Male Hormonal Control of Reproduction and Infertility Flashcards

1
Q

where is GnRH produced?

A

median eminence of hypothalamus.

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2
Q

what happens to GnRH after it is secreted?

A

GnRH diffuses to pituitary

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3
Q

what does GnRH cause?

A

release of gonadotropins (luteinising hormone (LH) & follicle stimulating hormone (FSH)).

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4
Q

what does overstimulation of GnRH lead to?

A

gonadotropin depletion & deficiency.

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5
Q

what does under stimulation of GnRH lead to?

A

inadequate gonadotropin production & deficiency.

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6
Q

what cells does FSH act on in the male reproductive system?

A

Sertoli cells

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7
Q

what are the effects of FSH on the male reproductive system?

A

production of Androgen Binding Protein (ABP) for transport of testosterone around blood. Also has a direct effect on germ cells (via the S. cells).

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8
Q

what cells does LH act on in the male reproductive system?

A

Leydig cells

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9
Q

what do the Leydig cells do?

A

produce testosterone

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10
Q

what does testosterone act on?

A

testosterone stimulates germ cells directly but also acts on bone, skin, hair and accessory sexual organs

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11
Q

what is testosterone converted to?

A

dihydrotestosterone

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12
Q

what are the actions of dihydrotestosterone?

A

effects on prostate; and oestradiol – important in epiphysial closure and reproductive system.

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13
Q

what is FHS negatively regulated by?

A

inhibin

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14
Q

where is inhibin produced?

A

Sertoli cells at the level of pituitary

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15
Q

what positively regulates FSH?

A

activin & follistatin

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16
Q

what negatively regulates LH?

A

testosterone acting at level of pituitary and hypothalamus

17
Q

what is the cause of Kallman’s syndrome?

A

Defect – deletion or point mutation – in kal-1 gene, on X-chromosome.

18
Q

what is the function the kal-1 gene?

A

produces anosmin. Regulator of outgrowth of axons

19
Q

what happens to GnRH neurones in foetal life?

A

migrate from olfactory epith –> pituitary.

20
Q

what are the symptoms of Kallman Syndrome?

A

No release of gonadotropins –> hypogonadism – lack of secondary sexual characteristics. Azoospermia. Anosmia.

21
Q

what is the treatment for Kallmann syndrome?

A

Testosterone substitution

Pulsatile GnRH

22
Q

what is the cause of Kleinfelter syndrome?

A

XXY (Non-disjunction during meiosis.)

23
Q

what are the symptoms of Kleinfelter syndrome?

A

(Usually only after puberty)

Hypogonadism –> azoospermia

Androgen deficiency

Gynaecomastia (~50% of cases)

Learning difficulties

24
Q

how is Kleinfelter syndrome treated?

A

Life-long testosterone substitution.

25
Q

what is the cause of complete testicular feminisation?

A

X-linked recessive condition. Inactivation of androgen receptor. (Androgen resistance)

26
Q

what are the symptoms of complete testicular feminisation?

A

Small inguinal testes

Lack of axillary or pubic hair

1º amenorrhea

Phenotypically ♀; genotypically ♂

27
Q

how can complete testicular feminisation be treated?

A

Orchidectomy (to remove risk of testicular cancer)

Oestrogen substitution after puberty