Skeletal Muscle – Anatomy and Physiology (2023)

Muscle tissue

OpenStaxCollege

learning objectives

At the end of this section, you will be able to:

  • Describe the connective tissue layers that surround skeletal muscle
  • Explain how muscles work with tendons to move the body
  • Identify areas of skeletal muscle fibers
  • Describe excitation-contraction coupling

The best-known characteristic of skeletal muscle is its ability to contract and cause movement. Skeletal muscles act not only to produce movement but also to stop it, such as resisting gravity to maintain posture. Small and constant adjustments of the skeletal muscles are necessary to keep the body upright or balanced in any position. Muscles also prevent excessive movement of bones and joints, maintaining skeletal stability and preventing damage or deformation of the skeletal structure. Joints can become misaligned or completely dislocated by pulling on associated bones; the muscles work to keep the 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 the internal organs (particularly the abdominal and pelvic organs) by acting as an external barrier or shield against external trauma and by supporting the weight of the organs.

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

Each skeletal muscle is an organ consisting of several integrated tissues. These tissues include skeletal muscle fibers, blood vessels, nerve fibers, and connective tissue. Each skeletal muscle has three layers of connective tissue (called “mysia”) that surround it and provide structure to the muscle as a whole, and also compartmentalize the muscle fibers within the muscle ([link]). Each muscle is surrounded by a sheath of dense, irregular connective tissue called theepimysium, which allows a muscle to contract and move with force while maintaining its structural integrity. The epimysium also separates the muscle from other tissues and organs in the area, allowing the muscle to move independently.

The three layers of connective tissue

Bundles of muscle fibers, called fascicles, are covered by the perimysium. Muscle fibers are covered by endomysium.

Within each skeletal muscle, muscle fibers are organized into individual bundles, each called afascicle, by an intermediate layer of connective tissue calledperimysium. This fascicular organization is common in limb muscles; allows the nervous system to trigger a specific movement of a muscle by activating a subset of muscle fibers within a muscle bundle or fascicle. Within each fasciculus, each muscle fiber is surrounded by a thin connective tissue layer of collagen and reticular fibers calledendomysium. The endomysium contains the extracellular fluid and nutrients to support the muscle fiber. These nutrients are delivered through the blood to muscle tissue.

In skeletal muscles that work with tendons to pull bones together, collagen in the three layers of tissue (the mysia) intertwines with the collagen in a tendon. At the other end of the tendon, it fuses with the periosteum that covers the bone. The tension created by muscle fiber contraction is then transferred through the mysia, to the tendon and then to the periosteum to pull on the bone to move the skeleton. Elsewhere, mysia may fuse with a broad, tendon-like blade called aaponeurosis, or the fascia, the connective tissue between the skin and bones. The broad layer of connective tissue in the lower back into which the latissimus dorsi muscles (the “lats”) fuse is an example of an aponeurosis.

Each skeletal muscle is also richly supplied with blood vessels for nourishment, oxygen delivery, and waste removal. In addition, each muscle fiber of a skeletal muscle is supplied by the axonal branch of a somatic motor neuron, which signals the fiber to contract. Unlike cardiac and smooth muscle, the only way skeletal muscle can functionally contract is through signaling from the nervous system.

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

Some other terminology associated with muscle fibers is rooted in the Greeksarco, which means "flesh". The plasma membrane of muscle fibers is calledsarcolema, the cytoplasm is referred to assarcoplasma, and the specialized smooth endoplasmic reticulum, which stores, releases, and retrieves calcium ions (Ca++) it's calledsarcoplasmic reticulum (SR)([link]). As will be described shortly, the functional unit of a skeletal muscle fiber is the sarcomere, a highly organized arrangement of contractile myofilaments.actin(fine strand) emyosin(thick filament), along with other supporting proteins.

muscle fiber

A skeletal muscle fiber is surrounded by a plasma membrane called the sarcolemma, which contains sarcoplasm, the cytoplasm of muscle cells. A muscle fiber is made up of many fibrils, which give the cell its striated appearance.

The striated appearance of skeletal muscle fibers is due to the arrangement of actin and myosin myofilaments in sequential order from one end of the muscle fiber to the other. Each bundle of these microfilaments and their regulatory proteins,troponinetropomiosina(along with other proteins) is calledsarcômero.

See thisvideoto learn more about the macro and microstructures of skeletal muscle. (a) What are the names of the “junction points” between sarcomeres? (b) What are the names of the “subunits” within the myofibrils that run the length of skeletal muscle fibers? (c) What is the “double string of pearls” described in the video? (d) What gives skeletal muscle fiber its striated appearance?

The sarcomere is the functional unit of the muscle fiber. The sarcomere itself is clustered within the myofibril that runs the length of the muscle fiber and attaches to the sarcolemma at its end. As the myofibrils contract, the entire muscle cell contracts. Because myofibrils are only about 1.2eum in diameter, hundreds to thousands (each with thousands of sarcomeres) can be found within a muscle fiber. Each sarcomere has approximately 2eum long with a three-dimensional arrangement similar to a cylinder and is bounded by structures called Z disks (also called Z lines, because the images are two-dimensional), to which the actin myofilaments are anchored ([link]). Because actin and its troponin-tropomyosin complex (projecting from the Z disks toward the center of the sarcomere) form thinner filaments than myosin, it is calledfine filamentof the sarcomere. Likewise, because the myosin filaments and their multiple heads (projecting from the center of the sarcomere, towards the Z disks, but not all towards them) have more mass and are thicker, they are calledthick filamentdo sarcômero.

O Sarcômero

The sarcomere, the region from one Z line to the next Z line, is the functional unit of a skeletal muscle fiber.

Another specialization of skeletal muscle is the location where the motor neuron terminal meets the muscle fiber – called theneuromuscular junction (JNM). It is here that the muscle fiber first responds to motor neuron signaling. Each skeletal muscle fiber in each skeletal muscle is innervated by a motor neuron in the JNM. Neuron excitation signals are the only way to functionally trigger fiber contraction.

Each skeletal muscle fiber is supplied by a motor neuron in the JNM. See thisvideoto find out more about what's happening at NMJ. (a) What is the definition of a motor unit? (b) What is the structural and functional difference between a large motor unit and a small motor unit? (c) Can you give an example of each? (d) Why is the neurotransmitter acetylcholine degraded after binding to its receptor?

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 known as the cell 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 specialized proteins in the membrane called ion channels. Although the currents generated by ions moving through these protein channels are very small, they form the basis of both neural signaling and muscle contraction.

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

although the termalternation excitation-contractionconfuses or frightens some students, it boils down to this: for a skeletal muscle fiber to contract, its membrane must first be “excited” – in other words, it must be stimulated to fire an action potential. The action potential of the muscle fiber, which travels through the sarcolemma like a wave, is “coupled” to the actual contraction through the release of calcium ions (Ca++) of RS. Once released, Ca++interacts with the protective proteins, forcing them apart so that the actin-binding sites are available for attachment by the myosin heads. Myosin then pulls the actin filaments toward the center, shortening the muscle fiber.

In skeletal muscle, this sequence begins with signals from the somatic motor division of the nervous system. In other words, the “arousal” step in skeletal muscles is always triggered by nervous system signaling ([link]).

Motor plate and innervation

In JNM, the axon terminal releases ACh. The motor endplate is the location of ACh receptors in the sarcolemma of the muscle fiber. When ACh molecules are released, they diffuse across a tiny gap called the synaptic cleft and bind to receptors.

Motor neurons that instruct skeletal muscle fibers 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, that are specialized for transmitting action potentials over long distances – in this case, from the spinal cord to the muscle itself (which can be up to a meter away). The axons of several neurons group together to form nerves, like wires grouped together in a cable.

Signaling begins when a neuronalaction potentialtravels along the axon of a motor neuron and then along individual branches to terminate at the JNM. In JNM, the axon terminal releases a chemical messenger, orneurotransmitter, calledacetylcholine (ACh). ACh molecules diffuse through a tiny space calledsynaptic cleftand bind to ACh receptors located within theengine end plateof the sarcolemma on the other side of the synapse. Once ACh binds, a channel on the ACh receptor opens and positively charged ions can pass into the muscle fiber, causing it to shift.depolarize, which means that the muscle fiber membrane potential becomes less negative (closer to zero).

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

Things happen very quickly in the world of excitable membranes (think how fast you can snap your fingers once you decide to do so). Immediately after the membrane depolarizes, it repolarizes, restoring the negative membrane potential. Meanwhile, ACh in the synaptic cleft is degraded by the enzyme acetylcholinesterase (AChE), so that ACh cannot rebind to a receptor and reopen its channel, which would cause excitation and unwanted prolonged muscle contraction.

The propagation of an action potential along the sarcolemma is the excitation portion of the excitation-contraction coupling. Recall that this excitation actually triggers the release of calcium ions (Ca++) from its storage in the cell's SR. For the action potential to reach the SR membrane, periodic invaginations occur in the sarcolemma, calledTubules T(“T” stands for “across”). You must remember that the diameter of a muscle fiber can reach 100eum, 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 RS membranes on either side is called atriad([link]). The triad surrounds the cylindrical structure calledmyofibrils, which contains actin and myosin.

The T tubule

Narrow T tubules allow the conduction of electrical impulses. The SR functions to regulate intracellular calcium levels. Two terminal cisternae (where the enlarged RS connects to the T-tubule) and a T-tubule make up a triad—a “three” of membranes, with those of the RS on two sides and the T-tubule sandwiched between them.

T tubules carry the action potential into the cell, which triggers the opening of calcium channels in the adjacent SR membrane, causing Ca++diffuse out of the SR and into the sarcoplasm. It's the arrival of Ca++in the sarcoplasm that initiates muscle fiber contraction by its contractile units, or sarcomeres.

Skeletal muscles contain connective tissue, blood vessels and nerves. There are three layers of connective tissue: epimysium, perimysium, and endomysium. Skeletal muscle fibers are organized into groups called fascicles. Blood vessels and nerves enter the connective tissue and branch into the cell. Muscles attach to bones either directly or through tendons or aponeuroses. Skeletal muscles maintain posture, stabilize bones and joints, control internal movements, and generate heat.

Skeletal muscle fibers are long, multinucleated cells. The cell membrane is the sarcolemma; the cytoplasm of the cell is the sarcoplasm. The sarcoplasmic reticulum (SR) is a form of endoplasmic reticulum. Muscle fibers are composed of myofibrils. Striae are created by the organization of actin and myosin, resulting in the banding pattern of myofibrils.

See thisvideoto learn more about the macro and microstructures of skeletal muscle. (a) What are the names of the “junction points” between sarcomeres? (b) What are the names of the “subunits” within the myofibrils that run the length of skeletal muscle fibers? (c) What is the “double string of pearls” described in the video? (d) What gives skeletal muscle fiber its striated appearance?

(a) Z lines. (b) Sarcomeres. (c) This is the arrangement of actin and myosin filaments in a sarcomere. (d) The alternating filaments of actin and myosin filaments.

Each skeletal muscle fiber is supplied by a motor neuron in the JNM. See thisvideoto learn more about what happens at the neuromuscular junction. (a) What is the definition of a motor unit? (b) What is the structural and functional difference between a large motor unit and a small motor unit? Can you give an example of each? (c) Why is the neurotransmitter acetylcholine degraded after binding to its receptor?

(a) It is the number of skeletal muscle fibers supplied by a single motor neuron. (b) A large motor unit has one neuron that supplies many skeletal muscle fibers for gross movement, such as the temporalis muscle, where 1000 fibers are supplied by one neuron. A small motor has one neuron that supplies a few skeletal muscle fibers for very fine movements, such as the extraocular ocular muscles, where six fibers are supplied by one neuron. (c) To prevent prolonged muscle contraction.

The correct order from smallest to largest unit of organization in muscle tissue is ________.

  1. fascicle, filament, muscle fiber, myofibril
  2. filament, myofibril, muscle fiber, fascicle
  3. muscle fiber, fascicle, filament, myofibril
  4. myofibril, muscle fiber, filament, fascicle

B

Depolarization of the sarcolemma means ________.

  1. the inside of the membrane has become less negative as sodium ions accumulate
  2. the outside of the membrane has become less negative as sodium ions accumulate
  3. the inside of the membrane has become more negative as sodium ions accumulate
  4. the sarcolemma has completely lost any electrical charge

A

What would happen to skeletal muscle if the epimysium were destroyed?

Muscles would lose their integrity during powerful movements resulting in muscle damage.

Describe how tendons facilitate body movement.

When a muscle contracts, the force of movement is transmitted through the tendon, which pulls on the bone to produce skeletal movement.

What are the five main functions of skeletal muscle?

They produce skeletal movement, maintain body posture and position, support soft tissues, surround the openings of the digestive, urinary, and other tracts, and maintain body temperature.

What are the opposite functions of voltage-gated sodium channels and voltage-gated potassium channels?

Opening of voltage-gated sodium channels, followed by Na influx+, transmits an action potential after the membrane has been sufficiently depolarized. Delayed opening of potassium channels allows K+to get out of the cell, to repolarize the membrane.

Glossary

acetylcholine (ACh)
neurotransmitter that binds to a motor end plate to trigger depolarization
actin
protein that makes up most of the thin myofilaments in a sarcomere muscle fiber
action potential
change in voltage of a cell membrane in response to a stimulus that results in the transmission of an electrical signal; exclusive to neurons and muscle fibers
aponeurosis
broad sheet of tendon-like connective tissue that connects a skeletal muscle to another skeletal muscle or to a bone
depolarize
to reduce the voltage difference between the inside and outside of a cell's plasma membrane (the sarcolemma of a muscle fiber), making the inside less negative than at rest
endomysium
loose, well-hydrated connective tissue covering each muscle fiber in a skeletal muscle
epimysium
outer layer of connective tissue around a skeletal muscle
alternation excitation-contraction
sequence of events from motor neuron signaling to a skeletal muscle fiber to contraction of the fiber's sarcomeres
fascicle
bundle of muscle fibers within a skeletal muscle
engine end plate
muscle fiber sarcolemma at the neuromuscular junction, with receptors for the neurotransmitter acetylcholine
myofibrils
long, cylindrical organelle that runs parallel within the muscle fiber and contains the sarcomeres
myosin
protein that makes up most of the thick cylindrical myofilament within a sarcomere muscle fiber
neuromuscular junction (JNM)
synapse between the axon terminal of a motor neuron and the membrane section of a muscle fiber with receptors for acetylcholine released from the terminal
neurotransmitter
signaling chemical released by nerve endings that bind to and activate receptors on target cells
perimysium
connective tissue that groups skeletal muscle fibers into fascicles within a skeletal muscle
sarcômero
longitudinally, repeating the functional unit of skeletal muscle, with all contractile and associated proteins involved in contraction
sarcolema
plasma membrane of a skeletal muscle fiber
sarcoplasma
cytoplasm of a muscle cell
sarcoplasmic reticulum (SR)
Specialized smooth endoplasmic reticulum, which stores, releases, and retrieves Ca++
synaptic cleft
space between a nerve terminal (axon) and a motor end plate
Tubulo T
projection of the sarcolemma into the interior of the cell
thick filament
the thick myosin filaments and their multiple heads projecting from the center of the sarcomere toward, but not toward, the Z disks
fine filament
thin filaments of actin and its troponin-tropomyosin complex projecting from the Z disks towards the center of the sarcomere
triad
the grouping of a T tubule and two terminal cisterns
troponin
regulatory protein that binds actin, tropomyosin, and calcium
tropomiosina
regulatory protein that covers myosin binding sites to prevent actin from binding to myosin
voltage gated sodium channels
membrane proteins that open sodium channels in response to a sufficient voltage change and initiate and transmit the action potential as Na+enter through the channel

References

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