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Vocabulary flashcard set covering blood components, plasma proteins, erythrocyte function, blood typing, leukocyte classification, platelets, and hemostasis.
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Erythrocytes (RBCs)
Biconcave blood cells lacking a nucleus and mitochondria that contain high amounts of hemoglobin and function primarily to transport O2 and CO2.
Leukocytes (WBCs)
Nucleated blood cells with organelles that provide immune defense and protection, functioning primarily in tissues after leaving the bloodstream.
Platelets (Thrombocytes)
Small cell fragments (2–4μm in diameter) without a nucleus, derived from megakaryocytes, that play a central role in hemostasis and blood clotting.
Blood Plasma Composition
The liquid matrix of blood, constituting 47–63% of total blood volume, consisting of 90% water, 9% plasma proteins, and 1% other solutes.
Albumin
The most abundant plasma protein (60%), synthesized by the liver, which maintains blood fluid balance, blood volume, and blood viscosity.
Globulins
Plasma proteins (36%) produced by plasma cells that function as antibodies to provide immune protection.
Fibrinogen
A soluble plasma protein (4%) synthesized by the liver that is converted into insoluble fibrin threads during blood coagulation.
Blood Viscosity
The thickness or resistance to flow of blood, which is approximately 2× greater than water due to plasma proteins like albumin.
Blood Osmolarity
The concentration of dissolved particles in the blood that determines its water-pulling power, with a normal value of approximately 300osmoles (isotonic).
Erythropoiesis
The process of red blood cell production occurring in the red bone marrow, taking about 3–5days to complete.
Erythropoietin (EPO)
A hormone released primarily by the kidneys (85%) and liver (15%) in response to hypoxemia to stimulate red bone marrow to produce RBCs.
Hemolysis
The rupture and breakdown of old or fragile red blood cells (after their ∼120day lifespan), carried out by macrophages in the spleen and liver.
Carbonic Anhydrase (CA)
An enzyme in erythrocyte cytoplasm that catalyzes the conversion of carbon dioxide and water into carbonic acid: CO2+H2O→H2CO3.
Hematocrit (Hct)
The percentage of total blood volume composed of red blood cells, normally 42–52% in men and 37–48% in women.
Polycythemia
A condition characterized by an excess of red blood cells, causing increased blood viscosity, blood volume, and blood pressure.
Anemia
A deficiency of red blood cells or hemoglobin leading to reduced oxygen delivery to tissues, decreased blood viscosity, and fatigue.
Agglutinogens
Surface antigens (glycoproteins and glycolipids) located on red blood cell membranes that determine ABO and Rh blood types.
Agglutinins
Antibodies present in blood plasma (such as Anti-A or Anti-B) that react against foreign RBC antigens.
Agglutination
The clumping reaction that occurs when plasma agglutinins bind to corresponding foreign agglutinogens on red blood cells.
Hemolytic Disease of the Newborn (HDN)
A condition in which maternal Anti-D antibodies cross the placenta and attack the RBCs of an Rh+ fetus in an sensitized Rh− mother.
Neutrophils
The most abundant granulocytes (1st in abundance) whose primary function is to fight bacterial infections.
Lymphocytes
Agranulocytes (2nd in abundance) that provide immune defense, destroy infected/cancer cells, produce antibodies, and serve immune memory.
Monocytes
Large agranulocytes (3rd in abundance) that leave blood vessels to become macrophages and phagocytose pathogens and tissue debris.
Eosinophils
Granulocytes (4th in abundance) specialized in fighting parasitic infections and involved in allergic reactions.
Basophils
The least abundant granulocytes (5th in abundance) that secrete histamine and heparin to promote inflammation.
Megakaryocyte
A giant bone marrow cell with a multi-lobed nucleus that extends proplatelet projections into blood vessels to release platelets into circulation.
Hemostasis
The three-step process that stops bleeding from a damaged vessel: vascular spasm, platelet plug formation, and blood coagulation.
Vascular Spasm
The initial rapid constriction of a injured blood vessel to minimize blood loss, facilitated by serotonin released from platelets.
Platelet Plug Formation
The second step of hemostasis where platelets adhere to exposed collagen, release ADP and thromboxane A2, and aggregate into a temporary seal.
Coagulation
The third step of hemostasis where a cascade of reactions converts fibrinogen into a mesh of insoluble fibrin threads to form a stable blood clot.
Plasmin
An active fibrin-dissolving enzyme formed from plasminogen via kallikrein and Factor XII that breaks down clots (thrombolysis/fibrinolysis).
Heparin
A natural anticoagulant produced by the body that interferes with the formation of prothrombin activator to inhibit blood clotting.
Warfarin (Coumadin)
A synthetic anticoagulant medication that acts as a vitamin K antagonist, reducing liver synthesis of blood clotting factors.
Hemophilia
An inherited bleeding disorder caused by a deficiency in a specific clotting factor (e.g., Hemophilia A lacking Factor VIII; Hemophilia B lacking Factor IX).
Embolus
A blood clot or intravascular debris that breaks free from its site of origin and travels in the bloodstream until it blocks a smaller vessel.