androgens and anabolic steroids Flashcards

1
Q

leydg cells are

A

interstitial cells responsible for the production of testosterone

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2
Q

anabolic androgen steroids AAS

A

are steroid hormones
endogenous and synthetic
based on testosterone structure

testosterone, DHEA, androstenedione

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3
Q

leydg cells lie

A

between the seminiferous tubules

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4
Q

GnRH triggers

A

anterior pituitary to produce LH and FSH

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5
Q

LH

A

acts on leydig cells to produce testosterone

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6
Q

FSH

A

acts on Sertoli cells in seminiferous tubules to support spermatogenesis

and to secrete ABP - androgen binding protein

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7
Q

secreted testosterone binds to

A

ABP

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8
Q

testosterone effects

A

androgenic - masculinising - foetal male organ development, pubertal maturation, maintenance of sex characteristics, spermatogenesis
anabolic - growth stimulating - increased proton synthesis in growing tissues, maintenance of muscle and bone

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9
Q

testosterone function in foetus/neonate

A

promote wolffian ducts to form epididymis/vas deferens/seminal vessicles
external genitalia

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10
Q

5a-reductase

A

converts testosterone to dihydrotestosterone DHT
more potent than testosterone
regulated maturation of external genitalia

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11
Q

DHT also drives

A

prostate gland hypserplasia

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12
Q

DHT mediates testosterone effects everywhere but the

A

testis - where testosterone concentration is much higher

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13
Q

aromatase

A

converts testosterone 17b oestradiol
important for healthy motile sperm and bone
men who have an aromatase mutation are osteopaenic

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14
Q

androgen receptor

A
ligands are testosterone and DHT 
gene encoding the androgen receptor is on the X chromosome 
widely expressed 
nucelar receptor 
DHT binds it more avidly
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15
Q

androgen binding

A

homodimerisation of the receptors and nuclear translocation

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16
Q

testosterone levels peak

A

in the morning

17
Q

androgen deficiency

A

male hypogonadism

clinical diagnosis confirmed by hormone assays

18
Q

primary hypogonadism

A

testicular problem - high LH, ls testosterone

sometimes chromosomal, cryptorchidism, trauma, chemo, radiotherapy

19
Q

secondary hypogonadism

A

low LH and testosterone
pituitary insufficiency - adenoma, surgery, trauma
kallman syndrome, prader-willi

20
Q

treatment of androgen deficiency

A

adrogen replacement therapy
for life
give testosterone esters

21
Q

testosterone esters

A

given by IM injection
bioconverted into testosterone
lasts 2-3 weeks
subcutaneous impacts, transdermal gels and patches

22
Q

contraindicated of androgen therapy

A

prostate cancer

breast cancer

23
Q

precautions of androgen replacement therapy

A

older men - urinary obstruction, libido
puberty - early epiphyseal closure, short stature
androgen sensitive epilepsy, migraine, polycythaemia
bleeding disorders

24
Q

misuse of AAS

A

prescribing androgens with no acceptable medical indication
eg.
adult male infertility - causes further suppression of spermatogenesis
erectile dysfunction - increase libido with no change in capacity
adrenopause - little to no benefit with CVS harm

25
Q

when should ART be prescribed

A
  • testicular or hypothalamic-pituitary disorders with severe androgen deficiency
    other conditions involving partial androgen defieicny
26
Q

partial androgen deficiency

A

boys experiencing delayed onset of puberty
chronic conditions such as HIV/AIDS to reverse catabolic state
older men and post menopausal women for prevent bone and muscle loss

27
Q

andropause

A

menopause for men

androgen levels steadily decline in males as they age

28
Q

symptoms and signs of andropause

A

decrease muscle mass and strength
decreased bone mass and osteoporosis
increased central body fat
decreased libido

29
Q

abuse of AAS

A

use without legal prescription
increases muscle strength, repairs soft tissue micro injury
recover faster from workout

30
Q

who benefits more from testosterone abuse

A

women

31
Q

designer steroids

A

aim to maximise anabolic effects of AAS
ie. not converted to oestradiol (less feminising effects) or DHT (less androgenic effects)

not absolutely selective and high doses needed

32
Q

women staking steroids

A

hirsutism, decreased breast tissue and mensrtuation,

effects female foetuses during preganancy

33
Q

men taking steroids

A

acne
testicual atrophy and reduction in spermatogenesis
short stature in premature epiphyseal closure
mood disturbance, agression and cognition
dylipdameia and hypertension
polycythaemia
hapentitie and hepatic tumours

34
Q

cognitive effects of AAS

A

aggression, impulse control and roid rage

35
Q

CVS effects of AAS

A

difficult to identify users and unethical to conduct studies
adverse cardiovascular effects

36
Q

SARMS

A

selective androgen receptor modulators
stimulate anabolic effects without androgenic effects
developed to treat cancer related muscle less and osteoporosis