EXAM3_L27_Metabolism Flashcards

1
Q

What 4 processes inside the mitochondrial matrix?

A
  1. Acetyl CoA Synthesis
  2. TCA Cycle
  3. Beta Oxidation of FA’s
  4. Ketogenesis
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2
Q

What process of Inner mitochondrial membrane?

A

Oxidative phosphorylation

ETC?

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3
Q

What are the 7 Processes of the Cytosol

A
  1. Glycolysis
  2. Glycogenesis
  3. Glycogenolysis
  4. Pentose phosphate shunt
  5. FA synthesis
  6. Steroid Synthesis (SER)
  7. Protein Synthesis (RER)
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4
Q

What 3 Processes in both the Cytosol and Mitochondria?

A
  1. Gluconeogenesis
  2. Urea Cycle
  3. Heme Synthesis
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5
Q

Why can’t Red Blood Cells oxidize pyruvate or acetyl CoA?

A

RBC’s and Platelets lack mitochondria

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6
Q

What are the 5 vitamin precursors of the TCA Cycle?

A
  1. Niacin –>NAD+
  2. Riboflavin (b2) –> FAD
  3. Thiamine (b1) –> TPP
  4. Pantothenate–> Coenzyme A
  5. Vitamin B12 (cobalamin) –> Succinyl CoA via FAox
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7
Q

Citrate synthase is activated and inhibited by?

A

Activated by INSULIN

Inhibited by ATP, NADH, Succinyl CoA

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8
Q

Isocitrate dehydrogenase Activated and inhibited by?

A

Activated by ADP

Inhibited by ATP, NADH

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9
Q

Alpha ketogluterate dehydrogenase activated by and inhibited by?

A
NO ACTIVATION
Inhibited by:
1. NADH,
2, Succinyl CoA,
3. ATP
4. GTP
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10
Q

What are the two water soluble electron carriers?
(Cytosol and mitochondrial matrix)

What are their precursor?

Which one is CATABOLIC?
WHICH ONE IS ANABOLIC?

A

NAD+ (ox form) NADH (reduced form) - NIACIN (VitB3)
CATABOLIC 700:1 nad:nadh

NADP+/NADPH - Niacin (VitB3)
ANABOLIC

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11
Q

What are the two membrane associated electron carriers? (inner mitochondrial membrane)
what is the precursor?

A

FAD/FADH2

FMN/FMNH2– (RIBOFLAVIN VitB2)

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12
Q

FMN/FMNH2 are a redox pair part of which complex in the ETC?

A

Complex 1— FMNH2

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13
Q

What processes make NADH?

What processes oxidize NADH to NAD+?

A

Glycolysis
TCA
Beta Oxidation

Mainly ETC oxidizes NADH to NAD but also
Lactate dehydrogenase in anaerobic glycolysis

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14
Q

What processes Synthesize NADPH?

What is NADPH used for/oxidized by?

What ratio of NADP+ to NADPH?

A

Made by HMP Shunt-oxidative (in All cells)
Made by Malic Enzyme (in cells with mitochondria)

Oxidized in ANABOLIC reactions making new molecules

1:10 NADP+ : NADPH

NADPH is used to donate energy to anabolic reactions so the reduced form is preferred

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15
Q

What are the 6 active processes of the FED STATE?

(0-4 hours post mixed meal)

A
  1. GLYCOLYSIS (glucose-> Acetyl CoA)
  2. TCA (Acetyl CoA -> NADH + FADH2 + GTP)
  3. ETC (NADH + FADH2 –> ATP + HEAT)
  4. OX PHOS (with above)
  5. GLYCOGENESIS (G6P -> Glycogen)
  6. FA Synth de novo- (Acetyl CoA cyto –> Fat acyl-CoA)
  7. TG synth- (Fat Acyl-CoA + glycerol -> TG)
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16
Q

Gluconeogenesis

A
Service 2 (glucose for export)
- Using precursors that are not from carbohydrates to make glucose

PYRUVATE–> Acetyl coA -> OAA >PEP> Glucose

17
Q

Liver Glycogenolysis

A

Glycogen –> Glucose (for export)

18
Q

Lipolysis

A

TG’s –> FA’s + Glycerol

19
Q

Beta oxidation

A

FA’s –> Acetyl CoA + NADH + FADH2

20
Q

Ketogenesis

A

Acetyl CoA -> ketones (for export)

Acetyl coa > Acetoacetate> bhydroxybutyrate

21
Q

What is the only organ that can Export or remove glucose from our blood?

What is it dependent upon?

A

LIVER

Dependent on hepatic portal blood glucose

22
Q

What is Portal Blood Glucose post prandial?

A

10-20mM

180-360mg/DL

23
Q

What is normal Blood Glucose post prandial?

A

5-8mM

90-140mg/DL

24
Q

What is FASTING blood glucose?

A

3-5mM

70-100mg/DL

25
Q

What are the two sources of blood going into the liver?

Where does all the blood drain?

Describe the blood leaving the liver.

A
Hepatic portal vein (nutrient rich, oxygen poor)
Hepatic Artery (oxygenated blood from general circulation)

they mix

All blood leaves via HEPATIC VEIN
- deoxygenated, detoxified, normal nutrient levels

26
Q

What cells have Insulin receptors?
What type of receptors are they?
When signal activated what happens?

A

Liver, Adipose, Muscle
Receptor Tyrosine Kinase

Increases phosphatase activity > overall dephosphorylated state for metabolism specific enzyme
altered gene expression

27
Q

What cells have glucagon receptors?

What kind of receptors are they? What effect?

A

LIVER ONLY!!!!
Gas-coupled receptor

cAMP> INCREASED PKA activity
INCREASED OVERALL PHOSPHORYLATED STATE

28
Q

What cells have Epinephrine receptors?

What kind of receptors are they? What effect?

A

Liver, Adipose, Muscle

cAMP> INCREASED PKA activity
INCREASED OVERALL PHOSPHORYLATED STATE

29
Q

how is energy stored?

A

Stored in electrons as reducing equivalents

NADH (reduced- energy rich)
NAD+ (oxidized- energy poor)

30
Q

Does the TCA make ATP?

A

NO!

31
Q

If there is too much glucose in the TCA what happens?

A

Fat synthesis pathway!

32
Q

When fasting, where does the pyruvate come from to undergo gluconeogenesis?

A

MUSCLE BREAKDOWN-

makes glucose and ketone bodies

can’t use the pyruvate form fat