P4: AST, ALT, ALP, ACP Flashcards
Product of AST
○ oxaloacetate and glutamate
AST
● Former Name: _________________
○ Serum glutamic-oxaloacetic transaminase (SGOT or
GOT)
AST
Cofactor: ______________
○ Pyridoxal phosphate (Vitamin B6)
_________________will serve as the amino group donor and the amino
group of aspartate will be given to Oxoglutarate
aspartate
_________________will become Glutamate upon acquiring the amino
group from aspartate
Oxoglutarate
● Aspartate becomes Oxaloacetate after giving up the ______________
amino group.
ALT
Product: _____________
○ glutamate and pyruvate
ALT
● Former Name: ______________
○ Serum glutamic-pyruvic transaminase (SGPT or
GPT)
ALT
● Cofactor: ______________
○ Pyridoxal phosphate (Vitamin B6)
_______________ is the amino group donor. The amino group will be given
to Oxoglutarate
Alanine
● Oxoglutatrate upon acquiring NH2 becomes__________________
Glutamate.
● Functions in the synthesis and degradation of Amino acids
Aspartate aminotransferase
Glutamate will be
synthesized with the breakdown of aspartate
Forward reaction
Glutamate will be
degraded to form aspartate
Reverse reaction
_______________regulates the number of amino acids in
our system
Transaminase
___________________are ultimately oxidized by the tricarboxylic acid
cycle to provide a source of energy
Ketoacids formed
The highest in AST
Cardiac tissue
highest in ALT
Liver
AST
Intracellular level: ___________times than
plasma
7000
ALT
Intracellular level: 3000 times than
plasma
3000
__________is not used in the diagnosis of heart disorders because of its
non-specificity. It’s highest in the heart but it is not solely produced
by the heart
AST
Inside our hepatocytes, both ________ and _______ are in high levels
therefore their presence in the blood is ____________
ALT and AST
very low.
● AST occurs in 2 forms:
1.
2.
○ Cytoplasmic AST
○ Mitochondrial AST
Predominant form in serum
● Cell cytoplasm
Increased in disorders producing CELLULAR
NECROSIS
Mitochondria
○ Diseases that damage the hepatocyte directly.
● Hepatocellular (ALT & AST)
● Hepatobiliary (ALP)
○ Common example: _________________ or __________________
gallstone or obstruction of the bile duct
AST
○ Rise: ___________
○ Peak: __________
○ Normalizes within __________
○ Rise: 6-8 hours
○ Peak: 24 hours
○ Normalizes within 5 DAYS
○ Viral hepatitis: _________ upper limit of Normal (ULN)
○ Liver Cirrhosis: ________ ULN
● Muscular Dystrophies: _________ULN
100 times
4 times
4-8 times
ALT elevation is frequently higher than (cytoplasmic)
AST due to its ______________
longer half-life in blood
■ ALT: ________
■ Cytoplasmic AST: _________
■ mitochondrial AST: half-life of ___________;
■ ALT: 47 hours
■ Cytoplasmic AST: 17 hours
■ mitochondrial AST: half-life of 87 hours;
_________ - How long it would take for enzyme
decrease to 50% of concentration
Half life
■ De Ritis ratio (ratio of AST:ALT): _________
3-4:1
Catalyze the hydrolysis of various phosphomonoesters at a
certain pH
Phosphatases
○ need water to break down substrate
hydrolases
ALP
Systemic Name: _____________
Orthophosphoric Monoester Phosphohydrolase
(Alkaline Optimum)
ALP
Product: _____________
○ alcohol and phosphate ion
ALP
● Optimum pH: _____________
○ pH 9.0 - 10.0
ALP
● Cofactor: _______________
○ Magnesium and Zinc