ED Pharmacology Flashcards

1
Q

What is BPH

A

prostate enlargement can cause symptomatic obstruction of the male urethra, causing the sensation of not fully emptying the bladder, increased frequency in urination, unintended interruptions in stream while urinating, and urinary straining.

May be caused by too much DHT or too many androgen. receptors

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2
Q

How do alpha 1 antagonists work

A

Alpha-1 Antagonists act to improve urine flow by means of partial reversal of smooth muscle contraction within the enlarged prostate

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3
Q

What are the main alpha 1 inhibitors

A

doxazosin, terazosin and tamsulosin

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4
Q

Impact of Alpha 1 antagonists on blood pressure

A

Can cause hypotension and reflexive tachycardia, can be good if patient has BPH and hypertension

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5
Q

Which alpha 1 antagonist has the least impact on bp

A

Tamsulosin is different from other alpha-1 antagonists because it targets one particular subtype of receptor

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6
Q

Other side effects of a1 antagonists besides impacts on bp

A

Can negatively effect ejaculation

Floppy iris syndrome

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7
Q

Most common 5 a reductase inhibitors for BPH

A

FInasteride and dutasteride

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8
Q

Common side effects of 5 a reductase inhibitors

A

sexual dysfunction and depression

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9
Q

Which is frist-line treatment for BPH

A

Alpha-1-adrenergic antagonists provide immediate therapeutic benefits and are usually considered first line treatment for BPH. 5-alpha-reductase inhibitors require long-term treatment for efficacy, taking 6-12 months before causing a “symptom-relieving” decrease in prostate size.

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10
Q

What two things are needed for erection

A

parasympathetic innervation and nitric oxide

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11
Q

How does NO cause erection

A

Nitric oxide activates guanylyl cyclase, thus increasing the concentration of cGMP, leading to second messenger activation, dephosphorylation of myosin light chains and finally relaxation of smooth muscle

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12
Q

How do most medications for ED work

A

Work to increase cGMP

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13
Q

How do Phosphodiesterase 5-Inhibitors work

A

act to increase cGMP by inhibition of its metabolism by phosphodiesterase isoform 5 (PDE-5), allowing prolonged effect of smooth muscle relaxation. Remember, increased cGMP is initiated by nitric oxide release from cholinergic motor input. Thus, in order for this drug to work, there has to be an intact nervous system with stimulating signals.

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14
Q

Most common Phosphodiesterase-5 inhibitors

A

tadalafil, sidenafil, and vardenafil

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15
Q

Side effects of PDE-5 inhibitors

A

PDE-5 inhibitors as a whole have vasodilatory effects and can potentiate the actions of nitrates (potent vasodilators used to treat chest pain, more on this in future lectures). Severe hypotension can occur, which may lead to myocardial infarction as the heart is unable to be adequately perfused. It is recommended that at least 6 hours pass between usage of these drugs together.

Lastly, Sildenafil is known to potentially effect color vision, particularly in blue-green discrimination. This effect is easily remembered if you recognize that sildenafil’s brand name is Viagra (“the little blue pill”).

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16
Q

How do synthetic prostoglandins work

A

Vasoactive drugs, when injected into the corpora cavernosa, inhibit or override sympathetic inhibition and act as direct smooth muscle vasodilators

17
Q

What is the main PGE1 analog

A

he PGE 1 analog alprostadil can be administered by intracavernosal injection or transurethral suppository to cause this effect.

18
Q

Side effects of PGE analogs

A

Side effects include penile pain (likely caused by pain-inducing derivatives of metabolized PGE) and penile bleeding. Prolonged erection and/or priapism are also possible side effects of these methods.

19
Q

What are the causes for ED (acronym and words)

A