ch 19 + 20

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Biology

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134 Terms

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cardiovascular system
consists of a pump (the heart), series of conducting hoses (blood vessels), fluid connective tissue (blood)
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functions of blood
transporting dissolved gases, nutrients, hormones and metabolic wastes

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regulating pH, ion composition of interstitial fluids

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restricting fluid losses at injury sites (hemorrhage)

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defending against toxins and pathogens (carries immune system to various parts of the body)

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stabilizing body temperature
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blood volume
approximately 5.25 liters
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whole blood
refers to a mix of plasma and formed elements
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plasma
fluid and proteins
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formed elements
cells and cell fragments

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red blood cells, white blood cells, platelets
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dissolved gases in blood
O2 — ATP production (cellular respiration)

CO2 — removed waste and acts like an acid to maintain pH
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plasma proteins
albumins, globulins, fibrinogen
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albumins
provide plasma osmolarity

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transports fatty acids, thyroid hormones (T3, T4), some steroid hormones
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plasma osmolarity
blood vessel concentration vs. interstitial fluid concentration → controls which direction fluids will be pulled

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albumins pull fluid into blood vessels from the interstitial fluid due to the higher particle concentration
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globulins
antibodies (immunoglobulins) released by plasma cells

or transport globulins (that work like albumin)
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fibrinogen
soluble protein that functions in clotting
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hemopoiesis
process of producing formed elements
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platelets
small, membrane-bound cell fragments that contains enzymes and other substances that contribute to clotting
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erythrocytes
aka red blood cells, contain hemoglobin
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hemoglobin
red pigment, binds and transports oxygen and carbon dioxide
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red blood cell count
number of erythrocytes per cubic millimeter or microliter of blood

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males have slightly higher ranges/values than females
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hematocrit
percentage of formed elements in blood or packed cell volume (PCV)
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PCV
centrifuged blood → white, gray layer where all RBCs are packed from the sample
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RBC, HCT, Hgb
provide the same clinical information and are related to each other (if one is low, the other values will also be low)

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measure of RBC in the blood
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structure of RBCs
small, highly specialized cells

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biconcave discs (indentation on both sides) → thin central region and thicker outer margin

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disease would result in variation in the shape and size
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mature RBC
anuclei, lack mitochondria and ribosomes, unable to divide/synthesize proteins/repair damage

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live about 120 days (it can't synthesize anything)

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last stage of RBC maturation
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hemoglobin structure
two alpha chains and two beta chains → each has a molecule of heme → each heme contains one iron ion
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iron
attaches to oxygen (HbO2), dissociates easily as well
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hemoglobin function
each RBC contains millions of Hb molecules → each can carry billions of O2 molecules

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deoxygenated (in peripheral capillaries) → Hb releases O2 and binds CO2


oxygenated (lungs) → Hb binds O2 and releases CO2
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erythropoiesis
red blood cell formation

only occurs in myeloid tissue (red bone marrow)
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reticulocyte
day 5-7 stage of RBC maturation

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low Hb synthesis and still contains RNA

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do the same things as mature RBC but not as efficient due to smaller size and less Hb

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high % = body compensating for lack of mature RBC
low % = body is producing enough of either
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erythropoietin
hormone that stimulates erythropoiesis → secreted by kidneys/liver when O2 is low in peripheral tissues

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released into blood → red blood marrow → stem cells and developing RBCs (speeds up RBC maturation)
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release of EPO
released due to :

* anemia
* decreased blood to kidneys (part of negative feedback loop)
* decreased air O2 content and damaged lungs (need more RBCs to attach to more O2)

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takes a couple days - weeks to take effect
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hemoglobin recycling
spleen, liver and red bone marrow macrophages engulf old RBCs

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remove Hb molecules from hemolysed RBCs and break Hb into components (only the iron is recycled)
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anemia
low RBC count

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microcytic, normal cytic, macrocytic depending on the size of RBC
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hemolysis
the rupture or destruction of red blood cells
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bilirubin
orange-yellow pigment in bile; produced from the iron recycled by the breakdown of hemoglobin during hemolysis
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jaundice
caused by the buildup of bilirubin, results in a yellow appearance
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hemoglobinuria
free floating heme/hemoglobin in urine (broken down RBCs), results in red/brown urine

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due to abnormally high hemolysis in bloodstream (could be due to artificial heart valve, capillary clot, sickle anemia)
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hematuria
whole RBCs in urine (heme still inside the RBC), due to kidney or blood vessel damage (UTI, inflammation)
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surface antigens
substances on plasma membranes that identify cells to immune system

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normal cells are ignored and foreign cells are attacked
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blood type
determined by presence or absence of surface antigen on RBCs (A, B, and Rh)
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type A
surface antigen A, anti-B antibodies
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type B
surface antigen B, anti-A antibodies
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type AB
antigens A and B
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type O
neither A or B antigens, anti-A and anti-B antibodies
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Rh positive
Rh surface antigen is present
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Rh negative
Rh antigen is absent, anti-Rh antibodies
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hypoxemia
low O2 in blood
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hypoxia
low O2 in peripheral tissues
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agglutinogens
surface antigens on RBCs (A, B, D) and screened by immune system
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agglutinins
antibodies in plasma that attack antigens on foreign RBCs (activates the clotting system) → causes agglutination
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agglutination
clumping of foreign cells
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cross-reaction
may occur in a transfusion of blood or plasma from one person to another when donor/recipient blood types aren't compatible

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plasma antibody meets its specific surface antigen → RBCs agglutinate and hemolysis may occur
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compatibility/cross-match testing
performed before transfusions → reveals cross-reactions between donor's RBCs and recipient's plasma
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white blood cells
also called leukocytes
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functions of WBC
defending body against pathogens (fungi, bacteria, virus, prion), removing toxins and wastes, attacking abnormal or damaged cells
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WBC types
neutrophils, eosinophils, basophils, monocytes, lymphocytes
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neutrophil
multinuclei, polymorphonuclear leukocytes, pale cytoplasmic granules that contain lysosomal enzymes and bactericide (bacteria-killing compounds)

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very active, phagocytic cells that attack/digest bacteria
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degranulation
occurs when vesicle containing pathogen fuses with lysosomes containing enzymes and defensins

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dead neutrophils contribute to pus
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eosinophils
attack large parasites by releasing toxic compounds, sensitive to allergens

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release enzymes that reduce inflammation caused by mast cells and neutrophils
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basophils
cross capillary endothelium and accumulate in damaged tissues

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release histamine → dilate blood vessels

release heparin → prevent blood clotting
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monocytes
enter peripheral tissues to become macrophages that engulf large pathogens

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release chemicals that attract other phagocytic cells and fibroblasts to injured area
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lymphocytes
continuously migrate in and out of bloodstream, part of body's specific defense system

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T cells, B cells, natural killer cells
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T cells
cell mediated immunity, attack foreign cells or control other lymphocytes
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B cells
differentiate into plasma cells and form antibodies
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natural killer cells
detect and destroy abnormal cells
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platelet
thrombocytes, cells fragments involved in clotting system
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platelet functions
release important clotting chemicals and temporarily patch damaged vessel walls
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thrombocytopoiesis
platelet production from megakaryocytes, occurs in red bone marrow
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megakaryocyte
giant cells in red bone marrow that produce platelets by shedding membrane-enclosed packets of cytoplasm
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hemostasis
cessation of bleeding, separated into 3 phases: vascular, platelet, coagulation
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vascular phase
a cut triggers vascular spasm → contraction of smooth muscle fibers of vessel wall aka vasoconstriction for 30 min

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endothelial cells contract and expose basement membrane to bloodstream, release chemical factors and local hormones → smooth muscle contraction and cell division

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endothelial plasma membranes become "sticky" → adhere to platelets and seal off tear to prevent blood flow
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platelet phase
adhesion → attach to exposed surfaces

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aggregation → stick to each other and endothelium/collagen with von willebrand factor to form a platelet plug

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activated platelets release clotting compounds
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coagulation phase
involves chain reactions of extrinsic, intrinsic, common pathway → creates a fibrin mesh
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extrinsic/intrinsic pathways
activates prothrombinase
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common pathway
prothrombinase activates prothrombin → thrombin
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thrombin
activates fibrinogen to fibrin

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forms a positive feedback loop that accelerates clotting process, leading to an exponential increase in speed
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fibrin
creates a fibrin mesh between clot to make it more stable
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clot retraction
pulls torn edges of vessel closer together (reduces residual bleeding and stabilizes injury site)

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reduce size of damaged area → makes it easier for repair cells to complete repairs
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pulmonary circuit
arteries carry deoxygenated blood and veins carry oxygenated blood

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(opposite of systemic circuit)
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arteries
carry blood away from heart, oxygenated for systemic circuit

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larger than capillaries and are visible with naked eye
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veins
return blood to heart, deoxygenated for systemic circuit
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capillaries
exchange vessels that are 1 cell thick, interconnect the smallest arteries and veins

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exchange dissolved gases, nutrients, wastes between blood and surrounding tissues
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heart
great vessels connect at base (superior) and pointed tip is the apex (inferior)

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sit between 2 pleural cavities in mediastinum
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pericardium
surrounds heart, consists of outer fibrous layer and inner serous layer
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pericardial cavity
space between parietal and visceral layers, contains pericardial fluid
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serous pericardium
consists outer parietal layer and inner visceral layer (epicardium)
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epicardium
covers surface of the heart (outermost layer), covered by parietal layer of serous pericardium
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myocardium
cardiac muscle tissue
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endocardium
covers inner surfaces of heart
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tricuspid valve
right atrioventricular valve, has 3 cusps to prevent back flow of blood

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blood flows from right atrium to right ventricle
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door to balloon time
90 minutes
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bicuspid valve
left atrioventricular valve separating the left atrium and ventricle

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aka mitral valve
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right ventricle
pumps deoxygenated blood to the lungs

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compared to the left ventricle, it holds and pumps the same amount of blood but has thinner walls and develops less pressure
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heart valves
prevent back flow of blood
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atrioventricular valves
between atria and ventricles → when ventricles contract, blood pressure closes valves

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papillary muscles contract and tense chordae tendineae to prevent regurgitation of blood back into atria

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when open (ventricles are relaxed), semilunar valves are closed
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semilunar valves
pulmonary and aortic valves to prevent back flow of blood into ventricles

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when ventricles are contracting, they are opened
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heartbeat
a single cardiac contract, atria contract first then ventricles contract
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autorhythmic cells
pacemaker cells, control and coordinate heart (similar to neurons)
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contractile cells
make up muscles in the heart and produce contractions that propel blood
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great vessels
first vessels leaving the heart (aorta and pulmonary)
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conducting system
electrical impulse that stimulate contraction

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components include pacemaker cells and conducting cells
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autorhythmicity
cardiac muscle tissue contracts without neural or hormonal stimulation