Skeletal Muscle
Voluntary control, striated
Individual fibers can be selectively activated
Capable of sustaining contraction, generating a large range of force.
Smooth Muscle
Involuntary control, non-striated
Regulated by the autonomic nervous system
Functions through myosin/actin cross bridges activated by calcium
Exhibits slow, sustained contractions, changes lumen diameter.
Cardiac Muscle
Like skeletal muscle (striated, sarcomere structure)
Functions as a unit, heart acts as a pump with contraction and relaxation cycles.
Myocytes contract simultaneously due to electrical coupling (gap junctions).
Skeletal Muscle
Activated by somatic motor neurons; action potentials (AP) lead to muscle contraction.
Smooth Muscle
Uses myosin/actin interaction regulated by calcium.
Lacks sarcomeres but contains actin and myosin arranged around dense bodies.
Can change shape and volume without losing tension due to its unique filament arrangement.
Neurons: Divided based on direction of impulse conduction.
Sensory Neurons: Convey information from sensory receptors to CNS.
Motor Neurons: Transmit signals from CNS to target organs (muscles/glands).
Somatic Motor Neurons: Control skeletal muscle with AP leading to muscle activation; no AP means muscle is off.
Autonomic Motor Neurons: Modulates contraction strength by tuning AP activity.
Structure and Function
Located in blood vessels, airways, digestive organs, urinary and reproductive tracts.
Lacks distinct striations yet functions via actin and myosin interactions.
Primarily contracts in a coordinated fashion (single-unit) through gap junctions.
Length-Tension Relationship
Maximum tension occurs when muscle is 100-120% of resting length.
Tension decreases outside this optimal range due to fewer interactions between myosin and actin filaments.
Single-unit Smooth Muscle
Multiple gap junctions ensure synchronized contractions.
Exhibits pacemaker activity, moderated by stretch or neural input.
Multi-unit Smooth Muscle
Requires individual nerve innervation for contraction, behaves more independently.
Examples include arrector pili muscles and ciliary muscles.
Calcium Source
Calcium primarily enters from the extracellular fluid via voltage-gated channels.
Calcium binds to calmodulin (not troponin as in skeletal muscle) and activates myosin light-chain kinase (MLCK).
MLCK phosphorylates myosin light chains allowing for cross-bridge formation, leading to contraction.
Key Components to Relaxation
Calcium removal is essential for muscle relaxation.
Decrease in cytosolic calcium occurs via pumping out of the cell or back into the sarcoplasmic reticulum.
Myosin light chain phosphatase removes phosphate from myosin light chains, decreasing myosin ATPase activity and muscle tension.
Parasympathetic Regulation
Ach binding to muscarinic receptors increases calcium influx, causing constriction and reduced airway radius.
Sympathetic Regulation
Epi binding to beta-2 adrenergic receptors decreases smooth muscle contraction, increasing airway radius.
Comparison to Skeletal Muscle
Structures are striated; smaller cells with a single nucleus.
Cells are electrically linked through gap junctions for synchronous contractions.
Action Potential (AP)
AP is longer, facilitating twitch contractions.
Pacemaker potentials allow automatic generation of heartbeat without nervous system input.
AP from adjacent cells triggers calcium influx through T-tubules.
Entry of Ca2+ activates ryanodine receptors for calcium release from SR, resulting in muscle contraction.
Skeletal Muscle: Voluntary, striated, requires nerve stimulation.
Cardiac Muscle: Involuntary, striated, cells contract as a unit without motor neuron input but modulated by autonomic nerves.
Smooth Muscle: Involuntary, non-striated, may contract on its own or be modulated by nerve activity.