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Blood

125 cards·by browncl4
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______Strucrure-->Blood + Cardiovascular System
Circulatory System
In the _________, it functions in aiding respiratory sytem(O2+CO2 transport)
circulatory system
In the circulatory system also functions in____(digestive system)
nutritive
In the _____ system, it functions in excretion,homeostasis,regulation of body temp.
circulatory system
Finally, the circulatory system functions in___.
chemical communication chromosome and protection of immune system
How many liters of whole blood are in a man 70 kg (155lb.)?
5.6 liters
In the whole blood there are three components that make them up, what are they?
plasma, cells and hematocrit
___ are non-cellular and pH is neutral 7.35-7.45.
Plasma
_____varies in pH levels which lead tometabolic problems with protein, ions, enzymes, antibodies and hormones.
plasma
In cells there's____(erythrocytes)
RBC
In cells there's____(leukocytes)
WBC
____ is 91-92% of water
Plasma
In cells there's___(thrombocytes)
Platlets
___ is % of solids in blood, mostly cells
Hematocrit
In a test tube there's 1% white coat and ~45%___
solids of hematocrit
In blood plasma there's blood plasma proteins such as_____,___,___.
Albumins, Globulins and Fibrinogen
In___ 60% is produced by the liver.
Albumins
In ____36% is produced mostly by liver.
Globulins
____ is osmotic pressure and also control direct effect on blood volume.
Albumins
In_____high BP= cut out of salts and soon enough you'll need a water pill which transport ions, drugs & hormones.
Albumins
In ___ there are alpha, beta and gamma.
Globulin
_____transport lipids and fats.
alpha
_____soluble vitamins (A,D,C,K)
beta
What are the two types of WBCs?
Granulocytes and Agranulocytes
______ are 70% of WBCs
Granulocytes
____ are composed of Neutrophils, Eosinophils and Basophils
Granulocytes
Granulocytes are composed of 15-60% of ___, which fight bacterial infections
Neutrophils
Granulocytes are composed of > 1% of ___hepanin and histamine,which promote inflammation and inhibit blood clotting
Basophils
____ are composed of monocytes and lymphocytes
Agranulocytes
Agranulocytes are composed of 3-9%____ which become macrophages
monocytes
What are the three irregularities/diseases of WBC Counts?
Leukocytosis, Leukpenia and Leukemia
____has greater than 10,000/mm3 leukocytes
Leukocytosis
____has less than 5,000/mm3 of leukocytes
Leukopenia
__ have granular cytoplasm in a drop of blood.
granular cytoplasma
____ are platlets, in btwn RBC & WBC formed from megakarycytes
Thrombocytes
___are non nucleated and repair damage of blood vessels
Thrombocytes
There's are a few more____ in male than female
RBCs
Main function of RBC and carrying oxygen through body depends on the amount of____.
hemoglobin
1/3 by volume of RBCs are ____
hemoglobin
_____ release oxygen, is darker and cyanosis from hypoxia.
deoxyhemoglobin
____ is a defincency of RBC or hemoglobin where you can't carry enough oxygen properly to body for metabolism
Anemia
Nutritional, Hemorrhagic, Aplastic, Pernicious, Hemolytic and Sickle Cell are all the different types of ________.
Anemia
____ is not enough iron in diet.
Nutritional Anemia
____is excess bleeding internally or externally and not creating enough RBC.
Hemorrhagic Anemia
_____ is where parasites and cemotherapy effects RBC production.
Aplastic Anemia
In aplastic anemia,____is where there's not enough RBC and oxygen being produced
cemotherapy
____ is where there's not enough astrinsic factor, can't absorb enough vitamin B12 for proper RBC function.
Pernicious Anemia
During___RBC rupture.
Hemolytic Anemia
The problem with_____ is that not enough RBC work fast enough for oxygen to work properly.
Hemolytic Anemia
______is from parasitic and drug reaction
Hemolytic Anemia
____ is another type of anemia that's a defective gene and harder to correct
Thalosemma
______is a aggregated deoxyhemoglobin at low PO2 from decreased pH of RBC
Sickle Cell Anemia
People with____ are more resistant to malaria.
Sickle Cell Anemia
_____is known as Erythropoiesis
RBC Production
In____,there are 2.5 million ___produced per sec.
RBC Production, RBCs
Where are new RBC being produced?
in red bone marrow of spongy bone
Bones in skull, pelvis, vertebrae, sternum are producing alot if____.
RBCs
____ bone is found in ends of long bone such as femur, radius, ulna, humerus, all areas at epithelial end
Spongy
_____ is a stem cell that allows RBC or WBC to be driven out of Red Bone marrow.
Hemoblast
_____follow a pathway to create a leukocyte, create RBC or to carry thrombocyte structures
Hemoblast
_____form a erythroblast
Hemoblast
_____has a nucleus,replicate,reproduce, form mitosis erythrocyte (RBC)
erythroblast
_____is a hormone that controls RBC formation
Erythropoietin
_____monitored by liver and kidneys when oxygen concentrations drop and when PO2 drops to low
Erythropoietin
____stimulates erythropoietin
erythropoiesis
____ get red marrow, which increases the rate of erythroblasts being formed
erythropoietin
Once erthroblasts rate increases, then they create more__, increasing oxygen carrying capacity that are eventually shut down through___.
RBC, negative feedback
_____stop bleeding
Hemostatis
What are the three parts to Hemostatis?
Blood Vessel Spasm, Platelet Plug Formation, and Blood Coagulation
_____is a cut blood vessel and smooth muscle around these vessels constrict rapidly
Blood Vessel Spasm
In ____, cells and platlets around this area start to release a neurotransmitter called sertonin
Blood Vessel Spasm
___ causes an even greater spasm of smooth muscle in an area that's damaged
sertonin
During_______,which is rapid reaction and first blood vessel is damaged,erythrocytescomethrough and spasm occurs.
Platlet Plug Formation
Second in _______after spasm occurs, shut things down, Platlets start to come in contact with damaged ends of vessel
Platelet Plug Formation
Then finally in____after we contact damaged ends, ends start to stick together and all exposed collagen of RBCs form a platelet plug
Platelet Plug Formation
If damage is not too severe the ____maybe enough to stop bleeding (hemostatis)
platelet plug
____is the last line of defense which is a stronger plug, using a protein that's soluble that becomes insoluble after damage.
Blood Coagulation (Blood Clotting)
____form a strong sticky insoluble fiber called fibrin
Blood Clotting
______is the final pathway where blood clot is formed.
prothrombin activator
______does not require platelets.
Extrinsic Clotting Mechanism
____starts at tissue damage,release tissue thromboplastin(factor III), release Ca+ and cause prothrombin activator to get blood clot.
Extrinsic Clotting Mechanism
____is blood clotting that occurs in the tissue or skin; bruise.
Hematoma
____blood clotting occurs in intact blood vessel, that can exceed blood flow.
Thrombus
_______occurs in intrinsic clotting mechanism.
thrombus
____can be promblematic if repeat blood flow, and oxygen flow farther down.
thrombus
Clavitis in lower leg are blood clots from ____ in blood vessels
thrombus
____breaks off wall of blood vessel and travels through the whole circulatory system, which can be problematic b/c could lodge farther down
Thrombus
During____ thrombus lodges in a blood vessel in brain or heart, causing heart attack or stroke
embolus
During_____thrombus becomes dislodged and moves through circulation
embolus
_________(plasmin)
fibrolysin
______turns into plasmin.
plasminogen
_____eats up clot
plasma
What is a active protein that breaks up clot?
plasmin
In the_____ of inhibiting blood clot formation there's endothelium(thin layer of epipthelial cells).
Smooth lining of blood vessel
A way to inhibit a blood clotting is to have a ___pathway to go through
smooth
_____prevents activation of intrinsic blood clot.
Smooth lining of blood vessel
In inhibiting blood clotting______have prostacyclin that repel platelets so they don't stick to blood vessel wall.
negative charge on vessel lining
_____is a transfusion reaction,where RBC react with antigens and cause blood to clump together
agglutination
In inhibiting blood clot formation_______where thrombin stick and stay with fibrin threads once their formed
Fibrin threads adsorb thrombin
In inhibiting blood clot formation____which are combatted by alpha globulin proteins produced by liver
Antithrombin inactivation of thrombin
In inhibiting whole blood clot formation_____have basophils and mast cells to do this
Heparin
_____major anticoagulin, have mast cells produced in lungs and liver and interferes with forming prothrombin activator
Heparin
_______is lack of specific clotting factor causes bleeding
Hemophilia
In inhibiting blood clotting______ is red-green color blindness, recessive x-linked traits and keep blood clotting to aminimum.
Hemophilia
_____are specific proteins in blood plasma that work against antigens
Antibodies
An individual with type A with type A antigens that is not type A and have antigens against type A, what happens to blood?
blood cells clump up causing problems with transfusion reaction
______ have type A antigens and anti-B antibodies and it's ideal tranfusion is type A blood
Type A blood
____have neither antigens and produce anti-A and anti-B antibodies
Type O blood
During the ABO system_____person never seen a type B antigen, they still use antibodies against type B, spontaneous a few months after birth
Type A
Type AB (rarest blood type) is the_________.
Universal Receipient
If type AB has A-antigens that could react with type B anti-A bodies if type B is donated to AB causing a slight problem called the___
dilution effect
Why can't we give someone that is type AB, type O blood?
Antibodies in type O attack every RBC in type a type AB person
Rh is either on_ or not
RBC
___rarest blood type
AB-
___is 85% of population
Rh+
____(D Immune Globulin)
Rh Factor
If your Rh- and never come in contact with Rh+ & antigen you_____antibody
don't have
Rh+(father) x Rh-(mother)=Possibility of ___ baby
Rh+
In ____mother gets antibodies circling her system to Rh factor,which crosses barrier,protecting developing fetus.
Erythroblastosis Fetalis or Hemolytic Disease of the Newborn
developing fetus produces___.
Erythroblastosis
If mother is ____ and baby is Rh-, baby should be fine if mother hasn't produced any antibodies, which is found in ___.
Rh+, Erythroblastosis Fetalis
____ is gamma-globulin immune serum containing Rh antibodies
RhoGAM
____counters or neutralizes Rh Factor
RhoGAM
____inactivates the Rh antigen in the fetus
RhoGAM
During____mother's body can't become synthesized, so pregnancy's not an issue
RhoGAM