Normal growth & clinical aspects Flashcards

1
Q

does insulin stimulate or inhibit growth?

A

stimulates growth

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2
Q

what is the functions of growth hormone and is this direct and indirect effects?

A
growth and development (indirect)
regulates metabolism (direct)
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3
Q

what is required to allow GH to stimulate growth?

A

thyroid hormones & insulin

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4
Q

in adulthood when we stop growing, what is GH required for?

A

GH is required for maintenance and repair of tissues

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5
Q

what is responsible for the indirect action of GH on growth?

A

somatomedian C

IGF-1

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6
Q

where is IGF-1 secreted from and what promotes its release?

A

GH stimulates IGF-1 release from the liver

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7
Q

how does IGF-1 provide a negative feedback loop to GH?

A

IGF-1 inhibits the release of GHRH and stimulates GHIH

can also have an effect on the release of GH from the anterior pituitary

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8
Q

during puberty when there is massive spikes in GH production, what provides a buffering mechanism so that adolescences don’t grow in dramatic bursts?

A

50% of GH is bound to carrier proteins which helps to smooth out the erratic pattern of secretion
also provides a reservoir of GH in the blood when required

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9
Q

the closure of the epiphyseal plates after puberty is due to what hormone?

A

sex hormones

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10
Q

what is responsible for the production of cartilage in bone growth?

A

GH stimulates the differentiation of chondrocyte precursors to form chondrocytes.
these cells then begin to secret IGF-1 which they then respond to
IGF-1 lays down the cartilage which is the foundation for bone growth

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11
Q

how does GH have a direct effect on metabolism?

A

GH increases gluconeogenesis in the liver to increase glucose
it also reduces the ability of insulin to stimulate glucose uptake by muscle and adipose tissue
this causes hyperglycaemia making glucose readily available to cells needing it for growth

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12
Q

in patients who have an increase in GH release, how might they present with diabetogenic signs?

A

GH increases blood glucose in order to mobilise energy stores to make it readily available for cells who require glucose for growth

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13
Q

what effect does GH have on muscle, liver and adipose tissue?

A

GH decreases insulin’s ability to stimulate glucose uptake by muscle, liver and adipose tissue
however GH increases the amino acid uptake and protein synthesis

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14
Q

because GH inhibits the actions of insulin, how does it increase the uptake of glucose by other cells who require it for growth?

A

GH inhibits insulin to increase blood glucose to make it readily available for tissues who require it for growth
but liver, muscle and adipose tissue are the only tissues that are insulin sensitive
therefore other cells are able to uptake the glucose without insulin

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15
Q

when is release of GHRH at it highest and why?

A

during deep delta sleep because this is when we have our lowest energy requirements

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16
Q

what provides the buffering qualities to GH release during sleep and how?

A

IGF-1

levels remain constant during sleep despite the dramatic fluctuations of GH

17
Q

what are stimuli that increase GHIH?

A

glucose
FFA
REM sleep
cortisol

18
Q

what stimuli increase GHRH?

A
decrease in energy supply to cells
increased AA in plasma 
stressful stimuli e.g. infection 
delta sleep
oestrogen and testosterone
19
Q

why does an increase of AA stimulate GHRH but an increase in glucose stimulates GHIH?

A

GH promotes AA uptake and protein uptake by muscle and liver

whereas GH promotes an increase in blood glucose by reducing the ability of insulin to stimulate glucose uptake

20
Q

for growth and development, IGF-1 promotes the uptake of glucose into what type of tissue?

A

muscle

21
Q

what is cretinism?

A

a condition where a child is hypothyroid from birth

22
Q

why does hypothyroidism from both cause stunted growth?

A

thyroid hormone is permissive to the actions of GH

therefore with no TH the GH won’t be stimulated despite normal levels

23
Q

what is the cause of gigantism and acromegaly ?

A

gigantism is caused by an over secretion of GH before the epiphyseal plate closes
Acromegaly is over production after it closes

24
Q

how would you treat gigantism or acromegaly?

A

resection of pituitary tumour

somatostatin analogues

25
Q

what may be some of the causes of dwarfism?

A

deficiency in GHRH
abnormal GH secretory cells so less GH released in response to GHRH
end organ unresponsive to GH ( = high GH in plasma)
genetic mutations
precocious puberty (excess GnRH so long bones fuse early due to early influence of sex hormones)
hypothyroid (permissive effects of TH on GH)