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40 Cards in this Set

  • Front
  • Back
Treatment Strategies for:
-DM1
-DM2
-Low sugar diet, insulin replacement
-dietary modification & exercise for wt loss; oral hypoglyemics
Insulin types:
name them(5)
long/short/intermediate acting?
1. Lispro (short-acting)
2. Insulin (short-acting)
3. NPH (intermediate)
4. Lente (long-acting)
5. Ultralente (long-acting)
Insulin:
-mechanism
-effects on liver, mm, fat
-Binds insulin receptor (tyrosine kinase activity)
-Liver: increase glucose sotred as glycogen
-Muscle: increase glycogen and protein synthesis, K+ uptake
-Fat: aids TG storage
Insulin:
-clinical use
-for Type 1 DM
-for life-threatening hyperkalemia
-for stress-induced hyperglycemia
Insulin:
-toxicity
-hypoglycemia
-hypersensitivity reaction (v. rare)
Sulfonylureas: name them
-1st generation (2)
-2nd generation (3)
1st: Tolbutamide, Chlorpropamide
2nd: Glyburide, Glimepiride, Glipizide
Sulfonylurea
-mechanism
Close K+ channel in beta cell membrane -> depolarizes -> Ca2+ influx -> trigger insulin release
Sulfonylurea
-clinical use
-stim release of endogenous insulin in DM2
-require some islet function (useless in DM1!)
Sulfonylurea
-toxicity
1st gen: disulfiram-like effects
2nd gen; hypoglycemia
Disulfiram-like reaction:
sxs

what is disulfiram
flushing, nausea, vomiting, thirst, palpitations, chest pain, vertigo, and hypotension

-disulfiram is an aldehyde dehydrogenase inhibitor
Bigaunide - name it (1)
Metformin
Metformin
-mechanism
-exact mech unknown
-possibly decreases gluconeogenesis, increases glycolysis, decreases serum glucose levels
Metformin
-clinical use
-oral hypoglycemic
-can be used in pts without islet function
Metformin
-toxicity
LACTIC ACIDOSIS (most grave effect)
Glitazones: name them (2)
-pioglitazone
-rosiglitazone
Glitazone
-mechanism
-increases target cell response to insulin
Glitazone
-clinical use
used as monotherapy in DM2 or combined with other agents
Glitazone
-toxicity

which one is no longer use?
-weight gain
-edema

*Troglitaozone - no longer used
alpha-Glucosidase inhibitors:
name them (2)
Acarbose
Miglitol
Acarbose, miglitol:
-mechanism
-inhibit intestinal brush border alpha-glucosidases
-delayed sugar hydrolysis and glucose absorption lead to decreased postprandial hyperglycemia
Acarbose, miglitol:
-clinical use
Used as monotherapy in DM2 or in combination with other agents
Acarbose, miglitol:
-toxicity
GI disturbance
Orlistat
-mechanism (inhibits which enzymes?)
Alters fat metabolism by inhibiting PANCREATIC LIPASES
Orlistat
-clinical use
Long-term obesity mgmt (in conjunction with modified diet)
Orlistat
-toxicity
-steatorrhea
-GI discomfort
-reduced fat-soluble vitamin absorption
-HA
Sibutramine
-mechanism
sympathomimetic serotonin and norepinephrine reuptake inhibitor (SNRI)
Sibutramine
-clinical use
Short term and long term obesity management
Sibutramine
-Toxicity
HTN
tachycardia
Propylthiouracil, Methimazole
-Mechanism

-extra effect of PTU?
inhibit organification and coupling of thyroid hormone synthesis

PTU also decreases peripheral conversion of T4 to T3
GH
-clinical use
-GH deficiency
-Turner's syndrome
Somatostatin
-other name?
Octreotide
Somatostatin
-clinical uses
-acromegaly
-carcinoid
-gastrinoma
-glucagonoma
Oxytocin
-clinical uses
-stimulates labor
-uterine contractions
-milk-letdown
-controls uterine hemorrhage
ADH
-other name (exogenously given)
Desmopressin
Desmopression
-clinical use
Pituitary diabetes insipidus (central, not nephrogenic)
Levothyroxine, Triiodothyronine
-mechanism
-clinical use
-toxicity
-thyroxine replacement
-for hypothyroidism
-for myxedema
-toxicity: tachycardia, heat intolerance, tremors
Glucocorticoids
-name them (5)
- hydrocortisone
- prednisone
- triamcinolone
- dexamethasone
- beclomethasone
Glucocorticoid
-mechanism
-decreases the production of LTs and PGs by inhibiting phospholipase A2 and expression of COX-2
Glucocorticoid
-clinical use
-Addison's disease
-inflammation
-immune suppresion
-asthma
Glucocorticoid
-toxicity
Iatrogenic Cushing's syndrome:
-buffalo hump
-moon facies
-truncal obesity
-mm wasting
-thin skin
-easy bruisability
-osteoperosis
-adrenocortical atrophy
-PUD
-Diabetes (if chronic)