DRUG INTERACTIONS I Lecture #36
Drug Interactions Terms Therapeutic Drug Interaction ADR Additive Synergism
DDIs PD – complementary responses – opposing responses PK – induce metabolism – inhibit metabolism – reduce absorption – decrease volume distribution – alter renal clearance
PD nAChR = nicotinic acetylcholine receptor GABA A = - aminobutyric acid receptor Mutual Sedative Effects No Counter Ion competitive antagonist GABA A agonist
PD μ-opioid receptor competitive antagonist μ-opioid receptor agonist NMDA = N-methyl-D-aspartate receptor for opioid overdose opioid analgesic
PK: Induce Metabolism CYP2C9 anticoagulant antibiotic warfarin
PK: Inhibit Metabolism Sedative HIV protease inhibitor
PK: Inhibit Metabolism antibiotic Metabolites CYP3A4 inhibits
PK: Reduced Absorption antacid log P = reduce gastric pH hydrophobic drug = Decreased Absorption
PK: Decrease Volume Distribution log P = 3.44 log P = 1.26 Quinidine displaces digoxin from tissues Reduces volume distribution (V)
PK: Renal Clearance Na + Lithium
Drug Combinations: Inhibit Metabolism HIV protease inhibitor CYP3A4 inhibitor Decrease Clearance Increase Oral Bioavailability = 12 hr = 8 hr
Drug Combinations: Inhibit Metabolism Parkinson’s Disease
Drug Combinations: Inhibit Metabolism Metabolites renal dehydropeptidase penicillin antibiotic dehydropeptidase inhibitor
PK: Inhibit Bacterial Enzymes -lactam antibiotic bacterial -lactamase Inactive antibiotic mechanism-based β-lactamase inhibitor
Interaction Types Mutual Effects – Competing for the same target Bidirectional Effects – Unidirectional Effects – A B Beneficial Interactions
Mutual Effects
D = Displaced C = Control Total Unbound
Mutual Effects anti-seizure Extraction Ratio?
Bidirectional anti-seizure diuretic Absorption diuretic anti-seizure Renal Clearance
Unidirectional Antibiotic Metabolites Chronic Obstructive Pulmonary Disease CYP1A2 Antibiotic Metabolites No Effect
Unidirectional
enoxacin