Respiratory Pharmacology-2 (1) Flashcards

1
Q

What type of antibiotics can be used for patients with uncomplicated COPD?

A
  • Advanced Macrolide (azithromycin, clarithromycin)
  • Ketolide (telithromycin)
  • Cephalosporin (cefuroxime, cefpodoxime, cefdinir)
  • Doxycycline
  • Trimethoprim/sulfamethoxazole

Concern over resistance with chronic use

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2
Q

Why are asthma patients not treated with antibiotics?

A

Bacteria is not the cause of the inflammation of the airways

Antibiotics may be beneficial in COPD patients during acute exacerbation

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3
Q

What is the mechanism of action for mucolytics?

A

Break up mucus by reducing viscosity and elasticity

Examples include N-acetylcysteine (NAC)

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4
Q

What is the only PDE-4 inhibitor currently approved for severe COPD treatment?

A

Roflumilast

Administered orally with systemic side effects

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5
Q

What are the two groups of leukotrienes?

A
  • Leukotriene B4 (LTB4)
  • Cysteinyl leukotrienes (LTC4, LTD4, LTE4)

LTB4 binds to BLT receptors; Cysteinyl leukotrienes bind to CysLT1 and CysLT2 receptors

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6
Q

What is the role of Zileuton in asthma treatment?

A

Inhibits 5-Lipoxygenase, used for prophylaxis and treatment of chronic asthma

Not effective for managing acute asthma attacks

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7
Q

What are leukotriene receptor antagonists used for?

A

Asthma prophylaxis and chronic treatment

Prototype: Montelukast

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8
Q

What are the advantages of monoclonal antibodies (MAbs)?

A
  • Greater selectivity
  • Better efficacy (possibly)
  • Less toxicity (possibly)

Limitations include high cost and administration methods

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9
Q

What is the prototype IgE inhibitor monoclonal antibody?

A

Omalizumab

Prevents interaction of allergen with IgE

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10
Q

What is the function of IL-5 inhibitors in asthma treatment?

A

Reduce eosinophil production and survival

Example: Mepolizumab

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11
Q

What is the genetic basis of Cystic Fibrosis (CF)?

A

Defective CF transmembrane conductance regulator (CFTR) gene

CFTR is an ion channel affecting ion and fluid transport

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12
Q

What is the main issue with CFTR gene defects in Cystic Fibrosis?

A
  • Misfolding of CFTR
  • Dysfunctional CFTR that reaches the cell membrane

Results in impaired chloride secretion and sodium reabsorption

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13
Q

What are the two pharmacological approaches needed for Cystic Fibrosis?

A
  • Correctors (correct misfolded protein)
  • Activators (activate CFTR in cell membrane)

Triple therapy includes Elexacaftor, Tezacaftor, and Ivacaftor

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14
Q

What is the mechanism of action of cough suppressants like Dextromethorphan?

A

Antagonists of NMDA-type glutamate receptors

Inhibits the cough reflex in the CNS

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15
Q

What is the mechanism of action for expectorants like Guaifenesin?

A

Reduces viscosity of mucus in the upper respiratory tract

Helps clear irritants/microbes

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16
Q

What are common side effects of Guaifenesin?

A
  • Dizziness
  • Nausea
  • Vomiting
  • Allergic reaction
  • Rash itching
  • Swelling

Side effects can vary among individuals

17
Q

What are the side effects of Dupilumab?

A
  • Elevated eosinophils
  • Eye disorders (conjunctivitis, keratitis)

Dupilumab blocks both IL-4 and IL-13