021015 male pharm Flashcards

1
Q

testosterone has a high first pass effect: true or false

A

true

most preps are designed to bypass hepatic catabolism (transdermal patch, gels)

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2
Q

testosterone esters (cypionate)

A

has esterified fatty acid-lipophilic analog of testosterone

the ester is hydrolyzed resulting in slow testosterone release. lasts 1 week, IM injection

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3
Q

17 alpha alklyated compounds

A

stanozolol (oral)
has alkyl group added to testosterone to retard hepatic catabolism

causes hepatotoxicity

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4
Q

uses of androgens

A

MALE HYPOGONADISM (due to testosterone deficiency)

male senescence
athletic performance abuse
women w low serum testosterone (to enhance libido and sk musc to fat ratio)
etc

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5
Q

adverse effects of androgens

A

similar to those in puberty-acne, gynecomastia, more aggressive sexual behavior

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6
Q

what should be considered in using androgens?

A

height and growth hormone status, b/c you don’t want to limit long bone growth via estrogen

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7
Q

risks of testosterone therapy

A

in men with pre-existing heart disease-risk of cardiovascular events

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8
Q

how does testosterone therapy impact spermatogenesis?

A

it decreases sperm count

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9
Q

testosterone precursors

A

androstenedione
dehydroepiandrosterone (DHEA)

weak androgens
no longer manufactured

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10
Q

adverse effects of androgen abuse

A

decreased endogneous testosterone and sperm production

decreased testicular size (after many years)

high doses-erythryocytosis

gynecomastia (testos is converted to estrogen)

17 alkylated androgens-HEPATOTOXIC

in women and children-virilization (increased hirsutism, male pattern hair loss, acne)

phallic enlargement, clitoral enlargement

stunting of linear growth (in children)

cardiac dis

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11
Q

antiandrogens and androgen antagnoists

A

leuprolide
finasteride
flutamide

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12
Q

inhibitors of androgen synthesis

A

GnRH analog-leuprolide (continuous GnRH)

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13
Q

5alpha-reductase inhibitor

A

finasteride

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14
Q

androgen receptor antagonist

A

flutamide (competitive inhibitor of androgen receptor)

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15
Q

uses of leuprolide

A

tx of advanced prostate cancer
endometriosis
central precocious puberty

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16
Q

androgen receptor antagonists’ efficacy

A

alone, have limited efficacy because they increase LH secretion and endogenous androgen production. they are used in CONJUNCTION with GnRH analog

17
Q

use of flutamide

A

metastatic prostate cancer

hirsutism in women

18
Q

use of finasteride

A

BPH

male pattern baldness

19
Q

tx for erectile dysfxn

A

alprostadil (PGE1)

sildenafil, vardenafil, tadalafil (PDE5 inhibitors)

20
Q

MOA of alprostadil

A

dilation of cavernosal arteries

21
Q

PDE5 inhibitors-MOA

A

cGMP is normally metabolized by PDE, so inhibition of cyclic GMP specific PDE5 causes accumulation of cGMP

cGMP relaxes the corpus cavernosum smooth muscle resulting in engorgement and erection

22
Q

which PDE5 inhibitor can be active for up to 36 hrs

A

tadalafil

23
Q

what are PDE5 inhibitors contraindicated in?

A

in pts taking nitrates (combo can cause extreme hypotension)