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Low-intensity training adaptations

Low-intensity training adaptations

Sloth M, Sloth Muscle protein synthesis, Overgaard Low-intensity training adaptations, Low-inteensity al. Energy-boosting for busy professionals Trainng. Sports Med. Physiological adaptations to interval training and the role of exercise intensity. Bishop D, Edge J, Goodman C. Keywords: metabolism, exercise prescription, mitochondria, cardiovascular, exercise physiology, human performance Citation: Langan SP and Grosicki GJ Exercise Is Medicine…and the Dose Matters.

Low-intensity training adaptations -

Training increased the content of the transcriptional regulatory protein peroxisome proliferator-activated receptor γ co-activator PGC -1α measured in nuclear fractions Fig. PGC-1α has emerged as an important regulator of mitochondrial and metabolic gene expression by virtue of its ability to co-activate numerous transcription factors in the nucleus.

The increase in nuclear PGC-1α suggests that low-volume HIT increases the activation of this critical regulatory protein. Evidence suggests that PGC-1α activation is reduced in conditions of obesity, insulin resistance, T2D and ageing. The ability of low-volume HIT to increase PGC-1α activation provides mechanistic support for the potential health benefits of this type of time-efficient exercise training.

Despite evidence for low-volume HIT to promote metabolic adaptations linked with improved health, more research is required to determine whether HIT elicits all of the benefits associated with traditional endurance training.

An accumulating body of research indicates that interval-based exercise induces superior cardiovascular benefits compared with continuous aerobic training matched for total work Wisloff et al. Whether low-volume HIT is of similar benefit to cardiovascular health requires further investigation.

In addition, most of the low-volume HIT research published to date has involved relatively short-term training protocols up to 6 weeks and additional studies are warranted to examine the long-term adaptations to this type of training. Finally, it remains to be determined whether our practical low-volume HIT model Little et al.

Encouragingly, recent unpublished work from our laboratory suggests that this HIT model is well-tolerated and can improve muscle oxidative capacity and markers of glycaemic control in sedentary, middle-aged adults as well as individuals with T2D. Low-volume HIT may therefore represent an attractive time-efficient exercise alternative for reducing the risk of metabolic disease.

Short-term sprint interval versus traditional endurance training: similar initial adaptations in human skeletal muscle and exercise performance. J Physiol , — Metabolic adaptations to short-term high-intensity interval training: a little pain for a lot of gain?

Exerc Sport Sci Rev 36 , 58— A practical model of low-volume high-intensity interval training induces mitochondrial biogenesis in human skeletal muscle: potential mechanisms.

Short-term sprint interval training increases insulin sensitivity In healthy adults but does not affect the thermogenic response to β-adrenergic stimulation. J Physiol. Published online 14 June High-intensity interval training to maximize cardiac benefits of exercise training? Exerc Sport Sci Rev 37 , — Supporting your next career move Research Teaching Science communication Sport and exercise science Healthcare Industry Jobs What we do What is physiology?

Physiology News Magazine. Download this issue. Thus, when considering the effects of low-volume interval training on insulin sensitivity and glycemic control in women, it is important to consider both acute and chronic responses.

The acute effects of low-volume interval training on insulin sensitivity and glycemic control are not well established in women, and available evidence in response to SIT as compared to HIIT is conflicting. To the best of our knowledge, acute effects of low-volume SIT on estimates of insulin sensitivity or glycemic control have yet to be investigated in an independent cohort of women.

Thus, while it is possible that the low exercise volume of SIT is insufficient to acutely improve insulin sensitivity independent of sex, comparisons between men and women are warranted in this regard. HOMA-IR primarily reflects hepatic insulin sensitivity, and therefore, the sex-specific results may not be generalizable to estimates of peripheral insulin sensitivity obtained from methods such as OGTTs or hyperinsulinemic-euglycemic clamps.

However, sex-based comparisons involving measurement of peripheral insulin sensitivity have not been conducted, and the efficacy of low-volume HIIT to improve peripheral insulin sensitivity and glycemic control in women can only be ascertained from mixed-sex cohorts. The potency of HIIT in this regard has been attributed to high rates of muscle glycogen utilization during exercise [ 91 ].

Fasting-derived estimates of insulin sensitivity and glycemic control have been widely reported following 6—15 weeks of low-volume interval training in women-only cohorts.

Trapp et al. More recently, Sun and colleagues [ 61 ] have used a similar low-volume SIT protocol in women with overweight and demonstrated greater reductions in HOMA-IR after 12 weeks of SIT than in response to a MICT protocol involving a threefold greater exercise volume.

Encouraging findings in this regard have also been reported among women and girls across the lifespan who are understudied in exercise physiology. Women with polycystic ovary syndrome, a condition commonly associated with insulin resistance, have also been reported to improve HOMA-IR following 12 weeks of thrice-weekly aquatic-based low-volume HIIT [ ].

Available evidence also suggests that the improvement in HOMA-IR following 6 weeks of low-volume HIIT is similar between sexes [ 76 ]. In contrast to fasting-derived indices of insulin sensitivity, estimates of peripheral insulin sensitivity are generally reported to be unchanged in women following low-volume interval training, which is different from findings in men.

Gillen et al. The authors also observed greater increases in skeletal muscle glucose transporter 4 GLUT4 protein content in men [ 53 ], providing a potential mechanism for the sex difference in training-induced changes in glycemic control.

More recently, Søgaard et al. Considering that these authors did not describe any sex differences when presenting the mixed-cohort results, it is possible that women do indeed improve indices of peripheral insulin sensitivity and glycemic control following low-volume interval training. Indeed, a more recent study from Metcalfe and colleagues [ 71 ] suggests that the previously reported differences between men and women might in fact be attributed to differences in baseline insulin sensitivity of participants, rather than sex, which corroborates other data suggesting that the degree of insulin resistance pre-training influences the adaptive response to HIIT [ ].

Clearly, additional well-controlled sex-comparison studies are needed, including those that evaluate potential mechanisms. Given the generally unchanged peripheral insulin sensitivity in women following low-volume interval training, it is possible that exercise protocols involving higher volumes of interval or continuous exercise are needed for more consistent improvements.

Recently, a high volume HIIT protocol involving 1 h of cycling three times per week has been shown to improve insulin sensitivity, measured via the hyperinsulinemic-euglycemic clamp, in healthy premenopausal and early postmenopausal women after 12 weeks [ ], perhaps suggesting a dose—response threshold may exist.

A training program that includes both high- and low-volume HIIT may also be an efficacious and more time-efficient option. Continued research is needed to decipher the minimal exercise dose necessary to improve insulin sensitivity in women.

Exercise training-induced increases in skeletal muscle mitochondrial volume can enhance skeletal muscle oxidative capacity and thereby improve submaximal fuel metabolism, lactate threshold and ultimately endurance performance [ 43 , ].

Another well-documented physiological adaptation to low-volume interval training is an increase in skeletal muscle mitochondrial content, as reviewed by others [ 1 , 11 ].

As little as 2 weeks of SIT or HIIT has been demonstrated to increase mitochondrial content in human skeletal muscle [ , , , , ], which is most often assessed using biochemical measurements such as the maximal activity or protein content of mitochondrial enzymes including citrate synthase CS , cytochrome c oxidase subunit IV COXIV and succinate dehydrogenase SDH [ , ].

However, as recently acknowledged in a narrative review by Bishop and colleagues [ 11 ], this area of research is predominantly supported by studies conducted in men. Nonetheless, there is evidence from a limited number of women-only cohorts demonstrating HIIT-induced improvements in biomarkers of mitochondrial content.

To our knowledge, Gillen et al. A companion paper from the same cohort [ ] further demonstrated increases in COXIV activity in type 1 and 2 muscle fibers using immunofluorescence.

More recently, Nyberg and colleagues [ ] have demonstrated 12 weeks of interval training 1-h cycling classes involving high-intensity intervals , three times per week, increased mitochondrial protein content in pre- and postmenopausal women.

Notably, the improvements following training were more pronounced in postmenopausal women compared to premenopausal women, suggesting that menopausal status may impact mitochondrial responses to interval training.

Future work should explore the influence of menopausal status on mitochondrial responses to low-volume interval training. Given the limited number of low-volume HIIT or SIT studies conducted in women, it is perhaps unsurprising that we know relatively little with regard to how mitochondrial adaptations in response to low-volume interval training compare to traditional forms of aerobic training e.

When considering mixed-sex cohorts, however, similar improvements in mitochondrial content have been observed following 6 weeks of low-volume SIT and MICT in young healthy men and women. Specifically, Burgomaster et al. This finding is consistent with recent studies demonstrating no difference in training-induced improvements in biomarkers of mitochondrial content or total mitochondrial volume following 6—12 weeks of low-volume HIIT and MICT in adults with overweight or obesity [ 91 , , ] or T2D [ ].

Thus, based on these mixed-sex studies it is plausible that low-volume interval training and MICT similarly increase mitochondrial content in women, consistent with several studies in men-only cohorts [ , , , ]; however, this notion has not been examined in an independent cohort of women.

The importance of investigating mitochondrial adaptations in women-only cohorts is bolstered by recent evidence demonstrating sex-based differences in the adaptive response to low-volume interval training. A sex-specific response to low-volume interval training was also observed in a recent study by Chrøis et al.

The mechanistic basis for the reported greater mitochondrial responses in men compared to women remains unclear. Interval training-induced mitochondrial biogenesis is initiated by repeated, transient disturbances in metabolic homeostasis that activate signaling pathways which promote the transcription of genes and translation of mitochondrial proteins [ 1 , ].

Additional work that examines acute molecular responses to low-volume interval training in women of varying age and health status, including sex-based comparisons, may provide insight into the observed greater rates of mitochondrial biogenesis [ 70 ] and improvements in mitochondrial respiration [ ] in men relative to women.

There is also evidence that low-volume interval training elicits comparable mitochondrial adaptations between sexes, specifically with respect to biomarkers of mitochondrial content. Training-induced increases in the maximal activity or protein content of CS following 3 or 6 weeks of low-volume SIT did not differ between men and women who were recreationally active [ 70 ], inactive with overweight or obesity [ 53 ] or inactive and older [ ].

The similar net change in mitochondrial content, despite the aforementioned tendency for greater rates of mitochondrial protein synthesis in men [ 70 ], may be explained by higher rates of mitochondrial protein breakdown in men compared with women. Future research in larger sample sizes that examines a comprehensive set of mitochondrial measures i.

Reasons for the lower representation of women as participants in exercise research studies [ 14 , 15 , 16 ] are numerous and complex and may include investigator-driven decisions and sex-based differences in willingness to participate [ , ].

Regardless, more research in women is needed that evaluates the impact of population characteristics e. Progress in this regard will require targeted recruitment strategies and careful consideration of women-specific methodological factors in study design.

For example, in premenopausal women, menstrual cycle phase has been demonstrated to influence resting insulin sensitivity [ ] and exercise-induced mitochondrial gene expression [ ].

Thus, careful consideration of these factors is necessary for the proper design of future studies that include women as participants, and recommendations in this regard have recently been made by others [ , , ]. While controlling for menstrual cycle phase and hormonal contraceptive use are generally recommended and would improve the quality of women-specific data, this approach may also introduce limitations such as decreased generalizability of the results and increased timescale [ ].

Thus, methodological decisions in this regard should be carefully considered for each study and guided by the specific research question. Nonetheless, enhanced documentation and reporting of hormonal parameter s , using consistent definitions, as provided by others [ ], are needed to reduce ambiguity and help clarify conflicting findings between studies.

Properly matching both participant characteristics and the exercise stimulus remains a challenging issue for sex-based comparison studies. There is evidence of greater baseline insulin sensitivity [ ] and mitochondrial volume [ ] in women relative to men, which may impact training-induced responses.

It is also well known that V̇O 2 peak relative to body mass is lower in women compared to men of a similar training background [ , , ]. Given this sex-based difference, and the greater body fat percentage in women compared with men, it has been suggested to match men and women for fitness levels using V̇O 2 peak relative to fat free mass [ ].

The optimal method for matching the interval exercise stimulus in sex-comparison studies, however, is an unresolved issue, as noted by Bishop and colleagues [ 11 ]. Some authors have compared power outputs during SIT relative to whole body fat-free mass to account for sex-based differences in body composition and found no sex differences in relative power output [ 53 , 70 , 93 , ].

However, this outcome may need to be interpreted with caution since cycling is a lower body exercise and there may be sex differences in the relative contribution of lower body fat free mass to total fat free mass [ ].

Moreover, there is large between-participant variability in the homeostatic disturbance elicited by reference points commonly used to determine exercise intensity in interval training protocols [e.

As such, it has been suggested that prescribing exercise intensity relative to metabolic thresholds may be more appropriate for sex-based comparisons [ 17 ]. The methodological decisions related to matching the interval exercise stimulus between men and women may also depend on the study objective s and whether the findings will address a more applied or basic science research question.

Manipulation of the interval exercise prescription variables e. For example, women have been reported to have faster metabolic recovery following repeated Wingate sprints relative to men [ 93 , ] and therefore may require shorter recovery periods between high-intensity intervals [ 17 ].

Indeed, a recent study by Schmitz and colleagues found that 4 weeks of SIT involving shorter 30 s rather than longer s active recovery periods improved repeated running ability in women [ ]. Whether altering the recovery duration during low-volume interval training modifies improvements in CRF, insulin sensitivity and mitochondrial content in women remains largely unexplored.

Interestingly, when 8 weeks of low-volume HIIT was combined with caffeine supplementation in women with obesity, larger improvements in glycemic control during an OGTT were observed compared to those who underwent training without caffeine supplementation [ ].

Additional research that examines the potential for nutrition to modify chronic responses to low-volume interval training in women would advance the field further. Studies that assess the mechanisms by which low-volume interval training improves physiological responses in women are also warranted and will provide insight into how to optimize the interval exercise stimulus for women.

There is a relative lack of data regarding physiological responses to low-volume interval training in women as compared to men. Nonetheless, given the wealth of research conducted over the past two decades, the efficacy of low-volume HIIT and SIT to improve select outcome variables in women, such as CRF, has been consistently demonstrated.

However, research that explores peripheral adaptations to low-volume interval training in women-only cohorts, such as skeletal muscle mitochondrial responses and insulin sensitivity, is limited and conflicting, with some evidence demonstrating blunted improvements in women relative to men.

Further research is needed to clarify and advance our knowledge of these interval training-induced responses in women of various ages, activity levels and health statuses, including studies that provide direct comparisons to traditional MICT. Additional sex-comparison studies that utilize best practice guidelines for matching men and women are also needed, as are studies that evaluate a mechanistic basis for previously reported sex-specific adaptations to low-volume interval training.

To increase our understanding of physiological adaptations to low-volume interval training in women, it is also necessary to evaluate the influence of training variables e.

These research efforts are important and necessary from both a basic science and translational perspective, and will support sex and gender equity in research while strengthening the evidence-base for physical activity recommendations in women.

MacInnis MJ, Gibala MJ. Physiological adaptations to interval training and the role of exercise intensity. J Physiol. Article CAS PubMed Google Scholar.

Batacan RB Jr, Duncan MJ, Dalbo VJ, Tucker PS, Fenning AS. Effects of high-intensity interval training on cardiometabolic health: a systematic review and meta-analysis of intervention studies. Br J Sports Med. Article PubMed Google Scholar. The effects of high-intensity interval training on glucose regulation and insulin resistance: a meta-analysis.

Obes Rev. Campbell WW, Kraus WE, Powell KE, Haskell WL, Janz KF, Jakicic JM, et al. High-intensity interval training for cardiometabolic disease prevention.

Med Sci Sports Exerc. Article PubMed PubMed Central Google Scholar. Sabag A, Little JP, Johnson NA. Low-volume high-intensity interval training for cardiometabolic health. Colberg SR, Sigal RJ, Yardley JE, Riddell MC, Dunstan DW, Dempsey PC, et al.

Diabetes Care. Department of Health and Social Care. United Kingdom Thompson WR. Worldwide survey of fitness trends for Article Google Scholar. Trost SG, Owen N, Bauman AE, Sallis JF, Brown W.

Bagley L, Slevin M, Bradburn S, Liu D, Murgatroyd C, Morrissey G, et al. Sex differences in the effects of 12 weeks sprint interval training on body fat mass and the rates of fatty acid oxidation and VO2max during exercise. BMJ Open Sport Exerc Med. Bishop DJ, Botella J, Genders AJ, Lee MJ, Saner NJ, Kuang J, et al.

High-intensity exercise and mitochondrial biogenesis: current controversies and future research directions. Physiology Bethesda. Article CAS Google Scholar. Way KL, Vidal-Almela S, Moholdt T, Currie KD, Aksetoy IA, Boidin M, et al.

Sex differences in cardiometabolic health indicators following HIIT in patients with coronary artery disease. Atakan MM, Li Y, Kosar SN, Turnagol HH, Yan X. Evidence-based effects of high-intensity interval training on exercise capacity and health: a review with historical perspective.

Int J Environ Res Public Health. Article CAS PubMed PubMed Central Google Scholar. Mind the gap: widening the demographic to establish new norms in human physiology. Costello JT, Bieuzen F, Bleakley CM. Where are all the female participants in Sports and Exercise Medicine research?

Eur J Sport Sci. Devries MC, Jakobi JM. Importance of considering sex and gender in exercise and nutrition research. Appl Physiol Nutr Metab. Ansdell P, Thomas K, Hicks KM, Hunter SK, Howatson G, Goodall S. Physiological sex differences affect the integrative response to exercise: acute and chronic implications.

Exp Physiol. Devries MC. Sex-based differences in endurance exercise muscle metabolism: impact on exercise and nutritional strategies to optimize health and performance in women.

Wohlgemuth KJ, Arieta LR, Brewer GJ, Hoselton AL, Gould LM, Smith-Ryan AE. Sex differences and considerations for female specific nutritional strategies: a narrative review.

J Int Soc Sports Nutr. Brockman N, Yardley J. Sex-related differences in fuel utilization and hormonal response to exercise: implications for individuals with type 1 diabetes.

Dominelli PB, Molgat-Seon Y, Sheel AW. Sex differences in the pulmonary system influence the integrative response to exercise.

Exerc Sport Sci Rev. Tiller NB, Elliott-Sale KJ, Knechtle B, Wilson PB, Roberts JD, Millet GY. Do sex differences in physiology confer a female advantage in ultra-endurance sport?

Sports Med. Williams JS, Dunford EC, Cheng JL, Moncion K, Valentino SE, Droog CA, et al. The impact of the h movement spectrum on vascular remodeling in older men and women: a review. Am J Physiol Heart Circ Physiol. Forbes SC, Candow DG, Smith-Ryan AE, Hirsch KR, Roberts MD, VanDusseldorp TA, et al.

Supplements and nutritional interventions to augment high-intensity interval training physiological and performance adaptations-a narrative review. Article CAS PubMed Central Google Scholar. Gibala MJ, Little JP. Physiological basis of brief vigorous exercise to improve health.

Weston KS, Wisloff U, Coombes JS. High-intensity interval training in patients with lifestyle-induced cardiometabolic disease: a systematic review and meta-analysis. Taylor JL, Holland DJ, Spathis JG, Beetham KS, Wisloff U, Keating SE, et al.

Guidelines for the delivery and monitoring of high intensity interval training in clinical populations. Prog Cardiovasc Dis. Gist NH, Fedewa MV, Dishman RK, Cureton KJ. Sprint interval training effects on aerobic capacity: a systematic review and meta-analysis.

Bacon AP, Carter RE, Ogle EA, Joyner MJ. VO2max trainability and high intensity interval training in humans: a meta-analysis. PLoS ONE. Bouaziz W, Malgoyre A, Schmitt E, Lang PO, Vogel T, Kanagaratnam L. Effect of high-intensity interval training and continuous endurance training on peak oxygen uptake among seniors aged 65 or older: a meta-analysis of randomized controlled trials.

Int J Clin Pract. Effects of cardiovascular interval training in healthy elderly subjects: a systematic review.

Front Physiol. Milanovic Z, Sporis G, Weston M. Effectiveness of High-Intensity Interval Training HIT and continuous endurance training for VO2max improvements: a systematic review and meta-analysis of controlled trials. Sloth M, Sloth D, Overgaard K, Dalgas U.

Effects of sprint interval training on VO2max and aerobic exercise performance: a systematic review and meta-analysis. Scand J Med Sci Sports. Vollaard NBJ, Metcalfe RS, Williams S. Effect of number of sprints in an SIT session on change in V O2max: a meta-analysis.

Su L, Fu J, Sun S, Zhao G, Cheng W, Dou C, et al. Sultana RN, Sabag A, Keating SE, Johnson NA. The effect of low-volume high-intensity interval training on body composition and cardiorespiratory fitness: a systematic review and meta-analysis.

Lora-Pozo I, Lucena-Anton D, Salazar A, Galan-Mercant A, Moral-Munoz JA. Anthropometric, cardiopulmonary and metabolic benefits of the high-intensity interval training versus moderate, low-intensity or control for type 2 diabetes: systematic review and meta-analysis.

Article PubMed Central Google Scholar. Liu JX, Zhu L, Li PJ, Li N, Xu YB. Effectiveness of high-intensity interval training on glycemic control and cardiorespiratory fitness in patients with type 2 diabetes: a systematic review and meta-analysis. Aging Clin Exp Res.

Qiu S, Cai X, Sun Z, Zugel M, Steinacker JM, Schumann U. Aerobic interval training and cardiometabolic health in patients with type 2 diabetes: a meta-analysis. Weston M, Taylor KL, Batterham AM, Hopkins WG. Effects of low-volume high-intensity interval training HIT on fitness in adults: a meta-analysis of controlled and non-controlled trials.

Ross R, Blair SN, Arena R, Church TS, Despres JP, Franklin BA, et al. Importance of assessing cardiorespiratory fitness in clinical practice: a case for fitness as a clinical vital sign: a scientific statement from the American Heart Association. Kodama S, Saito K, Tanaka S, Maki M, Yachi Y, Asumi M, et al.

Cardiorespiratory fitness as a quantitative predictor of all-cause mortality and cardiovascular events in healthy men and women: a meta-analysis. Joyner MJ, Coyle EF. Endurance exercise performance: the physiology of champions. Trilk JL, Singhal A, Bigelman KA, Cureton KJ.

Eur J Appl Physiol. Walter AA, Smith AE, Kendall KL, Stout JR, Cramer JT. Six weeks of high-intensity interval training with and without beta-alanine supplementation for improving cardiovascular fitness in women.

J Strength Cond Res. De Revere JL, Clausen RD, Astorino TA. Changes in VO2max and cardiac output in response to short-term high-intensity interval training in Caucasian and Hispanic young women: a pilot study.

Naves JPA, Viana RB, Rebelo ACS, de Lira CAB, Pimentel GD, Lobo PCB, et al. Effects of high-intensity interval training vs.

sprint interval training on anthropometric measures and cardiorespiratory fitness in healthy young women. Forbes SC, Sletten N, Durrer C, Myette-Cote E, Candow D, Little JP. Creatine monohydrate supplementation does not augment fitness, performance, or body composition adaptations in response to four weeks of high-intensity interval training in young females.

Int J Sport Nutr Exerc Metab. Astorino TA, Schubert MM, Palumbo E, Stirling D, McMillan DW, Cooper C, et al. Magnitude and time course of changes in maximal oxygen uptake in response to distinct regimens of chronic interval training in sedentary women.

Gillen JB, Percival ME, Ludzki A, Tarnopolsky MA, Gibala MJ. Interval training in the fed or fasted state improves body composition and muscle oxidative capacity in overweight women. Obesity Silver Spring. Boutcher SH, Park Y, Dunn SL, Boutcher YN.

The relationship between cardiac autonomic function and maximal oxygen uptake response to high-intensity intermittent-exercise training. J Sports Sci. Allison MK, Baglole JH, Martin BJ, Macinnis MJ, Gurd BJ, Gibala MJ. Brief intense stair climbing improves cardiorespiratory fitness.

Gillen JB, Percival ME, Skelly LE, Martin BJ, Tan RB, Tarnopolsky MA, et al. Three minutes of all-out intermittent exercise per week increases skeletal muscle oxidative capacity and improves cardiometabolic health.

Hazell TJ, Hamilton CD, Olver TD, Lemon PW. Running sprint interval training induces fat loss in women. Rowley TW, Espinoza JL, Akers JD, Wenos DL, Edwards ES, Couillard C. Marcotte-Chenard A, Tremblay D, Mony MM, Brochu M, Dionne IJ, Langlois MF, et al.

Low-volume walking HIIT: Efficient strategy to improve physical capacity and reduce the risk of cardiovascular disease in older women with type 2 diabetes. Diabetes Metab Syndr.

Boukabous I, Marcotte-Chenard A, Amamou T, Boulay P, Brochu M, Tessier D, et al. Low-volume High-Intensity Interval Training HIIT versus moderate-intensity continuous training on body composition, cardiometabolic profile and physical capacity in older women.

J Aging Phys Act. Lionett S, Kiel IA, Camera DM, Vanky E, Parr EB, Lydersen S, et al. Circulating and adipose tissue miRNAs in women with polycystic ovary syndrome and responses to high-intensity interval training.

Bonafiglia JT, Islam H, Preobrazenski N, Gurd BJ. Risk of bias and reporting practices in studies comparing VO2max responses to sprint interval vs. continuous training: a systematic review and meta-analysis. J Sport Health Sci. Kong Z, Fan X, Sun S, Song L, Shi Q, Nie J. Comparison of high-intensity interval training and moderate-to-vigorous continuous training for cardiometabolic health and exercise enjoyment in obese young women: a randomized controlled trial.

Sun S, Zhang H, Kong Z, Shi Q, Tong TK, Nie J. Twelve weeks of low volume sprint interval training improves cardio-metabolic health outcomes in overweight females. Sun S, Kong Z, Shi Q, Hu M, Zhang H, Zhang D, et al. Non-energy-restricted low-carbohydrate diet combined with exercise intervention improved cardiometabolic health in overweight Chinese females.

Hu M, Kong Z, Sun S, Zou L, Shi Q, Chow BC, et al. Interval training causes the same exercise enjoyment as moderate-intensity training to improve cardiorespiratory fitness and body composition in young Chinese women with elevated BMI.

Klonizakis M, Moss J, Gilbert S, Broom D, Foster J, Tew GA. Low-volume high-intensity interval training rapidly improves cardiopulmonary function in postmenopausal women.

Trapp EG, Chisholm DJ, Freund J, Boutcher SH. The effects of high-intensity intermittent exercise training on fat loss and fasting insulin levels of young women. Int J Obes Lond. Dupuit M, Rance M, Morel C, Bouillon P, Pereira B, Bonnet A, et al.

Moderate-intensity continuous training or high-intensity interval training with or without resistance training for altering body composition in postmenopausal women.

Higgins S, Fedewa MV, Hathaway ED, Schmidt MD, Evans EM. Sprint interval and moderate-intensity cycling training differentially affect adiposity and aerobic capacity in overweight young-adult women.

Astorino TA, Allen RP, Roberson DW, Jurancich M, Lewis R, McCarthy K, et al. Adaptations to high-intensity training are independent of gender. Metcalfe RS, Babraj JA, Fawkner SG, Vollaard NB. Towards the minimal amount of exercise for improving metabolic health: beneficial effects of reduced-exertion high-intensity interval training.

Scalzo RL, Peltonen GL, Binns SE, Shankaran M, Giordano GR, Hartley DA, et al. Greater muscle protein synthesis and mitochondrial biogenesis in males compared with females during sprint interval training.

FASEB J. Metcalfe RS, Tardif N, Thompson D, Vollaard NB. Changes in aerobic capacity and glycaemic control in response to reduced-exertion high-intensity interval training REHIT are not different between sedentary men and women. Bonafiglia JT, Rotundo MP, Whittall JP, Scribbans TD, Graham RB, Gurd BJ.

Inter-individual variability in the adaptive responses to endurance and sprint interval training: a randomized crossover study. Sogaard D, Lund MT, Scheuer CM, Dehlbaek MS, Dideriksen SG, Abildskov CV, et al. High-intensity interval training improves insulin sensitivity in older individuals.

Acta Physiol Oxf. Weber CL, Schneider DA. Increases in maximal accumulated oxygen deficit after high-intensity interval training are not gender dependent.

J Appl Physiol Bostad W, Valentino SE, McCarthy DG, Richards DL, MacInnis MJ, MacDonald MJ, et al. Twelve weeks of sprint interval training increases peak cardiac output in previously untrained individuals. Phillips BE, Kelly BM, Lilja M, Ponce-Gonzalez JG, Brogan RJ, Morris DL, et al.

A practical and time-efficient high-intensity interval training program modifies cardio-metabolic risk factors in adults with risk factors for type II diabetes.

Front Endocrinol Lausanne. Lundby C, Montero D, Joyner M. Biology of VO2 max: looking under the physiology lamp. Astorino TA, Edmunds RM, Clark A, King L, Gallant RA, Namm S, et al. High-intensity interval training increases cardiac output and VO2max.

Schaumberg MA, Jenkins DG, Janse DEJXA, Emmerton LM, Skinner TL. Oral contraceptive use dampens physiological adaptations to sprint interval training.

Munan M, Oliveira CLP, Marcotte-Chenard A, Rees JL, Prado CM, Riesco E, et al. Acute and chronic effects of exercise on continuous glucose monitoring outcomes in type 2 diabetes: a meta-analysis. Sylow L, Richter EA. Current advances in our understanding of exercise as medicine in metabolic disease.

Curr Opin Physio. Brestoff JR, Clippinger B, Spinella T, von Duvillard SP, Nindl BC, Arciero PJ. An acute bout of endurance exercise but not sprint interval exercise enhances insulin sensitivity. Richards JC, Johnson TK, Kuzma JN, Lonac MC, Schweder MM, Voyles WF, et al. Short-term sprint interval training increases insulin sensitivity in healthy adults but does not affect the thermogenic response to beta-adrenergic stimulation.

Metcalfe R, Fawkner S, Vollaard N. No acute effect of reduced-exertion high-intensity interval training REHIT on insulin sensitivity. Int J Sports Med. Ortega JF, Fernandez-Elias VE, Hamouti N, Pallares JG, Mora-Rodriguez R.

Higher insulin-sensitizing response after sprint interval compared to continuous exercise. Whyte LJ, Ferguson C, Wilson J, Scott RA, Gill JM.

Durrer C, Robinson E, Wan Z, Martinez N, Hummel ML, Jenkins NT, et al. Little JP, Jung ME, Wright AE, Wright W, Manders RJF. Effects of high-intensity interval exercise versus continuous moderate-intensity exercise on postprandial glycemic control assessed by continuous glucose monitoring in obese adults.

Parker L, Shaw CS, Banting L, Levinger I, Hill KM, McAinch AJ, et al. Acute low-volume high-intensity interval exercise and continuous moderate-intensity exercise elicit a similar improvement in h glycemic control in overweight and obese adults. Gillen JB, Little JP, Punthakee Z, Tarnopolsky MA, Ridell MC, Gibala MJ.

Acute high-intensity interval exercise reduces the postprandial glucose response and prevalence of hyperglycaemia in patients with type 2 diabetes. Diabetes Obes Metab. Ryan BJ, Schleh MW, Ahn C, Ludzki AC, Gillen JB, Varshney P, et al. Moderate-intensity exercise and high-intensity interval training affect insulin sensitivity similarly in obese adults.

J Clin Endocrinol Metab. Esbjörnsson-Liljedahl M, Sundberg CJ, Norman B, Jansson E. Metabolic response in type I and type II muscle fibers during a s cycle sprint in men and women.

Esbjörnsson-Liljedahl M, Bodin K, Jansson E. Smaller muscle ATP reduction in women than in men by repeated bouts of sprint exercise.

Tarnopolsky LJ, MacDougall JD, Atkinson SA, Tarnopolsky MA, Sutton JR. Gender differences in substrate for endurance exercise. Hamadeh MJ, Devries MC, Tarnopolsky MA. Estrogen supplementation reduces whole body leucine and carbohydrate oxidation and increases lipid oxidation in men during endurance exercise.

Oosthuyse T, Bosch AN. The effect of the menstrual cycle on exercise metabolism: implications for exercise performance in eumenorrhoeic women.

Devries MC, Hamadeh MJ, Graham TE, Tarnopolsky MA. Devries MC, Hamadeh MJ, Phillips SM, Tarnopolsky MA. Menstrual cycle phase and sex influence muscle glycogen utilization and glucose turnover during moderate-intensity endurance exercise.

Am J Physiol Regul Integr Comp Physiol. Racil G, Ben Ounis O, Hammouda O, Kallel A, Zouhal H, Chamari K, et al. Effects of high vs. moderate exercise intensity during interval training on lipids and adiponectin levels in obese young females.

Maillard F, Rousset S, Pereira B, Traore A, de Pradel Del Amaze P, Boirie Y, et al. High-intensity interval training reduces abdominal fat mass in postmenopausal women with type 2 diabetes. Diabetes Metab. Samadi Z, Bambaeichi E, Valiani M, Shahshahan Z. Evaluation of changes in levels of hyperandrogenism, hirsutism and menstrual regulation after a period of aquatic high intensity interval training in women with polycystic ovary syndrome.

Int J Prev Med. Arad AD, DiMenna FJ, Thomas N, Tamis-Holland J, Weil R, Geliebter A, et al. Sandvei M, Jeppesen PB, Stoen L, Litleskare S, Johansen E, Stensrud T, et al.

Sprint interval running increases insulin sensitivity in young healthy subjects. Arch Physiol Biochem. Shepherd SO, Wilson OJ, Taylor AS, Thogersen-Ntoumani C, Adlan AM, Wagenmakers AJ, et al.

Low-volume high-intensity interval training in a gym setting improves cardio-metabolic and psychological health. Scott SN, Shepherd SO, Hopkins N, Dawson EA, Strauss JA, Wright DJ, et al.

Francois ME, Durrer C, Pistawka KJ, Halperin FA, Chang C, Little JP. Combined interval training and post-exercise nutrition in type 2 diabetes: a randomized control trial. Little JP, Gillen JB, Percival ME, Safdar A, Tarnopolsky MA, Punthakee Z, et al.

Low-volume high-intensity interval training reduces hyperglycemia and increases muscle mitochondrial capacity in patients with type 2 diabetes.

Madsen SM, Thorup AC, Overgaard K, Jeppesen PB. High intensity interval training improves glycaemic control and pancreatic beta cell function of type 2 diabetes patients. Winding KM, Munch GW, Iepsen UW, Van Hall G, Pedersen BK, Mortensen SP. The effect on glycaemic control of low-volume high-intensity interval training versus endurance training in individuals with type 2 diabetes.

Alvarez C, Ramirez-Campillo R, Ramirez-Velez R, Izquierdo M. Effects and prevalence of nonresponders after 12 weeks of high-intensity interval or resistance training in women with insulin resistance: a randomized trial.

Mandrup CM, Egelund J, Nyberg M, Enevoldsen LH, Kjaer A, Clemmensen AE, et al. Effects of menopause and high-intensity training on insulin sensitivity and muscle metabolism.

Kiel IA, Lundgren KM, Morkved S, Kjotrod SB, Salvesen O, Romundstad LB, et al. Women undergoing assisted fertilisation and high-intensity interval training: a pilot randomised controlled trial. Holloszy JO. Biochemical adaptations in muscle. J Biol Chem. Burgomaster KA, Hughes SC, Heigenhauser GJ, Bradwell SN, Gibala MJ.

Six sessions of sprint interval training increases muscle oxidative potential and cycle endurance capacity in humans. Burgomaster KA, Heigenhauser GJ, Gibala MJ. Effect of short-term sprint interval training on human skeletal muscle carbohydrate metabolism during exercise and time-trial performance.

Gibala MJ, Little JP, van Essen M, Wilkin GP, Burgomaster KA, Safdar A, et al. Short-term sprint interval versus traditional endurance training: similar initial adaptations in human skeletal muscle and exercise performance.

Little JP, Safdar A, Wilkin GP, Tarnopolsky MA, Gibala MJ. A practical model of low-volume high-intensity interval training induces mitochondrial biogenesis in human skeletal muscle: potential mechanisms.

Jacobs RA, Fluck D, Bonne TC, Burgi S, Christensen PM, Toigo M, et al. Improvements in exercise performance with high-intensity interval training coincide with an increase in skeletal muscle mitochondrial content and function. Larsen S, Nielsen J, Hansen CN, Nielsen LB, Wibrand F, Stride N, et al.

Biomarkers of mitochondrial content in skeletal muscle of healthy young human subjects. Medeiros DM. Assessing mitochondria biogenesis. Tan R, Nederveen JP, Gillen JB, Joanisse S, Parise G, Tarnopolsky MA, et al.

Skeletal muscle fiber-type-specific changes in markers of capillary and mitochondrial content after low-volume interval training in overweight women. Physiol Rep. Edgett BA, Bonafiglia JT, Baechler BL, Quadrilatero J, Gurd BJ. The effect of acute and chronic sprint-interval training on LRP, SIRT3, and PGC-1alpha expression in human skeletal muscle.

Granata C, Oliveira RS, Little JP, Renner K, Bishop DJ. Training intensity modulates changes in PGC-1alpha and p53 protein content and mitochondrial respiration, but not markers of mitochondrial content in human skeletal muscle. Fiorenza M, Lemminger AK, Marker M, Eibye K, Iaia FM, Bangsbo J, et al.

High-intensity exercise training enhances mitochondrial oxidative phosphorylation efficiency in a temperature-dependent manner in human skeletal muscle: implications for exercise performance.

Gillen JB, Martin BJ, MacInnis MJ, Skelly LE, Tarnopolsky MA, Gibala MJ. Twelve weeks of sprint interval training improves indices of cardiometabolic health similar to traditional endurance training despite a five-fold lower exercise volume and time commitment.

Cocks M, Shaw CS, Shepherd SO, Fisher JP, Ranasinghe AM, Barker TA, et al. Sprint interval and endurance training are equally effective in increasing muscle microvascular density and eNOS content in sedentary males.

Boyd JC, Simpson CA, Jung ME, Gurd BJ.

Jonathan Energy-boosting for busy professionals Little and Martin J Gibala Department of Kinesiology, McMaster University, Diabetic retinopathy health education, Ontario, Energy-boosting for busy professionals 4K1, Trainimg. Regular endurance exercise training induces sdaptations adaptations that enhance functional Energy-boosting for busy professionals, improve health Low-ingensity reduce the risk for chronic disease. Low-intensty the physiological changes are complex and involve multiple organ systems, metabolic adaptations in skeletal muscle play a critical role in the beneficial effects of endurance training. In particular, exercise-induced increases in muscle oxidative and glucose transport capacities are believed to contribute to the reduced risk of diseases such as insulin resistance and type 2 diabetes T2D. Jonathan Little Martin Gibala What is HIT? The training impulse i. interval intensity, duration and number is infinitely variable, with single efforts lasting from a few seconds up to several minutes. For more Energy-boosting for busy professionals fraining PLOS Subject Areas, Energy-boosting for busy professionals here. The current study involved the Coenzyme Q and periodontal health of two distinct experiments. Experiment 1 compared Low-intensitty specific and Loa-intensity muscle responses to acute bouts of either low-volume high-intensity interval training LV-HIT or moderate-intensity continuous endurance exercise END in a randomized crossover design. Six recreationally active men Age: After 6 weeks, both training protocols induced comparable increases in aerobic capacity END: Pre: Interestingly, only LV-HIT induced greater improvements in anaerobic performance and estimated whole-muscle glycolytic capacity.

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