2.1-Secondary Carb Pathways Flashcards

1
Q

Where are the three steps in glycolysis that Fructose can enter (what tissue type for each?)

A
  1. Step to Fructose-6-Phosphate (from adipose tissue-Burning Fat goes to Fructose!) 2. Step 4b DHAP (Liver) 3. Step 4a G-3-P (Liver)
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2
Q

What are the three sources of Fructose in our diet? How is High Fructose Corn Syrup different from Sucrose?

A
  1. Pure Fructose 2. High Fructose Corn Syrup 3. Sucrose. HFC=NO covalent bonds; Sucrose=Covalently bonded
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3
Q

Which enzyme hydrolyses Sucrose in the small intestine? What “type” of enzyme is it?

A

A “Brush Border” Enzyme-Sucrase Isomaltase (S.I.)

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4
Q

What happens with an SI deficiency? Think Biome taking over…

A

osmotic-fermentive diarrhea

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5
Q

Which GLUT transporter absorbs Fructose from the Gut into the cell? Which GLUT transports Fructose from the cell to the Blood?

A

Gut to Cell= GLUT5; Cell to Blood= GLUT2

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6
Q

Is there a limit to Fructose absorption in the Small Intestine?

A

Yes, Excess goes to the colon and causes Diarrhea

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7
Q

What are the two locations for Fructose catabolism? What is the bigger one?

A

Muscle & Liver… MUCH more going on in the liver

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8
Q

What is the step that gets Fructose into Glycolysis in muscle cells? What is the enzyme used?

A

Fructose ——->Fructose-6-Phosphate. The enzyme that does this is HEXOKINASE (WEIRD, I know. Phosphorylating a 6 carbon molecule…)

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9
Q

What are the two key enzymes in getting Fructose into glycolysis in the LIVER? Which one is “fast”, which one is “slow”?

A
  1. FructoKinase 2. Aldolase B
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10
Q

What does FructoKinase do?

A

Phosphorylates Fructose—->Fructose-1-Phosphate. WHAAA?

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11
Q

What does Aldolase B do?

A

Splits Fructose-1-Phosphate into 1.G-3-P and 2.DiHydroxyAcetonePhosphate (DHAP)

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12
Q

What gets by bypassed in Fructose metabolism in the liver? What is the consequence? THIS HITS HOME :)

A

PFK1 gets bypassed making more Acetyl-CoA which will then start making FAT

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13
Q

What is the result of high Fructose intake and then sequestering of inorganic Phosphate?

A

HyperUricemia and therefore GOUT. LOOK OUT cause its comin for ya! (ALDOLASE B gets backed up and saturated)

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14
Q

Which is more severe a FructoKinase deficiency or an Aldolase B deficiency? Why?

A

Aldolase B deficiency is more severe because the F-1-P gets stuck in the cell and gathers iPhosphate. (FructoKinase deficiency just excretes fructose from the body)

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15
Q

How does the less popular monosaccharide MANNOSE enter glycolysis?

A

Mannose—->Fructose-6-Phosphate (by a couple of enzymes) and you’re good to go!

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16
Q

What is the sugar alcohol made from glucose in the cell? What unique function does this have?

A

Sorbitol! Helps trap glucose in the cell!

17
Q

Which enzyme is lacking in the lens, nerves, and kidney that causes a build up of sorbitol?

A

Sorbitol DeHydrogenase

18
Q

What are the 4 enzymes that participate in the conversion of Galactose to G-6-P?

A
  1. GalactoKinase 2. Galactose-1-Phosphate Uridylyl Transferase 3. UDP-Galactose-4-Epimerase 4.PhosphoGlucoMutase
19
Q

What are the two alternate names for the Pentose Phosphate Pathway?

A

1.Hexose MonoPhosphate Shunt 2. PhosphoGluconate Pathway

20
Q

What are the two main products of the Pentose Phosphate Pathway?

A
  1. NADPH (for anabolism of things-steriods,complex carbs) 2. Ribose-5-Phosphate (for NucleoTides!)
21
Q

What fatty acid synthesis areas are really active in PPP? What is the important area that IS NOT active in PPP?

A

MammaryGlands, Adipose Tissue, Adrenal Cortex, Liver…..MUSCLE dont care

22
Q

What is the key reaction in the oxidative PPP pathway?

A

Glucose-6-P—–>Lactone USING: Glucose-6-Phosphate Dehydgrogenase

23
Q

How many NADPHs are yielded from the oxidative PPP pathway?

A

2 NADPH’s

24
Q

What is the key of the NON oxidative pathway?

A

If cell needs NADPH to build things, it can recycle Ribose-5-Phosphate

25
Q

What happens when you are low on Ribose-5-Phosphate? What are the two starting ingredients?

A

Reverse PPP and make more from Fructose-6-Phosphate and Glyceraldehyde-3-Phospahte?

26
Q

Which part of PPP is dominant when NADPH and Ribose-5-Phosphate are balanced your cell?

A

The Oxidative Part

27
Q

What happens when you are low on NADPH?

A

GlucoNeoGenesis will make more Glucose-6-Phosphate to then go through the Oxidative PPP!

28
Q

What happens when BOTH NADPH and Ribose-5-Phosphate are low?

A

Couple PPP with Glycolysis!

29
Q

What is the enzyme that detoxifies H2O2 to H2O? What enzyme rejuvenates this enzyme to get back to work?

A

Glut-A-Thione Peroxidase…Reduced by GlutAThione Reductase

30
Q

What is the antioxidant GlutAThione made of?

A

3 amino acids (a tripeptide!)

31
Q

What is the #1 genetic deficiency in all Z world?! Where is the first place you will see it??

A

Glucose-6-P Dehydrogenase Deficiency..in the RBCs

32
Q

Why is the #1 genetic deficiency a problem in RBCs?

A

There is lots of Free Radical Oxygen in RBCs and they do not have the enzyme to take care of it!

33
Q

What is the clinical name for the deficiency of the enzyme Glucose-6-Phosphotase Dehydrogenase in a RBC?

A

Hemolytic Anemia

34
Q

Which enzyme converts Glucose to Sorbitol?

A

Aldose Reductase

35
Q

Is G6DP inhibited by NADPH?

A

NO

36
Q

Why is reduced glutathione used in RBCs?

A

To produce NADPH