Dietary lipids • Foods like meat, animal fat, butter, milk, cheese, egg yolk and cooking oils and ghee contain lipids. • The lipids present in them are mainly triglycerides, phospholipids, glycolipids, cholesterol and its esters, fatty acids, sterols and carotenes. • An adult may consume 50-150 gms of lipid per day. • Triglycerides accounts for 90% of dietary lipids. Digestion of Lipids • Hydrolysis of triglycerides, compound lipids and cholesterol esters to glycerol, free fatty acids, mono acylglycerols and free cholesterol constitutes the process of digestion.
• Since the lipids are water insoluble hydrolysis
of dietary lipids by enzymes in aqueous environment of GI tract poses a problem.
• The problem is solved by the emulsification
of lipids by the bile salts present in bile. Bile salts 1) Sodium and potassium glycocholate, 2) sodium and potassium taurocholate, 3) sodium and potassium glyco chenodeoxy cholate and 4) sodium and potassium taurochenodeoxy cholate. Bile salts form emulsions with lipids by reducing surface tension of water. An emulsion consist of water insoluble lipids dispersed in water. They can reduce surface tension of water because they are amphipathic molecules. The emulsification of lipids by bile salts increases surface area of lipid at water lipid interphase for the action of enzymes. Lipid Digestion In the mouth • Due to lack of favourable conditions like emulsification and PH, no digestion of lipid occurs in the mouth. In the stomach • In humans, initiation of fat digestion occurs in stomach with mechanical emulsification. • Gastric lipase hydrolyzes dietary triglycerides to diacylglycerol and fatty acids. • About 10-30% of dietary triglycerides are hydrolyzed by gastric lipase. In the small intestine • Small intestine is the major site of lipid digestion due to the pancreatic lipase. • It requires colipase and bile salts for its activity. • Colipase is a protein present in pancreatic juice along with lipase. • As such lipase has no affinity towards emulsion particles of dietary lipids and bile salts. • Hence, colipase forms complex with emulsion particle initially. • Then the lipase attaches to emulsion particle by forming ternary complex . • In the ternary complex lipase and colipase are bound to each other. • Pancreatic lipase, is an α-lipase and an esterase. Formation of lipase, colipase and emulsion complex • It hydrolyzes the ester linkages of triglyceride at α, α′ or (1, 3)- positions and forms 2-monoacylglycerol and free fatty acids. • It can not hydrolyze the ester bond of triglyceride at 2(β) position . • About 72% of 2-monoacylglycerol leaves emulsion particle and forms mixed micelles. • The rest (about 28%) of 2-monoacylglycerol is converted to 1-monoacylglycerol by an isomerase. • Now α-lipase converts 1-monoacylglycerol to glycerol and free fatty acids (22%). • The rest of 1-monoacylglycerol (about 6%) is absorbed as such. • Cholesterol esterase is another esterase present in pancreatic juice.
• It converts cholesterol esters to
cholesterol and free fatty acids.
• Human cholesterol esterase also acts on
triglycerides, phospholipids and lipid vitamin esters in presence of bile salts. Digestion and absorption of lipids. R–COOH indicates free fatty acids (FFA) Recycling of bile salts Pancreatic juice also contains some esterases, which acts on phospholipids 1. Phosphoplipase A2 It is secreted in proform and activated by trypsin. It hydrolyzes ester bond at β position of phospholipid and forms lysophospholipid and fatty acid . 2. Lysophospholipase It acts on lysophospholipid and forms glycerophosphocholine and free fatty acid. Enzymes of lipid digestion and bile secretion are hormonally regulated. In response to dietary lipids, lower part of duodenum and jejunum produces hormone cholecystokinin. It acts on pancreatic cells to release enzymes and causes contraction of gall bladder for the release of bile. Absorption of Lipids • Proximal part of jejunum is the major site of absorption of products of lipid digestion. • The monoacylglycerols, free fatty acids, cholesterol and lysophospholipids combine with bile salt micelles and form mixed micelles. • These mixed micelles carry the products of lipid digestion to the brush border of mucosal cells where they are absorbed into intestinal epithelium. • Under normal conditions over 98% of dietary lipid is absorbed. Fate of absorbed lipids in the intestine. FA-Fatty acid Action of pancreatic lipase. Fatty acids (FA) are cleaved from positions 1 and 3 of the triacylglycerol, and a monoacylglycerol with a fatty acid at position 2 is produced.
Action of pancreatic esterases
Disorders of Lipid Absorption 1. Chyluria
It is characterized by excretion of milky urine.
It is due to abnormal connection between
urinary tract and lymphatics of small intestine.
It is also called as chylous fistula.
It disappears when dietary fat is replaced
with fat containing short chain and medium chain fatty acids. 2. Congenital abeta lipoproteinemia
It is of genetic origin.
Triglycerides accumulates in intestinal
cells due to lack of apo B-48 required for lipoprotein formation (chylomicrons). 4. Cholestasis Lipid digestion and absorption is impaired in intra or extra hepatic cholestasis due to non availability of adequate amounts of bile salts, phospholipids and cholesterol.
In cholestatic patients, liquid crystal
vesicles are formed instead of mixed micelles.
Proper biliary secretion of phospholipid is
necessary for chylomicron formation in enterocyte and secretion of lipids into lymph. 5. Essential fatty acid deficiency (EFAD)
It occurs in cholestatic patients due to
malabsorption of lipids.
EFAD during cholestasis itself can impair
efficient lipid absorption and transport.
Because proper biliary secretion of
phospholipid is necessary for formation of mixed micelles and chylomicrons. Thank you