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201 Cards in this Set

  • Front
  • Back
autocrine
hormone acts on releasing cell
paracrine
hormone acts on cell near releasing cell
endocrine
hormone acts on cell distant from releasing cell
antidiuretic hormone secreted by...
posterior pituitary
oxytocin secreted by...
posterior pituitary
growth hormone secreted by...
anterior pituitary
prolactin secreted by...
anterior pituitary
FSH (__________) secreted by...
follicle stimulating hormone; anterior pituitary
LH (__________) secreted by...
luteinizing hormone; anterior pituitary
insulin secreted by...
pancreas
glucagon secreted by...
pancreas
somatostatin secreted by...
pancreas
parathyroid hormone secreted by...
parathyroid gland
T3/T4 secreted by...
thryoid gland
calcitonin secreted by...
thyroid gland
catecholamines secreted by...
adrenal gland
aldosterone secreted by...
adrenal gland
cortisol secreted by...
adrenal gland
estradiol (__________) secreted by...
estrogen; ovary
progesterone secreted by...
ovary
testosterone secreted by...
ovaries, testes, adrenal glands
posterior pituitary hormones
antidiuretic hormone, oxytocin
anterior pituitary hormones
GH, PRL, FSH, LH, ACTH, TSH
pancreas hormones
insulin, glucagon, somatostatin, digestive enzymes
parathyroid gland hormones
parathyroid hormone
thyroid gland hormones
T3/T4, calcitonin
adrenal gland hormones
catecholamines, aldosterone, cortisol, testosterone
ovary hormones
estradiol, progesterone, testosterone
testes hormones
testosterone
__________-__________-__________ __________ axis
hypothalamic-pituitary-target organ axis
GnRH name, pathway, & function
-gonadotropin-releasing hormone
-hypothalamus > ant. pituitary gonadotrophs (LH, FSH) > testes/ovaries (testosterone, estrogen, progesterone)
-spermatogenesis/ovulation
TRH name & pathway
-thyrotropin-releasing hormone
-hypothalamus > pituitary thyrotrophs (TSH) > thyroid > T3/T4
CRH name & pathway
-corticotropin-releasing hormone
-hypothalamus > pituitary corticotrophs (ACTH) > adrenal glands > glucocorticoids
GHRH name & pathway
-growth hormone-releasing
hormone
-hypothalamus > ant. pituitary somatotrophs (GH) > throughout body
PRF name, pathway, & function
-prolactin-releasing factor
-hypothalamus > ant. pituitary lactotrophs/mammotrophs (PRL) > breasts
-lactation
TSH
thyroid-stimulating hormone
ACTH
adrenocorticotropic hormone
GH
growth hormone
PRL
prolactin
gonadotrophic hormones
LH, FSH (leuteinizing hormone, follicle-stimulating hormone)
thyrotrophic hormones
TSH (thyroid-stimulating hormone)
corticotrophic hormones
ACTH (adrenocorticotropic hormone)
somatotrophic hormones
GH (growth hormone)
mammotrophic/lactotrophic hormones
PRL (prolactin)
hypothalamic factors (secreted by hypothalamus)
GnRH, TRH, CRH, GHRH, PRF, dopamine
pituitary cell types
gonadotroph
corticotroph
somatotroph
thyrotroph
lactotroph/mammotroph
1°/2°/3° hyperthyroidism is caused by a problem in the...
throid gland / pituitary gland / hypothalamus
anterior pituitary name
adenohypophysis
posterior pituitary name
neurohypophysis
oxytocin function
stimulates uterine contraction, promotes milk release during lactation
enuresis (bedwetting) probable etiology
lack of ADH secretion at night
diabetes insipidous def., etiology, and symptoms
-symptoms look like diabetes
-inadequate ADH secretion or renal receptors (V2) don't respond
-nocturia, polyuria, polydipsia
thyroid feedback mechanism (+/-)
-prolonged cold exposure, acute psychosis, and circadian rhythms induce TRH secretion
-severe stress inhibits TRH secretion
-T3/T4 inhibit TRH & TSH secretion
___% of thyroid hormones are ___
99.5%+; PPB
hypo/hyperthyroidism S/S
-hypo: ↓BMR
-hyper: ↑BMR, exophthalmos
-both: goiter, infertility
Hashimoto's disease
-chronic autoimmune thyroiditis (hyopthyroidism)
-T-cells attack antigen-like proteins on thyroid membrane, stimulating B-cells to produce Ab's against normal thyroid tissue
chronic autoimmune thyroiditis
Hashimoto's disease
myxedema
-end-stage of long-standing uncorrected hypothyroidism
-lethargy, stupor, hypothermia, delirium > coma > death
end-stage of long-standing uncorrected hypothyroidism
myxedema
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
__________ ↓ orbital edema
diuretics
methimazole-Tapazole & propylthiouracil-PTU

Indications / Pcol
-Graves disease
-inhibit biosynthesis of thyroid hormones by irreversibly inactivating peroxidase enzyme system in thyroid follicular cells
Graves disease pathophys
-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
hyperthyroidism Tx
-immunosuppressives: cyclosporine & cyclophosphamide
-corticosteroids
-surgical ablation
-radioactive I
proptosis (Graves) Tx
-α-adrenergic blockers (topical & oral) to reverse upper eyelid retraction
-Botox
-tape eyes closed at night
-diuretics
-topical ABx
-lubricants
Ca++ required for...
-neurotransmitter release
-muscle contraction
-blood coagulation
-second messengers
___% Ca++ stored in bone
99
PTH name & function
-parathyroid hormone
-stimulates resorption (bone breakdown) > ↑ [Ca++]pl
-↑ reabsorption of Ca++ in kidneys
-↑ Ca++ absorption in GI
osteoporosis pathophys & S/S
-universal, gradual ↓ in bone mass > skeleton compromised and fractures with minimal trauma
-shortened stature, fractures, pain, vertebral body collapse, widow's hump
osteoporosis etiology
-drug induced (>7.5mg prednisone equiv.)
-estrogen deficiency > ↑ bone breakdown
-↓Ca++ absorption with ↑ age
-↓ sun exposure
-↓ kidney/liver function
primary regulators of adult bone mass
-physical activity
-Ca++ intake
-reproductive/hormonal endocrine status
-genetics
HRT
hormone replacement therapy
___% of dietary Ca++ absorbed normally, absorption ↑ with excess...
25-35; vitamin D
body cannot absorb more than ___ elemental Ca++ at one time
500-600mg
body cannot absorb more than 500-600mg __________ at one time
elemental Ca++
Ca++ indications & DI
-prevention/Tx osteoporosis, neutralize stomach acid
-↓ absorption of ABx
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)
alendronate-Fosamax & risendronate-Actonel

Pcol
-suppresses osteoclast activity
-binds to and becomes permanent part of bone > ↑ bone mass, resistant to enzymatic hydrolysis
bisphosphanates

Drugs / Indications
-alendronate-Fosamax & risendronate-Actonel
-prevention/Tx osteoporosis, corticosteroid induced osteoporosis, Paget's disease
Paget's disease def. & S/S
-disorder of bone remodeling (good quantity, poor quality)
-deformity, pain
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
vasomotor symptoms (menopause)
"hot flashes"
gastroesophageal reflux disease (GERD) def., pathophys, & S/S
-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
peptic ulcer disease location & etiology
-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
PG role in GI
stimulate gastric epithelial cells to secrete mucous & HCO3
HCO3
bicarbonate; protective buffer against gastric acids
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
antacids

Drugs
-Mg OH
-Al OH-Alternagel
-Ca++ carbonate-Tums
-Mg OH + Al OH-Gelusil II, Mylanta II
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
histamine H2 receptor antagonists

Drugs / Use
-cimetidine-Tagamet, ranitidine-Zantac, famotidine-Pepcid
-antacids
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
proton pump inhibitors

Drugs / Use
-lansoprazole-Prevacid, omeprazole-Prilosec, esomeprazole-Nexium
-antacids
Prevpac

Dosage / Use
-BID 10-14 days
-elimination of helicobacter pylori in peptic ulcer disease
drug used for elimination of helicobacter pylori in peptic ulcer disease
Prevpac
effect of pepsin in GI
stimulates HCl secretion
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)
drug that forms sticky gel that binds to and coats ulcer site
sucralfate-Carafate
vitamin A / β-carotene source and ophthalmic & systemic function
-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
vitamins C & E ophthalmic & systemic functions
-potentially ↓ARMD and cataract development, ↓ intraocular inflammation
-anti-oxidants
zinc functions & gen. info
-antibacterial actions, neuroprotective
-causes Cu depletion, must supplement
ARMD (wet) etiology & vit./mineral Tx
-oxidative damage due to reactive O2 species
-preventative (antioxidants): A, C, E, zinc, lutein
-B vitamins ↓ homocysteine levels which may be elevated in ARMD
night blindness vit./mineral Tx
vitamin A
optic neuritis vit./mineral Tx
B6 & B12
dry eye keratitis vit./mineral Tx
vitamin A
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
herbal carotenoids with potential benefit for ARMD
-lutein
-zeaxanthin
acute pain is typically...
nociceptive
chronic pain is typically __________, has an __________ component, and involves pain __________
neuropathic; inflammatory; sensitization (know it's coming)
nociceptive pain receptor stimuli (molecules) & neurotransmitters
-substance P, bradykinin, leukotrienes
-glutamate**, substance P, serotonin (5-HT)
allodynia
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)
gamma aminobutyric acid (GABA) function
inhibitory NT in pain pathways
glutamate function
stimulatory NT in pain pathways
opioid pain receptor subtypes
mu, delta, kappa
opioid pain receptor subtype with the most analgesic effects
mu
sites of opioid action include receptor stimulation in the...
PNS and in specific regions of the CNS
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...
↓; nociceptive primary afferents
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
50ug estrogen/progestin combination drug
Ortho-Cyclen, Loestrin/Minestrin
sub-50ug monophasic estrogen/progestin combination drugs
Tri-Cyclen
sub-50ug multiphasic estrogen/progestin combination drug
Ovrette
progestin drug
estrogen/progestin combination drugs
-Ovral
-Ortho-Cyclen
-Loestrin/Minestrin
-Tri-Cyclen
progestin drugs
-Ovrette
-medroxyprogesterone-Provera/Cycrin/Amen/Curretab
-norethindrone-Micronor/Nor-QD/Aygestin/Ortho-Novum
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
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)
progestin only slightly {more/less} effective than combination drugs
less
combination oral contraceptive benefits & ADRs
-↓ ovarian & endometrial cancer, acne, and abnormal menstrual cycles, no ↑ in breast cancer
-↑ clotting disorders, women over 35 who smoke ↑ risk of MI and stroke
androgen production
testes > (5-α-reductase) > 5-α-dihydrotestosterone (DHT) production in prostate gland & seminal vesicles
DHT
5-α-dihydrotestosterone
androgen physiological effects
-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)
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)
testosterone ADR
-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%)
long-term androgen use leads to _________ through what mechanism?
sterility; ↓GnRH, LH, & FSH secretion > ↓ testis size & sperm production
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