inflammation and tissue repair

1. inflammation and tissue repair Definition of inflammation Cardinal signs of inflammation Stages of inflammatory response Tissue repair Inflammatory mediators

2. Introduction • The human immune system is designed to protect the body against foreign substances, bacteria and viruses as well as any abnormal cells that might arise within the body itself.

3. The first line of defense against invading microorganisms involves the physical barriers presented by the skin on the body surfaces and the mucous membranes that protect openings into the body. • These mucous membranes are covered by secretions such as sticky mucus that can trap invading organisms.

4. Organisms that are able to penetrate this first line of defense must now face circulating phagocytic white blood cells, antimicrobial substances and natural killer cells • In addition, the entry of these foreign organisms into the body will trigger a significant inflammatory response and possibly fever, both of which are also protective.

5. The inflammatory reaction • Inflammation is the response of a tissue to injury. • the inflammatory reaction is essential for preventing infection of the injured area as well as for initiating the process of healing.

6. What is Inflammation? • The reaction of vascularized tissue to injury that attempts to destroy or limit the injurious agent and prepare for repair of the damaged tissue. What is the Purpose of Inflammation? • Protection of the body against any injurious stimulus

7. What can cause Inflammation? 1. Pathogenic organisms : bacteria , myobacteria , fungi , virus and parasites. 2. Trauma : - Mechanical - Thermal ( e.g. burns , frostbite) - Radiant energy - Electrical - Chemical / toxic 3. Ischemia 4. Immunologic

8. Cardinal Signs There are five “cardinal signs” of inflammation: • Rubor — The redness that occurs as a result of the increased blood flow to the inflamed area. • Tumor — Swelling of the inflamed tissue as a result of increased capillary permeability and fluid accumulation.

9. Calor — The increase in temperature (heat) that occurs in the inflamed area as a result of increased blood flow. • Dolor — Pain that occurs in the inflamed area as a result of stimulation of sensory neurons. • Functio laesa — Alteration or loss of function in the inflamed tissues.

10. The inflammatory response may be divided into main two stages: - the vascular response stage - the cellular response stage

11. 1. Vascular response stage • Rapid vasoconstriction of blood vessels occurs in the injured area and is followed by rapid vasodilatation. • An increase in capillary permeability occurs in the injured area leading to swelling and edema. The fluids that enter the injured area are useful for diluting out any bacterial toxins or irritants present in the tissue.

13. 2. Cellular response stage • The cellular stage of acut inflammation is marked by movement of phagocytic white blood cells (leukocytes) into the area of injury. • Two types of leukocytes participate in the acute inflammatory response—the granulocytes and monocytes.

14. Granulocytes • Granulocytes are identifiable because of their characteristic cytoplasmic granules. These white blood cells have distinctive multilobed nuclei. • The granulocytes are divided into three types (i.e., neutrophils, eosinophils, and basophils) according to the staining properties of the granules. • The neutrophil is the primary phagocyte that arrives early at the site of inflammation, usually within 90 minutes of injury.

15. The neutrophils’ cytoplasmic granules contain enzymes and other antibacterial substances that are used in destroying and degrading the engulfed particles. • The cytoplasmic granules of the eosinophilsstain red with the acid dye eosin. These granulocytes increase in the blood during allergic reactions and parasitic infections. • The granules of the basophilsstain blue with a basic dye. The granules of these granulocytes contain histamine and other bioactive mediators of inflammation.

16. Monocytes • The monocytes are the largest of the white blood cells and constitute 3% to 8% of the total blood leukocytes. The circulating life span of the monocyte is three to four times longer than that of the granulocytes, and these cells survive for a longer time in the tissues. • The monocytes, which migrate in increased numbers into the tissues in response to inflammatory stimuli, mature into macrophages. Within 24 hours, mononuclear cells arrive at the inflammatory site, and by 48 hours, monocytes and macrophages are the predominant cell types.

17. Cellular Response of leukocytes • The sequence of events in the cellular response to inflammation includes: • (1) pavementing, • (2) emigration, • (3) chemotaxis, and • (4) phagocytosis. • Leukocytes undergo a change in shape and squeeze through the now more permeable capillaries into the tissues) diapedesis(.

18. During the early stages of the inflammatory response, fluid leaves the capillaries, causing blood viscosity to increase. • The release of chemical mediators and cytokines affect the endothelial cells of the capillaries and cause the leukocytes to increase their expression of adhesion molecules. • As this occurs, the leukocytes slow their migration and begin pavementing or moving to along the periphery of the blood vessels.

19. Emigration is a mechanism by which the leukocytes extend pseudopodia, pass through the capillary walls by ameboid movement, and then migrate into the tissue spaces. The emigration of leukocytes also may be accompanied by an escape of red blood cells.

20. The process by which leukocytes migrate in response to a chemical signal is called chemotaxis. • During the next and final stage of the cellular response, the neutrophils and macrophages engulf and degrade the bacteria and cellular debris in a process called phagocytosis.

23. Outcomes of acute inflammation 1. resolution – restoration to normal , limited injury - chemical substances neutralization - normalization of vascular permeability - apoptosis of inflammatory cells - lymphatic drainage 2. healing by scar 3. Progression into chronic inflammation

24. Chronic Inflammation • Inflammation of prolonged duration ( weeks to months ) with active inflammation , tissue destruction and repair proceeding simultaneously. • Develops secondary to : 1- persistent infection 2. Repeated episodes of acute inflammation 3. Persistence of injurious agent

26. Local Manifestations of Inflammation • swelling • formation of exudates • abscess formation or • Ulceration: epithelial surface (e.g., skin or gastrointestinal epithelium) has become necrotic.

28. Tissue Repair & Wound Healing • Body organs and structures contain two types of tissues: parenchymal and stromal. The parenchymal tissues contain the functioning cells of an organ or body part (e.g., hepatocytes, renal tubular cells).

29. The stromal tissues consist of the supporting connective tissues, blood vessels, and nerve fibers. • Injured tissues are repaired by regeneration of parenchymal cells or by connective tissue repair in which scar tissue is substituted for the parenchymal cells of the injured tissue. • The primary objective of the healing process is to fill the gap created by tissue destruction and to restore the structural continuity of the injured part.

30. Regeneration • Regeneration involves replacement of the injured tissue with cells of the same parenchymal type, leaving little or no evidence of the previous injury. • The ability to regenerate varies with the tissue and cell type. • Body cells are divided into three types according to their ability to undergo regeneration: labile, stable, or permanent cells.

31. Labile cellsare those that continue to divide and replicate throughout life, replacing cells that are continually being destroyed. • Labile cells can be found in tissues that have a daily turnover of cells. E.g. epithelial cells of the skin, oral cavity, etc • Stable cellsare those that normally stop dividing when growth ceases. However, these cells are capable of undergoing regeneration when confronted with an appropriate stimulus. E.g. hepatocytes of the liver are one form of stable cell, • Permanent or fixed cellscannot undergo mitotic division. The fixed cells include nerve cells, skeletal muscle cells, and cardiac muscle cells. These cells cannot regenerate; once destroyed, they are replaced with fibrous scar tissue that lacks the functional characteristics of the destroyed tissue.

32. Connective Tissue Repair • Connective tissue replacement is an important process in the repair of tissue. • It allows replacement of nonregenerated parenchymal cells by a connective tissue scar.

33. Phases of Wound Healing • (1) the inflammatory phase, • (2) the proliferative phase, • (3) the maturational or remodeling phase

35. Factors That Affect Wound Healing • Malnutrition • Blood Flow and Oxygen Delivery • Impaired Inflammatory and Immune Responses • Infection, Wound Separation, and Foreign Bodies

36. Inflammatory Mediators

37. Inflammatory Mediators • Signs and symptoms of inflammation are produced by chemical mediators. Mediators can be classified by function: • (1) those with vasoactiveand smooth muscle–constricting properties such as histamine, prostaglandins, leukotrienes, and platelet-activating factor (PAF); • (2) chemotactic factors such as complement fragments and cytokines; • (3) plasma proteases that can activate complement and components of the clotting system; and • (4) reactive molecules and cytokines liberated from leukocytes, which when released into the extracellular environment can damage the surrounding tissue

38. Although inflammation is precipitated by injury, its signs and symptoms are produced by chemical mediators.

40. Histamine. • It is found mostly in the lung, skin and gastro-intestinal tract. It is stored in granules of mastocytes or basophils from which it is released • Histamine causes dilation and increased permeability of capillaries. • It is one of the first mediators of an inflammatory response. • Antihistamine drugs inhibit this immediate, transient response.

41. Plasma Proteases. • The plasma proteases consist of the • kinins, • activated complement proteins, and • clotting factors. • One kinin, bradykinin, causes increased capillary permeability and pain. • The clotting system contributes to the vascular phase of inflammation, mainly through fibrinopeptides that are formed during the final steps of the clotting process.

42. The complement system consistsof a cascade of plasma proteins that plays an importantrole in both immunity and inflammation. • Complementfragments contribute to the inflammatory response • by (1) causing vasodilation and increasing vascular permeability; • (2) promoting leukocyte activation, adhesion,and chemotaxis; and • (3) augmenting phagocytosis

43. Prostaglandins. • The prostaglandins are ubiquitous, lipidsoluble molecules derived from arachidonic acid, a fatty acid liberated from cell membrane phospholipids. • prostaglandins are synthesized from arachidonic acid through the cyclooxygenase metabolic pathway . • Prostaglandins contribute to vasodilation, capillary permeability, and the pain and fever that accompany inflammation. • The stable prostaglandins (PGE1 and PGE2) induce inflammation and potentiate the effects of histamine and other inflammatory mediators.

44. The prostaglandin thromboxane A2 promotes platelet aggregation and vasoconstriction • Aspirin and the nonsteroidal anti-inflammatory drugs (NSAIDs) reduce inflammation by inactivating the first enzyme in the cyclooxygenase pathway for prostaglandin synthesis.

45. Leukotrienes • Like the prostaglandins, the leukotrienes are formed from arachidonic acid, but through the lipoxygenase pathway. • Histamine and leukotrienes are complementary in action in that they have similar functions. • Histamine is produced rapidly and transiently while the more potent leukotrienes are being synthesized. • Leukotrienes C4 and D4 are recognized as the primary components of the slow reacting substance of anaphylaxis (SRS-A) that causes slow and sustained constriction of the bronchioles and is an important inflammatory mediator in bronchial asthma and anaphylaxis.

47. The leukotrienes also have been reported to affect the • permeability of the post capillary venules, • the adhesion properties of endothelial cells, and • the chemotaxis and extravascularization of neutrophils, eosinophils, and monocytes.

48. Platelet-Activating Factor • Platelet-activating factor (PAF), which is generated from a complex lipid stored in cell membranes, affects a variety of cell types and induces platelet aggregation. • It activates neutrophils and is a potent eosinophil chemo attractant. When injected into the skin, PAF causes a wheal-and-flare reaction and the leukocyte infiltrate characteristic of immediate hypersensitivity reactions. • When inhaled, PAF causes bronchospasm, eosinophil infiltration, and nonspecific bronchial hyperreactivity.

49. Cytokines • CYTOKINES are peptides produced by immune cells, which play key roles in regulating virtually all mechanisms of inflammation, including • INNATE IMMUNITY, • antigen presentation, • cellular differentiation, as well as • repair processes. • They are produced primarily by MACROPHAGES and LYMPHOCYTES, but also by other leukocytes, endothelial cells and fibroblasts.

50. Substances considered as CYTOKINES include • INTERLEUKINS (IL)- • INTERFERONS (IFNs), • TUMOUR NECROSIS FACTORS (TNFs), • COLONY-STIMULATING FACTORS