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Chapter 3

EXERCISE PHYSIOLOGY
Theory and Application to Fitness and Performance 10th Edition
Scott K. Powers and Edward T. Howley

Bioenergetics

Chapter 3

Presentation prepared by:


Brian B. Parr, Ph.D., Scott K. Powers, Ph.D., Ed.D., and Edward T. Howley, Ph.D.

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Chapter 3

Lecture Outline
 Cell Structure
 Biological Energy Transformation
 Fuels for Exercise
 High-Energy Phosphates
 Bioenergetics
 Aerobic ATP Tally
 Efficiency of Oxidative Phosphorylation
 Control of Bioenergetics
 Interaction Between Aerobic/Anaerobic ATP Production

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Chapter 3

Introduction-key terms
 Metabolism
– Sum of all chemical reactions that occur in the body
– Anabolic reactions
 Synthesis of molecules
– Catabolic reactions
 Breakdown of molecules
 Bioenergetics
– Process of converting foodstuffs (fats, proteins,
carbohydrates) into usable energy for cell work

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Chapter 3 Cell Structure

Cell Structure
 Cell membrane (sarcolemma)
– Semipermeable membrane that separates the cell from
the extracellular environment
 Nucleus
– Contains genes that regulate protein synthesis
 Molecular biology
 Cytoplasm (sarcoplasm)
– Fluid portion of cell
– Contains organelles
 Mitochondria

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Chapter 3 Cell Structure

A Muscle Cell and Its Major


Organelles

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Chapter 3 A Closer Look 3.1

Molecular Biology and Exercise Science


 Study of molecular structures and events underlying biological
processes
– Relationship between genes and cellular characteristics they
control
 Genes code for specific cellular proteins
– Process of protein synthesis
 Exercise training results in modifications in protein synthesis
– Strength training results in increased synthesis of muscle
contractile protein
 Molecular biology provides “tools” for understanding the cellular
response to exercise

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Chapter 3 Biological Energy Transformation

Cellular Chemical Reactions


 Endergonic reactions
– Require energy to be added to the reactants
– Endothermic
 Exergonic reactions
– Release energy
– Exothermic
 Coupled reactions
– Liberation of energy in an exergonic reaction drives an
endergonic reaction

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Chapter 3 Biological Energy Transformation

The Breakdown of Glucose:


An Exergonic Reaction

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Chapter 3 Biological Energy Transformation

Coupled Reactions

The energy given off by the exergonic reaction


powers the endergonic reaction

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Chapter 3 Cell Structure

Take home messages (1)


 Metabolism is defined as the total of all cellular reactions that occur in the
body; this includes both the synthesis of molecules and the breakdown of
molecules.
 Cell structure includes the following three major parts: (1) cell membrane
(called sarcolemma in muscle), (2) nucleus, and (3) cytoplasm (called
sarcoplasm in muscle).
 The cell membrane provides a protective barrier between the interior of
the cell and the extracellular fluid.
 Genes located within the nucleus regulate protein synthesis within the
cell.

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Chapter 3 Cell Structure

Take home messages (2)


 Cytoplasm: fluid portion of the cell that contains
numerous organelles and enzymes.
 Endergonic reactions require energy to be
added.
 Exergonic reactions are reactions that give off
energy.
 Coupled reactions are reactions that are
connected, with the release of energy in one
reaction being used to drive the second reaction.
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Chapter 3 Biological Energy Transformation

Oxidation-Reduction Reactions
 Oxidation
– Removing an electron
 Reduction
– Addition of an electron
 Oxidation and reduction are always coupled
reactions
 Often involves the transfer of hydrogen atoms rather
than free electrons
– Hydrogen atom contains one electron
– A molecule that loses both a hydrogen and an electron;
therefore, this molecule is oxidized

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Chapter 3 Biological Energy Transformation

Roles of NAD and FAD in electron


transport
 Nicotinamide adenine dinucleotide (NAD)
– Oxidized form: NAD+
– Reduced form: NADH
 Flavin adenine dinucleotide (FAD)
– Oxidized form: FAD
– Reduced form: FADH2
 Both play an important role in transfer of electrons
– Carrier molecules during bioenergetic reactions

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Chapter 3 Biological Energy Transformation

Structural Formulas for NAD+, NADH,


FAD, and FADH2

(a) When NAD reacts


with 2 H, it binds to
one of them and
accepts the
electron from the
other to form
NADH.

(b) When FAD reacts


with 2 H, it binds to
both of them to
form FADH2.

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Chapter 3 Biological Energy Transformation

Enzymes
 Catalysts that regulate the speed of reactions
– Lower the energy of activation
 Factors that regulate enzyme activity
– Temperature
– pH
 Interact with specific substrates
– Lock and key model

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Chapter 3 Biological Energy Transformation

Enzymes Catalyze Reactions

Enzymes lower the energy of activation

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Chapter 3 Biological Energy Transformation

Factors That Alter Enzyme Activity


 Temperature
– A small rise in body temperature increases enzyme
activity
– Exercise results in increased body temperature
– Large increase in body temperature (>41oC) can
denature enzymes and decrease activity
 pH
– Changes in pH (increase or decrease) can decrease
enzyme activity
– High intensity exercise decreases muscle pH
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Chapter 3 Biological Energy Transformation

The Effect of Body Temperature on


Enzyme Activity

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Chapter 3 Biological Energy Transformation

The Effect of pH on Enzyme Activity

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Chapter 3 Biological Energy Transformation

Enzyme-catalyzed reaction

Two substrates Enzyme catalyzes Product molecule


fit into enzyme’s the chemical produced and
active site reaction enzyme is unaltered
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Chapter 3 Biological Energy Transformation

Classification of Enzymes
 Almost all enzyme names end in –ase
 Kinases
– Add a phosphate group
 Dehydrogenases
– Remove hydrogen atoms
 Oxidases
– Catalyze oxidation-reduction reactions involving
oxygen
 Isomerases
– Rearrangement of the structure of molecules
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Chapter 3 Clinical Applications 3.1

Diagnostic Value of Measuring


Enzyme Activity in the Blood

 Damaged cells release enzymes into the blood


– Enzyme levels in blood serve as “biomarkers” of
disease and/or tissue damage
 Diagnostic application
– Elevated lactate dehydogenase or creatine kinase
in the blood may indicate a myocardial infarction

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Chapter 3 Clinical Applications 3.1

Examples of the Diagnostic Value of


Enzymes in Blood

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Chapter 3 Biological Energy Transformation

Take home messages


 Oxidation is the process of removing an electron from an atom or
molecule.
 Reduction is the addition of an electron to an atom or molecule.
 Oxidation-reduction reactions are always coupled because a molecule
cannot be oxidized unless it donates and electron to another atom.
 Enzymes serve as catalysts for chemical reactions and therefore, regulate
the speed of chemical reactions.
 Enzymes are classified into categories based upon the type of reaction
that the enzyme performs.
 Temperature and pH are key factors that regulate enzyme activity.
Individual enzymes have an optimal temperature and pH at which they are
most active.

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Chapter 3 Fuels for Exercise

Fuels for exercise-Carbohydrates


 Include monosaccharides, disaccharides, and
polysaccharides
 Glucose
– Blood sugar
 Glycogen
– Storage form of glucose in liver and muscle
 Synthesized by enzyme glycogen synthase
– Glycogenolysis
 Breakdown of glycogen to glucose
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Chapter 3 Fuels for Exercise

Fuels for exercise-Fats


 Fatty acids
– Primary type of fat used by skeletal muscle
 Triglycerides
– Storage form of fat in muscle and adipose tissue
– Broken down into glycerol and fatty acids via lipolysis
 Phospholipids
– Not used as an energy source
 Steroids
– Derived from cholesterol-not an energy source
– Needed to synthesize sex hormones
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Chapter 3 Fuels for Exercise

Fuels for exercise-Protein


 Composed of amino acids
 Some can be converted to glucose in the liver
– Gluconeogenesis
 Others can be converted to metabolic
intermediates
– Contribute as a fuel in muscle
 Overall, protein is not a primary energy source
during exercise

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Chapter 3 Fuels for Exercise

Take home messages


 The body uses carbohydrate, fat, and protein nutrients consumed in the
diet to provide the necessary energy to maintain cellular activities both at
rest and during exercise.
 During exercise, the primary nutrients used for energy are fats and
carbohydrates, with protein contributing a relatively small amount of the
total energy used.
 Glucose is stored in animal cells as a polysaccharide called glycogen.
 Fatty acids are the primary form of fat used as an energy source in cells.
Fatty acids are stored as triglycerides in muscle and fat cells.
 Proteins are composed of amino acids, and 20 different amino acids are
required to form the various proteins contained in cells. The use of protein
as an energy source requires that cellular proteins be broken down to
amino acids.
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Chapter 3 High-Energy Phosphates

High-Energy Phosphates
 Adenosine triphosphate (ATP)
– Consists of adenine, ribose, and three linked
phosphates
 Synthesis

ADP + Pi  ATP

 Breakdown

ATP ATPase
ADP + Pi + Energy

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Chapter 3 High-Energy Phosphates

Structure of ATP

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Chapter 3 High-Energy Phosphates

ATP is the Universal Energy Donor


in Cells

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Chapter 3 Bioenergetics

Bioenergetics
 Formation of ATP
– Phosphocreatine (PC) breakdown
– Degradation of glucose and glycogen
 Glycolysis
– Oxidative formation of ATP
 Anaerobic pathways
– Do not involve O2
– PC breakdown and glycolysis
 Aerobic pathways
– Require O2
– Oxidative phosphorylation
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Chapter 3 Bioenergetics

Anaerobic ATP Production

 ATP-PC system or “phosphagen system”


– Immediate source of ATP

PC + ADP Creatine kinase


ATP + C

 Glycolysis
– Glucose  2 pyruvic acid or 2 lactic acid
– Energy investment phase
 Requires 2 ATP
– Energy generation phase
 Produces 4 ATP, 2 NADH, and 2 pyruvate or 2 lactate
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Chapter 3 The Winning Edge 3.1

Does Creatine Supplementation


Improve Exercise Performance?
 Depletion of PC may limit short-term, high-intensity exercise
 Creatine monohydrate supplementation
– Increased muscle PC stores
– Some studies show improved performance in short-term, high-
intensity exercise
 Inconsistent results may be due to water retention and weight gain
– Increased strength and fat-free mass with resistance training
 Creatine supplementation does not appear to pose health risks
 Variability in supplement purity exists

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Chapter 3 Bioenergetics

The Two Phases of Glycolysis

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Chapter 3 Bioenergetics

Interaction Between Blood Glucose


and Muscle Glycogen in Glycolysis

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Chapter 3 Bioenergetics

Glycolysis: Energy Investment Phase

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Chapter 3 Bioenergetics

Glycolysis: Energy Generation Phase

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Chapter 3

Glycolysis

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Chapter 3 Bioenergetics

Hydrogen and Electron Carrier


Molecules
 Transport hydrogens and associated electrons
– To mitochondria for ATP generation (aerobic)
– To convert pyruvic acid to lactic acid (anaerobic)
 Nicotinamide adenine dinucleotide (NAD)
NAD+ + 2H  NADH

 Flavin adenine dinucleotide (FAD)


FAD + 2H  FADH2

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Chapter 3 A Closer Look 3.3

NADH is “Shuttled” into Mitochondria

 NADH produced in glycolysis must be converted


back to NAD
– By converting pyruvic acid to lactic acid
– By “shuttling” H+ into the mitochondria
 A specific transport system shuttles H+ across
the mitochondrial membrane
– Located in the mitochondrial membrane

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Chapter 3 Bioenergetics

Conversion of Pyruvic Acid to


Lactic Acid

The addition of two H to pyruvic acid forms NAD


and lactic acid

Catalyzed by lactate dehydrogenase (LDH)


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Chapter 3 A Closer Look 3.2

Lactic Acid or Lactate?


 Terms lactic acid and lactate used interchangeably
– Lactate is the conjugate base of lactic acid
 Lactic acid is produced in glycolysis
– Rapidly disassociates to lactate and H+

The ionization of lactic acid forms the


conjugate base called lactate

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Chapter 3 Bioenergetics

Take homes messages


 The immediate source of energy for muscular contraction is the high-
energy phosphate ATP. ATP is degraded via the enzyme ATPase as
follows:

ATP ADP + Pi + Energy


ATPase
 Formation of ATP without the use of O2 is termed anaerobic metabolism.
The production of ATP using O2 is referred to as aerobic metabolism.
 Muscle cells can produce ATP by any one or a combination of three
metabolic pathways: (1) ATP-PC system, (2) glycolysis, (3) oxidative
formation of ATP.
 The ATP-PC system and glycolysis are two anaerobic metabolic pathways
that produce ATP without O2.

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Chapter 3 Bioenergetics

Aerobic ATP Production


 Krebs cycle (citric acid cycle)
– Pyruvic acid (3 C) is converted to acetyl-CoA (2 C)
 CO2 is given off
– Acetyl-CoA combines with oxaloacetate (4 C) to form citrate
(6 C)
– Citrate is metabolized to oxaloacetate
 Two CO2 molecules given off
– Produces three molecules of NADH and one FADH2
– Also forms one molecule of GTP
 Produces one ATP

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Chapter 3 Bioenergetics

Steps Leading to
Oxidative Phosphorylation

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Chapter 3 Bioenergetics

The Citric acid (aka, Krebs Cycle)

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Chapter 3 Bioenergetics

Fats and Proteins in Aerobic Metabolism

 Fats
– Triglycerides  glycerol and fatty acids
– Fatty acids  acetyl-CoA
 Beta-oxidation
– Glycerol is not an important muscle fuel during
exercise
 Protein
– Broken down into amino acids
– Converted to glucose, pyruvic acid, acetyl-CoA, and
Krebs cycle intermediates
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Chapter 3 Bioenergetics

Relationship Between the Metabolism


of Proteins, Carbohydrates, and Fats

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Chapter 3 Bioenergetics

Aerobic ATP Production


 Electron transport chain
– Oxidative phosphorylation occurs in the
mitochondria
– Electrons removed from NADH and FADH are
passed along a series of carriers (cytochromes) to
produce ATP
 Each NADH produces 2.5 ATP
 Each FADH produces 1.5 ATP
– Called the chemiosmotic hypothesis
– H+ from NADH and FADH are accepted by O2 to
form water
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Chapter 3 Bioenergetics

The Chemiosmotic Hypothesis of ATP


Formation
 Electron transport chain results in pumping of H+
ions across inner mitochondrial membrane
– Results in electrochemical (i.e., H+) gradient across
membrane
 Energy released to form ATP as H+ ions diffuse
back across the membrane
ADP + Pi  ATP

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Chapter 3 Bioenergetics

Oxidative Phosphorylation

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Chapter 3

Electron Transport Chain

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Chapter 3 A Closer Look 3.4

Beta Oxidation is the Process of


Converting Fatty Acids to Acetyl-CoA
 Breakdown of triglycerides releases fatty acids
 Fatty acids must be converted to acetyl-CoA to be
used as a fuel
– Activated fatty acid (fatty acyl-CoA) enters mitochondrion
– Fatty acid “chopped” into 2 carbon fragments forming
acetyl-CoA
 Acetyl-CoA enters the citric acid cycle and is used for
energy

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Chapter 3 A Closer Look 3.4

Beta Oxidation

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Chapter 3

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Chapter 3 Bioenergetics

Take homes messages


 Oxidative phosphorylation (i.e., aerobic ATP production) occurs in the
mitochondria as a result of a complex interaction between the Citric acid
cycle and the electron transport chain.
 The primary role of the Citric acid cycle is to complete the oxidation of
substrates and form NADH and FADH to enter the electron transport
chain.
 The end result of the electron transport chain is the formation of ATP and
water. Water is formed by oxygen-accepting electrons and the
associated hydrogens.
 Therefore, oxygen consumption in the body occurs because oxygen is
used as the final acceptor of electrons during aerobic metabolism.

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Chapter 3 Research Focus 3.1

Free Radicals are Formed in the Mitochondria


 Free radicals are molecules with an unpaired electron in outer orbital
 Free radicals can be produced by the leakage of electrons along the
electron transport chain
 Free radicals react with other molecules in the cell
– Damages the molecule combining with the radical
 Aerobic exercise promotes the production of free radicals in the working
muscles
– Exercise-induced free radical production is not due to oxidative
phosphorylation in the mitochondria

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Chapter 3 A Closer Look 3.5

A New Look at the ATP Balance Sheet


 Historically, 1 glucose produced 38 ATP
 Recent research indicates that 1 glucose
produces 32 ATP
– Energy provided by NADH and FADH also used
to transport ATP out of mitochondria
– 3 H+ must pass through H+ channels to produce
1 ATP
– Another H+ needed to move the ATP across the
mitochondrial membrane
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Chapter 3 Aerobic ATP Tally

Aerobic ATP Tally Per Glucose


Molecule

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Chapter 3

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Chapter 3 Efficiency of Oxidative Phosphorylation

Efficiency of Oxidative
Phosphorylation
 One mole of ATP has energy yield of 7.3 kcal
 32 moles of ATP are formed from one mole of glucose
 Potential energy released from one mole of glucose is 686 kcal/mole

32 moles ATP/mole glucose x 7.3 kcal/mole ATP


 Overall efficiency of aerobic respiration is 34% x 100 = 34%
– 66% of energy686 kcal/mole glucose
released as heat

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Chapter 3 Efficiency of Oxidative Phosphorylation

Take home messages


 The aerobic metabolism of one molecule of
glucose results in the production of 32 ATP
molecules, whereas the aerobic yield for
glycogen breakdown results in net production of
33 ATP.
 The overall efficiency of aerobic respiration is
approximately 34%, with the remaining 66% of
energy being released as heat.

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Chapter 3 Control of Bioenergetics

Control of Bioenergetics
 Rate-limiting enzymes
– An enzyme that regulates the rate of a metabolic
pathway
 Modulators of rate-limiting enzymes
– Levels of ATP and ADP+Pi
 High levels of ATP inhibit ATP production
 Low levels of ATP and high levels of ADP+Pi stimulate
ATP production
– Calcium stimulates aerobic ATP production

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Chapter 3 Control of Bioenergetics

Example of a Rate-Limiting Enzyme

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Chapter 3

Feedback Inhibition

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Chapter 3 Control of Bioenergetics

Rate-Limiting Enzymes of Metabolic


Pathways

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Chapter 3

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Chapter 3

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Chapter 3 Control of Bioenergetics

Take home messages


 Metabolism is regulated by enzymatic activity. An enzyme that regulates a
metabolic pathway is termed the rate-limiting enzyme.
 The rate-limiting enzyme for glycolysis is phosphofructokinase, while the
rate-limiting enzymes for the Citric acid cycle and electron transport chain
are isocitrate dehydrogenase and cytochrome oxidase, respectively.
 In general, cellular levels of ATP and ADP+Pi regulate the rate of metabolic
pathways involved in the production of ATP.
 Increases in free calcium can stimulate aerobic energy metabolism by
activating enzymes in the Citric acid cycle.

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Chapter 3 Interaction Between Aerobic/Anaerobic ATP Production

Interaction Between Aerobic/Anaerobic


ATP Production
 Energy to perform exercise comes from an interaction
between aerobic and anaerobic pathways
 Depends on duration and intensity of exercise
– Short-term, high-intensity activities
 Greater contribution of anaerobic energy systems
– Long-term, low to moderate-intensity exercise
 Majority of ATP produced from aerobic sources

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Chapter 3 The Winning Edge 3.2

Contribution of Aerobic/Anaerobic ATP


Production During Sporting Events

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Chapter 3 Interaction Between Aerobic/Anaerobic ATP Production

Take home messages

 Energy to perform exercise is derived from an


interaction of anaerobic and aerobic pathways.
 In general, the shorter the activity (high
intensity), the greater the contribution of
anaerobic energy production.
 Long-duration activities (e.g., low to moderate
intensity) utilize ATP produced from aerobic
sources.

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Chapter 3

Study Questions
1. List and briefly discuss the functions of the three major
components of cell structure.
2. Briefly explain the concept of coupled reactions.
3. Define the following terms: (1) bioenergetics, (2) endergonic
reactions, and (3) exergonic reactions.
4. Discuss the role of enzymes as catalysts. What is meant by the
expression “energy of activation”?
5. Where do glycolysis, the Krebs cycle, and oxidative
phosphorylation take place in the cell?
6. Define the terms glycogen, glycogenolysis, and glycolysis.

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Chapter 3

Study Questions
7. What are high-energy phosphates? Explain the statement that
“ATP is the universal energy donor.”
8. Define the terms aerobic and anaerobic.
9. Briefly discuss the function of glycolysis in bioenergetics. What
role does NAD+ play in glycolysis?
10. Discuss the operation of the Krebs cycle and the electron
transport chain in the aerobic production of ATP. What is the
function of NAD+ and FAD in these pathways?
11. What is the efficiency of the aerobic degradation of glucose?

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Chapter 3

Study Questions
12. What is the role of oxygen in aerobic metabolism?
13. What are the rate-limiting enzymes for the following metabolic
pathways? ATP-PC system? Glycolysis? Krebs cycle? Electron
transport chain?
14. Briefly discuss the interaction of anaerobic versus aerobic ATP
production during exercise.
15. Discuss the chemiosmotic theory of ATP production.
16. Briefly discuss the impact of changes in both temperature and pH
on enzyme activity.
17. Discuss the relationship between lactic acid and lactate.

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Chapter 3

Lab: Resting Blood Pressure and Heart


Rate
 HR is generally expressed as  Bradycardia- defined as
# of ventricular contractions Resting HR less than 60
 Expressed at BPM (Beats per – Commonly found in
Minute) aerobically trained
 Normal range: 60-100 individuals
– Avg. Sedentary Men: 72 – Due to a shift towards
Women: 76 parasympathetic nervous
system on the heart rather
than sympathetic
– Can result from drugs,
injury, or diseases

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Chapter 3

Lab

 Tachycardia- defined as  Heart Rate can be affected by:


resting HR greater than 100 – Drugs
– May indicate underlying – Body position
heart disease – Dietary and hydration
– Supplements or drugs may – Noise, temp, humidity, etc.
cause this

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Chapter 3

Lab

 Measure HR
– Palpate- touch
 Radial- thumb side of wrist, we will use this site especially during exercise
 Carotid- groove on side of neck
– Auscultation- listen

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Chapter 3

Lab

 Blood Pressure
– Depends on volume of blood moving through blood vessels
– Diameter or size of blood vessel
 This determines vascular resistance

– Expressed as Systolic/Diastolic (mmHg)


 Systolic- pressure of blood against vessel walls when ventricles are
contracting
 Diastolic- pressure of blood against vessel walls when ventricles relax to
fill with blood

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Chapter 3

Lab

 Blood Pressure Guidelines at Rest


– Normal: <120/80
– Prehypertension: 120-139/80-89
– Stage 1 Hypertension: 140-159/90-99
– Stage 2 Hypertension: ≥160/≥100

 Measure using stethoscope

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Chapter 3

Lab

 Place blood pressure cuff on left upper arm


 Purpose of cuff is to deform the brachial artery
 Listen to Korotokoff sounds

 At Rest: pump pressure up to ~200


– Slowly release pressure at about 4mmHg/sec
– After you hear the last Korotokoff sound completely release
pressure.
– Blood pressure is recorded in even numbers, round up to even
numbers

Copyright © 2018 McGraw-Hill Education. All rights reserved. No reproduction or distribution without the prior written consent of McGraw-Hill Education.
Chapter 3

Lab
 Systolic- is the first thump you hear (1st Korotokoff Sound)
 Diastolic- is the last thump you hear (4th Korotokoff Sound)
– You can use 5th Korotokoff Sound which is the absence of sound

 Sources of error
– Acuity of hearing, background noise, level of experience,
improper cuff size, improper placement of stethoscope or ear
pieces, inaccurate sphygmomanometer, improper rate of
release, slow reaction time, etc.

Copyright © 2018 McGraw-Hill Education. All rights reserved. No reproduction or distribution without the prior written consent of McGraw-Hill Education.

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