ADRENAL CORTEX Flashcards

1
Q

Cholesterol → Pregnenolone → Progesterone (21-hydroxylase) → Deoxycorticosterone → 11B-hydroxylase → Corticosterone to Aldosterone

A

Aldosterone Formation (Mineralocorticoid)

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2
Q

Pregnenolone → 17-OH Pregnenolone → 21-hydroxylase → Deoxycortisol → 11B-hydroxylase → Cortisol

A

Cortisol Formation (Glucocorticoid)

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3
Q

DHEA → Androstenedione → Testosterone, Estradiol

A

DHEA Formation (Sex Hormones)

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4
Q

Tyrosine → L-3,4-dihydroxyphenylalanine (L-DOPA) → Dopamine (HVA) → Norepinephrine (normetanephrine) → epinephrine (metanephrine)

A

Catecholamine Synthesis Pathway

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5
Q

Metabolite for Norepinephrine and Epinephrine

A

VMA

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6
Q

Source: Zona glomerulosa; Target: Kidneys; Major function: Blood pressure and electrolyte regulation (under RAAS control)

A

Aldosterone

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7
Q

Source: Zona fasciculata; Target: Liver or adipose; Major function: Carbohydrate, protein, and lipid metabolism

A

Cortisol

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8
Q

Source: Zona reticularis; Target: Gonads, muscles, and bones; Major function: Precursor to androgens; growth and maturation

A

Sex steroids

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9
Q

Source: Medulla; Target: Liver and adipose; Major function: Stimulates sympathetic nerves, promotes glycogenolysis and lipolysis

A

Epinephrine

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10
Q

Source: Medulla; Target: SNS; Major function: Stimulates sympathetic nerves

A

Norepinephrine

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11
Q

Confirmatory test for primary aldosteronism (Conn’s disease)

A

Captopril suppression test

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12
Q

Test for Conn’s disease

A

Urinary potassium excretion, Captopril suppression, upright PA (plasma aldosterone)/PRA (plasma renin activity) ratio, 18-Hydroxycorticosterone

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13
Q

Condition with increased aldosterone, plasma sodium, and decreased plasma potassium

A

Hyperaldosteronism (Conn’s)

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14
Q

Condition characterized by primary hypercorticotism

A

Cushing’s syndrome

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15
Q

Condition characterized by secondary hypercorticotism

A

Cushing’s disease

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16
Q

Tests for diagnosing Cushing’s syndrome and disease

A

Urine free cortisol over 24 hours, Midnight salivary cortisol, Dexamethasone suppression test (LD=1mg overnight or 2mg over 48 hours, HD=8mg), Plasma ACTH (requires pre-chilled tube)

17
Q

Plasma cortisol ↑, Plasma ACTH ↓

A

Cushing syndrome

18
Q

Plasma cortisol and ACTH ↑

A

Cushing disease

19
Q

Test result in Cushing disease with high dose DST

A

Suppressed plasma cortisol

20
Q

Plasma cortisol and ACTH ↑↑↑, High dose DST results

A

Ectopic Cushing syndrome (ACTH-producing tumors)

21
Q

Tests for Addison’s disease (primary adrenal insufficiency)

A

ACTH stimulation (Cortrosyn) test, Insulin tolerance test, Metyrapone test

22
Q

Condition with decreased aldosterone and cortisol, increased androgen

A

Congenital adrenal hyperplasia

23
Q

Enzyme deficiency associated with congenital adrenal hyperplasia

A

21-Hydroxylase

24
Q

Plasma and urinary tests for diagnosing congenital adrenal hyperplasia

A

Plasma 17-hydroxyprogesterone, Pregnanetriol, Urinary pregnanetriol, 17-ketosteroids

25
Q

Development of overt male secondary sexual features

A

Virilization

26
Q

Non-typically appearing female external genitalia

A

Genital ambiguity

27
Q

Excessive hair growth due to increased ovarian androgens in women

A

Hirsutism

28
Q

Scale used for grading hirsutism

A

Ferriman-Gallwey scale