From Jen: Endocrine Flashcards

1
Q

Short acting insulin

A

Lispro
Aspart
Regular

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2
Q

Intermediate acting insulin

A

NPH

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3
Q

Long acting insulin

A

Glargine

Detemir

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4
Q

Insulin action and clinical use:

A

Bind insulin receptor (tyrosine kinase activity)

Liver: ↑ glucose stored as glycogen
Muscle: ↑ glycogen and protein synthesis; K+uptake
Fat: aids TG storage

Use: Type I and 2 DM, stress induced hyperglycemia

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5
Q

Insulin toxicity

A

Hypoglycemia

Hypersensitivity rxns are rare

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6
Q

Sulfonylurea

Drugs/toxicity

A

1st Gen: tolbutamide, chlorpropamide
***disulfiram-like rxn

2nd Gen: glyburide, glimepiride, glipizide
***hypoglycemia

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7
Q

Sulfonylurea

MOA

A

MOA: Close K+ channel in beta-cell membrane so cell depolarized, triggering insulin release via Ca2+ influx

Use: stimulate release of endogenous insulin in DM type 2
**requires islet cell function so useless in DM type 1

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8
Q

Biguanides

A

Metformin

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9
Q

Biguanide

MOA
Toxicity

A

(Metformin)

MOA: unknown, poss ↓ gluconeogenesis, ↑ glycolysis, overall ↓ serum glucose
*** insulin sensitizer

Use: oral hypoglycemic in pts without islet cell function

Toxicity: lactic acidosis

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10
Q

Glitazones

A

Pioglitazone

Rosiglitazone

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11
Q

Glitazone

MOA
Toxicity

A

(pioglitazone, rosiglitazone)

MOA: ↑ target cell response to insulin

Use: monotherapy in DM type 2 or combined with metformin and/or sulfonylureas

Toxicity: weight gain, edema, hepatotoxicity, CV toxicity

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12
Q

alpha-glucosidase inhibitors

A

acarbose

miglitol

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13
Q

alpha-glucosidase inhibitors

MOA
Toxicity

A

(acarbose, miglitol)

MOA: inhibit brush border at alpha-glucosidases. Delayed sugar hydrolysis and glucose absorption leading to ↓ post-prandial hyperglycemia

Use: Monotherapy or combined for DM type 2

Toxicity: GI upset

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14
Q

Pramlintide

A

MOA: ↓ glucagon

Use: DM type 2

Toxicity: hypoglycemia, nausea, diarrhea

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15
Q

GLP-1 mimetics

A

Exenetide

MOA: ↑ insulin, ↓ glucagon

Use: DM type 2

Toxicity: Nausea, vomiting, pancreatitis (?)

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16
Q

Orlistat

A

MOA: alters fat metabolism by inhibiting pancreatic lipases

Use: long-term obesity management

Toxicity: steatorrhea, GI discomfort, reduced absorption of fat soluble vitamins, headache

17
Q

Sibutramine

A

MOA: sympathomimetic serotonin and NE reuptake inhibitor

Use: long term obesity management

Toxicity: HTN and tachycardia

18
Q

Propylthiouracil

Methimazole

A

MOA: inhibit organification and coupling of thyroid hormone synthesis
PTU also ↓ peripheral conversion of T4 to T3

Use: hyperthyroidism

Toxicity: skin rash, agranulocytosis, aplastic anemia

19
Q

Growth hormone

A

Use: growth hormone deficiency

Turner syndrome

20
Q

Octreotide

A

Somatostatin analog

Use: acromegaly
carcinoid
gastrinoma
glucagonoma

21
Q

Oxytocin

A

Use: stimulate labor, uterine contractions, milk let-down, controls uterine hemorrhage

22
Q

ADH

A

Desmopressin

Use Central diabetes insipidus

23
Q

Triiodothyronine

Levothyroxine

A

MOA: Thyroxine replacement

Use: hypothyroidism, myxedema

Toxicity: tachycardia, heat intolerance, tremors, arrhythmia

24
Q

Glucocorticoids

A

Hydrocortisone, prednisone, triamcinolone, dexamethasone, beclomethasone

MOA: ↓ production of leukotrienes and prostaglandins by inhibiting phospholipase A2 and expression of COX-2

Use: Addison’s disease, inflammation, immune suppression, asthma

25
Q

Glucocorticoid

Toxicity

A

Iatrogenic Cushing’s Syndrome:

  • buffalo hump
  • moon facies
  • truncal obesity
  • muscle wasting
  • thin skin
  • easy bruising
  • osteoporosis
  • adrenocortical atrophy
  • peptic ulcers
  • diabetes
26
Q

Demeclocycline

A

MOA: ADH antagonist (tetracycline family)

Use: SIADH

Toxicity: Photosensitivity, abnormalities of bone and teeth, nephrogenic DI