Lecture 9 - Fatty Acid Metabolism
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Transcript Lecture 9 - Fatty Acid Metabolism
فیزیولوژی تولید و ترشح شیر
Lactation Physiology
(part 1)
By: A. Riasi
(PhD in Animal Nutrition & Physiology)
What
is a mammary gland?
Serves a reproductive function; nourishment of the neonate.
The mammary gland is one of a few tissues in mammals, which
can repeatedly undergo growth, functional differentiation, and
regression
Relies on same endocrine (hormonal) support for development
and function.
Example: gonadal steroids, prolactin, etc.
What
is the difference between the animal udder?
Cow: Four glands and four teats
Sheep and goats: Two glands and two teats
Sow: 12-14 teats and two glands per teat.
Mare: Four glands and only two teats.
The
udder is a complex system
A supportive system.
A secretory system composed of epithelial cells.
A duct system for storage and conveyance of milk.
Blood, lymph, and nerve systems.
The
udder of cows
The
weight of empty cows udder is about 12-30 kg.
The
udder weight is affected by:
Age
Stage of lactation
Amount of milk in the udder
Inherited differences among cows
The
supportive system of udder
There
are seven tissues that provide support for the udder:
Skin covering the gland is only of very minor support.
Superficial fascia or Areolar subcutaneous tissue
Coarse areolar or cordlike tissue
Subpelvic tendon
Superficial layers of lateral suspensory ligament
Deep lateral suspensory ligament
Median Suspensory Ligament
An illustrated view of the ligaments that permit udder suspension
(Courtesy of Iowa State University)
Teat
structure
Interior anatomy of the Mammary Gland
The interior structure of mammary gland:
Connective tissue
Ductular system
Secretory tissue
Mammary duct system
Secretory tissue
Secretory tissue
A lactating secretory cell is the basic unit of milk synthesis
Milk precursors are taken from the blood into the cell
The secretory cell have two kind of junctions with neighbor cells:
Tight junction around the apical portion
Gap junction in lateral portion
Major component of a secretory epithelial cell
Apical membrane
Secretory vesicles
Golgi apparatus
Tight junction
Endoplasmic Reticulum
Gap junction
Nucleus
Lysosomes
Cytoplasm
Basement membrane
Basal and lateral membranes
Precursors of Milk
Precursors of milk come from the bloodstream and the primary
substrates extracted from blood include:
Glucose
Amino acids
Fatty acids
Minerals
Acetate *
βHB *
Precursors of Milk
Several materials in milk come unchanged from the blood:
Minerals
Hormones
Immunoglobulins
Synthesis of milk proteins
There are several specific systems for amino acids are absorption
through the basal membrane.
Inside the cell, amino acids are covalently bound together to
form proteins at the polysomes (Poly-ribosomes).
Proteins sythesized at RER include:
Casein
β-lactoglobulin, and α-lactalbumin
Membrane bound proteins
Synthesis of milk proteins
Synthesized proteins are transferred the golgi apparatues (GA).
Casein is secreted as micelle, which is formed in the GA from:
Casein molecues
Calcium
Phosphorus
Synthesis of milk lactose
Glucose enters the cells via the basolateral membrane via
specific transport system.
Some glucose is converted to galactose in the cell.
Both glucose and galactose enter the GA and react resulting in the
formation of lactose.
Synthesis of milk fat
In ruminant, acetate and β-hydroxybutyrate are important
precursors of fatty acids (FA) synthesis in mammary cells.
Preformed FA, glycerol and monoacylglyceride are absorbed at
the basolateral membrane.
Milk
fat
triglycerides
are
synthesized
endoplasmic reticulum and form small droplet.
on
the
smooth
Synthesis of milk fat
Under certain circumstances, fat droplets fuse with each other to
form cytoplasmic vacuoles.
The protein coat on the milk fat globule membrane comprises:
Mainly butyrophilin (BTN) *
Xanthine oxidoreductase (XDH) *
Adipophilin (ADPH)
Mucin 1
CD36
Periodic acid/Schiff
PAS III, and FABP
Pathways for milk fat globule transit and secretion from mammary epithelial cells
Synthesis of milk fat
The properties of milk fat:
Milk fat composed of different fatty acids:
Short chains (4-8 C)
Medium chains (10-14 C)
Long chains (≥16 C)
More than 95% of milk fat is TAG
Around 70% of FA by weight in milk fat are saturated
Approximately 25% of the milk FA are monounsaturated
PUFA only account for a small portion of total FA in milk
Synthesis of milk fat
There are two sources of FA for milk fat synthesis:
The de novo FA synthesis in mammary epithelial cells
Short chain (4-8 C)
Medium chain (10-14 C)
About 50% of 16 C
Preformed FA uptake from blood circulation
De novo fatty acid synthesis
In ruminants, the substrates for de novo FA synthesis in
mammary epithelial cells are:
Acetate produced by rumen fermentation
β- hydroxybutyrate produced by the rumen epithelium
Preformed fatty acid uptake
Long-chain FA taken up by the mammary gland are imported
from plasma:
Released from circulating lipoproteins by lipoprotein lipase
NEFA bound to albumin
There is evidence showing that the membrane transport of long-
chain FA is a facilitated process.
Some factors might play a role in FA uptake and transport:
Cluster of differentiation 36 (CD36)
Fatty acid binding protein 3 (FABP3)
Properties of milk TAG
Fatty acids are not esterified randomly to the sn-1, -2, and -3
positions of glycerol backbone.
The distribution of FA is dependent on the distinct binding
affinities of the acyltransferase enzymes for substrate FA.
Milk fat depression (MFD)
Several theories have been proposed to explain the physiology
behind this reduction in fat synthesis.
Lower production of acetic and butyric acids in the rumen caused
less fat production in mammary gland.
The greater proportionate production in rumen increases the blood
insulin, which partitions nutrients away from the mammary gland.
A more current theory is that the combination of high grain and
high unsaturated fatty acids in the diet causes the microorganisms in
the rumen to produce more trans fatty acids.
Milk fat depression (MFD)
Avoiding milk fat depression
Proper cooling of cows
Control the amount of polyunsaturated fatty acids in the diet
Balance dietary carbohydrates
Buffer and alkalinizing agents
Ionophores
Feeding Management
Transport
of milk components not synthesized in the
epithelial cells
Some milk components pass across the epithelial cell barrier
essentially unchanged:
Immunoglobulins
Serum albumim
Paracellular pathways for transport components
This occurs when substances and molecules are allowed to pass
through the junctional complexes.
This condition resulting in a change in electrical conductivity of
milk (used in detection of mastitis)
This condition increase concentration of lactose and other milk
components in the blood.
Mammary blood supply
Milk synthetic rate is depended to the rate of blood flow to the
mammary gland.
There is a 2-6 fold increase in blood flow in the mammary gland
staring 2-3 days prepartum.
The efficiency of extraction of the components from the blood
while it passes through the udder is very important.
Mammary blood supply
Mammary lymphatic network
The extracellular fluids are drained from the tissue and
conducted back to the circulatory system via the lymphatic
network.
The lymphatics contain concentrated areas of leukocytes
(particularly lymphocytes and macrophages) in lymph nodes
The lymphatic network serves to transport some things in the
body (vitamin K, lipids absorbed in the intestine).
Mammary lymphatic network
Mammary nervous system
The efferent innervation of the mammary gland is entirely
sympathetic in origin.
The efferent nerves innervate the muscle fibres within the
connective tissue surrounding the lobules, lobes, and the blood
vessels.
Mammary nervous system
Innervation of the udder is sparse compared with other tissues.
Sensory (afferent) nerves are involved in milk ejection and found
in the teats and skins.
Similar to other skin glands, there is no parasympathetic
innervation to the gland.
Sympathetic nerves are associated with the arteries but not with
alveoli.
There is no innervation of the secretory system.
Few nerves go to the interior of the udder.
Milk ejection
Oxytocin has the main role in milk ejection.
Oxytocin causes contraction of the myoepithelial cells.
Without frequent emptying of the mammary gland, milk
synthesis will not persist in spite of adequate hormonal status.
The time from the start of a tactile stimulation until the
occurrence of milk ejection spans between 40 s to >2 min and
increases with decreasing degree of udder filling.
Milk ejection
Milk ejection reflex actually is a neuroendocrine reflex.
The reflex has two pathways:
Afferent Pathway (neural)
Efferent Pathway (hormonal, blood-borne)
Milk ejection
Other mechanisms of milk ejection:
Myoepithelial cells will also contract in response to vasopressin
(ADH or antidiuretic hormone).
Visual or auditory stimuli can cause milk ejection. Milk ejection is
a condition response.
Stimulation of the genital tract such as vaginal distention causes
release of large amounts of oxytocin.
The mechanical tap stimulus does not involve oxytocin.
Effect of stress on milk ejection
Various stressful stimuli that inhibit milk ejection are associated
with increased activity of the sympathetic nervous system.
Role of autonomic nervous system
Sympathetic
nerves,
sympathetic nerves are:
Epinephrine
Norepinephrine
The
neuroendocrine
components
of
Colostrum production
In mammals, colostrum is known to contain larger amounts of
specific proteins than milk:
Immunoglobulins
Antimicrobial peptides (eg, lactoferrin and lactoperoxidase)
Other bioactive molecules, including growth factors
Under certain circumstances, the maternal antibodies may also
attack and destroy the newborns red blood cells, thereby causing
fatal incompatability reactions known as hemolysis of the newborn
or neonatal isoerythrolysis (NI).
Immunoglobulin transport in the mammary gland
The IgG1 and IgG2 make up the majority of immunoglobulin in
cow colostrum and primarily come from the blood.
Most of the IgA and IgM that are transported into colostrum are
synthesized by the plasma cells (B lymphocytes) that reside in the
mammary tissue.
Transport of the IgGs and the IgA/IgM occurs through the
epithelial cells by a process involving small transport vesicles.
Intestinal protective factors in colostrums and milk
The gastrointestinal tract is constantly under attack from acid,
proteolytic enzymes, and ingested noxious agents, such as aspirin
or alcohol.
The presence of multiple defense mechanisms— including the
mucus-bicarbonate layer in the stomach, a rapid mucosal turnover,
and a good blood supply—ensure that the mucosa remains intact
most of the time.
Bioactive factors in colostrums and milk
Colostrum and milk contain many factors that can influence cell
growth, differentiation, and function:
Glutamine
Polyamines
Nucleotides
Galactopoeisis
Galactopoeisis is the maintenance of lactation once lactation has
been established.
Two key interrelated components contribute to the maintenance
of lactation:
Galactopoietic hormones
Prolactin
Growth hormone
Removal of accumulated milk
Galactopoeisis
Local mammary factors play a major role in regulating milk
secretion in many species.
Feedback inhibitor of lactation (FIL) found in milk. FIL is
thought to be produced by the mammary cells as they synthesize
and secrete milk.