Biochem Final Review
Card Set Information
Biochem Final Review
What is the purpose of bile salts? Where are they synthesized? Where are they secreted from?
To mix with intestinal lipids to make them water soluble
Synthesized in the Liver
Secreted from Gallbladder
Where is lipase & phospholipaseA2 secreted from?
Pancreas - these mix with bile salt / lipid mix to prepare them to be absorbed by Intestinal walls; this mix becomes triacylglycerols
Where are chylomicrons found?
Small Intestine - they are the "foamy part of detergent"
Chylomicrons are also known as apolipoproteins
Once apolipoproteins are made, where do they go?
Into the Lymph System where it travels to other parts of the body as storage or to create energy through oxidation
The release through the Lymph System limits the rate this material is released into the blood (a protection system)
What is the function of lipoproteins?
They transport fat and cholesterol in the blood
What determines the whether lipoprotiens are called HDL / LDL / etc?
The protein density
HDL's have high protein density
LDL's have low protein density
Chylomicrons are majors carriers of what?
What is the difference between cholesterol and cholesterol esters?
Cholesterol esters are more hydrophobic (non water soluble)
What transports ingested fat from intestinal walls to adipose and liver?
Where is VLDL made? What is its purpose?
VLDL is made in the Liver
Its function is to transport fat to other tissues (such as adipocytes)
Which lipoprotein contains the major source of cholesterol?
What does cholesterol used for?
Making cell membranes, cortisol, testosterone, estrogen, aldosterone, etc
LDL's are only considered "bad" in large quantities which lead to atherosclerosis (hardening of vessels and build-up of obstruction in the vessels leading to heart disease and stroke
What is the purpose of HDL's? Where is it produced?
Transport / gather cholesterol from peripheral tissue back to the Liver where it is used and excreted as bile
It is produced by the Liver and enterocytes
If you have a genetic disorder or enzyme disorder, what are these disorders due to?
What is the difference between acquired hyperlipoproteinemia and and genetic hyperlipoproteinemia?
Acquired - non familial
Genetic - familial
What is the pathway of Triglycerides?
What is the pathway of Cholesterol?
What inhibits HMG-CoA reductase?
What is the central intermediate in lipid metabolism?
What is the most dominate protein the the blood stream?
Albumins - it is also a water soluble protein that transports fatty acids
This is the key enzyme for causing fatty acid release from adipocytes?
This transports fatty acids into the mitochondria during the breakdown of lipids for the generation of metabolic energy
Carnitine (like a boat)
This enzyme stimulates reverse cholesterol transport from tissues that have excessive amounts of cholesterol into HDL molecules.
Lecithin-cholesterol acyl transferase (LCAT)
What is this condition called when you have an increase in lipoproteins concentration in the blood?
What is this condition when you have large amounts of chylomicrons and triglycerides in the the plasma for a normal diet?
Hyperlipoproteinemia Type I
What condition is this when one has increased plasma levels of β-lipoproteins and cholesterol as well as elevated LDL but normal triglycerides?
Hyperlipoproteinemia Type IIA
What condition is this when one has increased plasma levels of β-lipoproteins and cholesterol as well as elevated LDL, cholesterol and triglycerides?
Hyperlipoproteinemia Type IIB
What is the difference between Homozygous and Heterozygous Hyperlipoproteinemia?
Homzygous - severe lipid changes, with manifestations on the body (xanthomatosis, xanthelesma, corneal arcus, atherosclerosis)
Heterozygous - mild lipid changes
The process of removing amine groups from molecules due to excess protein intake
The process of muscle cells using amino acids as an energy source while eliminating nitrogen
Glucose / Alanine Cycle
What is the purpose of the Alanine Cycle?
Shuttle to Liver to make glucose
Recycles carbon skeletons to between Muscle and Liver
to Liver and is converted to urea (where expelled)
A sequence of DNA that has been altered or mutated from its original form
Responsible for normal cell growth and proliferation. However, subtle changes can alter their ability to function normally thereby activating their cancer-causing potential
What is the name of the group of enzymes invovled in the detoxification process of Phase I?
Cytochrome P450 family
What does Phase II detoxification typically involve to neutralize toxins and reactivate intermediates left over from Phase I?
A significant pathway in the Phase II detoxification mechanism. It combines glucuronic acid with toxins.
This is excreted from bile. It is responsible for the yellow color of bruises and yellow discoloration in jaundice.
When RBC's get old or damages, what system gets rid of them?
Is unconjugated bilirubin water soluble?
No - it is bound to albumin and sent to the liver where it gets conjugated
Unconjugated hyperbilirubinemia can lead to accumulation of bilirubin in certain brain regions in new-born babies is know as?
Period when ingested nutrients are entering the blood from the GI tract
Period when the GI Tract is empty of nutrients and energy must be supplied from the stores in the body
Going without food for 24 hours
The catabolism of triaclglycerols yields glycerol and fatty acids. This occurs mainly in adipose tissue and the released glycerol is converted into glucose in the liver.
The utilization of fat instead of glucose