Diabetic Drugs Flashcards
Sulfonylureas 1st Gen
chlorpropamide and tolbutamide
Sulfonylureas 2nd Gen
glimepiride
glipizide
glyburide
Sulfonylureas MOA
block K voltage channels in the pancreatic Beta-cell membrane which makes the cell depolarizes and release insulin via increase of Ca influx
2nd gen enhances peripheral glucose uptake
Sulfonylureas ADR 1st and 2nd gen
In general hypoglycemia and wt gain
1st - disulfiram reaction
2nd - hypoglycemia
Dipeptidyl Peptidase-4 (DPP4) inhibitors and MOA
Sitaglipitin
Vildaglipitin
MOA: inhibits degradation of endogenous GLP1
They are weight neutral and have low risk of hypoglycemia.
They increased glucose-dependent insulin release.
Amylin analog and MOA
prAMLINtide
MOA: decrease glucagon release and gastric emptying but increases satiety
Glucagon-Like Peptide-1 analog (incretin mimetics) and MOA
Exenatide, liraglutide
MOA:
- inhibit glucagon release,
- inhibit GI secretion and motility ( decrease gastric emptying)
- increases glucose-dependent insulin release (glucose-induced insulin release)
LEADS TO WEIGHT LOSS
Glitazones
Pioglitazone
Rosiglitazone
MOA - activate PPAR-y (nuclear receptor)
increase insulin sensitivity and levels of adiponectin
ADR: weight gain and HF
Sodium-Glucose cotransporter 2 (SGLT2)
Canagliflozin
Dapagliflozin
MOA:
block reabsorption of glucose in proximal convoluted tubule
alpha-glucosidase inhibitors and MOA
Acarbose
miglitol
block a1 glucosidase on GI brush border
inhibits glucose absorption postprandial