Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
28 Cards in this Set
- Front
- Back
The role of hepatocytes are:
Manufacture _____ including _____. Synthesize, store, and process _____. Metabolize and store _____. Form and secrete _____. Eliminate _____ and other harmful biproducts of the body. _____, by metabolizing and/or secreting, drugs, alcohol, and environmental toxins. |
Proteins, albumin
Fats Carbohydrates Bile Bilirubin Detoxify |
|
_____ is the name given to a special liver form of the enzyme hexokinase.
How does it differ from hexokinase? |
Glucokinase
Has a higher Km for a sugar substrate (Important for the liver being the major source of glucose in the body) |
|
What two processes does glucokinase facilitate?
|
Creates glucose-6-phosphate as well as glycogen synthesis
|
|
Glukokinase is also the predominant enzyme for the phosphorylation of glucose _____ cells of the _____.
|
Beta, Pancreas
|
|
What are the three regulatory enzymes of glycolysis?
|
Hexokinase
Phosphofructokinase Pyruvate kinase |
|
What two organs take up the extra glucose released back into circulation from the liver?
|
Muscle
Brain |
|
What is the major fuel for the brain?
Why does it rely solely on the availability of it through the blood? |
Glucose
It has no significant glycogen stores |
|
What do RBC's oxidize glucose into?
|
Pyruvate
Lactate |
|
When does the liver release glucose into the blood?
Where is this released glucose derived from? |
Muscular activity and interval between meals
Breakdown of stored glycogen Formation of glucose through gluconeogenesis |
|
Fasting leads to decreased liver _____.
|
Glycogen
|
|
What is another name for the Urea cycle?
|
Ornithine cycle
|
|
What is the overall reaction of the Urea cycle?
|
2 Ammonia + Carbon Dioxide + 3 ATP = Urea + water + 3 ADP
|
|
The two nitrogens enter the urea cycle as _____ and _____.
|
Ammonia
Aspartate |
|
Urea is produced by the hydrolysis of _____.
|
Arginine
|
|
The cleavage of _____ does not require ATP.
|
Argininosuccinate
|
|
The urea cycle occurs partly in the _____.
|
Mitochondria
|
|
Why is a complete block in the urea cycle fatal?
|
There is no known alternative pathway for the synthesis of Urea.
|
|
Inherited disorders from defective enzymes may cause a partial block in some of the reactions and results in _____, which can lead to what?
|
Hyperammonia
Mental retardation |
|
Extensive ammonia accumulation leads to extensive _____ damage and _____.
|
Liver
death |
|
What disease creates an interface in the enzymes that produce _____ _____ in the first step of the urea cycle?
|
Carbamyl phosphate
Liver cirrhosis |
|
The level of nonprotein nitrogen in the blood is due primarily to the level of _____.
|
Urea
|
|
What is the major regulatory enzyme of cholesterol synthesis?
|
HMG-CoA reductase
|
|
What is cholesterol synthesized from?
|
acetyl-CoA
|
|
What are the intermediates of cholesterol?
|
HMG-CoA, mevalonic acid, isopentenyl pyrophosphate, squalene
|
|
What vitamin is formed from cholesterol?
|
Vitamin D
|
|
Cholesterol absorption depends upon the presence of _____ _____ in the intestinal lumen.
|
Bile Salts
|
|
What is the feedback control of cholesterol synthesis?
|
Cholesterol is in a negative feedback loop and causes allosteric inhibition of HMG-CoA reductase
|
|
What are the enzymes involved in cholesterol synthesis that are reversible and do not commit the cell to the synthesis of cholesterol?
|
Thiolase and HMG-CoA synthase
|