Biomedical subjects

Brian R MacIntosh

Publications and source records attributed to Brian R MacIntosh.

10 recordsLinked to original sources

PubMed2004

The length dependence of muscle active force: considerations for parallel elastic properties.

The purpose of this study was to choose between two popular models of skeletal muscle: one with the parallel elastic component in parallel with both the contractile element and the series elastic component (model A), and the other in which it is in parallel with only the contractile element (model B). Passive and total forces were obtained at a variety of muscle lengths for the medial gastrocnemius muscle in anesthetized rats. Passive force was measured before the contraction (passive A) or was estimated for the fascicle length at which peak total force occurred (passive B). Fascicle length was measured with sonomicrometry. Active force was calculated by subtracting passive (A or B) force from peak total force at each fascicle or muscle length. Optimal length, that fascicle length at which active force is maximized, was 13.1 +/- 1.2 mm when passive A was subtracted and 14.0 +/- 1.1 mm with passive B (P < 0.01). Furthermore, the relationship between double-pulse contraction force and length was broader when calculated with passive B than with passive A. When the muscle was held at a long length, passive force decreased due to stress relaxation. This was accompanied by no change in fascicle length at the peak of the contraction and only a small corresponding decrease in peak total force. There is no explanation for the apparent increase in active force that would be obtained when subtracting passive A from the peak total force. Therefore, to calculate active force, it is appropriate to subtract passive force measured at the fascicle length corresponding to the length at which peak total force occurs, rather than passive force measured at the length at which the contraction begins.

Animals↗

PubMed2004

Fatigue and optimal conditions for short-term work capacity.

There is an optimal load and corresponding velocity at which peak power output occurs. It is reasonable to expect that these conditions will change as a result of fatigue during 30 s of all-out cycling. This study evaluated optimal velocity after 30 s of maximal isokinetic cycle ergometer exercise and tested the hypothesis that progressive adjustment of velocity (optimized) during 30 s of all-out cycling would permit greater short-term work capacity (STWC). Non-fatigued optimal cadence [NF(OC), 109.6 (2.5) rpm] was determined for ten males on an SRM ergometer using regression analysis of the torque-angular velocity relation during a 7-s maximal acceleration. Fatigued optimal cadence [73.4 (2.4) rpm] was determined in the same way, immediately after a 30-s isokinetic test at NF(OC). A subsequent trial with cadence decreasing in steps from NF(OC) to a conservative estimate of fatigued optimal cadence [83.9 (2.8) rpm] was completed to see if more work could be done with a more optimal cadence during the test. STWC was not different ( P=0.50) between the constant [23,681 (764) J] and optimized [23,679 (708) J] conditions. Another more radical progressive change in cadence with four subjects yielded the same result (no increase in STWC). Extraneous factors apparently contribute more to variability in STWC than differences between constant and adjusted optimization of conditions.

Adult↗

PubMed2003

Anaerobic threshold: the concept and methods of measurement.

The anaerobic threshold (AnT) is defined as the highest sustained intensity of exercise for which measurement of oxygen uptake can account for the entire energy requirement. At the AnT, the rate at which lactate appears in the blood will be equal to the rate of its disappearance. Although inadequate oxygen delivery may facilitate lactic acid production, there is no evidence that lactic acid production above the AnT results from inadequate oxygen delivery. There are many reasons for trying to quantify this intensity of exercise, including assessment of cardiovascular or pulmonary health, evaluation of training programs, and categorization of the intensity of exercise as mild, moderate, or intense. Several tests have been developed to determine the intensity of exercise associated with AnT: maximal lactate steady state, lactate minimum test, lactate threshold, OBLA, individual anaerobic threshold, and ventilatory threshold. Each approach permits an estimate of the intensity of exercise associated with AnT, but also has consistent and predictable error depending on protocol and the criteria used to identify the appropriate intensity of exercise. These tests are valuable, but when used to predict AnT, the term that describes the approach taken should be used to refer to the intensity that has been identified, rather than to refer to this intensity as the AnT.

Anaerobic Threshold↗

PubMed2003

Role of calcium sensitivity modulation in skeletal muscle performance.

A common mechanism affecting Ca(2+) sensitivity in skeletal muscle is the proximity of myosin heads with actin filaments, a function of myofilament lattice spacing and myosin head mobility with respect to the myosin filament. This is an important mechanism of pCa(2+)(50) modulation by length, pH, regulatory light-chain phosphorylation, and temperature.

Animals↗

PubMed2002

Sarcomere length-dependence of activity-dependent twitch potentiation in mouse skeletal muscle.

BACKGROUND: It has been reported that potentiation of a skeletal muscle twitch response is proportional to muscle length with a negative slope during staircase, and a positive slope during posttetanic potentiation. This study was done to directly compare staircase and posttetanic responses with measurement of sarcomere length to compare their length-dependence. METHODS: Mouse extensor digitorum longus (EDL) muscles were dissected to small bundles of fibers, which permit measurement of sarcomere length (SL), by laser diffraction. In vitro fixed-end contractions of EDL fiber bundles were elicited at 22 degrees C and 35 degrees C at sarcomere lengths ranging from 2.35 microm to 3.85 microm. Twitch contractions were assessed before and after 1.5 s of 75 Hz stimulation at 22 degrees C or during 10 s of 10 Hz stimulation at 22 degrees C or 35 degrees C. RESULTS: Staircase potentiation was greater at 35 degrees C than 22 degrees C, and the relative magnitude of the twitch contraction (Pt*/Pt) was proportional to sarcomere length with a negative slope, over the range 2.3 microm - 3.7 microm. Linear regression yielded the following: Pt*/Pt = -0.59 x SL+3.27 (r2 = 0.74); Pt*/Pt = -0.39 x SL+2.34 (r2 = 0.48); and Pt*/Pt = -0.50 x SL+2.45 (r2 = 0.80) for staircase at 35 degrees C, and 22 degrees C and posttetanic response respectively. Posttetanic depression rather than potentiation was present at long SL. This indicates that there may be two processes operating in these muscles to modulate the force: one that enhances and a second that depresses the force. Either or both of these processes may have a length-dependence of its mechanism. CONCLUSION: There is no evidence that posttetanic potentiation is fundamentally different from staircase in these muscles.

Animals↗

PubMed2002

Assessment of peak power and short-term work capacity.

The purpose of this study was to evaluate conditions for conducting a 30 s Wingate test such as load selection, and the method of starting the test (stationary or flying start). Nine male and four female athletes volunteered to be tested on four laboratory visits. Tests were performed on a modified Monark cycle ergometer (Varberg, Sweden) equipped with force transducers on the friction belt and an optical encoder for velocity measurement. Power was calculated with the moment of inertia (I) of the flywheel taken into consideration. One laboratory visit was used to determine individualized optimal resistance conditions. The other three visits were for performance of one of three Wingate tests: a flying start with 0.834 N x kg(-1) [85 g x kg(-1) body weight (BW)] resistance (FLY-0.8); a stationary start with 0.834 N x kg(-1) BW resistance (ST-0.8), or a stationary start with optimal resistance (ST-OPT). FLY-0.8 gave a lower (P<0.05) value for short-term work capacity [19,986 (827) J] than either ST-OPT [23,014 (1,167) J] or ST-0.8 [22,321 (1075) J]. Peak power output per pedal revolution was lower ( P<0.005) for FLY-0.8 [833 (40) W] than for either ST-0.8 [974 (57) W] or ST-OPT [989 (61) W]. The results of this study demonstrate that higher values for peak power and short-term work capacity are obtained with a test from a stationary start. It is apparently not necessary to use an individualized optimal resistance when I is considered in a Wingate test initiated from a standstill.

Energy Metabolism↗

PubMed2002

What is fatigue?

Fatigue and potentiation are two forms of force modulation. A general definition of fatigue is "a circumstance where less than the anticipated contractile response is obtained." Fatigue is associated with depressed Ca2+ release and possibly decreased Ca2+ sensitivity. Potentiation results from increased Ca2+ sensitivity due to regulatory light chain phosphorylation. Muscle fatigue and potentiation can coexist, making it difficult to quantify these processes. With repetitive 10Hz stimulation, the developed tension first increases, then decreases. Is fatigue present when developed tension first begins to decrease or when it falls below the developed tension of the first response? Intermittent incompletely fused tetanic contractions for which peak developed tension first decreases, then increases, is another unusual example of fatigue. A third example is when twitch contractions following a tetanic contraction decrease to a level below the pretetanic twitch amplitude, indicating that fatigue may have been coexistent with posttetanic potentiation. These observations illustrate the complexity of detecting fatigue, based on the simple, but commonly accepted definition presented above. Care must be taken in interpreting "before vs. after" contractile responses. Even when the contraction amplitude is greater than the initial response, there is no guarantee that mechanisms associated with fatigue are not present.

Calcium↗

PubMed2002

The lactate minimum test for cycling: estimation of the maximal lactate steady state.

This study evaluated the reliability and validity of the lactate minimum test (LMT), an incremental test given after lactic acidosis was induced by sprint exercise. This test is purported to accurately estimate the intensity of exercise at which the transport of lactate into and out of the blood is in equilibrium (maximal lactate steady state or MLSS) and should be a good predictor of endurance performance. Fourteen athletes (mean age 27.2 +/- 3.7 yrs) completed the following on Kreitler rollers: (a) two 20-km time-trials (35.1 +/- 3.3 and 35.7 +/- 3.5 km.hr-1, p < .05); (b) two LMTs yielding lactate minimum speeds (LMS) of 33.6 +/- 3.4 and 33.4 +/- 3.1 km.hr-1 (p > 0.6); and (c) four constant intensity rides, at speeds bracketing the LMS. At 33.5 +/- 3.1 km.hr-1 plasma lactate concentration decreased 0.4 +/- 1.6 mM from 10 to 30 min. Plasma lactate increased 1.6 +/- 0.7 mM while riding 0.9 +/- 0.9 km.hr-1 faster. The LMT is a reliable (r2 = 0.904) and valid method to predict MLSS and a good predictor of endurance performance (LMT vs. 20-km time-trial, r2 = 0.86).

Adult↗

PubMed2002

Length-dependent twitch contractile characteristics of skeletal muscle.

The length dependence of force development of mammalian skeletal muscles was evaluated during twitch, double-pulse, and tetanic contractions, and the relation between muscle length and the time-dependent characteristics of twitch and double-pulse contractions were determined. In situ isometric contractions of the rat gastrocnemius muscle were analyzed at seven different lengths, based on a reference length at which the maximal response to double-pulse contractions occurred (Lopt-2P). Twitch and double-pulse contractions were analyzed for developed tension (DT), contraction time (tC), average rate of force development (DT-tC(-1)), half-relaxation time (t50%R), peak rate of relaxation (DT x dtmin(-1)), and 90%-relaxation time (t90%R). Considering the length at which maximal tetanic DT occurred to be the optimal length (Lo-TET), the peak DT for twitch contractions and double-pulse contractions was observed at Lo-TET + 0.75 mm (p < 0.05) and Lo-TET + 0.1 mm (p > 0.05), respectively. When measured at the length for which maximal twitch and double-pulse contractions were obtained, tetanic DT was 95.2 +/- 3 and 99.0 +/- 2% of the maximal value, respectively. These observations suggest that double-pulse contractions are more suitable for setting length for experimental studies than twitch contractions. Twitch and double-pulse contraction tC were 15.53 +/- 1.14 and 25.0 +/- 0.6 ms, respectively, at Lopt-2P, and increased above Lopt-2P and decreased below Lopt-2P. Twitch t50%R was 12.18 +/- 0.90 ms at Lopt-2P, and increased above Lopt-2P and below Lopt-2P. Corresponding changes for double-pulse contractions were greater. Stretching the muscle leads to slower twitch contractions and double-pulse contractions, but the mechanisms of this change in time course remain unclear.

Animals↗

PubMed2001

Potentiation of shortening and velocity of shortening during repeated isotonic tetanic contractions in mammalian skeletal muscle.

The purpose of this study was to investigate the enhancement of shortening and of the velocity of shortening during repeated incompletely fused isotonic tetanic contractions. The medial gastrocnemius muscle of anesthetized rats was isolated in situ and the motor nerve stimulated with supramaximal pulses, 50 micros duration, at optimal length. Estimated maximal velocity of shortening (V(max)) was 210 +/- 6 mm x s(-1) (mean +/- SEM). Repeated incompletely fused tetanic contractions (three pulses at 80 Hz) resulted in initial shortening which was 1.5 +/- 0.1 mm, and this increased to 2.7 +/- 0.2 mm after 7 s of 4 s(-1) contractions. Peak velocity of shortening for intermittent 80 Hz stimulation increased from 60.5 +/- 4 mm x s(-1) to 91.8 +/- plus minus 6 mm x s(-1). The initial velocity of shortening for 80 Hz stimulation was substantially less than the velocity of shortening observed with 200 Hz stimulation, but increased to 72 +/- 3% of the load-specific value for 200 Hz stimulation. Myosin regulatory light chain phosphorylation increased from 11.1 +/- 1.5% at rest to 32.9 +/- 5.4% after 4 s of intermittent 80 Hz stimulation and 50.4 +/- 8.8% after 7 s ( P<0.01). The ascending limb of the length-force relationship was determined with tetanic contractions, 200 Hz for 100 ms. At the length corresponding to peak shortening after 7 s of repeated 80 Hz contractions, the maximal isometric force was five times greater than the isotonic load. The rate of phosphorylation was sustained from 4 to 7 s, but the rate of increase in shortening and velocity decreased. The slower rate of change in shortening and velocity may be due to approaching maximal velocity for this short duration of contraction, but is not due to slowing of the rate of phosphorylation of the myosin regulatory light chains.

Animals↗