Skeletal muscle is a type of striated muscle tissue that is under voluntary control, primarily responsible for moving bones and facilitating locomotion.
Skeletal muscle contraction is driven by a series of complex molecular interactions that involve proteins like actin and myosin.
The interaction of these proteins is at the heart of muscle contraction and is regulated by calcium ions (Ca2+) and ATP.
The tractile cycle describes the sequence of events during muscle contraction. It includes the attachment, power stroke, and detachment of myosin heads from actin filaments.
This cycle is ATP-dependent and is crucial for sustained muscle contraction and relaxation.
Excitation-contraction coupling is the physiological process linking an action potential in the muscle cell membrane to muscle contraction.
An action potential causes calcium ions to be released from the sarcoplasmic reticulum into the cytosol, enabling the contractile proteins to interact and produce muscle contraction.
A muscle twitch is the response of a muscle fiber to a single action potential, resulting in a quick, brief contraction followed by relaxation.
It has three phases: the latent period, contraction phase, and relaxation phase.
Muscle twitches can combine through a process known as summation, where successive action potentials lead to increased muscle tension.
If the stimuli are rapid enough, the muscle does not have time to relax completely, resulting in tetanus, a sustained muscle contraction that can lead to fatigue if prolonged.
Asynchronous recruitment is a phenomenon where motor units are activated at different times to optimize force production while minimizing fatigue.
This allows certain muscle fibers to recover while others are contracting, facilitating endurance and sustained activity.