reproductive Flashcards
(26 cards)
menotropin
hMG(human menopausal gonadotropin)
acts as FSH and LH
stimulates hormone release and follicle relase->fertilization
Leuprolide
- GnRH analog with agonist properties when used in pulsatile fashion
Ex. infertiliy - antagonist when used in continuous fashion(down regulate receptor in pituitary–>decrease GSH/LH)
Ex. prostate cancer(with flutamide), uterine fibroids (continous), precocious puberty (continous)
Tox: antiandrogen, N/V(男女不分让人恶心)
tesosterone
1.agonist at androgen receptor
2.treats hypogonadism and development of 2ndary sex characteristics
stimulation of anabolism to promote recovery after burn or injury
3. causes masculinization in females,
reduces intratesticular testosterone in male by inhibiting release of LH(-feedback)–>gonadal atrophy
premature closure of epiphyseal plattes, increase LDL,decrease HDL.
methyltestosterone
1.agonist at androgen receptor
2.treats hypogonadism and development of 2ndary sex characteristics
stimulation of anabolism to promote recovery after burn or injury
3. causes masculinization in females,
reduces intratesticular testosterone in male by inhibiting release of LH(-feedback)–>gonadal atrophy
premature closure of epiphyseal plattes, increase LDL,decrease HDL.
finasteride
5-alpha-reductase inhibitor(decrease conversion of testosterone to DHT)
useful in BPH
also promotes hair growth-used to treat male-pattern baldness
flutamide
nonsteriodal competitive inhibitor of androgens at testosterone receptor
used in prostate carcinoma
ketoconazole
inhibits steroid synthesis (inhibits 17,20-desmolase)
ketoconazole and spironolactone are used in the treatment of polycystic ovarian syndrome to prevent hirsutism
sideeffect: gynecomastia and amenorrhea
sipronolactone
inhibits steroid binding
aldosterone receptor antagonist in the cortical collecting tubule
used to treat polycystic ovarian syndrome to prevent hirsutism
sideeffect: gynecomastia and amenorrhea
Spironolactone and eplerenone
estrogen
ethinyl estradiol, DES,mestranol
- bind estrogen receptors
- hypogonadism or ovarian failure, menstrual abnormalities, HRT in postmenopausal women; use in men with androgen-dependent prostate cancer
- increase risk of endometrial cancer, bleeding in postmenopausal, clear cell adenocarcinoma of vagina in female exposed to DES in utero
increase risk of thrombi
CI:ER+ breast cancer, history of DVTs
Clomiphene
partial agonist at estrogen receptor in hypothalamus
prevents normal feedback inhibition and increase release of LH and FSH from pituitary, stimulates ovulation
used to treat infertility and polycystic ovarian syndrome
hot flashes, ovarian enlargment, multiple stimultaneous pregnancies and visual disturbance
Tamoxifen
antagonist on breast tissue
used to treat and prevent recurrence of ER+ breast cancer
Raloxifene
agonist on bone, antagonist on breast and uterus
reduces resorption of bone
used to treat osteoporosis
hormone replacement therapy
relief or prevention of menopausal symptoms (hot flashs, vaginal atrophy) and osteoporosis (increase estrogen, decrease osteoclast activities);
unopposed estrogen replacement therapy (ERT), increase risk of endometrial cancer, so progesterone is added.
possible increase CV risk
anastrozole
aromatase inhibitors used in postmenopausal women with breast cancer
exemestane
aromatase inhibitors used in postmenopausal women with breast cancer
progestins
- binds progesterone receptor, reduce growth and increase vascularization of endometrium
- used in oral contraceptives and in the treatment of endometrial cancer and abnormal uterine bleeding
mifepristone
RU-486
- competitive inhibitor of progestins at progesterone receptor
- termination of pregnancy. administered with misoprosol (PGE1)
- heavy bleeding, GI effects (N/V, anorexia), abdominal pain
oral contraception
synthetic progestins, estrogen
estrogen and progestin inhibits LH/FSH –> prevent estrogen surge–> no LH surge–> no ovulation
progestins cause thickening of the cervical mucus, limiting access of sperm; also thickening of endometrial is less suitable for the implant.
CI: smoker>35yrs (increase risk for cardiovascular disease), pt with history of thromboembolism and stroke or E-dependent tumor
terbutaline
beta2-agonist that relaxes the uterus
reduces premature uterine contractions
tamsulosin
alpha1-antagonist used to treat BPH by inhibiting smooth muscle contraction
selective for Alpha1A,D receptor(found in prostate)vs vascular alpha1 B receptor
ritodrine
beta2-agonist that relaxes the uterus
reduces premature uterine contractions
metaproterenol
beta2-agonist that relaxes the uterus
reduces premature uterine contractions
TERAZOSIN
alpha1 blocker
BPH
sildenafil
inhibit phosphodiesterase 5, causing increase of cGMP, smooth muscle relaxation in the corpus cavernosum
increase blood flow, and penile erection
tox: headache, flushing, dyspepsia,
impaired blue-green color vision.
risk of life-threatening hypotension in patients taking nitrates