9.2 Skeletal Muscle – Fundamentals of Anatomy and Physiology (2024)

The best-known feature of skeletal muscle is its ability to contract and cause movement. Skeletal muscles act not only to produce movement but also to stop movement, such as resisting gravity to maintain posture. Small, constant adjustments of the skeletal muscles are needed to hold a body upright or balanced in any position. Muscles also prevent excess movement of the bones and joints, maintaining skeletal stability and preventing skeletal structure damage or deformation. Joints can become misaligned or dislocated entirely by pulling on the associated bones; muscles work to keep joints stable. Skeletal muscles are located throughout the body at the openings of internal tracts to control the movement of various substances. These muscles allow functions, such as swallowing, urination, and defecation, to be under voluntary control. Skeletal muscles also protect internal organs (particularly abdominal and pelvic organs) by acting as an external barrier or shield to external trauma and by supporting the weight of the organs.

Skeletal muscles contribute to the maintenance of homeostasis in the body by generating heat. Muscle contraction requires energy, and when ATP is broken down, heat is produced. This heat is very noticeable during exercise, when sustained muscle movement causes body temperature to rise, and in cases of extreme cold, when shivering produces random skeletal muscle contractions to generate heat.

Each skeletal muscle is an organ that consists of various integrated tissues. These tissues include the skeletal muscle fibres, blood vessels, nerve fibres, and connective tissue. Each skeletal muscle has three layers of connective tissue (called “mysia”) that enclose it and provide structure to the muscle as a whole, and compartmentalise the muscle fibres within the muscle (Figure 9.2.1). Each muscle is wrapped in a sheath of dense, irregular connective tissue called theepimysium, which allows a muscle to contract and move powerfully while maintaining its structural integrity. The epimysium also separates muscle from other tissues and organs in the area, allowing the muscle to move independently.

Inside each skeletal muscle, muscle fibres are organised into individual bundles, each called afascicle, by a middle layer of connective tissue called theperimysium. This fascicular organisation is common in muscles of the limbs; it allows the nervous system to trigger a specific movement of a muscle by activating a subset of muscle fibres within a bundle, or fascicle of the muscle. Inside each fascicle, each muscle fibre is encased in a thin connective tissue layer of collagen and reticular fibres called theendomysium. The endomysium contains the extracellular fluid and nutrients to support the muscle fibre. These nutrients are supplied via blood to the muscle tissue.

In skeletal muscles that work with tendons to pull on bones, the collagen in the three tissue layers (the mysia) intertwines with the collagen of a tendon. At the other end of the tendon, it fuses with the periosteum coating the bone. The tension created by contraction of the muscle fibres is then transferred though the mysia, to the tendon, and then to the periosteum to pull on the bone for movement of the skeleton. In other places, the mysia may fuse with a broad, tendon-like sheet called anaponeurosis, or fascia, the connective tissue between skin and bones. The broad sheet of connective tissue in the lower back that the latissimus dorsi muscles (the “lats”) fuse into is an example of an aponeurosis.

Every skeletal muscle is also richly supplied by blood vessels for nourishment, oxygen delivery, and waste removal. In addition, every muscle fibre in a skeletal muscle is supplied by the axon branch of a somatic motor neuron, which signals the fibre to contract. Unlike cardiac and smooth muscle, the only way to functionally contract a skeletal muscle is through signalling from the nervous system.

Skeletal Muscle Fibres

Because skeletal muscle cells are long and cylindrical, they are commonly referred to as muscle fibres. Skeletal muscle fibres can be quite large for human cells, with diameters up to 100μm and lengths up to 30 cm (11.8 in) in the Sartorius of the upper leg. During early development, embryonic myoblasts, each with its own nucleus, fuse with up to hundreds of other myoblasts to form the multinucleated skeletal muscle fibres. Multiple nuclei mean multiple copies of genes, permitting the production of the large amounts of proteins and enzymes needed for muscle contraction.

Some other terminology associated with muscle fibres is rooted in the Greeksarco, which means “flesh.” The plasma membrane of muscle fibres is called thesarcolemma, the cytoplasm is referred to assarcoplasm, and the specialised smooth endoplasmic reticulum, which stores, releases, and retrieves calcium ions (Ca²⁺) is called thesarcoplasmic reticulum (SR)(Figure 9.2.2). As will soon be described, the functional unit of a skeletal muscle fibre is the sarcomere, a highly organised arrangement of the contractile myofilamentsactin(thin filament) andmyosin(thick filament), along with other support proteins.

The Sarcomere

The sarcomere is the functional unit of the muscle fibre. The sarcomere itself is bundled within the myofibril that runs the entire length of the muscle fibre and attaches to the sarcolemma at its end. As myofibrils contract, the entire muscle cell contracts. Because myofibrils are only approximately 1.2μm in diameter, hundreds to thousands (each with thousands of sarcomeres) can be found inside one muscle fibre. Each sarcomere is approximately 2μm in length with a three-dimensional cylinder-like arrangement and is bordered by structures called Z-discs (also called Z-lines, because pictures are two-dimensional), to which the actin myofilaments are anchored (Figure 9.2.3). Because the actin and its troponin-tropomyosin complex (projecting from the Z-discs toward the centre of the sarcomere) form strands that are thinner than the myosin, it is called thethin filamentof the sarcomere. Likewise, because the myosin strands and their multiple heads (projecting from the centre of the sarcomere, toward but not all to way to, the Z-discs) have more mass and are thicker, they are called thethick filamentof the sarcomere.

The Neuromuscular Junction

Another specialisation of the skeletal muscle is the site where a motor neuron’s terminal meets the muscle fibre — called theneuromuscular junction (NMJ). This is where the muscle fibre first responds to signalling by the motor neuron. Every skeletal muscle fibre in every skeletal muscle is innervated by a motor neuron at the NMJ. Excitation signals from the neuron are the only way to functionally activate the fibre to contract.

Excitation–Contraction Coupling

All living cells have membrane potentials, or electrical gradients across their membranes. The inside of the membrane is usually around -60 to -90 mV, relative to the outside. This is referred to as a cell’s membrane potential. Neurons and muscle cells can use their membrane potentials to generate electrical signals. They do this by controlling the movement of charged particles, called ions, across their membranes to create electrical currents. This is achieved by opening and closing specialised proteins in the membrane called ion channels. Although the currents generated by ions moving through these channel proteins are very small, they form the basis of both neural signalling and muscle contraction.

Both neurons and skeletal muscle cells are electrically excitable, meaning that they can generate action potentials. An action potential is a special type of electrical signal that can travel along a cell membrane as a wave. This allows a signal to be transmitted quickly and faithfully over long distances.

Although the termexcitation-contraction couplingconfuses or scares some students, it comes down to this: for a skeletal muscle fibre to contract, its membrane must first be “excited”—in other words, it must be stimulated to fire an action potential. The muscle fibre action potential, which sweeps along the sarcolemma as a wave, is “coupled” to the actual contraction through the release of calcium ions (Ca2+) from the SR. Once released, the Ca2+interacts with the shielding proteins, forcing them to move aside so that the actin-binding sites are available for attachment by myosin heads. The myosin then pulls the actin filaments toward the centre, shortening the muscle fibre.

In skeletal muscle, this sequence begins with signals from the somatic motor division of the nervous system. In other words, the “excitation” step in skeletal muscles is always triggered by signalling from the nervous system (Figure 9.2.4).

The motor neurons that tell the skeletal muscle fibres to contract originate in the spinal cord, with a smaller number located in the brainstem for activation of skeletal muscles of the face, head, and neck. These neurons have long processes, called axons, which are specialised to transmit action potentials long distances— in this case, all the way from the spinal cord to the muscle itself (which may be up to three feet away). The axons of multiple neurons bundle together to form nerves, like wires bundled together in a cable.

Signalling begins when a neuronalaction potentialtravels along the axon of a motor neuron, and then along the individual branches to terminate at the NMJ. At the NMJ, the axon terminal releases a chemical messenger, orneurotransmitter, calledacetylcholine (ACh). The ACh molecules diffuse across a minute space called thesynaptic cleftand bind to ACh receptors located within themotor end-plateof the sarcolemma on the other side of the synapse. Once ACh binds, a channel in the ACh receptor opens and positively charged ions can pass through into the muscle fibre, causing it todepolarise, meaning that the membrane potential of the muscle fibre becomes less negative (closer to zero.)

As the membrane depolarises, another set of ion channels calledvoltage-gated sodium channelsare triggered to open. Sodium ions enter the muscle fibre, and an action potential rapidly spreads (or “fires”) along the entire membrane to initiate excitation-contraction coupling.

Things happen very quickly in the world of excitable membranes (just think about how quickly you can snap your fingers as soon as you decide to do it). Immediately following depolarisation of the membrane, it repolarises, re-establishing the negative membrane potential. Meanwhile, the ACh in the synaptic cleft is degraded by the enzyme acetylcholinesterase (AChE) so that the ACh cannot rebind to a receptor and reopen its channel, which would cause unwanted extended muscle excitation and contraction.

Propagation of an action potential along the sarcolemma is the excitation portion of excitation-contraction coupling. Recall that this excitation triggers the release of calcium ions (Ca²⁺) from its storage in the cell’s SR. For the action potential to reach the membrane of the SR, there are periodic invagin*tions in the sarcolemma, calledT-tubules(“T” stands for “transverse”). You will recall that the diameter of a muscle fibre can be up to 100μm, so these T-tubules ensure that the membrane can get close to the SR in the sarcoplasm. The arrangement of a T-tubule with the membranes of SR on either side is called atriad(Figure 9.2.5). The triad surrounds the cylindrical structure called amyofibril, which contains actin and myosin.

The T-tubules carry the action potential into the interior of the cell, which triggers the opening of calcium channels in the membrane of the adjacent SR, causing Ca²⁺to diffuse out of the SR and into the sarcoplasm. It is the arrival of Ca²⁺in the sarcoplasm that initiates contraction of the muscle fibre by its contractile units, or sarcomeres.

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