Adrenocortical Function and Dysfunction Flashcards

1
Q

What is the embryological origin of the adrenal medulla?

A

Modified sympathetic ganglion (catecholamines/neurohormones)

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2
Q

What is the embryological origin of the adrenal cortex?

A

Endocrine

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3
Q

What are the functions mediated by CRH?

A

inflammation and immune responses; inhibition of appetite; signals onset of labour from placenta; linked to mood

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4
Q

What is pro-opiomelanocortin (POMC)?

A

large protein that yields several bioactive peptides: ACTH (a. pit), beta-endorphin (a. pit), alpha-melanocyte-stimulating hormone (systemic ACTH)

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5
Q

What is the function of beta-endorphin?

A

blocks pain perception

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6
Q

What is the function of alpha-MSH?

A

decrease food intake, increase skin melanin

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7
Q

What are melanocortins?

A

MSH hormones and ACTH

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8
Q

What are the functions of cortisol?

A

essential; coping with long term stress; protects against hypoglycaemia by increasing catabolism of energy; permissive for glucagon and catecholamine actions

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9
Q

What are the effects of long-term cortisol use?

A

inhibition of ACTH secretion and atrophy of cortisol-secreting cells - tf need to taper doses on and off so body can physiologically adapt

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10
Q

A primary adrenal cortex disorder would be the result of

A

an adrenal cortex defect (primary = defect of the gland)

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11
Q

A secondary adrenal cortex disorder would be a result of

A

defect of the hypothalamus or anterior pituitary

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12
Q

What are the catecholamines?

A

Epinephrine (adrenal medulla only), norepinephrine, dopamine

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13
Q

Why is epinephrine only made in the adrenal medulla?

A

phenylethanolamine-N-methyltransferase (PMNT) that converts norepinephrine to epinephrine is only found here

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14
Q

What is the physiological result of hyperaldosteronism?

A

hypernatremia, hypokalemia, hypertension

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15
Q

Cushing’s syndrome is what type of hypercortisolism?

A

Primary - adrenal cortex tumours secreting cortisol (ACTH independent)

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16
Q

Cushing’s disease is what type of hypercortisolism?

A

Secondary - pituitary tumour secreting ACTH (ACTH-dependent)

17
Q

What is the most common cause of hypercortisolism?

A

Iatrogenic from prescription cortisol therapy

18
Q

What is adrenogenital syndrome?

A

Excess androgen and estrogen production due to lack of enzyme in the cortisol steroidogenic pathway shunting away from cortisol production towards sex hormones

19
Q

What is the effect of adrenogenital syndrome?

A

Inappropriate masculinisation (or early) of all but adult males

20
Q

What causes hyperglycaemia in Cushing’s syndrome?

A

Excess gluconeogenesis and glycogenolysis

21
Q

Decreased production of aldosterone (Addison’s, hypocortisolism) causes

A

K+ retention (cardiac arrhythmia) and Na+ and water depletion (hypotension)

22
Q

What causes salt and water retention in Cushing’s syndrome?

A

excess cortisol crossing over to react with mineralocorticoid receptors

23
Q

Secondary adrenal hyposecretion is caused by

A

abnormal hypothalamus or pituitary function causing decreased ACTH and cortisol production (aldosterone is normal)

24
Q

PMNT

A

phenylethanolamine-N-methyltransferase; converts norepinephrine to epinephrine in the adrenal medulla

25
Q

Pheochromocytomas

A

tumour of adrenal medulla causing hypersecretion of catecholamines and deadly prolonged hypertension

26
Q

Acute stress results in

A

activation of the fight or flight response

27
Q

Chronic stress results in

A

elevation of cortisol levels - this suppresses immune responses