<p>Dependence of total oxygen consumption (), related to proton leak, related to ATP synthesis, Δp, NADH (% of total NAD) and phenomenological ATP/O<sub>2</sub> ratio on relative activity of ATP usage (relative rate constant, k<sub>UT</sub>, or its activation in relation to rest, A<sub>UT</sub>) in skeletal muscle for ‘standard’ proton leak activity.</p
This article presents the biochemical intra-skeletal-muscle basis of exercise intensity domains: mod...
Estimation de la consommation d'ATP dans la fibre du muscle vaste latéral au cours de contractions i...
rates over broad dynamic work ranges in skeletal muscles. J. Appl. Physiol. 73(5): 1697-1703, 1992.-...
A computer model was used to simulate the dependence of protonmotive force (Δp), proton leak and phe...
<p>A. Original (not re-scaled) dependence of PCr, P<sub>i</sub>, ADP, ATP, pH after 8–12 min of stim...
AbstractThe distribution of control over the resting respiration rate (and other variables) was asse...
Purpose: The consequences of the assumption that the additional ATP usage, underlying the slow compo...
<p>The FRL was calculated as the ratio of H<sub>2</sub>O<sub>2</sub> production rate to twice the O<...
Tissues such as skeletal and cardiac muscles must sustain very large-scale changes in ATP turnover r...
A computer model of the skeletal muscle bioenergetic system was used to study the regulation of oxid...
<p>State 4, state 3, rest, moderate work and heavy/severe work in skeletal muscle are indicated. vLK...
The energy required for muscle contraction is provided by the breakdown of ATP but the amount of ATP...
<p>V’O<sub>2</sub> in state 4<sub>id</sub>, intermediate state and state 3 <sub>id</sub> is scaled f...
<p>A, dependence of , ADP and pH; B, dependence of PCr, P<sub>i</sub> and ATP; C, dependence of ATP ...
More than 30 years ago, it was proposed that adenosine was released from skeletal muscle in response...
This article presents the biochemical intra-skeletal-muscle basis of exercise intensity domains: mod...
Estimation de la consommation d'ATP dans la fibre du muscle vaste latéral au cours de contractions i...
rates over broad dynamic work ranges in skeletal muscles. J. Appl. Physiol. 73(5): 1697-1703, 1992.-...
A computer model was used to simulate the dependence of protonmotive force (Δp), proton leak and phe...
<p>A. Original (not re-scaled) dependence of PCr, P<sub>i</sub>, ADP, ATP, pH after 8–12 min of stim...
AbstractThe distribution of control over the resting respiration rate (and other variables) was asse...
Purpose: The consequences of the assumption that the additional ATP usage, underlying the slow compo...
<p>The FRL was calculated as the ratio of H<sub>2</sub>O<sub>2</sub> production rate to twice the O<...
Tissues such as skeletal and cardiac muscles must sustain very large-scale changes in ATP turnover r...
A computer model of the skeletal muscle bioenergetic system was used to study the regulation of oxid...
<p>State 4, state 3, rest, moderate work and heavy/severe work in skeletal muscle are indicated. vLK...
The energy required for muscle contraction is provided by the breakdown of ATP but the amount of ATP...
<p>V’O<sub>2</sub> in state 4<sub>id</sub>, intermediate state and state 3 <sub>id</sub> is scaled f...
<p>A, dependence of , ADP and pH; B, dependence of PCr, P<sub>i</sub> and ATP; C, dependence of ATP ...
More than 30 years ago, it was proposed that adenosine was released from skeletal muscle in response...
This article presents the biochemical intra-skeletal-muscle basis of exercise intensity domains: mod...
Estimation de la consommation d'ATP dans la fibre du muscle vaste latéral au cours de contractions i...
rates over broad dynamic work ranges in skeletal muscles. J. Appl. Physiol. 73(5): 1697-1703, 1992.-...