Consists of blood cells & plasma Blood cells = Erythrocytes (RBC’s), Leukocytes (WBC’s), & Thrombocytes (Platelets) Blood is 55% plasma & 45% blood cells Woman has ≈ 5 liters Man has ≈ 6 liters Transport Nutrients, waste, hormones, enzymes, O2 & CO2 Regulation of body temp due to high volume of H2O in plasma Helps regulate body pH Helps regulate water content of cells/Osmosis Clotting: prevents fluid loss Protection against pathogens (immune response, production of antibodies, destruction of bacteria/viruses, removal of cellular debris & allergic reactions) 91% water 7% proteins: 1. 2. 3. Albumin: maintains osmotic pressure & water balance Globulins: antibodies, complements (immune response) & transport molecules Fibrinogens: important role in clotting 2% solutes: Ions, nutrients, waste products, gases, enzymes & hormones 95% of blood cell volume; biconcave disks No nucleus, simple structures, don’t divide & live ≈ 120 days Composed of a network of protein called stroma, cytoplasm, lipids (cholesterol) & hemoglobin (red pigment ≈ 33% of cell’s volume) Function: Transport O2 & CO2 →→ Hemoglobin allows this Hemoglobin: Globin = protein Heme = pigment containing 4 iron atoms Iron combines with O2 in the lungs & releases it in tissues; Bright red in color Globin at tissues combines with CO2 & releases it at lungs; Dark red in color 2 subcategories: Granular & Nongranular Have nuclei & no pigment; larger than RBC’s General function in immune response: Combat inflammation & infection Can leave the blood stream & move into tissues via ameboid movement Phagocytosis: “cell eating” Neutrophils: 60% - 70% of WBC’s 1. Most active in WBC’s response to tissue destruction by bacteria Stay in blood for 12 hours & then move to tissues where they phagocytize (eat) foreign substances Secrete enzyme Lysozyme that destroys certain bacteria Pus contains dead neutrophils, cell debris & fluids Eosinophils: 2% - 4% of WBC’s 2. Combat irritants (pollen, dust, pet dander, etc) that causes allergies Produce antihistamines Basophils: 0.5% - 1% of WBC’s 3. Involved in allergic reactions Releases heparin (anticoagulant), histamine (inflammatory substance) & serotonin (a vasoconstrictor) Monocytes: 3% - 8% of WBC’s 1. Phagocytotic: eat bacteria, dead cells &/or cellular debris Largest; after they leave blood & enter tissue, they increase in size & are called Macrophages Lymphocytes: 20% - 25% of WBC’s 2. Production of antibodies & play important role in immune response Smallest; several types: B & T lymphocytes Control cancer cells, destroy microorganisms & reject foreign tissues Disk-shaped cellular fragments with a nucleus Prevent fluid loss when blood vessels are damaged When larger blood vessels are damaged, clotting mechanism takes over 3 Cut vessel is rough & irregular shaped stages to clotting/coagulation Rough surface of vessel causes platelets to clump together at the site of the injury 1. Tissue releases thromboplastin which produces prothrombin activator Requires Ca2+, certain proteins & phospholipids Ca2+ & prothrombin activator converts prothrombin into thrombin Soluble fibrinogen is converted into insoluble fibrin 2. 3. Thrombin catalyzes the reaction Fibrin forms long threads that act like a net = CLOT Clot forms & traps blood cells & platelets in the fibrin threads & bleeding stops Syneresis: clot retraction; tightening of clot so wound gets smaller & smaller Serum (blood plasma minus clotting factors) surrounds wound under clot & hemorrhage is stopped Blood vessel repairs itself Fibronolysis occurs: blood clot dissolves Build up of cholesterol mass (Plaque) on smooth walls of UNDAMAGED blood vessels can cause clot formation Called Thrombosis & clot is called a Thrombus Thrombus may dissolve or a piece can dislodge & get transported in blood = Embolus Embolus can get stuck in a vessel & cut-off circulation = Embolism If tissues are killed = Infarction Agglutination: clumping of RBC’s, A.K.A transfusion reaction Caused by reaction between antibodies in plasma & surface antigens on RBC’s Caused by mismatched blood types Headache, difficulty breathing, face flushed, pain in neck, chest & lower back, jaundice & kidney failure Presence or absence of antigens on RBC surface: antigen A & antigen B Inherited; 4 possible antigen combinations: A only: Type A B only: Type B A & B : Type AB Neither A nor B: Type O Antibodies are formed during infancy against the ABO antigens NOT present on our own RBC’s Type A: antibody anti-B Universal Type B: antibody anti-A Recipient Type AB: neither antibody → Type O: both anti-A & anti-B Universal Donor Inherited; named after Rhesus monkey where antigen 1st discovered If antigen D is found on RBC, the blood is Rh positive If the RBC lacks the antigen, blood is Rh negative Anti-Rh antibodies only develop after initial exposure to Rh-positive blood Rh-negative person receives transfusion from Rh-positive person = no reaction (1st time) but anti-Rh antibodies form If 2nd exposure happens, agglutination occurs
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