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11 Cards in this Set

  • Front
  • Back
What are the components of blood?
-Plasma
-Erythrocytes
-Leukocytes
-Platelets
Functions of blood
-Transports:
-______ from lungs to organs/cells
-______ from cells to lungs
-______ from digestive system & storage
-______ to liver & kidneys
-_______
-Regulates body ________
-______ (white blood cells)
-_______ (platelets)
-Stabilizes _______ balance
-Stabilizes ________-buffer for acids & bases
Functions of blood
-Transports
-Oxygen from lungs to organs/cells
-Carbon dioxide from cells to lungs
-Nutrients from digestive system & storage
-Wastes to liver & kidneys
-Hormones
-Regulates body temperature
-Immunity (white blood cells)
-Clotting (platelets)
-Stabilizes water balance
-Stabilizes pH-buffer for acids & bases
Viscosity:_____ _____ _____
(thickness/stickyness)
-Blood is 4.5-5.5 times _____ viscous than water
-Plasma alone is 2 times ______ viscous than water
-Too many or too few ______ ____ _____ changes the viscosity of blood and puts a strain on the heart
Viscosity: Resistance to flow (Thickness/stickyness)
-Blood is 4.5-5.5 times more viscous than water
-Plasma alone is 2 times more viscous than water
-Too many or too few red blood cells puts a strain on the heart
Osmolarity: Total molar concentration of dissolved particles in 1 L of solution due to transfer of nutrients and wastes between the _____ & ______ _____
-If too high: blood stream absorbs too much fluid from the tissues, thus causing _______
-If too low: bloodstream transfers too much fluid to tissues, resulting in ______ & _______
Osmolarity: Total molar concentration of dissolved particles in 1 L of solution due to transfer of nutrients and wastes between the blood & tissue fluids
-If too high: bloodstream absorbs too much fluid from the tissues, thus causing hypertension
-If too low: bloodstream transfers too much fluid to tissues, resulting in edema & hypotension
What are the functions of hemoglobin?
Transports oxygen & carbon dioxide
Polycythemia: _____ of RBCs
-Primary polycythemia is due to _____ of erythropoietic cell line in red bone marrow
-RBC count as high as _____
million; hematocrit of ____%
-Secondary Polycythemia: RBC count up to ______ million
-_______-more RBCs due to
less plasma
-_____ _____-extended stay->
RBC count rises to 7-8 million
-_____ _____-endurance
trained athletes have 6.6
million RBC due to higher
oxygen requirements
-_______-less lung tissue, but
RBC can't correct for this, but
erythropoietin is still released,
causing excess RBC production
-Dangers of polycythemia
-increased blood _____,
_____, & _____ can lead to
______ _____, _____ _____ &
_____ _____ which in turn lead
to _____, ______, _____
_____
Polycythemia: Excess of RBCs
-Primary Polycythemia is due to cancer of erythropoietic cell line in red bone marrow
-RBC count as high as 11
million; hematocrit of 80%
-Secondary Polycythemia-RBC count up to 8 million
-dehydration-more RBC due to
less plasma
-High altitude-extended stay at
high altitude->RBC count rises
to 7-8 million RBCs
-Physical conditioning:
endurance trained athletes
have 6.5 million RBC due to
higher oxygen requirements
-Emphysema-less lung tissue,
but RBCs can't correct for this,
but erythropoietin is still
released, causing RBC
production
-Dangers of polycythemia
-increased blood volume,
pressure and viscosity can lead
to poor circulation, heart strain
& clogged capillaries
-which in turn leads to
embolism, stroke, heart
failure
Anemia: Deficiency of _____ or ____
-Iron-deficiency anemia: dietary iron deficiency=______ ______
Pernicious Anemia: Inadequate ______ ______
-______ ______: Lack of
intrinsic factor
Anemia: Deficiency of RBCs or Hb
-Iron-deficiency anemia: dietary iron deficiency=less Hb
-Pernicious anemia: inadequate B12
-Poor nutrition: lack of intrinsic
factor (facilitates B12
absorption)
Sickle-cell is hereditary _____ defect
-Recessive allele modifies _____ structure
-_____ _____ for HbS have
sickle-cell disease
-______ for HbS have sickle-
cell trait
-sickle cell disease individual has shortened life
-Die by age ____ without
treatment; some live to ____
years with treatment
-HbS turns to gel in _____
oxygen concentrations
-RBCs become deformed
______, thus blocking blood
vessels
-HbS in indigestible to malaria
parasites so gene persists
despite its harmful effects to
the ______ individuals
Sickle cell is hereditary Hb defect
-Recessive allele modifies hemoglobin structure
-homozygous recessive for HbS
have sickle-cell disease
-heterozygous for HbS have
sickle-cell trait
-Sickle cell disease individual has shortened life
-Die by age 2 without
treatment; some live to 50 yrs
with treatment
-HbS turns gel in low oxygen
concentrations
-RBCs become deformed
and agglutinate, thus
blocking blood vessels
-HbS is indigestible to malaria parasites so gene persists despite its harmful effects to the homozygous individuals
Hemophilia
-genetic lack of _____ _____ affects coagulation
-sex-linked recessive in _____ (inherit from mother)
-Hemophilia A is missing clotting factor _____
-Hemophilia B is missing clotting factor _____
-Physical exertion causes _____ & _____ ______
-transfusion of ______ or
______ _______ ______
-Factor VIII now produced by
______ bacteria
Hemophilia
-genetic lack of any clotting factor affects coagulation
-sex-linked recessive in males (inherit from mother)
-hemophilia A is missing clotting factor VIII
-hemophilia B is missing clotting factor IV
-Physical exertion causes bleeding & excruciating pain
-transfusion of plasma or
purified clotting factors
-Factor VIII now produced by
transgenic bacteria
Disseminated intravascular coagulation (DIC)
-Widespread _____ of blood with unbroken vessels
-Triggered by ______ (septicemia) or if blood slows down or stops as in ______ ______
Disseminated intravascular coagulation
-Widespread clotting of blood within unbroken vessels
-Triggered by bacteria (septicemia) or if blood slows down or stops as in cardiac arrest
Prevention of Inappropriate Coagulation
-______ Repulsion
-Platelets do not adhere to
_____-coating
-______ Dilution
-Normally diluted by _____
flowing blood
-Heart slowing in shock can
result in _____ _____
-Natural anticoagulants
-_______: produced by the
liver deactivates thrombin
before it can act on fibrinogin
-_____ secreted by basophils &
mast cells interferes with
formation of prothrombin
activator
Prevention of Inappropriate Coagulation
-Platelet repulsion
-platelets do not adhere to
prostacyclin-coating
-Thrombin dilution
-normally diluted by rapidly
flowing blood
-heart slowing in shock can
result in clot formation
-Natural Coagulants
-antithrombin produced by the
liver deactivates thrombin
before it can act on fibrinogen
-Heparin secreted by basophils
& mast cells interferes with
formation of prothrombin
activator