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201 Cards in this Set
- Front
- Back
autocrine
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hormone acts on releasing cell
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paracrine
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hormone acts on cell near releasing cell
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endocrine
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hormone acts on cell distant from releasing cell
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antidiuretic hormone secreted by...
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posterior pituitary
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oxytocin secreted by...
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posterior pituitary
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growth hormone secreted by...
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anterior pituitary
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prolactin secreted by...
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anterior pituitary
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FSH (__________) secreted by...
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follicle stimulating hormone; anterior pituitary
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LH (__________) secreted by...
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luteinizing hormone; anterior pituitary
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insulin secreted by...
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pancreas
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glucagon secreted by...
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pancreas
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somatostatin secreted by...
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pancreas
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parathyroid hormone secreted by...
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parathyroid gland
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T3/T4 secreted by...
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thryoid gland
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calcitonin secreted by...
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thyroid gland
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catecholamines secreted by...
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adrenal gland
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aldosterone secreted by...
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adrenal gland
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cortisol secreted by...
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adrenal gland
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estradiol (__________) secreted by...
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estrogen; ovary
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progesterone secreted by...
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ovary
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testosterone secreted by...
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ovaries, testes, adrenal glands
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posterior pituitary hormones
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antidiuretic hormone, oxytocin
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anterior pituitary hormones
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GH, PRL, FSH, LH, ACTH, TSH
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pancreas hormones
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insulin, glucagon, somatostatin, digestive enzymes
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parathyroid gland hormones
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parathyroid hormone
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thyroid gland hormones
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T3/T4, calcitonin
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adrenal gland hormones
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catecholamines, aldosterone, cortisol, testosterone
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ovary hormones
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estradiol, progesterone, testosterone
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testes hormones
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testosterone
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__________-__________-__________ __________ axis
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hypothalamic-pituitary-target organ axis
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GnRH name, pathway, & function
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-gonadotropin-releasing hormone
-hypothalamus > ant. pituitary gonadotrophs (LH, FSH) > testes/ovaries (testosterone, estrogen, progesterone) -spermatogenesis/ovulation |
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TRH name & pathway
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-thyrotropin-releasing hormone
-hypothalamus > pituitary thyrotrophs (TSH) > thyroid > T3/T4 |
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CRH name & pathway
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-corticotropin-releasing hormone
-hypothalamus > pituitary corticotrophs (ACTH) > adrenal glands > glucocorticoids |
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GHRH name & pathway
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-growth hormone-releasing
hormone -hypothalamus > ant. pituitary somatotrophs (GH) > throughout body |
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PRF name, pathway, & function
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-prolactin-releasing factor
-hypothalamus > ant. pituitary lactotrophs/mammotrophs (PRL) > breasts -lactation |
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TSH
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thyroid-stimulating hormone
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ACTH
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adrenocorticotropic hormone
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GH
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growth hormone
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PRL
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prolactin
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gonadotrophic hormones
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LH, FSH (leuteinizing hormone, follicle-stimulating hormone)
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thyrotrophic hormones
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TSH (thyroid-stimulating hormone)
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corticotrophic hormones
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ACTH (adrenocorticotropic hormone)
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somatotrophic hormones
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GH (growth hormone)
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mammotrophic/lactotrophic hormones
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PRL (prolactin)
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hypothalamic factors (secreted by hypothalamus)
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GnRH, TRH, CRH, GHRH, PRF, dopamine
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pituitary cell types
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gonadotroph
corticotroph somatotroph thyrotroph lactotroph/mammotroph |
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1°/2°/3° hyperthyroidism is caused by a problem in the...
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throid gland / pituitary gland / hypothalamus
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anterior pituitary name
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adenohypophysis
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posterior pituitary name
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neurohypophysis
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oxytocin function
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stimulates uterine contraction, promotes milk release during lactation
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enuresis (bedwetting) probable etiology
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lack of ADH secretion at night
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diabetes insipidous def., etiology, and symptoms
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-symptoms look like diabetes
-inadequate ADH secretion or renal receptors (V2) don't respond -nocturia, polyuria, polydipsia |
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thyroid feedback mechanism (+/-)
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-prolonged cold exposure, acute psychosis, and circadian rhythms induce TRH secretion
-severe stress inhibits TRH secretion -T3/T4 inhibit TRH & TSH secretion |
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___% of thyroid hormones are ___
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99.5%+; PPB
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hypo/hyperthyroidism S/S
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-hypo: ↓BMR
-hyper: ↑BMR, exophthalmos -both: goiter, infertility |
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Hashimoto's disease
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-chronic autoimmune thyroiditis (hyopthyroidism)
-T-cells attack antigen-like proteins on thyroid membrane, stimulating B-cells to produce Ab's against normal thyroid tissue |
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chronic autoimmune thyroiditis
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Hashimoto's disease
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myxedema
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-end-stage of long-standing uncorrected hypothyroidism
-lethargy, stupor, hypothermia, delirium > coma > death |
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end-stage of long-standing uncorrected hypothyroidism
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myxedema
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levothyroxine (L-thyroxine)-Synthroid
Pcol / Pharmacology / ADR |
-synthetic T4 > T3 in vivo
-↑BMR, ↑O2 consumption, ↑HR, ↑ cardiac hypertrophy, ↑BP, ↑ fat breakdown -tachycardia, palpations, nervousness, insomnia, weight loss |
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__________ ↓ orbital edema
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diuretics
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methimazole-Tapazole & propylthiouracil-PTU
Indications / Pcol |
-Graves disease
-inhibit biosynthesis of thyroid hormones by irreversibly inactivating peroxidase enzyme system in thyroid follicular cells |
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Graves disease pathophys
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-autoimmune production of thyroid stimulating antibodies (IgG) > stimulate TSH receptor on surface of the thyroid cell > ↑ T3/T4 secretion (hyperthyroidism)
-75% have some ocular involvement |
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hyperthyroidism Tx
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-immunosuppressives: cyclosporine & cyclophosphamide
-corticosteroids -surgical ablation -radioactive I |
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proptosis (Graves) Tx
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-α-adrenergic blockers (topical & oral) to reverse upper eyelid retraction
-Botox -tape eyes closed at night -diuretics -topical ABx -lubricants |
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Ca++ required for...
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-neurotransmitter release
-muscle contraction -blood coagulation -second messengers |
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___% Ca++ stored in bone
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99
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PTH name & function
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-parathyroid hormone
-stimulates resorption (bone breakdown) > ↑ [Ca++]pl -↑ reabsorption of Ca++ in kidneys -↑ Ca++ absorption in GI |
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osteoporosis pathophys & S/S
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-universal, gradual ↓ in bone mass > skeleton compromised and fractures with minimal trauma
-shortened stature, fractures, pain, vertebral body collapse, widow's hump |
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osteoporosis etiology
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-drug induced (>7.5mg prednisone equiv.)
-estrogen deficiency > ↑ bone breakdown -↓Ca++ absorption with ↑ age -↓ sun exposure -↓ kidney/liver function |
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primary regulators of adult bone mass
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-physical activity
-Ca++ intake -reproductive/hormonal endocrine status -genetics |
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HRT
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hormone replacement therapy
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___% of dietary Ca++ absorbed normally, absorption ↑ with excess...
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25-35; vitamin D
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body cannot absorb more than ___ elemental Ca++ at one time
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500-600mg
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body cannot absorb more than 500-600mg __________ at one time
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elemental Ca++
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Ca++ indications & DI
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-prevention/Tx osteoporosis, neutralize stomach acid
-↓ absorption of ABx |
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alendronate-Fosamax & risendronate-Actonel
Class / Indications / DI |
-bisphosphanates
-prevention/Tx osteoporosis, corticosteroid induced osteoporosis, Paget's disease -don't take within 1/2-1hr of other meds (bind to everything, including other drugs) |
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alendronate-Fosamax & risendronate-Actonel
Pcol |
-suppresses osteoclast activity
-binds to and becomes permanent part of bone > ↑ bone mass, resistant to enzymatic hydrolysis |
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bisphosphanates
Drugs / Indications |
-alendronate-Fosamax & risendronate-Actonel
-prevention/Tx osteoporosis, corticosteroid induced osteoporosis, Paget's disease |
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Paget's disease def. & S/S
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-disorder of bone remodeling (good quantity, poor quality)
-deformity, pain |
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calcitonin-Miacalcin/Calcimar
Indications / Pcol |
-post-menopausal Tx (not preventative) of osteoporosis, hypercalcemia
-synthesized and secreted by thyroid parafollicular cells; inhibits osteoclast activity > ↓ [Ca++]pl |
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vasomotor symptoms (menopause)
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"hot flashes"
|
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gastroesophageal reflux disease (GERD) def., pathophys, & S/S
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-gastric acid reflux > esophageal mucosal damage
-weak lower esophageal sphincter; anatomical alterations in obesity & pregnancy -burning pain radiating into chest/throat during/after meals, reflex burping; asthma type symptoms: wheezing, coughing, SoB |
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peptic ulcer disease location & etiology
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-duodenum 5-10x more than gastric
-helicobactor pylori > secrete inflammatory enzymes; ulcerogenic drugs (NSAIDs, ASA, corticosteroids) > ↓ PG synthesis > ↓ gastric epithelial cell secretion of mucous & HCO3 |
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PG role in GI
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stimulate gastric epithelial cells to secrete mucous & HCO3
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HCO3
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bicarbonate; protective buffer against gastric acids
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Mg OH, Al OH-Alternagel, Ca++ carbonate-Tums, Mg OH + Al OH-Gelusil II/Mylanta II
Class / Gen. info / Pcol / DI |
-antacids
-not first line but work well, available OTC in many forms (chews, liquid, powder, gum) -neutralize acid effectively by buffering excessive H+ with OH- -don't stop acid secretion > short-term -interfere with absorption of many drugs |
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antacids
Drugs |
-Mg OH
-Al OH-Alternagel -Ca++ carbonate-Tums -Mg OH + Al OH-Gelusil II, Mylanta II |
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cimetidine-Tagamet, ranitidine-Zantac, famotidine-Pepcid
Class / Gen. info / Pcol |
-histamine H2 receptor antagonists
-available OTC & OTC combinations -competitive reversible blockade of H2 receptors on parietal cells > ↓HCl secretion |
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histamine H2 receptor antagonists
Drugs / Use |
-cimetidine-Tagamet, ranitidine-Zantac, famotidine-Pepcid
-antacids |
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lansoprazole-Prevacid, omeprazole-Prilosec, esomeprazole-Nexium
Class / Pcol |
-proton pump inhibitors (PPIs)
-forms irreversible bond with & inhibits H+/K+ ATPase (proton pump) in gastric parietal cells for 24hr; proton pumps last stage of HCl secretion > ↓ regardless of stimulation |
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proton pump inhibitors
Drugs / Use |
-lansoprazole-Prevacid, omeprazole-Prilosec, esomeprazole-Nexium
-antacids |
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Prevpac
Dosage / Use |
-BID 10-14 days
-elimination of helicobacter pylori in peptic ulcer disease |
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drug used for elimination of helicobacter pylori in peptic ulcer disease
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Prevpac
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effect of pepsin in GI
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stimulates HCl secretion
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sucralfate-Carafate
Pcol |
cytoprotective actions: complex of AlOH and sucrose form sticky gel that binds to and coats ulcer site, protecting from HCl & aiding in healing; complexes & inactivates pepsin (stimulates HCl secretion)
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|
drug that forms sticky gel that binds to and coats ulcer site
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sucralfate-Carafate
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vitamin A / β-carotene source and ophthalmic & systemic function
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-carotenes from plants, vit A from animals; β-carotene precursor to vit A
-retinal epithelial tissue growth & differentiation; mucin layer of tear film; retinol active form in rods (retinol + opsin = rhodopsin) -↑ immune function, ↓ certain malignancies |
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vitamins C & E ophthalmic & systemic functions
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-potentially ↓ARMD and cataract development, ↓ intraocular inflammation
-anti-oxidants |
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zinc functions & gen. info
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-antibacterial actions, neuroprotective
-causes Cu depletion, must supplement |
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ARMD (wet) etiology & vit./mineral Tx
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-oxidative damage due to reactive O2 species
-preventative (antioxidants): A, C, E, zinc, lutein -B vitamins ↓ homocysteine levels which may be elevated in ARMD |
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night blindness vit./mineral Tx
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vitamin A
|
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optic neuritis vit./mineral Tx
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B6 & B12
|
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dry eye keratitis vit./mineral Tx
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vitamin A
|
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ranibizumab-Lucentis & pegaptanib-Macugen
Class / Indications / Pcol / Admin |
-monoclonal antibodies (MABs)
-ARMD (wet) -selective vascular endothelial growth factor (VEGF) antagonist -intravitreal |
|
lutein
Class / Ingredients / Proposed benefits / Gen. info |
-herbal
-carotenoid -anti-oxidant, improve vision with cataracts & AMRD, stop phototoxic blue light from hitting macula -provides pigment to macula |
|
zeaxanthin
Class / Ingredients / Proposed benefits / Gen. info |
-herbal
-carotenoid -anti-oxidant, stop phototoxic blue light from hitting macula -provides pigment to macula |
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herbal carotenoids with potential benefit for ARMD
|
-lutein
-zeaxanthin |
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acute pain is typically...
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nociceptive
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chronic pain is typically __________, has an __________ component, and involves pain __________
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neuropathic; inflammatory; sensitization (know it's coming)
|
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nociceptive pain receptor stimuli (molecules) & neurotransmitters
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-substance P, bradykinin, leukotrienes
-glutamate**, substance P, serotonin (5-HT) |
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allodynia
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pain from a stimulus not normally painful
|
|
"wind-up" phenomenon
|
-constant pain from peripheral nerves can lead to CNS sensitization to pain
-with hyperalgesia, new pain circuits form -the longer pain goes untreated, the harder it becomes to treat |
|
neuropathic pain examples
|
-fibromyalgia
-peripheral neuropathies -post-herpetic neuralgia |
|
CNS modulation of pain
|
-descending pathway activation ↓ perception of pain by inhibiting nerve excitatory impulses
-endogenous opioids found throughout descending spinal cord pathways |
|
opioids def. & examples
|
-endogenous NTs
-endorphins, enkephalins, dynrophin |
|
opiates def.
|
exogenous compounds with opioid function
|
|
antinociception def. & physiology
|
-↓ in pain by a descending pathway through spinal cord periaqueductal gray area
-activated by release of opioids > act on opioid receptors in CNS > stimulate release of GABA (inhibitory NT in pain pathways) |
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gamma aminobutyric acid (GABA) function
|
inhibitory NT in pain pathways
|
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glutamate function
|
stimulatory NT in pain pathways
|
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opioid pain receptor subtypes
|
mu, delta, kappa
|
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opioid pain receptor subtype with the most analgesic effects
|
mu
|
|
sites of opioid action include receptor stimulation in the...
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PNS and in specific regions of the CNS
|
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opioid systemic physiological actions
|
-analgesia: ↑ pain threshold & alter brain's perception of pain
-euphoria -resp. depression (esp. mu receptors) -sedation & mental depression -↓ cough reflex -↓ GI contractions & secretions -histamine release: itching, urticaria |
|
opioid ocular physiological actions
|
-excitation of parasympathetic NS > miosis (pinpoint pupils with toxicity, pathognomonic), ↑ accomm., ↓IOP
|
|
pain management levels 1 & 2
|
1) non-opioid analgesics (APAP, ASA, NSAIDs): short-term, non-severe relief
2) opioids (codeine, morphine, oxycodone, etc): moderate to severe pain; short-term preferred due to addiction; efficacy not good in chronic pain Tx, body develops tolerance |
|
pain management levels 3 & 4
|
3)adjuvant analgesics (antidepressants, anticonvulsants, corticosteroids, local anesthetics): main Tx for neuropathic pain
4) palliative care: comfortable at end of life |
|
acetaminophen (APAP)-Tylenol
MOA / Pcol |
-exact MOA unknown, suspect COX-3 involvement in brain
-CNS acting to ↑ pain threshold; antipyretic (↓ fever); lacks anti-inflammatory and antiplatelet effects |
|
acetaminophen (APAP)-Tylenol
ADR |
-hepatic toxicity / potentially fatal (g/day): 4/7 acute, 2.6/4 chronic
-alcoholics: toxicity at normal doses -toxicity in narcotic analgesic combinations (e.g. Vicodin) -nausea & vomiting in hours; jaundice, hepatic & renal failure days to weeks |
|
mu receptor functions
|
-supraspinal and spinal analgesia
-sedation -inhibition of respiration -slowed GI transit |
|
delta receptor functions
|
-supraspinal and spinal analgesia
|
|
kappa receptor functions
|
-supraspinal and spinal analgesia
-slowed GI transit |
|
glutamate acts on _____ and _____ receptors
|
AMPA (α-amino-methyl-proprionic acid); NMDA (n-methyl D-aspartate)
|
|
opioid mu, delta, and kappa agonists __________ transmitter release from presynaptic terminals of...
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↓; nociceptive primary afferents
|
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opioid mu agonists can __________ secondary afferent neurons directly and inhibit transmission of pain impulse going to the...
|
hyperpolarize; somatosensory areas of the forebrain
|
|
drug schedules I-III
|
I: no medical use, high abuse risk; LSD, heroin, ecstacy
II: high abuse risk, may lead to severe dependence; fentanyl, morphine, oxycodone III: abuse may lead to low/moderate dependence; codeine & hydrocodone combinations, anabolic steroids |
|
drug schedules IV-V
|
IV: abuse may lead to limited dependence; alprazolam-Xanax, diazepam-Valium, propoxyphene-Darvon
V: least potential for abuse, may lead to limited dependence; codeine cough syrups, diphenoxylate + atropine-Lomotil |
|
WHO 3-Step ladder
|
1: mild; ASA, APAP, NSAIDs
2: moderate; APAP combinations, tramadol 3: severe; morphine, hydromorphone, methadone, levorphanol, fentanyl, oxycodone |
|
opium derived from __________, contains __________, and is synthesized into __________
|
poppys; morphine; heroin
|
|
analgesic layering
|
sustained release analgesics combined with short-acting analgesics for breakthrough pain
|
|
opioid analgesic general pcol
|
-agonist, partial agonist, or antagonist on the 3 opioid receptor subtypes
-majority agonists on mu receptor |
|
spinal analgesia
|
opioid agonists act on primary afferent neurons and inhibit release of excitatory NTs (e.g. glutamate)
|
|
mu opioid agonists bind to mu receptors on __________ tract neurons to...
|
spinothalamic; ↓ excitatory impulse/action potential generation
|
|
opioid analgesic general ADR
|
-GI (10%): nausea (21%), vomiting, constipation (15%)
-CNS (10%): sedation, dizziness -respiratory depression in overdose -avoid alcohol & sedatives when on opioids |
|
opioid tolerance manifests within __________ and can be limited by...
|
2-3 weeks; opioid rotation -> cross-tolerance to other opioids can be minimal
|
|
psychological dependence
|
desire without physiological manifestations
|
|
withdrawal syndrome S/S
|
intense dysphoria (anxiety, restlessness, depression), nausea/vomiting, muscle aches, lacrimation, rhinorrhea, mydriasis, piloerection (erection of hair on skin), sweating, diarrhea, yawning, fever
|
|
withdrawal syndrome usually lasts no more than...
|
2-4 days
|
|
opioid use in recommended doses may result in __________ but rarely results in __________
|
withdrawal syndrome; addiction
|
|
morphine-MS Contin/Kadian, meperidine-Demerol, oxycodone-Oxycontin, methadone-Dolophine
Class / Gen. info |
-full (strong) opioid agonists, schedule II
-most efficacious, high abuse risk |
|
full (strong) opioid agonist drugs
|
-morphine-MS Contin/Kadian
-meperidine-Demerol -oxycodone-Oxycontin -methadone-Dolophine |
|
methadone-Dolophine
Pcol / Indications |
-mu opioid agonist, NMDA receptor antagonist, inhibits serotonin & NE reuptake
-Tx of opioid addiction, tolerance & dependency develop more slowly |
|
hydrocodone + APAP-Vicodin
Class / Gen. info |
-mild to moderate opioid agonist, schedule III
-#1 selling drug and abused narcotic analgesic |
|
codeine + APAP-Tylenol #3
Class / Gen. info / ADR |
-mild to moderate opioid agonist, schedule III
-antitussive (cough suppressant) -codeine synthesized from morphine, requires liver metabolism, ~8% of Caucasions lack CYP isoenzymes required -CNS (>10%): drowsiness -GI (>10%): neasea, constipation |
|
mild to moderate opioid agonists
|
-hydrocodone + APAP-Vicodin
-codeine + APAP-Tylenol #3 |
|
tramadol-Ultram, tramadol + APAP-Ultracet
Class / Gen. info / Contraindications |
-weak opioid agonists, not controlled
-moderate to severe pain; much less potential for respiratory depression; can be layered with other opioids -can cause seizures in epileptics |
|
tramadol-Ultram, tramadol + APAP-Ultracet
Pcol |
-weak mu receptor agonist
-primary mechanism: inhibits reuptake of serotonin (mainly) and NE (somewhat) |
|
propoxyphene + APAP-Darvocet
Class / Gen. info / Contraindications / ADR |
-weak opioid agonists
-low efficacy, low abuse risk -avoid in elderly -↑ risk of arrhythmia and seizures |
|
weak opioid agonists
|
-tramadol-Ultram
-tramadol + APAP-Ultracet -propoxyphene + APAP-Darvocet |
|
dextromethorphan-Benyln/Robitussin, Vicks Formula 44, hydrocodone + Hycodan/Hydrotuss/Codiclear/Tussionex
Class / Indications / Pcol |
-Antitussives (cough suppressant)
-COPD patients with persistent, irritating, non-productive cough -depresses cough centers in medulla oblongata |
|
dextromethorphan-Benyln/Robitussin, Vicks Formula 44, hydrocodone + Hycodan/Hydrotuss/Codiclear/Tussionex
Gen. info |
-chemically related to morphine, lacks narcotic properties in therapeutic doses
-OTC as liquid, capsules, lozenges, syrup -abuse: "dexing;" hallucinations, intox, out of body experience; brain damage, death |
|
antitussives
Use / Drugs |
-cough suppressants
-dextromethorphan-Benyln/Robitussin, Vicks Formula 44, hydrocodone + Hycodan/Hydrotuss/Codiclear/Tussionex |
|
naloxone-Narcan
Class / Indications / Pcol / Gen. info |
-opioid receptor antagonist
-Tx of opioid dependence; can reverse coma & respiratory depression from opioid overdose; no analgesia -mu, kappa, & delta receptor antagonist -initiates withdrawal symptoms w/in minutes |
|
opioid receptor antagonist drugs
|
naloxone-Narcan
|
|
estrone pathway
|
pituitary (ACTH) > adrenal glands (testosterone) > adipose > estrone
|
|
estrogen physiologic effects
|
-reproductive organ & 2° sexual development
-improves lipid profiles > delays atherosclerotic diseases (until menopause) -↓ bone breakdown, ↑ intestinal Ca++ absorption |
|
menopause ↓ in __________ and __________ secretion by the __________ is a __________ process
|
estrogen; progesterone; ovary; slow and gradual
|
|
effects of estrogen loss
|
-↑ CV disease, bone loss, skin dryness & loss of elasticity
-genitourinary: infections, vaginal dryness or atrophy, urinary incontinence -CNS: vasomotor symptoms, insomnia, emotional lability, cognitive function change |
|
estradiol def.
|
natural estrogen produced in body
|
|
17β estradiol, phytoestrogens, conjugated equine estrogens (CEE)-Premarin, ethinyl estradiol
Class |
-estrogen replacements
-birth control (ethinyl estradiol) |
|
raloxifene-Evista, tamoxifen-Nolvadex
Class / Indications / Pcol / ADR |
-selective estrogen receptor modulator (SERM)
-osteoporosis, HRT, breast cancer prevention (only use for tamoxifen) -bind to diff. parts of estrogen receptor in diff. organs w/ diff. affinities > variable pcol effects -↓VA, CME |
|
__________ has most benefit for osteoporosis but has ↑ __________
|
Premarin; CV disease risk
|
|
Premarin
|
conjugated equine estrogens (CEE)
|
|
progestin physiologic effects
|
-↓ gonadotropin secretion (esp. LH) > ↓ follicle development
-preps endometrium for implantation -↓ endometrial proliferation & cancer; secretory endometrium development -maintains pregnancy: ↓ uterine contractility, ↑ mammary gland proliferation |
|
medroxyprogesterone-Provera/Cycrin/Amen/Curretab
Gen. info / Use |
-most similar to endogenous progesterone, highly selective for progesterone receptors
-HRT |
|
norethindrone-Micronor/Nor-Qd/Aygestin/Ortho-Novum
Gen. info / Use |
-resemble testosterone; more andronergic effects
-birth control |
|
progestin indications
|
-post-menopausal HRT, contraception w/ or w/out estrogens, endometriosis (endometrial-like tissue grows in other areas of the body, causing pain and irregular bleeding
|
|
progestin Pcol
|
-binds to progesterone receptors > antagonizes estrogen-induced effects (e.g. endometrial hypertrophy in uterus)
-↓ FSH/LH secretion > ↓ endometrial cell stimulation (endometriosis Tx) |
|
progesterone/progestin opposes the actions of __________
|
estrogen
|
|
post-menopausal Tx
|
-w/out uterus: estrogen alone (raloxifene); progestin for endometrial cancer, no uterus = no endometrial tissue
-w/ uterus: estrogen + progestin -HRT combination drugs (Prempro) |
|
Prempro
|
HRT combination drug: conj. estrogen + medroxyprogesterone
|
|
HRT combination drug: conj. estrogen + medroxyprogesterone
|
Prempro
|
|
pre-menopausal estrogen seems to prevent __________ while post-menopausal estrogen HRT significantly...
|
major disease states; ↓ menopausal symptoms but ↑ many major disease states
|
|
estrogen / estrogen + progestin HRT effects on breast cancer, endometrial cancer, osteoporosis/fractures, & CVD
|
↑ , ↑↑ , ↓ , ↑
↑- , ↓ , ↓ , ↑- |
|
Ovral
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50ug estrogen/progestin combination drug
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Ortho-Cyclen, Loestrin/Minestrin
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sub-50ug monophasic estrogen/progestin combination drugs
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Tri-Cyclen
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sub-50ug multiphasic estrogen/progestin combination drug
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Ovrette
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progestin drug
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estrogen/progestin combination drugs
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-Ovral
-Ortho-Cyclen -Loestrin/Minestrin -Tri-Cyclen |
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progestin drugs
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-Ovrette
-medroxyprogesterone-Provera/Cycrin/Amen/Curretab -norethindrone-Micronor/Nor-QD/Aygestin/Ortho-Novum |
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oral contraceptive
Pcol / Alternate use |
-continuous estrogens and progestins inhibit release of GnRH, FSH, and LH; ↑ cervical mucous > ↓ sperm movement
-regulating menstrual cycles, e.g. for irregular bleeding, endometriosis |
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oral contraceptive
Gen. info / Administration |
-synthetic estrogens used more frequently; very effective (pregnancy rates 1-2%)
-oral monophasic, bi-phasic, tri-phasic, and seasonal; transdermal; progestin only (Ovrette, Plan B) |
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progestin only slightly {more/less} effective than combination drugs
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less
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combination oral contraceptive benefits & ADRs
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-↓ ovarian & endometrial cancer, acne, and abnormal menstrual cycles, no ↑ in breast cancer
-↑ clotting disorders, women over 35 who smoke ↑ risk of MI and stroke |
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androgen production
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testes > (5-α-reductase) > 5-α-dihydrotestosterone (DHT) production in prostate gland & seminal vesicles
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DHT
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5-α-dihydrotestosterone
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androgen physiological effects
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-androgenic actions of testosterone & DHT: maturation, virilization, libido, ↑ aggression
-anabolic actions of testosterone: ↑ protein synthesis, muscle mass, bone growth; ↑ renal retention of N & electrolytes; ↑ erythropoiesis; atherogenic (↑LDL, ↓HDL) |
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testosterone
Gen. info / Pcol / Indications |
-abuse: anabolic steroids
-bind to intracellular androgen receptors -androgen HRT: impotence, growth, hypogonadism, male menopause; levels ↓ w/ age; anabolic effects (↑ muscle after injury) |
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testosterone ADR
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-virtually every organ affected by androgens
-masculinization (>10%); CV (>10%): edema, Na+ retention, atherogenic; hepatic dysfunction (1-10%); CNS: paranoia, mania, delirium, homicidal rage; sterility (1-10%) |
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long-term androgen use leads to _________ through what mechanism?
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sterility; ↓GnRH, LH, & FSH secretion > ↓ testis size & sperm production
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finasterid-Proscar
Class / Indications / Pcol |
-antiandrogen
-benign prostatic hyperplasia (BPH, not a cancer); alopecia (loss of hair) -synthetic testosterone analog, competitive inhibitor of 5-α-reductase > ↓DHT production > ↓ prostate hyperplasia |