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17 Cards in this Set
- Front
- Back
insulin analogs:
lispro (short acting) aspart (short) regular (short) NPH (immediate) glargine (long) detemir (long) |
- bind insulin receptor
-allows liver to store ↑ glucose as glycogen - ↑ glycogen & protein synthesis in muscle - K uptake, aids TG storage - used for Type 1 & 2 DM, can also be used for hyperkalemia and hyperglycemia |
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sulfonylureas
first generation: tolbutamide, chlorpropamide 2nd generation: glyburide, glimepiride, glipizide |
- close K channel in beta cell membrane so cell depolarizes which leads to triggering of insulin release via Ca influx
-used to stimulate release of endogenous insulin in Type 2 DM. useless in type 1 - hypoglycemia, DISULFRAM like rxn so take w/ alcohol |
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biguanides: metformin
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- overall acts as an insulin sensitizer, possibly ↓ gluconeogenesis, increase glycolysis, ↓ serum glucose
-used as an oral hypoglycemic. can be used in patients w/o islet function so good for type 1 - tox: LACTIC ACIDOSIS, avoid in pts with CHF |
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glitazones
pioglitazone rosiglitazone |
- increase target cell response to insulin. increase target cell response by regualting the release of adipokines (resistin & adiponectin) Adiponectin secretion is stimulated and it sensitizes tissues to insulin. resistin secretion is inhibited thereby reducing insulin resistance
- used as montherapy in type 2 DM tox: weight gain, edema, hepatotoxicity, CV tox |
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alpha glucosidase inhibitors
acarbose miglitol note: alpha glucosidase catalzes a step in glycogen breakdown |
- inhibit intestinal brush border alpha glucosidases. delayed sugar hydrolysis and glucose absorption leads to ↓ postprandial hyperglycemia
- used for type 2 DM tox: Gi disturbances |
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mimetics
pramlintide |
- ↓ glucagon
type 2 DM tox: hypoglycemia, nausea, diarrhea |
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GLP-1 mimetics
exenatide |
- increase insulin, ↓ glucagon release
- type 2 DM - nausea, vomiting, pancreatitis |
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orlistat
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"orlistat gets rid of fat"
- alters fat metabolism by inhibiting pancreatic lipases - used for long term obesity management -tox: steatorrhea, Gi discomfort, reduced absorption of fat soluble vitamins, headache |
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sibutramine
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- sympathomimetic serotonin and NE reuptake inhibitor
- used for short term & long term obesity management tox: HTN, tachycardia |
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propylthiuracil, methimazole
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- inhibit organification and coupling of thyroid hormone sythesis. PTU also ↓ conversion of T4 to T3, also inhibit thyroid peroxidase
- used for hyperthyroidism - tox; skin rash, agranulocytosis, aplastic anema |
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GH
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- used for GH deficiency, Turner's syndrome
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somatostatin (octreotide)
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- somatostatin analogue (↓ gastric acid/ pepsin secretion, ↓ pancreatic secretion, ↓ SI fluid secretion, ↓ gall bladder contraction), ↓ insulin & glucagon release. INHIBITS GH
- used for acromegaly, CARCINOID, gastrinoma, glucagonoma |
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oxytocin
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used for stimulating labor, uterine contractions, milk let down, controls uterine hemorrhage
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ADH
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used for central diabetes insipidus
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levothyroxine, triiodothyronine
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- thyroxine replacement
- used for hypothyroidism, myxedema - tox: tachycardia, heat intolerance, tremors, arrythmias |
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glucocorticoids
hydrocortisone, prednisone, triamcinolone, dexamethasone, beclomethasone |
- decrease the production of leukotrienes, and prostaglandins by inhibiting phospholipase A2 and expression of COX-2
- used for addison's disease, inflammation, immune supppression, asthma tox: cushings syndrome |
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demeclocycline
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- tetracycline antibiotic that also works as an ADH antagonist
- SIADH tox: photosensitivity, abnormalities of bone & teeth |