Pituitary Physiology Flashcards

1
Q

what does the posterior pituitary gland secrete

A

oxytocin and ADH

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2
Q

oxytocin function

A

allows the milk to be released when women breast feed

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3
Q

where are the posterior pituitary gland secretions formed

A
  • These hormones are synthesized in the body of the nerve cells in the hypothalamus, the gland is an extension of these nerve cells
  • Secretions controlled by neurons
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4
Q

describe the formation and storage of ADH

A
  • An octapeptide that is synthesised in the hypothalamus in neuron cell bodies. It is transported down neuron axons to nerve terminal in the posterior pituitary gland, where it is stored in granules.
  • It is released into the blood when action potentials down the nerves lead to Ca2+ dependent exocytosis.
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5
Q

what does the anterior pituitary gland secrete

A

ACTH, TSH, FSH, LH, PRL and STH

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6
Q

what are secretions to the anterior pituitary gland controlled by

A

inhibitory and releasing hormones - secretions first absorbed by capillaries at the base of the hypothalamus and then to pituitary

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7
Q

gonadotropins

A

eg LH and FSH

regulate growth, sexual development and normal reproductive function

stimulate production of testosterone and E2 (oestrogen)

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8
Q

E2

A

estradiol

an oestrogen

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9
Q

steroids - pituitary and peripheral hormones

A

pituitary - ACTH

peripheral - cortisol

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10
Q

GH - pituitary and peripheral hormones

A

pituitary: GH
peripheral: IGF-1

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11
Q

suppression test

A

performed if it is suspected that too much hormone produced

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12
Q

stimulation test

A

performed if it is suspected that too little hormone is produced

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13
Q

insulin stress test

A

suspected glucose, cortisol, GH deficiency

involves giving the patient IV insulin to make the hypoglycaemic, this stress should stimulate the hypothalamus and cause glucose, GH and cortisol levels to rise

eg if werent producing GH that curve wouldnt rise

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14
Q

synacthen test

A

Synthetic ACTH, performed when there is a suspected lack of cortisol

cortisol levels checked at 0, 30 and 60 minute intervals

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15
Q

what test is the gold standard for assessing the integrity of the HPA

A

insulin stress test

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16
Q

what is a non functioning pituitary adenoma

A

one that doesnt secrete any hormones

17
Q

complications of NFPA if extends upwards

A

compression of optic chiasma - bitemporal hemianopia

18
Q

complicationsof NFPA if it extends laterally

A

cavernous system

  • CNIII - several eye movements and dialted pupil
  • CNIV and CNVI - problems with specific eye movements

CNV (I and II)

internal carotid artery

cavernous sinus

19
Q

complications of NFPA if it affects the pitutiary

A

hypo - adrenalism, thyroidism, gonadism

diabetes insipidus if posterior pituitary affected

GH deficiency

20
Q

difference in size between a micro and macro adenoma

A

1cm

21
Q

pituitary carcinoma

A

rare, and often functional

metastasize late after multiple recurrences

22
Q

craniopharyngioma

  • what is it derived from
A
  • brain tumour derived from pituitary gland embryonic tissue - Rathke’s pouch
  • most common childhood intracranial tumour
  • most arise in the sella
23
Q

who do craniopharyngiomas most commonly occur in

A

children

also adults in 50s and 60s

24
Q

describe the progression of a craniopharyngioma

A

slow growing, cystic and may calcify

25
Q

clinical features of craniopharyngiomas

  • presentation in adult and child
A

over 50% present in children with growth failure

headaches and visual disturbances (compression of optic chiasma)

adults may present with amenorrhoea

26
Q

investigation of craniopharyngiomas

A

CT/MRI

27
Q

treatment and prognosis of craniopharyngiomas

A

surgery ± post-op radiation

prognosis is excellent, especially if it is <5cm