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Roughly 5 liters per person Blood is heavier than water (components are made primarily of water with other biochemicals added in!) Varies with: ◦ Body size ◦ Changes in fluid and electrolytes/salt ◦ Amount of adipose fat tissue ◦ Gender (males have more than females!)
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Def: % of formed elements in blood ◦ Mostly red blood cells (RBCs) ◦ WBCs and platelets– less than 1% Normal values ◦ In males- mid to high 40’s ◦ In females- low 40’s When centrifuged/spun: ◦ White blood cells (WBCs) and platelets form a thin very thin layer on top – called “buffy coat” – between plasma and RBCs
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Hematopoiesis ◦ Def: process by which immature stem cells become specialized ◦ Become either RBC, WBC or platelets ◦ Location: Occurs in red bone marrow
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Also called erythrocytes Biconcave shape ◦ Increases surface area/volume ratio Mature cells lack nuclei 1/3 filled with hemoglobin ◦ Oxygen carrying polypeptide molecule
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Composed of four chains (polypeptides) Also has iron or “heme” group attached Called oxyhemoglobin when oxygen is bound to it (bright red color) Called deoxyhemoglobin when oxygen is released (darker color)
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The higher the # of RBCs = higher oxygen carrying capacity ◦ Change in # affects health – greatly! ◦ Used, in part, to help diagnose and evaluate diseases Typical range ◦ Males: 4,600,000 – 6,200,000 cells per mm 3 ◦ Females: 4,200,000 – 5,400,000 cells per mm 3
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Hematopoiesis (red blood cell formation) ◦ Before Birth: yolk sac, liver, and spleen ◦ After Birth: red marrow ◦ Controlled very precisely by homeostatic mechanisms Production influenced by: ◦ Vitamin B 12 ◦ Folic acid ◦ iron
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Circulate for 120 days Old or damaged RBC’s are destroyed (removed from blood circulation daily) ◦ Phagocytized by macrophages in liver or spleen ◦ Hemoglobin is broken into heme and globin ◦ Heme is broken into iron and biliverdin (greenish pigment) ◦ Biliverdin is converted to bilirubin ◦ Iron is stored in liver or brought to marrow ◦ Biliverdin and bilirubin are secreted in bile
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Also called leukocytes Production stimulated by interleukins and colony-stimulating factors Two groups: ◦ 1) Granulocytes - have granular cytoplasm Neutrophils Eosinophils Basophils ◦ 2) Agranulocytes - no cytoplasmic granules Monocytes Lymphocytes WBC animation WBC animation
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Granulocyte Average 54-62% of leukocytes Fine cytoplasmic granules that are light purple in neutral stain Nucleus: 2-5 lobes Lifespan: about 12 hours Function: phagocytize bacteria and other particlesphagocytize bacteria
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Granulocyte Average 1-3% of leukocytes Coarse cytoplasmic granules that are deep red in acid stain Nucleus: 2 lobes Lifespan: about 12 hours Function: destroy certain parasites and control inflammation or allergic reactions
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Granulocyte Average ‹1 % of leukocytes Relatively few, irregularly shaped cytoplasmic granules that are deep blue in basic stain Nucleus: 2 lobes Lifespan: about 12 hours Function: release heparin and histamine
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Agranulocyte Average 3-9 % of leukocytes Nucleus: Varied shape Lifespan: several weeks or months Function: phagocytize materials
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Agranulocyte Average 25-33 % of leukocytes Nucleus: Large and round Lifespan: may live for years Function: function in immune response
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Normal range: 5,000-10,000 mm 3 Differential White Blood Cell Count ◦ Distinguish how many of each type ◦ Can be important for diagnosing some disorders/problems ◦ Excessive: If your WBC count exceeds 10,000, this is leukocytosis (infection) Ex: Appendicitis ◦ Deficiency: If you WBC count is below 5,000, this is leukopenia (low count) Ex: typhoid fever, influenza, measles, mumps, chickenpox, AIDS, polio WBC animation WBC animation
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White blood cells are also called leukocytes ◦ UP!!! ◦ UP!!! When discussing hematocrit, WBCs make up the majority of your blood. ◦ DOWN!!! The more WBCs you have, the better you’re probably feeling. ◦ DOWN! Lymphocytes function to assist your immune system ◦ UP!!! ◦ UP!!!
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Neutrophils are granulocytes. ◦ YES!!! ◦ YES!!! Basophils phagocytize materials. ◦ NO!!! Monocytes make up the majority of your WBCs. ◦ NO!!! Have an excessive WBC count can mean an infection like appendicitis. ◦ YES!!! ◦ YES!!!
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Also celled thrombocytes Made from megokaryocyte ◦ Large cells in red bone marrow Production stimulated by thrombopoietin (hormone) Lack nucleus ½ the size of RBC Lifespan: about 10 days Function: form blood clots, help close breaks in damaged blood vessels Normal range: 130,000-360,000
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91-2% water Remainder is mixture of biochemicals ◦ Proteins, nutrients, hormones, electrolytes Function: ◦ Transporting nutrients, gases and vitamins ◦ Regulate fluid and electrolyte balance ◦ Maintain proper pH
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Main component of dissolved substances Remain in plasma (not metabolized/broken down) Types: ◦ 1) Albumin (60%) Help establish colloid osmotic pressure Transports lipids and steroid hormones ◦ 2) Globulins (36%) Transport of ions, lipids and fat-soluble vitamins and some antibodies ◦ 3) Fibrinogen (4%) Function in blood coagulation and clotting
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Most important blood gases: ◦ Oxygen ◦ Carbon dioxide Plasma nutrients: ◦ Materials absorbed from digestive tract Ex: Amino acids, simple sugars, nucleotides, lipids ◦ Fats (triglycerides) ◦ Phospholipids ◦ Cholesterol ◦ Lipoproteins When Fats, phospholipids, cholesterol combine with proteins Large size
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Nonprotein Nitrogenous Substances ◦ Amino acids ◦ Urea and uric acid Electrolytes ◦ Various ions (K+, Ca+, Cl-)
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Def: the stoppage of bleeding Important when blood vessels are damaged (following injury) Vasospasm ◦ Contraction of blood vessel walls in response to small break Platelet plug ◦ Platelets adhere to damage and to each other to create a plug; may release serotonin to cause vasoconstriction If previous two are unsuccessful, blood clot may form (through coagulation)
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Def: formation of blood clot Damaged tissue releases tissue thromboplastin (hormone) After series of rxns, prothrombin activator is created Prothrombin activator (with Calcium) converts prothrombin to thrombin Thrombin cuts fibrinogen into fibrin fibers that form a meshwork over the damage
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Hemophilia ◦ Uncontrolled bleeding (hemorrhaging) following injury, frequent nosebleeds, blood in urine ◦ Inherited clotting disorder ◦ Carried on X chromosome (recessive) Von Willebrand Disease ◦ Tendency to bleed and bruise easily ◦ Inherited clotting disorder ◦ Far less severe than hemophilia
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Leukemia Leukemia ◦ Symptoms: Fatigue, frequent colds/fevers, chills, sweats, bruising, bone pain ◦ Diagnosing: Few RBCs and platelets, TOO many WBCs (notice the prefix “leuk” from leukocytes) ◦ Cause: Red bone marrow producing too many granulocytes cancer cells are not controlled – spread ◦ Treatment: Stem cell transplants, chemotherapy drugs
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Normal smear Leukemia smear
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Types: A, B, AB, O Typing is based on antigens found on RBC’s Two most important groups: ◦ 1) ABO group ◦ 2) Rh group + and – of each type Ex: A-, B-, AB-, O-; A+, B+, AB+, O+
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Blood type is codominant (A and B are BOTH equally dominant) Possible blood type genotypes (genetic code) ◦ A (I A I A or I A i) ◦ B (I B I B or I B i) ◦ AB (I A I B ) ◦ O (ii)
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Mixing blood types can cause agglutination
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Possible Rh Blood Types: ◦ + (++ or +-) ◦ - (--)
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Condition cause by Rh incompatibility between mother and fetus
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I have O- blood. What type can I receive? ◦ O- ONLY I have AB+ blood. What type can I receive? ◦ ANY!!! I have B- blood. Who can take my blood? ◦ B+ or B-; AB+ or AB-
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