scholarly journals Power fatigue of the rat diaphragm muscle

2000 ◽  
Vol 89 (6) ◽  
pp. 2215-2219 ◽  
Author(s):  
Bill T. Ameredes ◽  
Wen-Zhi Zhan ◽  
Y. S. Prakash ◽  
Rene Vandenboom ◽  
Gary C. Sieck
Keyword(s):  
Diaphragm Muscle ◽  
Fiber Types ◽  
Rat Diaphragm ◽  
Shortening Velocity ◽  
Reduction In Force ◽  
Novel Technique ◽  
Velocity Relationship ◽  
Stimulus Train ◽  
Force Velocity

We hypothesized that decrements in maximum power output (W˙max) of the rat diaphragm (Dia) muscle with repetitive activation are due to a disproportionate reduction in force (force fatigue) compared with a slowing of shortening velocity (velocity fatigue). Segments of midcostal Dia muscle were mounted in vitro (26°C) and stimulated directly at 75 Hz in 400-ms-duration trains repeated each second (duty cycle = 0.4) for 120 s. A novel technique was used to monitor instantaneous reductions in maximum specific force (Po) andW˙max during fatigue. During each stimulus train, activation was isometric for the initial 360 ms during which Po was measured; the muscle was then allowed to shorten at a constant velocity (30% V max) for the final 40 ms, and W˙max was determined. Compared with initial values, after 120 s of repetitive activation, Po andW˙max decreased by 75 and 73%, respectively. Maximum shortening velocity was measured in two ways: by extrapolation of the force-velocity relationship ( V max) and using the slack test [maximum unloaded shortening velocity ( V o)]. After 120 s of repetitive activation, V max slowed by 44%, whereas V o slowed by 22%. Thus the decrease inW˙max with repetitive activation was dominated by force fatigue, with velocity fatigue playing a secondary role. On the basis of a greater slowing of V max vs. V o, we also conclude that force and power fatigue cannot be attributed simply to the total inactivation of the most fatigable fiber types.

Salbutamol enhances isotonic contractile properties of rat diaphragm muscle

1998 ◽  
Vol 85 (2) ◽  
pp. 525-529 ◽  
Author(s):  
H. F. M. Van Der Heijden ◽  
W. Z. Zhan ◽  
Y. S. Prakash ◽  
P. N. R. Dekhuijzen ◽  
G. C. Sieck
Keyword(s):  
Power Output ◽  
Maximum Power ◽  
Contractile Properties ◽  
Diaphragm Muscle ◽  
Rat Diaphragm ◽  
Shortening Velocity ◽  
Maximum Power Output ◽  
Isometric Twitch ◽  
Camp Levels

The effects of the β2-adrenoceptor agonist salbutamol (Slb) on isometric and isotonic contractile properties of the rat diaphragm muscle (Diamus) were examined. A loading dose of 25 μg/kg Slb was administered intracardially before Diamus excision to ensure adequate diffusion. Studies were then performed with 0.05 μM Slb in the in vitro tissue chamber. cAMP levels were determined by radioimmunoassay. Compared with controls (Ctl), cAMP levels were elevated after Slb treatment. In Slb-treated rats, isometric twitch and maximum tetanic force were increased by ∼40 and ∼20%, respectively. Maximum shortening velocity increased by ∼15% after Slb treatment, and maximum power output increased by ∼25%. During repeated isotonic activation, the rate of fatigue was faster in the Slb-treated Diamus, but both Slb-treated and Ctl Diamusfatigued to the same maximum power output. Still, endurance time during repetitive isotonic contractions was ∼10% shorter in the Slb-treated Diamus. These results are consistent with the hypothesis that β-adrenoceptor stimulation by Slb enhances Diamus contractility and that these effects of Slb are likely mediated, at least in part, by elevated cAMP.

Effects of postnatal maturation on energetics and cross-bridge properties in rat diaphragm

2002 ◽  
Vol 92 (3) ◽  
pp. 1074-1082 ◽  
Author(s):  
Gilles Orliaguet ◽  
Olivier Langeron ◽  
Belaid Bouhemad ◽  
Pierre Coriat ◽  
Yves LeCarpentier ◽  
...  
Keyword(s):  
Mechanical Efficiency ◽  
Total Force ◽  
Rat Diaphragm ◽  
Shortening Velocity ◽  
Cross Sectional ◽  
Muscle Energetics ◽  
Postnatal Maturation ◽  
Cross Bridge ◽  
Velocity Relationship ◽  
Force Velocity

The effects of maturation on cross-bridge (CB) properties were studied in rat diaphragm strips obtained at postnatal days 3, 10, and 17 and in adults (10–12 wk old). Calculations of muscle energetics and characteristics of CBs were determined from standard Huxley equations. Maturation did not change the curvature of the force-velocity relationship or the peak of mechanical efficiency. There was a significant increase in the total number of CBs per cross-sectional area (m) with aging but not in single CB force. The turnover rate of myosin ATPase increased, the duration of the CB cycle decreased, and the velocity of CBs decreased significantly only after the first week postpartum. There was a linear relationship between maximum total force and m ( r = 0.969, P < 0.001), and between maximum unloaded shortening velocity and m ( r = 0.728, P < 0.001). When this study in the rat and previous study in the hamster are compared, it appears that there are few species differences in the postnatal maturation process of the diaphragm.

Hypothyroidism alters diaphragm muscle development

1996 ◽  
Vol 81 (5) ◽  
pp. 1965-1972 ◽  
Author(s):  
Gary C. Sieck ◽  
Louise E. Wilson ◽  
Bruce D. Johnson ◽  
Wen-Zhi Zhan
Keyword(s):  
Muscle Development ◽  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Diaphragm Muscle ◽  
Rat Diaphragm ◽  
Shortening Velocity ◽  
Pregnant Rats ◽  
Isoform Expression ◽  
The Impact

Sieck, Gary C., Louise E. Wilson, Bruce D. Johnson, and Wen-Zhi Zhan. Hypothyroidism alters diaphragm muscle development. J. Appl. Physiol. 81(5): 1965–1972, 1996.—The impact of hypothyroidism (Hyp) on myosin heavy chain (MHC) isoform expression, maximum specific force (Po), fatigability, and maximum unloaded shortening velocity ( V o) was determined in the rat diaphragm muscle (Dia) at 0, 7, 14, 21, and 28 days of age. Hyp was induced by treating pregnant rats with 6- n-propyl-2-thiouracil (0.05% in drinking water) beginning at gestational day 10 and was confirmed by reduced plasma levels of 3,5,3′-triiodothyronine and thyroxine. MHC isoforms were separated on sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels and analyzed by densitometry. Isometric Po and fatigue resistance of the Dia were measured in vitro at 26°C, and V o was determined at 15°C with the slack test. Compared with control muscles, expression of MHC-slow was higher and expression of adult fast MHC isoforms was lower in Hyp Dia at all ages. The neonatal isoform of MHC continued to be expressed in the Hyp Dia until day 28. At each age, Po and fatigability were reduced and V o was slower in the Hyp Dia. We conclude that Hyp-induced alterations in MHC isoform expression do not fully predict the changes in Dia contractile properties.

Effects of Acute Respiratory and Metabolic Acidosis on Diaphragm Muscle Obtained from Rats

2015 ◽  
Vol 122 (4) ◽  
pp. 876-883 ◽  
Author(s):  
Pierre Michelet ◽  
Serge Carreira ◽  
Alexandre Demoule ◽  
Julien Amour ◽  
Olivier Langeron ◽  
...  
Keyword(s):  
Metabolic Acidosis ◽  
Isometric Force ◽  
Respiratory Acidosis ◽  
Diaphragm Muscle ◽  
Peak Power Output ◽  
Control Group ◽  
Rat Diaphragm ◽  
Shortening Velocity ◽  
Cross Bridge

Abstract Background: Acute respiratory acidosis is associated with alterations in diaphragm performance. The authors compared the effects of respiratory acidosis and metabolic acidosis in the rat diaphragm in vitro. Methods: Diaphragmatic strips were stimulated in vitro, and mechanical and energetic variables were measured, cross-bridge kinetics calculated, and the effects of fatigue evaluated. An extracellular pH of 7.00 was obtained by increasing carbon dioxide tension (from 25 to 104 mmHg) in the respiratory acidosis group (n = 12) or lowering bicarbonate concentration (from 24.5 to 5.5 mM) in the metabolic acidosis group (n = 12) and the results compared with a control group (n = 12, pH = 7.40) after 20-min exposure. Results: Respiratory acidosis induced a significant decrease in maximum shortening velocity (−33%, P &lt; 0.001), active isometric force (−36%, P &lt; 0.001), and peak power output (−59%, P &lt; 0.001), slowed relaxation, and decreased the number of cross-bridges (−35%, P &lt; 0.001) but not the force per cross-bridge, and impaired recovery from fatigue. Respiratory acidosis impaired more relaxation than contraction, as shown by impairment in contraction–relaxation coupling under isotonic (−26%, P &lt; 0.001) or isometric (−44%, P &lt; 0.001) conditions. In contrast, no significant differences in diaphragmatic contraction, relaxation, or contraction–relaxation coupling were observed in the metabolic acidosis group. Conclusions: In rat diaphragm, acute (20 min) respiratory acidosis induced a marked decrease in the diaphragm contractility, which was not observed in metabolic acidosis.

Fatigue of mouse soleus muscle, using the work loop technique.

1997 ◽  
Vol 200 (22) ◽  
pp. 2907-2912 ◽  
Author(s):  
G N Askew ◽  
I S Young ◽  
J D Altringham
Keyword(s):  
Soleus Muscle ◽  
Power Output ◽  
Cycle Frequency ◽  
Reduction In Force ◽  
Negative Work ◽  
Loop Shape ◽  
Force Velocity ◽  
Positive Work ◽  
Work Loop

The function of many muscles requires that they perform work. Fatigue of mouse soleus muscle was studied in vitro by subjecting it to repeated work loop cycles. Fatigue resulted in a reduction in force, a slowing of relaxation and in changes in the force-velocity properties of the muscle (indicated by changes in work loop shape). These effects interacted to reduce the positive work and to increase the negative work performed by the muscle, producing a decline in net work. Power output was sustained for longer and more cumulative work was performed with decreasing cycle frequency. However, absolute power output was highest at 5 Hz (the cycle frequency for maximum power output) until power fell below 20% of peak power. As cycle frequency increased, slowing of relaxation had greater effects in reducing the positive work and increasing the negative work performed by the muscle, compared with lower cycle frequencies.

scholarly journals Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle

1997 ◽  
Vol 83 (4) ◽  
pp. 1062-1067 ◽  
Author(s):  
Roland H. H. Van Balkom ◽  
Wen-Zhi Zhan ◽  
Y. S. Prakash ◽  
P. N. Richard Dekhuijzen ◽  
Gary C. Sieck
Keyword(s):  
Isometric Force ◽  
Contractile Properties ◽  
Diaphragm Muscle ◽  
Peak Power Output ◽  
Rat Diaphragm ◽  
Fiber Morphology ◽  
Shortening Velocity ◽  
Maximum Isometric Force ◽  
Induced Changes ◽  
Isotonic Contractions

Van Balkom, Roland H. H., Wen-Zhi Zhan, Y. S. Prakash, P. N. Richard Dekhuijzen, and Gary C. Sieck. Corticosteroid effects on isotonic contractile properties of rat diaphragm muscle. J. Appl. Physiol. 83(4): 1062–1067, 1997.—The effects of corticosteroids (CS) on diaphragm muscle (Diam) fiber morphology and contractile properties were evaluated in three groups of rats: controls (Ctl), surgical sham and weight-matched controls (Sham), and CS-treated (6 mg ⋅ kg−1 ⋅ day−1prednisolone at 2.5 ml/h for 3 wk). In the CS-treated Diam, there was a selective atrophy of type IIx and IIb fibers, compared with a generalized atrophy of all fibers in the Sham group. Maximum isometric force was reduced by 20% in the CS group compared with both Ctl and Sham. Maximum shortening velocity in the CS Diamwas slowed by ∼20% compared with Ctl and Sham. Peak power output of the CS Diam was only 60% of Ctl and 70% of Sham. Endurance to repeated isotonic contractions improved in the CS-treated Diam compared with Ctl. We conclude that the atrophy of type IIx and IIb fibers in the Diam can only partially account for the CS-induced changes in isotonic contractile properties. Other factors such as reduced myofibrillar density or altered cross-bridge cycling kinetics are also likely to contribute to the effects of CS treatment.

Age-related increases in diaphragmatic maximal shortening velocity

1996 ◽  
Vol 80 (2) ◽  
pp. 445-451 ◽  
Author(s):  
S. K. Powers ◽  
D. Criswell ◽  
R. A. Herb ◽  
H. Demirel ◽  
S. Dodd
Keyword(s):  
Force Production ◽  
Specific Force ◽  
Fischer 344 Rats ◽  
Rat Diaphragm ◽  
Shortening Velocity ◽  
Fischer 344 ◽  
Age Related ◽  
Highly Correlated ◽  
Related Increase

Recent evidence demonstrates that aging results in an increase in fast (type IIB) myosin heavy chain (MHC) in the rat diaphragm. It is unknown whether this age-related change in fast MHC influences the diaphragmatic maximal shortening velocity (Vmax). Therefore, we tested the hypothesis that aging is associated with an increase in the diaphragmatic Vmax and that the increase in the Vmax is highly correlated with the percentage of type IIb MHC. In vitro contractile properties were measured with costal diaphragm strips obtained from young (4 mo old; n = 8) and (old 24 mo old; n = 8) male Fischer-344 rats. Diaphragmatic maximal tetanic specific force production was 14.5% lower in the old compared with the young animals (23.0 +/- 0.4 vs. 19.7 +/- 0.8 N/cm2; P < 0.05). In contrast, the diaphragmatic Vmax was significantly higher in the old compared with the young animals (5.5 +/- 0.1 vs. 4.4 +/- 0.3 lengths/s; P < 0.05). Although the percent type IIb MHC was significantly higher (approximately +14%; P < 0.05) in the old compared with the young animals, the correlation between Vmax and percent type IIb MHC was relatively low (r = 0.50; P = 0.05). These data support the hypothesis that an age-related increase in diaphragmatic Vmax occurs; however, factors in addition to type IIb MHC are involved in regulating diaphragmatic Vmax. Interestingly, although aging resulted in a decrease in diaphragmatic maximal specific force production, power output at all muscle loads was maintained in the old animals due to the increase in diaphragmatic shortening velocity.

THE WATER AND ELECTROLYTE METABOLISM OF RAT DIAPHRAGM IN VITRO

1956 ◽  
Vol 34 (1) ◽  
pp. 1069-1083 ◽  
Author(s):  
R. H. Rixon ◽  
J. A. F. Stevenson
Keyword(s):  
Intracellular Water ◽  
Diaphragm Muscle ◽  
Optimal Conditions ◽  
Rat Diaphragm ◽  
Concentration Gradients ◽  
Hypoxic Conditions ◽  
Diaphragm In Vitro ◽  
Sodium And Potassium

The distribution of water and of sodium and potassium between the cell and synthetic environments has been studied in rat diaphragm muscle. It has been found that: (1) the amount of intracellular water is markedly increased at 0 °C. in oxygen and at 37 °C. in nitrogen compared to that of tissue at 37 °C. in oxygen, in media up to 0.75 osmolar; (2) optimal conditions of temperature and oxygen are necessary to prevent or reduce the uptake of water; (3) swelling at reduced temperatures and under hypoxic conditions is related to the oxygen uptake; (4) the loss of tissue solids during incubation does not have any significant effect on the calculation of the total tissue and intracellular water; (5) the concentration of total sodium and potassium in the tissue, in vivo and in vitro at optimal conditions is slightly in excess of that in the plasma water or incubating medium—this is believed not to represent an active hypertonicity; (6) concomitant with the uptake of water there are marked redistributions of sodium and potassium, the gain of sodium being greater than the loss of potassium. It is concluded that the swelling of tissue cells under conditions that inhibit oxidative metabolism is primarily due to the redistribution of electrolytes and that the natural distribution of water in muscle is determined by active maintenance of the concentration gradients of sodium and potassium across the cell membrane.

Force-velocity relationship of expiratory muscles in normal subjects

1982 ◽  
Vol 52 (4) ◽  
pp. 930-938 ◽  
Author(s):  
Y. Kikuchi ◽  
H. Sasaki ◽  
K. Sekizawa ◽  
K. Aihara ◽  
T. Takishima
Keyword(s):  
Respiratory Muscles ◽  
Normal Subjects ◽  
Contractile Element ◽  
Shortening Velocity ◽  
Mean Values ◽  
Significant Difference ◽  
Velocity Relationship ◽  
Force Velocity ◽  
Expiratory Muscles ◽  
Relationship Of

We examined the force-velocity relationship of the respiratory muscles in normal subjects under nearly isotonic conditions, taking into consideration the pleural pressure (Ppl) changes during maximum forced expirations (MFE). We used an electromagnetic valve (EMV) to select the Ppl value at the onset of mouth flow; and both a pressure reservoir and a variable resistance to control the Ppl changes after the opening of the EMV during MFE. To simulate isotonic conditions and to obtain the shortening velocity of the contractile element (CE), we mathematically corrected the velocity of the series elastic component (SEC), using a modified version of Hill's equation. Although the maximum tension at total lung capacity (TLC) [1,156 +/- 215 (SD) g/cm] was larger than that at functional residual capacity (FRC) (782 +/- 97 g/cm) there was no significant difference in the maximum shortening velocity, 3.4 +/- 1.0 and 3.2 +/- 0.8 circumference/s at TLC and FRC, respectively. The mean values of k (slope) for the SEC at TLC and FRC were 19 +/- 4 and 18 +/- 5 circumference-1, respectively, and they were not significantly different. We concluded that the force-velocity relationship of the expiratory muscles exhibited the same mechanical properties as that of the other skeletal muscles.

Isotonic contractile and fatigue properties of developing rat diaphragm muscle

1998 ◽  
Vol 84 (4) ◽  
pp. 1260-1268 ◽  
Author(s):  
Wen-Zhi Zhan ◽  
Jon F. Watchko ◽  
Y. S. Prakash ◽  
Gary C. Sieck
Keyword(s):  
Power Output ◽  
Supply And Demand ◽  
Maximum Power ◽  
Diaphragm Muscle ◽  
Fatigue Properties ◽  
Rat Diaphragm ◽  
Shortening Velocity ◽  
Endurance Time ◽  
Early Postnatal Development ◽  
Maximum Power Output

Postnatal transitions in myosin heavy chain (MHC) isoform expression were found to be associated with changes in both isometric and isotonic contractile properties of rat diaphragm muscle (Diam). Expression of MHCneo predominated in neonatal Diam fibers but was usually coexpressed with MHCslow or MHC2A isoforms. Expression of MHCneo disappeared by day 28. Expression of MHC2X and MHC2B emerged at day 14 and increased thereafter. Associated with these MHC transitions in the Diam, maximum isometric tetanic force (Po), maximum shortening velocity, and maximum power output progressively increased during early postnatal development. Maximum power output of the Diam occurred at ∼40% Po at days 0 and 7 and at ∼30% Po in older animals. Susceptibility to isometric and isotonic fatigue, defined as a decline in force and power output during repetitive activation, respectively, increased with maturation. Isotonic endurance time, defined as the time for maximum power output to decline to zero, progressively decreased with maturation. In contrast, isometric endurance time, defined as the time for force to decline to 30–40% Po, remained >300 s until after day 28. We speculate that with the postnatal transition to MHC2X and MHC2Bexpression energy requirements for contraction increase, especially during isotonic shortening, leading to a greater imbalance between energy supply and demand.

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