Adrenalcorticoids Summary Flashcards

1
Q

How are adrenal steroids synthesized?

A

By enzymatic modification of cholesterol (like all steroid hormones)

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2
Q

Where does cholesterol come from for steroidogeneisis?

A

Acquired from dietary sources or synthesized in liver. De novo synthesis also possible.

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3
Q

What is the primary glucocorticoid? What does it have negative feedback control of?

A

Cortisol. Hypothalamic (CRF) and anterior pituitary hormone (POMC/ACTH) release.

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4
Q

What regulates glucocorticoid production?

A

ACTH. Side chain cleavage enzyme is under ACTH regulation making the production of pregnenolone the rate limiting step.

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5
Q

What enzyme is responsible for progesterone conversion to glucocorticoids?

A

21 hydroxylase.

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6
Q

What happens if 21 hydroxylase is defective?

A

There is a lack of glucocorticoids AND mineralocorticoids and an excess of androgens. Hypotension is seen with this. It is the most common genetic defect.

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7
Q

What is the function of 11B-hydroxylase (11 B hydroxysteroid dehydrogenase)?

A

It converts deoxycorticosteroids to glucocorticoids and mineralcorticoids.

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8
Q

What happens when 11B hydroxylase is defective?

A

There is a lack of cortisol and aldosterone. However, deoxycorticosterone and 11 deoxycortisol are made which have weak mineralocorticoid activity. HTN seen with 11B-hydroxylase defects.

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9
Q

What does Aldosterone regulate?

A

Sodium and K balance

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10
Q

How does Aldosterone influence ACTH?

A

Has no effect on ACTH.

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11
Q

What is hypercortisolism (cushing syndrome) usually due to?

A

Cushing disease

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12
Q

What is hypocortisolism (adrenal insufficiency) usually due to?

A

Addison’s disease or congenital adrenal hyperplasia.

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13
Q

What is co-incident with production of high levels of POMC (ACTH and MSH)?

A

Hyperpigmentation

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14
Q

What stimulates melanocyte production of melanin?

A

ACTH and MSH isoforms bind to skin MC1-R and stimulates this.

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