Muscular system anatomy and physiology

Last updated: February 24, 2023

Muscular system anatomy and physiology

MSKS

MSKS

Introduction to the skeletal system
Introduction to the muscular system
Bone histology
Cartilage histology
Skeletal muscle histology
Bone remodeling and repair
Cartilage structure and growth
Fibrous, cartilage, and synovial joints
Radial head subluxation (Nursemaid elbow)
Developmental dysplasia of the hip
Legg-Calve-Perthes disease
Slipped capital femoral epiphysis
Transient synovitis
Osgood-Schlatter disease (traction apophysitis)
Rotator cuff tear
Klumpke paralysis
Spondylolysis
Spondylolisthesis
Degenerative disc disease
Spinal disc herniation
Sciatica
Compartment syndrome
Rhabdomyolysis
Craniosynostosis
Osteogenesis imperfecta
Cleidocranial dysplasia
Achondroplasia
Osteomyelitis
Bone tumors
Osteochondroma
Chondrosarcoma
Osteoporosis
Osteomalacia and rickets
Paget disease of bone
Osteopetrosis
Osteoarthritis
Spondylosis
Spinal stenosis
Rheumatoid arthritis
Juvenile idiopathic arthritis
Gout
Calcium pyrophosphate deposition disease (pseudogout)
Psoriatic arthritis
Ankylosing spondylitis
Reactive arthritis
Spondylitis
Septic arthritis
Bursitis
Baker cyst
Polymyositis
Dermatomyositis
Inclusion body myopathy
Polymyalgia rheumatica
Fibromyalgia
Rhabdomyosarcoma
Myasthenia gravis
Lambert-Eaton myasthenic syndrome
Citric acid cycle
Slow twitch and fast twitch muscle fibers
Electron transport chain and oxidative phosphorylation
Glycolysis
Selective permeability of the cell membrane
Resting membrane potential
Neuron action potential
Fatty acid oxidation
Amino acid metabolism
Ketone body metabolism
Skeletal system anatomy and physiology
Muscular system anatomy and physiology
Brachial plexus
Neuromuscular junction and motor unit
Sliding filament model of muscle contraction
Muscle contraction
Muscle spindles and golgi tendon organs
Neuromuscular blockers
Neuromuscular junction disorders: Pathology review
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Glycogen storage disease type II (NORD)
Glycogen storage disease type I
Glycogen storage disease type V
Glycogen storage disease type IV
Glycogen storage disease type III
Muscular dystrophies and mitochondrial myopathies: Pathology review
Myalgias and myositis: Pathology review
Shock
Escherichia coli
Staphylococcus aureus
Clostridium tetani (Tetanus)
Clostridium botulinum (Botulism)
Abdominal trauma: Clinical
Neck trauma: Clinical
Chest trauma: Clinical
Traumatic brain injury: Clinical
Complement system
Clostridium perfringens
Streptococcus pyogenes (Group A Strep)
Neisseria gonorrhoeae
Non-steroidal anti-inflammatory drugs
Acetaminophen (Paracetamol)
Rheumatoid arthritis and osteoarthritis: Pathology review
Rheumatoid arthritis: Clinical
Seronegative arthritis: Clinical
Gout and pseudogout: Pathology review
Pseudomonas aeruginosa
Salmonella (non-typhoidal)
Pediatric bone and joint infections: Clinical
Back pain: Pathology review
Lower back pain: Clinical
Skin and soft tissue infections: Clinical
Bone tumors: Pathology review
Pediatric orthopedic conditions: Clinical
Uterine fibroid
Erb-Duchenne palsy
Seronegative and septic arthritis: Pathology review
Vaccinations: Clinical
Vaccinations
Cardiac muscle histology
Cardiac excitation-contraction coupling
Positive inotropic medications
cGMP mediated smooth muscle vasodilators
Calcium channel blockers
Adrenergic antagonists: Beta blockers
Marfan syndrome
Ehlers-Danlos syndrome

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Muscular system anatomy and physiology

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The muscular system is made up of three types of muscle tissue: skeletal, smooth, and cardiac muscle tissue.

They differ in terms of their location, cell structure, and innervation. But they also share some characteristics: they’re all excitable, meaning that the cells react to a stimulus, they all contract--meaning that the cells will shorten, they all have extensibility--meaning that the cells can be stretched, and they’re all elastic--meaning that they can recoil or bounce back to their original length.

Let’s start with skeletal muscles. Skeletal muscles usually attach to bones, but in some cases, they attach to the skin, like the muscles in our face that control facial expression.

Skeletal muscles are voluntary muscles, meaning that they can be controlled consciously, but some skeletal muscles are also controlled subconsciously.

Your diaphragm, for example, you can contract consciously when you take a big breath, but it also continues to contract and relax without conscious effort when you’re fast asleep or thinking about other things.

Skeletal muscles help you maintain your posture and stabilize joints, and because skeletal muscles use up a lot of energy as they contract and relax, they also generate a lot of heat as a byproduct. That’s why we shiver to stay warm when it’s really cold.

Now let’s take a look at the biceps brachii, a skeletal muscle in your upper arm. Like most muscles there’s the belly of the muscle and the muscle tendons.

The muscle belly is the part that contracts and it’s wrapped in a layer of connective tissue called the epimysium.

Now let’s take a look at the cross-section of the muscle belly, there are thin layers of connective tissue called the perimysium that separate the muscle into fascicles.

Each muscle fascicle consists of a bundle of muscle fibers, and each muscle fiber is a muscle cell, or myocyte.

Every myocyte is surrounded by a smaller connective tissue sheath called the endomysium.

Together, the endomysium, perimysium and epimysium, bundle together thousands of muscle fibers which give the muscle structure and strength - similar to how it’s easy to snap a single twig, but hard to break a big bundle of sticks.

Together these three layers of connective tissue extend beyond the muscle belly, and become the tough cord-like tendon which attach the muscle to the bone.

When a tendon attaches to a bone that’s not moving it’s called an origin, and when a tendon attaches to a bone that’s moving it’s called an insertion.

Now, let’s zoom in and look at a single myocyte. Myocytes are long cylindrical cells with multiple nuclei located just below the cell membrane which is called the sarcolemma.

The sarcolemma is unique because it makes these tiny tunnels that project downwards from the surface into the center of the muscle fiber. These tunnels are called transverse tubules, or T tubules.

The cytoplasm of a myocyte is called sarcoplasm, and it contains smooth endoplasmic reticulum which is called sarcoplasmic reticulum.

The sarcoplasmic reticulum stores lots of calcium and runs parallel to the T tubules.

Now, the sarcoplasm is filled with stacks of long filaments called myofibrils.

Each myofibril has thin actin filaments, and thick myosin filaments that don’t extend through the entire length of the myocyte, but instead they’re arranged into shorter segments called sarcomeres.

Each myocyte is made up of hundreds sarcomeres, and under a microscope, the thick myosin filaments look dark, while the thin actin filaments look light. This is why skeletal muscles look striated or striped.

Okay - so when we want to move, a motor signal is sent from the brain, down the spinal cord and then travels through a motor neuron.

The motor neuron releases the neurotransmitter acetylcholine onto the sarcolemma which has acetylcholine receptors. This causes rapid shifts in ions to occur across the sarcolemma and down the T tubules, which brings some calcium into the myocyte.

Key Takeaways

The muscular system is composed of specialized cells called muscle fibers, which contain contractile proteins that enable them to contract and relax. The main types of muscle tissue are: skeletal, cardiac and smooth muscles.

Skeletal muscles are voluntary muscles attached to bones, which enable movement of the skeleton, and maintain body temperature by generating heat. The cardiac muscle is present only in the heart and is responsible for cardiac contraction that pumps blood throughout the body. Smooth muscles lie mainly in the walls of hollow viscera, such as the stomach and intestines, where they help to propel substances through these organs.

Sources

  1. "Medical Physiology" Elsevier (2016)
  2. "Physiology" Elsevier (2017)
  3. "Human Anatomy & Physiology" Pearson (2018)
  4. "Principles of Anatomy and Physiology" Wiley (2014)
  5. "MHC composition and enzyme-histochemical and physiological properties of a novel fast-twitch motor unit type" American Journal of Physiology-Cell Physiology (1991)
  6. "Exercise induced increases in muscle fiber number" European Journal of Applied Physiology and Occupational Physiology (1986)
  7. "Enzyme activity and fiber composition in skeletal muscle of untrained and trained men" J Appl Physiol (1972)