Circulatory System: Blood Components, Hemostasis, and Blood Typing Flashcards

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Vocabulary flashcard set covering blood components, plasma proteins, erythrocyte function, blood typing, leukocyte classification, platelets, and hemostasis.

Last updated 6:44 AM on 9/3/26
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35 Terms

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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 O2O_2 and CO2CO_2.

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Leukocytes (WBCs)

Nucleated blood cells with organelles that provide immune defense and protection, functioning primarily in tissues after leaving the bloodstream.

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Platelets (Thrombocytes)

Small cell fragments (24μm2\text{--}4\,\mu\text{m} in diameter) without a nucleus, derived from megakaryocytes, that play a central role in hemostasis and blood clotting.

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Blood Plasma Composition

The liquid matrix of blood, constituting 4763%47\text{--}63\% of total blood volume, consisting of 90%90\% water, 9%9\% plasma proteins, and 1%1\% other solutes.

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Albumin

The most abundant plasma protein (60%60\%), synthesized by the liver, which maintains blood fluid balance, blood volume, and blood viscosity.

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Globulins

Plasma proteins (36%36\%) produced by plasma cells that function as antibodies to provide immune protection.

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Fibrinogen

A soluble plasma protein (4%4\%) synthesized by the liver that is converted into insoluble fibrin threads during blood coagulation.

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Blood Viscosity

The thickness or resistance to flow of blood, which is approximately 2×2\times greater than water due to plasma proteins like albumin.

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Blood Osmolarity

The concentration of dissolved particles in the blood that determines its water-pulling power, with a normal value of approximately 300osmoles300\,\text{osmoles} (isotonic).

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Erythropoiesis

The process of red blood cell production occurring in the red bone marrow, taking about 35days3\text{--}5\,\text{days} to complete.

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Erythropoietin (EPO)

A hormone released primarily by the kidneys (85%85\%) and liver (15%15\%) in response to hypoxemia to stimulate red bone marrow to produce RBCs.

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Hemolysis

The rupture and breakdown of old or fragile red blood cells (after their 120day\sim 120\,\text{day} lifespan), carried out by macrophages in the spleen and liver.

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Carbonic Anhydrase (CA)

An enzyme in erythrocyte cytoplasm that catalyzes the conversion of carbon dioxide and water into carbonic acid: CO2+H2OH2CO3CO_2 + H_2O \rightarrow H_2CO_3.

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Hematocrit (Hct)

The percentage of total blood volume composed of red blood cells, normally 4252%42\text{--}52\% in men and 3748%37\text{--}48\% in women.

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Polycythemia

A condition characterized by an excess of red blood cells, causing increased blood viscosity, blood volume, and blood pressure.

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Anemia

A deficiency of red blood cells or hemoglobin leading to reduced oxygen delivery to tissues, decreased blood viscosity, and fatigue.

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Agglutinogens

Surface antigens (glycoproteins and glycolipids) located on red blood cell membranes that determine ABO and Rh blood types.

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Agglutinins

Antibodies present in blood plasma (such as Anti-A or Anti-B) that react against foreign RBC antigens.

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Agglutination

The clumping reaction that occurs when plasma agglutinins bind to corresponding foreign agglutinogens on red blood cells.

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Hemolytic Disease of the Newborn (HDN)

A condition in which maternal Anti-D antibodies cross the placenta and attack the RBCs of an Rh+Rh^+ fetus in an sensitized RhRh^- mother.

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Neutrophils

The most abundant granulocytes (1st1\text{st} in abundance) whose primary function is to fight bacterial infections.

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Lymphocytes

Agranulocytes (2nd2\text{nd} in abundance) that provide immune defense, destroy infected/cancer cells, produce antibodies, and serve immune memory.

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Monocytes

Large agranulocytes (3rd3\text{rd} in abundance) that leave blood vessels to become macrophages and phagocytose pathogens and tissue debris.

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Eosinophils

Granulocytes (4th4\text{th} in abundance) specialized in fighting parasitic infections and involved in allergic reactions.

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Basophils

The least abundant granulocytes (5th5\text{th} in abundance) that secrete histamine and heparin to promote inflammation.

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Megakaryocyte

A giant bone marrow cell with a multi-lobed nucleus that extends proplatelet projections into blood vessels to release platelets into circulation.

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Hemostasis

The three-step process that stops bleeding from a damaged vessel: vascular spasm, platelet plug formation, and blood coagulation.

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Vascular Spasm

The initial rapid constriction of a injured blood vessel to minimize blood loss, facilitated by serotonin released from platelets.

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Platelet Plug Formation

The second step of hemostasis where platelets adhere to exposed collagen, release ADPADP and thromboxane A2A_2, and aggregate into a temporary seal.

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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.

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Plasmin

An active fibrin-dissolving enzyme formed from plasminogen via kallikrein and Factor XII that breaks down clots (thrombolysis/fibrinolysis).

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Heparin

A natural anticoagulant produced by the body that interferes with the formation of prothrombin activator to inhibit blood clotting.

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Warfarin (Coumadin)

A synthetic anticoagulant medication that acts as a vitamin K antagonist, reducing liver synthesis of blood clotting factors.

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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).

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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.