Treatment of endocrine conditions Flashcards
(26 cards)
treatments for hyperthyroidism
radioactive iodine
thioureylene drugs
iodine
treatments for hypothyroidism
HRT
levothyroxine (synthetic T4)
liothyronine (synthetic T3)
treatments for diabetes
insulin sensitisers
insulin secretagogues
incretin mimetics
glucose-reabsorption inhibitors
insulin sensitisers
increase sensitivity to insulin in muscle, liver and fat
metformin
thiazolidinediones
insulin secretagogues
stimulate insulin secretion from beta-cells (require functional beta-cells so only used in type 2) by blocking K+ channels to cause depolarisation
sulphonylureas
meglitinides
incretin mimetics
mimic GLP-1 and GIP released during digestion which induce insulin release (require functional beta-cells)
gliptins
GLP-1 receptor agonists
glucose-reabsorption inhibitors
promotes excretion of glucose in urine to decrease blood sugar levels
glifozins
metformin
insulin sensitiser
reduces gluconeogenesis and increases glucose uptake by skeletal muscle by activating affecting nuclear (II) receptors through increased AMP production, thus AMP kinases too.
nuclear receptor activation causes a decrease in expression in genes for gluconeogenesis
may be used with insulin sensitisers
thiazolidinediones
reduced hepatic glucose output , increases glucose uptake into muscle
decreases blood glucose, insulin and FFAs by acting as a PPAR agonists to alter gene expression
alters:
- lipoprotein lipase
- fatty acid transporters
- glut 4
rosiglitazone
pioglitazone
rosiglitazone
pioglitazone
thiazolidinediones
- alters gene expression
sulphonylureas
insulin secretagogue
blocks K+ channels to induce beta-cell depolarisation for insulin release
tolbutamide
glibenclamide
glipizide
tolbutamide
glibenclamide
glipizide
sulphonylureas
- beta-cell depolarisation
meglitinides
insulin secretagogue
blocks K+ channels to induce beta-cell depolarisation for insulin release
regalinide
nateglinide
regalinide
nateglinide
meglitinides
- beta-cell depolarisation
gliptins
incretin-mimetic
competitively inhibitor of DDP-4 which breaks down GLP-1 and GIP, increasing blood insulin
sitagliptin
vildagliptin
saxagliptin
sitagliptin
vildagliptin
saxagliptin
gliptins
- reduces incretin breakdown
GLP-1 receptor agonists
incretin-mimetic
GLP-1 agonist to stimulate SGLT2 on the proximal tubule nephron
exenatide
liraglutide
lixisenatide
exenatide
liraglutide
lixisenatide
GLP-1 receptor agonists
glifozins
glucose-reabsorption inhibitor
blocks sodium/glucose co-transporter on the proximal tubule nephron to increase insulin secretion
dapaglifozin
canaglifozin
empaglifozin
dapaglifozin
canaglifozin
empaglifozin
glifozins
- blocks glucose co-transporter
addisons disease
insufficient steroid hormone from adrenal cortex
cushing’s syndrome
over-production of steroid hormones
treatments for addisons disease
cortisol replacement:
hydrocortisone/prednisone/dexmethaxone
aldosterone replacement:
fludrocortisone
androgens replacement:
dehydroepiandrosterone
treatments for cushings syndrome
ketoconazole = reduce cortisol production
mitepristone = reduce cortisol effects