Review 1 Glycolysis Flashcards

1
Q

Liver

A

Fatty acid, glucose, amino acid

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2
Q

Adipose Tissue

A

Fatty acid

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3
Q

Skeletal Muscle

A

At rest: Fatty acid

Exertion: Glucose

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4
Q

Heart Muscle

A

Fatty acid

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5
Q

Brain

A

Fed state: glucose

Starvation: ketone bodies/glucose

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6
Q

Kcal/cal (dry)
Carb
Protein
Fat

A

Carb=4
Protein=4
Fat=9

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7
Q

Glycogenolysis

A

Glycogen–>Glucose

Stim: Glucagon, Epinephrine, Starve State

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8
Q

Glycogenesis

A

Glucose–>Glycogen

Stim: Insulin, Fed State

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9
Q

Glycolysis

A

Glucose–>Lactate and Pyruvate

Stim: Insulin, Fed State

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10
Q

Gluconeogenesis

A

Non carb products–>Glucose

Stim: Glucagon, Epinephrine, Starve State

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11
Q

3 stages to glycolysis

A
Priming Stage(ATP investment)
Splitting Stage
Oxidoreduction-phosphorylation stage (ATP earnings)
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12
Q

3 irreversible enzymes of glycolysis

A
  1. Hexokinase/Glucokinase
    Glucose–>Glucose 6 phosphate
  2. PFK-1
    Fructose 6-phosphate–>Fructose 1,6 bisphosphate
  3. Pyruvate Kinase
    Phosphoenolpyruvate–>
    2 Pyruvate
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13
Q

Hexokinase vs. Glucokinase

A

Hexokinase: All cell types, inhibited by glucose-6-phosphate, constitutive enzyme, low Km

Glucokinase: Liver and pancreas, Translocation between nucleus and cytosol, Fructose 6-P promotes translocation to nucleus(inactive), Glucose promotes translocation to cytosol(active), Inducible enzyme: enzyme synthesis increased by insulin, High Km

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14
Q

Pyruvate Carboxylase Genetic Deficiency

A

increase in blood alanine, lactate and pyruvate levels

Diagnosis: Developmental Delay, Recurrent Seizures, Metabolic Acidosis

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15
Q

Pyruvate Dehydrogenase Deficiency (PDH) genetic deficiency

A

Increases circulatory pyruvate and lactate concentration

Diagnosis: reduced head circumference (microcephaly), poor muscle coordination, and mental retardation

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16
Q

What is the glyceraldehyde-3-P dehydrogenase reaction require? What is it used in?

A

NAD+

Glycolysis

17
Q

Anaerobic Respiration and replenishing NAD+

A

reduction reaction

Lactate or ethanol

18
Q

Aerobic respiration and replenishing NAD+

A

metabolite shuttle system

19
Q

NAD+ Regenerated by

A

Lactate Dehydrogenase (cytosolic reaction)

Malate-aspartate shuttle(cytosol and mitochondria)

Glycerol-phosphate shuttle (cytosol and mitochondria)

20
Q

Lactate Dehydrogenase

A

Pyruvate to Lactate

21
Q

Pyruvate dehydrogenase

A

Multienzyme Complex (E1, E2, E3) catalyzes the conversion of pyruvate and coenzyme A to acetyl coA

22
Q

Cofactors needed for pyruvate dehydrogenase

A

Thiamine(TTP, B1)
Riboflavin (FAD, B2)
Niacin (NAD, B3)
Lipoate CoA (B5)

23
Q

Lactate Dehydrogenase A Deficiency

A
  • NAD+ levels insufficient
  • Glyceraldehyde 3-P-Dehydrogenase reaction inhibited
  • ->Cant use glycolysis to produce ATP
24
Q

Glycolysis output

A

2 ATP net gain

25
Oxygen is required for what two processes, which leads to anaerobic conditions to favor the formation of lactate
Reoxidation of mitochondrial NADH, formed in the reactions catalyzed by the PDH enzyme complex Reoxidation of cytosolic NADH by mitochondrial linked shuttles Low levels NADH-->decrease lactate formation
26
enzymes deficient in Galactosemia
Galactokinase or Galactose 1-phosphate uridyltransferase (most severe, and common)
27
Galactosemia symptoms
Cant have Galactose (or Lactose) | Cataracts, Brain Damage, Jaundice, Enlarged Liver, Kidney Damage
28
Hereditary Fructose Intolerance
Deficiency of Aldolase B (fructose bisphosphate aldolase-B) -role in both glycolysis and gluconeogensis -autosomal recessive Symptoms -hypoglycemia, fructose accumulation, high uric acid and lactic acid, fructose toxicity, vomiting, jaundice, hepatic failure Treatment: avoid fructose