Hypothalamus and Pituitary Tutorial Flashcards

1
Q

what is a ENdocrine gland

A

secretes its hormones directly into the bloostream

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2
Q

what is an EXocrine gland

A

secrete their hormones into a collection of ducts which are carried around the body

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3
Q

what is the difference in onset and duration of action of endo vs exocrine glands

A

exocrine quicker response

endocrine longer duration as taken to kidney to made available for absorption

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4
Q

match each hormone to its class:
steroid
protein and peptide
amine

insulin
adrenaline
testosterone

A

steroid- testosterone
protein and peptide- insulin
amine- adrenaline

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5
Q

true or false- amine peptides and proteins are only synthesised on demand

A

false

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6
Q

true or false- steroid hormones are mainly bound to proteins in the plasma

A

true

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7
Q

true or false- amines, peptides and proteins stimulate and act on intracellular receptors

A

false - have cell surface receptors

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8
Q

list these from shortest to longest half lives:
steroid
amine
peptide

A

amine- seconds
peptide- minutes
steroid- hours

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9
Q

what connects the hypothalamus to the pituitary

A

the pituitary stalk

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10
Q

what is the adenohypophysis

A

anterior pituitary

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11
Q

what in the neurohypophysis

A

posterior pituitary

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12
Q

what synthesises posterior hormones in the hypothalamus

A

supraoptic and paraventricular nuclei (neuroendocrine)

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13
Q

how do hormones from the hypothalamus get to the anterior pituitary

A

cell bodies secrete into via portal veins

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14
Q

what are the ‘releasing’ stimulatory hypothalamic hormones

A
growth hormone releasing hormone (GHRH)
prolactin releasing hormone (PRH)
thyrotrophin releasing hormone (TRH)
corticotrophin releasing hormone (CRH)
gonadotrophin releasing hormone (GnRH)
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15
Q

what are the inhibitory hypothamalic hormones

A

somatostatin and dopamine

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16
Q

what class are the hypothamalic hormones

A

all peptides except dopamine which is an amine

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17
Q

what does dopamine inhibit

A

the release of prolactin (ant pit)

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18
Q

what does somatostatin inhibit

A

growth hormone (ant pit)

19
Q

what is released from the anterior pituitary

A
GH 
ACTH (andenocorticotrophic hormone)
TSH
PRL
FSH (follicle)
LH (lutenising)
20
Q

what is released from the posterior pituitary

A

oxytocin

anti-diuretic hormone (ADH)

21
Q

what is the function of oxytocin

A

milk secretion and uterine contractions

22
Q

what is the function of ADH

A

increases water reabsorption at kidneys

vasoconstriction at vascular smooth muscle

23
Q

what are the actions of growth hormone

A

increases blood glucose by increasing gluoneogenesis in the liver
releases insulin GF (IGF-1) from the liver
decreases glucose uptake in muscles cells- increases it in brain cells
increases the rate of lipolysis in fat cells
has anabolic effect on the body
increase glucose and fatty acids
increased protein synthesis
decreased fat storage
increased soft tissue growth
increased bone growth

24
Q

what are common conditions in growth hormone excess

A

diabetes (T2), carpal tunnel syndrome, hypertension

25
what does IGF-1 cause
increased bone growth increased soft tissue growth increased protein synthesis
26
what changes can be seen in acrogmegaly
``` increase in hand and foot size prominent brow large nose and jaw pronounced cheekbones skin changes (thickens, sweating, acne) oral manifestations (enlargement of tongue and swelling of larynx, interdental separation) ```
27
how can acromegaly's oral manifestations cause presentations
deep or coarser voice | obstructive sleep apnoea
28
how is movement affected in acromegaly
joint pain, proximal muscle weakness, lethargy decreases movement decreased movement in hands and pain/ tingling sensations
29
what behavioural problems arise in acromegaly
lethargy | polydispsia and uria
30
why do you get hypertension in acromegaly
increased plasma fatty acids causes patty plaques
31
what nerve is affected in carpal tunnel
median nerve
32
what provides negative feedback for GH
IGF-1 negative on ant pit | GH negative on Hypothalamus
33
what causes acromegaly
``` pituitary tumour (micro <1cm or macroadenoma >1cm) ectopic tumour ```
34
what is gigantism
when children have a growth hormone secreting tumour of the pituitary gland- epiphyseal plates not closed so large bone growth
35
in acrogmegaly what hormone can also be secreted in excess
prolactin (in one 1/3rd of patients)
36
why can GH nnot diagnose acromegaly
as released in pulsatile manner - highest when asleep and in times of stress
37
when is growth hormone low normally
in pregnancy
38
what is the definitive test for acromegaly
oral glucose tolerance test
39
how does oral glucose tolerance test diagnose acromegaly
oral glucose should suppress GH to <1 microgram/litre if no suppression then acromegaly
40
what can IGF-1 test show
mean 24 hour secretion of growth hormone
41
what scan is done to see if there is a tumour in acromegaly
MRI of the pituitary fossa
42
what is the treatment for acrogmegaly
surgery- trans-sphenoidal radiotherapy- (with/without surgery) dopamine agonists (bromocriptine and cabergoline) somatostatin receptor agonists (octreotide and lanreotide) growth hormone antagonists (pegvisomant)- works on GH receptors not on tumour
43
what can cause hypopituitarism
pituitary tumour radiation damage trauma infective (meningitis, syphilis, encephalitis) immunological (autoimmune) infiltrative (haemachromoatosis, sarcoidosis, secondary mets lesions)