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Blood: Structure, Function, and Disorders (Anatomy & Physiology Chapter 17 Study Notes)

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Blood: Structure, Function, and Disorders

17.1 Functions of Blood

Blood is the life-sustaining transport vehicle of the cardiovascular system, performing essential roles in transport, regulation, and protection.

  • Transport

    • Delivers O2 and nutrients to body cells

    • Transports metabolic wastes to lungs and kidneys for elimination

    • Transports hormones from endocrine organs to target organs

  • Regulation

    • Maintains body temperature by absorbing and distributing heat

    • Maintains normal pH using buffers, especially the alkaline reserve of bicarbonate ions

    • Maintains adequate fluid volume in the circulatory system

  • Protection

    • Prevents blood loss via plasma proteins and platelets that initiate clot formation

    • Prevents infection via antibodies and white blood cells

17.2 Composition of Blood

Blood is the only fluid tissue in the body and is classified as a connective tissue. It consists of a nonliving fluid matrix called plasma and living cells called formed elements.

  • Plasma: Straw-colored, sticky fluid; about 90% water

    • Contains over 100 dissolved solutes: nutrients, gases, hormones, wastes, proteins, inorganic ions

    • Plasma proteins are the most abundant solutes

      • Remain in blood; not taken up by cells

      • Produced mostly by the liver

      • Albumin: Makes up 60% of plasma proteins; functions as a carrier, blood buffer, and contributes to plasma osmotic pressure

  • Formed Elements:

    • Erythrocytes (red blood cells, RBCs)

    • Leukocytes (white blood cells, WBCs)

    • Platelets

  • Spun tube of blood yields three layers:

    • Erythrocytes on bottom (~45% of whole blood) – measured as hematocrit

      • Normal values: Males 47% ± 5%, Females 42% ± 5%

    • Buffy coat (<1%): thin, whitish layer between RBCs and plasma; contains WBCs and platelets

    • Plasma on top (~55%)

  • Physical Characteristics and Volume:

    • Blood is sticky, opaque, with metallic taste

    • Color varies with O2 content: high O2 = scarlet red, low O2 = dark red

    • pH: 7.35–7.45

    • Volume: Males 5–6 L, Females 4–5 L

17.3 Erythrocytes (Red Blood Cells)

Erythrocytes are specialized cells responsible for the transport of respiratory gases, primarily oxygen and carbon dioxide.

  • Structural Characteristics:

    • Small-diameter (7.5 μm), biconcave disc shape

    • Anucleate and lack organelles

    • Filled with hemoglobin (Hb) for gas transport

    • Contain plasma membrane protein spectrin and other proteins

    • ATP production is anaerobic; RBCs do not consume the O2 they transport

  • Features for Efficient Gas Transport:

    • Biconcave shape offers large surface area relative to volume

    • Hemoglobin makes up 97% of cell volume (excluding water)

    • No mitochondria

  • Function:

    • Dedicated to respiratory gas transport

    • Hemoglobin binds reversibly with oxygen

  • Hemoglobin Structure:

    • Consists of red heme pigment bound to the protein globin

    • Globin: four polypeptide chains (two alpha, two beta)

    • Each heme group contains central iron atom that binds one O2

    • Each RBC contains ~250 million Hb molecules

  • Oxygen and Carbon Dioxide Transport:

    • O2 loading in lungs: produces oxyhemoglobin (ruby red)

    • O2 unloading in tissues: produces deoxyhemoglobin (dark red)

    • CO2 loading in tissues: 20% of CO2 in blood binds to Hb, producing carbaminohemoglobin

  • Production of Erythrocytes:

    • Hematopoiesis: formation of all blood cells; occurs in red bone marrow

    • Hematopoietic stem cells: stem cells that give rise to all formed elements

    • Hormones and growth factors push cells toward specific pathways of development

    • Committed cells cannot change

    • New blood cells enter blood sinusoids

  • Regulation and Requirements of Erythropoiesis:

    • Too few RBCs lead to tissue hypoxia

    • Too many RBCs increase blood viscosity

    • Balance between RBC production and destruction depends on:

      • Hormonal controls

      • Dietary requirements

    • Erythropoietin (EPO): hormone that stimulates formation of RBCs

      • Released by kidneys (and some by liver) in response to hypoxia (low O2 levels)

      • Testosterone enhances EPO production

  • Dietary Requirements:

    • Nutrients: amino acids, lipids, carbohydrates

    • Iron: essential for hemoglobin synthesis

    • Vitamin B12 and folic acid: necessary for DNA synthesis and cell division

  • Fate and Destruction of Erythrocytes:

    • Life span: 100–120 days

    • Old RBCs become fragile; hemoglobin degenerates

    • Macrophages in spleen engulf and break down dying RBCs

Erythrocyte Disorders

Most erythrocyte disorders are classified as either anemia or polycythemia.

  • Anemia: Blood has abnormally low O2-carrying capacity, insufficient to support normal metabolism.

    • Symptoms: fatigue, pallor, dyspnea, chills

    • Three groups based on cause:

      1. Blood loss

        • Rapid blood loss (e.g., severe wound): treated by blood replacement

        • Chronic hemorrhagic anemia (e.g., bleeding ulcer): treated by addressing primary problem

      2. Not enough RBCs produced

        • Iron-deficiency anemia: microcytes (small, pale RBCs); cannot synthesize hemoglobin due to lack of iron; treated with iron supplements

        • Pernicious anemia: autoimmune disease destroying stomach mucosa that produces intrinsic factor (needed for B12 absorption); results in macrocytes (large RBCs); treated with B12 injections or nasal gel

        • Renal anemia: lack of EPO; treated with synthetic EPO

        • Aplastic anemia: destruction/inhibition of red bone marrow by drugs, chemicals, radiation, or viruses; all formed elements affected; treated with transfusions or stem cell transplants

      3. Too many RBCs destroyed

        • Hemolytic anemias: premature lysis of RBCs due to incompatible transfusions, infections, or genetic abnormalities

        • Thalassemias: typically found in people of Mediterranean ancestry; one globin chain absent or faulty; RBCs are thin, delicate, and deficient in hemoglobin; severity varies

        • Sickle-cell anemia: mutated hemoglobin S; one amino acid wrong in a globin beta chain; RBCs become crescent-shaped under low O2; rupture easily and block small vessels; prevalent in people of African descent; confers resistance to malaria

  • Polycythemia: Excess of RBCs increases blood viscosity; can be caused by bone marrow cancer (polycythemia vera) or secondary to low O2 levels (e.g., high altitude)

Table: Comparison of Major Anemia Types

Anemia Type

Main Cause

RBC Appearance

Treatment

Iron-deficiency

Low iron intake or absorption

Microcytic, pale

Iron supplements

Pernicious

Lack of intrinsic factor (B12 absorption)

Macrocytic, large

B12 injections/nasal gel

Aplastic

Bone marrow destruction/inhibition

All formed elements affected

Transfusions, stem cell transplant

Hemolytic

RBC rupture (genetic, infection, transfusion)

Varies

Treat underlying cause

Thalassemia

Faulty globin chain (genetic)

Thin, delicate

Transfusions (severe cases)

Sickle-cell

Mutated hemoglobin S (genetic)

Crescent-shaped

Transfusions, stem cell transplant

Key Equations and Scientific Terms

  • Hematocrit:

  • Oxygen transport by hemoglobin:

  • Carbaminohemoglobin formation:

Additional info: These notes expand on the provided slides and images, adding definitions, examples, and a comparison table for anemia types to aid in exam preparation.

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