Lecture 9: Steroid Biosynthesis Flashcards

1
Q

Where does steroid hormone synthesis occur?

A

Adrenal Cortex

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2
Q

What are the classic and non-classic forms of Adrenal Hyperplasia caused by?

A

Deficiencies in the adrenal enzymes that are used to synthesize glucocorticoids

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3
Q

Women with mild congenital adrenal hyperplasia often present with?

A
  • Hirsutism
  • Excessive body hair in men and women on parts of the body where hair is normally absent or minimal, such as on the chin or chest in particular
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4
Q

Other than Hirsutism what else do female patients with Adrenal Hyperplasia present with?

A

General oligomenorrhea = infrequent (or, in occasional usage, very light) menstruation

  • Menstrual periods occuring at intervals of >35 days
  • Infertility
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5
Q

How is it determined if a fetus is at risk for congenital adreanl hyperplasia?

A
  • Using human leukocyte antigen halotype
  • Demonstration of excess cortisol precursors in amniotic fluid
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6
Q

What is the treatment for Adrenal Hyperplasia?

A

Carefully monitored hormone replacement therapy (HRT)

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7
Q

What occurs in 21-hydroxylase deficiency?

A
  • Accumulation of progesterone and 17-hydroxyprogesterone
  • Results in shunting of substrates to the pathway for the production of testosterone
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8
Q

What accumulates as a result of 11-β hydroxylase deficiency?

A
  • Accumulation of Deoxycorticosterone and 11-Deoxycortisol
  • Both of which have MR activity
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9
Q

The production of aldosterone from corticosterone occurs in which part of the adrenal cortex?

A

Zone Glomerulosa

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10
Q

Aldosterone is a mineralcorticoid that binds what; and regulates?

A
  • Binds mineralocorticoid receptor
  • Promotes the retention of Na+ and H2O in the kidneys, as well as excretion of H+ and K+
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11
Q

Increased levels of aldosterone are seen in what pathology; what dpo these patients experience?

A

Conn syndrome = increased blood volume and hypertension

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12
Q

An 11-β-hydroxylase deficiency leads to what?

A
  • Decrease in serum cortisol, aldosterone, and corticosterone
  • Increased production of 11-deoxycorticosterone causes fluid retention because this hormone suppresses the renin/angiotensin system, it causes low-renin hypertension
  • Overproduction of androgens causes masculinization and virilization as with 21-α-hydroxylase deficiency
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13
Q

Which substrate that buildsup from 11-β-hydroxylase deficiency has the greatest MR affinity?

A

11-deoxycorticosterone

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14
Q

Which molecule signals and stimulates production of steroid hormones from cholesterol; what is the first step in this pathway?

A
  • ACTH signals and regulates Desmolase activity
  • Desmolase is the enzyme that produces pregnenolone from cholesterol
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15
Q

What happens when cortisol levels are low; describe the pathway?

A
  • Signals to the hypothalamus to produce CRH
  • CRH stimulates the anterior pituitary gland to produce ACTH (polypeptide tropic hormone - 39 AA’s long)
  • ACTH stimulates the production of cortisol
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16
Q

What type of receptors does ACTH bind and where does the production of glucocorticoids occur?

A
  • Binds a GPCR located on adrenocortical cells of the adrenal cortex
  • Zone Fasciculata
17
Q

What is the significance of a tumor cell in terms of its ACTH activity?

A
  • Does not require ACTH as a signal
  • Uncoupling occurs and PKA is stuck in active state
  • Leads to cell proliferation and increased cortisol production
18
Q

What are the short-term mechanisms of ACTH binding its receptor in the adrenal cortex?

A
  • Stimualtion of cholesterol delivery to the mitochrondria where the P450scc enzyme is located
  • P450scc catalyzed the first step of steroidogenesis that is cleavage of the side-chain of cholesterol
19
Q

What are the long-term actions of ACTH binding its receptor on the adrenal cortex?

A
  • Stimulation of the transcription of the genes coding for steroidogenic enzymes (feed-forward loop):
  • P450scc
  • Steroid 11-β-Hydroxylase
  • Associated electron transfer proteins
20
Q

What is a key enzyme in the steroidogenic pathway that produces progestins, mineralocorticoids, glucocorticoids, androgens, and estrogens (sex hormones)?

A

17, 20-lyase = CYP17A1

21
Q

What do mutations of 17, 20-lyase (CYP17A1) lead to?

A
  • Pseudohermaphroditism
  • Adrenal Hyperplasia
22
Q

What 2 ways is cholecalciferol (D3) obtained?

A

1) Via the diet-Ergocalcifrol (Vitamin D2) is absorbed in the intestine
2) Converted from 7-dehydrocholesterol in the skin via UV radiation

23
Q

What is found exclusively in the liver pertaining to vitamin D and what does it do?

A
  • 25-hydroxylase (CYP2R1) only found in LIVER
  • Converts Cholecalciferol (D3) to 25-hydroxycholecalciferol