Glucocorticoids Flashcards

1
Q

What are the different zones of the adrenal cortex and what do each of them secrete?

A

Glomerulosa: aldosterone

Fasciculata: cortisol

Reticularis: testosterone, estrogen, cortisol

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2
Q

Describe the pathway of cortisol release.

A

The hypothalamus releases CRH –> CRH causes anterior pituitary to release ACTH –> ACTH causes the adrenal cortex to release cortisol.

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3
Q

What are the metabolic effects of cortisol? What is cortisol’s main purpose?

A
  • Increase gluconeogenesis
  • Release amino acids via muscle catabolism
  • Inhibit peripheral glucose uptake
  • Stimulate lipolysis.

All these things serve to maintain an adequate supply of glucose to the brain.

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4
Q

Describe the anti-inflammatory and immunosuppressive effects of glucocorticoids.

A

Upregulation of anti-inflammatory and downregulation of pro-inflammatory proteins.

Decreased leukocyte presence and function. Inhibition of lymphocyte mitosis.

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5
Q

How is cortisol prevented from binding to mineralocorticoid receptors?

A

Cortisol gets converted to cortisone by 11beta-HSD2.

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6
Q

What are 2 things that stimulate aldosterone release?

A
  1. Angiotensin II

2. High ECF potassium levels

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7
Q

Which corticosteroid has the longest duration of action?

A

Dexamethasone

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8
Q

Which corticosteroid has the strongest relative anti-inflammatory activity?

A

Dexamethasone

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9
Q

Which corticosteroid has the strongest relative mineralocorticoid activity?

A

Fludrocortisone

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10
Q

How can you distinguish primary and secondary adrenocortical insufficiencies?

A

Primary: high ACTH (due to anatomic destruction of adrenal gland) -leads to skin discoloration.

Secondary: low ACTH (due to decreased pituitary function) -cortisol is primarily affected (ACTH has minimal effect on aldosterone)

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11
Q

What are the signs/symptoms of an Adrenal Crisis (acute adrenal insufficiency)?

A

-Mineralocorticoid deficiency –> Hyperkalemia, hyponatremia, increased ADH, hypotension, nausea/vomiting

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12
Q

How do you treat Chronic Primary Adrenal Insufficiency?

A

Replace glucocorticoids with Hydrocortisone and mineralocorticoids with Fludrocortisone.

If a minor febrile illness occurs, increase the glucocorticoid dose.

In an emergency, inject dexamethasone.

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13
Q

How do you diagnose Cushing’s Syndrome?

A

Use a low-dose dexamethasone test. This will cause a decrease in cortisol release via negative feedback in a normal patient. Cushing’s patients will still have elevated cortisol the next morning.

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14
Q

If surgery is not an option, what treatments are available for Cushing’s Syndrome?

A

Aminoglutethimide, Ketoconazole, Mitotane, Metyrapone, Mifepristone

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15
Q

What does Aminoglutethimide do?

A

Blocks conversion of cholesterol to pregnenolone.

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16
Q

What does ketoconazole do?

A

It is a potent, nonselective inhibitor of adrenal and gonadal steroid synthesis.

17
Q

What does mitotane do?

A

It has a nonselective cytotoxic action on the adrenal cortex. Bad side effect profile.

18
Q

How does metyrapone work?

A

Inhibits 11-hydroxylation, interfering with cortisol and corticosterone synthesis.

19
Q

What is the metyrapone test?

A

It tests anterior pituitary function. The metyrapone results in decreased cortisol and corticosterone synthesis, which causes an increase in ACTH (in a normal patient) and 11-deoxycortisol (the precursor to cortisol).

20
Q

How does mifepristone work?

A

It’s a glucocorticoid receptor antagonist.

21
Q

What is the treatment plan for primary aldosteronism?

A

Surgery: unilateral adenoma

Spironolactone, eplerenone: bilateral adrenal hyperplasia

22
Q

Describe what is going on in 21-hydroxylase deficiency (Congenital Adrenal Hyperplasia)

A

The absence of this enzyme shunts away from aldosterone and cortisol production to androgen production.

The decreased cortisol increases ACTH and the increased androgen causes hirsutism and virilization.

23
Q

What is something very important to consider when ending steroid therapy?

A

NEVER stop abruptly. Always taper off.

24
Q

How is 21-hydroxylase deficiency diagnosed?

A

Increased response of plasma 17-OH-Progesterone to ACTH stimulation (Cosyntropin stimulation test)

25
Q

How is 21-hydroxylase deficiency treated?

A

Dexamethasone, prednisone or hydrocortisone.

If salt-wasting, add fludrocortisone.