Physiology - Endocrinology of Testis and Male Reproduction Flashcards

1
Q

Is positive feedback involved in the male reproductive system? Why? What does this mean?

A

NOPE High levels of testosterone in the male eliminates the possibility of positive feedback at the level of the median preoptic nucleus in the hypo => In the absence of testosterone, the default configuration is female!

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2
Q

Describe the hormonal regulation of the male reproductive system.

A
  1. GnRH stimulates LH release => LH reaches the testes and binds to LH receptors onLeydig cell => stimulates testosterone production in Leydig cells, and to a minor extent estradiol => testosterone then feedbacks negatively to the anterior pituitary to reduce sensitivity to GnRH + feedbacks negatively to the level of the hypothalamus, reducing GnRH release (high GABA/low glutamate) 2. GnRH stimulates FSH release => FSH reaches the testes and binds to FSH receptors on Sertoli cells in seminiferous tubules => in the presence of testosterone from the Leydig cells, the Sertoli cells will provide an environment for appropriate spermatogenesis => Sertoli cells produce inhibin => inhibin negatively feedbacks on the anterior pituitary to stop FSH release
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3
Q

Does inhibin feedback to the level of the hypothalamus?

A

NOPE

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4
Q

In what manner are LHRH and therefore LH and FSH secreted in the male? What to note?

A

Pulsatile circhoral rhythm every 1-2 hrs like in females BUT FSH has lower baseline and peak values due to the inhibitory effects of inhibin

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5
Q

Describe the Leydig cell LH receptor. How does it work?

A

GCPRAdenylyl cyclease: ATP => cAMP => activates PKA => phosphorylates enzymatic systems => stimulation of conversion of cholesterol into testosterone production

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6
Q

How does testosterone exit the Leydig cell?

A

Diffuses down its concentration gradient through the lipid bilayer because they are lipid based (just like all other steroid hormones)

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7
Q

What happens to testosterone once it is released in the blood by Leydig cells? Consequence?

A

Bound by 2 plasma proteins:1. Sex hormone binding globulin2. Albumin Inactive once bound

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8
Q

Does testosterone decrease FSH levels?

A

NOPE

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9
Q

Does inhibin decrease LH levels?

A

NOPE

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10
Q

What determines whether testosterone or DHT will bind to the androgen receptor if both are present?

A

Whichever is present in higher concentrations

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11
Q

Effect of estrogen secreted by Leydig cells?

A

Overwhelmed by testosterone effects, so none

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12
Q

In what tissues is testosterone not converted to DHT?

A

Penis

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13
Q

In what tissues can testosterone be converted to estrogen?

A
  1. Brain2. Hypo3. Pituitary4. Breast
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14
Q

In what tissues is testosterone converted to DHT?

A
  1. Hair follicles2. Prostate
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15
Q

What can testosterone be converted into at target tissues?

A
  1. DHT2. Estrogen
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16
Q

What % of testosterone in blood is bound by plasma proteins?

A

97%

17
Q

How do steroid hormones induce their effects?

A

Bind to nuclear receptor complex which then binds to chromatin to impact transcription/translation

18
Q

Can testosterone bind plasma membrane receptors?

A

In some instances

19
Q

Describe the structure of inhibin. Where can it be produced? What to note?

A

2 subunits: alpha and beta (2 types for each)Can be produced in Sertoli cells, but also the subunits can be made in FSH producing cells => 2 beta subunits can come together to make activin => stimulates FSH releaseNote: these subunits have nothing to do with glycoproteins secreted by the pituitary

20
Q

Differences between inhibin and activin?

A
  1. Inhibin: blood-borne and inhibits FSH release2. Activin: not blood-borned (LOCAL) and stimulates FSH release
21
Q

Major actions of testosterone?

A

FETAL DEVELOPMENT OF:1. Epididymis2. Vas deferens3. Seminal vesiclesPUBERTAL GROWTH OF:4. Penis5. Seminal vesicles6. Musculature7. Skeleton8. Larynx SPERMATOGENESIS

22
Q

Major actions of DHT?

A

FETAL DEVELOPMENT OF:1. Penis2. Penile urethra 3. Scrotum4. ProstatePUBERTAL GROWTH OF:5. Scrotum6. Prostate7. Sexual hair8. Sebaceous glandsPROSTATIC SECRETION

23
Q

How does testosterone promote the growth of the skeleton at puberty?

A
  1. Stimulates GH secretion2. Stimulates proliferation of bone cells3. Stimulates closure of epiphyseal end plates of bones to terminate growth at the end of puberty
24
Q

How does testosterone promote the growth of the larynx at puberty?

A

Anabolic effects causing thickening of the vocal chords

25
Q

How do drugs against prostate enlargement or cancer work?

A

Block DHT by either:1. Inhibiting 5-alpha reductase2. Androgen receptor blocker

26
Q

Describe the changes in testosterone levels over the lifetime of a male.

A
  1. 3 month of fetal development: peak due to hCG (analog of LH) and the early temporary activation of the hypo to produce LHRH and therefore LH => organizes the future male brain to eliminate the default positive feedback loop that is found in females2. Peak shortly before, after, or during birth: hypothalamus becomes temporarily activated, driving testosterone production => essential in ensuring testicle descent3. Very low levels from birth to puberty due to exquisite sensitivity of low levels of testosterone inhibiting LHRH/LH secretion by the hypo-pit unit 4. At puberty increased glutamate/decreased GABA in hypo + nocturnal LH levels rise => induce gonadotropic cells in the median preoptic nucleus to release LHRH, which then causes more LH to be produced => increased production of testosterone => by the end of puberty, a new, higher set point of testosterone is present = “resetting of the gonadostat”5. Around age 60: decreased sensitivity of pituitary to LHRH stimulation, BUT enough to drive spermatogenesis (until about 90)
27
Q

What are variations in the height and slope of the 3 month fetal testosterone peak associated with?

A

Associated with variations in gender identity and sexuality

28
Q

Kallman syndrome: 8 symptoms?

A
  1. Diminished muscle mass around shoulders2. Fat deposition around hips3. Scant pubic hair4. Small penis and scrotum5. “Milk-toast” personality (shy, lacking self-confidence, etc.)6. ANOSMIA (inability to smell, key differential for this disease)7. Overall under-virilized8. Infertility
29
Q

Kallman syndrome: cause? Note?

A

Failure of migration of LHRH/GnRH neurons during fetal development from the olfactory bulbs where they are formed, due to many reasons such as genetic or diseased tissue in bulb or issues with proteins necessary to the migration Note: this is why it is accompanied by anosmia!Note: can also be partial

30
Q

Kallman syndrome: treatment? What to note?

A

Testosterone to restore secondary sex characteristics:1. Get rid of fat deposits because testosterone is a lipolytic hormone 2. Enlarge muscle mass3. Growth of pubic hair4. Lengthening of penis and enlargement of scrotumNote: treatment not able to restore fertility because still lacks FSH

31
Q

What is Kallman syndrome an example of?

A

Subset of conditions called hypogonadotropic hypogonadism

32
Q

Symptoms of precocious puberty in males? What to note?

A
  1. Tall2. Overdeveloped genitals3. Increased sexual behavior Note: cause and treatment are the same as for females