{"id":519,"date":"2021-01-17T23:14:11","date_gmt":"2021-01-17T23:14:11","guid":{"rendered":"https:\/\/pressbooks.publishdot.com\/anatomyphysiology\/chapter\/9-2-skeletal-muscle\/"},"modified":"2021-12-07T09:26:33","modified_gmt":"2021-12-07T09:26:33","slug":"9-2-skeletal-muscle","status":"publish","type":"chapter","link":"https:\/\/pressbooks.publishdot.com\/anatomyphysiology\/chapter\/9-2-skeletal-muscle\/","title":{"raw":"9.2 Skeletal Muscle","rendered":"9.2 Skeletal Muscle"},"content":{"raw":"
\n

Learning Objectives<\/strong><\/p>\n\n<\/header>\n

\n\nBy the end of this section, you will be able to:\n
    \n \t
  • Describe the layers of connective tissues packaging skeletal muscle<\/li>\n \t
  • Explain how muscles work with tendons to move the body<\/li>\n \t
  • Identify areas of the skeletal muscle fibres<\/li>\n \t
  • Describe excitation-contraction coupling<\/li>\n<\/ul>\n<\/div>\n<\/div>\nThe 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.\n\nSkeletal 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.\n\nEach 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 \u201cmysia\u201d) 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 the\u00a0epimysium<\/strong>, 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.\n\n[caption id=\"attachment_518\" align=\"aligncenter\" width=\"841\"]\"The Figure 9.2.1. The Three connective tissue layers.<\/strong> Bundles of muscle fibres, called fascicles, are covered by the perimysium. Muscle fibres are covered by the endomysium.[\/caption]\n\nInside each skeletal muscle, muscle fibres are organised into individual bundles, each called a\u00a0fascicle, by a middle layer of connective tissue called the\u00a0perimysium. 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 the\u00a0endomysium. The endomysium contains the extracellular fluid and nutrients to support the muscle fibre. These nutrients are supplied via blood to the muscle tissue.\n\nIn 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 an\u00a0aponeurosis, 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 \u201clats\u201d) fuse into is an example of an aponeurosis.\n\nEvery 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.\n

    Skeletal Muscle Fibres<\/h2>\nBecause 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 100\u00a0\u03bc<\/em>m 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.\n\nSome other terminology associated with muscle fibres is rooted in the Greek\u00a0sarco<\/em>, which means \u201cflesh.\u201d The plasma membrane of muscle fibres is called the\u00a0sarcolemma<\/strong>, the cytoplasm is referred to as\u00a0sarcoplasm<\/strong>, and the specialised smooth endoplasmic reticulum, which stores, releases, and retrieves calcium ions (Ca2+<\/sup>) is called the\u00a0sarcoplasmic reticulum (SR)<\/strong>\u00a0(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 myofilaments\u00a0actin<\/strong>\u00a0(thin filament) and\u00a0myosin<\/strong>\u00a0(thick filament), along with other support proteins.\n\n \n\n[caption id=\"attachment_518\" align=\"aligncenter\" width=\"801\"]\"A Figure 9.2.2. Muscle fibre.<\/strong> A skeletal muscle fibre is surrounded by a plasma membrane called the sarcolemma, which contains sarcoplasm, the cytoplasm of muscle cells. A muscle fibre is composed of many fibrils, which give the cell its striated appearance.[\/caption]\n

    The Sarcomere<\/h2>\nThe 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 1.2\u00a0\u03bc<\/em>m in diameter, hundreds to thousands (each with thousands of sarcomeres) can be found inside one muscle fibre. Each sarcomere is approximately 2\u00a0\u03bc<\/em>m 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 the\u00a0thin filament<\/strong>\u00a0of 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 the\u00a0thick filament<\/strong>\u00a0of the sarcomere.\n\n \n\n[caption id=\"attachment_518\" align=\"aligncenter\" width=\"940\"]\"Diagram Figure 9.2.3. The sarcomere.<\/strong> The sarcomere, the region from one Z-line to the next Z-line, is the functional unit of a skeletal muscle fibre.[\/caption]\n

    The Neuromuscular Junction<\/h2>\nAnother specialisation of the skeletal muscle is the site where a motor neuron\u2019s terminal meets the muscle fibre \u2014 called the\u00a0neuromuscular junction (NMJ)<\/strong>. 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.\n

    Excitation\u2013Contraction Coupling<\/h2>\nAll 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\u2019s 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.\n\nBoth 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.\n\nAlthough the term\u00a0excitation-contraction coupling<\/strong>\u00a0confuses or scares some students, it comes down to this: for a skeletal muscle fibre to contract, its membrane must first be \u201cexcited\u201d\u2014in 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 \u201ccoupled\u201d to the actual contraction through the release of calcium ions (Ca2+) from the SR. Once released, the Ca2+\u00a0interacts 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.\n\nIn skeletal muscle, this sequence begins with signals from the somatic motor division of the nervous system. In other words, the \u201cexcitation\u201d step in skeletal muscles is always triggered by signalling from the nervous system (Figure 9.2.4).\n\n[caption id=\"attachment_518\" align=\"aligncenter\" width=\"440\"]\"Motor Figure 9.2.4. Motor end-plate and innervation.<\/strong> At the NMJ, the axon terminal releases ACh. The motor end-plate is the location of the ACh-receptors in the muscle fibre sarcolemma. When ACh molecules are released, they diffuse across a minute space called the synaptic cleft and bind to the receptors.[\/caption]\n\nThe 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\u2014 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.\n\nSignalling begins when a neuronal\u00a0action potential<\/strong>\u00a0travels 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, or\u00a0neurotransmitter<\/strong>, called\u00a0acetylcholine (ACh)<\/strong>. The ACh molecules diffuse across a minute space called the\u00a0synaptic cleft<\/strong>\u00a0and bind to ACh receptors located within the\u00a0motor end-plate<\/strong>\u00a0of 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 to\u00a0depolarise<\/strong>, meaning that the membrane potential of the muscle fibre becomes less negative (closer to zero.)\n\nAs the membrane depolarises, another set of ion channels called\u00a0voltage-gated sodium channels<\/strong>\u00a0are triggered to open. Sodium ions enter the muscle fibre, and an action potential rapidly spreads (or \u201cfires\u201d) along the entire membrane to initiate excitation-contraction coupling.\n\nThings 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.\n\nPropagation 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+<\/sup>) from its storage in the cell\u2019s SR. For the action potential to reach the membrane of the SR, there are periodic invaginations in the sarcolemma, called\u00a0T-tubules<\/strong>\u00a0(\u201cT\u201d stands for \u201ctransverse\u201d). You will recall that the diameter of a muscle fibre can be up to 100\u00a0\u03bc<\/em>m, 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 a\u00a0triad<\/strong>\u00a0(Figure 9.2.5). The triad surrounds the cylindrical structure called a\u00a0myofibril<\/strong>, which contains actin and myosin.\n\n[caption id=\"attachment_518\" align=\"aligncenter\" width=\"467\"]\"The Figure 9.2.5. The T-tubule.<\/strong> Narrow T-tubules permit the conduction of electrical impulses. The SR functions to regulate intracellular levels of calcium. Two terminal cisternae (where enlarged SR connects to the T-tubule) and one T-tubule comprise a triad\u2014a \u201cthreesome\u201d of membranes, with those of SR on two sides and the T-tubule sandwiched between them.[\/caption]\n\nThe 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+<\/sup>\u00a0to diffuse out of the SR and into the sarcoplasm. It is the arrival of Ca2+<\/sup>\u00a0in the sarcoplasm that initiates contraction of the muscle fibre by its contractile units, or sarcomeres.\n
    \n

    Section Review<\/strong><\/p>\n\n<\/header>\n

    \n\nSkeletal muscles contain connective tissue, blood vessels and nerves. There are three layers of connective tissue: epimysium, perimysium, and endomysium. Skeletal muscle fibres are organised into groups called fascicles. Blood vessels and nerves enter the connective tissue and branch in the cell. Muscles attach to bones directly or through tendons or aponeuroses. Skeletal muscles maintain posture, stabilise bones and joints, control internal movement, and generate heat.\n\nSkeletal muscle fibres are long, multinucleated cells. The membrane of the cell is the sarcolemma; the cytoplasm of the cell is the sarcoplasm. The sarcoplasmic reticulum (SR) is a form of endoplasmic reticulum. Muscle fibres are composed of myofibrils. The striations are created by the organisation of actin and myosin resulting in the banding pattern of myofibrils.\n\n<\/div>\n<\/div>\n
    \n

    Review Questions<\/strong><\/p>\n\n<\/header>\n

    \n\n[h5p id=\"246\"]\n\n<\/div>\n<\/div>\n
    \n

    Critical Thinking Questions<\/strong><\/p>\n\n<\/header>\n

    \n\n[h5p id=\"247\"]\n\n[h5p id=\"248\"]\n\n[h5p id=\"249\"]\n\n[h5p id=\"250\"]\n\n<\/div>\n<\/div>\nClick the drop down below to review the terms learned from this chapter.\n\n[h5p id=\"251\"]","rendered":"
    \n
    \n

    Learning Objectives<\/strong><\/p>\n<\/header>\n

    \n

    By the end of this section, you will be able to:<\/p>\n

      \n
    • Describe the layers of connective tissues packaging skeletal muscle<\/li>\n
    • Explain how muscles work with tendons to move the body<\/li>\n
    • Identify areas of the skeletal muscle fibres<\/li>\n
    • Describe excitation-contraction coupling<\/li>\n<\/ul>\n<\/div>\n<\/div>\n

      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.<\/p>\n

      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.<\/p>\n

      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 \u201cmysia\u201d) 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 the\u00a0epimysium<\/strong>, 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.<\/p>\n

      \"The
      Figure 9.2.1. The Three connective tissue layers.<\/strong> Bundles of muscle fibres, called fascicles, are covered by the perimysium. Muscle fibres are covered by the endomysium.<\/figcaption><\/figure>\n

      Inside each skeletal muscle, muscle fibres are organised into individual bundles, each called a\u00a0fascicle, by a middle layer of connective tissue called the\u00a0perimysium. 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 the\u00a0endomysium. The endomysium contains the extracellular fluid and nutrients to support the muscle fibre. These nutrients are supplied via blood to the muscle tissue.<\/p>\n

      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 an\u00a0aponeurosis, 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 \u201clats\u201d) fuse into is an example of an aponeurosis.<\/p>\n

      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.<\/p>\n

      Skeletal Muscle Fibres<\/h2>\n

      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 100\u00a0\u03bc<\/em>m 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.<\/p>\n

      Some other terminology associated with muscle fibres is rooted in the Greek\u00a0sarco<\/em>, which means \u201cflesh.\u201d The plasma membrane of muscle fibres is called the\u00a0sarcolemma<\/strong>, the cytoplasm is referred to as\u00a0sarcoplasm<\/strong>, and the specialised smooth endoplasmic reticulum, which stores, releases, and retrieves calcium ions (Ca2+<\/sup>) is called the\u00a0sarcoplasmic reticulum (SR)<\/strong>\u00a0(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 myofilaments\u00a0actin<\/strong>\u00a0(thin filament) and\u00a0myosin<\/strong>\u00a0(thick filament), along with other support proteins.<\/p>\n

       <\/p>\n

      \"A
      Figure 9.2.2. Muscle fibre.<\/strong> A skeletal muscle fibre is surrounded by a plasma membrane called the sarcolemma, which contains sarcoplasm, the cytoplasm of muscle cells. A muscle fibre is composed of many fibrils, which give the cell its striated appearance.<\/figcaption><\/figure>\n

      The Sarcomere<\/h2>\n

      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 1.2\u00a0\u03bc<\/em>m in diameter, hundreds to thousands (each with thousands of sarcomeres) can be found inside one muscle fibre. Each sarcomere is approximately 2\u00a0\u03bc<\/em>m 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 the\u00a0thin filament<\/strong>\u00a0of 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 the\u00a0thick filament<\/strong>\u00a0of the sarcomere.<\/p>\n

       <\/p>\n

      \"Diagram
      Figure 9.2.3. The sarcomere.<\/strong> The sarcomere, the region from one Z-line to the next Z-line, is the functional unit of a skeletal muscle fibre.<\/figcaption><\/figure>\n

      The Neuromuscular Junction<\/h2>\n

      Another specialisation of the skeletal muscle is the site where a motor neuron\u2019s terminal meets the muscle fibre \u2014 called the\u00a0neuromuscular junction (NMJ)<\/strong>. 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.<\/p>\n

      Excitation\u2013Contraction Coupling<\/h2>\n

      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\u2019s 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.<\/p>\n

      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.<\/p>\n

      Although the term\u00a0excitation-contraction coupling<\/strong>\u00a0confuses or scares some students, it comes down to this: for a skeletal muscle fibre to contract, its membrane must first be \u201cexcited\u201d\u2014in 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 \u201ccoupled\u201d to the actual contraction through the release of calcium ions (Ca2+) from the SR. Once released, the Ca2+\u00a0interacts 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.<\/p>\n

      In skeletal muscle, this sequence begins with signals from the somatic motor division of the nervous system. In other words, the \u201cexcitation\u201d step in skeletal muscles is always triggered by signalling from the nervous system (Figure 9.2.4).<\/p>\n

      \"Motor
      Figure 9.2.4. Motor end-plate and innervation.<\/strong> At the NMJ, the axon terminal releases ACh. The motor end-plate is the location of the ACh-receptors in the muscle fibre sarcolemma. When ACh molecules are released, they diffuse across a minute space called the synaptic cleft and bind to the receptors.<\/figcaption><\/figure>\n

      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\u2014 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.<\/p>\n

      Signalling begins when a neuronal\u00a0action potential<\/strong>\u00a0travels 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, or\u00a0neurotransmitter<\/strong>, called\u00a0acetylcholine (ACh)<\/strong>. The ACh molecules diffuse across a minute space called the\u00a0synaptic cleft<\/strong>\u00a0and bind to ACh receptors located within the\u00a0motor end-plate<\/strong>\u00a0of 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 to\u00a0depolarise<\/strong>, meaning that the membrane potential of the muscle fibre becomes less negative (closer to zero.)<\/p>\n

      As the membrane depolarises, another set of ion channels called\u00a0voltage-gated sodium channels<\/strong>\u00a0are triggered to open. Sodium ions enter the muscle fibre, and an action potential rapidly spreads (or \u201cfires\u201d) along the entire membrane to initiate excitation-contraction coupling.<\/p>\n

      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.<\/p>\n

      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+<\/sup>) from its storage in the cell\u2019s SR. For the action potential to reach the membrane of the SR, there are periodic invaginations in the sarcolemma, called\u00a0T-tubules<\/strong>\u00a0(\u201cT\u201d stands for \u201ctransverse\u201d). You will recall that the diameter of a muscle fibre can be up to 100\u00a0\u03bc<\/em>m, 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 a\u00a0triad<\/strong>\u00a0(Figure 9.2.5). The triad surrounds the cylindrical structure called a\u00a0myofibril<\/strong>, which contains actin and myosin.<\/p>\n

      \"The
      Figure 9.2.5. The T-tubule.<\/strong> Narrow T-tubules permit the conduction of electrical impulses. The SR functions to regulate intracellular levels of calcium. Two terminal cisternae (where enlarged SR connects to the T-tubule) and one T-tubule comprise a triad\u2014a \u201cthreesome\u201d of membranes, with those of SR on two sides and the T-tubule sandwiched between them.<\/figcaption><\/figure>\n

      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+<\/sup>\u00a0to diffuse out of the SR and into the sarcoplasm. It is the arrival of Ca2+<\/sup>\u00a0in the sarcoplasm that initiates contraction of the muscle fibre by its contractile units, or sarcomeres.<\/p>\n

      \n
      \n

      Section Review<\/strong><\/p>\n<\/header>\n

      \n

      Skeletal muscles contain connective tissue, blood vessels and nerves. There are three layers of connective tissue: epimysium, perimysium, and endomysium. Skeletal muscle fibres are organised into groups called fascicles. Blood vessels and nerves enter the connective tissue and branch in the cell. Muscles attach to bones directly or through tendons or aponeuroses. Skeletal muscles maintain posture, stabilise bones and joints, control internal movement, and generate heat.<\/p>\n

      Skeletal muscle fibres are long, multinucleated cells. The membrane of the cell is the sarcolemma; the cytoplasm of the cell is the sarcoplasm. The sarcoplasmic reticulum (SR) is a form of endoplasmic reticulum. Muscle fibres are composed of myofibrils. The striations are created by the organisation of actin and myosin resulting in the banding pattern of myofibrils.<\/p>\n<\/div>\n<\/div>\n

      \n
      \n

      Review Questions<\/strong><\/p>\n<\/header>\n

      \n
      \n