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a&p test 1

chapters 17

TermDefinition
Blood functions distribution, regulation, prevention
blood formed elements are suspended in a non living fluid matrix called plasma
erythrocytes red blood cells that binds, carries, and relseases oxygen. 45% of total blood volume. have no nuclei or organells.
leukocytes white blood cells that protect the body and platelets to help stop bleeding.
hematocrit
plasma 90% water, straw colored, sticky. contains electrocytes, proteins, nutrients, respiratory gases, non-protein nitrigenous substances.
plasma proteins albumin, globulin, gamma, fibrinogen
albumin 60% pof plamasma proteins, produced by the liver, osmotic pressure
globulins 36% of plasma proteins. alpha and beta. produced by the liver. transport proteins to lipids, metal ions, and fat soluble vitamins
gamma antibodies released by plasma cells during immune responce
fibrinogen 4% of plasma proteins. produced by the liver. forms fibrin threads of blood clot
hemoglobin the protein that makes red blood cells, binds easily and reversibly with oxygen. made up of red heme pigment pound to the protein globulin.
oxyhemoglobin oxygen binds to iron at the center of heme
deoxyhemoglobin reduced hemoglobin, no oxygen bound to heme
carbaminohemirooglobin happens when hemoglobin is in the reduced state. direction of transport of carbon dioxide is from tissues to lungs, where carbon dioxide is eliminated from the body.
hematopoiesis blood cell formation. happens in red blood marrow (network of reticular of connective tissue with blood sinusoids
hematopoietic stem cell (hemocytoblast) forms all blood cells. differentiation or maturation involves irreversible commitment to a pathway of development
erythropoiesis erythrocyte formation
life span of erythrocyte 120 days. in spleen, liver, and marrow.
anemia erythrocyte disorder. low oxygen carrying capacity due to blood loss, low production, and high destruction.
hemorrhagic anemia blood loss
iron-deficiency anemia low iron in diet
pernicious anemia immune system destroys stomach mucosa reducing intristic factor secretion necessary for B12 intake or low B12 diet.
polycythemia too many red blood cells, high viscosity, low oxygen delivery
granulocytes phagocytic, lobed nuclei, shorter lived than erythrocytes.
neutrophil most numerous, attracted to inflammations, very phagocytotic
eoisinophil attack parasitic worms, 2 lobed nuclei
basophil inflammatory responces, u or s shaped nucleus
agranulocytes lack cytoplasmic granules, kidney shaped nuclei
lymphocytes very large, dark purple nucleus
T-lymphocyte disrupt virus infected cells, and tumor cells
B-lymphocyte produce plasma cells, produce antibodies. cellular and humoral immunity
monocyte less numerus, kidney shaped nucleus. phagoctyize bacteria
leukopoiesis paracrine/hormonal controls.
leukocyte disorders leukemia, infectious mononucleosus
platelets blood clotting,
homeostasis vascular spasm, platelt plug formation, coagulation
vascular spasm damaged blood vessels respond to injury by constricting
platelet plug formation platelets stick together to form a plug that seals the break in the vessel wall
coagulation blodd clotting, fibrin threads reinforce platelet plug to form clot trapping addition cells in frbrin mesh. 3 phases
phase 1: activation of prothrombin intristic pathway (freely circulating in blood) extrinstic pathway (tissue factors from damaged tissues)
phase 2: thrombin activation prothrombin to thrombin
phase 3: fibrin mesh formation thrombin converts fibrinogen to fibrin, then polymerizes
clot retractionbilit stabilizes the clot, platelets contain contractile protein and contract like smooth muscle cells.
platelet derived growth factor released by platelets stimulates smooth muscle cells and fibroblasts to divide and rebuild the vessel wall
fibrinolysis keeps vessels from blocking. endothelial cells near clot secrete tissue plasminogen activator(tPA).
thrombus disorder in which a clot within an unbroken blood vessel attatched to the wall
embolus a clot wihtin an unbroken vessel, floating freely
thrombocyopenia platelet deficiency, causes spontaneous bleeding, caused by destruction of marrow
impaired liver function clot is unable to form
hemophilia genetic disorder, lacking 1 clotting factor
disseminated intravascular coagulation wide spread clotting formed by the inibility to form clots
antigens glyco and lipprotein markers on the cell membrane surface (IMMUNE RESPONCE)
agglutination clumping together of cells
Created by: 593740774
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