MedChem of Asthma, COPD, and Cystic Fibrosis Flashcards

1
Q

Outline the 6 steps of the stepwise approach to treatment of asthma.

A

(1) SABA prn
(2) low-dose ICS (or cromolyn, LTRA, theophylline)
(3) low-dose ICS + LABA (or others)
(4) medium-dose ICS + LABA
(5) high-dose ICS + LABA, consider Xolair
(6) high-dose ICS + LABA, oral CS, consider Xolair

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2
Q

Describe the biochemical mechanism for bronchial smooth muscle relaxation induce by beta-2 agonists.

A

Beta adrenergic receptors activate cytoplasmic G-proteins, which ultimately increase intracellular cAMP levels. cAMP activates protein kinase A. PKA, then, phosphorylates a myosin LC kinase that normally allows smooth muscle contraction by phosphorylating myosin. Myosin is now not properly oriented for contraction, and the smooth muscle will relax.

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3
Q

Which two examples of SABAs were given in lecture?

A

albuterol and terbutaline

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4
Q

Of the two SABAs, which is more beta-2 selective? What is the consequence of this?

A

terbutaline, causes increased palpitations

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5
Q

Name three LABAs.

A

formoterol (Foradil), Arformoterol (Brovana), and Salmeterol (Serevent)

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6
Q

Which LABAs have the greatest beta-2 selectivity?

A

formoterol and arformoterol

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7
Q

SABAs are resistant to metabolism by ______, while LABAs are resistant to ________ and ________.

A

COMT, COMT, MAO

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8
Q

Of the beta-agonists, which are confined to use for regular dosing?

A

the LABAs, (ar)formoterol and salmeterol

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9
Q

Between the two LABAs, _______ has the quicker onset of action due to its increased ________. Its decreased _________ keeps it in the lungs longer.

A

formoterol, hydrophilicity (allows it to get to receptor sites faster), lipophilicity

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10
Q

Outside of use for EIA, what is the suggested weekly limit for SABA use?

A

no more than 2x/week, not including EIA use

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11
Q

List three of the main effects of inhaled glucocorticoids.

A

(1) decr. eosinophils, macrophages, mast cells
(2) inhibition of leukotriene/prostaglandin synthesis
(3) decreased airway hyperresponsiveness

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12
Q

How often are inhaled glucocorticoids dosed?

A

once daily

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13
Q

What are the three inhaled glucocorticoids mentioned in lecture?

A

fluticasone, budesonide, mometasone

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14
Q

Outline the biochemical mechanism of action of methylxanthines.

A

There are two ways by which methylxanthines cause bronchodilation. The first is by inhibition of PDE4, which normally hydrolyzes cAMP intracellularly. cAMP levels are increased by this effect, and relaxation occurs by the same mechanism as with beta agonists. Methylxanthines also block the adenosine receptor, paired with Gq. The normal signaling cascade that follows increased intracellular calcium, allowing smooth muscle contraction. This is now blocked.

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15
Q

Why is theophylline use becoming less common in practice?

A

has a very narrow therapeutic range, more extensive adverse effect profile

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16
Q

theophylline drug interactions/precautions

A

(1) magnesium/aluminum will delay absorption
(2) half-life prolonged in CHF patients
(3) may aggravate pre-existing seizure disorders
(4) monitor for agents metabolized by P450

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17
Q

What are some stimulants that can cause degranulation of mast cells?

A

(1) antigens
(2) thermal/mechanical stress
(3) venoms
(4) various drugs, like high dose morphine

18
Q

Degranulation is mediated by _____ antibodies and requires that they be bound to the ______ receptor on the surface of mast cells.

A

IgE, FCεR

19
Q

What are the three primary mediators of the late phase reaction of asthma?

A

eosinophils cationic protein (ECP)
platelet activating factor (PAF)
neutrophil proteases

20
Q

Cromolyn salts are only useful in the treatment of asthma when taken _____________.

A

prophylactically

21
Q

T or F: The cromolyn salts are stable but extremely insoluble, and therefore must be taken via inhalation rather than orally.

A

True

22
Q

How frequently is cromolyn taken in asthma prophylaxis?

A

daily

23
Q

What are the side effects of inhaled cromolyn?

A

very well tolerated drug, few side effects that are minor and local

24
Q

How does omalizumab (Xolair) prevent mast cell degranulation?

A

It is a humanized mouse anti-human anti-IgE antibody. It binds IgE and prevents the necessary binding to FCεR1 receptors on mast cells.

25
Q

Xolair carries a boxed warning for _________.

A

anaphylaxis

26
Q

To what class does Zileuton belong? What is its role in the treatment of asthma?

A

selective inhibition of 5-lipoxygenase (decreases leukotriene production)

It is, like cromolyn, a prophylactic drug used in prevention of asthma attacks in chronic asthma patients.

27
Q

Zileuton is metabolized by P450. Because of this fact, which drug must we be cautious of another drug used to treat asthma, ________.

A

theophylline

Zileuton doubles the blood levels of theophylline due to competition for P450.

28
Q

What other therapy monitoring is necessary for patients taking Zileuton?

A

warfarin

Zileuton increases prothrombin time.

29
Q

What are the most common side effects noted with Zileuton?

A

headache, dyspepsia, some cases of liver toxicity

30
Q

In addition to blocking their production, you can block leukotrienes at the receptor site as well. Which receptor are we talking about, and which two drugs currently on the market do this?

A

CysLT-1 receptor (cysteine leukotriene 1)

Monelukast (Singulair) and Zariflukast (Accolate)

31
Q

Do leukotriene modifiers mainly inhibit the early or the late phase of bronchoconstriction?

A

late phase

Remember, they are prophylactic drugs with no acute use. Also, leukotrienes do not play a role in the early phase of asthma bronchoconstriction, which is mediated by mast cells (histamine).

32
Q

What is the biochemical mechanism by which CysLT-1 inhibitors inhibit bronchoconstriction?

A

It is the similar to one of the mechanisms used by methylxanthines, but at a different receptor. Like the adenosine receptor blocked by methylxanthines, the leukotriene receptor is couple to Gq. Inhibition, therefore, reduces intracellular calcium and prevents smooth muscle contraction.

33
Q

Which four classes of drugs are used to treat COPD? (#4 is only for a rare form of COPD)

A

(1) LAMA
(2) LABA
(3) SABA
(4) alpha-1 antitrypsin replacement

34
Q

Two LAMAs were given. What are they, and how do they differ in their duration of action?

A

Ipratropium (Atrovent, short acting) and Tiotropium (Spiriva, long acting)

35
Q

Describe the biochemical mechanism of action of LAMAs.

A

As seen with methylxanthines, and leukotriene receptor antagonists, a Gq coupled receptor is blocked (the Ach receptor). Intracellular calcium is decreased, and contraction is inhibited.

36
Q

What structural aspect of the LAMAs keeps them localized in the lungs?

A

quaternary ammonium salt prevents systemic absorption

37
Q

What is the newest LAMA approved for use in COPD patients?

A

Seebri (glycopyrollate)

38
Q

Describe the difference in use of LABAs in COPD vs. asthma patients.

A

LABAs are not contraindicated as mono therapy in COPD patients, as they are in asthma treatment.

39
Q

What are three examples of LABAs used in treatment of COPD?

A

salmeterol, formoterol, indacaterol (Arcapta)

40
Q

Ivacaftor (Kalydeco)

use, patients who can use it, dosing frequency

A

CFTR potentiator used in the treatment of CF, only for patients with certain mutations of CFTR, taken orally BID

41
Q

What are three other classes of drugs often used in the treatment of CF?

A

(1) mucolytics
(2) bronchodilators
(3) antibiotics