scholarly journals The relationship between initial creatine phosphate breakdown and recovery oxygen consumption for a single isometric tetanus of the frog sartorius muscle at 20 degrees C.

1979 ◽  
Vol 73 (2) ◽  
pp. 159-174 ◽  
Author(s):  
M Mahler
Keyword(s):  
Oxygen Consumption ◽  
Time Course ◽  
Atp Hydrolysis ◽  
Creatine Phosphate ◽  
Sartorius Muscle ◽  
Exothermic Reactions ◽  
Rate Of Oxygen Consumption ◽  
The Relationship ◽  
Frog Sartorius

A previous paper (Mahler, M. 1978 J. Gen. Physiol. 71:559--580) describes the time-course of the suprabasal rate of oxygen consumption (delta QO2) in the sartorius muscle of R. pipiens after isometric tetani of 0.1--1.0 s at 20 degrees C. To test whether these were the responses to impulse changes in the rate of ATP hydrolysis, we compared the total suprabasal oxygen consumption during recovery (delta[O2]) with the amount of ATP hydrolyzed during a contraction, measured indirectly as the decrease in creatine phosphate (delta[CP]O). If suprabasal ATP hydrolysis during recovery is negligible in comparison with that during contraction, delta[CP]0/delta[O2] should approximate the P:O2 ratio for oxidative metabolism, which has an expected value of 6.1--6.5. We found: formula; see text. We conclude that in this muscle at 20 degrees C: (a) after a tetanus of 0.2--1.0 s, delta QO2(t) can be considered the response to an impulse increase in the rate of ATP hydrolysis; (b) the reversal during recovery of unidentified exothermic reactions occurring during the contraction (Woledge, R. C. 1971. Prog. Biophys. Mol. Biol. 22:39--74) can be coupled to an ATP hydrolysis that is at most a small fraction of delta[CP]0; (c) the pooled mean for delta[CP]0/delta[O2], 6.58 +/- 0.55, sets an experimental lower bound for the P:O2 ratio in vivo.

scholarly journals Kinetics of oxygen consumption after a single isometric tetanus of frog sartorius muscle at 20 degrees C.

1978 ◽  
Vol 71 (5) ◽  
pp. 559-580 ◽  
Author(s):  
M Mahler
Keyword(s):  
Oxygen Consumption ◽  
Time Course ◽  
Atp Hydrolysis ◽  
Preceding Paper ◽  
Nonlinear Process ◽  
Forthcoming Paper ◽  
Sartorius Muscle ◽  
Frog Sartorius Muscle ◽  
Kinetics Of ◽  
Frog Sartorius

The time-course of the rate of oxygen consumption (QO2) has been measured in the excised frog sartorius muscle after single isometric tetani of 0.1-1.0 s at 20 degrees C. To measure deltaQO2(t), the change in QO2 from its basal level, a novel method was devised, based on the validity in this tissue of the one-dimensional diffusion equation for oxygen, established in the preceding paper. After a tetanus, deltaQO2 reached a peak within 45-90 s, then declined exponentially, and could be well fit by deltaQO2(t) = QO + Q1(epsilon -k1t - epsilon-k2t). tau2 (= 1/k2), which characterized the rise of deltaQO2, was a decreasing function of tetanus duration (range: from 1.1 +/- 0.28 min [nu = 5] for a 0.1-s tetanus, to 0.34 +/- 0.05 min [nu = 8] for a 1.0-sec tetanus). tau1 (= 1/k1), which characterized the decline of deltaQO2, was not dependent on tetanus duration, with mean 3.68 +/- -.24 min (nu = 46). A forthcoming paper in this series shows that these kinetics of deltaQO2 are the responses to impulse-like changes in the rate of ATP hydrolysis. The variation of tau2 with tetanus duration thus indicates the involvement of a nonlinear process in the coupling of O2 consumption to ATP hydrolysis. However, the monoexponential decline of deltaQO2(t), with time constant independent of tetanus duration, suggests that during this phase, the coupling is rate-limited by a single reaction with apparent first order kinetics.

scholarly journals Reappraisal of diffusion, solubility, and consumption of oxygen in frog skeletal muscle, with applications to muscle energy balance.

1985 ◽  
Vol 86 (1) ◽  
pp. 105-134 ◽  
Author(s):  
M Mahler ◽  
C Louy ◽  
E Homsher ◽  
A Peskoff
Keyword(s):  
Diffusion Equation ◽  
Time Course ◽  
Atp Hydrolysis ◽  
Rana Temporaria ◽  
Direct Method ◽  
Diffusion Method ◽  
Sartorius Muscle ◽  
O2 Consumption ◽  
Dimensional Diffusion ◽  
Frog Sartorius

Previously we tested the validity of the one-dimensional diffusion equation for O2 in the excised frog sartorius muscle and used it to measure the diffusion coefficient (D) for O2 in this muscle and the time course of its rate of O2 consumption (Qo2) after a tetanus (Mahler, 1978, 1979, J. Gen. Physiol., 71:533-557, 559-580, 73:159-174). A transverse section of the frog sartorius is in fact well fit by a hemi-ellipse with width divided by maximum thickness averaging 5.1 +/- 0.2. Using the previous techniques with the two-dimensional diffusion equation and this hemi-elliptical boundary yields a value for D that is 30% smaller than reported previously; the revised values at 0, 10, and 22.8 degrees C are 6.2, 7.9, and 10.8 X 10(-6) cm2/s, respectively. After a tetanus at 20 degrees C, Qo2 rose quickly to a peak and then declined exponentially, with a time constant (tau) approximately 15% faster than that reported previously; tau averaged 2.1 min in Rana temporaria and 2.6 min in Rana pipiens. A technique was devised to measure the solubility (alpha) of O2 in intact, respiring muscles, and yielded alpha (muscle)/alpha (H2O) = 1.26 +/- 0.04. With these modifications, the values for O2 consumption obtained with the diffusion method were in agreement with those measured by the direct method of Kushmerick and Paul (1976, J. Physiol. [Lond.]., 254:693-709). Using results from both methods, at 20 degrees C the ratio of phosphorylcreatine split during a tetanus to O2 consumption during recovery ranged from 5.2 to 6.2 mumol/mumol, and postcontractile ATP hydrolysis was estimated to be 13.6 +/- 4.1 (n = 3) nmol/mumol total creatine.

scholarly journals The Variation of Muscle Oxygen Consumption With Velocity of Shortening

1965 ◽  
Vol 49 (1) ◽  
pp. 9-15 ◽  
Author(s):  
R. J. Baskin
Keyword(s):  
Oxygen Consumption ◽  
Mechanical Efficiency ◽  
Sartorius Muscle ◽  
Maximum Oxygen Consumption ◽  
Shortening Velocity ◽  
Muscle Oxygen ◽  
Velocity Of Shortening ◽  
Muscle Oxygen Consumption ◽  
The Relationship ◽  
Frog Sartorius

Total oxygen consumption following contraction at controlled shortening velocities was determined for ten twitches of frog sartorius muscle. Under the conditions of this investigation maximum oxygen consumption occurred at approximately 30 mm/sec. shortening velocity and decreased for larger and smaller velocities. Mechanical efficiency was calculated and found to show a maximum at approximately 20 mm/sec. shortening velocity. The relationship between this study and a similar investigation in which heat changes are measured as a function of shortening velocity is discussed.

Relation between phosphate metabolites and oxygen consumption of heart in vivo

1989 ◽  
Vol 256 (1) ◽  
pp. H265-H274 ◽  
Author(s):  
L. A. Katz ◽  
J. A. Swain ◽  
M. A. Portman ◽  
R. S. Balaban
Keyword(s):  
Oxygen Consumption ◽  
Atp Hydrolysis ◽  
Respiratory Control ◽  
Creatine Phosphate ◽  
Canine Heart ◽  
Hydrolysis Products ◽  
Threefold Increase ◽  
Cooperativity Effects

The relation between induced increases in cardiac work and phosphate metabolites was investigated in the canine heart in vivo to evaluate the role of ATP hydrolysis products, ADP and inorganic phosphate (Pi), in the control of myocardial oxygen consumption (MVO2). In these studies, myocardial blood flow and oxygen consumption were simultaneously measured with the 31P-nuclear magnetic resonance (NMR)-detected phosphate metabolites. Three protocols were used to increase myocardial work: pacing, epinephrine, and phenylephrine infusions. When these protocols were used, no or only slight changes in myocardial ATP, Pi, and creatine phosphate were observed with a greater than threefold increase in MVO2. The calculated intracellular free Mg concentration, ADP, and pH were also only slightly affected by these increases in work. These data indicate that a simple model involving the feedback of cytosolic ADP and Pi to the mitochondria regulating respiration is inadequate to explain respiratory control in vivo. These data suggest that some other parameters or cooperativity effects involving the phosphate metabolites must play a role in the feedback between respiration and work in the heart in vivo.

On Respiration in the Dragonet Callionymus Lyra L

1968 ◽  
Vol 49 (3) ◽  
pp. 565-582
Author(s):  
G. M. HUGHES ◽  
SHUN-ICHI UMEZAWA
Keyword(s):  
Heart Rate ◽  
Oxygen Consumption ◽  
Time Course ◽  
Water Pressure ◽  
Minute Volume ◽  
Individual Variations ◽  
Wide Range ◽  
The Relationship ◽  
Respiratory Rhythms ◽  
Normal Ventilation

1. The usefulness of a bottom-living fish, the dragonet (Callionymus lyra), in experiments on fish respiration is described. The position and nature of its opercular opening made it possible to determine directly the volume of water pumped over the gills and the PO2 of the mixed expired water. The normal ventilation volume for a 100 g. fish was about 30 c.c./min. 2. The relationship between cardiac and respiratory rhythms was investigated and showed a variety of ratios. The heart usually beats more than once during each respiratory cycle. Individual variations in the coupling between these rhythms was common and close couplings were observed in the absence of anaesthetic and at normal PO2s. 3. Changes in minute volume produced by altering the hydrostatic pressure across the respiratory system did not affect the heart rate. Percentage utilization fell at higher flow rates. Changes in flow per cm. of water pressure gradient was less with negative gradients than when the static pressure on the mouth side exceeded that in the opercular collecting chamber. 4. Oxygen consumption of the fish is directly related to the ambient PO2 over a wide range (30-120 mm. Hg). Sudden lowering of the PO2 in the inspired water leads to compensatory responses in which the minute volume is maintained or increased as a result of a rise in stroke volume and lowered respiratory frequency: there is also a marked bradycardia. During recovery the increased oxygen consumption of the fish resulted from a rise in utilization rather than a change in the respiratory rate or ventilation volume. 5. Analysis of the time course of the changes in heart rate and ventilation volume in experiments in which PO2 was changed supports the view that the receptors mediating bradycardia occur on the gills and respond directly to the change in PO2 rather than to the secondary increase in flow produced by the hypoxia.

The relationship between cirral activity and oxygen uptake in Balanus balanoides

1965 ◽  
Vol 45 (2) ◽  
pp. 387-403 ◽  
Author(s):  
R. C. Newell ◽  
H. R. Northcroft
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Mantle Cavity ◽  
The Body ◽  
Effect Of Temperature ◽  
Zero Rate ◽  
Rate Of Oxygen Consumption ◽  
The Relationship ◽  
Balanus Balanoides

The rate of cirral beat of Balanus balanoides is related to the logarithm of the body weight as an exponential function. In any one animal, there is little effect of temperature on cirral activity between 7·5° and 10° C. Between 10° and 20° C, however, there is a rapid increase in cirral beat with temperature followed by a fall at temperatures above 20° C.Balanus balanoides exhibits a fast, medium and zero rate of oxygen consumption. These rates of oxygen consumption correspond with (a) normal cirral beating, (b) ‘testing’ activity with no cirral movement, and (c) with the closure of the mantle cavity. Both of the possible levels of oxygen uptake are related to the logarithm of the body weight in a logarithmic fashion over the temperature range 7·5°–22·5° C. Temperature affects the two rates of oxygen consumption differently. In the slower rate (rate B) there is an increase in the rate of oxygen consumption between 7·5° and 14° C but there is no significant increase in the rate of oxygen consumption between 14° and 22·5 C°.

scholarly journals Studies on the activity of the hypoxia-inducible-factor hydroxylases using an oxygen consumption assay

2006 ◽  
Vol 401 (1) ◽  
pp. 227-234 ◽  
Author(s):  
Dominic Ehrismann ◽  
Emily Flashman ◽  
David N. Genn ◽  
Nicolas Mathioudakis ◽  
Kirsty S. Hewitson ◽  
...  
Keyword(s):  
Oxygen Consumption ◽  
Recombinant Protein ◽  
Synthetic Peptides ◽  
Hypoxia Inducible Factor ◽  
Oxygen Sensors ◽  
Hydroxylase Activity ◽  
Protein Substrates ◽  
Physiological Conditions ◽  
The Relationship

The activity and levels of the metazoan HIF (hypoxia-inducible factor) are regulated by its hydroxylation, catalysed by 2OG (2-oxoglutarate)- and Fe(II)-dependent dioxygenases. An oxygen consumption assay was developed and used to study the relationship between HIF hydroxylase activity and oxygen concentration for recombinant forms of two human HIF hydroxylases, PHD2 (prolyl hydroxylase domain-containing protein 2) and FIH (factor inhibiting HIF), and compared with two other 2OG-dependent dioxygenases. Although there are caveats on the absolute values, the apparent Km (oxygen) values for PHD2 and FIH were within the range observed for other 2OG oxygenases. Recombinant protein substrates were found to have lower apparent Km (oxygen) values compared with shorter synthetic peptides of HIF. The analyses also suggest that human PHD2 is selective for fragments of the C-terminal over the N-terminal oxygen-dependent degradation domain of HIF-1α. The present results, albeit obtained under non-physiological conditions, imply that the apparent Km (oxygen) values of the HIF hydroxylases enable them to act as oxygen sensors providing their in vivo capacity is appropriately matched to a hydroxylation-sensitive signalling pathway.

scholarly journals The Effect of Shortening on the Time-Course of Active State Decay

1972 ◽  
Vol 60 (2) ◽  
pp. 202-220 ◽  
Author(s):  
Kay L. Briden ◽  
Norman R. Alpert
Keyword(s):  
Time Course ◽  
Active State ◽  
Sartorius Muscle ◽  
Quick Release ◽  
State Decay ◽  
State Force ◽  
Contraction Cycle ◽  
Frog Sartorius ◽  
Isotonic Shortening

The active state describes the force developed in a muscle when the contractile elements are neither lengthening nor shortening. Recently it was suggested that perturbations used to measure the active state also alter the time-course of the active state. The present research was undertaken to assess quantitatively the effect of two such perturbations, isotonic shortening and quick release, on the active state in frog sartorius muscle. Methods were developed which allowed the determination of active state points following periods of controlled isotonic shortening or quick release early in the contraction cycle. All experiments were carried out within the plateau region of the length-tension curve. Both isotonic shortening and quick release altered the active state decay. The active state force decreased as the extent of shortening or release was increased. For each 0.1 mm of isotonic shortening there was a 2% decrease in active state force. Quick release produced a larger decrement. From this data we conclude that the time-course of active state can be measured only in relative terms because it is altered by the motion which takes place in the contractile machine while the active state is being measured. This finding helps to resolve paradoxes in the literature relating to the time-course of the active state, calculated and experimentally determined isometric tetanic myograms, and the heat of shortening.

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