Title: Digestion and absorption of dietary fats in non-ruminants
1- Digestion and absorption of dietary fats in
non-ruminants
2Background and Review
- Fatty acid nomenclature relevant to this advanced
nutrition class - 140Â myristic acid
- 160Â palmitic acid
- 180 stearic acid
- 181 cis ? 9 oleic acid
- 182 cis ? 9,12 linoleic acid
- 183 cis ? 9,12,15 linolenic acid
- 204 cis ? 5,8,11,14Â arachidonic acid
- 205 cis ? 5,8,11,14,17 eicosapentaenoic acid (an
omega-3 fatty acid because of double bond 3 C
from distal end)
3Nomenclature
- Chain length
- Medium chain caproic (C6), caprylic (C8), capric
(C10) and lauric acid (C12) - Long chain C14..
- Saturation
- Saturated (C160)
- Monounsaturated (C181)
- Polyunsaturated (C204)
4Nomenclature
- Position of first double bond relative to
carboxylic acid or methyl end - n-3 fatty acids referred to as n-3 (?-3 fatty
acids or omega-3 fatty acids) a family of
unsaturated fatty acids that have a double bond
in the n-3 position that is, the third carbon
from the methyl end of the fatty acid
C205, n-3 (eicosapentaenoic acid)
From the acid end, ? 5,8,11,14,17
5Nomenclature
- Position of first double bond relative to
carboxylic acid or methyl end - n-6 fatty acids referred to as n-6 (?-6 fatty
acids or omega-6 fatty acids) a family of
unsaturated fatty acids that have a double bond
in the n-6 position that is, the sixth carbon
from the methyl end of the fatty acid
C182, n-6 (linoleic acid)
If discuss with respect to the acid end, we would
use 182 cis ? 9,12
6Lipid Digestion-The Overview
- Digestion to component parts
- Absorption of component parts by enterocytes
- Reassembly of complex lipids
- Delivery to systemic circulation via blood (or
lymphatics) - Uptake by recipient peripheral tissues (liver,
adipose tissue, muscle) - Metabolism and utilization for energy or other
processes
7Fundamental Problem
- Fatty acids are not stored in feeds or animal
tissues as fatty acids, they are stored as
triglycerides (triacylglycerol esters),
phospholipids, etc. - Complexed lipids must be digested and the
constituent parts absorbed by the enterocyte
8Triacylglycerol ester
9Solution to problem
- Must hydrolyze to component parts before
molecules can traverse the lumen of the intestine
and be absorbed by the enterocyte - Must be able to accommodate hydrophobic molecules
in an aqueous/hydrophilic environment
10Digestion
11Triacylglycerol (TAG) digestion
- Gastric/Lingual Lipase (Acid Lipase)
- Sn-3 position? 1,2 DAG FA to help emulsify
additional fat - Active to pH 6.5 (through upper duodenum)
- Prefers triglycerides composed of medium chain FA
(milks are rich in MCT) - Particularly important for newborns and suckling
young due to slow development of pancreatic
lipase - No activity on PL or cholesterol esters
- Gastric lipase mixing/motility ? fine lipid
droplets less than 0.5 mm diameter
12Most fat digestion occurs in the small intestine
- Pancreatic lipase
- Sn-1 and 3 positions ? FFA 2-MAG
- Requires co-lipase to function in presence of
bile salts - pro-colipase trypsin ? co-lipase
- co-lipase lipase ? TAG hydrolysis
13Not all fatty acids are equally absorbed by the
enterocyte
- Lard saturated fatty acids esterified in the
sn-2 position lipase activity produces 2-MAG
free fatty acids, many of which are unsaturated - As the free fatty acid, unsaturated fatty acids
are more readily absorbed than are saturated
fatty acids
14Not all fatty acids are equally absorbed by the
enterocyte
- Beef Tallow saturated fatty acids esterified in
the sn-1 and sn-3 positions lipase activity
produces 2-MAG free fatty acids, many of which
are saturated - As the free fatty acid, saturated fatty acids are
less readily absorbed than are unsaturated fatty
acids
15Which has the higher metabolizable energy value,
lard or beef tallow?
- Lard less energy lost due to lack of absorption,
BECAUSE saturated fatty acids are more readily
absorbed as the 2-MAG, and because unsaturated
fatty acids are more readily absorbed than
saturated fatty acids
16Animals not consuming just TAG
17Phospholipid digestion
- Phospholipase A2
- - secreted by pancreas, some activity intrinsic
in intestinal mucosa depending on species - - activated by trypsin
- - targets sn-2 postion (FFA
Lyso- phosphatidyl choline)
18Digestion of Cholesteryl Esters
The R (fatty acid group) varies across plants and
across animals
19Digestion of Cholesteryl Esters
- Cholesterol esterase (carboxyl ester hydrolase,
bile salt-stimulated lipase, nonspecific
esterase) - Secreted by pancreas, no activation required
- Broad esterase activity (TAG, CE,
- phosphoglycerides, spingolipids, A, D, MAG)
- Bile salt micelles (sodium taurocholate) self
- aggregation to polymeric form (dimer) to protect
against proteolytic degradation
20How do we get lipid digestion products into the
blood for distribution to recipient tissues?
- Lipids have little solubility in water (minimal
polarity) - Unstirred water layer, presents a barrier even
with vigorous intestinal motility and mixing of
intestinal contents
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22Bile is crucial for absorption of lipids
- Bile is produced by hepatocytes in the liver, and
drains out through the many bile ducts that
penetrate the liver - The common bile duct in turn joins with the
pancreatic duct to empty into the duodenum If
the sphincter of Oddi is closed, bile is
prevented from draining into the intestine and
instead flows into the gall bladder, where it is
stored and concentrated - Cholesterol is released with the bile, dissolved
in the acids and fats found in the concentrated
bile solution - When food is released by the stomach into the
duodenum in the form of chyme, the gallbladder
releases the concentrated bile to provide bile
salts to aid in digestion
23Mixed Micelles at CMC (1-2 mM)
Micelles form from bile salts (acids) lipid
moieties (cholesterol, etc.), engulf hydrophobic
products of fat digestion, and provide the
polarity that enables these molecules to
penetrate the unstirred water barrier Increase
the concentration of lipid digestion products
(100-1000X) Diffusion is thus toward the
enterocyte
24Micelles
25Entering the Enterocyte
- Passive
- Lipid-rich brush border
- TAG, phospholipids, cholesterol esters reformed
to sustain gradient - Glycerol, short chain FA, readily diffuse through
unstirred water barrier and into enterocyte due
to gradient
Initial diffusion followed by
re-esterification at the endoplasmic reticulum
26Carrier-mediated active transport
Fatty acids
- High concentrations of FA in the lumen
- diffusion is likely major mechanism of
- uptake
- Importance of FATP-4 increases as the
- concentration of FA decreases
FATP-4
Fatty acids
27Intracellular Metabolism
- Must traverse an aqueous cytosol to get to ER
- FABP (Villi vs. crypt jejunum vs. ileum high
fat diet vs. low fat diet) - I-FABP (fatty acids only)
- L-FABP (lysophosphatidyl choline, retinoids,,
MAG) - SCP-1
- SCP-2 (cholesterol)
28Re-esterification
- Triacylglycerol complex on cytosolic surface of
the ER - Then TAG must penetrate the ER aided by a
transport protein - Abetalioproteinemia- chylomicrons not formed,
despite presence of apoB
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30Phospholipids
- Lysophatidyl choline, etc.
- Acylated
- Phosphatidyl choline
- Hydrolyzed
- glycerol 3-phosporyl choline
- liver
- fatty acids
- MAG TAG
- 2 lysophatidyl choline
- phosphatidyl choline
-
- Glycerol 3-phosporyl choline
31Cholesterol
Cholesterol (diet and endogenous)
Free Pool
LYMPH
32Chylomicrons
- Apo A-1, apo A-II, apo B-48
- apoE and C added in circulation
- Fatty acid composition diet
- (unlike phospholipids)
- ER Golgi prechylomicrons
- Exocytosis
- intracellular space
33Avian vs. Mammalian Species
- Mammals chylomicrons, enter circulation via the
lymphatics at the thoracic duct - Avian portomicrons, transported to the liver via
the portal vein, then delivered to systemic
circulation
34Summary
- Digestion lipases
- Micelle formation
- Uptake of component parts by diffusion and
carrier mediated (FATP) processes - Reassembly of triglyceride via MAG or glycerol
phosphate pathways - Incorporation of TAG, etc. and apo proteins into
lipoproteins called chylomicrons (or
portomicrons) in enterocyte - Secretion via exocytosis and entry in systemic
circulation via lymphatics or portal circulation
via liver