Endo 8: Therapeutic use of adrenal steroids Flashcards
Which 2 things affect ACTH release
Stress and circadian stimuli
Where is cortisol made within the adrenal cortex
Zona fasciculata
T/F production of sex steroids in the adrenal gland is responsive to ACTH control, but aldosterone is not
True! Aldosterone activated by renin angiotensin axis (e.g. renin secreted due to: high potassium, hyponatraemia and reduced renal blood flow in the JGA and b1-adrenoceptor stimulation)
Where are sex steroid produced in the adrenal cortex
zona reticularis
Compare MR and GR receptors
Distribution: MR discrete (kidney) GR everywhere
Selectivity: MR doesn’t distinguish cortisol and aldosterone, GR selective for glucocorticoids
Affinity for cortisol: GR low MR high
Which receptors can aldosterone and cortisol bind to
Aldosterone- only MR
Cortisol- GR and MR
Reason for hypokalaemia in cushings and hypertension
11B-HSD 2 overwhelmed so cortisol not converted to cortisone (the inactive form) thus can bind to the MR receptors in the kidneys and cause excretion of K+ and reabsorption of salt and water so hypertension
What is cortisol converted to in MR containing tissue
Cortisone (inactive form)
Treatment for addisonian crisis
NaCl and hydrocortisone and glucose
Impact of high dose hydrocortisone on BP in addisonian crisis
Such high level of cortisol that it overwhelms 11b-HSD 2and acts on MR to increase BP (so don’t worry about aldosterone acutely
What is fludrocortisone
aldosterone analogue- given to an addisons patient going home and also cortisol (hydrocortisone or prednisolone)
Which binds MR more: hydrocortisone or prednisolone
hydrocortisone
Routes of admin for cortisol/aldosterone replacement
Oral (hydrocrotisone, prenisolone, dexamethasone or fludrocortisone) and parenteral (i.v. or i.m.) (hydrocortisone or dex)
Where do corticosteroids bind (it said this is where they all bind I think?)
Corticosteroid binding globulin (CBG)
Differentiate the adrenal cortex function in secondary vs primary hypoadrenalism
Secondary- aldosterone and BP is fine but low cortisol and sex steroids, the only reason for low cortisol is lack of ACTH which doesn’t affect aldosterone as aldosterone is regulated by renin (which converts angiotensinogen to angiotensin I etc. etc.)
Primary- low aldosterone and low cortisol and sex steroids because the whole of the adrenal cortex is actually destroyed so there’s no ability to make aldosterone or cortisol
Which precursor starts to accumulate in 21 hydroxylase deficiency
17ahydroxyprogesterone accumulates, because it’s immediately before the enzyme block, and this is converted into the sex steroid arm so lots of adrenal androgens produced (leading to hirsutism and virilisation)
What will ACTH be like in 21 hydroxylase deficiency
ACTH high as no cortisol so no negative feedback
T/f The MR receptor has higher affinity for cortisol than GR
True, counterintuively
State the selectivity of the following drugs: Hydrocortisone Prednisolone Dexamethason Fludrocortisone
HC- GR and MR at high dose
Pred- GR and weak MR
Dex- glucorticoid with no mineralocorticoid activity
Fludrocortisone- aldosterone analogue
Duration of action of hydrocortisone, prednisolone and dexamethasone
HC: 8hrs
Pred: 12 hr
Dex: 40hr
How would you treat primary adrenocortical failure (not crisis)
Hydrocortisone and fludrocortisone by mouth –> mimicks glucocorticoid and mineralocorticoid respectively
How would you treat secondary adrenocortical failure (not crisis)
Adosterone is normal so no need to give fludrocortisone-
Just give hydrocortisone
How would you treat acute adrenocortical failure (addisonian crisis)
0.9% NaCl
High dose hydrocortisone i.v. or i.m every 6h-mineralocorticoid effect at high dose as 11bHSD 2 overwhelmed
5% dextrose if hypoglycaemic
What are the objectives of therapy in congenital adrenal hyperplasia
You want to;
Replace cortisol and aldosterone
And also suppress the very high ACTH (which is leading to lots of precursors which are being converted to the adrenal androgens and causing hirsutism and acne)
How do you treat congenital adrenal hyperplasia
Dexamethason 1/day pm or
Hydrocortison 2-3/day, high dose pm
AND
fludrocortisone
How do you monitor treatment for congenital adrenal hyperplasia
17-OH progesterone levels
And clinical assessment:
-if they are cushingoid then GC dose is too high
-If they have hirsutism it’s too low (so ACTH has risen)
This is a very fine balance and giving too much can make the patient cushingoid (too much cortisol), giving to little will fail to suppress ACTH and they will become hursuit.
What extra measures must be taken for patients taking corticosteroid replacement therapy
You need to increase glucocorticoid drugs when stressed (as happens physiogically), so take twice the normal dose for minor illness
If having surgery, a general anaesthetic is a major stress so cortisol would usually be really high, hydrocortisone i.m with pre-med and at 6-8 hour intervals. Can be taken oral once eating and drinking
Normal cortisol vs normal cortisol when stressed
20mg/day, in stress 200-300mg per day
How important is the cortisol, aldosterone and androgens/oestrogens as adrenal steroids
Cortisol – essential for life
Aldosterone
Promotes Na+ retention and K+ loss
Androgens/oestrogens
?
Main source of these are gonads
Give the 2 uses of hydrocortisone
In Addison’s patients with primary adrenocortical failure, you give hydrocortisone as REPLACEMENT. You also give fludrocortisone
For secondary adrenocortical failure, you give hydrocortisone as REPLACEMENT. You don’t give fludrocortisone because the zona glomerulosa (producing aldosterone) is intact and doesn’t respond to ACTH anyway
For someone with ACUTE adrenocortical failure (i.e. addisonian crisis, which is when your primary adrenocortial failure is really bad), you are giving HIGH DOSE HYDROCORTISONE to replace the cortisol, but also to replace aldosterone in the short term to get the blood pressure back up (because the cortisol can overwhelm 11b-HSD 2 and act on MR receptors to increase Na+ and water reabsorption), then when sent home, they would be put on the first arrangement here.
What happens in 21OH deficiency (in CAH) to:
cortisol
aldosterone
ACTH
Which hormone accumulates
It means that no cortisol or aldosterone can be made
ACTH starts to increase as there is no negative feedback
Progesterone/17OH progesterone cannot be converted into aldosterone and cortisol respectively, so it accumulates and is shuttled into sex steroid pathway
High ACTH drives further adrenal androgen production
Patients get hirsuitism and virilisation
Why does the adrenal gland grow in CAH
Because there is no production of cortisol in utero, then there is nothing to switch of ACTH.
ACTH causes the adrenal cortex to grow!