CHEMICAL MEDIATORS OF INFLAMMATION تحت اشراف أ.د/ كوكب طالب/ محمد محمود محمد مشالى عبد الحميد رقم/07274 Cairo University Faculty of Veterinary Medicine Department of Pathology

Introduction: Inflammation provoked response to tissue injury chemical agents cold, heat trauma invasion of microbes serves to destroy, dilute or wall off the injurious agent induces repair protective response can be potentially harmful

CARDINAL SIGNS OF ACUTE INFLAMMATION Heat Redness Swelling Pain Loss of function

Inflammation - Mechanism 1.Vaso dilatation 2.Exudation - Edema 3.Emigration of cells 4.Chemotaxis 5.Phagocytosis

CHEMICAL MEDIATORS OF INFLAMMATION Definition: Any messenger that acts on blood vessels, inflammatory cells, or other cells to contribute to an inflammatory response. (Pretty much anything...) Exogenous –Endotoxins Endogenous –Plasma –Leukocytes –Endothelial cells –Fibroblasts

Chemical Mediators of Inflammation: Locally produced Histamine Seratonin/5HT Interleukins. Prostaglandins Leukotrienes Plasma derived Kinins Complements Coagulation system Plasminolysis system Others: H2O2, NO

CHEMICAL MEDIATORS OF INFLAMMATION Facts Mechanism of action –Receptor-ligand interactions (1 o ) –Direct enzymatic activity –Mediate oxidative damage Extensive network of interacting chemicals High degree of redundancy Guarantees amplification and maintenance of inflammatory response Short t ½ and are harmful

CHEMICAL MEDIATORS Vasodilation –Prostaglandins, Nitric Oxide Increased Vascular Permeability –Vasoactive amines (histamine, serotonin), C3a and C5a, Bradykinin, Leukotrienes, PAF, Chemotaxic Leukocyte Activation –C5a, LTB 4, Chemokines

CHEMICAL MEDIATORS OF INFLAMMATION Fever –IL-1, IL-6, TNF, Prostaglandins Pain –Prostaglandins, Bradykinin Tissue Damage –Neutrophil and Macrophage products –Lysosomal enzymes –Oxygen metabolites –NO Bradykinin

VASOACTIVE AMINES Increase Vascular Permeability and Vascular Permeability Histamine and Serotonin –Mediators in the immediate active phase of increased permeability –Promotes contraction of smooth muscle –Stimulates to cells to produce eotaxins –Serotonin found in rodent mast cells

Vasoactive Amines Continued Releasing Stimulators –Direct physical or chemical injury –Binding of IgE- Ag- complexes –Fragments of C3a and C5a –Histamine releasing factors (pmn’s and θ) –Cytokines (IL-1, IL-8) –Neuropeptides

PLASMA PROTEASES 1. Kinin system –Highly vasoactive 2. Complement system Vasoactive Chemotactic 3.Clotting system Vasoactive Cleaves C3 3 interrelated systems are active within this category

Interaction of Kinin-, Coagulation- and Complement system during acute inflammation Kallikrein HMWK Plasminogen Prekallikrein Factor XII (Hageman) XIIa Collagen, basement membrane, platelets and microbial surfaces Kinin cascadeClotting cascade Fibrinolysis Plasmin Complement Bradykinin Acute Inflammation Fibrin Fibrinogen C3 C3a ProthrombinThrombin PAR* Intrinsic pathway * Protease activated receptors

COMPLEMENT SYSTEM Plasma proteins - act against microbial agents Products of activated complement –Vascular permeability –Chemotaxis –Opsonization –Lysis

COMPLEMENT SYSTEM Few reminders Classical pathway Alternate pathway Common pathway Important inflammatory mediators –C3a and C5a (anaphylatoxins) –Cause release of histamine from mast cells –Lysosomal enzyme release in inflammatory cells –C5a –Activates lipoxygenase pathway –Chemotactic many inflammatory cells –Increases adhesion of leukocytes

COMPLEMENT SYSTEM And Inflammation C5b-9 membrane attack complex –Lyses cells –Stimulates arachidonic acid metabolism –Produces reactive oxygen metabolites

Complement Cascade

KININ SYSTEM BRADYKININ Activated by Hageman factor (XIIa) Bradykinin –Release of vasoactive nonapeptide bradykinin –Generated from the plasma Potent vasodilator Increased vascular permeability Contraction of smooth muscle Produce pain Stimulates release of histamine Activates the arachidonic acid cascade

COAGULATION SYSTEM Clotting system Plasma proteins –Can be activated by Hageman factor Thrombin converts fibrinogen to fibrin –Fibrinopeptides are formed –↑vascular permeability –Chemotactic for leucocytes Plasmin is important in lysing fibrin clots, –Activates Hageman factor (XII) ⇨ bradykinin –Cleaves C3 ⇨ C3a –"fibrin-split products" formed from fibrin breakdown –↑ vascular permeability

COAGULATION CASCADE TF: tissue factor; HK: high-molecular-weight kininogen; PK: prekallikrein; PL: phospholipid; PT: prothrombin; TH: thrombin.

Clotting System

HAGEMAN FACTOR Dependent Factors Factor XII of intrinsic coagulation cascade Activated by –Negatively charged surfaces –Platelets –Proteases from inflammatory cells Causes –Coagulation –Activation of fibrinolytic system –Produces bradykinin –Activates complement –Provides an amplification system

IMPORTANT NOTE Activated Hageman factor (factor XIIA) initiates the clotting, fibrinolytic and kinin systems. The products of this initiation (kallikrein, factor XIIA, and plasmin, but particularly, kallikrein) can, by feedback, activate Hageman factor, resulting in significant amplification of the effects of the initial stimulus.

CYTOKINES Transmitters for cell-to-cell chatting –Modulate cell function Primarily from activated macrophages and lymphocytes IL-1, IL-8, TNF

IL-I and TNF “Master Cytokines” Origin –Monocytes –Macrophages Similar in action Endothelium Acute phase proteins Fibroblasts

Other Cytokines Chemokines??? IL-5 –Eosinophils IL-6 –B and T cells IL-8 –Neutrophils –Lesser degree monocytes and eosinophils

GROWTH FACTORS Platelet derived growth factor Transforming growth factor β –Chemokines -Leukocytes and Mesenchymal Cells Important in regeneration and repair

NITRIC OXIDE (NO) Just say NO! Nitric oxide is synthesized from L-arginine 2 enzymes and many factors produce NO 3 effects –♥♥ physical mediator of vascular tone –Host defense (forms perroxynitrite) –Signaling molecule – especially brain –Reduces platelet aggregation and adhesion –Inhibits several features of mast cell induced inflammation Uncontrolled NO production –Can lead to massive peripheral -Vasodilation -Shock

LYSOSOMAL CONSTITUENTS Neutrophils, Monocyte/Macrophages –Enzymes and proteins within granules Cationic proteins –↑ vascular permeability –Chemotactic Neutral proteases –Degrade ECM

OXYGEN-DERIVED FREE RADICALS Cause endothelial damage Protein destruction by inhibiting antiproteases Injury to variety of cells Don’t forget the antioxidants –Ceruloplasmin –Transferrin –Superoxide dismutase –Catalase –Glutathione peroxidase