Lecture #28: Metabolism--Carbohydrates, Lipids, and Proteins Flashcards

1
Q

What is catabolic?

A

reactions break down complex organic compounds, providing energy

Catabolic reactions transfer energy from complex molecules to ATP

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2
Q

What is Anabolic?

A

reactions synthesize complex molecules from small molecules, requiring energy

Anabolic reactions tranfer energy from ATP to complex molecules

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3
Q

How do catabolic and anabolic exchange energy?

A

Exchange of energy require use of ATP

  • Each cell has about 1 billion ATP molecules (equals ~2 sec of max contraction for skeletal muscle); rapid ADP-ATP turnover
  • Over half of the energy released from ATP is lost as heat.
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4
Q

What happens in Energy transfer?

A

• Energy is found in the bonds between atoms.

• Oxidation is a decrease in the energy content of a
molecule: electrons are lost, plus H+
.

• Reduction is the increase in the energy content of a
molecule: electrons gained, plus H+
.
• Oxidation-reduction reactions are always coupled
within the body.
– sometimes an intermediate molecule is involved in the
electron transfer: coenzyme (NAD + and FADH)

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5
Q

What the 4 steps of glucose catabolism?

A
  1. Glycolysis
  2. Formation of Acetyle Coenzyme A
  3. Krebs cycle
  4. Electron Transport Chain (ETC)
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6
Q

What is the electron transport chain?

A

• The ETC is a series of integral membrane protein complexes in the inner mitochondrial
membrane of mitochondria.

• The ETC complexes are capable of oxidation/reduction
(donating/receiving electrons).

• The small amounts of energy released w/ each transfer is
used to make an H+ gradient.

• The H+ gradient is used to form
ATP, a process termed chemiosmosis

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7
Q

What is Chemiosmosis?

A
  1. High-energy electrons are
    delivered to ETC complexes.
  2. Electrons are passed from
    ETC complex to ETC complex,
    releasing energy with each transfer that is used to
    pumps H+ ions into the space between the inner and outer
    membranes of mitochondria.
  3. H+ ions are only permitted to
    move back into the matrix through special H+ channels which use the energy of H+ diffusion to power synthesis
    of ATP from ADP and Pi
    .
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8
Q

In the presence of O2, what is broken down from glucose?

A

CO2,H2O, and captured high-energy electrons

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9
Q

What are high energy electrons used for?

A

Used by the ETC to pump H+ ions which are used to make ATP (via chemiosmosis)

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10
Q

What do all 3 (CO2, H20, and ATP) do once they reached the ETC?

A

Move out of the mitchondria and into the cell’s cytoplasm

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11
Q

What does Glycolysis do?

A

(Break down of glucose)

Glucose to pyruvate/lactate

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12
Q

What does glycogenolysis do?

A

(Break Down of glycogen)

Glycogen to glucose

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13
Q

What does Glycogenesis do?

A

Formation of glycogen

Glucose to glycogen

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14
Q

What does Gluconeogenesis do?

A

Formation of new glucose

–Other substrates to glucose

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15
Q

Are polar or non polar and what must they do first before they are transported in the blood stream?

A

Most lipids are nonpolar and must be combined with protein to be transported in blood

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16
Q

What are lipoproteins?

A

Are spheres containing hundreds of molecules

Are categorized by function and density

17
Q

What are the 4 major classses of lipoproteins?

A

chylomicrons,

very low-density of protein

lowdensity &high-density lipoproteins

18
Q

What is chylomicrons?

A

2% protein, 85% TG

– form in intestinal epithelial cells to transport dietary fats to adipose cells

19
Q

What is Very low density lipoprotein?

A

10% protein, 50% TG

– form in hepatocytes to transport triglycerides to adipose cells

20
Q

What is low density lipoprotein?

A

25% protein, 50% Chol.)
- bad cholesterol
–> carry blood cholesterol to body cells

21
Q

What is High density lipoprotein?

A

40% protein, 20% Chol.
- good cholesterol
– carry cholesterol from cells to liver for elimination

22
Q

What is the fate of lipids?

A
  • Oxidized to produce ATP
  • Excess stored in adipose tissue or liver

• Synthesize structural or other important molecules
– phospholipids of plasma membranes
– lipoproteins that transport cholesterol
– thromboplastin for blood clotting
– myelin sheaths to speed up nerve conduction
– cholesterol used to synthesize bile salts and steroid
hormones

23
Q

What is lipolysis?

A

triglycerides are broken down into
glycerol and fatty acids within liver or adipose cells
in the presence of epinephrine, norepinephrine,
cortisol

24
Q

What is lipogenesis?

A

triglycerides are synthesized from
amino acids or glucose within liver or adipose cells
in the presence of insulin

25
Q

In lipolysis, what do fatty acids undergo?

A

Beta-oxidation in mitchondria to produce Acetyle CoA and lots of ATP

26
Q

What is ketogenesis?

A

occurs in liver cells; ketone bodies are used by heart muscle & kidney cortex for ATP production

27
Q

What fuel sources are included for lipogenesis?

A
  1. amino acids, glycolysis metabolites, and ketone bodies for
    fatty acid production from Acetyl-CoA
  2. glycolysis metabolites for glycerol production
28
Q

What is the fate of proteins?

A

• Proteins are broken down into amino acids, which
are transported to the liver

• Amino acids may be
– deaminated to enter Krebs Cycle
– donate amino group to form new amino acids
(transamination)
– used to synthesize new proteins throughout the body

• Excess amino acids may be converted into glucose or
triglycerides (no storage)

• Absorption of AA into body cells is stimulated by
insulin-like growth factors (IGFs) & insulin

29
Q

What happens to metabolism during the absorptive state?

A

represents the time after a meal
when nutrients enter the blood and need to be
stored.

• The hepatic portal system is used for absorption of
glucose and amino acids. The liver is able to act on
these first.

• Lacteals are used for absorption of dietary fats which
are transported as lipoproteins through the lymphatic
system before reaching general circulation.

30
Q

What is the purpose of the absorptive state?

A

• Storage of excess fuels occurs in hepatocytes,
adipocytes, skeletal muscle

• Most glucose entering liver cells is converted to
glycogen (10%) or triglycerides (40%)

• Dietary lipids are stored in adipose tissue

31
Q

What happens to amino acids in the absorptive state?

A

• Amino acids are deaminated to enter Krebs cycle or
are converted to glucose or fatty acids

• Amino acids not taken up by hepatocytes are used by other cells for synthesis of proteins

32
Q

What happens to metabolism after postabsorptive state?

A
• 4 hours after a meal when absorption of all nutrients
is complete (similar to starvation)

– Maintaining normal blood glucose level (70 to 110 mg/dL
of blood) is major challenge  goal is to put glucose back into the blood or use alternative fuel sources

33
Q

What is the purpose of the postabsorptive state?

A

• Glucose enters blood from the liver
– glycogenolysis
– gluconeogenesis

  • glycerol from adipose tissue
  • amino acids and lactic acid from muscle

• Alternative fuel sources are
– fatty acids from adipose fed into Krebs as Acetyl CoA for
most cells*
– oxidation of ketone bodies by heart & kidney

• *Most body tissues switch to utilizing fatty acids,
except brain still prefers glucose