Blood Components and Physiology Flashcards

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Vocabulary flashcards covering blood composition, formed elements, WBC types, hemostasis, blood typing, and related blood pathologies.

Last updated 3:51 AM on 9/14/26
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30 Terms

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Hematocrit

The percentage of red blood cells in a blood sample, averaging about 45% in a normal centrifuged sample.

<p>The percentage of red blood cells in a blood sample, averaging about 45% in a normal centrifuged sample.</p>
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Hemoglobin

A tetramer metalloprotein found in red blood cells that comprises four globin subunits, each containing an iron atom bound to heme, responsible for delivering oxygen to tissues.

<p>A tetramer metalloprotein found in red blood cells that comprises four globin subunits, each containing an iron atom bound to heme, responsible for delivering oxygen to tissues.</p>
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Plasma

The clear, straw-colored liquid matrix of blood that constitutes approximately 55% of total blood volume and is 92% water.

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Serum

The liquid component of blood remaining after coagulation, devoid of clotting factors such as fibrinogen (serum=plasmafibrinogen\text{serum} = \text{plasma} - \text{fibrinogen}).

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Albumin

The most abundant plasma protein (60% of total), synthesized in the liver, which helps maintain colloid osmotic pressure.

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Non-protein Nitrogenous Substances

Molecules in plasma that contain nitrogen but are not proteins, including urea, uric acid, amino acids, creatine, and creatinine.

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Hematopoiesis

The process of blood cell formation, which occurs in red bone marrow from hemocytoblasts or hematopoietic stem cells.

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Erythrocytes

Red blood cells; non-nucleated biconcave discs containing hemoglobin that function in gas transport and have a lifespan of approximately 120 days.

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Erythropoietin

A hormone released by the kidneys and liver in response to low blood oxygen levels to stimulate red blood cell production.

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Anemia

A condition characterized by a reduced oxygen-carrying capacity of the blood due to a deficiency of red blood cells or hemoglobin.

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Sickle Cell Disease

An inherited red blood cell disorder caused by a genetic mutation in hemoglobin, resulting in abnormally shaped crescent/sickle red blood cells that can block blood flow.

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Granulocytes

A category of white blood cells with granular cytoplasm and short lifespans, comprising neutrophils, eosinophils, and basophils.

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Agranulocytes

A category of white blood cells that lack noticeable cytoplasmic granules, comprising monocytes and lymphocytes.

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Diapedesis

The process by which leukocytes squeeze between endothelial cells of capillary walls to exit the bloodstream and migrate toward infection sites.

<p>The process by which leukocytes squeeze between endothelial cells of capillary walls to exit the bloodstream and migrate toward infection sites.</p>
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Neutrophils

Phagocytic granulocytes with a 2–5 lobed nucleus that stain light purple, representing 54%–62% of leukocytes, and serving as the first responders to bacterial infections.

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Eosinophils

Granulocytes with bi-lobed nuclei and deep red granules, constituting 1%–3% of leukocytes, that defend against parasitic worm infestations and moderate allergic reactions.

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Basophils

Granulocytes with deep blue granules, representing less than 1% of leukocytes, that release histamine to promote inflammation and heparin to inhibit blood clotting.

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Monocytes

The largest white blood cells by size, making up 3%–9% of leukocytes, which leave the bloodstream to differentiate into macrophages that phagocytize large particles.

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Lymphocytes

Agranulocytes with a large spherical nucleus nearly filling the cell, comprising 25%–33% of leukocytes, that provide immunity via T cells and antibody-producing B cells.

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Platelets

Anucleated cellular fragments derived from megakaryocytes in red bone marrow that play a key role in hemostasis and release serotonin to induce vasoconstriction.

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Hemostasis

The physiological process that halts bleeding from a damaged blood vessel, involving vascular spasm, platelet plug formation, and blood coagulation.

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Extrinsic Clotting Mechanism

A coagulation pathway triggered by damaged blood vessel walls or external tissues releasing tissue thromboplastin (Factor III).

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Intrinsic Clotting Mechanism

A coagulation pathway triggered when blood contacts a foreign surface (such as collagen) without external tissue damage, initiating via Hageman factor XII.

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<p>Thrombus</p>

Thrombus

An abnormal blood clot that forms inside an intact blood vessel.

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Embolus

A blood clot or clot fragment that dislodges and travels through the bloodstream until it lodges in a narrower vessel.

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Universal Donor

Type O blood, which lacks A and B surface antigens on its red blood cells, allowing it to be transfused into recipients of any ABO blood type.

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Universal Recipient

Type AB blood, which lacks anti-A and anti-B antibodies in its plasma, enabling an individual with this type to receive red blood cells of any ABO blood group.

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<p>Rh Factor</p>

Rh Factor

An antigen protein (most importantly antigen D) located on the surface of red blood cells; individuals possessing it are Rh-positive, while those lacking it are Rh-negative.

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Erythroblastosis Fetalis

Also known as hemolytic disease of the newborn; a condition in which maternal anti-Rh antibodies cross the placenta and destroy the red blood cells of an Rh-positive fetus.

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Hemophilia A

An X-linked recessive hereditary clotting disorder characterized by a deficiency in Factor VIII (antihemophilic factor), resulting in abnormal bleeding tendencies.

<p>An X-linked recessive hereditary clotting disorder characterized by a deficiency in Factor VIII (antihemophilic factor), resulting in abnormal bleeding tendencies.</p>