Placenta and Implantation Flashcards

1
Q

Describe the main stages in the development of the physical link between mother and fetus.

A

• In the earliest stages of pregnancy the anatomical link between mother and foetus develops through a series of phases. The sequence of events is:

1) Invasion of conceptus to endometrium
2) Decidualisation ie endometrial remodeling including secretory transformation of the uterine glands, influx of specialised uterine natural killer cells, and vascular remodeling.
3) Placentation ie placenta formation

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2
Q

Describe the placental blood supply.

A

• Maternal blood
– Enters placental sinuses/pools via uterine artery.
– Flows through sinuses.
– Exits via uterine veins,

• Foetus blood
– Flows into capillaries of choronic villi via umbilical afteries
– And back to foetus via umbilical vein

(no mixing of the two blood supplies in
health)

• Umbilical cord connects foetus to placenta.

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3
Q

State each of the following occurs, following ovulation.

A
  • Fertilisation occurs : 24 hours post ovulation
  • Transport to uterus: 3 – 4 days
  • Formation of blastocyst: 4.5 days
  • Attachment: 7-9 days
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4
Q

Describe the events occurring to the blastocyst following its formation.

A

END OF WEEK 1 (ATTACHMENT AND IMPLANTATION)

• Day 6/7 the blastocyst leaves the zona pelucida and is bathed by uterine secretions for 2 days:
– progesterone prepares supportive uterine environment increasing glandular tissue
– oestrodiol is required to release the glandular secretion

• Attachment and Implantation:
– very limited time window (has to occur before next menstrual cycle happens)
– complex interactions between trophoblast and maternal epithelial tissue:
a) causes syncytiotrophoblast cells ‘flow’ into the endometrium
b) causing oedema, glycogen synthesis and increased
vascularisation (decidualisation) (all to provide nutrients and oxygen and support to fertilised blastocyst). The pregnant endometrium is now termed the decidua.

DAY 13 (FURTHER IMPLANTATION/TIME THE WOMAN EXPECTS HER NEXT PERIOD)

  • Syncytiotrophoblast cells erode through the walls of large maternal capillaries which then bleed into the spaces - primitive placental circulation (Breakthrough bleeding may occur)
  • Growth in the embryonic disk is slow and it remains very small (0.1 - 0.2 mm)

PLACENTAL DEVELOPMENT

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5
Q

As the Syncytiotrophoblast cells erode through the walls of large maternal capillaries, what does nutrition depend on ?

A

Nutrition still depends on uterine secretion and tissues.

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6
Q

Describe the development of the placenta.

A
  • Syncytiotrophoblast forms villi that project into the blood filled spaces (chorionic villi). In the core of the villus is a fetal capillary loop - dilated at the tip (slow flow rate).
  • Embryonic placental structure develops over several weeks. The villi eventually becoming localised at the embryonic pole and presenting a huge surface area for exchange of O2, nutrients and waste products
  • Maternal side of the placental circulation is restricted and is not functional until 10 – 12 weeks
  • Maternal and fetal circulations are separated by the placental membrane. There is no mixing of maternal and fetal blood
  • Syncytiotrophoblast is bathed in maternal blood
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7
Q

Describe the end result of placental development.

A
  • Embryonic portion of placenta supplied from outermost layers of trophoblast cells (ie the chorion).
  • Maternal portion by endometrium underlying the chorion.
  • Choronic villi * extend from chorion to endometrium.
  • Villi have network of capillaries – part of embryo’s circulatory system.
  • Endometrium around villi is changed by enzymes and paracrine agents so each villi is surrounded by a pool/sinus of maternal blood.
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8
Q

Describe how the embryo derives nutrients and O2 in the first semester.

A

Limited embryonic growth (complex differentiation) - nutrition of the embryo is largely based on uterine secretion and tissues.

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9
Q

Identify the main contents of chorionic vili.

A
  • Branches of the umbilical artery and umbilical vein grow into the inner core of extraembryonic mesoderm
  • Middle layer of cytotrophoblast
  • Outer layer of syncytiotrophoblast
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10
Q

How thick should the endometrium be for successful implantation ?

A

Endometrium should be at least 8mm thick for successful implantation.

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11
Q

What factor accounts for early pregnancy losses ?

A

Lack of appropriate hormonal support (luteal phase defect) may account for early pregnancy losses.

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12
Q

Describe the evolution in levels of estrogen and progesterone in the follicular phase, and luteal phase.

A

Steady, low levels of estrogen and progesterone in follicular phase. When one follicle chosen to mature fully then have increase in estrogen levels (then LH surge occurring and then ovulation occurring a little time after that).
If fertilisation occurs, takes few days to be transported into uterus then needs to be attached into maternal tissue before estrogen and progesterone levels fall too much and the next menstrual cycle starts.

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13
Q

Describe the evolution of LH levels in the luteal phase. What is the implication of this on attachment ?

A

LH supports coprus luteum for about 10 to 12 days and then regresses after that and new menstrual cycle if no fertilisation.
Attachment needs to happen before LH stops supporting CL.

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14
Q

Explain the function of the human chorionic gonadrotropin.

A
  • In a non-fertile cycle the CL will fail after 10 days and menstruation will occur
  • An implanting embryo must prevent menstruation, through production of hCG.
  • hCG mimics the action of LH and maintains progesterone secretion from the corpus luteum (and therefore prevents both menstruation and any further follicular development) until the placenta can synthesise its own progesterone.
  • hCG stimulates the Leydig cells of male fetuses to produce testosterone - important for development of the male duct system
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15
Q

Where and when is hCG produced ?

A

Syncytiotrophoblasts secrete hCG soon after implantation (peaks ~8-10 weeks of gestation)

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16
Q

How soon is hCG measurable ? By what test ?

A

hCG measurable by 7-8 days postconception/6-7 days post-fertilisation (in maternal blood by immunoassay) or by 14 days in commercial kits.

17
Q

What is the function of progesterone in pregnancy ? Does it increase or decrease throughout pregnancy ?

A

• Must have progesterone for the maintenance of pregnancy:

  • Suppression of follicular growth and ovulation
  • Suppression of the immune response
  • Maintenance of endometrium

Increases through out pregnancy

18
Q

How long is the CL required, in the case of a pregnancy ? Why ?

A

CL not required after 5 weeks, because after 4-5 weeks placenta is secreting all steroid hormones required for pregnancy (i.e. foetus is self sufficient).

19
Q

Once the CL is no longer required in pregnancy, how is progesterone produced ?

A

Cholesterol from the maternal circulation is the substrate for progesterone production.

20
Q

State the main estrogen of pregnancy.

A

Oestriol is the main oestrogen in pregnancy.

21
Q

How is estrogen produced in pregnancy ?

A

Foetus and placenta (feto-placental unit) cooperate to secrete oestrogens (mainly oestriol).

22
Q

Identify the main functions of estrogens (mainly oestriol) in pregnancy.

A

♦ Stimulate continuous growth of uterine myometrium
♦ Stimulates growth (with progesterone) of ductal tissue of breast
♦ Along with relaxin, relaxes and softens maternal pelvic
ligaments and symphysis pubis of pelvic bones – allows
expansion of uterus
♦ Stimulate LDL cholesterol uptake and activity of P450 enzymes
– Contribute to progesterone synthesis
♦ Foetal well being and placental function can be measured by monitoring oestrogen levels.

23
Q

Identify the main placental functions.

A

♦ FIRST TRIMESTER:
• 1st month - villus formation
• 2nd month - increasing surface area and circulation
• 3rd month - growing, becoming increasingly efficient

♦ Most importantly:
• Serves as the organ of exchange between mother and
foetus for remainder of pregnancy:
1. Foetal “gut”: supplying nutrients.
2. Foetal “lung”: exchanging O2 and CO2.
3. Foetal “kidney”: regulates fluid volumes and disposing of waste metabolites.
4. Endocrine gland: synthesises steroids and proteins that affect both maternal and foetal metabolism.

24
Q

Describe the permeability of the placental membrane.

A
  • Most molecules can pass through the membrane - after 20 weeks placental membrane thins even more with loss of cytotrophoblast (allowing for other things to pas as well)
  • 3rd trimester syncytiotrophoblastic cells may be lost into the maternal blood
25
Q

How long is the SA for diffusion in the placental membrane ?

A

• Surface area of the diffusion membrane is huge

26
Q

Graph placental conductivity, explaining your diagram.

A

Refer to page 4 of 5 in lecture slides.

Placenta not operating fully in early stages, then big and rapid increase in placental membrane conductivity once around 10 to 12 weeks.

Peaks a few of weeks prior to a full term pregnancy (i.e. 40 week pregnancy) around 36 weeks, then start to see reduction in conductivity.

27
Q

Explain the clinical significance of the reduction in placental conductivity following week 36 approx.

A

Source of concern if a baby has not been delivered yet, how long should the woman be allowed to wait for a natural delivery given the reduction in conductivity that may be happening ?

28
Q

Describe how different nutrients are exchanged across the placenta.

A
  • Water and electrolytes diffuse freely
  • Glucose passes via facilitated diffusion because foetus has little capacity for gluconeogenesis
  • Amino acids are actively transported for fetal growth
  • Lipids cross as free fatty acids
  • Vitamins also transported
29
Q

How quick is nutrient exchange in the placenta ? Does it increase or decrease as the pregnancy advances ?

A

• Nutrient exchange is rapid and increases as pregnancy advances

30
Q

Explain the clinical significance of the fact that glucose passes via facilitated diffusion across the placenta.

A

Babies of diabetic mothers are heavier than normal range.

31
Q

What is a use of glucose in the later stages of pregnancy in the fetus ?

A

Glucose also used for storage of glycogen in liver for postnatal requirements in later stages of pregnancy

32
Q

Describe the process of gas exchange across the placenta.

A
  • Simple diffusion of gases across the membrane (almost as efficient as the lungs)
  • Concentration gradients are influenced by blood flow rates (rates of blood exchange in the placenta)
  • Quantity of O2 reaching the foetus is flow limited
  • Fetal haemoglobin has a greater affinity for O2 than adult haemoglobin (which helps support transfer of oxygen)
  • Towards end of pregnancy exchange capacity decreases and placenta is less able to meet the demands of the foetus.
33
Q

Is the placenta an endocrine organ ?

A

Yes