Wize University Physiology Textbook > Blood
Chapter Intro
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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