, and speed at which the onset of blood lactate accumulation occurred during the VO2max test). Levels of mitochondrial complexes I-IV in the ET-only group increased 32-66%, while the RT+ET group increased 1-11%. Additionally, mixed fiber relative mitochondrial content increased 15% in the ET-only group but decreased 13% in the RT+ET group. In conclusion, RT performed prior to ET had no additional benefits to ET adaptations. Moreover, prior RT seemed to impair mitochondrial adaptations to ET. KEY POINTS SUMMARYO_LIResistance training is largely underappreciated as a method to improve endurance performance, despite reports showing it may improve mitochondrial function. C_LIO_LIAlthough several concurrent training studies are available, in this study we investigated the effects of performing a period resistance training on the performance and molecular adaptations to subsequent endurance training. C_LIO_LIPrior resistance training did not improve endurance performance and impaired most mitochondrial adaptations to subsequent endurance training, but that seemed to be a result of detraining from resistance training. C_LI

Ribosomal DNA (rDNA) copies are organized in tandem repeats across multiple chromosomes, and inter-individual variation in rDNA copy number has been speculated to be a modifier of the hypertrophic responses to resistance training. In the current study, 82 apparently healthy participants (n=53 males, 21{+/-}1 years old; n=29 females, 21{+/-}2 years old) performed 10-12 weeks of supervised full-body resistance training. Whole-body, mid-thigh, and histological skeletal muscle hypertrophy outcomes were determined, as was relative rDNA copy number from pre-intervention vastus lateralis (VL) biopsies. Pre- and post-intervention VL biopsy mRNA/rRNA markers of ribosome content and biogenesis were assayed in all participants, and these targets were also assayed in the 29 females 24 hours following their first workout bout. Across all 82 participants, no significant associations were evident between relative rDNA copy number and training-induced changes in whole body lean mass (r = -0.034, p=0.764), vastus lateralis thickness (r = 0.093, p=0.408), mean myofiber cross-sectional area (r = -0.128, p=0.259), or changes in muscle RNA concentrations (r = 0.026, p=0.818). Several significant, positive associations in females support ribosome biogenesis being linked to training-induced myofiber hypertrophy. Follow-up studies using LHCN-M2 myotubes demonstrate a reduction in relative rDNA copy number induced by bisphenol A (BPA). However, BPA did not significantly affect myotube diameter or prevent insulin-like-growth factor-induced hypertrophy. These findings provide strong evidence that relative rDNA copy number is not associated with myofiber anabolism and provide further mechanistic evidence for ribosome biogenesis being involved in this phenomenon.

The present study aimed to characterise the temporal recovery pattern of contralateral-homologous torque following a bout of unilateral resistance exercise (RE). Ten young, healthy, recreationally active, resistance-trained men performed 10 sets of 10 repetitions of knee extensor (KE) contractions at 50 % 1RM with 1 min rest between sets. Isometric maximal voluntary contraction (MVC) peak torque (PT), surface electromyography (sEMG), muscle soreness and serum creatine kinase (CK) levels were assessed immediately before and 5 min after RE cessation, and then +4 h, +24 h, +48 h and +72 h later. Data are presented as mean [95 % CI] % change from pre-exercise values. RE evoked a minor increase in CK and pain in the late recovery period (+24 h to +72 h) (P < 0.034) and decreases in ipsilateral KE PT were observed immediately post-exercise (-26 [-33, -18] %, P < 0.001) and up to +48 h (-12 [-19, -4] %, P = 0.006). Measurable decreases in PT were also observed in the non-exercised contralateral KE immediately post-exercise (-8 [-13, -3] %, P = 0.006) up to +24 h (-8 [-15, 0] %, P = 0.020), but were significantly lower than the ipsilateral KE PT (P < 0.05). These findings suggest the presence of crossover fatigue following RE in young, healthy, active, resistance-trained men, however, the magnitude and temporal recovery are substantially less severe and protracted in the contralateral homologous KE.

Intracellular accumulation of hydrogen ions (H+) and inorganic phosphate (Pi) have temperature-dependent effects on single fiber contractile function between 10-30{degrees}C. In vivo, human skeletal muscle temperatures range between 35-38{degrees}C, and although contractile function is highly dependent on temperature, the effects of fatigue-inducing [H+] and [Pi] on contractile mechanics at 37{degrees}C is unknown. Using sinusoidal analysis, the independent and combined effects of these metabolites on cellular and molecular contractile function were determined at 37{degrees}C in slow-contracting myosin heavy chain (MHC) I and fast-contracting MHC IIA fibers from vastus lateralis muscle of 13 older adults (8 females), under four conditions: maximal calcium activation ("control"; 5 mM Pi, pH 7.0), high Pi (30 mM), low pH (6.2), and fatigue (30 mM Pi and pH 6.2). Specific tension (force/cross-sectional area, mN/mm2) in both fiber types was reduced only under fatigue conditions (20-26%). MHC I fibers had slower cross-bridge kinetics with fewer or less stiff strongly-bound myosin-actin cross-bridges in high Pi, low pH, and fatigue. In contrast, fatigued MHC IIA fibers had faster cross-bridge kinetics with increased myofilament and/or cross-bridge viscosity. Single fiber oscillatory work was reduced in both fiber types when Pi or pH alone was altered. However, fatigue conditions returned oscillatory work values toward control through alterations to cross-bridge kinetics in MHC I fibers and changes to work absorption and production processes in MHC IIA fibers. These findings quantify fiber-type specific mechanical and kinetic mechanisms of fatigue in human skeletal muscle at 37{degrees}C, thus advancing our understanding of metabolite-based muscle fatigue in vivo. KEY POINTS SUMMARYO_LIWorking skeletal muscle increases intracellular concentrations of hydrogen ion and inorganic phosphate, leading to fatigue, or loss of force-generating capacity C_LIO_LITemperature plays a well-established role in the muscle response to hydrogen ion and/or inorganic phosphate accumulation, but has not previously been studied at human body temperature (37{degrees}C) C_LIO_LIAt 37{degrees}C, reduced force generation only occurs when high phosphate and hydrogen ions are combined, not when changed individually C_LIO_LIIn slow-contracting fibers, fatigue slowed myosin-actin cross-bridge kinetics and reduced the number or stiffness of strongly-bound cross-bridges. In fast-contracting fibers, fatigue increased myosin-actin cross-bridge kinetics and increased myofilament viscosity. C_LIO_LIThe distinct responses by fiber type to fatigue provides new insight into its mechanisms and advances our understanding of the whole muscle and body responses to fatigue C_LI Abstract Figure O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=125 SRC="FIGDIR/small/672942v1_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@e4ece3org.highwire.dtl.DTLVardef@17c62eforg.highwire.dtl.DTLVardef@1434e30org.highwire.dtl.DTLVardef@1c2446c_HPS_FORMAT_FIGEXP M_FIG C_FIG

BackgroundImmobilization, bed rest, or illness rapidly lead to weakness out of proportion to muscle atrophy. Although the contribution of muscle wasting to weakness is well described, the role of neuromuscular junction (NMJ) dysfunction in early disuse-related weakness is not well understood. ObjectiveWe investigated whether short-term unilateral hindlimb immobilization (HLI) in rats impairs NMJ transmission and contributes to muscle weakness out of proportion to atrophy. MethodsFour-month-old male Fischer-344/Brown Norway rats underwent 10 days of unilateral HLI (n=6) or remained mobile (n=6). Neuromuscular excitability and transmission were assessed using compound muscle action potentials (CMAP), repetitive nerve stimulation (RNS), and single-fiber electromyography (SFEMG). Muscle contractility testing quantified tetanic torque, and post-mortem analysis measured muscle mass. ResultsTen days of HLI reduced gastrocnemius, soleus, and plantaris muscle mass by [~]20-35%. Plantarflexion peak tetanic torque normalized to body weight declined by 23%, and torque-time integral was reduced by 36%, indicating disproportionate functional loss (muscle size versus contractile output) and supporting underlying neural impairment. CMAP amplitude decreased from 69 mV to 53.23 mV (a 22.9% reduction; p = 0.0109), indicating a loss of summated neuromuscular excitability. Furthermore, both RNS and SFEMG indicated features consistent with NMJ transmission defects. RNS revealed CMAP decrement from [~]0% pre-HLI to -9.15% at 40 Hz stimulation and -8.63% at 50 Hz post-HLI. Similarly, SFEMG confirmed marked NMJ transmission defects, with jitter increasing 103% and blocking increased from <1% to >11% of fibers. ConclusionsOur findings suggest that short-term immobilization produces rapid and pronounced impairments in NMJ transmission that contribute to weakness beyond the degree of muscle atrophy. These findings identify the NMJ as an early and vulnerable site of disuse-induced dysfunction and highlight the potential for synaptic-targeted therapies to preserve muscle performance during immobilization and recovery.

Runners with Achilles tendinopathy (AT) have reduced neural drive to the gastrocnemius lateralis (GL). This study investigated if the strategy of pointing feet-inward (feet-in) during isometric plantarflexion would increase gastrocnemius lateralis electromyography root mean square amplitude (RMS) and motor unit discharge rates, compared to feet-in neutral position (feet-neutral), in runners with Achilles Tendinopathy (AT). High-density electromyograms were recorded from gastrocnemius lateralis and medialis, during 20-s feet-in and feet-neutral isometric heel raise, in runners with (n=18) and without (n=19) AT. During feet-in, GL RMS was higher during feet-in in both groups and GM RMS was lower only during feet-in in the AT. Conversely, motor unit discharge rates were lower during feet-in in GL (p<0.001) and in GM in the AT group. The AT group had lower triceps surae endurance during single leg heel raise. In summary, feet-in increases GL RMS in both groups, conversely reducing motor unit discharge rates in the AT group, compared to feet-neutral. Additionally, feet-in reduces GM RMS and motor unit discharge rates only in the AT group, compared to feet-neutral. This would shift the gastrocnemius lateralis/medialis ratio excitation, favouring gastrocnemius lateralis. Nonetheless, while this strategy holds promise, it remains uncertain whether performing plantarflexion exercise with feet pointed inwards would provide additional benefits for the treatment of runners with Achilles tendinopathy. Our findings suggest that the increased GL RMS during feet-in is effective in increasing GL excitation but not as consequence of increased MUDR and, but it might be a result of recruitment of more motor units.

The reduction in mechanical loading applied on the lower limb has numerous detrimental consequences on neuromuscular function. The current study aimed to investigate the changes in knee extensors strength and spinal excitability induced by unilateral lower limb suspension (ULLS), providing new insights into the neuromuscular adaptations to muscle hypoactivity. Ten young healthy males (19-28 years old) underwent 10 days of ULLS to simulate muscle disuse. Modulation by unloading of knee extensors function (muscle morphology and strength, activation capacity and contractile properties) and spinal reflexes were explored before and after the ULLS. The knee extensors anatomical cross-sectional area (-4%, p = 0.007), maximal strength (-27%, p < 0.001) and central activation ratio (-3%, p = 0.006) were reduced after 10 days of ULLS. Vastus medialis H-reflex amplitude was enhanced both at rest (+33%, p = 0.038) and during a low-intensity contraction set at 10% of maximal strength (+103%, p = 0.038). No changes in muscle contractility and nerve conduction velocity were observed after the ULLS. The present study suggests that neural impairments mainly contribute to the decrease in knee extensors strength induced by short-term ULLS. The decrease in muscle activation after a short period of ULLS was accompanied by an increase in spinal excitability. However, the latter adaptation did not counterbalance the reduction in activation capacity and thus in maximal strength resulting from ULLS. These adaptations to short-term ULLS should be considered when aiming at improving the neuromuscular function of people experiencing muscle hypoactivity. NEW & NOTEWORTHYThis study provides new insights into the effects of muscle hypoactivity on neuromuscular function and spinal excitability in the major antigravity muscle group of the lower limb. Neural impairments primarily contribute to maximal strength loss after short-term unilateral lower limb suspension, while spinal excitability increased. These findings are crucial as they offer valuable understanding for developing effective interventions to improve health outcomes for individuals experiencing muscle inactivity.

The effects of higher-load (HL) versus higher-volume (HV) resistance training (RT) on various molecular outcomes are similar. However, mitochondrial responses remain understudied. Therefore, the purpose of this study was to interrogate mitochondrial mRNA and protein responses to acute and chronic HL versus HV RT. Vastus lateralis biopsies from resistance trained males in two prior studies were assessed. In STUDY 1, 11 college-aged men completed an acute bout of either HL or HV RT exercises to failure. Biopsies were collected at PRE, 3 hours post-, and 6 hours post-exercise. In STUDY 2, 15 college-aged men participated in six weeks of supervised unilateral RT where each leg was assigned to either HL or HV RT. Biopsies were collected from both legs prior to and 72 hours following last training bout of the intervention. Biopsies from both studies were used to assess mitochondrial mRNAs, and STUDY 2 biopsies were assayed for mitochondrial proteins and CS activity. Results from both studies revealed several significant main effects of time but no significant interactions. Additionally, CS activity, a surrogate of mitochondrial content, decreased following chronic RT (p=0.016) but no interaction was observed between the HV and HL leg over time (p=0.882). In conclusion, while RT resulted in both acute mitochondrial mRNA as well as chronic CS activity and mitochondrial protein responses, there were no differences in the HL versus HV paradigms on these outcomes.

Spinal cord injury (SCI) results in severe atrophy of skeletal muscle in paralyzed regions, and a decrease in the force generated by muscle per unit of cross-sectional area. Oxidation of skeletal muscle ryanodine 1 receptors (RyR1) reduces contractile force due to reduced binding of calstabin 1 to RyR1 together with altered gating of RyR1. One cause of RyR1 oxidation is NADPH oxidase 4 (Nox4). We have previously shown that in rats, RyR1 was oxidized and bound less calstabin 1 at 56 days after spinal cord injury (SCI) by transection. Here, we used a conditional knock-out mouse model of Nox4 in muscle to investigate the role of Nox4 in reduced muscle specific force after SCI. Peak twitch force in control mice after SCI was reduced by 42% compared to sham-operated controls but was increased by approximately 43% in SCI Nox4 conditional KO mice compared to SCI controls although it remained less than that for sham-operated controls. Unlike what observed in rats, after SCI the expression of Nox4 was not increased in gastrocnemius muscle and binding of calstabin 1 to RyR1 was not reduced in this muscle. The results suggest a link between Nox4 expression in muscle tissue and reduction in muscle twitch force, however further studies are needed to understand the mechanistic basis for this linkage.

ObjectiveAccentuated eccentric loading (AEL) involves higher load applied during the eccentric phase of a stretch-shortening cycle movement, followed by a sudden removal of load before the concentric phase. Previous studies suggest that AEL enhances human countermovement jump performance, however the mechanism is not fully understood. Here we explore whether isolating additional load during the countermovement is sufficient to increase ground reaction force, and hence elastic energy stored, at the start of the upward movement and whether this leads to increased jump height or power generation. MethodsWe conducted a trunk-constrained vertical jump test on a custom-built device to isolate the effect of additional load while controlling for effects of squat depth, arm swing, and coordination. Twelve healthy, recreationally active adults (7 males, 5 females) performed maximal jumps without AEL, followed by randomised AEL conditions prescribed as a percentage of body mass (10%, 20%, and 30%), before repeating jumps without AEL. Results. No significant changes in vertical ground reaction force at the turning point were observed. High load AEL conditions (20% and 30% body weight) led to slight reductions in jump height, primarily due to decreased hip joint and centre of mass work. AEL conditions did not alter peak or integrated activation levels of the knee extensor muscles. ConclusionThese findings suggest that increased elastic energy return may not be the primary mechanism behind the potentiating effects of AEL on jump performance, and other factors such as rate of descent, squat depth, or body configuration may contribute to effective AEL.

Non-invasive recordings of motor unit (MU) spike trains help us understand how the nervous system controls movement and how it adapts to various physiological conditions. The majority of study participants in human and non-human animal physiology studies are male, and it is assumed mechanisms uncovered in these studies are shared between males and females. However, sex differences in neurological impairment and physical performance warrant the study of sex as a biological variable in human physiology and performance. To begin addressing this gap in the study of biophysical properties of human motoneurons, we quantified MU discharge rates and estimates of persistent inward current (PIC) magnitude in both sexes by quantifying {Delta}F. We decomposed MU spike trains from the tibialis anterior (TA), medial gastrocnemius (MG), and soleus (SOL) using high-density surface electromyography and blind source separation algorithms. Ten participants of each sex performed slow triangular (10s up and down) isometric contractions to a peak of 30% of their maximum voluntary contraction. We then used linear mixed effects models to determine if peak discharge rate and {Delta}F were predicted by the fixed effects of sex, muscle, and their interaction. Despite a lack of significant sex-differences in peak discharge rates across all muscles, {Delta}F was larger ({chi}2(1) = 6.26, p = 0.012) in females (4.73 {+/-} 0.242 pps) than males (3.81 {+/-} 0.240 pps). These findings suggest that neuromodulatory drive, inhibitory input, and/or biophysical properties of motoneurons differ between the sexes and may contribute to differences in MU discharge patterns. KEY POINTS- Sex differences in motor unit studies have been revealed with greater inclusion of female participants, however, mechanisms for these differences remain unclear. - Estimates of persistent inward currents (i.e., {Delta}F) were greater in females than males in the tibialis anterior, medial gastrocnemius, and soleus muscles. - This suggests that neuromodulatory drive, monoaminergic signaling, or descending control may differ between the sexes. - Therefore, sex differences in estimates of PICs may provide a mechanism behind previously reported sex differences in motoneuron discharge patterns..

O_LIPhospholamban and sarcolipin are two key regulators of the sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) that have been shown to protect SERCA from thermal inactivation in muscle C_LIO_LIWe have recently detected neuronatin (NNAT) in murine skeletal muscle and have shown that it too regulates SERCA C_LIO_LIHere, we questioned whether NNAT would also protect SERCA from thermal inactivation C_LIO_LIIn response to 60 min of heat stress at 40{degrees}C, maximal SERCA activity was significantly reduced in soleus homogenates obtained from NNAT knockout mice (-23%) but not wild-type mice (-5%). C_LIO_LIOur results add further support for NNATs role in regulating SERCA function in murine muscle C_LI

Neuroinflammation affects dopamine metabolism and produces a set of symptoms known as sickness behavior, including fever, anhedonia, anorexia, weight loss, decreased sociability and mobility, and cognitive impairment. Motor and cognitive impairments related to sickness behavior are associated with dopamine (DA) metabolism imbalance in the prefrontal cortex. Lipopolysaccharide (LPS) administration induces neuroinflammation and causes sickness behavior in mice, while physical exercise has anti-inflammatory properties and may attenuate sickness behavior and DA impairment. We investigated the effect of exercise on DA levels and sickness behavior induced by LPS in mice. Adult Swiss male mice (8-10 weeks, 47.1 {+/-} 0.7 g, n=495) performed six weeks of voluntary exercise in free-running wheels (RW group) or had the blocked wheel in their cages (sedentary, SED group). After six weeks of exercise, both groups received an intraperitoneal injection (i.p.) of either saline (SAL) or LPS (0.33 mg/kg, i.p.). All animals were submitted to behavioral tests for sickness behavior assessment (fatigue, locomotion, anhedonia, and social interaction). Neuroinflammation markers and DA metabolism were assessed in the prefrontal cortex. LPS administration provoked anorexia, body weight loss, impaired motor function, social withdrawal, and anhedonia. This sickness behavior was accompanied by reduced cortical DA metabolism and its metabolite, 3,4-dihydroxyphenylacetic acid (DOPAC). Neuroinflammation was confirmed through increased levels of the proinflammatory cytokines IL-1{beta} and IL-6. Inflammation was also confirmed in the blood by an increased content of IL-1{beta}. Physical exercise intervention prevented animals from neurochemical, biochemical, and behavioral alterations. These findings provide new evidence of physical exercises potential as an environmental approach to treating neuroinflammatory conditions.

The muscular and myocellular adaptations to low-load resistance exercise training (LL-RET) remain incompletely understood, particularly in the trained state. The primary aim of this study was to examine adaptations to an LL-RET regimen and compare these to a high-load training regimen (HL-RET). Fourteen resistance-trained males and females (26.4 {+/-} 4.4 years) participated in a 9-week RET program (twice per week). Using a within-subject design, each individual trained one leg with HL-RET (3-5 repetitions), and the other with LL-RET (20-25 repetitions), all sets performed to volitional failure. Pre- and post-intervention, muscle endurance, maximal strength, and muscle thickness using ultrasound was assessed. Muscle biopsies were analyzed for fiber type composition, fiber cross-sectional area (fCSA), and satellite cell- and myonuclear content using immunofluorescence. The training regimens led to comparable increases in maximal strength in multi-joint movements (21%), but not in single-joint movements were HL-RET was superior. LL-RET induced superior improvements in local muscle endurance (9% vs -2.7%, p=0.013). Regardless of training regimen, muscle thickness increased by [~]7.4% at the mid-thigh site and [~]8.5% at the distal site pre-to post-intervention. However, no changes were observed in fiber type composition or fCSA. Satellite cell content increased by [~]25% in type I fibers, independent of training regimen, but no changes were noted in myonuclear content. Here we novelly show that LL-RET can replicate many aspects of HL-RET leading to similar increases in both muscle hypertrophy and strength. Our study thus supports the notion that comparable adaptations to RET can be achieved using distinct loading regimens. New and noteworthyThis study compared two distinct resistance exercise loading strategies (3-5 RM vs. 20-25 RM) in trained individuals, evaluating both muscular and myocellular adaptations. Our findings demonstrate that low-load resistance exercise training (LL-RET) is an effective alternative to traditional high-load strategies for increasing strength and muscle size. These results highlight that skeletal muscle growth can be achieved through various external stressors, offering valuable insights for individuals seeking hypertrophy but unable to tolerate high loads.

In a previous study by our group (Nold et al., 2025), we investigated exercise-induced pain modulation after high-intensity compared to low-intensity exercise in a heterogeneous sample of diverse fitness levels. Exploratory analyses suggested an interaction of sex, fitness level, and drug treatment, indicating that males showed increasing hypoalgesia after high-compared to low-intensity exercise with increasing fitness levels, which was diminished when naloxone was administered. In contrast, these effects were not evident in females. These exploratory findings warranted further investigation to determine if and to what extent exercise-induced hypoalgesia depends on fitness level and/or sex. In this current study, we investigated an all-female sample (N = 21) of high fitness levels using a similar paradigm as in the previous study, comparing heat and pressure pain ratings after high-intensity and low-intensity exercise. Our data show an interaction of exercise intensity and stimulus intensity in heat pain, with greater pain relief following high-intensity exercise, especially at the highest stimulus intensity. Despite results for pressure pain not reaching significance, a similar trend was evident. These results suggest that females at a high fitness level also show exercise-induced hypoalgesia for high-intensity compared to low-intensity exercise. Together with our previous findings, this suggests that exercise-induced hypoalgesia depends on fitness level but not on sex.

It is well documented that, in soleus, motoneuron output and the effectiveness of activated Ia afferents to discharge -motoneurons both decrease during eccentric contractions. Evidence suggests that these regulations can be explained by (1) recurrent inhibition and (2) greater post-activation depression by primary afferent depolarization. However, the influence of muscle length on the regulation of the effectiveness of Ia afferents to discharge -motoneurons observed during eccentric contractions remains unclear. We conducted a study on 16 healthy young individuals. We used simple and conditioned Hoffmann reflex with different conditioning techniques such as paired H reflex, D1 method and heteronymous Ia facilitation coupled with electromyography during eccentric, isometric and concentric contractions at long, intermediate and short soleus muscle lengths. Our results confirm that during eccentric contraction the effectiveness of Ia afferents to discharge U-motoneurons decreases only at intermediate and short muscle lengths but is similar between all contraction types at long muscle length. Findings are similar for recurrent inhibition. Post-activation depression is significantly more pronounced during eccentric contractions compared with isometric and concentric contractions at long muscle length. Our analysis also shows that recurrent inhibition and post-activation depression are greater at long muscle length compared with short muscle length, whatever the contraction type. These new findings demonstrate an important influence of muscle length on the activity of spinal regulatory mechanisms and the effectiveness of activated Ia afferents to discharge -motoneurons during eccentric contractions.