what happens when blood is centrifuged
formed elements (eukaryocytes, leukocytes, and platelets) sink to the bottom (45%), buffy layer in middle with leukocytes and platelets, plasma is at the top (55%)
what is in plasma
90% water, nutrients, salt (electrolytes), respiratory gases (oxygen, co2), hormones, plasma proteins, waste products from kidneys filtering,
plasma proteins
most abundant substance in plasma, made by liver, 3 kinds- albumin, clotting proteins (fibrinogens), antibodies (globulins)
albumin
plasma protein, regulates osmotic pressure
fibrinogen (clotting proteins)
plasma protein, converted to fibrin during clotting process, helps stem blood loss when a blood vessel is injured
globulins (antibodies)
plasma proteins, help protect the body from pathogens
formed elements
erythrocytes, leukocytes, platelets, cellular fragments
erythrocytes
most abundant formed element, 4-6 million per mm3, red biconcave disks, anucleate, sacs of hemoglobin, most organelles are ejected, transport oxygen to hemoglobin molecules, also move small amounts of o2
leukocytes
white blood cells, five kinds; neutrophils, lymphocytes, monocytes, eosinophils, basophils, 4-11,000 per mm3
platelets
50-500,000 per mm3, irregularly shaped deep purple cell fragments, needed for normal blood clotting, initiate clotting cascade by clinging to torn area, help control blood loss from broken blood vessels
hematocrit
the ratio of the volume of red blood cells to the total volume of blood
average number of hemoglobin
250 million per erythrocyte
red blood cell disorders
anemia, sickle cell anemia, polycythemia
anemia
decrease in oxygen-carrying ability of blood, 3 types- decrease in RBC #, inadequate hemoglobin content in RBC, abnormal hemoglobin in RBC
sickle cell anemia
abnormally shaped hemoglobin in RBC
polycythemia
excessive or abnormal increase in number of erythrocytes
hemoglobin
iron containing protein, binds strongly but can be reversed to oxygen, has four binding sites for oxygen, each erythrocyte has 250 million, normal blood has 12-18 g per 100 ml of blood
types of anemia from decrease in RBC
hemorrhagic anemia, hemolytic anemia, pernicious anemia, aplastic anemia
iron deficiency anemia
inadequate hemoglobin content in RBC
positive chemotaxis
response of leukocytes to chemicals released by damaged tissues
leukocytosis
WBC above 11,000 leukocytes per mm3, usually indicates an infection
leukopenia
abnormally low leukocyte level, commonly caused by certain drugs like corticosteroids or chemotherapy
leukemia
excessive WBC causes bone marrow to become dangerous
granulocytes
granules in cytoplasm, lobed nuclei; neutrophils, eosinophils, basophils
agranulocytes
no granules, spherical, oval, or kidney shaped nuclei; lymphocytes and monocytes
never let monkeys eat bananas
list of WBC from most to least abundant; neutrophils, lymphocytes, monocytes, eosinophils, basophils
neutrophils
multilobed nucleus with fine granules, destroy infection by ingesting them and killing them
lymphocytes
part of immune system, produces antibodies to fight infection
monocytes
agranular leukocyte that can migrate into tissues and transform into a macrophage.
eosinophils
large red cytoplasmic granules, found in response to allergies and worms
basophils
have histamine containing granules, initiate inflammation
hematopoiesis
blood cell formation, occurs in red bone marrow, all blood cells are derived from a hemocytoblast (common stem cell), lymphoid cells produce lymphocytes, myeloid stem cells produce everything else
formation of red blood cells
formation happens when erythrocytes are unable to grow, divide, or synthesize proteins (100-120 days), then are eliminated by the phagocytes in the liver and spleen, they are then replaced by division of hemocytoblasts in the red bone marrow
how is the rate of formation of red blood cells controlled
erythropoietin, a hormone produced by kidneys as a response to reduced oxygen levels in the blood, homeostasis is maintained by a negative feedback from blood oxygen levels
how are platelets formed
produced by cell fragments from a hormone called thrombopoietin controlling the production
thrombocytopenia
a bleeding disorder in which platelets are deficient, even normal movements can cause bleeding from small blood vessels that require platelets for clotting
when does shock begin in blood loss
15-30% causes weakness, over 30% causes hypovolemic shock
thrombus
a clot in an unbroken blood vessel, can potentially be deadly if it is in the heart area
embolus
thrombus that breaks away into the blood stream, can clog vessels in critical areas like the brain
hemophilia
hereditary bleeding disorder, noraml clotting factors are missing
ABO blood group
based on presence/absence of two antigens; type A or type B, if someone has neither they are called blood type O
agglutination
how blood is typed, put antibodies in a sample of blood, if the blood clumps up then they have that antigen in their body
antibody
part of immune system, searches for antigens, if they are bad then an immune response is triggered
antigen
marker on outside of cell, tells "what am i :)?"
universal donor
type O; they have no antigens and therefore cannot trigger any antibodies in other bodies
universal recipient
type AB; they have all antigens so no antibodies in their body are triggered
cross matching
testing for agglutination of donor RBCs by the recipients serum and vice versa
hemolytic disease of newborn
in second pregnance if the mother if Rh-, and the baby is Rh+, the mothers immune system creates antibodies to attack the second babies Rh+ blood
physiologic jaundice
in infants when the liver cannot rid the body of hemoglobin breakdown fast enough
Rh blood group
named by presence or absence of one of eight Rh antigens (agglutinogen D) that was in Rhesus monkeys, Rh+ blood doesnt make antibodies, Rh- blood does, but only after it is exposed to Rh+
RhoGam
shot given to pregnant mothers to prevent buildup of anti-Rh+ antibodies when the baby is Rh+ and mother is Rh-
hemostasis
vascular spasms contract blood vessel, platelets stick to damaged site on endothelium, they then release serotonin which attracts more platelets to form a platelet plug, then PF3 is released from platelets, tissue factor in damaged tissue and calcium and other clotting factors in blood plasma are released that create the prothrombin activator, which converts prothrombin into thrombin, which then joins soluble fibrinogen that converts into insoluble fibrin which forms the mesh