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Arachadonic Acid Metabolism

              M1 – Immunology Sequence
                 Joseph Fantone, MD


Winter 2009
How many take aspirin, ibuprofen,
      tylenol, naproxen ?



           Why???
INFLAMMATORY MEDIATORS

PLASMA DERIVED     
     
           
CELL-DERIVED

• COMPLEMENT CASCADE     
           
• VASOACTIVE AMINES
   C3a, C5a 
     
      
           
 histamine, serotonin

• COAGULATION CASCADE    
           
• OXYGEN METABOLITES                

   Thrombin, plasmin 
   
           
 hydrogen peroxide (H202)
      
     
      
     
                 superoxide anion (02-)
      
     
      
     
                 hypochlorous acid (HOCl-)

      
     
      
     
        • ARACHIDONIC ACID METABOLITES
      
     
      
     
          cyclooxygenase-derived
      
     
      
     
          lipoxygenase-derived

      
     
      
     
          • CYTOKINES
      
     
      
     
                 Interleukins  Chemokines
      
     
      
     
                Interferons   Growth Factors
      
     
      
     
                Tumor Necrosis Factor
Intended Learning Outcomes
          To Understand The:
•  Primary inflammatory mediators derived from the
   metabolism of arachidonic acid including their primary
   cellular source and biological activity.

•  Effects of nonsteroidal anti-inflammatory compounds
   on blocking the production of arachidonic acid
   metabolites during disease

•  Mechanism of aspirin therapy and diets rich in fish
   containing high levels of omega 3 fatty acids as
   potentially important in lowering the incidence of
   cardiovascular disease.
What is Arachidonic Acid?

                              COOH




J. Fantone
How And Where Is Arachidonic Acid Generated?




            chocolateBear (Wikispaces)
Lipid Mediators of Inflammation

                                    Cell membrane
   Stimulus
                                    Phospholipids
                +
                    Phospholipase


                                    Arachidonic acid




J. Fantone
Source Undetermined
What are the primary products
 derived from arachidonic acid?

•  Cyclooxygenase (COX)
•  Lipoxygenase (LO)
Acute inflammation: lipid mediators
                                  Cell membrane
Stimulus
                                  Phospholipids
           +
                  Phospholipase


                                  Arachidonic acid



      COX-1+2                       COX-1            Lipooxygenases (5-LO)

     Prostaglandins               Thromboxanes            Leukotrienes


   Prostaglandin E2                                         LTB4
   Prostacyclin PGI2                  TXB2                 LTC4, LTD4


     J. Fantone
Source Undetermined
CELL SPECIFICITY OF ARACHIDONIC
    ACID-DERIVED PRODUCTS

CELL 
      
     
   
   
PRODUCT
Neutrophils 
     
   
   
Leukotrienes

Macrophage/Monocyte   
   
Prostaglandins +
      
     
     
   
   
Leukotrienes

Platelets   
     
   
   
Thromboxane

Endothelial Cells 
   
   
Prostacyclin
In Vivo Effects of Arachidonic Acid
       Derived Products: Regulates

• Thermostatic Set Point (Fever)
• Pain (Interacts with pain receptors)
• Blood Flow
• Leukocyte Activity
•  Platelet Function
Biological Function of Arachidonic
                Acid Products

Cyclooxygenase-derived Products:

Prostaglandin E2/Prostacyclin
      
Immunoregulatory        
       
      
       
      
•Inhibits Immune cell activation
      
       
      
        
     
•Inhibits cytokine production
      
       
      
        
     
•Inhibits mast cell activation
      
       
      
        
     
Blocks platelet aggregation
      
       
      
        
     
Increases vasodilation
      
       
      
        
     

Thromboxane 
        
        
     
Causes vasoconstriction
      
       
      
        
     
Induces platelet aggregation
The Homeostatic
Balance
                                              
                                              




Endothelium                               Platelets 
   PGI2                                    TXA2 




  Regents of the University of Michigan
Production of Fever

                   Hypothalamus Thermoregulatory Area


                                        COX inhibitors
                                          (aspirin)
Endogenous pyrogens
  (Interleukins -1,-6)

                             Arachidonic acid X   Prostaglandins

Exogenous pyrogens
 (bacterial products)

                                          Increase temp set-point
      J. Fantone
Biological Function

Lipoxygenase-derived Products:

Leukotriene B4
       
   
Neutrophil Activation
      
       
       
   
       
       
      
- chemotaxis
      
       
       
   
- degranulation

      
       
       
   
 Mast cell activation
      
       
       
   
- degranulation

Leukotriene C,D,E     
   
Smooth muscle contraction
(SRS-A)       
       
   
Increase vascular permeability
Pharmacologic Regulation of Arachidonic

        Acid-Derived Products: Modulate
        

•  Phospholipase activity:
     –  Suppress the release of arachidonic acid (no substrate available)
     –  Blocks both COX and LO-derived products


•  Cyclooxygenase Activity:
     –  Blocks Cyclooxygenase-derived products
     –  COX-1 and COX-2 inhibitors


•  Specific enzymes down-stream from COX:
     –  Thromboxane synthetase inhibitors


•  Lipoxygenase activity:
     –  Block 5-lipoxygenase enzyme
     –  Small molecule receptor antagonists for cysteinyl leukotrienes
Non- Steroidal Anti-Inflammatory
          Compounds; NSAIDS    


•     Aspirin (acetysalicylic acid)
•     Ibuprofen (propionic acid derivatives)
•     Indomethacin (indole derivatives)
•     Tylenol (acetominophen)
•     COX-2 Inhibitors (Vioxx, celebrex,
      Bextra)
COX-2 Inhibitors

• CELEBREX (Celecoxib) Pfizer-(Pharmacia)
• BEXTRA (Valdecoxib) Pfizer
• VIOXX (Rofecoxib) Merck

     
Osteoarthritis
     
Rheumatoid arthritis
     
Primary dysmenorrhea
     
Pain management
Aspirin

• Irreversible inhibition of cyclooxygenase
• Acetylates active site of enzyme
• Decreased production of products (e.g.
prostaglandins, prostacylcins & thromboxanes)




    Source Undetermined
Source Undetermined




NSAIDS: Inhibit cyclooxygenase: reversible binding
            to active site of enzyme
AN ASPIRIN A DAY




 Regents of the University of Michigan
Regents of the University of Michigan
Aspirin Anti-thrombogenic Activity

• Inhibitsplatelet aggregation; blocks platelet-derived
thromoboxane production

• Blocks platelet cyclooxygenase for the life of the platelet; no
new protein synthesis

• Blocks endothelial cell-derived prostacyclin

• Suppression of endothelial cell-derived prostacyclin is short
lived as endothelial cells can generation new cyclooxygenase
enzyme

• Platelet activity is blocked more than endothelial cell activity
Acute inflammation: lipid mediators
               An important role in vascular homeostasis



             Endothelium                 Platelets




             Prostacyclin PGI2            TXB2




               Anti-thrombotic           Pro-thrombotic




J. Fantone
Acute inflammation: lipid mediators
                                          Therapeutic targets




                     Endothelium                         Platelets


Aspirin                           All cells but the platelet       Aspirin
                              X   can resynthesize the
inhibits COX-2 irreversibly
                                  enzymes
                                                               X   inhibits COX-1 irreversibly




                     Prostacyclin PGI2                    TXB2

                                                                        tic
                                                               thro mbo
                                                        Pro-

                                     botic
                              t hrom
        J. Fantone
                        Anti-
Acute inflammation: lipid mediators
                                  Therapeutic targets




              Endothelium                     Platelets



             COX-2                                  COX-1


              Prostacyclin PGI2                TXB2




                Anti-thrombotic               Pro-thrombotic

        NSAIDs inhibit both COX-1 and COX-2;       COXIBs inhibit COX-2
J. Fantone
Acute inflammation: lipid mediators
                                    Therapeutic targets




                Endothelium                       Platelets



             COX-2   X          Ibuprofen*           X   COX-1


               Prostacyclin PGI2                   TXB2




                  Anti-thrombotic                 Pro-thrombotic

* Classical NSAID, it inhibits both COX enzymes                    J. Fantone
COX-2 inhibitors work by blocking COX-2 enzyme which is
     involved ingastrointestinal toxicity is reduced
       the inflammation pathway. By sparing COX-1




      Source Undetermined
Acute inflammation: lipid mediators
                                     Therapeutic targets




               Endothelium                       Platelets



             COX-2   X           Vioxx®                 COX-1


               Prostacyclin PGI2                  TXB2


                 Anti-t
                       hrom
                             botic

                                                Pro-t
                                                     hrom
                                                         botic
J. Fantone
Fish Oil: Protective Effects


Eicosapentanoic Acid            Arachidonic Acid

                      Omega-3   Omega-6




     Source Undetermined           Source Undetermined
Acute inflammation: lipid mediators
                                     Cell membrane
Stimulus                             Phospholipids
                 +
                     Phospholipase

                                     Arachidonic acid


         COX-1+2                       COX-1            Lipooxigenases (5-LO)

        Prostaglandins               Thromboxanes             Leukotrienes


    Prostaglandin E2                                            LTB4
    Prostacyclin PGI2                    TXB2                  LTC4, LTD4


  Vasodilation . Increase vascular permeability. Control platelet aggregation .
                            Chemotaxis . Pain . Fever
    J. Fantone
Thank You
Additional Source Information
                           for more information see: http://open.umich.edu/wiki/CitationPolicy

Slide 7: J. Fantone
Slide 8: chocolateBear, Wikispaces, https://illnessesanimalsplants.wikispaces.com/Selectively%20Permeable%20Lipid%20Bilayer
Slide 9: J. Fantone
Slide 10: Source Undetermined
Slide 12: J. Fantone
Slide 13: Source Undetermined
Slide 17: Regents of the University of Michigan
Slide 18: J. Fantone
Slide 23: Source Undetermined
Slide 24: Source Undetermined
Slide 25: Regents of the University of Michigan
Slide 26: Regents of the University of Michigan
Slide 28: J. Fantone
Slide 29: J. Fantone
Slide 30: J. Fantone
Slide 31: J. Fantone
Slide 32: Source Undetermined
Slide 33: J. Fantone
Slide 34: Source Undetermined; Source Undetermined
Slide 35: J. Fantone

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02.10.09(c): Arachadonic Acid Metabolism

  • 1. Attribution: University of Michigan Medical School, Department of Microbiology and Immunology License: Unless otherwise noted, this material is made available under the terms of the Creative Commons Attribution–Noncommercial–Share Alike 3.0 License: http://creativecommons.org/licenses/by-nc-sa/3.0/ We have reviewed this material in accordance with U.S. Copyright Law and have tried to maximize your ability to use, share, and adapt it. The citation key on the following slide provides information about how you may share and adapt this material. Copyright holders of content included in this material should contact open.michigan@umich.edu with any questions, corrections, or clarification regarding the use of content. For more information about how to cite these materials visit http://open.umich.edu/education/about/terms-of-use. Any medical information in this material is intended to inform and educate and is not a tool for self-diagnosis or a replacement for medical evaluation, advice, diagnosis or treatment by a healthcare professional. Please speak to your physician if you have questions about your medical condition. Viewer discretion is advised: Some medical content is graphic and may not be suitable for all viewers.
  • 2. Citation Key for more information see: http://open.umich.edu/wiki/CitationPolicy Use + Share + Adapt { Content the copyright holder, author, or law permits you to use, share and adapt. } Public Domain – Government: Works that are produced by the U.S. Government. (USC 17 § 105) Public Domain – Expired: Works that are no longer protected due to an expired copyright term. Public Domain – Self Dedicated: Works that a copyright holder has dedicated to the public domain. Creative Commons – Zero Waiver Creative Commons – Attribution License Creative Commons – Attribution Share Alike License Creative Commons – Attribution Noncommercial License Creative Commons – Attribution Noncommercial Share Alike License GNU – Free Documentation License Make Your Own Assessment { Content Open.Michigan believes can be used, shared, and adapted because it is ineligible for copyright. } Public Domain – Ineligible: Works that are ineligible for copyright protection in the U.S. (USC 17 § 102(b)) *laws in your jurisdiction may differ { Content Open.Michigan has used under a Fair Use determination. } Fair Use: Use of works that is determined to be Fair consistent with the U.S. Copyright Act. (USC 17 § 107) *laws in your jurisdiction may differ Our determination DOES NOT mean that all uses of this 3rd-party content are Fair Uses and we DO NOT guarantee that your use of the content is Fair. To use this content you should do your own independent analysis to determine whether or not your use will be Fair.
  • 3. Arachadonic Acid Metabolism M1 – Immunology Sequence Joseph Fantone, MD Winter 2009
  • 4. How many take aspirin, ibuprofen, tylenol, naproxen ? Why???
  • 5. INFLAMMATORY MEDIATORS PLASMA DERIVED CELL-DERIVED • COMPLEMENT CASCADE • VASOACTIVE AMINES C3a, C5a histamine, serotonin • COAGULATION CASCADE • OXYGEN METABOLITES Thrombin, plasmin hydrogen peroxide (H202) superoxide anion (02-) hypochlorous acid (HOCl-) • ARACHIDONIC ACID METABOLITES cyclooxygenase-derived lipoxygenase-derived • CYTOKINES Interleukins Chemokines Interferons Growth Factors Tumor Necrosis Factor
  • 6. Intended Learning Outcomes To Understand The: •  Primary inflammatory mediators derived from the metabolism of arachidonic acid including their primary cellular source and biological activity. •  Effects of nonsteroidal anti-inflammatory compounds on blocking the production of arachidonic acid metabolites during disease •  Mechanism of aspirin therapy and diets rich in fish containing high levels of omega 3 fatty acids as potentially important in lowering the incidence of cardiovascular disease.
  • 7. What is Arachidonic Acid? COOH J. Fantone
  • 8. How And Where Is Arachidonic Acid Generated? chocolateBear (Wikispaces)
  • 9. Lipid Mediators of Inflammation Cell membrane Stimulus Phospholipids + Phospholipase Arachidonic acid J. Fantone
  • 11. What are the primary products derived from arachidonic acid? •  Cyclooxygenase (COX) •  Lipoxygenase (LO)
  • 12. Acute inflammation: lipid mediators Cell membrane Stimulus Phospholipids + Phospholipase Arachidonic acid COX-1+2 COX-1 Lipooxygenases (5-LO) Prostaglandins Thromboxanes Leukotrienes Prostaglandin E2 LTB4 Prostacyclin PGI2 TXB2 LTC4, LTD4 J. Fantone
  • 14. CELL SPECIFICITY OF ARACHIDONIC ACID-DERIVED PRODUCTS CELL PRODUCT Neutrophils Leukotrienes Macrophage/Monocyte Prostaglandins + Leukotrienes Platelets Thromboxane Endothelial Cells Prostacyclin
  • 15. In Vivo Effects of Arachidonic Acid Derived Products: Regulates • Thermostatic Set Point (Fever) • Pain (Interacts with pain receptors) • Blood Flow • Leukocyte Activity •  Platelet Function
  • 16. Biological Function of Arachidonic Acid Products Cyclooxygenase-derived Products: Prostaglandin E2/Prostacyclin Immunoregulatory •Inhibits Immune cell activation •Inhibits cytokine production •Inhibits mast cell activation Blocks platelet aggregation Increases vasodilation Thromboxane Causes vasoconstriction Induces platelet aggregation
  • 17. The Homeostatic Balance         Endothelium  Platelets  PGI2  TXA2  Regents of the University of Michigan
  • 18. Production of Fever Hypothalamus Thermoregulatory Area COX inhibitors (aspirin) Endogenous pyrogens (Interleukins -1,-6) Arachidonic acid X Prostaglandins Exogenous pyrogens (bacterial products) Increase temp set-point J. Fantone
  • 19. Biological Function Lipoxygenase-derived Products: Leukotriene B4 Neutrophil Activation - chemotaxis - degranulation Mast cell activation - degranulation Leukotriene C,D,E Smooth muscle contraction (SRS-A) Increase vascular permeability
  • 20. Pharmacologic Regulation of Arachidonic
 Acid-Derived Products: Modulate •  Phospholipase activity: –  Suppress the release of arachidonic acid (no substrate available) –  Blocks both COX and LO-derived products •  Cyclooxygenase Activity: –  Blocks Cyclooxygenase-derived products –  COX-1 and COX-2 inhibitors •  Specific enzymes down-stream from COX: –  Thromboxane synthetase inhibitors •  Lipoxygenase activity: –  Block 5-lipoxygenase enzyme –  Small molecule receptor antagonists for cysteinyl leukotrienes
  • 21. Non- Steroidal Anti-Inflammatory Compounds; NSAIDS •  Aspirin (acetysalicylic acid) •  Ibuprofen (propionic acid derivatives) •  Indomethacin (indole derivatives) •  Tylenol (acetominophen) •  COX-2 Inhibitors (Vioxx, celebrex, Bextra)
  • 22. COX-2 Inhibitors • CELEBREX (Celecoxib) Pfizer-(Pharmacia) • BEXTRA (Valdecoxib) Pfizer • VIOXX (Rofecoxib) Merck Osteoarthritis Rheumatoid arthritis Primary dysmenorrhea Pain management
  • 23. Aspirin • Irreversible inhibition of cyclooxygenase • Acetylates active site of enzyme • Decreased production of products (e.g. prostaglandins, prostacylcins & thromboxanes) Source Undetermined
  • 24. Source Undetermined NSAIDS: Inhibit cyclooxygenase: reversible binding to active site of enzyme
  • 25. AN ASPIRIN A DAY Regents of the University of Michigan
  • 26. Regents of the University of Michigan
  • 27. Aspirin Anti-thrombogenic Activity • Inhibitsplatelet aggregation; blocks platelet-derived thromoboxane production • Blocks platelet cyclooxygenase for the life of the platelet; no new protein synthesis • Blocks endothelial cell-derived prostacyclin • Suppression of endothelial cell-derived prostacyclin is short lived as endothelial cells can generation new cyclooxygenase enzyme • Platelet activity is blocked more than endothelial cell activity
  • 28. Acute inflammation: lipid mediators An important role in vascular homeostasis Endothelium Platelets Prostacyclin PGI2 TXB2 Anti-thrombotic Pro-thrombotic J. Fantone
  • 29. Acute inflammation: lipid mediators Therapeutic targets Endothelium Platelets Aspirin All cells but the platelet Aspirin X can resynthesize the inhibits COX-2 irreversibly enzymes X inhibits COX-1 irreversibly Prostacyclin PGI2 TXB2 tic thro mbo Pro- botic t hrom J. Fantone Anti-
  • 30. Acute inflammation: lipid mediators Therapeutic targets Endothelium Platelets COX-2 COX-1 Prostacyclin PGI2 TXB2 Anti-thrombotic Pro-thrombotic NSAIDs inhibit both COX-1 and COX-2; COXIBs inhibit COX-2 J. Fantone
  • 31. Acute inflammation: lipid mediators Therapeutic targets Endothelium Platelets COX-2 X Ibuprofen* X COX-1 Prostacyclin PGI2 TXB2 Anti-thrombotic Pro-thrombotic * Classical NSAID, it inhibits both COX enzymes J. Fantone
  • 32. COX-2 inhibitors work by blocking COX-2 enzyme which is involved ingastrointestinal toxicity is reduced the inflammation pathway. By sparing COX-1 Source Undetermined
  • 33. Acute inflammation: lipid mediators Therapeutic targets Endothelium Platelets COX-2 X Vioxx® COX-1 Prostacyclin PGI2 TXB2 Anti-t hrom botic Pro-t hrom botic J. Fantone
  • 34. Fish Oil: Protective Effects Eicosapentanoic Acid Arachidonic Acid Omega-3 Omega-6 Source Undetermined Source Undetermined
  • 35. Acute inflammation: lipid mediators Cell membrane Stimulus Phospholipids + Phospholipase Arachidonic acid COX-1+2 COX-1 Lipooxigenases (5-LO) Prostaglandins Thromboxanes Leukotrienes Prostaglandin E2 LTB4 Prostacyclin PGI2 TXB2 LTC4, LTD4 Vasodilation . Increase vascular permeability. Control platelet aggregation . Chemotaxis . Pain . Fever J. Fantone
  • 37. Additional Source Information for more information see: http://open.umich.edu/wiki/CitationPolicy Slide 7: J. Fantone Slide 8: chocolateBear, Wikispaces, https://illnessesanimalsplants.wikispaces.com/Selectively%20Permeable%20Lipid%20Bilayer Slide 9: J. Fantone Slide 10: Source Undetermined Slide 12: J. Fantone Slide 13: Source Undetermined Slide 17: Regents of the University of Michigan Slide 18: J. Fantone Slide 23: Source Undetermined Slide 24: Source Undetermined Slide 25: Regents of the University of Michigan Slide 26: Regents of the University of Michigan Slide 28: J. Fantone Slide 29: J. Fantone Slide 30: J. Fantone Slide 31: J. Fantone Slide 32: Source Undetermined Slide 33: J. Fantone Slide 34: Source Undetermined; Source Undetermined Slide 35: J. Fantone