Sweatman BPH Drugs Flashcards
(41 cards)
three drug classes used in BPH treatment
Alpha antagonist
PDE5 inhibitors
5 alpha reductase inhibitors
dynamic bladder-outles obstruction due to
signalling via Alpha 1a,b,d receptors
static bladder-outlet obstruction
5 alpha reductase-testosterone-enlargment of the prostate (hyperplasia)
bladder muscle is under what control
Muscarcinic (Acetylcholine) M3 selective and M2 non-selective
only alpha families that matter
alpha 1a
alpha 1d
detrussor muscle is under what receptor control
alpha-1d
Lower GI tract”–>Trigone, prostatic urethra, prostate gland penile urethra of bladder is under what receptor control
alpha 1a
blockade causes relaxation of all these entities and allows for easier urination
alpha blocker with great variation from patient to patient
prazosin
dose titration necessary
prazosin
all alpha blockers end in
- Zosin
- losin
- dozin
advantage of selective alpha 1a agents
no need for dose titration, less CV effects
disadvantages of alpha 1a agents
- retrograde ejactulation (tamsulosin, silodosin)
- blockade of dopa receptors in CNS
superior Alpha antagonist at the momen
Alfuzosin–> no CNS or ejaculatory effects
alpha 1 blockers in eye surgery
floppy iris syndrome
events in erection
(PNS S2-S4) via the cavernous nerve-ACH-NOS-NO-SOLUBLE GC–>cGMP–>active PKG–>efflux of calcium (dec intraceullualr concentration)–> vasodilation
MOA for PDE5i
inhibits PDE5 which allows cGMP to linger—>prolongs natural vasodilatory action of the endogenous molecule
name the PDE5i
tadalafil (cialis)
ADE’s for tadalafil
Nasopahrygitis, URTI, NON-arteric ischemic optic neuropathy, retinal artery occluson, hearling loss
contraindicated in tadalafil usage
nitrate-profoudn hypotension
worse with ETOH consumption
which androgen activate gene expression more efficiently
DHT»testosterone–> binds with higher affinity
distribution of type I/II 5 alpha reductase
type I: non genital skin, liver, bone
2–> urogenital tissue and genital skin in men and women
MOA for 5 alpha reductase inhibitors
reduce DHT driven proliferation of the prostate-providing relief for urinary evacuation
inhibits type I and 2
dutasteride
inhibits type 2 only
finasteride