Carbohydrate Metabolism Flashcards

(66 cards)

1
Q

What is the overall process of glycolysis?

A

1 mol Glucose -> 2 mols Pyruvate

Pyruvate -> Lactate (when there is low amounts of oxygen like when sprinting)

Pyruvate -> CO2 + H2O (when there is lots of oxygen like during a slow run)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How many ATPs does Glycolysis produce overall

A

2 ATP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

_____ is the only fuel that rbcs can use

_____ is the only fule that the brain uses under non-starvation conditions

A

Glucose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Where are each of the following GLUTs found? Describe the affinity/Km for each

GLUT1
GLUT2
GLUT3
GLUT4

A

GLUT1- rbcs and brain (High affinity, Km is low)
GLUT2- liver (Low affinity, Km is high)
GLUT3- neurons (High affinity, Km is low)
GLUT4- skeletal muscle, heart, adipose tissue (medium affinity, Km is medium)

remember that Km is inversely proportional to the affinity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Which GLUT is regulated by insulin?

A

GLUT4- skeletal muscle, adipose tissue, and heart

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Where does glycolysis occur?

A

Within the cytoplasm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the overall yield of glycolysis?

A

2 ATP
2 NADH
2 Pyruvate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the 3 regulatory steps of glycolysis and what is the rate limiting step?

A

Hexokinase(in all cells)/Glucokinase (in liver and pancreatic cells) trap glucose within the cell by using ATP

Phosphofructokinase is used as the rate limiting enzyme. ATP is also used here too

Pyruvate Kinase is the last enzyme for the regulatory step in glycolysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the 3-4 factors that govern whether glycolysis occurs or not?

A

ATP/AMP
Glucose
Insulin/Glucagon

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Glucokinase and Hexokinase both trap glucose within cells. For each, describe where they are found, the Km, and the Vmax

A

Hexokinase:
Location: All cells
Km: Low (High affinity)
Vmax- Low

Glucokinase:
Location- Liver and pancreas
Km- High (Low affinity)
Vmax- High

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What do glucokinase/hexokinase change glucose to?

A

G6P

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Phosphofructokinase-1 is the rate limiting step in glycolysis. Describe when it is in its active form and when it is in its inactive form in terms of insulin and glucagon levels.

A

Fed State: High Insulin/Low Glucagon -> Want more glycolysis -> Dephosphorylation of PFK-2 -> Increases F-2,6 BP -> Increases PFK-1 activity

Fasting State: Low Insulin/High Glucagon -> Decreases Glycolysis -> Phosphorylates PFK-2 -> Decreases F-2,6-BP -> Decreases PFK-1 activity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is deficient in Tarui’s disease?

A

Phosphofructokinase is deficient

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Does a high G6P activate or inhibit Hexokinase?

A

Inhibits because that is the product

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

G6P that is produced in glycolysis is also a precursor for what pathway?

A

The pentose phosphate pathway

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

If glycolytic enzymes are defective, what clinical diagnosis occurs? What kind of cells does this mostly impact?

A

Hemolytic anemia, which mostly impacts rbcs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

rbcs lack mitochondria, therefore _____ is the only mechanism that produces ATP

A

Glycolysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is mutated that causes Fanconi-Bickel Syndrome

A

Mutation in the GLUT2 transporter, which causes an inability to take up glucose, fructose, and galactose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

How many grams of glucose does your body need on the daily to survive? How much from the brain, how much from the bodily fluids?

A

160 grams

120 grams from brain
20 form bodily fluids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

How many grams of glucose do we have in reserve?

A

190 grams glucose in reserve, which means we can only store enough glucose to survive for one day

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Describe the overall process of gluconeogenesis. In what 3 tissues does this occur?

A

Converts pyruvate into glucose (almost an exact opposite to glycolysis, but not exactly)

Occurs in the liver, kidneys, and small intestines

*Note that energy is being used, not made during gluconeogenesis. This is because the point of gluconeogenesis is to make glucose when we are fasting.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What are the 4 main enzymes of gluconeogenesis? Which one is the rate limiting step?

A

Glucose 6 Phosphatase
Fructose 1,6 bisphsphate (rate limiting step)
PEP carboxykinase
Pyruvate carboxylase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

How does Glucagon and ADP/AMP affect gluconeogenesis?

A

Glucagon increases it

ADP/AMP decreases it

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

How does Glucose, insulin, and AMP affect glycolysis?

A

They all increase it

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
How does Glucagon and ATP affect Glycolysis?
They both decrease it
26
Compare the net yield/use of ATP for glycolysis and gluconeogensis?
Glycolysis: Net yield it 2 ATP Gluconeogenesis: Net use is 6 ATP, 0 Net yield
27
Describe the Cori Cycle.
This links the lactate produced from anaerobic glycolysis in RBC and exercising muscle to gluconeogenesis in the liver
28
What are the 3 precursors of gluconeogenesis?
Carbohydrates, lipids, and proteins
29
If a patient had a disorder of the molecule Fructose 1,6 bisphosphatase, what pathway would be affected? What is this similar to?
F 1,6 Bisphosphatase deficiency is a disorder of gluconeogenesis This is similar to Tarui's disease in glycolysis- deficiency in PFK-1
30
What is Von Gierke's disease?
Deficiency in Glucose-6-phosphatase
31
What are the monosaccharides that make up sucrose?
fructose and glucose
32
What are the monosaccharides that make up lactose?
galactose and glucose
33
What is the issue with high amounts of fructose intake within your diet?
This bypasses the rate limiting step of glycolysis due to the absence of PFK-1 and therefore causes an increase in triacylglycerides
34
What is the rate limiting step of galactose metabolism?
Glalactose-1-phosphate uridyltransferase (GALT)
35
What is caused by galactosemia? What does this cause?
Deficiency in glucose- 1 phosphate uridyltransferase (GALT) Causes liver failure
36
What does a deficiency in Galactokinase cause?
an accumulation of galactitol in the eye, which leads to cataracts
37
What is the purpose of the pentose phosphate pathway?
Produce NADPH that is needed for reductive biosynthesis It also is used to produce ribose
38
What is the rate limiting step of the pentose phosphate pathway?
G6P Dehydrogenase
39
What is the purpose of NADPH?
It regenerates glutathione, which is an important antioxidant
40
What are the 2 phases of the pentose phosphate pathway? Which one has a high demand for Ribose and which has a high demand for NADPH
Oxidative Pathway- High demand for Ribose 5 Phosphate | Non-oxidative pathway- High demand for NADPH
41
Describe the structure of glycogen?
Glycogenin is the beginning part | chains of glucose are connected
42
What 2 tissues store glycogen?
Liver and Muscle
43
What is the function of liver glycogen?
Regulates blood glucose levels
44
What is the function of muscle glycogen?
Provides reservoir of fuel for physical activity
45
What attaches glycogen in a linear fashion?
Glycogen synthase
46
What attaches glycogen in an branched pattern?
Glucosyl (4,6) transferase
47
When glycogen is debranched what is the yield of glucose1phosphate and glucose
10 G1P 1 Glucose
48
What are the 2 reasons why we regulate glycogen metabolism?
Maintain blood sugar | Provide energy to muscle
49
What are the 2 key enzymes of glycogen metabolism?
Glycogen Synthase- the rate limiting step of synthesis | Glycogen Phosphorylase- the rate limiting step of degradation
50
What is the active form of glycogen synthase and glycogen phosphorylase?
Glycogen Synthase: Dephosphorylated is active form Phosphorylated is the inactive form Glycogen Phosphorylase: Dephosphorylated is the inactive form Phosphprylated is the active form
51
What are the 3 factors that favor the fed state of glycogenesis?
High blood glucose High insulin High ATP
52
What are the 2 factors that favor glycogenolysis in the fasting state?
Low blood glucose | High glucagon
53
What 2 factors favor glycogenolysis during exercise?
High calcium | High AMP
54
Does Glucagon act on muscles?
NO
55
What are the 4 key proteins involved in regulation by insulin?
GLUT4 Protein Kinase B Protein Phosphatase 1 Glycogen Synthase Kinase 3
56
What are the blood glucose criteria for the following: Normal Prediabetic Diabetes Mellitus
Normal: 70-100 (fasting), ≤140 (fed) Prediabetic: 100-125 (fasting), >140 (fed) Diabetes Mellitus: ≥125 (fasting), ≥199 (fed)
57
What is the overall result of insulin being used?
Glycogen Synthesis via activation of glycogen synthase and inactivation of glycogen phosphorylase
58
What is the overall result of glucagon being used?
Glycogen breakdown via inactivation of glycogen synthase and activation of glycogen phosphorylase
59
What molecule is deficient in GSD 0?
Glycogen Synthase
60
What molecule is deficient in GSD 1 Von Gierke Disease?
Glucose 6 Phosphatase
61
What molecule is deficient in GSD 2 Pompe Disease? What does this result in?
Acid Glucosidase, which results in the impairment of lysosomal glycogenolysis. This causes the accumulation of glycogen in lysosomes
62
What molecule is deficient in GSD 3? Cori Disease
Deficiency in alpha-1,6- glucosidase (the debranching enzyme) This causes patients to have glycogen with a large number of short branches
63
What molecule is deficient in GSD 4? Andersens Disease
Deficiency in glucosyl (4:6) transferase (the branching enzyme) This causes patients to have longer chain glycogens with fewer branches
64
What molecule is deficient in GSD 5? McArdle disease
Deficiency in MUSCLE glycogen phosphorylase, which is the rate limiting step of glycogen breakdown
65
What molecule is deficient in GSD 6? Hers Disease
Deficiency in LIVER glycogen phosphorylase, which is the rate limiting step of glycogen breakdown
66
What are the 5 key enzymes regulated by Glucagon?
``` GPCR Adenylyl Cyclase Protein Kinase A Protein Phosphatase 1 Phosphorylase Kinase ```