Chapter 23: Endocrine System Drugs
insulin
required as replacement therapy for Type 1 diabetics with insufficient production of insulin from the islets of Langerhans in the pancreas required in patients with Type 2 who have failed to maintain satisfactory concentrations of blood glucose with therapy including dietary regulation and oral antidiabetic agents
meglitinides
starlix and prandin stimulate beta cells to produce insulin
endocrine
the body's "slow" chemical communication system; a set of glands that secrete hormones into the bloodstream
pituitary gland
the master gland regulates the function of the other glands secretes several hormones somatotropin (human growth hormone): -secreted by the anterior pituitary lobe -regulates growth -insufficient production will result in growth abnormalities associated disorders treated via corticosteroids
biguanides
work by decreasing hepatic glucose production and enhancing insulin uptake in muscle glucophage (Metformin)
thyroid
endocrine gland located in the front part of the neck responsible for regulating the rate of metabolism when thyroid levels are low, the pituitary gland releases TSH, which promotes the synthesis of T4 (thyroxine) and T3 (triiodothyronine), the active form of thyroid hormone thyroxine is later converted in the body to T3
hyperthryoidism
can be caused by Graves disease treated with anythryroid agents -Tapazole and propylthiouracil (PTU) Methimazole (treatment of choice)
alpha-glucosidase inhibitors
precose delay digestion of complex carbohydrates (e.g., starch) and subsequent absorption of glucose, resulting in a smaller rise in blood glucose concentrations following meals
thiazolidinediones (TZDs)
Actos and Avandia lower blood glucose by decreasing insulin resistance and improving sensitivity to insulin in muscle, liver, and adipose tissue
replacement therapy
administration of a naturally occurring substance that the body is not able to produce in adequate amounts to maintain normal function
adrenal corticosteroids
adrenal glands secrete hormones called corticosteroids act on the immune system to suppress the body's response to infection or trauma relieve inflammation, reduce swelling, and suppress symptoms in acute conditions two broad categories: replacement therapy and immunosuppressant agents
immunosuppressant agents
agents that decrease or prevent immune response used in the treatment of organ rejection
incretin therapies
agents that mimic actions of incretin hormones Byetta, (a GLP-1), Januvia and Onglyza
conditions treated with corticosteroids
allergic reactions acute flare-ups of rheumatic or collagen disorders acute flare-ups of severe skin conditions acute respiratory disorders long-term prevention of symptoms in severe persistent asthma or chronic management of COPD cancer brain swelling organ transplant life-threatening shock acute flare-ups of ulcerative colitis
diabetes mellitus
characterized by impaired metabolism of carbohydrates, fats, and proteins that results in elevated levels of blood glucose Type 1: insulin dependence; destruction of pancreatic beta cells Type 2: insulin resistance and deficiency
hormones
chemical messengers with specialized functions in regulating activities of specific cells or organs
sulfonylureas
consist of first-generation agents (e.g., chlorpropamide, tolbutamide) and second-generation agents (e.g., glipizide, glyburide) increaase insulin production from the pancreas
hypothyroidism
most common thyroid problem in the U.S. causes slowed metabolism treated with thyroid agents
SGLT2 inhibitors
newest class decrease the reabsorption of glucose in the kidney Invokana
