Fetoplacental unit
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Transcript of Fetoplacental unit
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FETOPLACENTAL UNIT
Presenter : Dr AnuPriya J
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Scheme
• Introduction• History • Corpus luteum• Luteal-placental shift• Fetoplacental unit
- Synthesis of hormones- Plasma levels- Metabolites- Functions of the hormones
• Applied aspects
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• The placenta
- major source of estrogens and progesterone during pregnancy
- cannot synthesize these hormones by itself
- requires the assistance of both mother and fetus.
Introduction
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Introduction
• The fetus, placenta, and mother are interdependent - functional unit – joint effort in steroid biosynthesis – lead to the concept of
feto-placento-maternal unit or simply, the fetoplacental unit.
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• Steroid hormones-
Estriol
17 β Estradiol
Estrone
Progesterone and
Pregnenolone.
Introduction
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HISTORY
• The concept of the functional “maternal-placental-fetalunit” or “complex” (Diczfalusy, 1964).
• These hormonal relationships are important in terms of fetal growth and development (Evseenko et al., 2007; Kingdom et al., 2000), the regulation of maternal blood volume in pregnancy (Longo, 1983)
• The role of the fetal-placental unit as a factor in the initiation of labor (Beshay et al., 2007; Challis et al., 2001; 2005)
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ESTROGEN AND PROGESTERONE IN A NON-CONCEPTION CYCLE
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CORPUS LUTEUM
• Following ovulation during a normal or nonconception cycle - the cells of the ovarian follicle functionally transform into luteal cells
• Progesterone(mainly) & estrogens.
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CORPUS LUTEUM
• Life span - lasts only ≈ 12 days – then - begins its demise in the presence of declining LH levels.
• Luteal demise - levels of both progesterone and estrogens decline
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ESTROGEN AND PROGESTERONE DURING PREGNANCY
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• During pregnancy - maternal levels of progesterone and estrogens(estradiols, estrone, estriol) increase - reach concentrations substantially higher than those achieved during a normal menstrual cycle.
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HOW ARE THESE ELEVATED LEVELS ACHIEVED?
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EARLY IN THE FIRST TRIMESTER
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Corpus luteum of pregnancy• Early in the first trimester (upto 7 wks after conception) - hCG
that is manufactured by the syncytiotrophoblast rescues the corpus luteum – source of estrogen and progesterone - untilfetoplacental unit is able to synthesize its own estrogen and progesterone.
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• hCG - also known as second luteotropichormone.
• Actions - similar to LH of anterior pituitary.
• Maintains functions of corpus luteum upto 7 weeks after conception
Corpus luteum of pregnancy
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• hCG converts corpus luteum of menstruation into corpus luteum of pregnancy - stimulates it to secrete 17 alpha hydroxy progesterone and lesser amount of progesterone.
ROLE OF hCG
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AFTER 8 WKS OF GESTATION
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LUTEAL-PLACENTAL SHIFT
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• Study by Caspo et al – to find the timing of luteal-placental shift - luteectomy before, but not after, the 7th week of gestation – usually resulted in subsequent abortion
LUTEAL-PLACENTAL SHIFT
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After 8 wks of gestation
- coordinated biosynthetic activity of the
maternal-placental-fetal unit maintains
high levels of progesterone and estrogens.
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•Corpus luteum – manufactures the hormones –without assistance from fetus or placenta .
•The placenta is an imperfect endocrine organ -shortcomings overcome by the fetoplacental unit - shuttling of many of the hormonal substrates.
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• Placenta - does not express SF-1 (Steroidogenic Factor-1) – a transcription factor – important regulator of genes involved in adrenal & gonadal steroidogenesis.
• Trophoblasts – reduced levels / lack of certain enzymes
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NEEDS CONTRIBUTES LACKS
MOTHER PROGESTERONEESTRONEESTRADIOLESTRIOL
LDL CHOLESTEROL ADEQUATE SYNTHETIC CAPACITY FOR PROGESTERONE & ESTROGENS
PLACENTA 3βHYDROXY STEROID DEHYROGENASE
AROMATASE
ADEQUATE CHOLESTEROLSYNTHESIZING CAPACITY17 α HYDROXYLASE17,20 DESMOLASE16 α HYDROXYLASE
FETUS 17 α HYDROXYLASE17,20 DESMOLASE16 α HYDROXYLASE
3βHYDROXY STEROID DEHYROGENASE
AROMATASE
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Cholesterol uptake by trophoblasts
• The trophoblast can synthesize cholesterol from acetate - but the amount of hydroxy-methyl-glutaryl-coenzyme A is low in placental microsomes.
• LDL & VLDL from maternal circulation – receptors in syncytiotrophoblast.
• Receptor mediated uptake – stimulated by estrogen.
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PROGESTERONE
MOTHER PLACENTA FETUSACETATE
↓
CHOLESTEROL
PROGESTERONE
CHOLESTEROL↓CYP11A1
PREGNENOLONE
↓3βHSD
PROGESTERONE
CORTISOL
→
DHEAS & 16-OH-DHEAS
CYP11A1 – CHOLESTEROL SIDE CHAIN CLEAVAGE / DESMOLASE ENZYME3BHSD – 3 β HYDROXY STEROID DEHYDROGENASE
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• Placenta lacks StAR (Steroidogenic Acute Regulatory protein) – mediates cholesterol transport from outer to inner mitochondrial membrane – the site where CYP11A1 acts in other sites of steroidogenesis.
• Therefore, there must be another mitochondrial transport mechanism present in the placenta
• Pregnancies with StAR mutations – no alterations in placental steroidogenesis.
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FORMATION OF DHEAS
FETUSPREGNENOLONE SULFATE
17 HYDROXY-PREGNENOLONE SULFATE
DEHYDROXYEPIANDROSTERONE SULFATE
17 α HYDROXYLASE
17,20 DESMOLASE
FETAL STEROID SULFOTRANSFERASE
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ESTRONE & ESTRADIOL
60%40%
E1 – EstroneE2 - Estradiol
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ESTRIOL
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ESTRIOL
• Major estrogen formed in pregnancy
• Increase to 12-20 ng/ml by term
• Low affinity for sex hormone binding globulin – cleared more rapidly – therefore, circulating level of estradiol > estriol.
Placental estrogens
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Placental estrogens
• During pregnancy – a woman produces more estrogen than a normal ovulatory woman produce in more than 150 yrs.(Tulchinsky & Hobel 1973)
• 90% of 17β estradiol & estriol secreted by placenta –enters maternal compartment
• Most of the estrone – enters fetal compartment
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ESTETROL
• An estrogen unique to pregnancy
• 15 α hydroxy derivative of estriol
• Synthesized in the fetal liver
Placental estrogens
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• Maternal environment is protected from testosterone produced by male fetus –placental aromatase enzyme – converts testosterone to estradiol.
Placental estrogens
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Fetal cortisol
• Fetal adrenal cortex – placental progesterone ----hydroxylated at C-17, C-21 & C-11 positions – form aldosterone, cortisone & cortisol respectively.
• Upto 10 weeks of gestation – Placental CRH needed
• After 10th week of gestation – Fetal CRH sufficient to produce corticosteroids.
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• Prior to term, there is an effective negative feedback mechanism by which cortisol inhibits fetal ACTH secretion. Estrogen selectively suppresses fetal zone growth during second half of pregnancy.
• At term, human placental estrogen leads to positive feedback cycle with progressive increase in fetal HPA activity resulting in increase in ACTH and cortisol.
Fetal cortisol
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Plasma levels
Progesterone
• Non-conception cycle
Follicular phase ≈ 2.5 mg/day
Luteal phase ≈ 25 mg/day
• By the end of pregnancy
Production ≈ 250 mg/day
Circulating level ≈ 130 ng/ml
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ESTROGENS
• Estriol – first detectable at 9 weeks (0.05 ng/ml) –increases gradually to about 30 ng/ml at term.
• Secretory curve parallels that of progesterone
• Maximum plateau – 30 to 40 weeks of gestation
• At term – oestrogen:progesterone ratio increases.
Plasma levels
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Metabolites
• Progesterone – pregnanenediol – glucuronisedand secreted by kidneys – urine
• Estrogen – glucuronised and sulfated – urine
• Catecholestrogens
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CATECHOLESTROGENS
• Hydroxylation at the C2 position of the phenolic A ring
• 2-hydroxy-estrone, 2-hydroxy estradiol, 2-hydroxy-estriol
• Major product of estrogen metabolism during pregnancy
• Act as antiestrogens – competes with estrogen for their receptors
Metabolites
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Placental ProgesteroneFunctions
• Helps to preserve the pregnancy by promoting growth of the endometrium
• Converts secretory endometrium of luteal phase of menstrual cycle to decidua during pregnancy
• Marked inhibitory effect on uterine contractions – by acting on uterine smooth muscle - maintains quiescence
• Development of alveolar system of breast
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Functions
• Inhibits uterine prostaglandin production - promotes uterine quiescence & delays cervical ripening.
• Antagonizes the effect of aldosterone – promotes renal excretion of sodium during pregnancy
• Precursor for corticosteroid synthesis by the fetal adrenal cortex – therefore helps in growth and development of fetus
• Inhibits lactation during pregnancy
Placental Progesterone
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Functions
• Immunosuppressive activity
• Contributes to the immunologically privileged status of the pregnant uterus – by inhibiting T lymphocyte mediated processes that play a role in tissue rejection.
Placental Progesterone
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Placental Estrogen
Functions
• Enlargement of the uterus, breasts and female external genitalia.
• Relaxes various pelvic ligaments and makes the pelvis more capacious
• Development of lactiferous ductal system of breast
• Stimulates prolactin secretion
• Production of hormone binding globulins in liver
• Enhance receptor mediated uptake of LDL
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Functions• Stimulates cell proliferation of fetal tissue
• Fetal development & organ maturation
• Helps in increasing fetal lung surfactant production
• Stimulates Leydig cells of male fetus to produce testosterone ( initial stimulus is by hCG)
• Increases uteroplacental blood flow – ensures adequate supply of oxygen & nutrients to the fetus.
Placental Estrogen
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Functions
Increase in oestrogen:progesterone ratio –progression of the stages of labour
• Due to the stimulatory effects of estrogen on:
- Phospholipid synthesis & turnover
- Prostaglandin production
- Increases formation of lysosomes in the uterine endometrium
- Stimulates synthesis of gap junctions between myometrial smooth muscle cells
Placental Estrogen
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• Plasma 17 α hydroxy progesterone level - excellent indicator of the activity of corpus luteum of pregnancy. Peak level - 3 to 4 wks after conception.
• Decrease in 17 α hydroxy progesterone & the dip in progesterone levels – 8 to 10 weeks of gestation – reflect luteal-placental shift
• Progesterone supplementation required if corpus luteum function is compromised before 9-10 weeks of gestation.
Applied aspects
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• Progesterone production continues after fetal death - Fetal adrenals not essential for progesterone production – lacks 3βHSD
Applied aspects
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Applied aspects Conditions – low estrogen production
Genetic disorders
- fetal & placental sulfatase deficiencies
- fetal & placental aromatase deficiencies
Absence of fetal signals from the fetal hypothalamic pituitary adrenal axis – no stimulus for fetal androgen production
• Absence of a fetus – molar pregnancy, pseudocyesis
• Fetal demise
• Anencephaly
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• Placental estrogen synthesis – not essential for maintenance of pregnancy - pregnancy proceeds to term .
• Changes in the reproductive tract that precede the
stages of labour do not occur.
Applied aspects
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Urinary estriol
• Index of function of fetoplacental unit
• Use is limited now because of various factors that affect estriol levels:
- Moment to moment fluctuations – single time plasma measurement is not very conclusive.
- Body position (bed rest, ambulation) affects blood flow to uterus & kidney.
- Drugs like glucocorticoids & penicillin.
Applied aspects
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• Aromatase deficiency – fetus and mother are virilized – due to diminished aromatization of androgens.
• Oocyte recipients who have no ovarian function - exogenous progesterone needed only in the first trimester
Applied aspects
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The major estrogen during pregnancy is
• Estrone
• Estradiol
• Estetrol
• Estriol
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Major source of estrogen & progesterone during the first 7 weeks of pregnancy
• Corpus luteum of pregnancy
• Endometrium
• Fetoplacental unit
• Fetal tissue
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The second luteotropic hormone is
• Human chorionic gonadotropin
• Luteinising hormone
• Human chorionic somatomammotropin
• Prolactin
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References
Robert K.Creasy, Robert Resnik, Jay D.Iams –
Maternal-Fetal medicine - Principles & practice
Williams Textbook of Endocrinology, 11th Edition
Ganong's Review of Medical Physiology, 24th Edition
Guyton and Hall Textbook of Medical Physiology, 12th
Edition
Best & Taylor's Physiological Basis Of Medical Practice, 13/ E.
Berne & Levy - Physiology, 6th Edition
Boron & Boulpaep - Medical Physiology, 2nd Edition
Internet References
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CORTISOL ---CONTINUED
• PLACENTAL CRH ALSO PLAYS A ROLE
• ROLE OF FETAL/MATERNAL STRESS IN PREGNANCY
• BEFORE TERM – COTISOL BINDING GLOBULIN – BINDS WT IT N PREV ITS ACTN
• LATER – DEC IN CORTISOL BINDING GLOBULIN – CORTISOL FREE TO ACT
• CRH BINDING PROTEIN – WILLIAMS ENDOCRINOLOGY
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• The progesterone antagonist mifepristone -terminate pregnancy because it blocks progesterone action and causes the uterus to contract.
• Supplemental progesterone - prevent preterm birth in women who have a history of preterm labor.
Applied aspects
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• The addition of mifepristone to the misoprostolregimen for induction increases effectiveness and decreases induction-to-abortion time. Mifepristone is a synthetic steroid that competitively binds to progesterone receptors, and also appears to increase myometrialsensitivity to misoprostol.19Administration of mifepristone 24 to 48 hours before misoprostoldecreases mean induction times by up to 45%, and it has been suggested that use of adjunctive mifepristone could make induction a day procedure.
Applied aspects
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(1) The placenta cannot synthesize cholesterol from acetate.
• However, both mother and fetus can do so and the cholesterol so formed diffuses into the placenta, which possesses the enzymes needed to convert cholesterol to progesterone via pregnenolone.
• The progesterone formed in the placenta diffuses back into the maternal circulation and exerts its physiological actions.
• Placental progesterone also diffuses into the fetus where it is converted to corticosteroids.
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• (2) The enzyme 17, 20 lyase is essential for the synthesis of DHEA (dehydroepiandrosterone), which is the precursor to all estrogens. 17, 20 lyase is absent in the placenta.
• Hence, for estrogen synthesis, the placenta obtains DHEAS from the maternal and fetalcirculation.
• DHEAS (dehydroepiandrosterone sulfate) is deconjugated to DHEA in the placenta before it is converted to estrone and estradiol.
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• (3) Estriol, the major circulating hormone in pregnancy is synthesized from 16-OH-DHEAS.
• The conversion requires mainly two enzymes: 16a hydroxylase and aromatase. However, 16a- hydroxylaseis absent in the placenta.
• The placenta therefore takes up 16 OH-DHEAS from maternal and fetal circulation, deconjugates it into 16 OH-DHEA and converts it into estriol.
• Fetal 16 OH-DHEA is the major source of placental estriol and therefore, the urinary excretion of estriol in mother is an index of the health of the fetus.
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SYNTHESIS OF PLACENTAL ESTROGENS - SUMMARY
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• Parturition• Parturition is the delivery of the infant followed by delivery of the placenta.
Estrogen is the most important hormone in preparation for parturition. Estrogenstimulates proliferation in the myometrium, accomplishing the considerable growth that is necessary for the forceful contractions of labor. Importantly, as the time for parturition nears, estrogen stimulates the synthesis of gap junctions between myometrial smooth muscle cells. Gap junctions allow electrical activity to travel between cells, so that coordinated contractions can occur.
• Near term, estrogen stimulates the synthesis of enzymes involved in prostaglandin synthesis. Before labor, prostaglandins stimulate cervical ripening, the breakdown of cervical connective tissue allowing it to become soft and flexible and capable of dilation. During labor, prostaglandins stimulate myometrial contractions.
• The posterior pituitary hormone oxytocin is the strongest stimulator of uterine contractions. As the time of delivery approaches, estrogen increases responsiveness to oxytocin by increasing expression of oxytocin receptors.
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