Reproductive Physiology Flashcards

1
Q

Give an overview of the events before and during puberty.

A
  • Repro system quiescent during early childhood.
  • Increased activity of repro system during adolescence.
  • When inihibition is withdrawn or overcome at puberty, phenotypic and behavioural changes occur.
  • Increases in GnRH (gonadotrophin-releasing hormone) lead to increases in LH and FSH secretion (both females and males).
  • Age of onset varies (according to various factors e.g. sex, nutritional state, race.
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2
Q

Describe adrenarche.

A
  • 6-8 years of age (adrenal gland secretes androgens (e.g. dehydroepiandrosterone, DEHA) - similar to male puberty).
    • Trigger not known - “pre-programmed”?
    • Androgens eventually cause growth spurt
    • Pubic hair growth starts
    • Breast development starts
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3
Q

Describe menarche.

A
  • Onset of menstrual cycle at 10-16 years old.
    • Ability to produce mature ova and an endometrium that could support a zygote.
    • Increased FSH and LH from pituitary (triggered by GnRH).
    • Ovaries respond to FSH and LH by producing steroids.
    • Oestrogen induces ovulation.
    • Onset related to critical level of body fat - triggers GnRH release.
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4
Q

Describe the phenotypic changes associated with female puberty.

A
  • Secondary sexual characteristics induced by ovarian oestrogens.
    • Pubic hair
    • Growth / maturation of reproductive tract (including uterus) and external genitalia.
    • Fat deposition - breasts, buttocks, thighs.
    • Closure of epiphyseal plates (stops growing) (at end of puberty).
  • Somatic growth
    • Begins ~2 years earlier in girls compared with boys.
    • Growth induced by gonadal sex steroids, growth hormone and insulin-like growth factor (as for males).
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5
Q

Describe the endocrinology of male puberty.

A
  • Bursts of GnRH release begin at 8-12 years (initially at night) to initiate puberty.
    • Exact trigger for GnRH production is not clear.
    • “Pre-programmed”? Critical body weight? Inhibition of melatonin secretion?
  • GnRH triggers bursts of FSH and LH release (as for females).
  • This triggers testes to produce androgens and sperm.
  • Frequency of bursts increases until levels of GnRH, LH, FSH and testosterone are the same as in the adult.
  • Rising levels of testosterone produce secondary sexual features.
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6
Q

Describe the phenotypic changes associated with male puberty.

A
  • Secondary sexual characteristics appear (caused by testosterone and metabolites).
    • Testicular enlargement
    • Pubic hair growth
    • Growth of larynx
    • Deepening of voice
    • Increased bone mass
    • Increased mass and strength of skeletal muscle
    • Thickened skin
    • Increased and thickened har on trunk, arms, legs, face
  • Somatic growth
    • Induced by gonadal sex steroids, growth hormone and insulin-like growth factor.
  • Puberty lasts many years - facial hair pattern may not mature until 20-25 years of age.
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7
Q

Describe the female monthly sexual cycle.

A
  • Ovarian cycle - production and release of ova.
  • Cycle lasts for 28 days (average).
  • Has 2 phases:
    • Follicular phase
      • 1st half of cycle.
      • Maturation of egg, ready for ovulation at midcycle - ovulation signals end of follicular phase.
    • Luteal phase
      • 2nd half of cycle.
      • Development of corpus luteum (yellow body).
      • Induces preparation of reproductive tract for pregnancy (if fertilisation occurs).
  • Menstrual cycle - signified by blood loss via vagina due to sloughing of uterine endometrial lining - if it is not required to maintain a pregnancy.
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8
Q

What effect does LH have during the menstrual cycle?

A

Triggers ovulation at ~ day 14.

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9
Q

What happens to oestrogen concentration in response to ovulation?

A

It falls.

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10
Q

Describe the concentrations of oestrogen, FSH and LH during the menstrual cycle?

How do these concentrations correlate to follicular development?

A
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11
Q

What effect does progesterone have on FSH and LH?

A

Inhibitory

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12
Q

Describe the female menopause.

A
  • Menopause - determined retrospectively: begins at 12 months after the end of last menstrual bleed.
  • Cessation of menstruation - commonly occurs between approximately 45 and 55 years.
  • Menopause manifests physically but isn’t a disease - it is a normal part of ageing.
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13
Q

What are the potential triggers of the female menopause?

A
  • Precise trigger still not known.
  • Oocyte depletion? Post-menopause there may still be some healthy oocytes so this can’t be the full picture.
  • Remaining follicles might not be as sensitive to LH and FSH? In the reproductive cycle, these gonadotrophins trigger ovaries to produce a follicle (containing the oocyte).
  • Age-related changes in CNS alter GnRH secretion?
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14
Q

Describe the physiological changes associated with menopause.

A
  • Before menopause (menopause transition):
    • Menstrual cycle may be irregular- may be shorter due to lack of complete follicular development, sometimes no ovulation occurs.
  • Progressively:
    • Ovaries atrophy - there are few or no healthy follicles.
    • Decrease in oestrogen secretion with concomitant increase in LH and FSH.
    • Increased LH stimulates ovaries to produce androstane-dione.
    • Androstene-dione is androgen precursor → hirsuteness and precursor for estrone.
      • Estrone becomes the dominant oestrogen post-menopause, beta-oestradiol was dominant pre-menopause.
    • Overall decrease in oestrogens → breast and reproductive tract atrophy, vaginal dryness.
    • LH pulses coincide with hot flushes but are not responsible for flushes. More likely to be due to temporary disturbances of hypothalamus thermoregulatory centres (linked somehow to GnRH pulse generator).
    • Increased bone mineral loss → decreased density.
    • Increased CV disease risk due to lack of protection due to oestrogen concentration falling.
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15
Q

Describe the male andropause.

A
  • There is no distinct andropause in males.
  • However, as men age:
    • Gonadal sensitivity to LH decreases.
    • Androgen production decreases.
    • Serum LH and FSH increase.
    • Sperm production typically declines after age ~50.
    • Many men maintain reproductive function and spermatogenesis throughout life.
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16
Q

What are the essential female reproductive functions?

What are the roles of the different parts of the female reproductive tract which carry out these functions?

A
  • Production of ova
  • Reception of sperm
  • Capacitation
  • Transport of sperm and ova to site of fertilisation
  • Gestation
  • Parturition
  • Nourishment of the infant by lactation
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17
Q

What are the basic phases of oogenesis?

A
  • Identical meiotic and mitotic divisions to male sperm production - but:
    • Oogenesis takes many years to complete (spermatogenesis takes 60-68 days).
    • Begins in utero.
    • Suspended for many years.
    • Begins again at puberty.
    • Completed at fertilisation.
    • Oogenesis ceases at menopause.
18
Q

What are the essential male reproductive functions?

What are the roles of the different parts of the male reproductive tract which carry out these functions?

A
  • Production of sperm (spermatogenesis).
  • Delivery of sperm to female.
  • Route of sperm: testes → epididymus → vas deferens → ejaculatory duct → urethra.
19
Q

How do the male accessory organs aid fertilisation?

A
  • Epididymus and vas deferens
    • Exit route from testes to urethra.
    • Concentrattion and storage of sperm.
    • Site for sperm maturation.
  • Seminal vesicles
    • Produce semen into ejaculatory duct.
    • Supply fructose.
    • Secrete prostaglandins (stimulates motility).
    • Secrete fibrinogen (clot precursor).
  • Prostate gland
    • Produces alkaline fluid (neutralises vaginal acidity).
    • Produces clotting enzymes to clot semen within female.
  • Bulbourethral glands
    • Secrete mucus to act as a lubricant.
20
Q

What are the 4 stages of sexual arousal?

A
  • Excitement
  • Plateau
  • Orgasm
  • Resolution
21
Q

Describe the excitement phase of sexual arousal in males and in females.

A
  • Males
    • Heightened sexual awareness.
    • Testicular vasocongestion.
    • Engorgement of penis → erection.
  • Female
    • Heightened sexual awareness.
    • Vasodilation of vagina and external genitalia → swelling of labia.
    • Erection of clitoris.
    • Lubrication of vagina.
    • Enlargement of breasts.
    • Flush to skin.
22
Q

Describe the erection reflex.

A
23
Q

Describe the plateau phase of sexual arousal in males and in females.

A
  • Male
    • Intensification of excitement.
    • Increased HR, BP, RR, muscle tension.
  • Female
    • As male.
    • Also vasodilation of lower 1/3 of vagina causes tightening around penis.
    • “Tenting effect”
      • Uterus raises
      • Lifts cervix
      • Enlarges upper 1/2 of vagina (makes room for ejaculate)
24
Q

Describe the orgasm phase of sexual arousal in males and in females.

A
  • Males
    • Intense physical pleasure.
    • Ejaculation.
    • Rhythmic contractions of pelvic muscles every 0.8 seconds.
    • Increased HR, BP, RR, muscle tension.
  • Females
    • Intense physical pleasure.
    • Rhythmic contractions of pelvic muscles every 0.8 seconds, especially in lower 1/3 of vagina (“orgasmic platform”).
    • Increased HR, BP, RR, muscle tension.
    • No ejaculation.
    • No refractory period → can have another orgasm immediately.
25
Q

Describe the ejaculation reflex.

A
26
Q

Describe the structure of a spermatozoon.

A

Plural = spermatozoa

27
Q

Describe the resolution phase of sexual arousal in males and in females.

A
  • Male
    • Temporal refractory period - men cannot have orgasms in quick succession.
    • Relaxation.
    • Return of body to pre-excitement state.
    • Slowing of blood flow to penis.
  • Female
    • ​No refractory period.
    • Relaxation.
    • Return of the body to pre-excitement state.
28
Q

Describe the pre-fertilisation stage of oocytes and spermatozoa.

A
  • Oocyte is viable approximately 6-24 hours after ovulation.
  • Spermatozoa is viable approximately 24-48 hours in the female reproductive tract.
  • Freshly ejaculated spermatozoa are incapable of fertilisation. They must undergo capacitation (in female reproductive tract - can be induced in vitro under correct conditions).
    • Surface of sperm altered by removal of glycoprotein coat.
    • Tail movements become whip-like.
    • Increased calcium sensitivity and cAMP levels rise to promote acrosomal reaction.
  • Allurin released by mature ovum to attract sperm.
    • Sperm “smell” this chemical using an olfactory receptor. Detection induced directed tail movements and swimming in direction of the signal. They have a long journey.
29
Q

Describe the journey of sperm after ejaculation.

A
  • Most sperm stay in the vagina (millions) and eventually leak out.
  • Some sperm found in the cervix (minutes).
  • If mucous is thin and watery and cervix is soft, some sperm can get into uterus.
  • Some sperm get to site of fertilisation (typically hours) (a few hundred).
30
Q

Describe the binding and penetration of sperm.

A
  • Fertilin (protein on sperm) binds to integrin (adhesion molecule on secondary oocyte).
  • Then, acrosomal reaction.
    • Enzymes in the acrosomal tip allow sperm to ‘burrow’ through the outer layers of ovum and enter cytoplasm.
    • Tail of sperm probably lost.
    • ‘Block to polyspermy’ membrane changes triggered.
31
Q

Describe the fusion of sperm and egg membranes.

A
  • Fusion of sperm and egg membranes triggers 3 events:
  • Block to polyspermy:
    1. ​Primary block
      • ​​Egg membrane depolarises, preventing other sperm fusing.
    2. Secondary block
      • Changes to zona pelucida making sperm binding difficult (known as cortical reaction).
    3. Second meiotic division of the egg
      • Second polar body formed and extruded from the egg, ensuring femal pronucleus is haploid.
        • Result = usually one sperm / one egg ratio (both haploid) → diploid conceptus.
        • Mostly “triploid” embryos are not viable.
32
Q

Describe the stages in the first phase of implantation.

A
  1. Initial contact with epithelium of uterus - blastocyst sticky.
  2. Proteases released from trophoblast.
  3. Pathways created allowing trophoblast cells to grow into endometrium.
  4. Trophoblast releases nutrients for embryo.
33
Q

Describe the stages in the second phase of implantation.

A
  1. Trophoblast cells tunnel into the endometrial lining.
  2. Boundaries between trophoblast cells disintegrate - “syncytiotrophoblast” will become fetal placenta.
  3. Trophoblast induces “decidualisation” of endometrium - increased local vascularisation and nutrient storage.
  4. Blastocyst becomes buried in uterine lining by day 12.
34
Q

Describe the development of the placenta.

A
  • Placenta derived from both trophoblast and decidual tissue.
  • Trophoblast cells (chorion) differentiate into multinucleate “syncytiotrophoblasts” which invade decidua and break down capillaries to form cavities filled with maternal blood.
  • Developing embryo sends capillaries into the syncytiotrophoblast projections to form placental villi.
  • Each villus contains fetal capillaries separated from maternal blood by a thin layer of tissue - no direct contact between fetal and maternal blood.
  • 2 way exchange of respiratory gases, nutrients, metabloites etc. between mother and fetus, largely down diffusion gradient.
  • Placenta (and fetal heart) are functional by the 5th week of pregnancy.
35
Q

What does HCG do?

A
  • hCG is responsible for maintenance of pregnancy.
  • In the first trimester.
  • Human chorionic gonadotrophin (hCG).
    • Produced by the blastocyst.
    • Prolongs life of corpus luteum (now called corpus luteum of pregnancy).
    • For further 10 weeks, corpus luteum of pregnancy grows and produces increasing concentrations of progesterone and oestrogen (first trimester).
    • After 10 weeks, the placents produces these hormones.
    • THEREFORE, the uterine lining is maintained during pregnancy.
  • Pregnancy test = hCG detected in urine.
  • Morning sickness = hCG may trigger vomiting centre.
  • At the end of the first trimester, hCG stimulates male fetal gonads to produce steroid hormones → genitalia differentiation.
  • Second and third trimester, oestrogen and progesterone take over.
36
Q

Describe the roles of oestrogens and progesterones during pregnancy.

A
  • Secreted by the corpus luteum of pregnancy in the 1st trimester and placenta in 2nd and 3rd trimesters.
  • Oestrogens
    • Stimulates growth of myometrium musculature - to expel fetus during labour.
    • Stimulates development of mammary gland ducts.
  • Progesterone
    • Suppresses contractions of uterine myometrium.
    • Promotes formation of mucous plug.
    • Stimulted development of mammary milk glands.
37
Q

What is the role of human chorionic somatomammotrophin (hCS) during pregnancy?

A
  • Decreased maternal glucose utilisation, increased plasma FA, increased glucose and FA availibility for fetus.
  • Prepares breast glands for lactation
38
Q

What is the role of parathyroid hormone-related peptide (PTHrp) during pregnancy?

A
  • Mobilises maternal Ca2+ for calcification of fetal bones (if mother’s diet does not contain enough Ca2+).
39
Q

What is the role of relaxin during pregnancy?

A
  • Softens cervix
  • Loosens pelvic connective tissue
40
Q

What is the role of placental corticotrophin releasing hormone (CRH) during pregnancy?

A
  • Stimulates DEHA (dehydroepiandrosterone) production by fetal adrenal cortex - important in initiation of parturition.
41
Q

Describe the interruption to menstruation associated with pregnancy.

A
  • Typically, pregnancy “full-term” (singleton) lasts for 40 weeks (counted from the first day of the woman’s last menstrual bleed).
  • Usually, menstrual cycle stops during pregnancy.
  • Usually, menstruation begins again after about 4-6 weeks post partum, if not breastfeeding.
  • If breastfeeding, menstruation begins again after about 4-6 weeks weaning.
    • Some mothers will menstruate throughout.
    • Pregnancy can still occur post-partum, even if menstruation has not yet begun.