Exam 1 2025 Flashcards

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
Q

What enzyme reduces pyruvate to lactate?

A

Lactate dehydrogenase

26
Q

What are the symptoms of Pyruvate Dehydrogenase Deficiency?

A

Lactic acidosis and neurological symptoms

27
Q

What pathway does galactose metabolism follow?

A

Galactose → Galactose-1-phosphate → UDP-Galactose → Glucose-1-phosphate

28
Q

What deficiency causes galactosemia?

A

Deficiency in galactose-1-phosphate uridyltransferase

29
Q

What are the symptoms of galactosemia?

A

Jaundice, hepatomegaly, and intellectual disability

30
Q

What pathway does fructose metabolism follow?

A

Fructose → Fructose-1-phosphate → Glyceraldehyde and DHAP

31
Q

What deficiency causes Hereditary Fructose Intolerance?

A

Deficiency in aldolase B

32
Q

What are the symptoms of Hereditary Fructose Intolerance?

A

Hypoglycemia, vomiting, and liver damage after fructose ingestion