Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
80 Cards in this Set
- Front
- Back
Closes K channels deep in pancreatic B-cells to depolarize them and cause release of insulin
|
Sulfonylureas
|
|
Closes K channels in B-cells to depolarize them and cause release of insulin, but not as well as SUF drugs. Short duration and rapid onset
|
Meglitinides
|
|
Increases target tissue sensitivity to insulin and prevents glucose production in liver
|
TZD
|
|
Inhibits conversion of complex carbohydrates by inhibiting a-glycosidase and decreases GI motility
|
a-glucosidase inhibitors
|
|
Neuroendocrine peptide hormone cosecreted by B-cells that stimulates satiety center, suppresses PP glucose release, and regulates gastric emptying
|
Amylin
|
|
Hormone secreted by L-cells in ileum that stimulates insulin secretion, suppresses glucagon release, regulates gastric emptying, and stimulates satiety center. Has a role in B-cell regeneration
|
GLP-1
|
|
Target the peroxisome proliferator-activated receptor-gamma (PPAR-g) in muscle, fat, and liver to increase insulin
|
TZD/Glitazones
|
|
Incretin-based hormone that regulates GI motility and decreases hepatic glucose production
|
DPP-4 Inhibitors
|
|
Hormone used to treat hypoglycemia reactions in Type I diabetics
|
Glucagon
|
|
Members of DPP-4 inhibitor
|
Sitagliptin
|
|
Members of GLP-1 analogues
|
Exenatide (injection only)
|
|
Members of Amyline analogue
|
Pramlintide
|
|
Members of TZD/glitazones
|
Pioglitazone
Rosiglitazone |
|
Members of Biguanide class
|
Metformin
|
|
Members of meglitinide class
|
Repaglinide
Nateglinide |
|
Members of a-glucosidase inhibitors
|
Acarbose
Miglitol |
|
Members of Sulfonylureas
|
Tolbutamide
Glyburide Glipizide Glimepiride |
|
Drugs that decrease both FASTING and POSTPRANDIAL glucose
|
SUF
TZDs/glitazones |
|
Drugs that decrease only POSTPRANDIAL glucose
|
DPP-4 inhibitors
GLP-1 analogues Meglitinides a-glucosidase inhibitors |
|
Drugs that decrease only FASTING glucose
|
Biguanides
|
|
Drugs that cause weight GAIN
|
SUF
TZDs |
|
Drugs that cause weight LOSS
|
Biguanides
GLP-1 |
|
AEs of SUF
|
weight gain
hypoglycemia |
|
AEs of inhaled-insulin Exubera
|
hypoglycemia
cough dyspnea sore throat dry mouth |
|
AEs of meglitinides
|
hypoglycemia
|
|
AEs of a-glucosidase inhibitors
|
stomach/GI discomfort
flatulence |
|
AEs of biguanides
|
stomach/GI distress
weight loss |
|
AEs of TZDs/glitazones
|
Edema
Weight gain Heart failure in some pts |
|
AEs of Amylin analogue (Pramlintide)
|
nausea, vomiting, abdominal pain, headache, fatigue
|
|
AEs of GLP-1 analogues (Exenatide)
|
weight loss
stomach upset |
|
AEs of DPP-4 inhibitors (Stigliptin)
|
stuffy runny nose
headache hypersensitivity rxn |
|
AEs of glucagon
|
nausea and vomiting
|
|
Class that takes up to 4 weeks to work
|
TZD
|
|
Duration of action of meglitinides
|
Short acting (1/2 to 4 hrs)
|
|
Fastest release of insulin
|
meglitinide
|
|
Short-acting glucocorticoids
|
Anything with, "Cort" or "Pred" and not "Flu"
|
|
Long-acting glucocorticoids
|
Betamethasone
Dexamethasone |
|
Mineralcorticoids
|
DOCA
Fludrocortisone |
|
AEs of glucocorticoid treatment
|
immune suppression
increased glucose release adiposity muscle atrophy Na/H2O retention osteoporosis |
|
Onset of action for corticoids
|
2-4 hours d/t multi-step process
|
|
Similar to DDT used in inoperable adrenal cancer
|
Mitotane
|
|
Inhibits 11B-hydroxylase
|
Metyrapone
|
|
Inhibits conversion of cholesterol to pregnolone. Used for a medical adrenalectomy
|
Aminoglutethamide
|
|
Inhibits conversion of pregnolone to progesterone; used in Cushing's syndrome
|
Trilostane
|
|
inhibits P450 enzyme and inhibits all steroid synthesis; used in Cushing's and prostate ca
|
Ketoconazole
|
|
Adrenal synthesis inhibitors
|
Mitotane
Trilostane Ketoconazole Aminoglutethamide Metryapone |
|
Stronger anti-inflammatory action than cortisol with no Na-retaining effects
|
Triamcinoline
|
|
30X more potent than cortisol with no water or Na retaining effects
|
Betamethasone
Dexamethasone |
|
AEs of DHEA
|
acne
testicular atrophy increased risk of prostate ca |
|
converted to testosterone by 17-dehydro or estradiol via aromatase
|
Androstenedione
|
|
Actions of thyroid
|
inotropic/chronotropic fx
normal respiratory control center response stimulates GI motility |
|
AEs of thyroid hormone
|
Same stuff as hypothyroidism
SOB cardiotoxicity impaired reproductive function |
|
Onset of action for liothyronine
|
very fast 48 - 72 hrs
|
|
Inhibits iodination and coupling in thyroid synthesis
|
PTU
Methimazole |
|
Also inhibits 5'-deiodinase
|
PTU
|
|
AEs of PTU/Methimazole
|
Agranulocytosis
Rash Edema |
|
Antithryoid with long duration of action
|
Methimazole
|
|
Antithyroid not highly protein bound
|
Methimazole
|
|
3 step tx for thyroid storm
|
1. Propanolol
2. KI 3. PTU |
|
AEs of iodide treatment
|
metallic taste
rashes sore mouth |
|
AE of radioactive iodine
|
delayed hypothyroidism
|
|
Antithyroids contraindicated in pregnancy
|
I-131
Methimazole |
|
Duration of effect for Iodine/Iodide
|
24 hours
|
|
Allosteric activator of PTH CaSR to increase sensitivity to Ca and decrease PTH without change in serum Ca or PO4
|
Cinacalcet
|
|
Intranasal drug that inhibits osteoclast Ca mobilization by binding Gi protein membrane receptors
|
Calcitonin
|
|
Antagonizes Vitamin D-stimulated intestinal Ca transport, stimulates renal Ca excretion, and blocks bone foromation
|
Glucocorticoids
|
|
Reduces bone-resorbing effects of PTH
|
Estrogen
|
|
Binds phosphate
|
Phosphate binders
(Al, Ca, Sevelamer) |
|
Decreases PTH, PO4, and Ca
|
Cinacalcet
|
|
Decreases PTH but raises Ca and PO4
|
Vitamin D analogue Calcitriol
(Doxicalciferol/paricalcitol used in tx of hyperPTH d/t renal failure) |
|
Inhibits bone resorption, reduces both Ca and PO4 reabsorption as well as Na, Mg, and K
|
Calcitonin
|
|
AEs of Calcitonin
|
nausea
facial flushing swelling of hands inflammatory rxns at injection site Uritcaria |
|
Decreases PTH and PO4 while increasing Ca
|
bisphosphonates
|
|
Indication for use of calcitonin
|
post-MP osteoporosis when HRT contraindicated
|
|
Chelating-type agent that inhibits FPP synthase to prohibit attachment of osteoclasts
|
N-bisphosphonates
|
|
Members of N-bisphosphonate class
|
alendronate
risedronate zoledronate pamidronate |
|
Antiadrenal drug used in prostate ca and cushing's
|
Ketoconazole
|
|
Antiadrenal used in Cushing's
|
Trilostane
|
|
Two drugs for tx of Gestational Diabetes
|
Insulin, SUF(Glyburide)
|
|
Given IV to partially inhibit conversion of T4 to T3
|
Hydrocortisone
|