Diabetes Flashcards
Lispro
- onset
- peak effect
- duration
- 0.3-0.5hrs
- 1-2hrs
- 3-4hrs
Aspart
- onset
- peak effect
- duration
- 0.3-0.5hrs
- 1-2hrs
- 3-4hrs
Glulisin
- onset
- peak effect
- duration
- 0.3-0.5hrs
- 1-2hrs
- 3-4hrs
Insulin
- onset
- peak effect
- duration
- 0.5-1hrs
- 2-4hrs
- 5-7hrs
NPH, NPL, NPA
- onset
- peak effect
- duration
- 1-4hrs
- 4-10hrs
- 14-24hrs
Glargine
- onset
- peak effect
- duration
- 2-3hrs
- no peak
- > 24hrs
Detemir
- onset
- peak effect
- duration
- 3-4hrs
- 4-8hrs
- 6-24hrs
Which insulin analog has no danger of hypoglycemia
glargine
Canagliflozin
- mechanism
- side effect
SGLT2 inhibitor
- reduce glucose reabsorption in kidney, increase urinary glucose excretion
- UTI’s genital mycotic infection, volume depletion, hyperkalemia, hypersensitivity
Dapaglifloxin
- mechanism
- side effect
SGLT2 inhibitor
- reduce glucose reabsorption in kidney, increase urinary glucose excretion
- UTI’s genital mycotic infection, volume depletion, hyperkalemia, hypersensitivity
Empaglifloxin
- mechanism
- side effect
SGLT2 inhibitor
- reduce glucose reabsorption in kidney, increase urinary glucose excretion
- UTI’s genital mycotic infection, volume depletion, hyperkalemia, hypersensitivity
Glipizide
- mechanism
- side effects
- *
sulfonylureas
- block K+ channels in beta cells > depolarize cell > open Ca channel > Ca enters cell > insulin release
- hypoglycemia (early morning), weight gain, drug interaction due to protein binding, allergies
- *decreased hepatic dysfunction
Glypuride
- mechanism
- side effects
- *
sulfonylureas
- block K+ channels in beta cells > depolarize cell > open Ca channel > Ca enters cell > insulin release
- hypoglycemia (early morning), weight gain, drug interaction due to protein binding, allergies
- *active metabolite, decreased dose in renal dysfunction
Glimepiride
- mechanism
- side effect
sulfonylureas
- block K+ channels in beta cells > depolarize cell > open Ca channel > Ca enters cell > insulin release
- hypoglycemia (early morning), weight gain, drug interaction due to protein binding, allergies
Name 3 sulfonylureas
glimepiride, glypuride, glipizide
Metformin
- mechanism
- side effects
- decrease postprandial glucose levels w/o causing hypoglycemia or weight gain, may involve increased tissue sensitivity to insulin (bypasses insulin receptor to enter cell and activate TFs) and/or decreased hepatic gluconeogenesis
- lactic acidosis, GI distress (most common)
What condition are oral sulfonylureas most effective for
Type II only! Type I doesn’t have beta cells for OSU’s to work on
Acarbose/Miglitol
- mechanism
- side effect
- inhibits alpha-glucosidase in brush borders of sm intestine > decreased formation of absorbable carbohydrate > decreased postprandial glucose > decreased demand for insulin
- GI discomfort, flatulence, diarrhea, potential hepatotoxicity
Pioglitazone
- mechanism
- side effect
thiazolidinediones
- binds to PPARs involved in transcription of insulin-responsive genes > increased sensitization of tissues to insulin
- less hypoglycemia than OSU’s, weight gain, edema
Rosiglitazone
- mechanism
- side effect
thiazolidinediones
- binds to PPARs involved in transcription of insulin-responsive genes > increased sensitization of tissues to insulin
- less hypoglycemia than OSU’s, weight gain, edema
What DM drugs decrease liver gluconeogenesis (2)
Metformin, glitazone
What DM drugs increase tissue sensitivity to insulin (3)
Glitazone, metformin, bromocriptine
What DM drugs increase pancreas production of insulin (2)
Repaglinide, OSU’s
What DM drugs act in the GI tract to limit uptake of carbs (4)
acarbose, miglitol, colesevelam, pramlintide