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components of blood
- red blood cells (erythrocytes) 45%
- white blood cells (leukocytes) <1%
- Platelets <1%
- plasma 55%
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Blood Plasma
- 55%
- 90-92% water
- electrlytes/ glucose
- clotting factors
- plasma proteins
- albumin-transport fatty substancesglubulins
- fibrinogen-blood clotting
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3 components of plasma
- albumin (liver)-osmotic pressure of plasma and carrier
- globulin(liver & lymphoid tissue)- clotting, enymes, antibodies and carriers
- fibrinogen(liver)- need for blood clotting
- transferrin- iron transport
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5 types of white blood cells
- lymphocytes-body immune system
- monocytes-evolve into macrophages which kill of bacteria
- neutrophils-phagocytes, first to move to point of inlfammation in an infection (chemotaxis)
- eosinophils-killing bacteria and parsites
- basophils- response to allergic symptoms, and contain vasodilator histamine which promotes blood flow
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what do megakaryocytes become
platelets
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whast comes from myeloid stem cell?
- megakaryocytes
- erythrocytes
- monocytes
- granulocytes
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what do erythropoietin and thrombopoietininfluence growth of?
- red blood cells
- megakaryocytes
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normal blood volume is :
5-6 litres
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WBC count and lifespan:
- 5000-10,000/mm3(mcl)
- lifespan 13-20 days
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lymphocytes
- specific immunity
- T-cells and B-cells
- 20-40%
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Monocytes
- macrphages(big eaters)
- 2-8%
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Eosinophils
- allergic reactions/ worms
- 1-4%
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Basophils
- histamine- runny nose, eyes. Stops entry of other pathogens
- <1%
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RBC count and lifespan
- 4.2-5.4 million/ mm3 (mcl)
- lifespan= 120days
- 2 million per sec
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Platelets count and lifespan
- 150,000-350,000
- lifespan= 5-9 days
- 5,000-10,000/ megakaryocyte
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hemoglobin values in male and females
- males: 13.5-17.5 g/dL
- females: 12-16 g/dL
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what is hematocrit?
- ratio of RBC's to total blood volume
- males: 40-54%
- females: 37-47%
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blood system organs:
- lymph nodes
- bone marrow- cell production
- liver- prothrombin and fibrinogen for blood clotting
- spleen- lymphocytes, plasma cells, and antibodies
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RBC production in bone marrow:
- erythropoietin- horomone that trigger red cell production
- w/o this not proper cell formation
- folic acid, B12- need for proper cell division
- iron- bind O2 and make hemoglobin
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erythropoiesis
low blood O2 in kidney cause secretion of erythropoietin which stimulates erythropoiesis by bone marrow. This increases RBC's, increase O2. This help relieve intial erythropoietin secretion.
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bi concave disks (RBC)
- no nucleus
- flexible
- more SA, more diffusion and more flexible
- when red blood cell old can lose felixibility and get stuck in capillaries which can cause problems
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osmotic changes to red blood cells
- cell shape changes with osmolarity of plasma
- hyoptonic- more water in cell
- isotonic- same # of particles in solution and cell
- hypertonic - crenated shrivel cell
- water move to outside
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red blood cells removed by ______ and ________
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iron homeostasis and metabolism
- 1,iron from diet
- 2. iron absorbed
- 3.transferrin transport Fe in plasma
- 4. liver store excess iron as ferritin
- 5. bone marrow use Fe to make hemoglobin
- 6. spleen converts to bilirubin
- 7.liver metabolize bilirubin and excrete in bile
- 8.bilirubin excreted in urine
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Anemia
- decrease O2
- decrease RBC count
- dreace Hb
- decrease Hct
iron defiency, folic acid deficiency, pernicious, hemolytic, sickle cell, aplastic
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symptoms of anemia
- pallor
- fatigue
- shortness breath
- headache
- irritability
- fast HR
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iron deficiency anemia (causes and treatment)
- low Fe-> low Hb-> decrease cell size (RBC count normal)
- casues:
- blood loss- lose iron that want to recycle
- low dietry intake
- microcytic cells
- low hctlow hbTreatment
- increase iron intake
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folic acid deficiency anemia
- need folic acid for maturation RBC/ DNA production
- causes:
- poor dietover cooked vegetables
- alchohol= decrease folic acidTreatment
- increase folic acid intake
- green and yellow vegetables; citrus fruits
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Pernicious Anemia
- not enough absorption vit B12
- B12 needed for cell division
- Macrocytic cells:
- Low RBC countHct and Hb normalRBC big in size
- Treatment:
- monthly injection vit B12
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Hemolytic Anemia
- destruction RBC
- antigen-antibody reaction, immune disorderjaundice- yellow skin and eyes
- Treatment:
- exchange tanfusion/ splenectomy
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Sickle cell anemia
- hereditary
- sickle shape RBC
- doesnt travel smotthly through vesselsno cure
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Aplastic Anemia
- bone marrow cannot produce blood components
- casues:
- chemotherapy
- radiation
- viruses
- toxins
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other RBC disorders
- polycythemia (primary, secondary, relative)
- symptoms:
- red skin and mucous membranes
- bloodshot eyes
- increased blood volume and pressure
- enlarged spleen
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primary polycythemia
- bone marrow tumor
- increase RBC b/c increase sensitivity to Epo
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secondary polycythemia
- high levels erythropoietin cause high level RBC
- RBC abnormal structure
- not enough oxygen cause high Epo
- ex: kidney tumor-> increase Epo-> increase RBC
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Relative polycythemia
- increase in Hct= less plasma so increase RBC volume
- number red blood cell normal
- ex dehydration
- danger include
- decreased oxygen
- decreased blood flow
- increased clotting
- treatment= blood doping
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percentage of hematocrit for normal, anemia, polycythemia and dehydration
- 45%=normal
- 30%=anemia
- 70%=polycythemia
- 70%=dehydration
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white blood cell disorders
- leukocytopenia
- leukocytosis
- neutropenia
- mononucleosis
- leukemia
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leukocytopenia
- decrease WBC
- weaken immune system
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leukocytosis
- increase WBC
- normal response to small infections
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neutropenia
- decrease neutrophils
- increase risk for bacterial and fungal infectionsdestruction neutrophils
- cancer therapyrheumatoid arthritis ( inflammation joint surrounding tissue)
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mononucleosis
- increase monocytes
- symptoms:
- fatigue, sore throat swollen glandstreatment:
- rest, analgesics( painkillers)
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leukemia
- cancer
- increase immature leukocytes
- acute or chronic
- myelegenous=affecting bone marrow
- lymphocyte= affect lymph nodes
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symptoms of leukemia
- anemia
- fatigue
- headache
- sore throat
- bleeding mucous membranes
- bone and joint pain
- enlarged lymph nodes, liver and spleen
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what is hemostasis and the threee mechanisms
- stopping bleeding
- 3mechanisms:
- vascular spasm-vasoconstrictionplatelet plugcoagulation
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Healing process
- clot formation (intrinsic)
- clot reaction
- clot destruction
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platelet plug
- get sticky and adhere to collagen
- activated platelets secrete chemotaxins
- -ADP,serotonin and thrombaxane A2attract other paltelets
- activate and aggregate
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platelet plug formation
- 1.collagen bind and activate platelet
- 2.release of platelet factors
- 3.factors attract platelet
- 4.platelet go into platelet plug
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undamaged tissue secrete;
- prostacyclin
- prevent platelet aggregationNitric Oxide
- vasodilator
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Effect of aspirin
Inhibit thrombaxane->decrease activation platelet->decrease clotting-> can cause heart attacks
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what you need for coagulation
- clotting factors-in the liver
- platelet factor- if dont have it can bruise easily
- clotting cofactor
- plasma calcium- dont have calcium slow down clotting
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extrinsic pathway
- shorter
- faster
- less fibrin
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Anti-clotting system
- tissue factor pathway inhibitor
- slows extrinsic pathwayProtein C
- activated by thrombinslow down both pathwaysAntithrombin
- secreted by undamaged endothheliuminactivates thrombinHeparin, coumadin
- inhibit plateletsturn of blood formation and intrinsic/extrinsic pathways
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fibronolysis
- break down of clot after healing
- secrete tPA(tissue plasminogen activator)- this comes from liver to convert to plasmin to make active and break down the clot
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disorders of platelets
- hemophelia
- thrombocytopenia
- disseminated intravascular coagulation
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hemophelia
- hereditary bleeding disorder common among males
- lack protein for clot formation
- symptoms:
- nosebleedsbruisinglots bleedingtreatment:blood transfusion, clotting proteins
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thrombocytopenia
- low platelet-> no platelet plug-> no coagulation
- know if you have this by platlelt vcount and bleeding time
- symptoms:
- abnormal bleedingpetechiae- small purple spot on skin from damaged blood vesselecchymoses-bruising hematuria
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treatment for thrombocytopenia
- avoid tissue trauma
- vitamin K
- transfusion of platelets
- splenectomy
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Disseminated intravascular coagulation
- abnormal clotting followed by abnormal bleeding
- followed by major trauma(surgery, complicated child birth)
- multiple clots in capillaries
- symptoms:
- Petechiae/ ecchymosishematoma
- hematuria/ hematamesisGI bleeding
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