20. Male hormonal control of reproduction and infertility Flashcards

1
Q

where is GnRH produced?

A

median eminence

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2
Q

where is the median eminence

A

between hypothalamus + pit gland

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3
Q

GnRh is released in a pulsatile manner - what does this mean?

A

periods when there is and when there is not Gn RH release

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4
Q

what occurs between the pulses of GnRh secretion?

A

GnRH is replenished

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5
Q

can GnRH secretion and replenishment occur at the samr time?

A

no

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6
Q

what effects would a GnRH agonist cause?

A

overstimulation of GnRH secretion - no production

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7
Q

what effects would a GnRH antagonist cause?

A

production of GnRH - but no secretion

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8
Q

what does GnRH cause the release of

A

FSH and LH

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9
Q

function of FSH

A

production of ABP

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10
Q

function of ABP

A

binds and transports testosterone

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11
Q

which cells does FSH act on

A

sertoli

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12
Q

what is FSH negatively regulated by?

A

inhibin and follistatin

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13
Q

what is FSH positively regulated by?

A

activin

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14
Q

function of LH

A

causes leydig cells to produce testosterone

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15
Q

what is LH negatively regulated by?

A

testosterone

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16
Q

3 functions of testosterone

A
  1. stimulate germ cells - sex differentiaiton
  2. bone, skin, hair and accessory sex organs - post puberty
  3. converted into dihydrotesotosterone (DHT)
17
Q

function of DHT

A

epiphysial closure of long bones

18
Q

3 diseases associated with this gonadotropins in males

A
  1. Kallman’s syndrome
  2. Kleinfelter syndrome
  3. Complete testicular feminisation
19
Q

which disease involves a gene defect?

A

kallman’s syndrome

20
Q

which disease is X-linked recessive?

A

complete tesicular feminisation

21
Q

what is Kleinfelter’s syndrome caused by?

A

XXY - non-disjunction during meiosis

22
Q

describe the genetic background of Kallman’s syndrome

A

genetic mutation of kal-1 gene - which is on X ch - failure to regulate outgrown axons in nasal olfactory epithelium. GnRH cannt be produced

23
Q

wheere do GnRH neurones migrate to and form in foetal life

A

nasal epithelium to hypothalamus

24
Q

describe cause of complete testicular feminisation

A

inactivation of androgen receptor - causing androgen resistance

25
Q

what is complete testicular feminsation

A

genetically = male

physically and psychosocially = female

26
Q

which 2 disease result in hypogonadism>

A

kallman’s and kleinfelters syndrome

27
Q

3 sxs of kallmans syndrome

A
  1. azoospermia
  2. anosmia
  3. lack of secondary sexual characteristics
28
Q

6 sxs of kleinfelters syndrome

A
  1. azoospermia
  2. underdevelopment of testes
  3. learning difficulties
  4. adipose build up
  5. androen deficiency
  6. gynaecomastia (enlargement of male breasts)
29
Q

3 sxs of complete testicular feminisation

A
  1. primary amenorrhoae
  2. lack of pubic hair
  3. small inguinal testes
30
Q

treatment of kallman and klienfelters syndrome

A

tesosterone substituion

31
Q

3 treatment options for complete testicular feminsation

A
  1. orchidectomy - surgical removal of testes
  2. oestrogen sub after puberty
  3. counselling