Quiz 3 Material Flashcards
Corticotropin (ACTH)
Hypothalamic and Anterior Pituitary Hormones: Binds to receptors in the adrenal cortex, which stimulates the release of adrenocorticosteriods and adrenal androgens (part of fight or flight response)
Gonadorelin
Hypothalamic and Anterior Pituitary Hormones: Essential for the release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) from the pituitary (in pulse dose)
Somatotropin
Hypothalamic and Anterior Pituitary Hormones: Promotes cell proliferation, bone growth, cartilage synthesis, and decreses adipose tissue
Somatostatin
Hypothalamic and Anterior Pituitary Hormones: Suppress GH and thyroid stimulating hormone release, also inhibits the release of insuling, glucagon, and gastrin
Gonadotropins
Hypothalamic and Anterior Pituitary Hormones: Regulates gonadal steriod hormones
Thyroid Stimulating Hormone
Hypothalamic and Anterior Pituitary Hormones: Results in the uptake of iodine and the synthesis of T3 and T4
Prolactin
Hypothalamic and Anterior Pituitary Hormones: Primary function is to stimulate and maintain lactation (also to decrease reproductive function)
Oxytocin
Hormones of the Posterior Pituitary: Stimulates uterine contraction and milk ejection
Vasopressin/ADH
Hormones of the Posterior Pituitary: Increases water permeability and reabsorption in the kidney, also causes constriction of vascular smooth muscle
Liothyronine
Thyroid Drugs: Act to replace/supplement the physiologic function of T3 (T3 replacement)
Levothyroxine
Thyroid Drugs: Act to replace/supplement the physiologic function of T4 (T4 replacement)
Methimazole
Thyroid Drugs: Inhibit a step in the production of thyroid hormone (some hormones already in storage, so there may be a delayed effect when first taking the drug)
Propylthiouracil
Thyroid Drugs: Inhibit a step in the production of thyroid hormone (some hormones already in storage, so there may be a delayed effect when first taking the drug)
Iodine, potassium iodide
Thyroid Drugs: Pharmacologic dose of iodide inhibits the production/release of hormone (MoA not known)
Estradiol
Estrogens: Diffuse across the cell membrane and bind to specific nuclear-receptor proteins, Activated complex interacts with nuclear chromatin to initiate RNA synthesis
Estrone
Estrogens: Diffuse across the cell membrane and bind to specific nuclear-receptor proteins, Activated complex interacts with nuclear chromatin to initiate RNA synthesis
Estriol
Estrogens: Diffuse across the cell membrane and bind to specific nuclear-receptor proteins, Activated complex interacts with nuclear chromatin to initiate RNA synthesis
Raloxifene
Selective Estrogen-Receptor Modulators (SERMs): Compete with estrogen for binding on estrogen receptors (in breast tumors); Different effects depending on tissue (agonism or antagonism)
Tamoxifen
Selective Estrogen-Receptor Modulators (SERMs): Compete with estrogen for binding on estrogen receptors (in breast tumors); Different effects depending on tissue (agonism or antagonism)
Drospirenone (with esteradiol = YAZ)
Progestogens: Promotes the development of secretory endometrium to accommodate the implantation of the embryo; Negative feedback on LH to prevent ovulation; Produced naturally in response to LH in males and females
Levonorgestrel
Progestogens: Promotes the development of secretory endometrium to accommodate the implantation of the embryo; Negative feedback on LH to prevent ovulation; Produced naturally in response to LH in males and females
Medroxyprogesterone
Progestogens: Promotes the development of secretory endometrium to accommodate the implantation of the embryo; Negative feedback on LH to prevent ovulation; Produced naturally in response to LH in males and females
Megestrol
Progestogens: Promotes the development of secretory endometrium to accommodate the implantation of the embryo; Negative feedback on LH to prevent ovulation; Produced naturally in response to LH in males and females
Norelgestromin
Progestogens: Promotes the development of secretory endometrium to accommodate the implantation of the embryo; Negative feedback on LH to prevent ovulation; Produced naturally in response to LH in males and females
Norethindrone
Progestogens: Promotes the development of secretory endometrium to accommodate the implantation of the embryo; Negative feedback on LH to prevent ovulation; Produced naturally in response to LH in males and females
Progesterone
Progestogens: Promotes the development of secretory endometrium to accommodate the implantation of the embryo; Negative feedback on LH to prevent ovulation; Produced naturally in response to LH in males and females
Mifepristone
Antiprogestin: Progesterone Antagonist
Testosterone
Androgens: Binds to a specific nuclear receptor; Testosterone itself is an active ligand in muscle and liver; Hormone-receptor complex binds to DNA and stimulates the synthesis of specific RNAs and proteins
Dutasteride
Anti-androgens: Interfere with the synthesis of androgens or block their receptors; Flutamide, Nilutamide, Bicalutamide = competitive antagonists
Finasteride
Anti-androgens: Interfere with the synthesis of androgens or block their receptors; Flutamide, Nilutamide, Bicalutamide = competitive antagonists
Flutamide
Anti-androgens: Interfere with the synthesis of androgens or block their receptors; Flutamide, Nilutamide, Bicalutamide = competitive antagonists
Nilutamide
Anti-androgens: Interfere with the synthesis of androgens or block their receptors; Flutamide, Nilutamide, Bicalutamide = competitive antagonists
Bicalutamide
Anti-androgens: Interfere with the synthesis of androgens or block their receptors; Flutamide, Nilutamide, Bicalutamide = competitive antagonists
Insulin
Insulin: Bind to insulin receptors in the body and mimic the actions of insulin
Acarbose
Alpha-glucosidase Inhibitors: These drugs prevent alpha-glucosidase from breaking down carbohydrates, minimizing upper intestinal digestion and absorption of carbs. Also decrease postprandial release of glucose.
Miglitol
Alpha-glucosidase Inhibitors: Alpha-glucosidase Inhibitors: These drugs prevent alpha-glucosidase from breaking down carbohydrates, minimizing upper intestinal digestion and absorption of carbs. Also decrease postprandial release of glucose.
Linagliptin
DPP-4 Inhibitors: Inhibite DPP-IV, an enzyme responsible for inactivation of incretin hormones. This results in an increase in glucose-mediated insulin secretion and a decrease in glucagon levels.
Saxagliptin
DPP-4 Inhibitors: Inhibite DPP-IV, an enzyme responsible for inactivation of incretin hormones. This results in an increase in glucose-mediated insulin secretion and a decrease in glucagon levels.
Sitagliptin
DPP-4 Inhibitors: Inhibite DPP-IV, an enzyme responsible for inactivation of incretin hormones. This results in an increase in glucose-mediated insulin secretion and a decrease in glucagon levels.
Exenatide
GLP-1 Agonists: Bind to GLP-1 receptors and help restore activity. Results in: potentiation of glucose-mediated insulin secretion, suppression of the postprandial glucagon release and slowed gastric emptying and loss of appetite
Liraglutide
GLP-1 Agonists: Bind to GLP-1 receptors and help restore activity. Results in: potentiation of glucose-mediated insulin secretion, suppression of the postprandial glucagon release and slowed gastric emptying and loss of appetite
Nateglinide
Meglitinides: Stimulate insulin secretion from the Beta cells; Similar to sulfonylureas but bind to a different site on the receptor
Repaglinide
Meglitinides: Stimulate insulin secretion from the Beta cells; Similar to sulfonylureas but bind to a different site on the receptor
Glimepiride
Sulfonylureas: Stimulate insulin secretion from the Beta cells; this bind to receptors which cause K channels to close and depolarized. This leads to the opening of the VG Ca channels which activates Ca-dependent proteins to lead to the release of insulin.
Glipizide
Sulfonylureas: Stimulate insulin secretion from the Beta cells; this bind to receptors which cause K channels to close and depolarized. This leads to the opening of the VG Ca channels which activates Ca-dependent proteins to lead to the release of insulin.
Glyburide
Sulfonylureas: Stimulate insulin secretion from the Beta cells; this bind to receptors which cause K channels to close and depolarized. This leads to the opening of the VG Ca channels which activates Ca-dependent proteins to lead to the release of insulin.
Pioglitazone
Thiazolidinediones: Improve whole-body insulin sensitivity by promoting or enhancing the local effects of insulin; Stimulates receptor in adipose tissue - resuling in transcription of a number of insulin-sensitive genes
Rosiglitazone
Thiazolidinediones: Improve whole-body insulin sensitivity by promoting or enhancing the local effects of insulin; Stimulates receptor in adipose tissue - resuling in transcription of a number of insulin-sensitive genes
Metformin
Other Diabetes Drug: Increases hepatic sensitivity to insulin (which decrease hepatic glucose production) and Increases insulin-stimulated glucose uptake in skeletal muscle; and suppresses the oxidation of fatty acids and reduces triglyceride levels
Pramlintide
Other Diabetes Drug: Delays gastric emptying and decreases glucagon secretion while improving satiety
Canagliflozin
Glucuretic: Sodium-glucose cotransporter 2 inhibitors, which prevent reabsorption of glucose in the kidney and increase urinary glucose excretion
Empagliflozin
Glucuretic: Sodium-glucose cotransporter 2 inhibitors, which prevent reabsorption of glucose in the kidney and increase urinary glucose excretion