Adrenal Cortex Flashcards
functional zonation of adrenal glands
Zona fasculata reticularis makes cort and androgens
zona glomerulosa makes aldosterone
Cell mechanism of activation of steroidogenisis in zona fasculata/reticularis
- ACTH binds to its G-coupled protein receptor
- low density lipoprotein (LDL) is taken up and cholesterol esters are stored in lipid droplets
- ACTH increases cAMP production to increase (cholesreol ester hydrolase) and increases STAR activity
- cholesterol is trasported from lipid droplet to mito via STAR (rate limiting step)
- steroidogenisis, cort is diffused right out of the cell via simple diffusion
STEROIDOGENISIS: look at RAFF ADRENAL SLIDES
synthetic cort
prednisones bind more tightly to CBGs
Mechanism of glucocorticoid receptor
- Cort dissociates from the CBG and diffuses right into the cytoplasm
- Cort binds to GR (glucocorticoid receptor) and causes it to dissociate from its HSP complex
- the 2x (cort/GR) enters the nucleus and attaches to 2x GRE (glucocorticoid response elements) right on the DNA–> transcription and translation–> change in cell response
POMC gene
ACTH etc are produced by post transcriptional modification of the POMC gene, by processing prohormone convertase 1 and 2 (PC1 and PC2)
Specific tissues express PC1 (ant pit) and PC2
primary adrenal insufficiency vs secondary
primary aka adissons disease: Adrenals are fucked up–> very low cort levels, which cause super high ACTH because of a lack of negative feedback
(weakness, fatigue, anorexia, wt loss)
secondary: messed up ant pit not making ACTH, so Adrenals atrophy, low cort levels
Causes of Primary adrenal insufficiency
Autoimmune (80%) TB(20%)
Top 4 symptoms of Adrenal insufficiency
Weakness, fatigue, anorexia, weight loss
Hyperpigmentation occurs in primary only (MSH receptor)
Hypotension is due to the loss of CORT maintenance of vasoconstriction (permissive because CORT is needed to help the vaso constrictors do their job)
Recovery from Gluccocorticoid therapy
patients need to be weaned off of gluccocorticoid therapy , because once GC is taken off, Plasma ACTH starts to increase due to loss of negative feedback, however it takes months for the hypothalamus and pituitary to wake up and for the Adrenals to regrow
Cushings Syndrome Subtypes
ACTH dependent (pituitary of ectopic tumor making tooo much ACTH, over stimulation of the Adrenals)
ACTH independent (adrenal tumor making cort in the absence of ACTH)