💀Anatomy and Physiology I Unit 18 – The Cardiovascular System – Blood
Blood is the vital fluid that sustains life, circulating through our bodies to deliver oxygen, nutrients, and hormones while removing waste. This complex connective tissue consists of plasma and formed elements, each playing crucial roles in maintaining homeostasis and defending against pathogens.
Understanding blood composition and function is essential for grasping how our bodies operate. From red blood cells carrying oxygen to white blood cells fighting infections, and platelets sealing wounds, blood's components work together to keep us alive and healthy.
Plasma constitutes ~55% of blood volume and consists primarily of water, proteins, and dissolved substances
Proteins in plasma include albumins, globulins, and fibrinogen
Dissolved substances encompass nutrients, electrolytes, hormones, and waste products
Formed elements comprise ~45% of blood volume and include red blood cells (erythrocytes), white blood cells (leukocytes), and platelets (thrombocytes)
Red blood cells are the most abundant formed elements (~5 million/μL) and contain hemoglobin for oxygen transport
White blood cells are less numerous (~5,000-10,000/μL) and play crucial roles in immune defense
Platelets are small, anucleate cell fragments (~150,000-400,000/μL) that participate in blood clotting
Hematocrit represents the percentage of blood volume occupied by red blood cells, typically ranging from 38-48% in adults
Blood pH is tightly regulated between 7.35-7.45 to ensure proper functioning of cells and enzymes
Blood viscosity, influenced by hematocrit and plasma proteins, affects blood flow resistance and pressure
Blood Composition and Functions
Blood is a connective tissue consisting of plasma and formed elements that serves vital functions in the body
Transports oxygen from the lungs to tissues and carbon dioxide from tissues back to the lungs for exhalation
Delivers nutrients (glucose, amino acids, lipids) absorbed from the digestive tract to cells throughout the body
Removes metabolic waste products (urea, creatinine, uric acid) from cells and transports them to excretory organs
Distributes hormones from endocrine glands to target tissues, enabling communication and regulation of body functions
Helps regulate body temperature by absorbing and redistributing heat through circulation
Maintains osmotic balance and pH homeostasis in tissues by adjusting plasma composition and buffering capacity
Plasma proteins contribute to colloid osmotic pressure, which helps retain fluid within blood vessels
Provides immune defense through white blood cells and circulating antibodies that combat pathogens and foreign substances
Red Blood Cells and Hemoglobin
Red blood cells (erythrocytes) are biconcave, anucleate cells that primarily function in oxygen transport
Lack of nucleus and organelles allows for maximum space for hemoglobin and enhances flexibility for capillary passage
Hemoglobin, the oxygen-binding protein in red blood cells, consists of four globin subunits, each with an iron-containing heme group
Iron in heme reversibly binds to oxygen, allowing for efficient oxygen loading in the lungs and unloading in tissues
Red blood cell production (erythropoiesis) occurs in the bone marrow and is regulated by the hormone erythropoietin (EPO)
EPO is produced by the kidneys in response to low blood oxygen levels (hypoxia)
Red blood cells have a lifespan of ~120 days and are removed from circulation by the liver and spleen when they become senescent or damaged
Anemia, a decrease in red blood cell count or hemoglobin concentration, can result from blood loss, decreased production, or increased destruction
Symptoms of anemia include fatigue, pallor, shortness of breath, and dizziness
Polycythemia, an increase in red blood cell count, can occur due to chronic hypoxia (high altitude) or bone marrow disorders
White Blood Cells and Immunity
White blood cells (leukocytes) are nucleated cells that defend the body against infections and foreign substances
Granulocytes, which contain cytoplasmic granules, include neutrophils, eosinophils, and basophils
Neutrophils (~60% of leukocytes) are phagocytic cells that engulf and destroy bacteria and fungi
Eosinophils (~2-4%) target parasitic infections and participate in allergic reactions
Basophils (<1%) release histamine and other mediators involved in inflammation and allergic responses
Agranulocytes, which lack cytoplasmic granules, include lymphocytes and monocytes
Lymphocytes (~30%) include T cells (cell-mediated immunity) and B cells (humoral immunity)
T cells directly attack infected or cancerous cells and regulate immune responses
B cells produce antibodies that neutralize pathogens and mark them for destruction
Monocytes (~5%) migrate into tissues and differentiate into macrophages, which phagocytose pathogens and cellular debris
Leukocytosis, an increase in white blood cell count, often indicates an ongoing infection or inflammatory process
Leukopenia, a decrease in white blood cell count, can result from bone marrow disorders or immunosuppressive conditions
Platelets and Coagulation
Platelets (thrombocytes) are small, anucleate cell fragments derived from megakaryocytes in the bone marrow
Play a critical role in hemostasis, the process of stopping blood loss from damaged blood vessels
Adhere to exposed collagen in damaged vessel walls and release chemicals that promote platelet aggregation and activation
Activated platelets change shape, express surface receptors, and release factors that amplify the coagulation cascade
Coagulation (blood clotting) involves a series of enzymatic reactions that convert fibrinogen into insoluble fibrin strands
Intrinsic pathway is initiated by contact with negatively charged surfaces and involves factors XII, XI, IX, and VIII
Extrinsic pathway is triggered by tissue factor released from damaged cells and involves factor VII
Both pathways converge on the common pathway, which includes factors X, V, and II (prothrombin), leading to fibrin formation
Anticoagulants, such as heparin and warfarin, are used to prevent excessive clotting in conditions like deep vein thrombosis and pulmonary embolism
Disorders of platelet function or coagulation factors can lead to bleeding disorders, such as hemophilia and von Willebrand disease
Hemophilia is caused by deficiencies in factors VIII (hemophilia A) or IX (hemophilia B), leading to prolonged bleeding
Von Willebrand disease results from a deficiency in von Willebrand factor, which helps platelets adhere to damaged vessel walls
Blood Types and Transfusions
Blood types are determined by the presence or absence of specific antigens on the surface of red blood cells
ABO blood group system is based on the expression of A and B antigens
Type A individuals have A antigens and produce anti-B antibodies
Type B individuals have B antigens and produce anti-A antibodies
Type AB individuals have both A and B antigens and do not produce antibodies against either
Type O individuals lack A and B antigens and produce both anti-A and anti-B antibodies
Rh blood group system is based on the presence (+) or absence (-) of the Rh factor (D antigen)
Rh incompatibility between an Rh-negative mother and Rh-positive fetus can lead to hemolytic disease of the newborn
Compatibility testing (cross-matching) is performed before transfusions to ensure donor and recipient compatibility
ABO incompatibility can cause immediate and severe transfusion reactions due to preformed antibodies
Rh incompatibility can lead to sensitization and future transfusion reactions or complications in pregnancy
Universal donors (Type O-) can donate to all blood types, while universal recipients (Type AB+) can receive from all types
Blood Disorders and Diseases
Anemias are characterized by decreased red blood cell count or hemoglobin concentration, leading to reduced oxygen-carrying capacity
Iron-deficiency anemia results from inadequate dietary iron intake or chronic blood loss
Pernicious anemia is caused by vitamin B12 deficiency due to lack of intrinsic factor production in the stomach
Sickle cell anemia is an inherited disorder caused by a mutation in the hemoglobin gene, leading to abnormally shaped red blood cells
Leukemias are cancers of the blood-forming tissues that result in the uncontrolled production of immature or abnormal white blood cells
Acute leukemias (lymphoblastic or myeloid) progress rapidly and require immediate treatment
Chronic leukemias (lymphocytic or myeloid) develop more slowly and may not require treatment in early stages
Lymphomas are cancers of the lymphatic system that arise from lymphocytes in lymph nodes, spleen, or other tissues
Hodgkin lymphoma is characterized by the presence of Reed-Sternberg cells and often presents with enlarged lymph nodes
Non-Hodgkin lymphomas encompass a diverse group of cancers with varying cell types and clinical presentations
Myeloproliferative disorders, such as polycythemia vera and essential thrombocythemia, involve the overproduction of red blood cells or platelets
Bleeding disorders, like hemophilia and von Willebrand disease, result from deficiencies in coagulation factors or platelet function
Treatment involves replacing the missing factors or using medications to promote clotting
Disseminated intravascular coagulation (DIC) is a life-threatening condition characterized by widespread, uncontrolled activation of the coagulation cascade
Can be triggered by severe infections, trauma, or certain cancers and leads to simultaneous clotting and bleeding
Clinical Applications and Lab Tests
Complete blood count (CBC) is a routine lab test that measures red blood cell count, white blood cell count, platelet count, and hemoglobin concentration
Used to diagnose anemia, infections, leukemia, and other blood disorders
Differential white blood cell count provides information on the relative proportions of different types of leukocytes
Coagulation tests, such as prothrombin time (PT) and activated partial thromboplastin time (aPTT), assess the function of the extrinsic and intrinsic pathways, respectively
Prolonged PT or aPTT may indicate deficiencies in coagulation factors or the presence of anticoagulants
Blood typing and antibody screening are performed before transfusions or during pregnancy to ensure compatibility and prevent complications
Hemoglobin electrophoresis is used to diagnose hemoglobinopathies, such as sickle cell anemia and thalassemia
Separates different types of hemoglobin based on their electrical charge and migration pattern
Flow cytometry is a technique that analyzes the expression of cell surface markers on blood cells
Used to diagnose and classify leukemias and lymphomas based on the immunophenotype of the abnormal cells
Bone marrow aspiration and biopsy are invasive procedures that involve collecting samples of bone marrow for microscopic examination
Performed to diagnose blood cancers, assess response to treatment, or evaluate unexplained anemia or thrombocytopenia
Therapeutic apheresis is a procedure that selectively removes specific components of blood, such as platelets or plasma, for treatment purposes
Plasmapheresis is used to remove antibodies in autoimmune disorders like Guillain-Barré syndrome and myasthenia gravis
Plateletpheresis is used to collect donor platelets for transfusion or to treat conditions like thrombotic thrombocytopenic purpura (TTP)