Repro7 - Puberty and the HPG Axis Flashcards

1
Q

5 features of secondary sexual characteristics in females

Age
3 Stages
Scale

A
  1. ) Age - appear between 9-13 years (puberty)
  2. ) Thelarche - stage where male and female breasts becomes distinct (breast buds form)
  3. ) Adrenarche - early stage in maturation
    - growth spurt, pubic hair growth
  4. ) Menarche Cycles - menstrual cycle begins
    - breasts and pubic hair fully grow and mature
  5. ) Tanner Scale - scale of physical development
    - 5 stages using breast size and pubic hair growth
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2
Q

5 features of secondary sexual characteristics in males

Age
3 Stages
Scale

A
  1. ) Age - appear between 10-14 years
  2. ) Genital Development
  3. ) Spermatogenesis and Pubic Hair Growth
  4. ) Growth Spurt
    - also, genitalia and pubic hair fully grow and mature
  5. ) Tanner Scale - scale of physical development
    - 5 stages using penis size, pubic hair growth, and scrotum growth
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3
Q

3 features of accelerated somatic growth in males and females

A

1.) Hormone Dependent - depends on GH, IGF-1 and sex steroids in both sexes

  1. ) Larger Males - starts later in males but the growth spurt is longer and slightly faster
    - genital development in boys depends on testosterone
  2. ) Epiphyseal Fusion - determines the end of accelerated somatic growth and depends on oestrogen
    - oestrogen closes epiphyses earlier in girls
    - males have less oestrogen so closes later in boys
    - males can testosterone –> oestrogen (aromatisation)
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4
Q

4 features of the HPG (hypothalamus-pituitary-gonadal) axis

Sequence
GnRH Release
Puberty Onset

A

1.) Sequence - Hypothalamus (GnRH) –> Anterior Pituitary (LH + FSH) –> Gonads (androgens + oestrogen)

  1. ) Nocturnal GnRH - causes LH secretions at night which precedes phenotypic changes (e.g. breast buds/testicular enlargement) by several years
    - amount of sleep is directed related to LH release which can cause early pubertal changes
  2. ) Pulsatile GnRH Release - released every 1-3 hours
    - if GnRH receptors are exposed to continuous presence of GnRH, they become desensitised, stopping FSH and LH production –> stopping gonadal steroid production
    - GnRH agonist can be used as a contraceptive

4.) Onset of Puberty - associated with steady rise in FSH/LH secretion

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5
Q

3 features/structures relating to male androgen production

Seminiferous Tubules
Leydig Cells
Sertoli Cells

A
  1. ) Seminiferous Tubules (ST) - spermatogenesis occurs
    - ST need functioning leydig cells
  2. ) Leydig Cells - produces majority of testosterone
    - stimulated by LH
    - production is affected by circadian rhythm (highest in early morning) and environmental stimuli
  3. ) Sertoli Cells - provides nutrition and hormonal support for sperm
    - stimulated by FSH
    - can secrete inhibin, producing -ve feedback on AP
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6
Q

6 features of female androgen production

2 Stimulatory Hormones
2 Types of Cells
3 Sex Steroids and their effect on HPG axis

A

1.) FSH and LH - bind to G(as)PCRs to activate AC

  1. ) Granulosa Cells - stimulated by FSH, LH and androgens produced by the theca interna cells
    - produce oestrogen, progesterone, and inhibin
  2. ) Theca Interna Cells - stimulated by LH
    - produce progesterone and androgens
  3. ) Oestrogen - produces +ve and -ve FB on GnRH
    - moderate/small levels promotes -ve feedback
    - high levels promote GnRH leading to an LH surge
    - it affects the amount of GnRH per pulse
  4. ) Progesterone - inhibits oestrogen
    - increases -ve feedback of moderate oestrogen
    - prevents +ve feedback of high oestrogen
    - it reduces the frequency of GnRH pulses

6.) Inhibin - inhibits secretion of FSH (-ve FB on AP)

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7
Q

4 features of leptin

Type of Hormone
Function
Type of Release
Relation with HPG Axis

A
  1. ) Hormone Type - adipocyte-derived protein hormone
  2. ) Function - signals info about energy stores to CNS
  3. ) Pulsatile Release - associated with variations in LH
  4. ) Regulate GnRH Levels - secretion may be influenced by gonadal steroids but it’s independent of LH control
    - can accelerate the onset of reproductive function, whilst deficiency can lead to reproductive dysfunction
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