Pituitary And Adrenal Gland Flashcards

1
Q

What hormones are excreted by the neurohypophysis (posterior pituitary)

A

ADH (anti diuretic hormone/ vasopressin) and oxytocin

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2
Q
The adenohypophysis (anterior) potion of the pituitary gland is controlled mostly by: 
Neurohypophysis?
A

Anterior: hypothalamus
Posterior: nervous tissue

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3
Q

The master gland

A

The pituitary gland

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4
Q

Where adrenal glands are located

A

On top of kidneys

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5
Q

ACTH (adrenocorticotropic hormone) controls what portion of the adrenal gland

A

The cortex: cortex hormones (glucocorticoids, minerlcorticoids, androgens) released based on ACTH levels (feedback loop)

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6
Q

What controls the medulla portion of the adrenal gland

A

Nervous system

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7
Q

The medulla of the adrenal gland is responsible for producing what

A

Catecholamines: epinephrine and norepinephrine

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8
Q

Role of glucocorticoids produces by cortex, give example

A
Ex: cortisol 
Promotes glycogenesis (production of glucose via breakdown for energy and storage)
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9
Q

What we would give steroids (glucocorticoids) for, what they do

A

Decreases inflammation, slows healing, inhibits immune system
Give for allergic reactions or swelling

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10
Q

Aldosterone is what kind of cortex hormone, what does it do

A

Mineralocorticoid: works at kidney level for water and Na retention, and K excretion

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11
Q

What are androgen cortex hormones

A

Sex hormones like testosterone

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12
Q

What is cushings disease

A

Hyperadrenocorticism

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13
Q

What is Addison’s disease

A

Hypoadrenocorticism

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14
Q

Possible causes of hyperadrenocorticism ( cushings)

A

Adrenal tumor (primary), pituitary tumor (secondary), iatrogenic cause (too many steroid hormones)

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15
Q

Signs of hyperadrenocorticism (cushings)

A

Pot belly, polyphagia, PU/PD, hair-loss (bi lateral symmetrical), skin changes (too many glucocorticoids, high energy in body)

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16
Q

What is Addison’s disease

A

Hypoadrenocorticism

17
Q

Possible causes of hypoadrenocorticism (Addison’s disease)

A

Tumor, infectious agent, or autoimmune disorder that damages the adrenal gland

18
Q

Signs of hypoadrenocorticism (Addison’s disease)

A

Weak, depressed, PU/PD, vomiting, poor hair coat, arrhythmia
(K retained, Na and Cl lost)

19
Q

What resting cortisol levels can diagnose

A

Hypoadrenocorticism (low)

Hyperadrenocorticism is not definitive w high levels Bc other things (like physiologic stress) can also increase

20
Q

What are provocative tests? What ones are used to diagnose hyper/hypoadrenocorticism

A

Administer drug to provoke a response from feedback loop: ACTH stimulation test or dexamethasone suppression test

21
Q

How a ACTH stim Test is done

A

Take baseline blood sample, administer ACTH, take a 2nd sample 1 hr later, measure cortisol samples in both (normally should increase 2-4x)

22
Q

in an ACTH stim test

What is indicative of hyperadrenocorticism and hypoadrenocorticism

A

Hyper- second sample v high (4-8x)

Hypo- no change from 1st or 2nd sample, both are low

23
Q

What is dexamethasone, and how is it used to diagnose hyperadrenocorticism

A

Synthetic cortisol, injected to suppress release of ACTH and thus suppress cortisol release

24
Q

Low dose v high dose dexamethasone suppression test (what they diagnose?)

A

Low dose: hyperadrenocorticism (confirm after resting cortisol test)
High dose: differentiate primary v secondary hyperadrenocorticism)

25
Q

After dexamethasone is given, the cortisol levels in blood samples should be

A

Lower than baseline (cortisol in blood tells ACTH to stop, cortisol is suppressed)

26
Q

What we would see for hyperadrenocorticism on a low dose dexamethasone suppression test

A

The low is not enough to turn off pituitary or adrenal hormones, all samples have same amounts of cortisol

27
Q

Primary v secondary hyperadrenocorticism high dose tests

A

Primary: baseline is high, other samples after dxm also high Bc adrenal gland continues making cortisol (no suppression)
Secondary: baseline high, others suppressed in cortisol (ACTH is suppressed, causing cortisol to be suppressed)

28
Q

Equine hyperadrenocorticism is also called

A

Pituitary Pars intermediate dysfunction (PPID) or Equine Cushing’s

29
Q

When does equine hyperadrenocorticism typically occur

A

Old horses 18+, usu benign pituitary tumors

30
Q

Signs of equine hyperadrenocorticism

A

Lethargy, pot belly, sweating, PU/PD, hirsutism (overgrowth of hair, fails to shed), prone to infections