are important dietary sources of energy. Fat also functions as a major form of energy storage (9 cal/g).
Lipids
Because it is water-insoluble, fat can be stored in larger quantities than carbohydrates.
Lipids
Carbohydrate reserves are depleted after about 1 day without food, but stored fat can provide needed calories for 30-40 days.
Digestion of Triglycerides
During digestion, triglycerides are hydrolyzed to glycerol, fatty acids, and monoglycerides:
Phosphoglycerides
are also hydrolyzed to their component substances (glycerol, fatty acids, phosphate groups, and aminoalcohols).
Chylomicrons
The smaller molecules that are produced, along with cholesterol.
Chylomicrons
modified by the liver into smaller lipoprotein particles.
phosphoglycerides, and cholesterol are complexed with proteins to form lipoprotein aggregates
The concentration of plasma lipids increases after a meal, and returns to normal as a result of storage in fat depots and oxidation to provide energy.
The concentration of plasma lipids rises within 2 hours after a meals, peaks after 4-6 hours, then drops to normal levels.
Lipoproteins may be classified by density.
Chylomicrons carry triglycerides from the intestines to the liver, skeletal muscle, and adipose tissue.
Very-low-density lipoproteins (VLDL)
carry newly synthesized triglycerides from the liver to adipose tissue.
Low-density lipoproteins (LDL)
carry cholesterol from the liver to cells of the body or bad cholesterol
High-density lipoproteins (HDL)
collect cholesterol from the body’s tissues, and bring it back to the liver or good cholesterol.
Cholesterol
is involved in the formation of cell membranes, the insulation of nerves, the synthesis of a number of hormones, and the digestion of food.
Resin drugs (Questran, Colestid)
bind with bile acids in the digestive tract and remove them from operation
Lopid, or large doses of niacin
reduce the production of triglycerides, whichare involved in the formation of LDL
Statins (Mevacor, Zocor, Pravachol, Lipitor)
block the synthesis of cholesterol in the liver by inhibiting HMG-CoA reductase
Brain cells do not obtain nutrients from blood.
Red blood cells do not have mitochondria, and cannot do fatty acid oxidation.
Glycogen and Glucose Stores
Carbohydrates from dietary sources and glycogen catabolism are used preferentially for energy production
Fat mobilization
When cells need fatty acids for energy, the endocrine system produces several hormones, including epinephrine which enter the bloodstream.
In the blood, mobilized fatty acids form a lipoprotein with the plasma protein called serum albumin.
Fat Mobalization
In this form, the fatty acids are transported to the tissue cells that need them.
The glycerol is water soluble, so it dissolves in the blood and is also transported to cells that need it.
Glycerol Metabolism
The glycerol hydrolyzed from triglycerides can provide energy to cells. It is converted to dihydroxyacetone phosphate in two steps:
Dihydroxyacetone phosphate is one of the chemical intermediates in glycolysis. It is converted to pyruvate, and thus contributes to cellular energy production.
The pyruvate can also be converted to glucose through gluconeogenesis.
Fatty Acid Oxidation
Fatty acids that enter tissue cells cannot be oxidized to produce energy until they pass through the membrane of the mitochondria.
Fatty Acid Oxidation
This reaction is catalyzed by acyl CoA synthetase.
This reaction is referred to as activation of the fatty acid because the fatty acyl CoA is a high energy compound
β-oxidation
The fatty acyl CoA molecules that enter the mitochondria then undergo a catabolic process
Plasma
Liquid portion of the blood
Blood Sugar
glucose part in the blood
RCBS - Erythrocytes
no nucleus and mitochondria
RCBS
cannot do fatty acid oxidation (atp production)
Four reaction
Dehydrogenation
Hydration
Dehydrogenation
Release of the acetyl unit
β-oxidation of Fatty acids
In the final step of b-oxidation (Step 4), the bond between the a- and b- carbons is broken by reaction with coenzyme A.
β-oxidation of Fatty acids
A new fatty acyl CoA is formed, which is two carbons shorter than the original molecule, and a unit of acetyl CoA is released
Thus, the breakdown of 18-C stearic acid requires 8 passes through the spiral, and produces 9 acetyl CoA’s, but only 8 FADH2 ’s and 8 NADH’s.
The activation of stearic acid by coenzyme A to form stearoyl CoA comes from the hydrolysis of 2 ATP’s
As a stearoyl CoA molecule (18 C’s) passes through the b-oxidation spiral, 9 acetyl CoA’s, 8 FADH2 ’s, and 8 NADH’s are produced.
Acetyl CoA can enter the citric acid cycle / electron transport chain and form 10 ATP’s = 90 ATP’s