Genitourinary Flashcards
Darifenacin
Anticholinergic
Reduce bladder muscle contractility, increase
bladder capacity
Oxybutynin
Anticholinergic
Reduce bladder muscle contractility, increase
bladder capacity
Propantheline
Anticholinergic
Reduce bladder muscle contractility, increase
bladder capacity
Solifenacin
Anticholinergic
Reduce bladder muscle contractility, increase
bladder capacity
Tolterodine
Anticholinergic
Reduce bladder muscle contractility, increase
bladder capacity
Mirabegon
Beta3-adrenoreceptor agonist; relaxes bladder muscle during the storage phase of micturition, increasing bladder capacity.
Desmopressin
Antidiuretic hormone analogue
Used in nocturnal enuresis in children
Alfuzosin
Block alpha1 receptors, relaxing smooth muscle in the bladder neck and prostate, and decreasing resistance to urinary flow.
Unlike nonselective alpha-blockers (eg phenoxybenzamine), they have little effect on presynaptic alpha2 receptors and are therefore less likely to cause reflex tachycardia.
Alfuzosin, silodosin and tamsulosin are more selective for the alpha1-receptor subtypes found in the bladder and prostate.
Silodosin
Block alpha1 receptors, relaxing smooth muscle in the bladder neck and prostate, and decreasing resistance to urinary flow.
Unlike nonselective alpha-blockers (eg phenoxybenzamine), they have little effect on presynaptic alpha2 receptors and are therefore less likely to cause reflex tachycardia.
Alfuzosin, silodosin and tamsulosin are more selective for the alpha1-receptor subtypes found in the bladder and prostate.
Tamsulosin
Block alpha1 receptors, relaxing smooth muscle in the bladder neck and prostate, and decreasing resistance to urinary flow.
Unlike nonselective alpha-blockers (eg phenoxybenzamine), they have little effect on presynaptic alpha2 receptors and are therefore less likely to cause reflex tachycardia.
Alfuzosin, silodosin and tamsulosin are more selective for the alpha1-receptor subtypes found in the bladder and prostate.
Dutasteride
Inhibit 5‑alpha-reductase, which converts testosterone to dihydrotestosterone (a potent cellular androgen that stimulates prostate growth). They reduce prostate size and improve symptoms and urinary flow rate.
Finasteride
Inhibit 5‑alpha-reductase, which converts testosterone to dihydrotestosterone (a potent cellular androgen that stimulates prostate growth). They reduce prostate size and improve symptoms and urinary flow rate.
Avanafil
Phosphodiesterase 5 inhibitor
Sexual stimulation increases cyclic guanosine monophosphate (cGMP) levels, resulting in smooth muscle relaxation, inflow of blood to the corpus cavernosum and penile erection.
These agents inhibit the breakdown of cGMP by phosphodiesterase 5 (PDE5), increasing blood flow to the penis during sexual stimulation.
Sildenafil
Phosphodiesterase 5 inhibitor
Sexual stimulation increases cyclic guanosine monophosphate (cGMP) levels, resulting in smooth muscle relaxation, inflow of blood to the corpus cavernosum and penile erection.
These agents inhibit the breakdown of cGMP by phosphodiesterase 5 (PDE5), increasing blood flow to the penis during sexual stimulation.
Tadalafil
Phosphodiesterase 5 inhibitor
Sexual stimulation increases cyclic guanosine monophosphate (cGMP) levels, resulting in smooth muscle relaxation, inflow of blood to the corpus cavernosum and penile erection.
These agents inhibit the breakdown of cGMP by phosphodiesterase 5 (PDE5), increasing blood flow to the penis during sexual stimulation.