platelets produce thromboxanes (stimulate vasoconstriction, clotting)
DESCRIPTION
Leukotrienes lead to inflammation (asthma, heart attack, anaphylaxis). Reduce inflammatory response, transmit pain, regulate allergy and immunity. Platelets produce thromboxanes (stimulate vasoconstriction, clotting). Blood vessels produce prostacyclins - PowerPoint PPT PresentationTRANSCRIPT
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Platelets produce thromboxanes(stimulate vasoconstriction, clotting)
Blood vessels produce prostacyclins(stimulate vasodilation, inhibit clotting)
Reduce inflammatory response, transmit pain, regulate allergy and immunity
Leukotrienes lead to inflammation (asthma, heart attack, anaphylaxis)
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Arachidonic acid
• Eicosanoid (C20) precursor from dietary essential polyunsaturated fatty acids (linoleic acid)
• Stored as C2-ester of phospholipids (released by phospholipase A2)
• Hormone-like molecules, decompose within seconds or minutes (have very local effects)
• Pain, fever, coagulation, blood pressure, and reproduction
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Prostaglandins
• Prostaglandin H2 synthase forms a cyclopentane ring in linear arachidonic acid
• Enzyme has 2 catalytic activities:– Cyclooxygenase (adds two O2)– Peroxidase (converts OOH group to OH)
• Commonly called COX• Aspirin is an irreversible inhibitor of COX
(inactivates enzyme by acetylating active site Ser and blocking active site from reacting with substrate– Analgesic, antipyretic, anti-inflammatory
Ser-ÖH
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COX
• NSAIDs (NonSteroidal Anti-Inflammatory Drugs)
• Acetaminophen and ibuprofen are noncovalent inhibitors of COX
• COX-1 and COX-2 isoforms (60% identical)• COX-2 inhibitors lack side effects of other NSAIDS
– COX-1 expressed ubiquitously, maintains homeostasis – COX-2 expressed in certain tissues during inflammation
response and is responsible for elevated prostaglandin levels
• Aspirin and ibuprofen are nonspecific NSAIDs, have side effects (gastrointestinal ulceration)
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COX-2•Structure-based drug design of selective COX-2 inhibitors•COX-2 active site ~20% larger than COX-1 (make a bigger inhibitor that cannot fit into COX-1 site)
•Rofecoxib (Vioxx) popular and effective, but withdrawn due to unanticipated cardiac side effects (mechanism may involve inhibition of prostacyclin synthesis (leaving thromboxane synthesis less affected)
•Acetaminophen effective, but low affinity for COX-1,2 (binds COX-3, which is expressed in the central nervous system)
COXinhibitor
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Drug Design
• Drug Discovery: How?Screening large numbers of compounds for inhibition
of enzymatic activity or receptor signaling
Measure KI(or KI’)
Good lead compound has KI < 1MWhy is high affinity necessary?-specificity!!!!!-dose!!!!!!!Design related compounds using combinatorial
chemical techniques
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Structure-based design
• X-ray, NMR• What does the active site
look like empty and with the substrate in it?
• Look at structural and electrostatic properties of active site and try to better fit/fill it.
For a candidate…• Quantum mechanical calculation of charge
distribution• Docking simulations• Determine structure of complex, revise inhibitor
structure and re-assay KI
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Bioavailability & ToxicityTo cause desired response:
– Drug must arrive at high enough concentration– Drug must arrive to the location of the target protein
Oral drugs (cheapest)– Acid-stable (stomach)– Membrane-permeable (gut-blood transfer, so can’t be highly charged))– Don’t bind tightly to other things (lipophilic drugs sequestered in
membrane/adipocytes)– Survive detoxifying enzymes in the liver (portal vein drains intestine
directly to liver)– Avoid rapid excretion by kidneys– Must pass from capillaries to tissues– (for brain) must pass blood-brain barrier, which blocks polar substances– (for intracellular protein) must pass plasma (and other) membrane(s)
Protein drugs poor oral drugs (acid, pepsin, trypsin, immune system, etc.)
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Bioavailability & Toxicity
How drug interacts with barriers is pharmacokinetics (Absorption, Distribution, Metabolism, Excretion measurements)
Bioavailability (extent to which it reaches proper site) depends on dose and pharmacokinetics
Best drugs a compromise: not too polar or lipophilic, neutral at pH 6-8 (pass through membrane in uncharged state)
Drugs with low KI for target are likely to be more specific and have fewer side effects
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Clinical trials
After in vitro (test tube) and in vivo (animal) studies:Phase I: test safety, dosage range and method (20-100
healthy volunteers, or if toxic drug then test very sick people)
Phase II: efficacy against target disease (100-500 volunteer patients). Refine dosage, check for side effects. Single-blind tests (docs know, patients don’t)
Control substance is a placebo (ethical caveat)Phase III: Monitor adverse effects from long-term use,
confirm efficacy (1000-5000 patients) through statistical analysis of double-blind, placebo-controlled tests
(double blind removes bias from subjective judgments of investigators…you see what you want to see…)
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Clinical trials
Few drug candidates survive preclinical testing (~5/5000, ~3 years)
Clinical trials 7-10 years, most fail in Phase II
~$500 million to bring drug to market!!!
Most difficult issue is identifying rare side effects (1/10000) and long-term effects
Out of Control, by Celia Farber (HIV clinical trial article… holiday reading)
http://www.harpers.org/archive/2006/03/0080961
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P450s
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Cytochromes P450
Well-tolerated drugs can be dangerous for others…
Genetic differences among individualsDifferent disease stateOther drugsSexAgeEnvironmental factors
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Cytochromes P450Detoxify xenobiotics (embedded in ER membrane)
Superfamily of heme-containing enzymes in nearly all living organisms
Fe(II), CO-bound enzyme absorbs at 450nmHumans have ~100 isozymes (isoforms)Monooxygenases (Fe undergoes reversible redox-state change
during catalytic cycle)
RH + O2 + 2H+ + 2e- ROH + H2Oe- from NADPH to the P450 heme via cytochrome P450
reductaseOxidize lipophilic compounds for conjugation to glucuronic acid
or sulfate.