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24 Cards in this Set
- Front
- Back
How is OAA made/regenerated in the cell? |
Glycolysis: Glucose --> 2 pyruvate
or from Gluconeogenic AAs
Or from Propionyl CoA --> Succinate, which will then be converted into OAA VIA the Kreb Cycle
Can also be made from Lactate and glycerol |
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What is the first step in the Krebs Cycle? |
Acetyl CoA ( 2C) condenses with Oxaloacetate(6C, OAA) +H2O to form Citrate + CoA
OAA + H20 + Acetyl-CoA---> Citrate + CoA |
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What Happens to OAA in liver cells during extreme Starvation, or untreated diabetes? |
There is no regeneration of OAA and TCA Cycle cannot continue. The OAA in the liver is used to produce Glucose, which is then consumed, and the resulting pyruvate is pushed through the kreb cycle for Energy. No regen of OAA |
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What happens to Acetyl CoA in the liver during Starvation, and a lack of OAA |
Acetyl CoAs are transformed into Ketone Bodies, blood soluble versions of Acetyl CoA |
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What are the three types of Ketone Bodies made in the liver? |
Acetone
AcetoAcetate
D-B-Hydroxybutyrate |
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What happens to Acetone when it is produced? |
exhaled |
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Why can't the Brain use FAs? |
Because the FAs cannot fit through the Blood Brain Barrier (BBB), which is composed of tight junction endothelial cells. |
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Where are Ketone Bodies produced? |
In the Mitochondrial Matrix of liver cells |
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Where does the Liver export Glucose to? |
The Brain, Renal Cortex, Heart, Adipose tissue, Skeletal muscle |
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Where does the liver export Ketone Bodies to? |
Brain, Heart, Skeletal muscle, renal Cortex (but not to Adipose tissue) |
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Where do FAs from Adipose tissues get shipped to? |
Liver, Heart, Renal Cortex, Skeletal muscle (but not brain, can't pass the BBB) |
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What enzyme catalyzes the condensation reaction of 2 Acetyl CoA --> Acetoacetyl-CoA |
Thiolase |
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What enzyme catalyzes the reaction AcetoAcetyl-CoA ---> HMG-CoA |
HMG-CoA synthase |
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What is the full name of the Molecule HMG-CoA? |
B-Hydroxy B-methylglutaryl CoA (co-enzyme A) |
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What molecule Cleave HMG-CoA (B-hydroxy B-methylglutaryl CoA) into Aceto Acetate?
HMG-Coa --> AcetoAcetate + Acetyl-CoA |
HMG-CoA lyase. |
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which enzyme catalyzes the reaction AcetoAcetate -->> acetone + Co2 |
Acetoacetate decarboxylase |
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which enzyme catalyzes the reaction Aceto-Acetate decarboxylase ---> D-B-Hydroxybutryate? |
D-B-hydroxybutyrate dehydrogenase |
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Which has more Energy, D-B-Hydroxybutyrate, or AcetoAcetate, and why? |
D-B-Hydroxybutyrate because it is more reduced. NADH reduces Acetoacetate to form D-B-Hydroxybutyrate. This rxn is catalyzed by D-B-Hydroxybutyrate dehydrogenase. |
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What determines whether Acetoacetate or D-B-Hydroxybutyrate is exported from the liver? |
The concentration of NADH in the cell. If [NADH]/[NAD+] <1, Acetoacetate will be predominantly made and exported. |
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What happens when D-B-HydroxyButyrate arrives at extra hepatic tissues? |
it is oxidized to form acetoacete. Once acetotoacetate is made, it is catalyzed by B-KetoAcyl CoA transferase to form Acetoacyl-CoA. Aceto Acyl CoA is then used to produce two Acetyl-CoA, which will then be pumped into the kerb cycle to make ATP |
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What is the enzyme that converts AcetoAcyl-CoA into 2 Acetyl CoAs? |
Thiolase (same one used in B-ox, and Ketone body synthesis) |
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Why does the liver produce very low levels of B-KetoAcyl transferase |
This would create a futile cycle. If B-Ketoacyl Transferase was produced in the liver, every time acetoAcete is produced, it would be converted back into Acetoacetate-CoA. |
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Which intermediate molecule is produced during the synthesis of Ketone bodies, but not during the catabolism of ketone bodies? |
HMG-CoA (B-Hydroxy B-Methylglutaryl-CoA) |
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What is a negative effect of a prolonged increase is acetyl-CoA concentration as a result of prolonged starvation? |
Keto Acidosis. Ketone bodies are acidic, and if there is no OAAs, Acetyl CoA will build up, causing ketone bodies to be created, which will decrease the pH of the blood. |