Musculoskeletal System

Musculoskeletal System

Learning Objectives

  • Understand the function of the human skeleton.

  • Describe the structures of bone, muscle, tendons, and ligaments.

  • Understand and discuss how muscles contract.

The Skeleton

Functions of the Skeletal System
  • Protection of Vital Organs:

    • Protects the heart, lungs, brain, and spinal cord.

  • Movement Support:

    • Provides anchor points for muscles.

    • Transmits forces generated by muscular contraction similar to a system of pulleys and levers.

  • Body Support:

    • Provides support for the entire body.

  • Mineral Storage and Release:

    • Stores essential minerals such as calcium and phosphorus.

    • Hematopoiesis: Formation of blood cells occurs in the marrow of some bones, with some white blood cells maturing outside of the bone.

Bone

What is Bone?
  • Bone is a living tissue made up of:

    • Cells

    • Fibres embedded in a hard matrix consisting of calcium phosphate and calcium hydroxide, collectively known as hydroxyapatite.

Types of Bone
  1. Cancellous (Trabecular or Spongy Bone)

  2. Compact Bone

  3. Classification by Shape:

    • Irregular Bone (e.g., vertebrae)

    • Long Bone (e.g., femur, humerus)

    • Sesamoid Bone (e.g., patella)

    • Short Bone (e.g., carpal and tarsal bones)

    • Flat Bone (e.g., sternum, skull bones)

Characteristics of Different Bone Types
  • Short Bones:

    • Cube-shaped, nearly equal in length and width.

    • Mostly consist of spongy bone with a compact bone surface.

    • Examples include carpal and tarsal bones (excluding phalanges).

  • Flat Bones:

    • Thin and protective with two parallel plates of compact bone enclosing spongy bone.

    • Examples include cranial bones, sternum, ribs, scapulae, and ilium.

  • Long Bones:

    • Central shaft (diaphysis) is thick compact bone.

    • Ends (epiphyses) consist of spongy bone covered by compact bone.

    • Examples include humerus and femur.

  • Irregular Bones:

    • Variable amounts of spongy and compact bone.

    • Examples include vertebrae, ischium, pubis, and sacrum.

  • Sesamoid Bones:

    • Develop in tendons under stress to protect tendons from wear.

    • Change the direction of tendon pulls and improve mechanical advantage.

    • Examples are patellae and sesamoid bones in palms and soles of feet.

Periosteum
  • The outer surface of bone is covered by the periosteum, a specialized connective tissue layer.

  • Functions of the periosteum:

    • Connector for tendons and ligaments to bone.

    • Enables new bone formation and repair.

Compact Bone
  • Forms a protective outer shell around every bone.

  • Constitutes roughly 80% of skeletal mass, providing strength against bending and torsion.

  • Structure: Comprised of osteons (Haversian systems) containing:

    • A central vascular channel (Haversian canal) that houses capillaries, venules, and nerves.

    • Surrounding concentric layers termed lamellae, which contain osteocytes embedded in fluid-filled lacunae, connected by canaliculi.

  • Osteocytes are the most abundant bone cell type, approximately 42 billion, with a half-life of about 25 years.

Trabecular (Spongy) Bone
  • Comprises 20% of skeletal mass yet occupies 80% of bone surface area.

  • Less dense and more elastic than compact bone

  • Contains a network of trabecular structures that maintain shape under compressive forces.

  • Predominantly found in the ends of long bones and throughout the interior of short bones.

Bone Formation (Ossification/Osteogenesis)

Overview of Bone Development
  • Different bones form through various mechanisms, largely dependent on their type and function.

  • Timeline: Long bones begin developing approximately 2 months into fetal development.

Developmental Mechanism
  1. Cartilage Model Formation:

    • Formation begins with mesenchymal cells creating a cartilaginous matrix, which later becomes calcified.

    • Establishment of perichondrium around the cartilage structure.

  2. Osteoblast Formation:

    • Some mesenchymal cells differentiate into osteoblasts that surround the cartilage model with a bony collar.

    • The periosteum contributes to bone formation via osteoblast generation.

  3. Center of Ossification:

    • The middle cartilage breaks down and is invaded by blood vessels and osteoblasts leading to bone tissue formation.

    • This progresses longitudinally toward the epiphyses, replacing cartilage with spongy bone.

  4. Secondary Ossification Centers:

    • These form in the epiphyses, eventually leading to a marrow cavity formation as spongy bone is resorbed.

  5. Epiphyseal Plate: Maintains cartilage for lengthening until adulthood (~20 years old), after which further growth stops.

Intramembranous Ossification
  • Process: Formation of flat bones via ossification of soft sheets of mesenchymal cells (membrane bones), featuring:

    • Mesenchymal cell condensation and blood capillary permeation.

    • Osteoid tissue deposition by osteoblasts, resulting in spongy bone formation before converting to compact bone.

Bone Remodeling and Renewal

  • Bone strength is maintained by continuous remodeling involving:

    • Resorption: Removal of old bone by osteoclasts.

    • Formation: Creation of new bone by osteoblasts.

  • As individuals age, resorption may outweigh formation, leading to conditions such as osteopenia or osteoporosis.

Cell Types in Bone Renewal

  1. Osteoblasts:

    • Cells responsible for bone formation

  2. Osteoclasts:

    • Cells responsible for bone resorption

Calcium Regulation
  • Bone resorption is regulated by parathyroid hormone (PTH):

    • Released in response to low calcium and phosphorus levels, stimulating osteoclasts for increased bone resorption and mineral release.

    • It also converts vitamin D, affecting intestinal calcium absorption.

    • Calcitonin acts oppositely, decreasing osteoclast activity and promoting osteoblast function while managing blood calcium levels.

Cartilage

  • A flexible tissue comprised of glycoprotein (chondroitin), collagen fibers, and cartilage cells.

  • Locations include:

    • Trachea and larynx

    • Nose and ear lobes

    • Between ribs and breastbone

    • Articular surfaces in joints.

Joints

  • Types of Joints According to Mobility:

    • Fibrous Joints: No movement (e.g., bones of the skull).

    • Cartilaginous Joints: Limited movement (e.g., between vertebrae).

    • Synovial Joints: Increased movement with lubricated cavities, allowing for flexibility at joints.

Ligaments and Tendons
  • Ligaments: Tough bands of fibrous tissue linking bones at joints, limiting joint mobility.

  • Tendons: Connect muscle to bone, facilitating movement.

Muscles

Types of Muscle
  1. Cardiac Muscle= smooth, involuntary, heart

  2. Skeletal Muscle= striated, voluntary, and responsible for movements of the skeleton. Composed of bundles of muscle cells (fascicles) with connective tissue envelops (epimysium and perimysium).

  3. Smooth Muscle= smooth, involuntary and found in the walls of hollow organs such as the intestines, bladder, and blood vessels.

Muscle Contraction Mechanism
  1. Thick Filaments: Composed of myosin.

  2. Thin Filaments: Comprised of actin along with troponin and tropomyosin.

  3. Sliding Filament Model:

    • Triggered by nervous action potentials causing Ca2+ release from the sarcoplasmic reticulum.

    • Calcium binding to troponin moves tropomyosin, exposing myosin binding sites on actin.

    • Myosin heads attach to actin and pivot to pull actin filaments, shortening the sarcomere.

    • ATP replaces ADP to detach myosin from actin, with the process repeating as long as calcium is present.

Muscle Strength Factors
  • Related to muscle cross-sectional area, with thicker muscles exerting more force but longer muscles allowing for more considerable movement.

  • Muscle fibers are fixed in number after early life; further development results from hypertrophy (thickening).

Anabolic Steroids
  • Often illegally used in sports to boost muscle mass; can cause severe health issues, including liver damage, kidney issues, and increased heart disease risk, mimicking testosterone effects.