Anatomy and Physiology I Q&A
Anatomy and Physiology I

Question 1

ST. AMBROSE SCHOOL OF NURSING AND MIDWIFERY - NO.10

  1. Define synovial joints.
  2. Explain six types of synovial joint.
  3. Outline 10 movements that occur at synovial joints.

Answer:

a) Definition: Synovial Joints
A joint is a site where two or more bones meet (articulate). Synovial joints are a type of joint that allows for a wide range of movement. They are characterized by having a space (synovial cavity) between the articulating bones. The ends of the bones are covered with smooth articular cartilage and are held together by a fibrous capsule. This capsule is lined by a synovial membrane which secretes synovial fluid, a lubricating fluid that reduces friction and nourishes the cartilage. Synovial joints are also known as freely movable joints or diarthroses.
b) Six Types of Synovial Joints:
  • 1. Ball and Socket Joints:The rounded head (ball) of one bone fits into a cup-shaped cavity (socket) of another bone. This allows for movement in many directions (multiaxial), including flexion, extension, abduction, adduction, rotation, and circumduction. Examples: Shoulder joint, hip joint.
  • 2. Hinge Joints:The convex surface of one bone fits into the concave surface of another, like a door hinge. These joints primarily allow movement in one plane (uniaxial) – flexion and extension. Examples: Elbow joint, knee joint, ankle joint, interphalangeal joints (fingers and toes), joint between atlas and occipital bone.
  • 3. Pivot Joints:A rounded or pointed surface of one bone articulates with a ring formed partly by another bone and partly by a ligament. This allows for rotation around a central axis (uniaxial). Examples: Joint between the atlas (C1) and axis (C2) vertebrae (allows head to turn side to side), proximal and distal radioulnar joints (allow forearm to supinate and pronate).
  • 4. Condyloid (Ellipsoidal) Joints:An oval-shaped condyle of one bone fits into an elliptical cavity of another. This allows for movement in two planes (biaxial) – flexion, extension, abduction, adduction, and circumduction (but not axial rotation). Examples: Wrist joint (radiocarpal joint), metacarpophalangeal joints (knuckles of the hand), metatarsophalangeal joints (base of toes), temporomandibular joint (TMJ).
  • 5. Saddle Joints:The articular surface of one bone is saddle-shaped, and the articular surface of the other bone fits into it like a rider sitting on a saddle. These are biaxial joints allowing flexion, extension, abduction, adduction, and circumduction. They offer more movement than condyloid joints. Example: Carpometacarpal joint at the base of the thumb (between the trapezium and the first metacarpal). This allows for opposition of the thumb.
  • 6. Gliding (Plane) Joints:The articulating surfaces are usually flat or slightly curved, allowing for side-to-side and back-and-forth gliding movements. These are typically nonaxial or multiaxial but with limited range. Examples: Intercarpal joints (between carpal bones in the wrist), intertarsal joints (between tarsal bones in the ankle), sternoclavicular joints, acromioclavicular joints, joints between vertebral articular processes.
[Image: Diagram showing different types of synovial joints and their location in a human skeleton]
c) 10 Movements That Occur at Synovial Joints:
  • Flexion:Decreasing the angle between two bones (bending a joint). Example: Bending the elbow.
  • Extension:Increasing the angle between two bones (straightening a joint). Example: Straightening the knee.
  • Abduction:Moving a limb away from the midline of the body. Example: Lifting the arm out to the side.
  • Adduction:Moving a limb towards the midline of the body. Example: Bringing the arm back to the side.
  • Circumduction:A conical movement of a limb extending from the joint, where the distal end of the limb moves in a circle while the proximal end remains relatively stable. It's a combination of flexion, extension, abduction, and adduction. Example: Circling the arm at the shoulder.
  • Rotation:Turning a bone around its own long axis. > Medial (Internal) Rotation: Turning the anterior surface of a limb towards the midline. > Lateral (External) Rotation: Turning the anterior surface of a limb away from the midline. Example: Turning the head side to side (at the atlantoaxial joint).
  • Supination:Rotating the forearm so the palm faces anteriorly or upwards (like holding a bowl of soup). Radius and ulna are parallel.
  • Pronation:Rotating the forearm so the palm faces posteriorly or downwards. Radius crosses over the ulna.
  • Inversion:Turning the sole of the foot inwards (medially).
  • Eversion:Turning the sole of the foot outwards (laterally).
  • Dorsiflexion:Bending the foot upwards at the ankle (toes pointing towards the shin).
  • Plantarflexion:Bending the foot downwards at the ankle (pointing the toes).
  • Protraction:Moving a body part anteriorly (forward) in the horizontal plane. Example: Jutting the jaw forward.
  • Retraction:Moving a body part posteriorly (backward) in the horizontal plane. Example: Pulling the jaw backward.
  • Elevation:Lifting a body part superiorly (upwards). Example: Shrugging the shoulders.
  • Depression:Moving a body part inferiorly (downwards). Example: Lowering the shoulders.
  • Opposition:Movement of the thumb to touch the fingertips of the same hand. Unique to the saddle joint of the thumb.
[Image: Diagram showing the main movements possible at synovial joints]

Source: Based on St. Ambrose School of Nursing and Midwifery answer sheet provided in the PDF (pages 81-84), adapted and simplified. General Anatomy & Physiology textbooks like Ross and Wilson would also cover this.

Question 2

ARUA SCHOOL OF COMPREHENSIVE NURSING AND MIDWIFERY - NO.15

  1. Define cardiac cycle.
  2. With a well labelled diagram, outline 3 events that occur during cardiac cycle.

Answer:

a) Definition: Cardiac Cycle
The cardiac cycle refers to the sequence of events that occurs in the heart from the beginning of one heartbeat to the beginning of the next. It includes the contraction (systole) and relaxation (diastole) of both the atria and the ventricles, and the associated changes in blood pressure and volume within the heart chambers.

A healthy adult heart at rest typically beats 60-90 times per minute (bpm). At an average rate of 74 bpm, each cardiac cycle lasts about 0.8 seconds.

b) 3 Events that Occur During Cardiac Cycle (with diagram placeholder):

The cardiac cycle involves several coordinated events. The main phases are often described as atrial systole, ventricular systole, and complete cardiac diastole.

  • 1. Atrial Systole (Atrial Contraction - approx. 0.1 seconds): This is the contraction of the atria (the upper chambers of the heart). The sinoatrial (SA) node (the heart's natural pacemaker) initiates an electrical impulse that spreads across both atria, causing them to contract. Before atrial systole, about 70% of blood flows passively from the atria into the ventricles (lower chambers) as the atrioventricular (AV) valves (tricuspid and mitral) are open. Atrial contraction then actively pumps the remaining 30% of blood from the atria into the already partially filled ventricles, completing ventricular filling. During atrial systole, the AV valves are open, and the semilunar valves (pulmonary and aortic) are closed to prevent backflow from the major arteries.
[Diagram: Heart showing Atrial Systole - Atria contracting, AV valves open, Semilunar valves closed, blood moving from atria to ventricles]
  • 2. Ventricular Systole (Ventricular Contraction - approx. 0.3 seconds): This is the contraction of the ventricles. It has two phases: Isovolumetric Contraction: After the electrical impulse passes from the atria through the AV node to the ventricles, the ventricles begin to contract. The pressure inside the ventricles rises rapidly. This increased pressure forces the AV valves (tricuspid and mitral) to snap shut, producing the first heart sound ("lubb"). For a brief moment, both AV and semilunar valves are closed, so no blood is leaving the ventricles, but pressure is building up (isovolumetric = same volume). Ventricular Ejection: As ventricular pressure continues to rise and exceeds the pressure in the aorta and pulmonary artery, the semilunar (aortic and pulmonary) valves are forced open. Blood is then powerfully ejected from the left ventricle into the aorta (to the body) and from the right ventricle into the pulmonary artery (to the lungs). During ventricular systole, the atria are in diastole (relaxed) and begin to refill with blood returning from the body (right atrium) and lungs (left atrium).
[Diagram: Heart showing Ventricular Systole - Ventricles contracting, AV valves closed, Semilunar valves open, blood being ejected into aorta and pulmonary artery]
  • 3. Complete Cardiac Diastole (Relaxation Phase - approx. 0.4 seconds): Both the atria and ventricles are relaxed during this phase. As the ventricles relax after ejecting blood, the pressure within them drops. When ventricular pressure falls below the pressure in the aorta and pulmonary artery, the semilunar valves snap shut, producing the second heart sound ("dupp"). This prevents backflow of blood from the arteries into the ventricles. For a short period, all four valves are closed (isovolumetric relaxation). As the ventricles continue to relax, their pressure drops below atrial pressure. The AV valves (tricuspid and mitral) then open, and blood that has been accumulating in the atria flows passively into the ventricles. Ventricular filling begins again. The entire heart is at rest, and the myocardium (heart muscle) recovers, preparing for the next cycle.
[Diagram: Heart showing Complete Cardiac Diastole - Atria and Ventricles relaxed, AV valves open (allowing passive filling of ventricles), Semilunar valves closed]

Source: Based on Arua School of Comprehensive Nursing and Midwifery answer sheet provided in the PDF (pages 85-87), adapted and simplified. General Anatomy & Physiology textbooks like Ross and Wilson or Gray's Anatomy would provide further detail.

Question 3

KAMPALA SCHOOL OF HEALTH SCIENCES - NO.11

  1. Outline six functions of blood.
  2. Describe the composition of plasma.
  3. List the classification of leucocytes.

Answer: (Researched)

a) Six Functions of Blood:

Blood is a vital fluid connective tissue that performs many essential functions for the body.

  • 1. Transportation: Blood is the primary transport medium in the body. Gases: Carries oxygen from the lungs to body tissues and carbon dioxide from tissues back to the lungs for exhalation. Nutrients: Transports absorbed nutrients (like glucose, amino acids, fatty acids, vitamins, minerals) from the digestive system to all body cells. Hormones: Carries hormones from endocrine glands to their target organs to regulate various body functions. Waste Products: Transports metabolic waste products (like urea, uric acid, creatinine) from cells to excretory organs (kidneys, liver, lungs) for removal. Heat: Helps distribute heat throughout the body, contributing to temperature regulation.
  • 2. Regulation (Homeostasis): Blood helps maintain a stable internal environment. pH Balance: Contains buffer systems (like bicarbonate) that help maintain the blood pH within a narrow, normal range (around 7.35-7.45). Body Temperature: Absorbs and distributes heat produced by metabolic activities, helping to regulate body temperature by diverting blood flow to or away from the skin surface. Fluid Balance (Osmotic Pressure): Plasma proteins, especially albumin, help maintain osmotic pressure, which influences the movement of water between blood and interstitial fluid, preventing excessive fluid loss from capillaries. Electrolyte Balance: Transports electrolytes and helps regulate their concentration in body fluids.
  • 3. Protection: Blood defends the body against disease and blood loss. Clotting (Hemostasis): Platelets and clotting factors in plasma prevent excessive blood loss from damaged blood vessels by forming blood clots. Immunity: White blood cells (leucocytes) defend against pathogens (bacteria, viruses, fungi, parasites) through phagocytosis and immune responses. Antibodies (immunoglobulins) in plasma also neutralize or mark pathogens for destruction.
  • 4. Maintenance of Water Balance:Blood volume is crucial for maintaining blood pressure and ensuring adequate hydration of tissues. The kidneys regulate blood volume by adjusting water excretion.
  • 5. Buffering Action:Plasma proteins and the bicarbonate buffer system in the blood help to resist changes in pH, keeping it stable for optimal enzyme function and cellular processes.
  • 6. Transport of Heat:As blood circulates, it picks up heat from active tissues (like muscles) and distributes it around the body or to the skin for dissipation, thus playing a role in thermoregulation.
  • 7. Nutrient Supply to Tissues:Delivers essential substances like glucose for energy, amino acids for protein synthesis, and fats for energy storage and cell structure directly to the cells.
  • 8. Waste Removal from Tissues:Collects waste products of cellular metabolism and transports them to organs like the kidneys and liver for processing and excretion.
b) Composition of Plasma:

Plasma is the liquid, straw-colored matrix of blood, making up about 55% of total blood volume. The remaining 45% consists of formed elements (red blood cells, white blood cells, and platelets). Plasma itself is about 90-92% water.

  • 1. Water (approx. 90-92%):Acts as a solvent for various solutes, transports substances, and absorbs heat.
  • 2. Plasma Proteins (approx. 7-8%): These are the most abundant solutes in plasma and perform various functions. They are mostly synthesized in the liver. Albumin (approx. 60% of plasma proteins): Maintains osmotic pressure of the blood (preventing excessive fluid loss from capillaries), acts as a carrier protein for hormones, fatty acids, and drugs, and contributes to blood viscosity. Globulins (approx. 36% of plasma proteins): > Alpha and Beta Globulins: Transport lipids (lipoproteins), metal ions (like iron via transferrin, copper via ceruloplasmin), and fat-soluble vitamins. > Gamma Globulins (Immunoglobulins or Antibodies): Produced by plasma cells (derived from B lymphocytes) and are crucial for the immune response by neutralizing or eliminating pathogens. Fibrinogen (approx. 4% of plasma proteins): A key clotting protein that is converted to insoluble fibrin threads during blood coagulation, forming the meshwork of a blood clot. (Serum is plasma without clotting factors like fibrinogen). Regulatory Proteins: Includes enzymes involved in various metabolic processes and hormones circulating in the blood.
  • 3. Other Solutes (approx. 1-2%): These are dissolved substances transported in the plasma. Electrolytes (Inorganic Salts/Ions): Include sodium (Na+), potassium (K+), calcium (Ca2+), magnesium (Mg2+), chloride (Cl-), bicarbonate (HCO3-), phosphate (PO43-), and sulfate (SO42-). They help maintain osmotic pressure, normal pH, and are essential for nerve and muscle function. Nutrients: Organic substances absorbed from the digestive tract, such as glucose, amino acids, fatty acids, glycerol, vitamins, and minerals. Waste Products: Substances transported to organs of excretion, including urea, uric acid, creatinine, bilirubin, and ammonia. Respiratory Gases: Small amounts of dissolved oxygen and carbon dioxide (most are carried by red blood cells or as bicarbonate). Hormones: Chemical messengers transported from endocrine glands to target cells.
c) Classification of Leucocytes (White Blood Cells - WBCs):

Leucocytes are the cells of the immune system involved in protecting the body against infectious diseases and foreign invaders. They are classified based on their appearance under a light microscope, particularly the presence or absence of granules in their cytoplasm.

  • I. Granulocytes (Polymorphonuclear Leucocytes - PMNs): Contain visible granules in their cytoplasm and have lobed nuclei. 1. Neutrophils (50-70% of WBCs): > Appearance: Multi-lobed nucleus (3-5 lobes), pale pink or lilac cytoplasmic granules. > Function: Primary phagocytes; first responders to bacterial infections and inflammation. Engulf and destroy bacteria and cellular debris. 2. Eosinophils (1-4% of WBCs): > Appearance: Bilobed nucleus, large red-orange cytoplasmic granules. > Function: Combat parasitic infections, play a role in allergic reactions by releasing enzymes that counteract inflammatory mediators. 3. Basophils (0.5-1% of WBCs): > Appearance: U or S-shaped nucleus often obscured by large, coarse, dark blue-purple cytoplasmic granules. > Function: Release histamine (promotes inflammation) and heparin (prevents blood clotting) during allergic reactions and inflammatory responses. Similar in function to mast cells.
  • II. Agranulocytes (Mononuclear Leucocytes): Lack visible cytoplasmic granules (or have very fine, non-specific granules) and have non-lobed, more regularly shaped nuclei. 1. Lymphocytes (20-40% of WBCs): > Appearance: Large, spherical or slightly indented nucleus that occupies most of the cell volume; thin rim of pale blue cytoplasm. > Function: Crucial for specific immunity. Subtypes include: › B Lymphocytes (B cells): Differentiate into plasma cells that produce antibodies. Responsible for humoral immunity. › T Lymphocytes (T cells): Directly attack infected cells or regulate immune responses. Responsible for cell-mediated immunity. (Includes Helper T cells, Cytotoxic T cells, Regulatory T cells). › Natural Killer (NK) cells: Attack virus-infected cells and tumor cells without prior sensitization. 2. Monocytes (2-8% of WBCs): > Appearance: Largest WBCs; kidney-shaped or U-shaped nucleus; abundant pale blue-gray cytoplasm, may appear foamy. > Function: Phagocytic cells. They migrate from the blood into tissues where they differentiate into macrophages (powerful phagocytes) or dendritic cells (antigen-presenting cells). They engulf pathogens, cellular debris, and present antigens to lymphocytes to initiate specific immune responses.

Question 4

KISIZI SCHOOL OF NURSING AND MIDWIFERY - NO.12

  1. Describe the classification of epithelial tissue.
  2. List the functions of epithelial tissue.

Answer: (Researched)

a) Classification of Epithelial Tissue:

Epithelial tissue (epithelium) is one of the four basic types of animal tissue, along with connective tissue, muscle tissue, and nervous tissue. It covers body surfaces, lines body cavities and hollow organs, and forms glands. Epithelial tissues are classified based on two main criteria: the shape of the cells and the number of cell layers.

  • I. Classification by Number of Cell Layers: 1. Simple Epithelium: > Consists of a single layer of cells. > Functions: Primarily involved in absorption, secretion, filtration, and diffusion because a single layer presents a minimal barrier. > Found where these processes are important, e.g., lining of blood vessels, air sacs of lungs, kidney tubules. 2. Stratified Epithelium: > Consists of two or more layers of cells stacked on top of each other. > Functions: Primarily protective, as the multiple layers provide a more robust barrier against abrasion, pathogens, and chemical stress. > Found in areas subjected to wear and tear, e.g., skin surface, lining of the mouth and esophagus. 3. Pseudostratified Epithelium: > Appears to be stratified (multiple layers) because the cell nuclei are at different levels, but all cells are actually attached to the basement membrane, so it's technically a single layer. > Functions: Often involved in secretion (especially of mucus) and absorption; may be ciliated to move substances. > Example: Lining of the trachea and much of the upper respiratory tract (ciliated form).
  • II. Classification by Cell Shape (of the apical/surface layer for stratified types): 1. Squamous Epithelium: > Cells are flattened, scale-like, and thin. The nucleus is also flattened. > Allows for rapid passage of substances (diffusion, filtration). 2. Cuboidal Epithelium: > Cells are cube-shaped, as tall as they are wide. The nucleus is spherical and centrally located. > Often involved in secretion and absorption. 3. Columnar Epithelium: > Cells are taller than they are wide, like columns. The nucleus is elongated and usually located near the base of the cell. > Specialized for secretion and absorption; may have cilia or microvilli on their apical surface. 4. Transitional Epithelium (Urothelium): > A type of stratified epithelium where the shape of the surface cells changes depending on the degree of stretch. When relaxed, surface cells may appear large and rounded (dome-shaped); when stretched, they flatten out. > Functions: Allows for distension (stretching) of urinary organs. > Found exclusively in the urinary system (lining of ureters, bladder, and part of the urethra).

Combining these two criteria gives specific types, e.g., Simple Squamous Epithelium, Stratified Cuboidal Epithelium, Pseudostratified Ciliated Columnar Epithelium.

[Image: Diagram illustrating different types of epithelial tissues based on cell shape and layers (e.g., simple squamous, stratified cuboidal, pseudostratified columnar)]
b) Functions of Epithelial Tissue:
  • Protection:Acts as a protective barrier for underlying tissues from mechanical injury, harmful chemicals, invading pathogens, and excessive water loss (e.g., epidermis of the skin, lining of the mouth).
  • Secretion:Epithelial cells in glands (glandular epithelium) are specialized to produce and secrete various substances such as hormones, mucus, enzymes, sweat, and saliva (e.g., cells of salivary glands, thyroid gland, sweat glands).
  • Absorption:Certain epithelial cells are adapted for absorbing substances from a lumen or the external environment into the body (e.g., lining of the small intestine which absorbs nutrients, lining of kidney tubules which reabsorbs water and solutes). Often have microvilli to increase surface area.
  • Excretion:Specialized epithelial cells help in the elimination of waste products from the body (e.g., epithelium of kidney tubules secretes waste products into urine).
  • Filtration:Allows selective passage of small molecules and water while preventing the passage of larger substances (e.g., endothelium lining blood capillaries, epithelium of Bowman's capsule in the kidney glomeruli).
  • Diffusion:Facilitates the movement of gases (like oxygen and carbon dioxide) down their concentration gradients across thin epithelial layers (e.g., simple squamous epithelium of alveoli in the lungs and lining capillaries).
  • Sensation (Sensory Reception):Some epithelial tissues contain specialized sensory nerve endings or are associated with sensory receptors that detect stimuli such as touch, taste, smell, temperature, and pain (e.g., taste buds on the tongue, olfactory epithelium in the nasal cavity, neuroepithelium in the inner ear).
  • Transport:Ciliated epithelium can move substances along its surface (e.g., cilia in the respiratory tract move mucus and trapped particles upwards; cilia in the fallopian tubes move the ovum towards the uterus).
  • Lubrication:Secretion of mucus by goblet cells (a type of epithelial cell) lubricates surfaces, reducing friction and protecting underlying tissues (e.g., lining of the digestive and respiratory tracts).
  • Forms Glands:Epithelial tissue invaginates to form both exocrine glands (secrete products into ducts) and endocrine glands (secrete hormones directly into the bloodstream).
  • Regeneration:Epithelial tissues have a high capacity for regeneration and repair after injury, as they are often subjected to wear and tear.

Question 5

BUNDIBUGYO SCHOOL OF NURSING AND MIDWIFERY - NO.13

  1. Describe a liver.
  2. Outline seven functions of the liver.

Answer: (Researched)

a) Description of the Liver:

The liver is the largest internal organ and the largest gland in the human body, weighing about 1.2-1.5 kg in an adult. It is a vital, reddish-brown, wedge-shaped organ located primarily in the upper right quadrant of the abdominal cavity, just below the diaphragm and superior (above) to the stomach, right kidney, and intestines. A small portion extends into the upper left quadrant.

  • Structure: The liver is divided into two main lobes: a larger right lobe and a smaller left lobe, separated by the falciform ligament. There are also two smaller, accessory lobes visible on the inferior surface: the quadrate lobe and the caudate lobe. It is covered by a fibrous connective tissue capsule called Glisson's capsule. The functional units of the liver are called hepatic lobules, which are hexagonal structures made up of hepatocytes (liver cells) arranged in plates around a central vein. Portal triads (containing a branch of the hepatic artery, a branch of the portal vein, and a bile ductule) are located at the corners of the lobules. Blood from both the hepatic artery (oxygen-rich) and the portal vein (nutrient-rich from the digestive system) flows through sinusoids (specialized capillaries) between the plates of hepatocytes towards the central vein. Kupffer cells, specialized macrophages, line the sinusoids and remove bacteria and debris from the blood. Bile, produced by hepatocytes, flows through tiny channels called bile canaliculi in the opposite direction to blood flow, eventually collecting into bile ducts.
  • Blood Supply:The liver has a dual blood supply: > Hepatic Artery: Supplies oxygenated blood from the aorta. > Portal Vein: Carries nutrient-rich (but deoxygenated) blood from the digestive organs (stomach, intestines, spleen, pancreas) to the liver for processing. Blood leaves the liver via hepatic veins, which drain into the inferior vena cava.
  • Gallbladder:The gallbladder, a small organ, is located beneath the right lobe of the liver. It stores and concentrates bile produced by the liver.
[Image: Anatomical illustration of the liver, showing its lobes, location, and associated structures like the gallbladder and major blood vessels]
b) Seven Functions of the Liver:

The liver performs over 500 vital functions. Here are seven key ones:

  • 1. Metabolic Functions: The liver plays a central role in carbohydrate, lipid (fat), and protein metabolism. Carbohydrate Metabolism: Maintains normal blood glucose levels by storing glucose as glycogen (glycogenesis), breaking down glycogen to release glucose (glycogenolysis), and forming new glucose from non-carbohydrate sources like amino acids (gluconeogenesis). Lipid Metabolism: Synthesizes cholesterol, lipoproteins (like LDL, HDL) for fat transport, triglycerides, and phospholipids. It also breaks down fatty acids for energy (beta-oxidation) and forms ketone bodies. Protein Metabolism: Synthesizes most plasma proteins (e.g., albumin, clotting factors, transport proteins). Deaminates amino acids (removing the amino group), converting the ammonia produced into urea for excretion by the kidneys. Converts amino acids from one type to another (transamination).
  • 2. Detoxification and Excretion:The liver detoxifies harmful substances, both endogenous (produced within the body, like ammonia) and exogenous (from outside, like drugs, alcohol, and environmental toxins). It converts them into less toxic or water-soluble forms that can be excreted in bile or urine. It also excretes bilirubin (a breakdown product of hemoglobin) in bile.
  • 3. Bile Production and Secretion:Hepatocytes produce bile, a greenish-yellow fluid containing bile salts, bilirubin, cholesterol, electrolytes, and water. Bile is stored and concentrated in the gallbladder and released into the small intestine to aid in the digestion and absorption of fats and fat-soluble vitamins.
  • 4. Storage:The liver stores several important substances: > Glycogen (a readily available source of glucose). > Vitamins: Fat-soluble vitamins (A, D, E, K) and water-soluble vitamin B12. > Minerals: Iron (as ferritin) and copper. > Blood: The liver can store a significant volume of blood, which can be released into circulation if needed (e.g., during hemorrhage).
  • 5. Synthesis of Clotting Factors:The liver produces most of the plasma proteins essential for blood clotting, including fibrinogen, prothrombin, and factors V, VII, IX, X, XI, and XII. Vitamin K is required for the synthesis of some of these factors.
  • 6. Phagocytosis (Immune Function):Kupffer cells, specialized macrophages located in the liver sinusoids, engulf and destroy old red blood cells, old white blood cells, bacteria, viruses, and other foreign particles that enter the liver via the portal blood from the intestines.
  • 7. Activation of Vitamin D:The liver (along with the kidneys) plays a role in converting inactive vitamin D into its active form, which is essential for calcium absorption and bone health.
  • 8. Hormone Metabolism:The liver inactivates or modifies hormones such as steroid hormones (e.g., estrogen, cortisol) and thyroid hormones, helping to regulate their levels in the body.

Question 6

INTERNATIONAL INSTITUTE OF NURSING AND MIDWIFERY MAYA - NO.14

  1. Describe the development of long bone.
  2. Outline the factors that determine bone growth.

Answer: (Researched)

a) Development of Long Bone (Endochondral Ossification):

Most long bones in the body (like the femur, humerus, tibia) develop through a process called endochondral ossification, which means bone formation "within cartilage." This process begins in the fetus and continues through adolescence.

  • 1. Hyaline Cartilage Model Formation:In the early embryo, the future long bone exists as a model made of hyaline cartilage, shaped like the bone it will become. This model is surrounded by a connective tissue membrane called the perichondrium.
  • 2. Formation of a Bone Collar:Cells in the perichondrium differentiate into osteoblasts (bone-forming cells). These osteoblasts begin to secrete bone matrix around the diaphysis (shaft) of the cartilage model, forming a compact bone collar. The perichondrium then becomes the periosteum.
  • 3. Development of the Primary Ossification Center: Chondrocytes (cartilage cells) within the center of the diaphysis enlarge (hypertrophy) and the surrounding cartilage matrix begins to calcify (harden). These hypertrophied chondrocytes die, leaving behind cavities within the calcified cartilage. Blood vessels from the periosteum (the periosteal bud) invade these cavities, bringing with them osteoblasts and osteoclasts (bone-resorbing cells). Osteoblasts deposit bone matrix over the calcified cartilage remnants, forming spongy bone. This region is the primary ossification center, and ossification spreads from here towards the ends of the bone. Osteoclasts break down some of the newly formed spongy bone in the center of the diaphysis, creating the medullary (marrow) cavity.
  • 4. Development of Secondary Ossification Centers:Around the time of birth or shortly after, blood vessels invade the epiphyses (ends of the long bone), and secondary ossification centers form here. Ossification proceeds outwards from the center of each epiphysis, similar to the primary center, forming spongy bone. However, in most secondary centers, a medullary cavity is not formed.
  • 5. Formation of Articular Cartilage and Epiphyseal Plate (Growth Plate): The hyaline cartilage covering the surface of the epiphyses where they articulate with other bones remains as articular cartilage, providing a smooth surface for joint movement. A region of hyaline cartilage also remains between the diaphysis and each epiphysis. This is the epiphyseal plate or growth plate. It is responsible for the lengthwise growth of the long bone during childhood and adolescence.
  • 6. Lengthening of the Bone (Interstitial Growth):Growth in length occurs at the epiphyseal plate. Chondrocytes in the plate divide and mature, pushing the epiphysis away from the diaphysis. The older cartilage on the diaphyseal side of the plate is replaced by bone.
  • 7. Widening of the Bone (Appositional Growth):Bones also grow in thickness (diameter) through appositional growth. Osteoblasts in the periosteum add new bone tissue to the outer surface of the diaphysis, while osteoclasts in the endosteum lining the medullary cavity resorb bone from the inner surface, enlarging the medullary cavity.
  • 8. Closure of Epiphyseal Plates:At the end of adolescence (typically between ages 18-25), the chondrocytes in the epiphyseal plates stop dividing, and the cartilage is completely replaced by bone. The epiphyseal plate becomes the epiphyseal line, and lengthwise growth stops.
[Image: Diagram illustrating the stages of endochondral ossification in a long bone]
b) Factors That Determine Bone Growth:

Bone growth is a complex process influenced by a combination of genetic, nutritional, and hormonal factors.

  • 1. Genetic Factors:An individual's genetic makeup inherited from parents plays a primary role in determining potential bone size, shape, and overall skeletal structure, including height.
  • 2. Nutritional Factors: Adequate intake of specific nutrients is essential for normal bone growth and development. Calcium and Phosphorus: These are the main minerals that make up bone matrix, providing hardness and strength. Deficiencies can lead to conditions like rickets (in children) or osteomalacia (in adults). Vitamin D: Essential for the absorption of calcium from the intestine. Deficiency impairs bone mineralization. Vitamin C: Required for the synthesis of collagen, a major protein component of bone matrix. Deficiency (scurvy) can result in poor bone growth and fragile bones. Vitamin A: Influences the activity of osteoblasts and osteoclasts, important for bone remodeling. Vitamin K and B12: Also play roles in bone protein synthesis and bone health. Proteins: Provide amino acids necessary for collagen synthesis and overall cell growth. Other Minerals: Magnesium, fluoride, and manganese are also important for bone health.
  • 3. Hormonal Factors: Various hormones regulate bone growth and remodeling. Growth Hormone (GH): Secreted by the anterior pituitary gland, GH is the single most important hormone for stimulating bone growth during childhood and adolescence, particularly by promoting chondrocyte proliferation at the epiphyseal plates. Thyroid Hormones (T3 and T4): Secreted by the thyroid gland, these hormones are essential for normal skeletal development and maturation. They work with GH to promote bone growth. Sex Hormones (Estrogen and Testosterone): Secreted by the gonads (ovaries and testes), these hormones are responsible for the growth spurt during puberty. They also promote ossification and eventual closure of the epiphyseal plates, thus ending lengthwise bone growth. Estrogen is particularly important for maintaining bone density throughout life. Parathyroid Hormone (PTH): Secreted by the parathyroid glands, PTH regulates blood calcium levels. It stimulates osteoclast activity to release calcium from bones when blood calcium is low. Calcitonin: Secreted by the thyroid gland, calcitonin inhibits osteoclast activity and promotes calcium deposition in bones when blood calcium is high (has a weaker effect than PTH in humans). Insulin-like Growth Factors (IGFs): Produced mainly by the liver in response to GH, IGFs mediate many of the growth-promoting effects of GH on bone and other tissues. Glucocorticoids (e.g., Cortisol): In excess, these can inhibit bone growth and increase bone resorption.
  • 4. Physical Activity and Mechanical Stress:Weight-bearing exercise and mechanical stress on bones stimulate osteoblast activity and bone deposition, leading to increased bone density and strength (Wolff's Law). Lack of physical activity can lead to bone loss.
  • 5. General Health and Disease:Certain chronic illnesses or conditions can affect bone growth, such as kidney disease (affecting vitamin D activation and mineral balance), malabsorption syndromes (affecting nutrient absorption), or endocrine disorders.
  • 6. Exposure to Sunlight:Sunlight is necessary for the skin to synthesize Vitamin D, which is crucial for calcium absorption.

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