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Plasma Composition

  • Proteins in blood: albumin, fibrinogen, globulin
  • Albumin contributes the most to plasma's colloidal osmotic pressure (c.o.p.)

Capillary Wall Transport

  • Capillaries are not permeable to plasma proteins --> creates colloidal osmotic pressure (c.o.p.)
  • C.o.p. opposes hydrostatic pressure
  • C.o.p. "holds" water in plasma
  • Hydrostatic pressure "pushes" water out

  • Edema can be caused by:
  • 1. Increases in hydrostatic pressure (e.g. traveling long hours)
  • 2. Decreases in c.o.p (oncotic) pressure (e.g. low protein production)
  • 3. Increases in capillary permeability
  • 4. Decreases in lymphatic drainage (e.g. accidental damage to lymphatics during cancer surgery)

Blood Cells

  • All blood cells are derived from hematopoietic stem cells
  • Location of blood production varies throughout life
  • Red Blood Cells:
  • No nuclei, no organelles, survive 120 days
  • NOTHING can increase their lifespan
  • Erythropoietin (EPO) (produced by kidney) stimulates its production in response to low oxygen
  • stimulates proliferation of erythrocyte progenitor cells AND their differentiation into mature RBCs
  • Have hemoglobin to carry oxygen
  • Can increase RBC production:
  • High altitude
  • Lung problems
  • Exercise
  • Taken out of circulation by macrophages --> production of pigmented molecule bilirubin
  • Too much bilirubin in blood = jaundice
  • Bilirubin goes into bile
  • Platelets:
  • Derived from megakaryocytes
  • Survive 7-10 days
  • No nucleus, many granules

Blood Disorders

  • Anemia = decreased ability of blood to carry oxygen to tissues
  • Look at hemoglobin amount, RBC count, hematocrit
  • Causes:
  • Decreased production of RBCs
  • Iron deficiency: hypochromic, microcytic RBCs
  • Aplastic anemia (bone marrow failure): normal looking RBCs
  • Low EPO: normal looking RBCs
  • Improper maturation of RBCs
  • Vitamin B12 deficiency (aka pernicious anemia): impaired DNA production = macrocytic, normochromic RBCs
  • Folic acid deficiency: impaired DNA production = macrocytic, normochromic RBCs

  • Polycythemia = increased amount of RBCs
  • Causes blood to be sluggish and viscous = bad
  • Can be normal = physiological
  • Living at high altitude
  • Athletes
  • Chronic lung problems (i.e. from smoking)
  • Can from disease = pathological
  • Tumors producing EPO
  • Bone marrow disease

Hemostasis

  • Process to stop bleeding
  • Primary Hemostasis
  • Platelet plug formation (white thrombus)
  • Secondary Hemostasis
  • Clotting cascade to stabilize clot (red thrombus) --> end goal is fibrinogen converted to fibrin (can be further crosslinked by F XIIIa)
  • Can be activated by intrinsic and extrinsic (faster) pathways
  • Platelets also involved, but not main "stars"
  • Requires Ca2+/phospholipid, and vitamin K at for certain factors
  • Problems:
  • In primary hemostasis
  • low platelets or platelets not functioning well
  • Aspirin
  • In secondary hemostasis
  • issues with clotting factors --> low production of factors, low vitamin K, anti-coagulant drugs, liver disease