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plasma protein contributes to colloid osmotic pressure causes water to move into blood |
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plasma protein defense against foreign invaders |
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plasma protein precursor to fibrin, clotting protein |
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plasma protein increase solubility of substances in blood Ex: transferrin-transports iron |
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plasma proteins able to travel in blood without carrier Ex: amine and peptide |
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Red Blood Cells 5 million cells/microL of blood function: transport of O2 and CO2 biconcave shape no nucleus no mitochondria glycolysis flexible membrane with spectrin |
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% of RBC in blood volume 45% for average person |
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protein in red blood cell membrane allows membrane to change shape due to changes in surrounding fluid, allow movement through small spaces, change shape due to diseases |
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plasma protein used for transport of O2 and CO2 4 polypeptide chains (2alpha, 2beta) each chain contains heme group (contains iron) O2 binds to heme group CO2 binds to chains 1 hemoglobulin can bind 4 O2 |
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White Blood Cells function: protect body from foreign invaders 4k-11k cell/microL blood contains nucleus! five types in order of abundance: NLMEB (neutrophils, lymphocytes, monocytes, eosinophils, basophils) |
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type of white blood cell phagocytic release cytokines to increase body temp and increase inflammation bacterial infection |
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located in lymphoid tissue (more likely to be exposed to antigens) tonsils, lymph nodes, spleen 2 types: B and T cells B cells=antibodies T cells=cytotoxic (kill infected cells) and helper (stimulate immune response) viral infection |
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type of white blood cell circulate in blood enter tissue become--> Macrophage phagocytes antigen presenting cells |
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white blood cell released during allergic reactions and to kill parasitic worms |
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white blood cells involved in allergic reactions and inflammation releases histamine=vasodilation and bronchoconstriction release heparin=inhibits blood clotting circulates in blood enter tissues become-->Mast cells skin, lungs, digestive tract |
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cell fragments from megakaryocytes (large cells located in bone marrow) 150k platelets/microL blood no nucleus contains granules filled with clotting proteins and cytokines always present in blood not active unless damage occurs plays a role in coagulation |
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bone marrow cell that fragments and gives rise to platelets |
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production and development of blood cells all blood cells derived from one precursor cell-->Hemocytoblast process is age dependent (as child ages, active regions of bone marrow decreases. adults: only areas of production is in bones of the hip, vertebrae, ribs, cranium, and proximal ends of long bones) hemocytoblast-->uncommitted stem cell-->committed stem cell |
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stem cell located in RED bone marrow can develop into any type of blood cell |
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production of red blood cells controlled by hormone erythropoietin |
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hormone that controls red blood cell production (erythropoiesis) made in kidneys synthesis of hormone is stimulated by hypoxia (low levels of O2 in tissues) more red blood cells=more oxygen transported |
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decreased oxygen carrying capacity due to defective hemoglobulin or low red blood cell numbers 2 possible causes 1. abnormal hemoglobuin=sickle cell causes RBC to be sicle cell shape and rupture at high rate 2. inadequate hemoglobulin sysnthetis=due to inadequate intake of dietary iron |
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production of white blood cells controlled by colony stimulating factor depending on need, differentiation of a particular white blood cell will occur Ex: bacterial infection=neutrophils viral infection=lymphocytes parasitic worms=eosinophils |
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production of megakaryocytes-->production of platelets controlled by thrombopoietin |
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hormone that controls megakaryocyte and platelet production produced in liver and kidneys |
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Colony Stimulating Factor |
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hormone that controls white blood cell production produced in endothelial cells, fibroblasts in bone marrow, and white blood cells |
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Prevention of blood loss steps |
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1. Vasoconstriction 2. Platelet Plug 3. Clot |
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Vasoconstriction in Prevention of Blood Loss |
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endothelium release chemicals that cause vasoconstriction of blood vessels to decrease blood flow, blood pressure, and blood loss |
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platelets adhere to collagen in damaged blood vessel wall platelets release chemicals to function in vasoconstriction (serotonin, thromboxane A2) and platelet aggregation (ADP, platelet activating factor) more platelets are attracted and adhere to each other to form platelet plug |
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inactive proteins are activated by the intrinsic or extrinsic pathway to contribute to the clotting process end result is the formation of fibrin protein from fibrinogen, which stabilizes platelet plug to become a clot |
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triggered by damage to blood vessel lining exposure to collagen collagen activates F12 to begin cascade F12: F11-->F11a F11a: F9-->F9a F9a+F8a: F10-->F10a
F12, F11, F9, F9+F8, F10 |
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triggered by damage to blood vessel lining exposes tissue factor 3 tissue factor 3 activates factor & to begin cascade F3a: F7-->F7a F3a+F7a: F10-->F10a
F3, F7, F3+F7, F10 |
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F10a causes prothrombin-->thrombin thrombin causes fibrinogen--> fibrin thrombin causes F8-->F8a F8a causes production of cross linking in fibrin thrombin acts in positive feedback loop to activate F11 and F7
*Calcium is required for activation of clotting factors *Vitamin K is required for synthesis of clotting factors and prothrombin |
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breakdown of fibrin in blood clot 1. thrombin and tPA (tissue plasminogen activator) activate plasminogen 2. plasminogen-->plasmin 3. plasmin breaks up fibrin in clots |
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inhibits thrombin formation |
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inhibits platelet aggregation inhibits release of clotting substances |
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binds to free calcium lowers the amt of calcium available for coagulation |
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disrupts vitamin K activity, which is needed for synthesis of clotting factors |
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