Pharmacology Flashcards
Albuterol
Selective short acting ß-2 adrenergic agonist.
first line agent for treatment of acute bronchial asthma episodes
induce bronchidilation, minimal effects on inflammation
ß2 agonists alone recomended for patients with mild episodic symptoms.
Fluticasone
Inhaled glucocorticoid. Most effective anti-inflammatory agent for chronic preventative treatment of bronchial asthma.
Long-term asthma treatment.
High dose glucocorticoids reserved for initial managment of acute asthma exacerbations. Inhaled glucocorticoids used to prevent acute exacerbations but do not have a role in acute episodes.
Corticosteroid, has the strongest and most predictable effects on inflammatory component of asthma.
MOA: after entering an epithelial cell, steroid binds to intracellular receptors, altering gene txn.
inhibit the formation of certain cytokines implicated in bronchial asthma
induce apoptosis of inflammatory cells, like Mø, lymphocytes and eos’s. after a few weeks, patients show significantly reduced airway inflammation.
Also decrease amount of mucus produced by goblet cells.
No direct bronchodilatory effects, but reduce hyperresponsiveness of airway by decreasing inflammation. Other drugs used in treatment of bronchial astham are less potent than glucocorticoids at reducing airway inflammation.
Theophylline
bronchodilator inhibits the enzyme phosphodiesterase, increasing intracellular cAMP.
has anti-inflammatory and bronchoprotective properties also. less effective than glucocorticoids
Ipratropium
blocks action of AcCh on M receptors when AcCh is released on vagal stimulation (leading to bronchoconstriction)
like ß2 agonists, has minimal effects on airway inflammation thorugh it does decrease mucus production by bronchial epithelial cells
Zileuton
leukotriene inhibitors (leukotrienes are potent inducers of airway bronchoconstriction and inflammation)
these are much less dramatic than glucocorticoids
Nifedipine
DHP calcium channel blocker used in treatment of hypertension.
blcokage of Ca influx into bronchial smooth muscle cells causes bronchodilation.
Has no anti-inflammatory effects
A: 4 groups of antifungals
B: their mechanisms of action
C: examples
Polyenes: (amphotericin B, Nystatin): bind ergosterol molecules in fungal cell membranes, creating pores and causing cell lysis.
Triazoles (ketoconazole, fluconazole, itraconazole, voriconazole): inhibit ergosterol synthesis.
Echinocandins (caspofungin and micafungin): inhibit glucan synthesis (component of fungal cell wall.)
Pyrimidines (Flucytosine): converted to 5-fluorouracil within the fungal cell and interferes with fungal RNA and protein synthesis.
only the polyenes (amphotericin B and nystatin) depend on amount of ergosterol incorporated into fungal cell membranes for efficacy. polyenes bind ergosterol molecules, form pores int he membrane and alow leakage of ions (K+) from cells –> leads to cell lysis. decreasing ergosterol in cell membrane reduces efficacy of polyenes. This is the major mechanism of polyene resistance.
Isoniazid chemical similar to ___ mechanism and use
chemically similar to B6/pyridoxine (which is depleted during isoniazid therapy).
inhibits mycolic acid syntehsis in mycobacterial cells: Mycobacterium species and has no effect on other microorgnaisms.
inhibiting mycolic acid creation prevents mycobacterial cell walll synthesia dn oformation of many virulence factors.
side efffect: neuopathy, hepatotoxicity, CYP450 inhibition in liver.
mycolic acid is long branched chain saturated fatty acid used in cell wall syntehsis of mycobacteria and formation of virulence factors.
isoniazid associated neuropathy
similarity to B6/pyridoxine causes isoniazid to compete with B6 for synthesis of neurotransmitters (like GABA) resulting in defective end products.
Isoniazid also increases excretion of pyridoxine.
B6 defiency most common in patients treated with Isoniazid who are elderly, alcoholics, or have other comorbidities (liver/kidney dysfunction)
usually manifests as peripheral neuropathy.
prevention: B6 supplementation with isoniazid therapy.
Varenicline
Chantix - partial agonist of nicotinic acetylcholine receptors. assists patients with cessation of tobacco use by reducing withdrawal cravings and attenuating the rewarding effects of nicotine.
partial agonist activity allows reduction of symptoms of nicotine withdrawal by mildly stimuling receptor. only limited downstream release of dopamine, so less stimluation of the reward pathways than nicotine.
reduces withdrawal cravings and attenuates rewarding effects.
Ethambutol
effective component of multi-agent antibiotic regimen used in treatment of M. tuberculosis and atypical mycobacterial infections. Most notabile side effect of ethambutol is optic neuritis - which manifests as decreased visual acuity, central scotoma, color-blindness and can be reversile with discontinuation of the drug.
drugs for TB that compromise hepatic function
Isoniazid, rifampin, pyrazinamide
TB drugs that affect hearing and vestibular function
aminoglycosides or vancomycin. ototoxicity from direct damage to 8th cranial nerve, can cause vertigo, tinnitus, deafness. can also cause renal toxicity.
Rarely, flaccid paralysis due to neuromuscular blockade.
antibiotics that cause blood problems
chloramphenicol, dapsone, trimethoprim-sulfamethoxazole.
Chlor.. can cause aplastic anemia
dapsone can cause agranulocytosis
trimeth-sulf.. can lead to megaloblastic anemia in some patients because its a folate antagonist
antibiotics with renal function side effects
aminoglycosides (tubular necrosis) and amphotericin B