DEVELOPMENT OF PLACENTA,PLACENTA AT TERM , DECIDUA,PLACENTAL MEMBRANE , PLACENTAL CICULATION,PLACENTAL ENDOCRINE SYNTHESIS,ABNORMAL PLACENTA,FUNCTIONS.
Hemostasis Physiology and Clinical correlations by Dr Faiza.pdf
PLACENTA
1. 1
PLACENTA
• This is a fetomaternal organ.
• It has two components:
– Fetal part – develops from the chorionic sac ( chorion
frondosum )
– Maternal part – derived from the endometrium ( functional
layer – decidua basalis )
• The placenta and the umbilical cord are a transport system for
substances between the mother and the fetus.( vessels in umbilical
cord )
• Function Of The Placenta:
1. Protection
2. Nutrition
3. Respiration
4. Excretion
5. Hormone production
3. Further Development of Chorionic
Villi
Early in the 3rd
week,
mesenchyme growth into the
primary villi forming a core of
mesenchymal tissue. Thus the
Secondary Chorionic Villi are
formed over the entire surface of
the chorionic sac.
Some mesenchymal cells in the
secondary villi differentiate into
capillaries and blood cells
forming the Tertiary Chorionic
Villi.
The capillaries in the villi fuse to
form arteriocapillary networks.
4. The previous formed
arteriocapillary networks
become connected with the
embryonic heart through
vessels which are formed in the
mesenchyme of the chorion and
connecting stalk.
By the end of the 3rd
week,
embryonic blood begins to flow
through the capillaries in the
chorionic villi.
Oxygen & nutrients in the
maternal blood in the intervillous
space diffuse through the walls
of the villi and enter the
embryo’s blood.
Carbon dioxide & waste
products diffuse from blood in
the fetal capillaries through the
wall of the chorionic villi into the
5.
6. 6
DECIDUA
• This is the endometrium
of the gravid (pregnant)
uterus.
• It has four parts:
– Decidua basalis: it
forms the maternal
part of the placenta
– Decidua capsularis:
it covers the
conceptus
– Decidua parietalis:
the rest of the
endometrium
– Decidua reflexa:
– Junction between
capsularis &
parietalis.
7. 7
DEVELOPMENT OF PLACENTA
• Until the beginning of the 8th
week, the entire chorionic
sac is covered with villi.
• After that, as the sac grows,
only the part that is
associated with Decidua
basalis retain its villi.
• Villi of Decidua capsularis
compressed by the
developing sac.
• Thus, two types of chorion
are formed:
– Chorion frondosum
(villous chorion)
– Chorion laeve – bare
(smooth) chorion
– About 18 weeks old, it
covers 15-30% of the
decidua and weights
about 1 6 of fetus
8. 8
DEVELOPMENT OF
PLACENTA
• The villous
chorion ( increase
in number, enlarge
and branch ) will
form the fetal part
of the placenta.
• The decidua
basalis will form
the maternal part
of the placenta.
• The placenta will
grow rapidly.
• By the end of the
4th
month, the
decidua basalis is
almost entirely
replaced by the
fetal part of the
placenta.
9. 9
FULL-TERM
PLACENTA
• Cotyledons –about 15 to 20
slightly bulging villous areas.
Their surface is covered by
shreds of decidua basalis
from the uterine wall.
• After birth, the placenta is
always inspeced for missing
cotyledons. Cotyledons
remaining attached to the
uterine wall after birth may
cause severe bleeding.
• Grooves – formerly occupied
by placental septa
• The fetal part of placenta;
fetal membranes called
developmental adnexa
• Placenta;fetal membranes
which are expelled are called
afterbirth or secundina
Maternal side
10. 10
FULL-TERM PLACENTA
( Discoid shape -500- 600 gm- Diameter 15-20 cm
– Thickness of 2-3 cm)
• Fetal surface:
• This side is smooth
and shiny. It is
covered by amnion.
• The umbilical cord is
attached close to the
center of the placenta.
• The umbilical vessels
radiate from the
umbilical cord.
• They branch on the
fetal surface to form
chorionic vessels.
• They enter the
chorionic villi to form
arteriocapillary-
venous system.
Fetal side
14. 14
PLACENTAL MEMBRANE
knot –syncytiotrophoblast
–Toward end of pregnancy –
phagocytic cells
• This is a composite structure
that consists of the extrafetal
tissues separating the fetal
blood from the maternal
blood.
• It has four layers:
– Syncytiotrophoblast
– Cytotrophoblast
– Connective tissue of
villus
– Endothelium of fetal
capillaries
• After the 20th
week, the
cytotrophoblastic cells
disappear and the placental
membrane consists only of
three layers.
21. When villi persist on the entire
surface of the chorionic sac ,a
thin layer of placenta attaches to
a large area of the uterus …… it
is a membranous placenta.
30. PLACENTAL FUNCTION
• Transfer of nutrients and waste products bn
the mother & fetus.
RESPIRATORY
EXCRETORY
NUTRITIVE
• Produces or metabolizes the hormones &
enzymes necessary to maintain the
pregnancy.
32. Transfer function
• Transport is facilitated by the close
approximation of maternal and fetal
vascular systems within the placenta.
• It is important to recognize that there
normally is no mixing of fetal and maternal
blood within the placenta.
33. • Respiratory function—Intake of o2 &
output of co2 takes place by simple
diffusion.o2 supply to fetus rate of
5ml/kg/min & this achieved with cord flow
of 165-330ml/min.
• Excretory function—waste products urea,
uric acid,creatinine are excreted to maternal
blood by simple diffusion.
34.
35. NUTRITIVE FUNCTION
• Glucose is the major energy substrate
provided to the placenta and fetus. It is
transported across the placenta by facilitated
diffusion via hexose transporters
• Although the fetus receives large amounts of
intact glucose, a large amount is oxidized
within the placenta to lactate, which is used
for fetal energy production.
36. • Amino acid concentrations in fetal blood
are higher than in maternal blood.
Amino acids are therefore transported
to the fetus by active transport .
• LIPIDS—TG`s & FA directly
transported from mother to fetus in early
pregnancy but synthesized in fetus later
in pregnancy. Thus, fetal fat has got
dual origin.
37. • Water & electrolytes—Na,K+,Cl- by
simple diffusion.Ca,Ph,iron by active
transport.
• BARRIER FUNCTION:-Protective
barrier to the fetus against noxious
agents circulating in maternal blood.
(High MW >500daltons.
38. IMMUNOLOGICAL
FUNCTION
• Fetus & placenta contain paternally determined
antigens,foreign to the mother . Inspite of this
,no evidence of graft rejection. Probably:
1. Fibrinoid & sialomucin coating of trophoblast
may suppress the troblastic antigen.
2. Placental hormones ,steroids, HCG have got
weak immunosuppressive effect, may be
responsible for producing sialomucin.
39. 3.Nitabuch`s layer which intervenes bn
decidua basalis &cytotrophoblast probably
inactivates the antigenic property of tissue.
4.There is little HLA & blood group antigens on
trophoblast surface. so antigenic stimulus is
poor.
5. Production of block antibodies by mother
,protects fetus from rejection.
40. • ENDOCRINE—hormones secreted
internally.
• HORMONE--Any organic chemical that is
secreted by a gland into the circulatory
system and is transported to some target
organ. The target may be either peripheral
tissue (such as muscle or other gland) or
brain.
41. Fetal, placental & maternal compartments
form an integrated hormonal unit
The feto-placental-maternal (FPM) unit
creates the
Endocrine Environment
that maintains and drives the processes of
pregnancy and pre-natal development.
43. To understand the FPM one should know:
1. The major hormones involved:
hCGn
Progesterone
Estrogen
Human Chorionic Somatomammotropin (hCS)
(placental lactogen)
2. How the FPM compartments work together
to produce the steroid hormones
3. The transfer of hormones between
the FPM compartments.
44.
45. Human Chorionic Gonadotropin (hCG)
• PREGNANCY HORMONE---
glycoprotein
• Half life –24hrsof hCG
• Levels peak at 60-70 days then remain at a low
plateau for the rest of pregnancy.
• Placental GnRH have control of hCG.
• FUNCTIONS:
1. RESCUE &MAINTENANCE of function of
corpus luteum.
46. • Prevents degeneration of corpus luteum
• Stimulates corpus luteum to secrete E + P which,
in turn, stimulate continual growth of
endometrium.
2.hCG stimulates leydig cells of male fetus to
produce testosterone in conjunction with fetal
pituitary gonadotrophins.Thus indirectly involed
in development of external genitalia.
3. Suppresses maternal immune function
& reduces possibility of fetus immunorejection
47. Human Chorionic Somammotropin (hCS)
or Placental Lactogen
• Structure similar to growth hormone
• Produced by the placenta
• Levels throughout pregnancy
• Large amounts in maternal blood but
DO NOT reach the fetus
48. Human Chorionic Somammotropin (hCS)
or Placental Lactogen
• Biological effects are reverse of those of insulin:
utilization of lipids;
• make glucose more readily available to fetus,
and for milk production.
• hCS levels proportionate to placental size
• hCS levels placental
insuffiency
49. Estrogen (E)
• FORMS-estriol,estradiol &estrone .
• Estriol most important .
• Levels increase throughout pregnancy
• 90% produced by placenta.
(syncytiotrophoblast)
• Placental production is transferred to both
maternal and fetal compartments
50.
51. • Two of the principle effects of placental
estrogens are:
• Stimulate growth of the myometrium and
antagonize the myometrial-suppressing activity of
progesterone. In many species, the high levels of
estrogen in late gestation induces myometrial
oxytocin receptors, thereby preparing the uterus
for parturition.
• Stimulate mammary gland development.
Estrogens are one in a battery of hormones
necessary for both ductal and alveolar growth in
the mammary gland.
52. Progesterone (P)
• Levels increase throughout pregnancy
• 80-90% is produced by placenta and
secreted to both fetus and mother
53. • Progestins, including progesterone, have two
major roles during pregnancy:
• Support of the endometrium to provide an
environment conducive to fetal survival. If the
endometrium is deprived of progestins, the
pregnancy will inevitably be terminated.
• Suppression of contractility in uterine smooth
muscle, which, if unchecked, would clearly be a
disaster. This is often called the "progesterone
block" on the myometrium. Toward the end of
gestation, this myometrial-quieting effect is
antagonized by rising levels of estrogens, thereby
facilitating parturition.
54. • Progesterone and other progestins also
potently inhibit secretion of the pituitary
gonadotropins luteinizing hormone and
follicle stimulating hormone. This effect
almost always prevents ovulation from
occuring during pregnancy
57. Adrenal Gland Development
• Adrenal Cortex
– Vital to organism survival
– Begins to develop at 4th
week of embryonic life
– Functional around 10th
to 12th
week of embryonic life
– Enzymes necessary for biosynthesis of adrenocortical
hormones do not develop simultaneously
– hCG may have a role in stimulating Adrenocortical
development
• Adrenal Medulla
– Originates from nervous system
– Ganglia of Autonomic Nervous System
58. Fetal Adrenal Cortex Function
– Adrenal Cortex
• Zona Glomerulosa
– Has enzymes to convert Pregnenalone to:
» Progesterone
» Deoxycorticosterone
» Corticosterone
» Aldosterone
• Zona Fasciculata
– Converts Pregnenalone and Progesterone to 17OH-Pre
and 17OH-Pro
– 17OH-Pro is converted to cortisol (major glucocorticoid)
• Zona Reticularis
– Converts 17OH-Pre into DHEA and Androstenedione
(androgens)