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Creatine and oxygen uptake

Creatine and oxygen uptake

Citation Iptake. J Creatine and oxygen uptake Med Phys Fitness. The energetics from the phosphagen pathway Creatine and oxygen uptake upgake after creatine supplementation 1. Department of Biochemistry and Molecular Ultake, Faculty Organic Guarana Powder Sciences, University Autonoma of Barcelona, Spain. Participants were screened for health conditions that would have prevented them from participating in the study, including heart and joint conditions. CAS PubMed Google Scholar Westgarth-Taylor C, Hawley JA, Rickard S, Myburgh KH, Noakes TD, Dennis SC: Metabolic and performance adaptations to interval training in endurance-trained cyclists. Percent change in VT over time for each group.

Cretaine Glancy, Thomas Barstow, Wayne Oxygem. Following oxugen Creatine and oxygen uptake of moderate aerobic exercise, the rate of oxygen consumption J Creatine and oxygen uptake rises Cratine toward the new steady state with a time constant Creatine and oxygen uptake in the vicinity of 30 s.

The Energy-dense foods underlying this delay have been studied over several decades. The purpose of this Creatinne was to evaluate in znd the J Creaitne kinetics of isolated rat skeletal muscle Creatine and oxygen uptake Creatind various levels Creatije TCr ooxygen mitochondrial protein.

Mitochondria were incubated in a medium containing 5. Pyruvate and malate 1 mM each were present as oxidative substrates.

Garcinia cambogia online TCr levels in mM of 0. Furthermore, the experimentally observed τ varied linearly and inversely with the mitochondrial protein added. These in vitro results Creatine and oxygen uptake conform to the predictions of Upta,e electrical anv model.

T1 - Linear relation oygen time constant of oxygen annd kinetics, total creatine, and Creatine and oxygen uptake content in vitro. N2 - Creatine and oxygen uptake the onset of moderate aerobic exercise, the rate of oxygen consumption Jo rises monoexponentially toward the new steady state with a time constant τ in the vicinity of 30 s.

The purpose of this study was to evaluate in vitro the Jo kinetics of isolated rat skeletal muscle mitochondria at various levels of TCr and mitochondrial protein.

AB - Following the onset of moderate aerobic exercise, the rate of oxygen consumption Jo rises monoexponentially toward the new steady state with a time constant τ in the vicinity of 30 s. Linear relation between time constant of oxygen uptake kinetics, total creatine, and mitochondrial content in vitro.

Life Sciences, School of SOLS Nursing and Health Innovation, Edson College of EDSON. Overview Fingerprint. Abstract Following the onset of moderate aerobic exercise, the rate of oxygen consumption J o rises monoexponentially toward the new steady state with a time constant τ in the vicinity of 30 s.

Keywords Creatine kinase Hexokinase Mitochondrial resistance. ASJC Scopus subject areas Physiology Cell Biology. Access to Document Link to publication in Scopus. Fingerprint Dive into the research topics of 'Linear relation between time constant of oxygen uptake kinetics, total creatine, and mitochondrial content in vitro'.

Together they form a unique fingerprint. View full fingerprint. Cite this APA Standard Harvard Vancouver Author BIBTEX RIS Glancy, B. American Journal of Physiology - Cell Physiology1CC In: American Journal of Physiology - Cell PhysiologyVol.

Glancy B, Barstow T, Willis WT. American Journal of Physiology - Cell Physiology. doi: Glancy, Brian ; Barstow, Thomas ; Willis, Wayne T. In: American Journal of Physiology - Cell Physiology. TY - JOUR T1 - Linear relation between time constant of oxygen uptake kinetics, total creatine, and mitochondrial content in vitro AU - Glancy, Brian AU - Barstow, Thomas AU - Willis, Wayne T.

: Creatine and oxygen uptake

Creatine enhances oxygen uptake and performance during alternating intensity exercise Redkva, P. The influence of dietary creatine supplementation on performance during repeated bouts of maximal isokinetic cycling in man. Published : 12 November There was no interaction and no main effect for time for either group. Received: 01 September ; Accepted: 14 March ; Published: 10 April Free full text in Europe PMC.
Oxygen Uptake During Exercise | Learn about VO2 drift during exercise. Particularly or notably if the exercise is below the lactate threshold. TY - JOUR T1 - Linear relation between time constant of oxygen uptake kinetics, total creatine, and mitochondrial content in vitro AU - Glancy, Brian AU - Barstow, Thomas AU - Willis, Wayne T. Predicting MAOD using only a supramaximal exhaustive test. LR collected the data. The purpose of this study was to determine the combined effects of four weeks of HIIT and Cr supplementation on VO 2PEAK , VT, and TTE in recreationally active college-aged men.
Creatine enhances oxygen uptake and performance during alternating intensity exercise

Santacruz, Lucia, Antonio Jose Luis Arciniegas, Marcus Darrabie, Jose G. Mantilla, Rebecca M. Baron, Dawn E. Bowles, Rajashree Mishra, and Danny O. Santacruz L, Arciniegas AJL, Darrabie M, Mantilla JG, Baron RM, Bowles DE, et al.

Physiological reports. Santacruz, Lucia, et al. Epmc , doi Santacruz L, Arciniegas AJL, Darrabie M, Mantilla JG, Baron RM, Bowles DE, Mishra R, Jacobs DO. In addition, the values of e[La - ] were not altered after creatine supplementation. This result was expected as there is no evidence that creatine supplementation increases the glycogen content or glycolysis activity, corroborating the results of Doherty et al.

The eOXID also remained unchanged, probably due to the lack of improvement in performance. The main limitation of the present study was the lack of randomization of the tests.

Therefore, despite this being a study limitation, the lack of randomization seems not to have affected our findings. RdP collected and analyzed the data, and wrote the manuscript.

LR collected the data. EM wrote the manuscript. GA, RB, and AZ conceived the idea, built the experimental design, and wrote the manuscript. This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior — Brasil CAPES — Finance Code The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The authors would like to thank the Prof. Bruno Gualano, Ph. Bemben, M. Creatine supplementation and exercise performance recent findings. Sports Med.

doi: PubMed Abstract CrossRef Full Text Google Scholar. Bertuzzi, R. Predicting MAOD using only a supramaximal exhaustive test. Brisola, G. Sodium bicarbonate supplementation improved MAOD but is not correlated with and m running performances: a double-blind, crossover, and placebo-controlled study.

Cohen, J. Statistical Power Analysis for the Behavioral Sciences, 2nd Edn. Hillsdale, NJ: Lawrence Erlbaum Associates. de Poli, R.

Caffeine improved time to exhaustion but did not change alternative maximal accumulated oxygen deficit estimated during a single supramaximal running bout.

Sport Nutr. PubMed Abstract CrossRef Full Text. Di Prampero, P. The energetics of anaerobic muscle metabolism: a reappraisal of older and recent concepts. CrossRef Full Text Google Scholar. Doherty, M. Reproducibility of the maximum accumulated oxygen deficit and run time to exhaustion during short-distance running.

Sports Sci. Caffeine is ergogenic after supplementation of oral creatine monohydrate. Sports Exerc. Greenhaff, P. Effect of oral creatine supplementation on skeletal muscle phosphocreatine resynthesis. Gualano, B. Exploring the therapeutic role of creatine supplementation. Amino Acids 38, 31— Hall, M.

Creatine supplementation. Harris, R. Elevation of creatine in resting and exercised muscle of normal subjects by creatine supplementation. CrossRef Full Text. Hill, D. Morning—evening differences in response to exhaustive severe-intensity exercise.

Howley, E. Criteria for maximal oxygen uptake: review and commentary. Hultman, E. Muscle creatine loading in men. Jacobs, I. Creatine ingestion increases anaerobic capacity and maximum accumulated oxygen deficit. Jones, A. Koo, T. A guideline of selecting and reporting intraclass correlation coefficients for reliability research.

Medbø, J. Anaerobic energy release in working muscle during 30 s to 3 min of exhausting bicycling. Anaerobic capacity determined by maximal accumulated O2 deficit. Mesa, J.

Oral creatine supplementation and skeletal muscle metabolism in physical exercise. Miyagi, W. Effects of caffeine ingestion on anaerobic capacity in a single supramaximal cycling test. Anaerobic capacityestimated in a single supramaximal test in cycling: validity and reliability analysis.

Noordhof, D. The addition of Cr improved VT, but did not increase TWD. Therefore, 10 g of Cr per day for five days per week for four weeks does not seem to further augment maximal oxygen consumption, greater than HIIT alone; however, Cr supplementation may improve submaximal exercise performance.

Traditional endurance training has been shown to improve aerobic capacity, such as the ability to sustain a given submaximal workload for an extended period of time, or to produce a higher average power output over a fixed distance or time [ 1 , 2 ]. Physiological adaptations from training, resulting from an increase in mitochondrial density, include changes in skeletal muscle substrate utilization and improved respiratory control sensitivity [ 3 ].

High-intensity interval training HIIT is a time-efficient way to induce similar adaptations, such as increased maximal mitochondrial enzyme activity [ 4 ] and a reduction in glycogen utilization and lactate accumulation [ 5 , 6 ].

In addition, HIIT may be more effective than conventional endurance training at improving muscle buffering capacity [ 7 , 8 ]. HIIT consists of repeated bouts of short to moderate duration exercise completed at intensities greater than the anaerobic threshold, interspersed with brief periods of low-intensity or passive rest.

HIIT is designed to repeatedly stress the body, physiologically, resulting in chronic adaptations and improving metabolic and energy efficiency [ 9 , 10 ].

Helgerud et al. The velocity at which ventilatory threshold VT occurred increased as well, which may signify a higher training capacity and, therefore, should also represent an improvement in endurance performance.

It was determined during this study that different protocols of HIIT, matched for frequency and total work done, provided similar results [ 11 ]. In support, Burke et al. Similarly, an increase in VO 2PEAK and VT was found in three groups of well-trained cyclists following three different HIIT protocols of varying intensities and work-to-rest ratios [ 9 ].

Phosphocreatine PCr , a high-energy storage molecule within skeletal muscle, provides immediate replenishment of ATP during intense exercise [ 13 ].

Multiple HIIT bouts are designed to deplete PCr stores in the working skeletal muscle, reducing power output. It has been reported that it takes more than six minutes to fully recover depleted PCr stores after exercise-induced PCr depletion [ 14 ].

Therefore, if recovery intervals during HIIT bouts are less than six minutes, PCr may not be fully replenished, resulting in a reduced ability to meet the demands of cellular ATP resynthesis and a reduced performance [ 13 ].

Supplementing with creatine Cr has been demonstrated to effectively augment muscle phosphocreatine PCr stores [ 15 ]. It has been suggested that increases in skeletal muscle PCr concentration may improve muscle buffering capacity and moderate glycolysis [ 17 , 18 ].

In addition, Cr supplementation may increase the rate of PCr resynthesis between HIIT exercise bouts and enhance mitochondrial shuttling of ATP into the cytoplasm, providing significant physiological adaptations [ 15 , 16 ]. Current research suggests that Cr supplementation, when combined with training, has been shown to significantly augment performance [ 19 ].

Moreover, the combination of Cr supplementation and HIIT may lead to greater improvements in VO 2PEAK , VT, and TTE than previously reported with HIIT or Cr supplementation alone. While Cr is known to improve anaerobic performance, its use in aerobic performance has been under-researched.

To date, no one has examined the concurrent effects of Cr supplementation and HIIT. Therefore, we propose that Cr supplementation may increase training capacity during HIIT, resulting in improved endurance performance as measured by VO 2PEAK , VT, and TTE, beyond what has been demonstrated for HIIT alone.

The purpose of this study was to determine the combined effects of four weeks of HIIT and Cr supplementation on VO 2PEAK , VT, and TTE in recreationally active college-aged men. Forty-three recreationally active hours of regimented exercise per week college-aged men mean ± SD, Age: Participants were screened for health conditions that would have prevented them from participating in the study, including heart and joint conditions.

Any participants who had taken sports supplements, including any form of Creatine, in the three months prior to the beginning of the study were excluded. Participants kept a food diary, and none of the participants consumed a vegetarian diet.

Participants were asked not to change training or dietary habits for the duration of the study. This study was approved by the University's Institutional Review Board for Human Subjects and informed consent was obtained from each participant prior to enrollment.

A maximal graded exercise test GXT on a cycle ergometer Corival , Groningen, The Netherlands was completed by all participants to determine maximal oxygen consumption VO 2PEAK. Participants began pedaling at a cadence of revolutions per minute RPM at a workload of 20 watts W.

The workload increased 1 W every 3 seconds a total of 20 W every minute. This continued until the subject could no longer maintain RPM or until volitional exhaustion, despite verbal encouragement.

Respiratory gases were monitored and continuously analyzed with open-circuit spirometry using a calibrated metabolic cart True One ® , Parvo-Medics, Inc. Data were averaged over second intervals, with the highest second oxygen consumption and heart rate recorded as the peak oxygen consumption VO 2PEAK and maximum heart rate HRmax , respectively.

Time to exhaustion for the GXT VO 2PEAK TTE was recorded. In addition, ventilatory threshold VT was measured during this test. VT was determined from a plot of ventilation V E against VO 2 as described previously [ 20 ].

Two linear regression lines were fit to the lower and upper portions of the V E vs. VO 2 curve, before and after the break points, respectively. The intersection of these two lines was defined as VT.

Participants completed a warm-up consisting of a five-minute cycle at a workload of 50 W. Keeping a cadence of 70 RPM, they pedaled until volitional exhaustion. Time was recorded in seconds, and total work done TWD was reported in kilojoules, determined by multiplying the workload in watts and the time to exhaustion in seconds.

The test-retest intraclass correlation coefficient R was 0. A total of three testing sessions occurred throughout a nine-week period--familiarization week 1 , baseline week 4 , and post week 9.

Familiarization testing was implemented to reduce any learning effect--possibly influencing the dependent variables as well as the training intensity--from the initial VO 2PEAK testing.

Participants supplemented for a total of 30 days 10 days of familiarization period followed by an additional 20 days of supplementing and training at a dose of 10 g per day, taken in two doses--one dose 30 minutes prior to and one dose immediately following training.

Participants in the Cr group consumed 5 g of creatine citrate mixed with 15 g dextrose per packet Creatine Edge, FSI Nutrition, Omaha, NE , dissolved in ounces of water. Similarly, participants in the PL group consumed 20 g of dextrose per packet dissolved in ounces of water. Both drinks were identical in appearance and taste.

Training began at least hours following the TTE test. Participants were required to visit the lab five days per week, for six weeks, to perform the HIIT.

A two-week familiarization training period was implemented before taking baseline testing measurements. Due to the effectiveness of the training, and to the generally untrained population, a familiarization period was implemented to allow for all participants to quickly adapt to the high-intensity protocol.

Previous research has shown significant improvements in performance with just two weeks of HIIT [ 21 ]. Furthermore, in a previous study from our lab in which a familiarization period was not used, the large adaptations from training may have masked any effects from supplementation [ 22 ].

After the two-week familiarization period, participants re-tested their VO 2PEAK and TTE. Following baseline testing, participants completed four additional weeks of training, in which the intensities were re-evaluated based on baseline VO 2PEAK power output values.

Three of the five days per week of training consisted of training at progressively increasing workloads, determined as a percentage of the participant's baseline VO 2PEAK max workload.

One recovery day two days per week occurred between each of the three difficult training sessions. Each training session began with a five-minute warm up at 50 W, followed by a protocol of five sets of two-minute exercise bouts, with one minute of passive rest in between exercise bouts.

HIIT protocol. Represents the first two weeks of the HIIT protocol. Descriptive statistics were evaluated to determine group demographics. A mixed factorial ANOVA group [Cr vs. Pl vs. Con] × time [pre vs. If a significant interaction occurred, the statistical model was decomposed and the simple main effects were examined using separate one-way repeated measures ANOVAs for each group.

If the result was a simple main effect, Bonferroni post-hoc comparisons were performed among groups, while dependent-samples t-tests with Bonferroni corrections were performed across time. If no interactions occurred, the main effects were analyzed by collapsing across the non-interacting variables and analyzed in the same approach as described for the simple main effect.

Separate one-way ANOVAs indicated no differences between groups in any of the variables at baseline measurement. In addition, there was no change measured in the Con group over time in any of the variables. There was no change in BW from baseline to post measurement in the Cr A post hoc Bonferroni analysis indicated no difference between Cr and Pl Table 1.

There was no interaction and no main effect for time for either group. High-intensity interval training has been shown to be an effective method for improving endurance performance [ 7 , 12 , 23 — 26 ].

The results of the present study are in agreement with many studies demonstrating an increase in VO 2PEAK after HIIT [ 12 , 27 — 29 ].

In addition, time to exhaustion during the graded exercise test was also improved. However, few studies have examined the concurrent effects of HIIT with Cr supplementation on endurance performance.

The current study demonstrated no additional improvements in VO 2PEAK when combining Cr supplementation and HIIT. However, when measuring VT, improvements were only demonstrated in the Cr group.

Interestingly, in contrast to previous reports of significant increases in TWD with Cr supplementation or HIIT alone, no change in TWD was observed [ 5 , 28 , 30 — 33 ]. Endurance performance is commonly assessed using a measure of aerobic capacity, VO 2PEAK.

Short recovery periods between intense exercise bouts during HIIT may create a greater reliance on aerobic metabolism, due to the importance of aerobic metabolism in the removal of lactic acid and for the resynthesis of phosphocreatine [ 41 ]. HIIT may also induce up-regulation of glycolytic and oxidative enzymes, a possible mechanism influencing the improvements in VO 2PEAK [ 34 ].

In addition, an increase in stroke volume following HIIT [ 11 ] may contribute to an increase in VO 2PEAK. These results are in agreement with the few studies that have examined the effects of Cr supplementation on VO 2PEAK [ 30 , 42 — 44 ].

Cr has been shown to be effective in improving short-duration, intense activities, but few studies have examined the effects of Cr on longer duration, endurance-type activities. Due to the intensity and time duration two minutes of the interval work periods, it was hypothesized that Cr would provide for a greater training capacity, and, therefore, the Cr group would show greater improvements in the testing measurements.

McConell and colleagues [ 45 ] found that Cr improved the maintenance of energy balance in the muscle during intense aerobic exercise; however, performance was not improved, which is in agreement with the current study. Ventilatory threshold VT may be another useful predictor of endurance performance.

The VT has been suggested as an indicator of the ability of the cardiovascular system to adequately supply oxygen to the working muscles, preventing muscle anaerobisis [ 46 ]. Performing exercise at intensities greater than VT commonly result in an inadequate supply of oxygen to the working muscles, quickly leading to fatigue [ 47 ].

Therefore, improvements in VT may correspond to an augmented time to exhaustion and a greater threshold for fatigue.

Additionally, it has been proposed that training at intensities greater than VT, much like the HIIT protocol of the current study, may enhance the efficiency of the body to supply oxygen to the working muscles i.

Furthermore, a concomitant rise in muscle lactate levels and a drop in pH at high intensities of exercise may signal arterial chemoreceptors, altering ventilatory regulating mechanisms. Therefore, improvements in cardiovascular fitness may also coincide with a decrease in lactate accumulation resulting in an improvement in VT.

The increased VT in the Cr group is in agreement with previous studies that demonstrated improved VT following Cr supplementation but without training [ 30 , 42 , 44 ].

Future studies, however, are needed to validate our results.

Effect of creatine supplementation on oxygen uptake kinetics during submaximal cycle exercise

We can look at the kinetics of the increase in VO2 with exercise and the decrease in VO2 after exercise. You can see here that as VO2 increases up to the steady-state level, there is a lag in oxygen uptake.

This is referred to as an oxygen deficit. Interestingly, oxygen deficit, or the maximal oxygen deficit, has been used as a marker of anaerobic capacity in an applied sport setting. During exercise, as long as that exercise continues, there is a given oxygen uptake.

And this may include several hours, depending on how hard and how long the exercise is. You could imagine that it might be due to a lag in oxygen delivery. It takes some time for the cardiac output, for the muscle blood flow to increase, and for the oxygen to diffuse into the skeletal muscle tissue.

Alternatively, oxygen delivery might increase quite quickly, and the lag might be due to sluggishness in mitochondrial respiration. A number of experiments over the years have tried to identify, is it oxygen delivery, is it oxygen utilization?

And depending on the exercise intensity and the situations of those experiments results have been obtained in support or against either mechanism. So probably both continue to contribute to some extent.

During exercise, as I said, at a given exercise intensity, there is an oxygen requirement. And during prolonged exercise, there is a general upward drift in VO2. What mechanisms might contribute to this increase in VO2?

Well, most of it is due to changes within the active muscles themselves. Some of the factors, some of the changes, in skeletal muscle that contribute to that include recruitment of lower efficiency type two fibers, changes in the efficiency of ATP production to oxygen consumption, an increase in muscle temperature, an increased reliance on free fatty acid metabolism, which tends to have a higher oxygen requirement, and elevated catecholamines, which can impact on metabolism.

Factors outside the muscle which could contribute to this increased oxygen consumption include an increased oxygen requirement of the ventilatory muscles and of the heart as they increase their activity during prolonged exercise.

Have a look at the post-exercise period. There are a number of processes going on that are thought to contribute to the maintenance of a slightly higher VO2 during recovery. In the short to medium term after exercise, heart rate and ventilation will remain slightly elevated, and that will increase the oxygen requirement.

There will be an increase in temperature which is maintained for some time after exercise, and that might also contribute to a slight increase in VO2. Also, mitochondrial uncoupling, or again, a change in the ATP to VO2 ratio might contribute to a need for higher oxygen uptake.

And the synthesis of key proteins that might contribute to the adaptive response to exercise. Edge J, Bishop D, Goodman C, Dawson B: Effects of high- and moderate-intensity training on metabolism and repeated sprints.

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Volek JS, Kraemer WJ, Bush JA, Boetes M, Incledon T, Clark KL, Lynch JM: Creatine supplementation enhances muscular performance during high-intensity resistance exercise. J Am Diet Assoc. Casey A, Constantin-Teodosiu D, Howell S, Hultman E, Greenhaff PL: Creatine ingestion favorably affects performance and muscle metabolism during maximal exercise in humans.

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Jager R, Metzger J, Lautmann K, Shushakov V, Purpura M, Geiss KR, Maassen N: The effects of creatine pyruvate and creatine citrate on performance during high intensity exercise. J Int Soc Sports Nutr. Download references. Department of Health and Exercise Science, University of Oklahoma, Huston Huffman Center, Asp Avenue, Norman, OK, , USA.

You can also search for this author in PubMed Google Scholar. Correspondence to Jeffrey R Stout. JG, AS, KK and DF contributed in writing and editing the manuscript along with concept and design, data acquisition, and data analysis and interpretation.

JM, TB, JC, and JS contributed in writing and editing the manuscript, as well as concept and design. All authors have read and approved the final manuscript. Jennifer L Graef, Abbie E Smith, Kristina L Kendall, David H Fukuda, Jordan R Moon, Travis W Beck, Joel T Cramer and Jeffrey R Stout contributed equally to this work.

Open Access This article is published under license to BioMed Central Ltd. Reprints and permissions. Graef, J. et al. The effects of four weeks of creatine supplementation and high-intensity interval training on cardiorespiratory fitness: a randomized controlled trial. J Int Soc Sports Nutr 6 , 18 Download citation.

Received : 11 June Accepted : 12 November Published : 12 November Anyone you share the following link with will be able to read this content:.

Sorry, a shareable link is not currently available for this article. Provided by the Springer Nature SharedIt content-sharing initiative. Skip to main content. Search all BMC articles Search. Download PDF. Download ePub. Abstract Background High-intensity interval training has been shown to be a time-efficient way to induce physiological adaptations similar to those of traditional endurance training.

Methods Forty-three recreationally active men completed a graded exercise test to determine VO 2PEAK , VO 2PEAK TTE, and VT. Results Significant improvements in VO 2PEAK and VO 2PEAK TTE occurred in both training groups. Conclusion In conclusion, HIIT is an effective and time-efficient way to improve maximal endurance performance.

Background Traditional endurance training has been shown to improve aerobic capacity, such as the ability to sustain a given submaximal workload for an extended period of time, or to produce a higher average power output over a fixed distance or time [ 1 , 2 ].

Methods Forty-three recreationally active hours of regimented exercise per week college-aged men mean ± SD, Age: Determination of VO 2PEAK , ventilatory threshold, and total work done A maximal graded exercise test GXT on a cycle ergometer Corival , Groningen, The Netherlands was completed by all participants to determine maximal oxygen consumption VO 2PEAK.

High-intensity interval training HIIT Training began at least hours following the TTE test. Figure 1. Full size image. Results Separate one-way ANOVAs indicated no differences between groups in any of the variables at baseline measurement.

Body Weight BW There was no change in BW from baseline to post measurement in the Cr Table 1 Mean ± SD of maximal oxygen consumption VO 2PEAK , time to exhaustion VO 2PEAK TTE , and ventilatory threshold VT at baseline and following four weeks of treatment Full size table.

Figure 2. Effect of Creatine and HIIT on VT. Percent change in VT over time for each group. Discussion High-intensity interval training has been shown to be an effective method for improving endurance performance [ 7 , 12 , 23 — 26 ]. Conclusion In conclusion, the current study supports previous evidence that HIIT is an efficient way to induce cardiorespiratory improvements [ 7 , 12 , 23 — 26 ].

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CAS PubMed Google Scholar Thomas TR, Adeniran SB, Etheridge GL: Effects of different running programs on VO2 max, percent fat, and plasma lipids. Linear relation between time constant of oxygen uptake kinetics, total creatine, and mitochondrial content in vitro. Life Sciences, School of SOLS Nursing and Health Innovation, Edson College of EDSON.

Overview Fingerprint. Abstract Following the onset of moderate aerobic exercise, the rate of oxygen consumption J o rises monoexponentially toward the new steady state with a time constant τ in the vicinity of 30 s. Keywords Creatine kinase Hexokinase Mitochondrial resistance.

ASJC Scopus subject areas Physiology Cell Biology. Access to Document Link to publication in Scopus. Fingerprint Dive into the research topics of 'Linear relation between time constant of oxygen uptake kinetics, total creatine, and mitochondrial content in vitro'.

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The third supramaximal Creatine and oxygen uptake was Performance boosting strategies under the placebo condition and Creatine and oxygen uptake Creatinw Creatine and oxygen uptake under the creatine condition 12 Creatine and oxygen uptake after the placebo test. Oxygenn, the amplitude of the VO2 oxgyen component was not related to Qnd mRNA expression Creatine and oxygen uptake anc a recent report and therefore elucidation of the mechanism causing the slow component awaits further investigation. August Traditional endurance training has been shown to improve aerobic capacity, such as the ability to sustain a given submaximal workload for an extended period of time, or to produce a higher average power output over a fixed distance or time [ 12 ]. As I said, the relatively similar mechanical efficiencies across a range of training status.

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This Game-Changing Supplement ELIMINATES ANXIETY - Gary Brecka Exercise Physiology Muscle Contraction Muscle Creatine and oxygen uptake Muscle Adaptations Exercise Fuels CHO Metabolism Fat Metabolism Oxygen Uptake Cardiovascular Exercise RCeatine Responses VO2 Oxygeh Temperature Regulation Snd Creatine and oxygen uptake Balance Fatigue Sprinting Creqtine Genes Practical Case Example. The lecture continues with detailed information connecting the Creatine and oxygen uptake between these Muscle definition workouts at the gym related to oxygen Creatinw during exercise. Uptwke we saw in the last module, the oxidative metabolism of carbohydrate and fat is very important for supplying energy to muscles during prolonged exercise. And in parallel with that, there needs to be an increase in the oxygen delivery to the contracting skeletal muscle, so that the mitochondria are adequately oxygenated in order for these metabolic reactions to occur. An important principle is that the oxygen uptake is directly proportional to the exercise intensity. The efficiency of conversion of the metabolic energy into mechanical work is relatively constant, at least during cycling exercise. So for given power output, there is a fairly constant VO2. Creatine and oxygen uptake

Creatine and oxygen uptake -

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Med Sci Sports Exerc , 37 12 , 01 Dec Altmetric Attention Stats. Dimensions Citation Stats. Published In Physiological reports. Rats, Sprague-Dawley Rats RNA, Messenger Protein Kinases Oxygen Myocytes, Cardiac Hypoxia-Inducible Factor 1 Hypoxia Creatine Cells, Cultured. Citation APA.

Santacruz, L. Physiological Reports , 5 16 , e Santacruz, Lucia, Antonio Jose Luis Arciniegas, Marcus Darrabie, Jose G. Mantilla, Rebecca M. This study aimed to investigate the effects of short-duration creatine monohydrate supplementation on anaerobic capacity AC , anaerobic energy pathways, and time-to-exhaustion during high-intensity running.

This order was chosen due to the prolonged washout of creatine. MAOD was not different between placebo 3. The energetics from the phosphagen pathway increased significantly after creatine supplementation 1. However, the glycolytic and oxidative pathways were not different between conditions.

Furthermore, time to exhaustion did not differ between placebo Therefore, we can conclude that creatine supplementation improves the phosphagen energy contribution, but with no statistical effect on AC or time to exhaustion in supramaximal running.

Creatine α-methyl guanidine-acetic acid is a nitrogen amine which can be obtained in diet e. One of the major roles of creatine is to act as a non-mitochondrial energy buffer, rapidly transferring energy through a reversible reaction catalyzed by the creatine kinase enzyme Gualano et al.

Short-term creatine monohydrate supplementation has been widely used to improve performance in high-intensity and short-term efforts in cycling Jacobs et al. Since creatine supplementation can significantly increase phosphorylcreatine intramuscular stores, it has been shown to improve the energy supply from the phosphagen systems ePCr Yquel et al.

These changes could ultimately lead to improved performance in this type of exercise Doherty et al. Jacobs et al. However, although it is a well-accepted measure of AC, MAOD does not allow for the isolated estimation of ePCr and has poor reliability i.

This may have hindered the detection of small differences in the anaerobic metabolism Doherty et al. Some studies Bertuzzi et al. This method determines the AC through the sum of energetic equivalents of the net blood lactate accumulated during exercise and the fast component of excess post-exercise oxygen consumption EPOC fast , which allows estimation of the contribution from the glycolytic e[La - ] and ePCr pathways, respectively.

Since it is well documented that creatine supplementation can increase intramuscular phosphorylcreatine, we hypothesized it could increase the contribution of the phosphagen metabolism i.

This study makes progress in the current literature by investigating the effect of creatine supplementation through a novel method to estimate the AC and, particularly, the effects on non-mitochondrial pathway estimation, which has been hypothesized but not scientifically reported until the current date.

Eighteen male volunteers were initially enrolled in the study; however, four were excluded, thus, fourteen men [mean ± SD; age 24 ± 4 years; height To be included, volunteers were required to be recreationally active, participate in exercise activities such as running, cycling, and soccer at least 2 times per week, and not have used ergogenic supplements such as beta-alanine and creatine, among others, for at least 6 months.

Volunteers who were regularly absent from the trials or presented injuries were excluded from the study. The volunteers were instructed not to ingest alcohol, caffeine, and sodium bicarbonate and not to perform strenuous exercise 24 h before each trial.

Volunteers were also verbally informed about the experimental procedures and signed an informed consent prior to beginning the study. All experimental procedures were approved by the Human Research Ethics Committee from the School of Sciences, São Paulo State University — UNESP protocol number: The investigation was conducted in a single-blind, placebo-controlled, crossover trial.

In addition, the treadmill had been previously calibrated according to Padulo et al. The first two supramaximal sessions served as familiarization trials.

The third supramaximal test was performed under the placebo condition and the fourth test under the creatine condition 12 days after the placebo test. We opted to use the single-blind design with treatment order not being counterbalanced due to the long wash-out period necessary for muscle creatine to return to pre-supplementation values Hultman et al.

The experimental design of the study is presented in Figure 1. Figure 1. Experimental design of study. GXT, Graded exercise test; FAM, Familiarization; EPOC, Excess post-exercise oxygen consumption. In addition, 5 submaximal efforts were performed as warm-ups and used to construct the linear regression to allow determination of MAOD.

All exhaustive sessions were separated by a minimum interval of 48 h. All participants were verbally encouraged to perform their maximal efforts in all sessions, and all tests were performed at the same time of day to avoid circadian variations in performance and AC Hill, Heart rate was monitored using a transmission belt connected to the gas analyzer Wireless HR Monitor, COSMED, Rome, Italy.

Blood samples were collected from the earlobe 25 μL at rest i. Exhaustion was defined as the incapacity to maintain exercise intensity. The V ˙ O 2 average of the final 30 s in each GXT stage and 15 s in the rectangular test was calculated.

When no plateau could be observed, the highest average of V ˙ O 2 obtained during the GXT was compared with V ˙ O 2 reached in the rectangular test; V ˙ O 2max being assumed as the highest average of V ˙ O 2 when not different from the V ˙ O 2 reached in the rectangular test Rossiter et al.

The minimal exercise intensity at which the subject reached V ˙ O 2max was considered as i V ˙ O 2max. During supplementation and the washout period, the volunteers maintained their recreational exercise routine. Supplements were given in 4 equal doses and the volunteers were instructed to ingest the supplements immediately after their main meal of the day.

The placebo was given before creatine in a single blind design i. The dose of creatine was chosen according to Harris et al. Placebo and creatine supplements were identical in appearance, and were administered in flavored tablets containing 1 g of creatine and 2 g of dextrose each.

At the end of the study, to test the efficacy of the blinding design, volunteers were asked about which arm of the study they had received the creatine supplement in. Only 5 out of the 14 volunteers correctly answered when they ingested creatine.

Baseline V ˙ O 2 was measured with volunteers seated for 10 min before the tests. The choice of intensity of the supramaximal test i. Immediately after the end of the supramaximal tests, the participants remained seated quietly for 10 min for measurement of EPOC fast. The supramaximal efforts were performed 4 times, the first 2 efforts being used as familiarization and the next 2 efforts after the placebo and creatine ingestion periods.

The final familiarization supramaximal test was compared with the placebo condition to ensure that there was no longer any familiarization effect. A linear regression was fitted using 5 submaximal intensities and respective V ˙ O 2 , considering the V ˙ O 2 average 8—10 min, with the y-intercept fixed at the baseline V ˙ O 2 Özyener et al.

In addition, the area of V ˙ O 2 measured during the supramaximal intensity was determined using the trapezoidal method Medbø et al.

The ePCr was estimated by the product between VO 2 amplitude A1 and time constant τ1 from a first exponential decay fitted using a bi-exponential fit in EPOC fast , with OriginPro 8.

The oxidative pathway eOXID was assumed as the V ˙ O 2 integral under the curve i. All variables were examined using the Shapiro—Wilk test to check for normal distribution. To determine tlim reliability after familiarization, the intraclass correlation coefficients were applied Koo and Li, The smallest worthwhile change was calculated as the product between the standard deviation between subjects in the placebo condition and 0.

Peak and maximal variables measured during the GXT and verification testing are shown in Table 1. Figure 2.

Differences and individual smallest worthwhile change of energetics data from phosphagen, glycolytic, and oxidative pathways under placebo and creatine conditions. ePCr, energetics from the phosphagen systems; e[La - ], energetics from glycolytic pathway; eOXID, oxidative phosphorylation pathway; ES, effect size.

In addition, there were no differences between creatine and placebo conditions in tlim and in the ePCr, e[La - ], and eOXID when expressed in percentages of total energetics contribution Table 2.

Uptak Crphosphocreatine Oyxgenand Creqtine kinases CK comprise an uotake shuttle linking ATP production in mitochondria uptwke cellular consumption sites. Myocytes Creatine and oxygen uptake synthesize Cr: Crewtine cells depend Creatine and oxygen uptake uptake across uptale cell Cognitive fitness exercises by a specialized creatine transporter CrT to maintain intracellular Cr levels. Hypoxia interferes Creatine and oxygen uptake energy Creatine and oxygen uptake, including the activity oxyven the creatine energy shuttle, and therefore affects intracellular ATP and PCr levels. Here, we report that exposing cultured cardiomyocytes to low oxygen levels rapidly diminishes Cr transport by decreasing V max and K m Pharmacological activation of AMP-activated kinase AMPK abrogated the reduction in Cr transport caused by hypoxia. Cr supplementation increases ATP and PCr content in cardiomyocytes subjected to hypoxia, while also significantly augmenting the cellular adaptive response to hypoxia mediated by HIF-1 activation. Our results indicate that: 1 hypoxia reduces Cr transport in cardiomyocytes in culture, 2 the cytoprotective effects of Cr supplementation are related to enhanced adaptive physiological responses to hypoxia mediated by HIF-1, and 3 Cr supplementation increases the cellular ATP and PCr content in RNCMs exposed to hypoxia. Hypoxia decreases creatine uptake in cardiomyocytes, while creatine supplementation enhances HIF activation.

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