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
Q

Oxygen is required for what two processes, which leads to anaerobic conditions to favor the formation of lactate

A

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
Q

enzymes deficient in Galactosemia

A

Galactokinase or Galactose 1-phosphate uridyltransferase (most severe, and common)

27
Q

Galactosemia symptoms

A

Cant have Galactose (or Lactose)

Cataracts, Brain Damage, Jaundice, Enlarged Liver, Kidney Damage

28
Q

Hereditary Fructose Intolerance

A

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