L1-Principles/Design Of Metabolism Flashcards

1
Q

LO10- list two major goals of metabolism

A
  • to extract energy and reducing power from the environment

- to synthesize building blocks needed to make more complex polymeric macromolecules

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2
Q

LO10- what type of pathways achieve each major goal of metabolism? Give examples of each.

A
Catabolic- degradation
Oxidative examples
- glycolysis
-fatty acid oxidation
Non oxidative examples
-glycogenolysis
-hydrolysis of triglycerides to fatty acids

Anabolic- synthesis

  • glycogen synthesis
  • fatty acid synthesis
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3
Q

LO1- how are metabolic pathways arranged and why? How are they controlled?

A
  • chemical pathways arranged in distinct sequences that are regulated, coordinated and interconnected to maintain homeostasis
  • pathways are distinct so they can occur independently/prevent futile cycling
  • pathways have regulatory steps/enzymes
  • pathways all use building blocks, ATP, electron carriers, reducers, and acyl carriers
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4
Q

LO2-skeletal muscle structure vs function (white/red fibers) + its metabolic capacities

A

F(x): intermittent mechanical work; white muscle fibers contract rapidly and are short acting while red muscle fibers are slow contracting and longer lasting

  • white: limited aerobic oxidation due to low mitochondria content, so they use glycogen (early in exertion) and glucose breakdown with lactate formation (short acting)
  • red: higher oxidative capacity due to high mitochondria content (slow contracting and longer lasting)
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5
Q

LO2: heart function + its metabolic capacities

A

Continuously contracting muscle->high oxidative capacity due to highest density of mitochondria (1/2 of heart volume=mitochondria and it has negligible energy reserves)

Mainly uses fatty acids (to help supply be continuous) but can also use glucose, lactate, and ketone bodies

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6
Q

LO2: liver function + its metabolic capacities (including list of processes it is involved in)

A

F(x)s: biosynthesis and detoxification, so lots of mitochondria and microsomes (can itself use glucose, fatty acids and amino acids)

Involved in: glucose homeostasis
glucose storage (as glycogen)
gluconeogenesis
urea synthesis
ketone synthesis
lipoprotein assembly (fatty acids)
coordination of fuel homeostasis (b/c it processes glucose and fats)
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7
Q

LO2: brain/nerve function + its metabolic capacities

A

F(x): electrochemical signaling
-high energy demands (O2 and ATP) to maintain membrane potentials for signaling

High glycolytic and oxidative capacity (more mitochondria than kidney or liver, second highest only to heart/skeletal muscle)

  • major fuel is glucose (~60% of our total glucose utilization at rest) but can convert to using ketones during starvation (can’t oxidize fatty acids however)
  • like heart, cannot store energy so supply of O2 (~20% of total oxygen consumed at rest) and glucose must be continuous
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8
Q

LO2: adipose tissue function + its metabolic capacities

A

F(x): storage, mobilization, synthesis of triglycerides (regulated by fasting/feeding hormone signals)

Adipocyte structure allows efficient storage of fuel in form of lipids (fats, excess carbs, excess proteins can all be stored in small amount of space)

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9
Q

LO2- kidney function + its metabolic capacities

A

F(x): fluid homeostasis (high rate of active transport), osmotic work, acid and base balance, excretion of waste, ammonia synthesis, gluconeogenesis (second to liver; 10% during overnight fast, up to 40% during starvation)

Similar levels of mitochondria as brain/nervous system, can use fatty acids, lactate and ketones as fuels

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10
Q

LO2: RBCS + their metabolic capacities

A

F(x): exchange O2 and C02, make 2,3-bisphosphoglycerate (BPG) to regulate O2 affinity to hemoglobin
-constitute 1/2 of blood volume and >99% of blood cells, so primary pathway in energy metabolism of blood

Mature RBCs have no mitochondria- get all energy from anaerobic glycolysis (no oxidative metabolism)

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11
Q

LO2- GI tract function + its metabolic capacities

A

Absorbs and transports nutrients

Contains specific enzymes and transporters

Uses glutamine/glutamate for its own energy (transport/to replace rapid turn-over of epithelial cell lining)

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12
Q

LO2: skeletal muscle function (at rest vs. during starvation) + its metabolic capacities

A

Skeletal muscle can use glucose, fatty acids, and ketone bodies, but at rest it uses fatty acids

Skeletal muscle stores about 3/4 of the total glycogen in humans, but it can’t be released from the cell for use by other tissues (except in starvation, when muscle protein can be degraded for use)

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13
Q

LO2: creative phosphate role in skeletal muscle function

A

Short term energy reserve- can generate ATP without metabolism of fuels (exhausted quickly in exertion)

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14
Q

LO8: list the caloric value of the three major metabolic fuels

A

Kcal/gram (1000 calories=1 Calorie=1 kcal)

Carbs: 4
Proteins: 4
Fat: 9
For comparison- EtOH: 7

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15
Q

LO9: Name four metabolites at major branch points in metabolism

A

Glucose-6-phosphate
Pyruvate
Acetyl-CoA
Glutamate

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16
Q

LO7: Name the circulating fuels and their key tissue intermediates

A

Carbs: glycogenglucose-6-phosphatepyruvate
Circulating forms: glucose, lactate

Proteinsamino acids (circulating form)

Fats: triglyceridestriglycerides or fatty acidsacetyl-Co-Aketones or ATP
Circulating forms: triglycerides, fatty acids, ketones

17
Q

LO6: List the three major stages of energy extraction (and where they occur-LO4)

A

Stage I: Degradation of macromolecules into smaller building blocks (no useful energy gained

Stage 2: Building blocks converted to common intermediates (small amount of energy extracted)

Stage 3: Terminal oxidation of acetyl-CoA to CO2 and H2O, O2 is required (most of energy extracted here)

18
Q

LO4: List the major metabolic processes that occur in the cell and what subcellular compartments they occur in: cytosol

A
Glycolysis
Pentose phosphate pathway
Fatty acid synthesis
Nucleotide synthesis
Protein synthesis
19
Q

LO4: List the major metabolic processes that occur in the cell and what subcellular compartments they occur in: mitochondria

A
TCA cycle
Oxidative phosphorylation
B-oxidation of fatty acids
Ketogenesis
Ketone oxidation
20
Q

LO4: List the major metabolic processes that occur in the cell and what subcellular compartments they occur in: cytoslic and mitochondrial enzymes used

A

Gluconeogenesis
Urea synthesis
Steroid hormone synthesis

21
Q

LO4: List the major metabolic processes that occur in the cell and what subcellular compartments they occur in: smooth ER

A
Triglyceride synthesis
Phospholipid synthesis
Glycolipid synthesis
Cholesterol synthesis
Hydroxylation reactions
Detoxification reactions
22
Q

LO3: Outline the major metabolic transitions and why some transitions aren’t permitted

A

*Evolutionary design: for when starvation was our greatest metabolic challenge

Fatty acids, ketones, acetyl-CoA: can be converted only into energy (purpose=storage, can’t be used to maintain blood glucose levels)

Glycogen/glucose: can be used for energy, converted into FAs etc via lipogensis or into proteins etc via synthesis of non-essential amino acids

Proteins/amino acids: can be used for energy, converted into FAs etc via ketogenesis, or into glucose etc via gluconeogenesis

23
Q

LO5: Describe the roles of ATP, NADH, NADPH, NAD+, NADP+, FAD and acetyl-CoA in metabolism integration

A

ATP: universal source of chemical energy generated by catabolic pathways and used in energy-requiring anabolic pathways
NADH: reduced form of NAD+
NADPH: supplies reducing power for biosynthetic rxns
NAD+: major carrier of electrons in oxidation rxns
NADP+: oxidized form of NADPH
-other major carrier of electrons in oxidation reactions
Acetyl-CoA: (coenzyme A), universal carrier of acyl groups, intermediate of pathways