Unit 1: Ch 18, 19, 20 Flashcards
ABO Blood Group Determination
- Hereditary presence or absence of antigens A and B on the RBCs
- Type O: doesn’t agglutinate in either one
- Type A or B: agglutinates only in the corresponding antiserum
- Blood type AB: exhibits agglutination in both antisera
- Wright stain test
- Determined by placing a drop of blood in a pool of anti-A serum and another drop in a pool of anti-B
Agglutination
- Description
- Antibody molecules that bind to antigens; “clumping of RBCs”
- Can attach to foreign antigens on different RBCs at the same time
- Agglutinated RBCs block small blood vessels, hemolyze, and release their hemoglobin over the next few hours or days
- Responsible for mismatched transfusion reaction
Anemia
- What causes it?
- How does it effect the body?
-
Causes
- Kidney failure
- Dietary deficiency
-
Effects
- Reduced blood osmolarity
- Reduced blood viscosity
- Hypoxia
- Lethargy
- Shortness of breath
- Necrosis of brain, heart, or kidney
Anemia Types
- List & describe
- Aplastic anemia: complete cessation of erythropoiesis
- Hypoplastic anemia: decline in erythropoiesis
- Iron-deficiency anemia: nutritional anemia
- Pernicious anemia: autoimmune disease in which antibodies destroy stomach tissue
Antibodies
- Description
- Types
- An immune system protein that aids in immune response
- Types
-
Anti-A and -B
- Appear 2 to 8 months after birth
- Maximum concentration by 10 YOA
- Do not form antibodies against your antigens
-
Anti-D
- Form only in Rh- individuals who are exposed to Rh+ blood (transfusion or birth)
-
Anti-A and -B
Antigens
- Description
- Any substance that is capable of causing an immune reaction
- Usually proteins, glycoproteins, or glycolipids
Basophils
- Cell type
- Secretions and their functions
- A type of granulocyte
- Fight fungal or bacterial infections and viruses
- Secrete heparin (anticoagulant): promotes the mobility of other WBCs in the area
- Secrete histamine (vasodilator): speeds flow of blood to an injured area
- Increased numbers found in chickenpox, sinusitis, diabetes
Blood Clot Dissolution
- List & describe the 3 approaches
- Hementin: produced by giant Amazon leech
-
Streptokinase: enzyme made by streptococci bacteria
- Used to dissolve clots in coronary vessels
- Digests almost any protein
- Tissue plasminogen activator (TPA): works faster, is more specific, and now made by transgenic bacteria
Blood Clot Prevention
- List & describe the 3 approaches
-
Aspirin
- Suppresses thromboxane A2
-
Vitamin K
- Required for formation of clotting factors
- Examples: Coumarin, warfarin (Coumadin)
-
Other anticoagulants discovered in animal research
- Medicinal leeches used since 1884 (hirudin)
- Snake venom from vipers (arvin)
Blood Clot Retraction
- Methods and descriptions
- Timing of clot retraction
- Methods
-
Platelet-derived growth factor secreted by platelets and endothelial cells
- Mitotic stimulant for fibroblasts and smooth muscle to multiply and repair damaged vessel
-
Fibrinolysis—dissolution of a clot
- Factor XII speeds up formation of kallikrein enzyme
- Kallikrein converts plasminogen into plasmin, a fibrin-dissolving enzyme that breaks up the clot
-
Platelet-derived growth factor secreted by platelets and endothelial cells
- Retraction occurs within 30 minutes
Blood Components
- Liquid connective tissue: adults have 4-6 L of blood
- Extracellular matrix: blood plasma
- Formed elements: RBC, WBC, and platelets
Blood Plasma
- Description
- The liquid portion of blood (serum) after blood clots and solids are removed
- Identical to plasma except for the absence of fibrinogen
Blood Production
(Daily for adults)
- 400 billion platelets
- 200 billion RBCs
- 10 billion WBCs
Blood Type Discovery
- Who discovered ABO blood types
- What is its significance
- Karl Landsteiner discovered blood types A, B, and O in 1900
- Won a Nobel Prize in 1930
- Type AB discovered later
- Blood types and transfusion compatibility are a matter of interactions between plasma proteins and erythrocytes
Blood Viscosity
- Description
- Ratio to water
- Ratio to plasma
- Resistance of fluid to flow, resulting from the cohesion of its particles
- Whole blood 4.5 - 5.5 times as viscous as water
- Plasma is 2x as viscous as water; important in circulatory function
Cardiovascular System Components
- Heart
- Blood Vessels
Centrifugation
- Description
- Separates the formed elements
- Determines hematocrit (packed cell volume)
Charles Drew
- Blood banking pioneer
- First black person to pursue advanced degree in medicine to study transfusion and blood banking
- Used plasma rather than whole blood; caused less transfusion reactions
Circulatory System Components
- Heart
- Blood vessels
- Blood
Circulatory System Functions
-
Transport
- O2, CO2, nutrients, wastes, hormones, and stem cells
-
Protection
- Inflammation, limit spread of infection, destroy microorganisms and cancer cells, neutralize toxins, and initiate clotting
-
Regulation
- Fluid balance, stabilizes pH of ECF, and temperature control
Coagulation Pathways
-
Extrinsic pathway
- Factors released by damaged tissues begin the cascade
- Initiated by release of tissue thromboplastin (factor III) from damaged tissue
- Cascades to factor VII, V, and X
-
Intrinsic pathway
- Factors found in blood begin the cascade (platelet degranulation)
- Initiated by platelets releasing Hageman factor (factor XII)
- Cascades to factor XI to IX to VIII to X
- Calcium required for both pathways
Coagulation Process
- Activation of factor X
- Production of prothrombin activator
- Prothrombin converted to thrombin
- Thrombin converts fibrinogen into fibrin
Positive feedback loop: thrombin speeds up formation of prothrombin activator
Disseminated Intravascular Coagulation (DIC)
- Widespread clotting within unbroken vessels
- Limited to one organ or occurring throughout the body
- Usually triggered by septicemia but also occurs when blood circulation slows markedly (as in cardiac arrest)
- Marked by wide-spread hemorrhaging, congestion of the vessels with clotted blood, and tissue necrosis in blood-deprived organs
Embolus
- Anything that can travel in the blood and block blood vessels
- Infarction (tissue death) may occur if clot blocks blood supply to an organ (MI or stroke)
- 650,000 Americans die annually of thromboembolism (traveling blood clots)
Eosinophils
- Type of granulocyte
- Increased numbers in parasitic infections, collagen diseases, allergies, diseases of spleen and CNS
- Phagocytosis of antigen–antibody complexes, allergens, and inflammatory chemicals
- Release enzymes to destroy large parasites
Erythrocyte death & disposal process
- RBCs & macrophages in spleen
- Separate heme from globin
- Globins hydrolyzed into amino acids
- Iron removed from heme
- Heme pigment converted to biliverdin (green)
- Biliverdin converted to bilirubin (yellow)
- Released into blood plasma (kidneys—yellow urine)
- Liver removes bilirubin and secretes into bile
- Concentrated in gallbladder: released into small intestine; bacteria create urobilinogen (brown feces)
Erythrocyte Disorders
- Description
- List and describe the 2 types
- Imbalance between the rates of erythropoiesis and RBC destruction
- Types
- Polycythemia: RBC excess
- Anemia: RBC or hemoglobin deficiency
Erythrocyte / RBC Functions
- Carry oxygen from the lungs and deliver it to tissues
- Pick up CO2 from tissues and bring to lungs
Erythrocytes / RBCs
- Shape
- Description
- Disc-shaped cell with thick rim
- Most abundant formed elements of the blood and most critical to survival
- It is the lack of life-giving oxygen, carried by erythrocytes, that leads rapidly to death in cases of major trauma
- The only human cells that carry on anaerobic fermentation indefinitely
- Lose nearly all organelles during development
- Lack mitochondria; rely exclusively on anaerobic fermentation to produce ATP
- Lack of nucleus and DNA; no protein synthesis or mitosis
Fibrinogen
- Becomes fibrin, the major component of blood clots
Formed Elements
- List various types
- Erythrocytes (RBC)
- Platelets
- Leukocytes (WBC)
-
Granulocytes (with granules)
- Basophils
- Eosinophils
- Neutrophils
-
Agranulocytes (without granules)
- Lymphocytes
- Monocytes
-
Granulocytes (with granules)
Fractionation
- Fractionation of blood into formed elements, plasma, and serum
Hematocrit
- The percentage by volume of red cells in your blood
- Packed cell volume
Hematology
- The study of blood
Hematomas
- Description
- Masses of clotted blood in the tissues
- Thrombosis: Abnormal clotting in unbroken vessel
- Thrombus: Clot most likely to occur in leg veins of inactive people
Hematopoiesis
- The production of blood, especially its formed elements
Hematopoietic stem cells (HSC)
- What do they produce?
- Differentiate into distinct types of colony-forming units (CFU) and then produce the following cell lines, each committed to a certain outcome
-
Myeloblasts: differentiate into 3 types of granulocytes
- basophils
- eosinophils
- neutrophils
- Monoblasts: lead ultimately to monocytes
- Lymphoblasts: produce all lymphocyte types
-
Myeloblasts: differentiate into 3 types of granulocytes
Hemoglobin Degradation
- 5 streams
- Heme → Biliverdin → Bilirubin → Bile → Feces
- Heme → Iron → Storage → Reuse
- Heme → Iron → Reuse
- Heme → Iron → Loss by menstruation, injury, etc
- Globin → Hydrolyzed to free amino acids
Hemolysis
- Rupture of RBCs
- Releases hemoglobin and leaves empty plasma membranes
- Membrane fragments digested by macrophages in the liver and spleen
Hemolytic disease of the newborn (HDN) / erythroblastosis fetalis
- Description
- Causes
- Can occur when a woman has a baby with a mismatched blood type, typically when she is Rh- and carries an Rh+ fetus
- Causes
- Mismatched Rh type (most severe)
- Mismatched ABO type
- Mismatched Kell blood group
- Mismatched Kidd
- Mismatched Duffy
Hemophilia
- Description
- Types
- A family of hereditary diseases characterized by deficiencies of one factor or another
- Occurs predominantly in males
- Can inherit it only from mothers
- Types
- Classical hemophilia (hemophilia A): Lack of factor VIII
- Hemophilia B: Lack of factor IX
- Hemophilia C: Lack of factor XI; autosomal and not sex-linked - occurs equally in both sexes
Hemostasis
The cessation of bleeding
Hemostatic Mechanisms
-
Vascular spasm
- Immediate protection against blood loss
- Constriction of broken blood vessels
-
Platelet plug formation
- Mass of formed platelets
-
Blood clotting (coagulation)
- The last but most effective defense against bleeding
- Converts fibrinogen into fibrin
- 2 reaction pathways
- Extrinsic mechanism: initiated by clotting factors released by the damaged blood vessel and perivascular tissues. Come from sources external to the blood itself
- Intrinsic mechanism: Uses only clotting factors found in the blood itself
Hypoproteinemia
- “Starvation” / deficiency of plasma proteins
- extreme starvation
- liver or kidney disease
- severe burns
Hypoxemia
- Description
- Causes
- Oxygen deficiency in the blood
- Causes
- Blood loss
- Low levels of oxygen in the atmosphere
- Abrupt increase in the body’s oxygen consumption
Infectious mononucleosis
- Infection of B lymphocytes with Epstein-Barr virus
Kernicterus
- Description & cause
- Treatments
- Syndrome of toxic brain damage that can be lethal or leave the child with motor, sensory, and mental deficiencies
- Caused by HDN; high bilirubin levels
- Treatments
- Phototherapy: exposes the infant to ultraviolet radiation
- Exchange transfusion: completely replaces an infant’s Rh+ blood with Rh-
Kwashiorkor
- Children with severe plasma protein deficiency
- Thin arms and legs
- Swollen abdomen
- Fed on cereals once weaned
Leukemia classifications
- List and describe the 4 types of leukemia
-
Acute leukemia
- Appears suddenly, progresses rapidly, and causes death if untreated
-
Chronic leukemia
- Develops more slowly and may go undetected
- If untreated, the typical survival time is 3 yrs
-
Lymphoid leukemia
- Uncontrolled lymphocyte or monocyte production
-
Myeloid leukemia
- Uncontrolled granulocyte production
Leukocyte disorders
- List and describe the 3 primary leukocyte disorders
-
Leukocytosis—high WBC count: above 10,000 WBCs/mL
- Causes: infection, allergy, disease
- Differential WBC count: identifies what percentage of the total WBC count consist of each type of leukocyte
-
Leukemia—cancer of hemopoietic tissue that usually produces an extraordinary high number of circulating leukocytes and their precursors
- Effects: normal cell percentages disrupted; impaired clotting; opportunistic infections
-
Leukopenia—low WBC count: below 5,000 WBCs/mL
- Causes: radiation, poisons, infectious disease
- Effects: elevated risk of infection
Leukocytes / WBCs
- Description
- Least abundant formed elements
- Protect against infection & other diseases
- Differ from RBCs in that they retain their organelles throughout their life
- Conspicuous nucleus
- Retain their organelles for protein synthesis
Lymphocytes
- Cell type
- Function
- Effect
- Type of agranulocyte
- Function
- Destroy cells (cancer, foreign, and virally infected cells)
- “Present” antigens to activate other immune cells
- Secrete antibodies and provide immune memory
- Increased numbers in diverse infections and immune responses
Monocytes
- Type of agranulocyte
- Increased numbers in viral infections and inflammation
- Leave bloodstream and transform into macrophages
- Phagocytize pathogens and debris
- “Present” antigens to activate other immune cells—antigen-presenting cells (APCs)
Myeloid
- Blood formation in the bone marrow
Neutrophils
- Type of granulocyte
- Increased numbers in bacterial infections
- Phagocytosis of bacteria
- Release antimicrobial chemicals
Opportunistic infection
- The establishment of pathogenic organisms that usually cannot get a foothold in people with healthy immune systems
- Caused by the deficiency of competent WBCs
Osmolarity of blood
- Description
- Effect if too high & low
- The total molarity of dissolved particles that cannot pass through the blood vessel wall
- If too high: blood absorbs too much water, increasing the blood pressure
- If too low: too much water stays in tissue, blood pressure drops, and edema occurs
- Optimum osmolarity is achieved by the body’s regulation of sodium ions, proteins, and RBCs
Other blood groups
- Description
- Types
- Rarely cause transfusion reactions
- Useful for legal purposes (paternity) and criminal cases
- Now that DNA sequencing is more economical, it has replaced blood typing in many applications
- Types
- Duffy
- Kell
- Kidd
- Lewis
- MNS
Plasma Proteins Role
- Clotting
- Defense against pathogens
- Transport of other solutes such as iron, copper, lipids, and hydrophobic hormones
Plasma Proteins
- Description
- Categories
- Formed by liver, except globulins which are produced by plasma cells
- Categories
- Albumins
- smallest and most abundant
- contribute to visosity and osmolarity
- influence blood pressure, flow and fluid balance
- Globulins
- antibodies
- provide immune system functions
- alpha, beta, and gamma globulins
- Fibinogen
- precursor of fibrin threads that help form blood clots
- Albumins
Platelet Functions
- Initiate the formation of a clot-dissolving enzyme
- Secrete vasoconstrictors
- Internalize and destroy bacteria
Platelet Production
- List & describe the 3 platelet cell types
-
Thrombopoiesis
- Stem cells (that develop receptors for thrombopoietin) become megakaryoblasts
-
Megakaryoblasts
- Repeatedly replicate DNA without dividing
- Megakaryocytes
Pulmonary Embolism
- When a blood clot breaks free and travels from veins to lungs
Reasons oxygen in blood are higher in women
- Androgens stimulate RBC production, and men have higher androgen levels than women
- Women of reproductive age have periodic menstrual losses
- The hematocrit is inversely proportional to % of body fat, which average higher in women
Red bone marrow
- Produces all 7 formed elements
Rh blood group
- Description
- Antigens
- Prevention
- Rh determination
- Description
- Named for the rhesus monkey
- ABO blood type has no influence on Rh type
- Occurs if Rh- mother has formed antibodies and is pregnant with second Rh+ child
- Anti-D antibodies can cross placenta
- Prevention
- RhoGAM given to pregnant Rh- women
- Binds fetal agglutinogens in her blood so she will not form anti-D antibodies
- RhoGAM given to pregnant Rh- women
- Antigens
- Principal RBC antigen types are C, D, and E
- Antigen D is the most reactive
- Determination
- Rh+ if a person has antigen D
- Rh- if someone does not have antigen D
Sickle-Cell Disease
- Hereditary hemoglobin defects that occur mostly among people of African descent
- Caused by a recessive allele that modifies the structure of the hemoglobin molecule (HbS)
- Differs only on the sixth amino acid of the beta chain
- HbS does not bind oxygen well
- RBCs become rigid, sticky, pointed at ends
- Clump together and block small blood vessels causing intense pain
- Can lead to kidney or heart failure, stroke, rheumatism, or paralysis
Thalassemia
- Hereditary anemias most common in Greeks, Italians, and others of Mediterranean descent
- Deficiency or absence of alpha or beta hemoglobin and RBC counts that may be less than 2 million
Thrombocytopenia
- Platelet counts below 100k
- Causes include bone marrow destruction by radiation, drugs, poisons, or leukemia
- Signs include small hemorrhagic spots in the skin or hematomas in response to minor trauma
Blood Type Compatibility
Universal Donor & Recipient
- Description of each
- Universal donor
- Type O: most common blood type
- Lacks RBC antigens
- Donor’s plasma may have both antibodies against recipient’s RBCs (anti-A and anti-B)
- May give packed cells (minimal plasma)
- Universal recipient
- Type AB: rarest blood type
- Lacks plasma antibodies; no anti-A or anti-B
Cardiovascular System Components
- Heart
- Blood vessels
Circulatory System Components
- Heart
- Blood vessels
- Blood
Circulatory System Divisions
- List and describe
-
Pulmonary circuit
- Right side of heart
- Carries blood to lungs for gas exchange and back to heart
- Lesser oxygenated blood arrives from inferior and superior venae cavae
- Blood sent to lungs via pulmonary trunk
-
Systemic circuit
- Left side of heart
- Supplies oxygenated blood to all tissues of the body and returns it to the heart
- Fully oxygenated blood arrives from lungs via pulmonary veins
- Blood sent to all organs of the body via aorta
Heart Base & Apex
- Describe
-
Base
- Wide, superior portion of heart
- Blood vessels attach here
-
Apex
- Inferior end
- Tilts to the left, tapers to point