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Transcript
Overview of Lipid Metabolism
Learning Objectives
By the end of this lecture the students should be able to understand:
•
Classification of Lipids
•
The digestion, absorption and utilization of dietary lipids
•
Lipogenesis and Lipolysis
•
Lipid malabsorption
•
•
•
The functions of cholesterol
Cholesterol synthesis and metabolism
Cholesterol transport
Classification of lipids
Fatty Acids
•
Fatty acids are long chain carboxylic acids having a terminal carboxyl
(COOH-) group
–
Saturated Fatty Acids: have no double bonds e.g. Palmitic acid and
Stearic acid
–
Unsaturated Fatty Acids: have one or more double bonds
•
Essential Fatty Acids
–
Fatty Acids that can not be synthesized de novo and have to supplied
in the diet
–
Linoleic acid
–
Linolenic acid
Triglycerides
•
When one, two or three fatty acids are esterified to a molecule of
glycerol; they form mono, di or triacylglycerols aka TGs
•
Lipids are stored within adipose tissue as fat droplets made up of TGs
Lipogenesis
•
Lipid synthesis:
–
From glycerol derived from Dihydroxyacetone phosphate from
glycolysis
–
Occurs in the liver and to a small extent in adipose tissue
–
Acetyl coA can form any fatty acid except for the essential FA
–
The main rate limiting enzyme of lipid synthesis is Fatty Acid
Synthase
Lipolysis
•
Lipid catabolism where lipids become:
–
Glycerol
–
Free fatty acids
•
Glycerol can be converted to pyruvic acid which enters TCA
•
Fatty Acids are degraded by beta oxidation, occurs in mitochondria of
liver, muscle and adipose tissue
The Dietary Lipids
•
An adult consumes about 60-150 g of lipid per day
•
Much of it is composed of Triglycerides
•
Remaining is made up of free Fatty acids, Cholesterol, cholesterol
esters and phospholipids
Digestion of Dietary Lipids
•
Digestion begins in the GIT with the action of Lipase
•
Gastric lipase requires neutral pH to emulsify fat
•
In adults much of the dietary lipids are transported unchanged to the
small intestine owing to acidic pH of the stomach
Emulsification of Dietary Lipids
•
In the small intestine the pancreatic secretions digest the dietary lipids
•
Bile Salts emulsify fat droplets
•
Pancreatic lipase digests triglycerides into monoglycerides and free
fatty acids
•
Pancreatic cholesterol esterase digests CE into cholesterol and FFA
Absorption of lipids across intestinal mucosa
•
FFA, cholesterol and monoacylglycrol together with bile salts,
constitute micelles to get absorbed across the intestinal mucosal cells
•
Micelles: amphipathic structures with hydrophobic core containing
the water insoluble lipids, and hydrophilic outer shell soluble in aqueous
medium of intestinal epithelium
Lipid transport from intestinal mucosa
•
Once inside the intestinal mucosal cells, the absorbed lipids are
resynthesized into TG and CE ( cholesterol esters )
•
Intestinal cells synthesize apolipoprotein B-48 and package TG and
CE into Chylomicrons
•
Chylomicrons are secreted first into the lymphatics and then into the
blood
Lipoproteins
•
TGs and Cholesterol are transported in blood as Lipoproteins.
•
According to density the lipoproteins are classified as
–
Chylomicrons
–
VLDL (very low density lipoproteins )
–
IDL (intermediate density lipoproteins )
–
LDL (low density lipoproteins )
–
HDL (high density lipoproteins )
Classes of lipoproteins with associated Apoproteins
Lipoprotein Function
Apoprotein
Chylomicrons
Transport dietary TG and CE from intestine to tissues
apoB-48
apoC-II
apoE
VLDL
Transport TG from liver to tissues
apoB-48
apoC-II
apoE
LDL Delivers cholesterol into cells apoB-100
IDL Picks up cholesterol from HDL to become LDL
Picked up by liver apoE
HDL Picks up cholesterol accumulating in blood vessels apoA1
Lipoproteins and their functions
Complex lipids
•
Phospholipids
–
Polar, amphipathic, ionic compounds composed of alcohol attached to
a diacylglycerol or sphingosine
•
Phosphoglycerides
–
Phospholipids containing glycerol
•
Sphingomylin
–
Phospholipids containing sphingosine
•
Fatty acid + sphingosine = Ceramide
Glycolipids
•
Derivatives of ceramide
•
Components of cell membranes
•
Serve as receptors of certain bacterial and viral toxins
•
Antigenic: tumor antigens, embryonal antigens and sources of blood
group antigens
Cholesterol
•
Component of cell membranes
•
Steroid synthesis
•
Precursor of steroid hormones e.g. corticosteroids, aldosterone,
estrogen and testosterone
•
Vitamin D precursor
•
bile acid precursor
Fat malabsorption
•
Syndrome of fat malabsorption consists of Diarrhea, steatorria,
malabsorption, wasting and vitamin deficiencies
•
Some common causes are:
–
Lactase deficiecy
–
Celiac sprue
–
Pernicious anemia
–
–
–
–
Blind loop syndrome
Lymphatic obstruction
Tuberculosis
lymphoma
Deficiencies in Fat malabsorption
•
Deficiency of Fat soluble vitamins: vitamin A, D, E and K
•
Iron deficiency-Anemia
•
Vitamin B12/ Folate deficiency- Megaloblastic anemia
•
Vitamin K deficiency- easy bruising
•
Vitamin D deficiency- osteopenia
Cholesterol Metabolism and CVS Function
Cholesterol
• The major sterol compose of four fused rings and an eight-membered,
branched hydrocarbon chain
Functions of Cholesterol
• Necessary part of cell membranes
• Precursor molecule for steroid synthesis
–
–
–
–
–
–
–
Aldosterone
Corticosteroids
Estrogens
Progesterone
Testosterone
Bile acid for digestion
Vitamin D
Sources of Cholesterol
Cholesterol Synthesis
•
•
•
•
•
Occurs in cytosol
Requires NADPH and ATP
Highly regulated
80 % in liver, ~10% intestine, ~5% skin
Hydroxymethylglutaryl-coenzyme A (HMG-CoA) is the precursor for
cholesterol synthesis.
• HMG-CoA is also an intermediate on the pathway for synthesis of ketone
bodies from acetyl-CoA.
Formation of HMG CoA-Rate Limiting step
 HMG-CoA is formed by condensation of acetyl-CoA & acetoacetyl-
CoA, catalyzed by HMG-CoA Synthase.
 HMG-CoA Reductase catalyzes production of mevalonate from HMGCoA
O
H3 C
H2 O  O
H3 C
C
CH2
C
SCoA
SCoA
HMG-CoA
Synthase
HSCoA
OH
O
O
C
acetoacetyl-CoA
acetyl-CoA

O
C
CH2
C
O
CH2
C
SCoA
CH3
hydroxymethylglutaryl-CoA
Regulation of Cholesterol Synthesis
Cholesterol Transport
• Chylomicrons:
– Chylomicrons transport triglycerides from intestine
• Very Low Density Lipoproteins (VLDL) and Intermediate Density
Lipoproteins (IDL) :
– VLDL produced in liver . Carry cholesterol and triglycerides
• Low Density Lipoproteins (LDL)
– LDL result from metabolism of VLDL and IDL and carry cholesterol.
LDL are important cause of heart disease
• High Density Lipoproteins(HDL)
– HDL is “good” cholesterol. It removes cholesterol and protects against
heart disease
Cholesterol
Transport
Hypercholestrolemia
Blood Cholesterol levels
• Total cholesterol
< 5.17 mmol/L = Good
5.17-6.19
= Borderline High
•
•
•
•
•
•
> 6.20
= High
LDL
< 2.58 mmol/L = Good
2.58-3.33 = Near Normal
3.34- 4.12 = Borderline High
4.13-4.88 = High
> 4.88
= Very High
Hypercholestrolemia
Hypercholestrolemia-Risk factor for
Atherosclerosis
Atherosclerosis
Hypercholesterolemia and Risk of Stroke
HDL-Cardio protective Lipoprotein
Management of Hypercholestrolemia
• Life style modifications
– Balanced diet
– Exercise
– Stress management
• Drug Therapy
REFERENCE
Lippincott’s Illustrated Review
Biochemistry
5th Edition
Page no. 219 to 224
THANKS