2. 22
To compare and contrast the different mechanisms by which
cholesterol biosynthesis are regulated.
To predict whether intracellular cholesterol synthesis will be
up- or down-regulated in response to energy availability as
influenced by diet, hormones and exercise.
To distinguish the different mechanisms by which plasma
cholesterol levels are controlled by clinically adminstrered
pharmacological agents.
OBJECTIVES
6. 6
26
hydrocarbon tail
steroid nucleusA
C D
B
cholesterolCholesterol
•27 carbons all derived from acetate
•C-3 hydroxyl group
•C-17 side chain with 8 carbons
Sources in the body
• synthesized primarily in liver and intestine
• not required in diet
• intestinal uptake from diet
Elimination
• converted into bile acids and bile salts in liver
• stored in gall bladder, secreted into intestine
• small % excreted in feces
21
3
cholesterol ester
fatty acid
A
C D
B
Cholesterol esters
• esterification at C-3 with fatty acid
• primary form transported in plasma
• packaged in lipoprotein particles
(e.g. LDL, HDL)
11. The transcription factor regulating cholesterol synthesis genes is
SREBP- sterol responsive element binding protein
11
12. SCAP- SREBP Cleavage Activating Protein
a transmembrane protein
has a sterol sensing domain
binds to SREBP in the ER
when ER sterols are low, SCAP-SREBP move to the Golgi
Protease 1 and Protease 2-
localized to the Golgi
responsible for the two step cleavage of SREBP resulting
in soluble, cytosolic SREBP
Mature, proteolytically-processed SREBP
translocates from the Golgi to the nucleus
activates the expression of cholesterol synthesis genes
SREBP- Sterol Regulatory Element Binding Protein
a transmembrane protein
has a DNA binding domain
has a SCAP interacting domain
Sterol-dependent regulation of cholesterol synthesis genes
12
25. Vytorin (ezetimibe + simvastatin)
• ezetimibe administered in combination with a
simavastatin (i.e. a statin)
• further reduces total cholesterol levels as compared
to statin alone
• blocks cholesterol absorption in the intestine and
cholesterol synthesis in the liver
• permits reduced doses of statins, which have
side effects
Zetia (ezetimibe)
Mechanism of action-
• acts at small intestine brush border
• does not enter the bloodstream, no side effects
• inhibits absorption of cholesterol
• does not block absorption of triglycerides or
fat-soluble vitamins
25
27. • cholesterol is the precursor of bile acids and bile salts
• synthesized in the liver
• stored in the gall bladder
• secreted into intestine
• aids digestion by emulsifying dietary lipids making them
accessible to pancreatic lipases
• aids intestinal absorption of fat-soluble vitamins (A, D, E, K)
• ~95% are reabsorbed in ileum and returned to liver
• ~5% of bile salts are excreted in feces
Bile acids and bile salts
Excretion of bile salts is the principal mechanism
for eliminating cholesterol from the body
Enterohepatic circuit
•synthesis in the liver
•storage in the gall bladder
•secretion into intestine
•re-circulation to liver
27
28. 28
cholic acid-
+ cholesterol
rate limiting step
Primary bile acids
are formed from
cholesterol
cholesterol
cholic acid chenodeoxycholic acid
7-a-hydroxylase hydroxylation of C7
addition of OH group
7-a-hydroxycholesterol
30. • Hypercholesterolemia is often treated with
“sequestrants” that bind bile acids in the intestine.
These compounds:
prevent reabsorbtion of bile acids
increase conversion of cholesterol to bile acids
increase bile salt elimination in feces
• Dietary fiber also sequesters bile acids
Secondary
bile acids
Secondary
bile acids
Primary
bile acids
7-a-hydroxylase
cholic acid-
+ cholesterol
30
Increased elimination of cholesterol from the body
31. Secondary
bile acids
Primary
bile acids
Bile salts-
glycine or taurine
conjugated to
bile acids in liver
5% lost in feces Recent R & D efforts focusing on bile acid receptors
as drug targets for treating liver disease, liver cancer,
metabolic disease.
32. Review- you tell me !!!!
•How many carbons are there in cholesterol?
•Which carbons are the business ends of the
cholesterol molecule?
•When cholesterol levels are high, HMG CoA reductase is
regulated by which of the following mechanisms?
•When cholesterol levels are high, HMG CoA reductase is
regulated by which of the following mechanisms?
•What organ STORES bile acids and bile salts?