Reproduction Flashcards

1
Q

How many oocytes are formed in embryonic development?
How many remain by birth?
How many are released into the fallopian tubes?

A

5 million form in embryonic development
0.5 million by birth
500 released into fallopian tubes

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2
Q

Primordial oocyte features

A

Quiescent
Incomplete meiotic division
lined by squamous follicle cells on basal lamina

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3
Q

Primary oocyte

A

Enlarged cuboidal follicle cells - form granulosa cells
Active and dividing
Striatum granulosum makes oestrogen
External stromal cells form thecal cells - Theca internal and theca externa
Theca interna makes androgens
Surrounded by zona pellucida

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4
Q

Secondary follicle

A

Stratum granulosa thickens; forms corona radiata
Antrum appears
Cumulus oophorus - stalk suspends oocyte in antrum
Thecal cells - outermost

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5
Q

Ovulation

A

Graafian follicle - mature follicle
Released due to LH surge –> follicle ruptures, SM contracts to squeeze egg out
Survives for 24hrs unfertilised

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6
Q

Uterus histology

A

Perimetrium
Myometrium - 3 SM layers
Endometrium - ciliated and secretory simple columnar cells

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7
Q

Cervix histology

A

Endocervix - Simple columnar epithelium, glandular

Ectocervix - Stratified squamous epithelium

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8
Q

Cervical transformation zone histology

A

Simple squamous epithelium and cervical glandular epithelium
Reproductive years - junction at external os
Oestrogens - expansion of cervical stroma - eversion of columnar epithelium near external os and exposure to hostile vaginal environment - metaplasia into durable stratified squamous epithelium
Location of boundary changes over menstrual cycle
Increased risk of tumerous change

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9
Q

Terminal duct lobular unit

A

Acini and intralobular collecting duct. Form functional metabolic unit

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10
Q

Leydig cells

A

Produce testosterone. Between seminiferous tubules

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11
Q

Sertoli cells

A

Support cells, in seminiferous tubulous. Fluid –> fluid flux

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12
Q

Origin of epididymis and vas deferens

A

Wolffian (mesonephric) duct

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13
Q

Clitoris histology

A

2 extra masses of cavernous tissue not present in males - bulbs of clitoris. Function unknown.

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14
Q

Fibrocystic change

A

Benign
Common - almost considered physiological
Mid-late reproductive years
Variable dilation of ducts - cysts may form
Fibrosis, adenosis (acini proliferation), apocrine metaplasia (epithelial cells become pink and granular)
Lumps may result from fibrosis/cysts

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15
Q

High pathogenic HPV types

A

16 and 18

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16
Q

HPV oncogenic potential

A

E6/E7

17
Q

Role of E2 in HPV

A

E2 encodes transcription factor which suppresses E6/E7
If there is a break in HPV DNA as it integrates into the host genome - dysregulation of E6/7
E6 binds p53 - deactivation
E7 binds Rb
Results in uncontrolled proliferation of squamous epithelial cells

18
Q

Spermatogenesis

A

Spermatogonia (present in foetal life)
Mitosis - 2 daughter cells; 1 remains on outer edge, replacing germinal stem cells. Other moves towards lumen.
Daughter spermagonium divides by mitosis to again - 2 spermagonia
Spermagonia divide by mitosis - primary spermatocytes
First meitotic division - secondary spermatocytes
Secondary meitotic division - spermatids
Maturation - spermatozoa

19
Q

Production of sex hormones

A

Testes - testosterone, DHT (dihydrotestosterone)
Ovary - oestrogen, progesterone
Adrenal gland - Small amounts of sex steroids

20
Q

Regulation of sex hormones - male

A

Hypothalamus - GnRH
Anterior pituitary - FSH and LH
FSH acts on Sertoli cells - Inhibin (Keep FSH/testosterone levels in check via negative feedback to anterior pituitary), Spermatogenesis, androgen-binding protein (required to bind testosterone)
LH acts on leydig cells - Testosterone

21
Q

Nutrients in semen and source

A

Seminal vesicles - fructose and vitamin C
Prostate - citric acid
Epididymis - Carnitine

22
Q

Testosterone

A

Before birth - sexual differentiation; promotes testicular descent
Continuous secretion from puberty - sex drive, control of gonadotropin secretion, secondary sexual characteristics, protein anabolic effects, bone growth and closure of epiphysis, sebaceous gland secretion

23
Q

Oestrogen

A

Breast developmetn and body fat distribution

24
Q

Adrenal androgens

A

Hair growth and libido

25
Q

Oogenesis

A

Oogonium divide - primary oocytes
Primary oocytes - arrest in first meiotic division
After puberty - 1 primary oocyte reaches maturity and ovulated 1ce a month
Primary oocyte complets first meiotic division prior to ovulation - secondary oocyte
Secondary oocyte completes second meiotic division after fertilization - mature ovum

26
Q

Menstrual cycle - phases

A

Follicular/proliferation phase
Ovulation
Luteal/secretory phase

27
Q

Early-mid follicular phase

A

Hypothalamus secretes GnRH - FSH and LH from anterior pituitary
LH - thecal cells to produce androgens
FSH - granulosa cells to convert androgens in estrogen
Oestrogen - negative feedback to hypothalamus and AP; positive feedback to granulosa cells

28
Q

Late follicular phase and ovulation

A

High oestrogen levels - negative feedback switches to positive feedback at the hypothalamus
Granulosa cells produce inhibin - negative feedback on FSH
Granulosa cells also produce small amount of progesterone (positive feedback on GnRH and LH)

29
Q

Early to mid luteal phase

A

Corpus luteum - high oestrogen, progesterone and inhibin
Negative feedback at hypothalamus and pituitary
Endometrium maintained
Cervical mucus thick, sticky and viscous
Increased basal body temperature

30
Q

Late luteal phase

A

Corpus luteum dies - decreased estrogen and progesterone
Blood vessels constrict - decrease trophic support of endometrium - dies and sloughs off - menses
Loss of negative feedback - Increased FSH and LH
Cycle begins again

31
Q

Fertilisation

A
Ovulation
Day 1 - fertilisation (sperm capacitation in vagina, swims upstream, reaches oocyte in fallopian tube, acrosomal reaction - digests zona pellucida and cell junctions, membranes fuse, sperm nucleus enters, cortical reaction blocks polyspermy, nuclear fusion - zygote produced, 2nd meiotic division completed producing polar body)
Day 2-4 - Cell division
Day 4-5 blastocyst reaches uterus
Day 5-9 Blastocyst implants
32
Q

Critical weeks

A
Early pregnacy (weeks 1-2) - not susceptible to teratogens, susceptible to chromosomal abnormalities
Embryonic period (weeks 3-8) - major organs develop. Susceptible to teratogens. 
Foetal period (week 9-40) - affected by genetic and environmental factors (multiple, pregnancy, maternal under nutrition, oxygenation, placental function, smoking, alcohol etc)