Adrenal Gland Fx And Diseases - 2/9 Lopez Flashcards

1
Q

A defect in 17a-hydroxylase results an increased production in what?

A

Aldosterone

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2
Q

A deficiency in 21B-hydroxylase results in what?

A

Directs the system towards androgen production

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3
Q

Deficit in 11B-hydroxylase results in what?

A

Directs system towards Androgens

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4
Q

How do steroid hormones work?

Where are the receptors located?

Slow or fast acting?

A

Lipophilic, easily cross CM

Cytoplasm or nucleus

Slow

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5
Q

What does ACTH contain?

What does it do?

A

alpha-MSH

Melanin synthesis

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6
Q

What are the target tissues of cortisol?

A

LIAM

Liver, immune system, adipose, muscle

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7
Q

What effect does cortisol have on the following?

Liver
Immune system
Adipose
Muscle

A

Gluconeogenesis
Immune suppression
Lipolysis
Protein catabolism

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8
Q

When are secretory rates of cortisol high?

Low?

A

In the morning

Night/midnight

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9
Q

Exogenous cortisol may cause what with prolonged exposure?

A

Atrophy of the adrenal cells

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10
Q

Cushing’s syndrome is caused by what?

Results in what?

A

Adrenal tumor

Hypercortisolism

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11
Q

What is Cushing’s disease?

Result?

A

Tumor in pituitary gland

Hypercortisolism

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12
Q

What is Addison’s disease?

Causes what?

A

Autoimmune disease of adrenal gland

Hypocortisolism

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13
Q

In Hypocortisolism cortisol levels are low, what does this mean regarding CRH and ACTH levels?

A

Elevated because it detects low levels of cortisol

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14
Q

What causes secondary adrenal insufficiency?

A

Glucocorticoid drugs

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15
Q

When does hyper pigmentation result?

A

When ACTH levels are elevated (secondary/pituitary excess and primary deficiency)

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16
Q

Describe the levels of the following in Cushing’s Syndrome

CRH
ACTH
Cortisol

17
Q

Describe the levels of the following in Cushing’s disease

CRH
ACTH
Cortisol

18
Q

Describe the levels of the following in Addison’s Disease

CRH
ACTH
Cortisol

19
Q

Describe the levels of the following in Secondary adrenal insufficiency

CRH
ACTH
Cortisol

20
Q

What kind of receptor does aldosterone have?

A

Cytoplasmic receptor

Will translocate to nucleus to initiate transcription

21
Q

What causes primary hyperaldosteronism?

A

Excessive secretion of aldosterone from adrenal cortex

22
Q

What causes secondary hyperaldosteronism?

A

Excessive secretion by the JG cells of the kidney

23
Q

What is Conn’s syndrome?

A

Adenomas in the adrenal cortex, primary hyperaldosteronism

24
Q

What causes hypoaldosteronism?

A

Destruction of adrenal cortex
Defects in aldosterone synthesis
Inadequate stimulation of aldosterone secretion

25
What are the clinical Sx of Addison's disease? Result of what?
Weakness, weight loss, hyperpigmentation Primary deficiency of cortisol and aldosterone due to atrophy of adrenal cortex
26
Describe the synthesis of epinephrine
Tyrosine -> dopa -> dopamine -> NE -> epinephrine
27
Synthesis of NE -> Epi via what enzyme? What stimulates production?
PNMT Cortisol
28
Where is NE synthesized in chromaffin cell? Epi?
Within the chromaffin granule Cytosol
29
What is the RLS of epinephrine synthesis? Give substrate, product, enzyme
Try -> L-dopa | Via enzyme Tyrosine hydroxylase
30
How is Epi transported from the cytosol to the granule?
VMAT
31
What are NE and Epi complexed with in the granule?
ATP, Ca, chromogranins
32
Epi can be broken by what enzymes? What is the ultimate breakdown product that can be measured in the urine?
COMT, MAO VMA
33
What receptor does epinephrine have higher affinity that NE for?
Beta-2
34
What is pheochromocytomas? Sx?
Tumor of chromaffin tissue Produces excess catecholamines Headaches, sweating, palpitation, hypertension
35
What regulates the activity of cholesterol desmolase? What does it regulate?
steroids genie acute regulatory protein (StAR) Cholesterol transport transfer within the mitochondria