Exam 1 2025 Flashcards

(32 cards)

1
Q

What is the function of GLUT1?

A

Transport glucose at a constant rate

Found in red blood cells and the blood-brain barrier

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2
Q

Where is GLUT2 primarily found?

A

Liver, pancreas, and kidney

Functions in glucose uptake and release, acting as a glucose sensor

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3
Q

What is the primary role of GLUT3?

A

High-affinity transporter for rapid glucose uptake

Predominantly in neurons

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4
Q

What type of glucose uptake does GLUT4 facilitate?

A

Insulin-dependent glucose uptake

Found in adipose tissue and muscle

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5
Q

What is the main function of GLUT5?

A

Transport of fructose

Primarily involved in the small intestine

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6
Q

What is the significance of glucose transporters?

A

Facilitate the passive transport of glucose across the cell membrane

Vary in affinity and capacity, matching the metabolic needs of different tissues

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7
Q

What syndrome is caused by GLUT1 deficiency?

A

GLUT1 Deficiency Syndrome

Leads to seizures, developmental delays, and motor dysfunction

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8
Q

What condition is associated with GLUT2 mutation?

A

Fanconi-Bickel Syndrome

Characterized by glycogen storage issues, hepatomegaly, and renal tubular dysfunction

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9
Q

What is linked to GLUT4 impairment?

A

Insulin resistance and Type 2 Diabetes

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10
Q

What is the primary function of the liver in glucose metabolism?

A

Central in glucose homeostasis, glycogen storage, and gluconeogenesis

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11
Q

What role does muscle play in glucose metabolism?

A

Glucose uptake and utilization for energy during contraction

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12
Q

What is the pancreas’s function in glucose regulation?

A

Sensing blood glucose levels and regulating insulin/glucagon secretion

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13
Q

Where does oxidative phosphorylation occur?

A

Mitochondria

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14
Q

What metabolic process occurs in the cytoplasm?

A

Glycolysis and initial steps of gluconeogenesis

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15
Q

What is the first intermediate in glycolysis?

A

Glucose

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16
Q

Which enzyme converts glucose to glucose-6-phosphate?

A

Hexokinase/Glucokinase

17
Q

What is the enzyme that converts fructose-6-phosphate to fructose-1,6-bisphosphate?

A

Phosphofructokinase-1

18
Q

What are the two products of aldolase in glycolysis?

A

Glyceraldehyde-3-phosphate and Dihydroxyacetone phosphate

19
Q

What is generated during glycolysis?

A

Net 2 ATP and 2 NADH

20
Q

What does gluconeogenesis consume per glucose molecule synthesized?

A

4 ATP, 2 GTP, and 2 NADH

21
Q

What inhibits hexokinase/glucokinase?

A

Glucose-6-phosphate

22
Q

What activates phosphofructokinase-1 (PFK-1)?

A

AMP

Inhibited by ATP and citrate

23
Q

What activates pyruvate kinase?

A

Fructose-1,6-bisphosphate

Inhibited by ATP and alanine

24
Q

What is the importance of lactic fermentation?

A

Allows for ATP generation under anaerobic conditions

25
What enzyme reduces pyruvate to lactate?
Lactate dehydrogenase
26
What are the symptoms of Pyruvate Dehydrogenase Deficiency?
Lactic acidosis and neurological symptoms
27
What pathway does galactose metabolism follow?
Galactose → Galactose-1-phosphate → UDP-Galactose → Glucose-1-phosphate
28
What deficiency causes galactosemia?
Deficiency in galactose-1-phosphate uridyltransferase
29
What are the symptoms of galactosemia?
Jaundice, hepatomegaly, and intellectual disability
30
What pathway does fructose metabolism follow?
Fructose → Fructose-1-phosphate → Glyceraldehyde and DHAP
31
What deficiency causes Hereditary Fructose Intolerance?
Deficiency in aldolase B
32
What are the symptoms of Hereditary Fructose Intolerance?
Hypoglycemia, vomiting, and liver damage after fructose ingestion