Endo Flashcards
1
Q
aspart
A
Short acting insulin Type 1 DM, type 2 DM, GDM (postprandial glucose control). Binds insulin receptor (tyrosine kinase activity). Liver: increase glucose stored as glycogen. Muscle: increase glycogen, protein synthesis; increase K+ uptake. Fat: increase TG storage.
2
Q
glulisine
A
Short acting insulin Type 1 DM, type 2 DM, GDM (postprandial glucose control). Binds insulin receptor (tyrosine kinase activity). Liver: increase glucose stored as glycogen. Muscle: increase glycogen, protein synthesis; increase K+ uptake. Fat: increase TG storage.
3
Q
tolbutamide
A
Sulfonylurea Stimulate release of endogenous insulin in type 2 DM. Require some islet function, so useless in type 1 DM. Close K+ channel in β cell membrane > cell depolarizes > insulin release via increased Ca2+ influx. Risk of hypoglycemia increased in renal failure, weight gain. First generation: disulfiram-like effects. Second generation: hypoglycemia.
4
Q
chlorpropamide,
A
1st gen Sulfonylurea Stimulate release of endogenous insulin in type 2 DM. Require some islet function, so useless in type 1 DM. Close K+ channel in β cell membrane > cell depolarizes > insulin release via increased Ca2+ influx. Risk of hypoglycemia increased in renal failure, weight gain. First generation: disulfiram-like effects. Second generation: hypoglycemia.
5
Q
glipizide,
A
Sulfonylurea Stimulate release of endogenous insulin in type 2 DM. Require some islet function, so useless in type 1 DM. Close K+ channel in β cell membrane > cell depolarizes > insulin release via increased Ca2+ influx. Risk of hypoglycemia increased in renal failure, weight gain. First generation: disulfiram-like effects. Second generation: hypoglycemia.
6
Q
repaglinide
A
meglitinide Used as monotherapy in type 2 DM or combined with metformin. Stimulate postprandial insulin release by binding to K+ channels on β cell membranes (site differs from sulfonylureas). Hypoglycemia (increased risk with renal failure), weight gain