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Kin 310 Exercise/Work Physiology

Kin 310 Exercise/Work Physiology. Office hours - K8621 W 10:30-12:20 or by appointment (ryand@sfu.ca) class email list announcements, questions and responses inform me of a preferred email account class notes will be posted on the web site in power point each week

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Kin 310 Exercise/Work Physiology

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  1. Kin 310Exercise/Work Physiology • Office hours - K8621 • W 10:30-12:20 • or by appointment (ryand@sfu.ca) • class email list • announcements, questions and responses • inform me of a preferred email account • class notes will be posted on the web site in power point each week • can be printed up to six per page • lecture schedule along with reading assignment on web site • www.sfu.ca/~ryand/kin310.htm

  2. Overview • Discussion of the physiological basis of exercise and work • Cellular bioenergetics • Providing ATP to meet demand • Cardiovascular and respiratory compensations and capacities • Limitations and adaptations to training • Molecular level adaptation • activity changes the cellular environment - stimulating adaptation to better meet demand • Fatigue - inability to sustain activity level • description of fatigue in the CNS, the neuromuscular junction and the muscle cell • Ageing - change in physiological capacities - impacts of disease and activity level • Assessment of work load and physical capacity for exercise and work • Exercise and the Environment • Heat and barometric pressure can create additional demands on physiological systems

  3. Energy Sources and Recovery from Exercise • Ch 2 Foss and Keteyian - Fox’s Physiological basis for Exercise and Sport- 6th edition • all human activity centers around the ability to provide energy (ATP) on a continuous basis • without energy cellular activity would cease • Main sources of energy • biomolecules - carbohydrate and fat • protein small contribution • lecture will review metabolic processes with an emphasis on regulation and recovery

  4. Energy • Energy - capacity or ability to perform work • Work - application of a force through a distance • Biological work - transport, mechanical and chemical work • Power - amount work performed over a specific time (rate of work) • Transformation of energy - forms of energy can be converted from one form to another • chemical energy in food is transformed into mechanical energy of movement or other biological work • Biological energy cycle

  5. ATP - adenosine tri-phosphate • Energy harnessed from molecular bonds in biomolecules - • used to resynthesize ATP - Fig 2.2 • only energy released from ATP can be utilized to perform cellular work • ATP in solution represents immediate source of energy available to muscle • enzyme (eg. ATPase) break high energy bonds between phosphate groups • Forming ADP + Pi + energy • Energy used to do biological work • Eg Calcium ATPase, myosin ATPase • Reaction is reversible (reform ATP) • CP -creatine phosphate (phosphocreatine) • Enzyme CK - Creatine Kinase • Kinases (eg glycolysis) • oxidative phosphorylation • form NADH, FADH2 then form ATP

  6. Sources of ATP • Limited quantity of ATP available • constant turnover (re-synthesis) - requires energy • 3 processes - use coupled reactions • ATP-PC system (phosphagen) • energy for re-synthesis from CP • Anaerobic Glycolysis • ATP from partial breakdown of glucose • Limited quantities of glucose • absence of oxygen • generates lactate as end product (*pH) • Aerobic System • requires oxygen • oxidation of carbohydrates, fatty acids and protein • Krebs cycle and Electron Transport

  7. Anaerobic sources • ATP -PC system (fig 2.4) • high energy phosphates • energy in CP bond is immediately available • as ATP is broken down it is continuously reformed • ADP + PC(Creatine Kinase) -> ATP • ADP + ADP (myokinase) -> ATP • CP reformed during recovery • from ATP formed through aerobic pathways • Table 2.1 - most rapidly available fuel source - very limited quantity • Depleted with 10 seconds of maximum activity • Recovers quickly

  8. Anaerobic Glycolysis • Incomplete breakdown of glucose or glycogen to lactate • 12 separate, sequential chemical reactions • breakdown molecular bonds • couple reaction to synthesis of ATP • yields 2 (glucose) or 3 (glycogen) ATP • Rapid but limited production • Limited glycogen stores • lactate accumulates -> acidity -> fatigue - unable to sustain demand • PFK - phosphofructokinase • rate limiting enzyme- slow step in reaction - inhibited by acidity • Table 2.2

  9. Anaerobic Glycolysis • Pyruvate is final product of glycolysis • pyruvate is converted to lactate when aerobic ATP production can not meet demand for ATP utilization • Inadequate O2 delivery (or high demand) • enzyme LDH - lactate dehydrogenase • Redox reaction (Fig 2.6) • *frees up NAD+ required in glycolysis • Allows rapid production of ATP through glycolysis - until acidity shuts it down • summary fig 2.7 • glycogen - endogenous fuel • within muscle • glucose - exogenous fuel • comes from blood glucose, released from liver glycogen

  10. Aerobic Sources of ATP • Acetyl groups - 2 carbon units • formed from pyruvate and from Beta oxidation of free fatty acids • NAD and FAD - electron carriers • become reduced when biomolecules are oxidized - form NADH, FADH2 • carry these hydrogen atoms to the electron transport chain • donated and passed down chain of carriers to form ATP • Oxidative - phosphorylation • oxygen is final acceptor of hydrogen, it is reduced to H2O • occurs in mitochondrial membrane system - cristae

  11. Krebs Cycle • Fig 2.12 - Krebs Cycle (Citric Acid cycle) • Key regulatory enzymes • ICDH(Iso citrate De-hydrogenase), CS (citrate synthase), KGDH (alpha ketoglutarate DH) • NADH - inhibits enzyme activity • High NADH - indicates ETC is behind in utilizing NADH already produced • Availability of ADP also regulates Krebs cycle activity • ADP and NAD+ are needed for reactions to occur • CO2 produced as molecules are oxidized ( H atoms are removed) • Krebs Cycle - produces • (per acetyl group-2 Carbons) • 1 GTP (ATP equivalent) • 3 NADH and 1 FADH2

  12. ETC • Electron Transport Chain (ETC) • H atoms passed down series of electron carriers by enzymatic reactions coupled to production of ATP • oxidative phosphorylation • each NADH - yields 3 ATP • each FADH2 - yields 2 ATP • for process to continue, must liberate NAD+ and FAD+ - • Process requires oxygen

  13. Aerobic Glycolysis • With sufficient oxygen pyruvate moves into mitochondria • Monocarboxylate transporter • law of mass action • 1 mole glycogen - • glycolysis • 2 moles pyruvate ; 3 moles ATP • 2 moles NADH (6 moles ATP after ETC) • Krebs - per pyruvate molecule • 4 moles NADH (one from PDH) • 12 ATP • 1 mole FADH2 • 2 ATP • 1 GTP • Multiplied by 2 = 30 moles of ATP • 39 ATP per mole of glycogen

  14. Fat Metabolism • Fat and Protein only oxidized • No anaerobic metabolism • Fatty acids - 16-18 carbon units • acetyl groups (2 carbons) broken off chain to enter Krebs cycle one at a time • Beta oxidation Fig. 2.15 • uses 1 ATP for first two carbons only • produces 1 NADH and 1 FADH2 • acetyl co-A through Krebs/ETC • Yields 12 ATP • total of 16 ATP for first acetyl group • 17 for each remaining acetyl group • last acetyl group only 12 ATP- as it is not produced by beta oxidation • 1 mole of palmitic acid-138 of moles ATP • Key enzymes - B-HAD, and lipases

  15. Comparing the Energy Systems • Table 2.6 • energy capacity - amount of ATP able to be produced independent of time • power - rate of production - time factor • *aerobic - table represents availability from glycogen only - fat is unlimited • Rest • aerobic - supplies all ATP • mainly fats and carbohydrates • some lactate ~10 mg/dl in blood • does not accumulate, but LDH active

  16. Exercise • Both anaerobic and aerobic • relative contribution to ATP production depends on • intensity and/or duration • state of training • Dietary factors (replenishment of stores) • Energy contribution vs time • (*Assumes all out activity for time frame ) • Mcardle, Katch and Katch - Exercise Physiology • Immediate - phosphagens - major contributor for up to 10 sec • Anaerobic Glycolysis - majro contributor for 30sec - 2.5 min • Aerobic metabolism major contributor for 3 min onward • Contribution of energy systems is a continuum, not an on or off situation

  17. Experimental evidence • Two types of exercise compared in most of the following experiments • near maximal - short duration • sub maximal - longer duration • Fig 2.18 glycogen depletion • activities below 60 % (VO2 max) and above 90% - limited glycogen depletion • At 75% significant depletion - leading to exhaustion (fatigue) • 2.18b • rate of depletion dependant on demand • Volume of depletion related to duration

  18. Short duration • 2-3 minutes high intensity exercise • fig 2.19 - major energy source CH2O • ATP and PC will drop rapidly • restored in recovery (rapidly) • Aerobic contribution limited by its low power output • also takes 2-3 min to increase output • oxygen deficit - period during which level of O2 consumption is below that necessary to supply all ATP required by exercise demands • ATP supplied by anaerobic systems to make up for aerobic shortfall • rapid accumulation of lactate • 200 mg/dl in blood / muscle

  19. Prolonged Exercise • 10 minutes or longer • Aerobic fat and carbohydrate metabolism are main sources of ATP • CHO dominate up to ~ 20 min • fats minor but supportive role • after ~1 hr fats become dominant source of ATP • at lower intensities (< 60% Hr max) fats also have greater contribution • fig. 2.20 • fatigue not associated with lactate, other factors - discussed later in semester • Fig 2-22 activities require blend of anaerobic and aerobic systems • energy continuum

  20. Control and Regulation • Matching provision of ATP to demand is needed so performer does not experience early or undue fatigue • Enzymes, hormones, substrates interact to modify flow through metabolic pathways of each system • Table 2.7 • Flow through different pathways is often modified by activating and inactivating key enzymes • Influences over enzymes include; • high vs low energy state of cell(NAD+) • Hormone levels (epinephrine, glucagon) • “amplification” of hormone effects • competition for ADP (between enzymes) • adequacy of oxygen supply • power output requirements relative to aerobic power (demand)

  21. Regulation • In general we observe; • regulation within muscle cell, • And influences from outside the cell • both serving to modify regulatory enzymes in each pathway • Fig 2.23 • Energy State regulation • ADP/ATP ratio • very quick - tightly linked to rate of energy expenditure • Hormone Amplification • cAMP 2nd messenger systems - amplification • Ep and Glucagon - activate phosphorylase - glycogen breakdown • lipase - fat breakdown

  22. Regulation • Substrates - • eg. NADH - buildup • In cytosol stimulates LDH - frees NAD+ • occurs when ETS is maximized • can not oxidize NADH fast enough • Also inhibitory in Krebs cycle (DH’s) • eg. Inc Pyruvate • stimulates PDH - entry into Krebs • PDH also influenced by phophorylation • Oxidative State Regulation • O2 and ADP availability • O2 stimulates cytochrome oxidase (CO) • final step in ETC • low O2 - inhibits Cytochrome Oxidase • Leads to build up of NADH, FADH2 • key factor is oxygen availability vs demand for ATP utilization

  23. Recovery from Exercise • Ch. 3 • process of recovery from exercise involves transition from catabolic to anabolic state • breakdown of glycogen and fats to replenishment of stores • breakdown of protein to protein synthesis for muscle growth and repair • Our discussion of recovery will include; • oxygen consumption post exercise • Replenishment of energy stores • Lactate metabolism(energy or glycogen) • Replenishment of oxygen stores • intensity and activity specific recovery • guidelines for recovery

  24. Recovery Oxygen • Recovery O2 - Net amount of oxygen consumed during recovery from exercise • excess above rest in Litres of O2 • Fast and Slow components • Based on slope of O2 curve • first 2-3 min of recovery - O2 consumption declines fast • then declines slowly to resting • Fig 3.1 • Fast Component - first 2-3 minutes • restore myoglobin and blood oxygen • energy cost of elevated ventilation • energy cost of elevate heart activity • replenishment of phosphagen • volume of O2 for fast component = area under curve • related to intensity not duration

  25. Recovery Oxygen • Slow Component • elevated body temperature • Q10 effect - inc metabolic activity • cost of ventilation and heart activity • ion redistribution Na+/K+ pump • glycogen re-synthesis • effect of catecholamines and thyroid hormone • oxidation of lactate serves as fuel for many of these processes • duration and intensity do not modify slow component until threshold of combined duration and intensity • After 20 min and 80% • We observe a 5 fold increase in the volume of the slow component

  26. Energy Stores • Both phosphagens (ATP, CP) and glycogen are depleted with exercise • ATP/CP - recover in fast component • measured by sterile biopsy, MRS • rate of PC recovery indicative of net oxidative ATP synthesis (VO2) • study of ATP production • 20-25 mmol/L/min glycogen and all fuels • during exercise • CP can drop to 20%, ATP to 70 % • CP lowest at fatigue, rises immediately with recovery • Fig 3.2 - very rapid recovery of CP • 30 sec 70%, 3-5 min 100% recovery

  27. Phosphagen Recovery(cont.) • Fig 3.3 • occlusion of blood flow - no phosphogen recovery • ** requires aerobic metabolism • estimate 1.5 L of oxygen for ATP-PC recovery • Energetics of Recovery • Fig 3.4 • breakdown carbs, fats some lactate • produce ATP which reforms CP • high degree of correlation between phosphagen depletion and volume of fast component oxygen • Fig. 3.5 • anaerobic power in athlete related to phosphagen potential - Wingate test

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