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Embryology
Embryology
Provides the efferent (motor) pathway linking areas of the brain concerned with the
regulation of the internal environment to specific effectors such as blood vessels, glands
and the heart
Axons of pre-ganglionic fibres emerge via the ventral root of the spinal cord together with
somatic motor fibres *
Shortly after the dorsal and ventral roots of the spinal cord fuse, sympathetic pre-ganglionic
fibres leave the spinal nerve trunk and travel to sympathetic ganglia via white rami
communicantes *
Sympathetic pre-ganglionic fibres synapse with post-ganglionic neurons in the sympathetic
ganglia *
Fibres entering the sympathetic ganglia high up in the thorax may travel up the sympathetic
trunk to cervical ganglia where they synapse with post-ganglionic neurons
Pre-ganglionic fibres may pass through the sympathetic ganglia without synapsing - these
myelinated fibres form splanchnic nerves of which there are three - greater splanchnic
nerve (5th - 9th thoracic ganglia - pierce the diaphragm and synapse in the celiac ganglion),
lesser splanchnic nerve (10thand 11th thoracic ganglia, pierce the diaphragm and synapse
with cells in the lower part of the celiac plexus) and lowest splanchnic nerve (12 th thoracic
ganglion, may be absent, pierces the diaphragm and synapses with cells in the renal
plexus) *
A few pre-ganglionic fibres travelling in the greater splanchnic nerve synapse directly with
cells in the adrenal medulla *
Sympathetic post-ganglionic fibres travel to target organs via grey rami communicantes and
segmental spinal nerves *
Sympathetic pre-ganglionic fibres may therefore terminate in the ganglion of the same
segment or pass to another ganglion in the sympathetic chain or to pre-vertebral ganglia
such as the celiac ganglion *
Sympathetic pre-ganglionic fibres are myelinated (white) while post-ganglionic fibres are
non-myelinated (grey) *
With the exception of the cervical region, sympathetic ganglia are distributed segmentally as
far as the coccyx *
The cervical sympathetic chain is represented by the superior, middle and inferior cervical
ganglia which supply the eyes, lacrimal, salivary glands (superior), heart and respiratory
tract (middle & inferior plus upper 3-4 thoracic ganglia) *
Sympathetic pre-ganglionic fibres to the abdominal organs form the splanchnic nerves
which are distributed to the celiac, superior and inferior mesenteric plexuses *
All pre-ganglionic fibres secrete acetylcholine *
1
AFFERENT myelinated fibres travel from the viscera through the sympathetic ganglia
without synapsing, enter the spinal nerve via the white rami communicantes and reach their
cell bodies in the posterior (dorsal) root ganglion of the corresponding spinal nerve. The
central axon then enters the spinal cord and may form the afferent component of a local
reflex arc or pass to higher autonomic centres in the brain *
Derived embryologically from the neuro-ectoderm (neural crest). During development, chromaffin
cells are widely scattered within the embryo but in the adult can only be found in the adrenal medulla*
Innervated by pre-ganglionic fibres from the thoracic spinal cord via the splanchnic nerves. These
fibres synapse directly with the chromaffin cells which are homologous to sympathetic post-ganglionic
neurons and can generate action potential *
Sympathetic pre-ganglionic fibres are myelinated while post-ganglionic fibres are non-myelinated. All
pre-ganglionic fibres secrete acetylcholine *
2
Adrenal medulla Secretion of adrenaline & No innervation
noradrenaline
There are thoracic, lumbar, sacral, and pelvic splanchnic nerves. "Splanchnic" refers to
nerves that supply viscera. *
Thoracic, lumbar and sacral splanchnic nerves emerge from sympathetic ganglia and
carry sympathetic fibers*
Pelvic splanchnic nerves arise from the ventral (anterior) primary rami of S2, 3, 4. *
These are the ways in which parasympathetic neurons reach the hypogastric plexus,
and therefore the pelvic viscera and distal colon.*
The parasympathetic part of the autonomic nervous system is the "craniosacral" part.
Parasympathetic innervation to most of the gut comes from the "cranio-" half of that, i.e., the
vagus nerve. The rest, to colon distal to the splenic flexure and to pelvic viscera, is from the
"-sacral" half, via the pelvic splanchnic nerves.
3
AFFERENT / EFFERENT FIBRES *****
Each spinal nerve is connected to the spinal cord by two roots - anterior (ventral) and
posterior (dorsal) roots
The anterior root contains nerves carrying impulses AWAY FROM the CNS - EFFERENT
fibres. Efferent fibres to skeletal muscles are called motor fibres - cell bodies located in the
anterior grey horn of the spinal cord *
Posterior roots contain fibres carrying impulses TO the CNS - AFFERENT fibres -
conveying information about sensation of touch, pain, temperature, vibration - SENSORY
fibres. Cell bodies are located in the posterior / dorsal root ganglion with a peripheral axon
to the viscera and a central axon to the CNS *
At each intervertebral foramen, the anterior and posterior roots unite to form a spinal nerve *
On emerging from the foramen, each spinal nerve divides into a large anterior ramus and a
smaller posterior ramus which passes posteriorly to supply the skin and muscle of the back.
The anterior ramus supplies the antero-lateral body wall and limbs *
At the root of the limbs, the anterior rami come together to form complex nerve plexuses
Secretion mediated directly by the activity of the splanchnic nerves and the gland
becomes non-functional if these nerves are cut
Secretion increased in stressful situations: *
1) Exercise
2) Hypoglycaemia
3) Cold
4) Haemorrhage
5) Hypotension
4
True False
c. Dilator fibres to the sphincter pupillae
True False
d. Constrictor fibres to the small intestine
True False
5
c. Contain adrenergic pre-ganglionic nerve terminals
True False
d. Receive non-myelinated pre-ganglionic fibres through the grey rami communicantes
True False
6
True False
d. Increases during acute haemorrhage
True False
7
d. Constrictor fibres to the coronary arteries
True False
a. Ejaculation
True False
b. Increased secretion by eccrine sweat glands
True False
c. Viscous secretion by the salivary glands
True False
d. Renal vasoconstriction and decreased urine out-put
True False
The Zygote begins a series of mitotic divisions within 24h of fertilization - cleavage. The
number of cells increases but the size of the embryo remains constant within the zona
pellucida - results in a decrease in mean cell volume. By the 32 cell stage, the embryo is
called a morula *
The cells (blastomeres) become segregated into the inner cell mass which forms the
embryo proper and the outer cell mass which forms the placenta and membranes *
Fluid collects between the cells of the inner cell mass, forming a blastocyst cavity - day 4 of
development
The blastocyst enters the uterine cavity ~day 4, hatches from the zona Pellucida *
Appears during the third week and is clearly visible by day 15-16
Narrow groove on the epiblast with slightly bulging sides
Cephalic end forms primitive node - elevated area surrounding a small pit, the primitive pit
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ells from the epiblast migrate towards the primitive streak, detach from and slip underneath
the epiblast to form a third layer between the epiblast and hypoblast - the intra-embryonic
mesoderm
These cells also form most, or all of the intra-embryonic endoderm
This process is known as gastrulation, at the end of which the remaining epiblast forms the
ectoderm
The ectoderm and endoderm remain in contact, without intervening mesoderm in two
regions - the buccopharyngeal membrane and the cloacal membrane
Ectodermal cells at the edge of the neural grove, become detached and located initially
between the closed neural tube and the overlying ectoderm *
Contribute to several important structures including
1) The truncoconal septum of the heart - migrate via pharyngeal arches. Form the connective
tissue , muscle and parasympathetic ganglia *
5) Sympathetic chain *
6) Parasympathetic ganglia *
7) Melanocytes *
9) Odontoblasts *
9
SPERMATOGENESIS
SPERMATOZOON *****
OOGENESIS *****
Begins during intra-uterine life. The primordial germ cells undergo mitosis and then
differentiate into oogonia *
By the 5th month in-utero, the number of oogonia is at a maximum - 7 million *
Oogonia enlarge into primary oocytes. These are surrounded by flattened follicular
cells forming primordial follicles
Primary oocyte enters prophase of meiosis I and becomes arrested at the dictyotene
stage. Meiosis I is not completed until puberty *
10
Primordial follicles begin to degenerate such that at birth, there are 700,000 - 2
million, and at puberty there are 40,000 *
Several primordial follicles (10-12) begin to mature with each menstrual cycle and one
dominant follicle becomes selected by mechanisms which are not fully
understood *
Follicular cells become cuboidal, forming the primary follicle. A layer of acellular
mucopolysaccharide becomes deposited between the developing oocyte and the
follicular cells, forming the zona pellucida
Resumption of meiosis is triggered by the ovulatory LH / FSH surge with formation of
the secondary oocyte with most of the cytoplasm and the first polar body *
Ovulation occurs the moment the secondary oocyte shows spindle formation and the
second meiotic division is only completed if fertilisation occurs *
The polar body also completes meiosis II, resulting in one definitive oocyte and three
polar bodies *
FERTILIZATION *****
The gonads do not develop male / female differentiation until the end of the 6th week *
Primordial germ cells develop from the yolk sac endoderm and migrate via the dorsal
mesentery of the hindgut to reach the gonadal ridge in the 6th week *
Failure of migration results in gonadal agenesis
The gonadal ridge develops medial to the mesonephros by proliferation of the coelomic
epithelium and condensation of the underlying mesenchyme, forming the primitive
sex cords
The sex-determining region of the Y chromosome has a testis determining factor,
transcription of which triggers male development *
Primitive sex cords proliferate into medullary cords with Sertoli cells which produce
Mullerian Inhibiting Factor which acts on the ipsilateral Mullerian tube only, causing
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degeneration. Mullerian remnants in the male include the appendix testis and the
Utriculus prostaticus *
Leydig (Interstitial) cells develop from the mesenchyme and produce testosterone,
influencing development of the duct system and external genitalia. The enzyme 5-
alpha reductase is essential for the development of the external genitalia but not for
the development of the duct system *
The distal excretory tubules of the mesonephros persist, forming the ductuli efferentes while
the mesonephric duct elongates and forms the eipdidymis and vas deferens *
The medullary cords remain solid until puberty when they become canalised, forming the
seminiferous tubules *
The first meiotic division and spermatogenesis do not commence until puberty *
The seminal vesicles develop as outgrowth of the mesonephric duct while the prostate and
bulbo-urethral glands develop from the prostatic urethra
During the 7th week, the testis begins to detach from the surrounding mesenchyme and
develops a tough connective tissue coat - tunica albuginae
A thickening of mesenchyme, the Gubernaculum testis runs from the testis to the genital
swellings
As a result of the growth of the body relative to the gubernaculums, the testis descends to
lie in the inguinal region during the 12th week *
During this process, an evagination of the coelomic epithelium forms the processus
vaginalis which follows the descent of the testis
The final descent of the testis into the scrotum occurs in the 7th-9th months*
The processus vaginalis is obliterated during the first year of life, forming the tunica
vaginalis
The primitive sex cords disintegrate and the centre of the developing ovary becomes
replaced by a vascular stroma, forming the ovarian medulla *
The surface epithelium continues to proliferate, producing cortical cords which split into
isolated cell clusters surrounding the primitive germ cells
The primitive germ cells differentiate into oogonia which undergo several mitotic divisions.
The number of oogonia reaches its maximum (~7 million) during the 5th month after
which degeneration begins *
The oogonia become surrounded by a layer of follicular cells from the surface epithelium
and develop into primary oocytes. Primary oocytes surrounded by follicular cells form
primordial follicles
The primary oocytes duplicate their DNA and enter the first meiotic division and become
arrested during Prophase I until puberty
There are 700,000 - 2 million primary oocytes at birth and 40,000 at puberty*
The descent of the ovary is less extensive, coming to lie within the pelvis. The round
ligaments of the ovary and uterus are the equivalent of the gubernaculums testis *
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PHARYNGEAL ARCHES
First arch - cartilage forms incus and malleus, mesenchyme gives rise to the maxilla,
mandible, zygomatic bone and part of the temporal bone
Second arch - cartilage forms the stapes and styloid process of the temporal bone and part
of the hyoid bone
Pharyngeal arches develop during the 4th-5th weeks. The arches receive neural crest cells
which form the skeletal components while the mesenchyme forms the muscle.
PHARYNGEAL POUCHES
Third pharyngeal pouch - inferior parathyroid gland and the thymus gland
The thyroid gland develops from an epithelial proliferation in the floor of the pharynx
(represented by the foramen cecum) and subsequently descends in front of the
pharyngeal gut, hyoid bone and laryngeal cartilages to reach its final position in the
7th week.
The first pharyngeal cleft forms the external auditory meatus. The others do not form any
definitive structures.
13
Each branchial arch receives its own artery during the 4-5th week - aortic arches
The first aortic arch disappears apart from a small part - maxillary artery
Third arch - common carotid artery and first part of internal carotid artery
The forth arch on the left forms part of the arch of the aorta. Right - proximal part of right
subclavian artery
Vitelline veins - carry blood from the yolk sac to the sinus venosus - develops into the post-
hepatic portion of the inferior vena cava, the portal vein and superior mesenteric vein
Umbilical veins - the proximal part of both umbilical veins and the remainder of the right vein
later disappear so that the left vein is the only one to carry blood from the placenta to the
liver
Cardinal veins: anterior cardinal veins anastomose to form the brachiocephalic vein. The
superior vena cava is formed from the right common cardinal vein and the proximal portion
of the right anterior cardinal vein. Anastomosis of the sacrocardinal veins forms the
common iliac veins. *
Extra-embryonic mesoderm
Two umbilical arteries and one umbilical vein with in the umbilical cord *
The umbilical vein carries oxygenated blood from the placenta to the fetus *
Oxygenated blood in the umbilical vein bypasses the liver, draining into the inferior vena
cava via the ductus venosus *
14
The obliterated umbilical vein forms the ligamentum teres while the obliterated ductus
venosus forms the ligamentum venosum. The ductus venosus is formed when a direct
communication develops between the left umbilical vein and the hepatocardiac channel *
Oxygenated blood entering the right atrium from the inferior vena cava is directed into the
left atrium through the foramen ovale *
Desaturated blood from the superior vena cava flows via the right ventricle to the pulmonary
artery *
Oxygenated blood then enters the aorta via the left ventricle
Some blood from the right atrium leaves via the pulmonary artery - mainly return from the
superior vena cava. As the pulmonary circulation has high resistance, the blood enters the
descending aorta through the ductus arteriosus which connects the pulmonary artery to the
aorta *
From the aorta, blood is supplied to the fetus, deoxygenated blood returns to the placenta
via two umbilical arteries - oxygen saturation here is ~58% *
The proximal part of the umbilical arteries form the superior vesical arteries. The obliterated
distal part form the medial umbilical ligaments *
Oxygenated and deoxygenated blood become mixed at the following points *
1) The liver, mixing with blood returning via the portal system
2) The inferior vena cava, mixing with venous blood from the lower extremities
3) The right atrium, mixing with venous blood from the superior vena cava
4) The descending aorta, mixing with blood from the ductus arteriosus
Blood in the ascending aorta has the highest oxygen saturation and supplies the heart and
brain *
Blood in the right ventricle is therefore mostly de-oxygenated blood from the superior vena
cava. Oxygenated blood passes directly into the left atrium via the foramen ovale and does
not enter the right ventricle *
Closure of the umbilical vein and ductus venosus - occurs shortly after closure of the
umbilical arteries. The umbilical vein forms the Ligamentum teres hepatis in the falciform
ligament while the ductus venosus forms the ligamentum venosum *
Loss of umbilical blood supply reduces venous return via the inferior vena cava - fall in
pressure *
Closure of the Ductus arteriosus - dependent on a rise in PaO2. Prostaglandin F, low
calcium, low glucose and high pulmonary pressure keep ductus arteriosus open in utero.
Hypoxia can cause ductus to become patent *
15
Closure of the foramen ovale - caused by decreased right atrial pressure and increased left
atrial pressure. Held shut by haemodynamic forces only for the first few weeks. Remains
potentially patent in 25-30% of normal adults *
The Mullerian ducts persist in the female while the Mesonephric ducts degenerate. The
Mullerian duct gives rise to the Fallopian tube, body of the uterus, cervix and
upper third of the vagina *
The Mullerian ducts fuse and grow into the urogenital sinus, forming the sinovaginal
bulb which proliferates to form a solid plate of tissue between the uterus and
the urogenital sinus. This becomes canalised at the end of the 5th month to
form the vagina *
The epoophron and paroophron and Gartner?s cyst are remnants of the Mesonephric
duct *
Urogenital septum divides the cloaca into the anorectal canal and the
primitive urogenital sinus - endodermal in origin *
The upper part of the urogenital sinus forms the bladder (except the trigone)
which is initially continuous with the allantois (obliterated to form the
urachus) *
The narrow pelvic part of the urogenital sinus forms the prostatic and
membranous urethra in the male *
Cloacal folds develop on either side of the cloacal ggmembrane during the
3rd week and fuse to form the genital tubercle cranial to the cloaca
With partitioning of the cloaca, the folds form the urethral folds anteriorly and
the anal folds posteriorly
The male / female genitalia are indistinguishable at the end of the 6th week *
16
The urethral groove closes over at the end of the 12th week, forming the penile
urethra. The lining is endodermal in origin. The external urethral meatus is formed
from ectodermal cells from the tip of the glans which penetrate inwards, forming a
cord which is later canalised *
The genital swellings, which form on either side of the urethral swellings form
the scrotum in the male and the labia majora in the female
In the female, there is only slight elongation of the genital tubercle, forming the
clitoris. The urethral folds do not fuse and form the labia minora. The urogenital
groove is open to the surface and forms the vestibule *
The epithelium of the male and female urethra is endodermal (urogenital sinus)
in origin apart from the most distal tip in the male which is ectodermal in origin.
The proximal part of the urethra in the female forms the urethral and paraurethral
glands and greater vestibular (Bartholin's) glands *
FOREGUT
The tracheo-bronchial diverticulum develops on the ventral wall of the foregut during the 4th
week and then becomes separated from it by the tracheo-oesophageal septum. The
respiratory primordium is therefore developed from the foregut
The stomach develops as a dilatation and rotates 90 degrees clockwise along its
longitudinal axis. The left side comes to lie anteriorly such that the left vagus nerve forms
the anterior vagal trunk
The liver develops as an outgrowth of the endoderm of the distal foregut, as does the gall
bladder, bile and cystic ducts. The haemopoietic cells, Kupffer cells and connective tissue
are derived from the mesoderm of the septum transversum
The pancreas develops from a dorsal and a ventral pancreatic bud from the distal foregut.
With rotation of the duodenum, the ventral pancreatic bud migrates dorsally.
The dorsal bud forms the head, body and tail while the ventral bud forms the uncinate
process of the pancreas.
The main pancreatic duct is formed from the distal part of the dorsal pancreatic duct and
the entire ventral duct. Exocrine pancreatic glands are derived from the foregut endoderm.
Insulin secretion begins in the fifth month. The origin of the Islets is controversial.
MIDGUT
Begins distal to the entrance of the bile duct into the duodenum and ends at the junction
between the proximal 2/3 and distal 1/3 of the transverse colon
17
During the 6th week, the midgut herniated into the extra-embryonic coelom in the umbilical
cord and rotates 90 degrees counter clockwise along the axis of the superior mesenteric
artery when viewed from in front
The apex of the intestinal loop remains in open connection with the yolk sac through the
vitelline duct, remnants of which form the Meckel?s diverticulum
During the 10th week, the midgut retracts into the abdomen, undergoing a further 180
degrees rotation
HINDGUT
Extends to the upper two thirds of the anal canal. The distal third of the anal canal is
formed from the ectoderm of the cloaca and the junction is marked by the pectinate line
The urogenital septum divides the cloaca into an anterior urogenital sinus (forming the
bladder, pelvic urethra and external genitalia) and the anorectal canal
The gut forms a solid cord during the 6th week with re-canalisation during the 7th - 8th
weeks
The smooth muscle and mesentery of the gut is derived from mesoderm
Pronephros
Vestigial - develops from cervical nephrotomes, disappears by the end of the 4th
week
Mesonephros *****
Develops from the intermediate mesoderm on either side of the upper thoracic
and lumbar vertebrae during the 4th week *
The mesonephros is functional between the 6th - 10th week, producing urine.
The mesonephros regresses after 10 weeks in the female *
In the male, the mesonephric duct and a few modified mesonephric tubules
persist forming the ductus deferens and ductuli efferentes of the testis. In the
female, Gartner?s duct cysts, epoophron and paroophron are mesonephric
remnants *
Mullerian remnants in the male include the appendix testis and the Utriculus
prostaticus *
Develops in the 5th-15th week from the metanephric mesoderm in the sacral
region *
Ureters - develop from the ureteric bud, an outgrowth of the mesonephric duct
close to its opening into the cloaca. Grows into the metanephric mesoderm,
successive divisions forming the renal pelvis, major and minor calyces and
collecting tubules *
The metanephric mesoderm develops into the excretory units under inductive
influence of the ureteric bud, forming the Bowman’s capsule and excretory tubules.
If the ureteric bud is missing, the kidney does not develop *
Metanephric development occurs in the pelvis and the kidney later ascends to its location
in the abdomen by the 10th week. Failure of this ascent leads to a pelvic kidney *
The cloaca becomes divided into the anorectal canal and the primitive urogenital
sinus during the 4th - 7th week by the urorectal septum *
The cloacal membrane is divided into the anal and urogenital membranes
The upper part of the primitive urogenital sinus forms the urinary bladder which
is initially continuous with the allantois *
The distal portions of the mesonephric ducts are absorbed into the urinary
bladder such that the ureters come to open directly into the bladder. With the
ascent of the kidneys, the mesonephric ducts come to open into the prostatic
urethra as the ejaculatory ducts *
The part of the mucosa of the bladder derived from the incorporation of the
mesonephric ducts is mesodermal in origin and forms the TRIGONE. The
mesodermal lining of the trigone is later replaced by cells of endodermal origin
such that at birth, the bladder is completely lined by cells of endodermal origin *
The narrow pelvic part of the urogenital sinus forms the prostatic and
membranous part of the urethra in the male (membranous urethra in the female).
Outgrowths of the endoderm of the prostatic urethra into the surrounding
mesoderm form the prostate gland (urethral and para-urethral glands in the
female)*
The definitive urogenital sinus develops into the distal urethra and external
genitalia *
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a. Appendix of the testis
True False
b. Efferent ductules of the testis
True False
c. Gartnet?s duct cyst
True False
d. Prostatic utricle
True False
a. Blood flows from the left atrium into the right atrium through the foramen ovale
True False
b. The resistance within the pulmonary vessels is high
True False
c. Oxygenated blood from the placenta is mixed with deoxygenated blood within the
right atrium
True False
d. Oxygenated blood from the placenta is mixed with deoxygenated blood in the inferior
vena cava
True False
20
Question 5: In the fetal circulatrion
a. Blood from the inferior vena cava is largely directed through the foramen ovale
True False
b. Most blood from the superior vena cava passes directly from the right to the left
atrium
True False
c. Out-put of the right ventricle is greater than that of the left ventricle
True False
d. Blood in the descending aorta is more oxygenated than that in the ascending aorta
True False
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Question 9: With respect to the development of the external genitalia
Question 10: With respect to the development of the female gonadal system
a. The ductus venosus delivers blood directly into the superior vena cava
True False
b. The umbilical artery returns blood from the placenta
True False
c. The ductus arteriosus carries blood to the lungs
True False
d. Blood returning from the lungs is 90% saturated with oxygen
True False
Question 12: The following are derived from the urogenital sinus
a. Paraurethral glands
True False
b. The greater vestibular glands
True False
c. Gartner?s duct
True False
d. Urachus
True False
22
a. There is an increase in the number of nephrons in each kidney after birth
True False
b. The mesonephric kidney develops in the pelvis
True False
c. The metanephric kidney develops in the pelvis and ascends into the abdomen
True False
d. The ureters are endonermal in origin
True False
a. The ureter develops as an outgrowth of the mesonephric duct close to its entrance
into the cloaca
True False
b. The ureter develops as an outgrowth of the paramesonephric duct close to its
entrance into the cloaca
True False
c. The ureteric bud gives rise to the renal collecting tubules
True False
d. The metanephric mesoderm gives rise to the excretory units of the kidney
True False
Question 15: With respect to the development of the female gonadal system
· Later formed from transudate from fetal skin and umbilical cord and diffusion across
the amniotic membrane *
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· Fetal skin becomes keratinised in the second trimester and amniotic fluid is mainly
formed from fetal urine and lung secretions. The term fetus passes 500-700ml urine
per day *
· Cells: at term, contains fetal epithelial cells, amniocytes and dermal fibroblasts.
Epithelial cells and amniocytes grow poorly in culture. Glial cells present if neural
tube defect *
· Protein: concentration increases with gestation but plateaus after 30 weeks. Mainly
albumin and globulins. Also contains AFP (1/10TH concentration in fetal blood -
rises until 12 weeks then declines). Virtually no fibrinogen. *
· Lipids: mainly free fatty acids. Also contains phospholipids, cholesterol and lecithin
(secreted by lungs during maturation) *
Fetal weight is related to placental weight. The fetal:placental weight ratio increases with
gestation age. At term, fetal weight is 5-6x placental weight. At 32 weeks gestation, fetal
weight ~ 4x placental weight
During implantation, the outer layer of the blastocyst proliferates to form the outer cell mass
from which the trophoblast and the placenta develop
The trophoblast differentiate into an inner layer of large clear mononuclear cells, the
cytotrophoblast and an outer layer of multi-nucleated cells, the syncytiotrophoblast which
forms a true syncytium
24
DNA synthesis and mitosis occurs only in the cytotrophoblast layer. The
syncytiotrophoblast is formed by fusion of cells from the cytotrophoblast layer *
Lacunae appear within the syncytiotrophoblast between days 10 - 13 post-ovulation and are
the precursors of the intervillous space. The lacunae are separated by columns of
syncytiotrophoblast called primary villous stems (These are not villi)
Primary villous stems become infiltrated by cytotrophoblasts between days 13-21 post-
ovulation
Villous stems are subsequently infiltrated by extra-embryonic mysenchyme which
differentiates into fetal blood vessels
The distal parts of the villous stems are not vascularised. Here, cytotrophoblasts proliferate
and spread laterally to form a cytotrophoblastic shell, splitting the syncytiotrophoblast into a
definitive syncytiotrophoblast on the fetal side and the peripheral syncytium on the decidual
side which degenerates and is replaced by fibrinoid material (Nitabuch's layer)
Sprouts extend from primary villous stems, initially made up of syncytiotrophoblast and
then infiltrated by cytotrophoblast and mesenchyme - these are primary stem villi and the
placenta is a true villous structure by day 21 of gestation. These villi grow and divide into
secondary, tertiary and terminal villi
The villi oriented towards the uterine cavity degenerate between day 21 and the 4th month
to form the chorion laeve. The overlying decidua degenerates and the chorion laeve comes
in contact with the deciduas of the opposite uterine wall
The rest of the villi form the chorion frondosum which develops into the definitive placenta
Division and modification of the villous tree continues until term. First trimester villi are
larger, have a complete layer of cytotrophoblasts and have a loose mysenchymal core
which is vascularised towards the end of the first trimester
At term, the villi are smaller, cytotrophoblasts are few in number, the syncytiotrophoblast is
irregularly thinned. Fetal vessels are sinusoidal and occupy most of the villous core and lie
close to the syncytiotrophoblast, forming vasculusyncytial membranes which maximise
materno-fetal transfer.
Sometimes, the syncytiotrophoblast nuclei appear in clusters called syncytial knots - more
common in placentas from IUGR / pre-eclamptic pregnancies *
Maternal blood is separated from fetal blood by the syncytiotrophoblast and the fetal
capillary endothelium *
OESTROGENS *
Mainly oestriol, but also oestradiol and oestrone in smaller amounts. Oestriol is
produces from DHES-sulphate from fetal zone of the fetal adrenal gland and also
from the maternal adrenals. Fetal DHEA-S is initially hydroxylated by the fetal liver
PROGESTERONE *
HCG
Human Placental Lactogen - has growth-hormone -like effects and decreases insulin-
sensitivity. *
Human chorionic thyrotropin and virtually all of the hypothalamic releasing hormones
Activin levels increase with gestation age and a marked increase occurs with the
onset of labour and in pre-eclampsia
PLACENTAL TRANSFER
Feto-placental blood-flow
Charge of solute
Protein binding
O2 / CO2 *****
Small lipid soluble molecules - transfer is by simple diffusion and rate of transfer
is dependent on maternal / fetal concentrations (partial pressure), rate of blood flow
and surface area
The fetal O2 - Hb dissociation curve lies to the left of the maternal curve - fetal
red cells have greater affinity for O2 - see respiratory physiology
A hypoxic fetus develops both respiratory and metabolic acidosis ? CO2 excretion
is impaired and anaerobic glucose metabolism results in lactate production
WATER TRANSFER
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3-4L of water is exchanged per hour between the mother and the fetus, placenta
and amniotic fluid
Fetal amino acid concentrations are generally higher than maternal levels *
Transfer of amino acids from the mother to the fetus is therefore against a
concentration gradient and energy (ATP) is required for this process *
Total and ionised calcium concentration - higher in fetal than maternal plasma.
Calcium transfer across the microvillous plasma membrane is magnesium
dependent and dependent on 1,25-dihydroxycholecalciferol *
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PTH, Calcitonin Not transferred
IgM No transfer
Free fatty acids Very limited transfer - essential fatty acids only
ACTH No transfer
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Question 1: With respect to the transfer of solutes across the placenta
Question 3: With respect to the transfer of water between the mother and the fetus
a. 3-4L of water are exchanged between the maternal and fetal compartments per 24h
True False
b. Water crosses the placenta by osmosis
True False
c. Net water accumulation by the fetus stops at 37 weeks gestation
True False
d. Maternal dehydration has no impact on net fetal water accumulation
True False
a. Trophoblasts initially invade the uterine spiral arterioles at 16-18 weeks gestation
True False
b. Villous cytotrophoblasts form a layer beneath the syncytiotrophoblast in early
pregnancy
True False
c. The syncytiotrophoblast is the only cellular layer between maternal and fetal blood
True False
d. Syncytial knots in the placenta are composed of aggregates of cytotrophoblasts
True False
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Question 5: The placenta
Question 6: The composition of amniotic fluid varies as normal pregnancy advances in the
following way
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Question 9: Amniotic fluid
Question 11: With respect to the transfer of electrolytes across the placenta
a. Na+ is taken up across the microvillous plasma membrane through the action of
Na+K+ ATPase
True False
b. The concentration of Na+ is higher within the syncytiotrophoblast than in maternal
plasma
True False
c. The concentration of K+ is lower in maternal plasma than in the syncytiotrophoblast
True False
d. Total calcium concentration is higher in fetal than in maternal plasma
True False
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Question 13: In the human placenta
Question 14: With respect to the transfer of electrolytes across the placenta
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