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THE MUSCULAR SYSTEM
Functions
1. Locomotion
2. Vasoconstriction & vasodilatation
3. Peristalsis
4. Cardiac motion
5. Posture maintenance
6. Heat generation
Properties
 Striations: only present in skeletal and cardiac
muscles. Absent in smooth muscle.
 Nucleus: smooth and cardiac muscles are
uninucleated; skeletal muscle is multinucleated.
 Transverse tubule (T tubule): well developed
in skeletal and cardiac muscles to transport
calcium. Absent in smooth muscle.
Properties
 Intercalated disk: specialized intercellular
junction that only occurs in cardiac muscle.
 Control: skeletal muscle is always under voluntary
control; smooth and cardiac muscles are under
involuntary control.
Characteristics
1. Excitability
2. Contractility
3. Elasticity
4. Extensibility
THE SKELETAL MUSCLE
Skeletal muscle fiber
 Each skeletal muscle fiber is a single muscle cell.
 Muscle fibers are cylindrical cells with many nuclei .
 The cell membrane is called sarcolemma; the
cytoplasm is called sarcoplasm.
 The sarcoplasm contains abundant , parallel thread
like myofibrils, that run in parallel fashion.
Neuromuscular junction
 The site where a motor neuron’s terminal meets the
muscle fiber.
 This is where the muscle fiber first responds to
signaling by the motor neuron.
 Every skeletal muscle fiber in every skeletal muscle
is innervated by a motor neuron at the NMJ.
T Tubules
 Carry the action potential into the interior of the
cell – triggers the opening of calcium channels in
the membrane of the adjacent SR, causing Ca++ to
diffuse out of the SR and into the sarcoplasm.
Muscle fiber contraction
 The Ca++ ions combine with troponin molecules of
the myofibrils*
 Binding of Ca++ to troponin shifts tropomyosin to
expose active sites on the actin molecules.
Mechanisms of Muscle
Contraction
POWER STROKE
VIDEO ON THE MECHANISM OF CROSS
BRIDGE
Relaxation of skeletal muscle
1. After the impulse is over, the SR begins actively
pumping Ca++ back into its sacs.
2. As Ca++ is stripped from troponin molecules,
tropomyosin returns to its position, blocking actin’s
active sites.
3. Myosin cross bridges are prevented from binding to
actin & can no longer sustain the contraction.
4. The muscle fiber return to its longer, resting length.
ATP as energy source
 ATP supplies the energy for muscle contraction –
cross bridge cycle*
 ATP also provides the energy for the active-
transport Ca++ pumps in the SR.
 The amount of ATP stored in muscle is very low;
ATP must therefore be regenerated and replaced
quickly to allow for sustained contraction.
ATP as Energy Source
 There are three mechanisms by which ATP can be
regenerated:
1. Creatine phosphate metabolism
2. Anaerobic glycolysis
3. Fermentation & aerobic respiration
Creatine phosphate metabolism
Muscle tension
 The force generated by the contraction of the
muscle (or shortening of the sarcomeres).
 Generated when moving a load or when the muscle
contract against a load that does not move.
 2 types of skeletal muscle contractions:
Isotonic contractions & isometric contractions
Concentric
Eccentric
Motor unit
 The actual group of muscle fibers in a muscle
innervated by a single motor neuron*
 Small motor unit is an arrangement where a single
motor neuron supplies a small number of muscle fibers
in a muscle**
 Large motor unit is an arrangement where a single
motor neuron supplies a large number of muscle fibers
in a muscle***
Motor unit. A motor unit consists of one somatic motor neuron and the
muscle fibers sup-plied by its branches.
Motor neuron
Myelin sheath
NMJ
Muscle fibers
Twitch
 An single (isolated) contraction in the muscle fibers
produced by the activation when a single action
potential from a motor neuron.
 A twitch can last for a few milliseconds or 100
milliseconds, depending on the muscle type.
A Myogram of a Muscle Twitch
Twitch
 Significance:
 A single twitch does not produce any significant muscle
activity in a living body.
 A series of action potentials to the muscle fibers is
necessary to produce a muscle contraction that can
produce work.
The Frequency of Motor Neuron Stimulation
Muscle tone
 Constant low-level contractions that allow for posture and
stability (joints)*
 Hypotonia
 The absence of low-level contractions that lead to muscle
tone**
 Hypertonia
 Excessive muscle tone; present with muscle rigidity or
spasticity***
Types of muscle fibers
1. Slow oxidative (SO) fibers
2. Fast oxidative (FO) fibers
3. Fast glycolytic (FG) fibers
Fast fibers vs. Slow fibers
 Fast & Slow – speed of contraction: dependent on how
quickly myosin’s ATPase hydrolyzes ATP to produce
cross-bridge.
 Fast fibers hydrolyze ATP approximately twice as
quickly as slow fibers, resulting in much quicker cross-
bridge cycling.
Oxidative vs. Glycolytic
 Oxidative fibers
 Produce more ATP during each metabolic cycle, making
it more resistant to fatigue.
 Contain more mitochondria*
 Glycolytic fibers
 Produce less ATP per cycle; fatigue at a quicker rate.
Slow oxidative (SO) fibers
 Possess a large number of mitochondria
 Capable of contracting for longer period*
 Extensively supplied with blood capillaries**
 Possess myoglobin (O2-carrying molecule)***
 Useful to maintain posture, stabilize bones and joints,
and make small movements that do not require large
amounts of energy.
Fast oxidative (FO) fibers
 Produce ATP relatively quickly – produce higher
amount of tension than SO fibers.
 Do not possess significant myoglobin*
 They produce more tension than SO fibers but they are
more fatigue-resistant than FG fibers.
 Used primarily: walking (require more energy than
postural control but less energy than an explosive
movement, such as sprinting)
Fast glycolytic (FG) fibers
 Use glycolysis as ATP source
 Produce high levels of tension*
 Produce rapid, forceful contractions to make quick,
powerful movements.
 Fatigue quickly, permitting them to only be used for
short periods.
The predominant fiber type in a muscle is determined by the
primary function of the muscle.
Terms (skeletal muscle)
 Hypertrophy
 An increase in muscle mass due to the additions of
structural proteins*
 Atrophy
 The loss of muscle mass due to breakdown of structural
proteins.
 Sarcopenia
 Age-related muscle atrophy.
Marathoners. Long-distance runners have a large number of SO fibers and relatively few FO and
FG fibers. (credit: “Tseo2”/Wikimedia Commons). SO fibers are capable to sustain low levels of
muscle contractions for greater periods without fatiguing.
Endurance Exercise
Body builders have a large number of FG fibers and
relatively few FO and SO fibers. (credit: Lin Mei/flickr)
Resistance Exercise
SMOOTH MUSCLE
 Present in the walls of hollow organs like the
urinary bladder, uterus, stomach, intestines, and in
the walls of passageways, such as the arteries and
veins and the tracts of the respiratory, urinary,
and reproductive systems.
Smooth muscle tissue is found around organs in the digestive, respiratory,
reproductive tracts and the iris of the eye. LM × 1600. (Micrograph provided by the
Regents of University of Michigan Medical School © 2012)
Smooth muscle
 Do not have striations, sarcomere & T tubules*
 Dense body – analogous to the Z-discs of skeletal
and cardiac muscle fibers (fastened to the
sarcolemma); anchor the thin filaments.
 Calveoli – membrane indentations that supplies
calcium ions from ECF.
 Limited SR**
The dense bodies and intermediate filaments are networked through the sarcoplasm, which cause
the muscle fiber to contract.
Smooth muscle
 Cross-bridge formation is regulated by the the regulatory
protein calmodulin.
 Ca++ bind to calmodulin.
 Ca++-calmodulin complex activates myosin kinase, which,
in turn, activates the myosin heads by phosphorylating
them*
 The heads can then attach to actin-binding sites and pull
on the thin filaments.
Relaxed
Contracted
Plasma
membrane
Thin myofilament
Thick myofilament
A
B
Latch-bridges
 Subset of cross-bridges between myosin heads and actin
that keep the thick and thin filaments linked together for a
prolonged period without the need for ATP.
 Allows for maintenance of muscle “tone” in SM with very
little energy expenditure.
Varicosity
 Series of neurotransmitter-filled bulges of axons
through smooth muscle; loosely forming motor units.
 Releases neurotransmitters into the synaptic cleft.
 Corresponds to the NMJ of the skeletal muscles.
A series of axon-like swelling, called varicosities or “boutons,” from autonomic neurons form motor
units through the smooth muscle.
Types of smooth muscle
1. Single-unit or visceral
2. Multiunit
Single unit muscle
 Has its muscle fibers joined by gap junctions so that the
muscle contracts as a single unit.
 Found in the walls of all visceral organs except the heart,
and so it is commonly called visceral muscle.
 Exhibit stress-relaxation response*
 Produces slow, steady contractions that allow substances,
such as food, to move through the body (peristalsis)
Multiunit muscle
 Does not act as a single unit but instead is
composed of may independent single-cell units.
 Stimuli come from autonomic nerves or hormones
but not from stretching.
 Found around large blood vessels, in the respiratory
airways, and in the eyes.
Hyperplasia
 Unlike other muscle, SM can divide to produce
more cells, a process called hyperplasia.
 Observed in the uterus at puberty, which responds
to increased estrogen levels by producing more
uterine smooth muscle fibers, and greatly increases
the size of the myometrium.

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Physiology of the Muscular System

  • 2. Functions 1. Locomotion 2. Vasoconstriction & vasodilatation 3. Peristalsis 4. Cardiac motion 5. Posture maintenance 6. Heat generation
  • 3. Properties  Striations: only present in skeletal and cardiac muscles. Absent in smooth muscle.  Nucleus: smooth and cardiac muscles are uninucleated; skeletal muscle is multinucleated.  Transverse tubule (T tubule): well developed in skeletal and cardiac muscles to transport calcium. Absent in smooth muscle.
  • 4. Properties  Intercalated disk: specialized intercellular junction that only occurs in cardiac muscle.  Control: skeletal muscle is always under voluntary control; smooth and cardiac muscles are under involuntary control.
  • 6.
  • 8.
  • 9. Skeletal muscle fiber  Each skeletal muscle fiber is a single muscle cell.  Muscle fibers are cylindrical cells with many nuclei .  The cell membrane is called sarcolemma; the cytoplasm is called sarcoplasm.  The sarcoplasm contains abundant , parallel thread like myofibrils, that run in parallel fashion.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16. Neuromuscular junction  The site where a motor neuron’s terminal meets the muscle fiber.  This is where the muscle fiber first responds to signaling by the motor neuron.  Every skeletal muscle fiber in every skeletal muscle is innervated by a motor neuron at the NMJ.
  • 17.
  • 18.
  • 19. T Tubules  Carry the action potential into the interior of the cell – triggers the opening of calcium channels in the membrane of the adjacent SR, causing Ca++ to diffuse out of the SR and into the sarcoplasm.
  • 20.
  • 21. Muscle fiber contraction  The Ca++ ions combine with troponin molecules of the myofibrils*  Binding of Ca++ to troponin shifts tropomyosin to expose active sites on the actin molecules.
  • 23.
  • 24.
  • 25.
  • 26.
  • 28.
  • 29.
  • 30. VIDEO ON THE MECHANISM OF CROSS BRIDGE
  • 31. Relaxation of skeletal muscle 1. After the impulse is over, the SR begins actively pumping Ca++ back into its sacs. 2. As Ca++ is stripped from troponin molecules, tropomyosin returns to its position, blocking actin’s active sites. 3. Myosin cross bridges are prevented from binding to actin & can no longer sustain the contraction. 4. The muscle fiber return to its longer, resting length.
  • 32. ATP as energy source  ATP supplies the energy for muscle contraction – cross bridge cycle*  ATP also provides the energy for the active- transport Ca++ pumps in the SR.  The amount of ATP stored in muscle is very low; ATP must therefore be regenerated and replaced quickly to allow for sustained contraction.
  • 33. ATP as Energy Source  There are three mechanisms by which ATP can be regenerated: 1. Creatine phosphate metabolism 2. Anaerobic glycolysis 3. Fermentation & aerobic respiration
  • 35.
  • 36.
  • 37. Muscle tension  The force generated by the contraction of the muscle (or shortening of the sarcomeres).  Generated when moving a load or when the muscle contract against a load that does not move.  2 types of skeletal muscle contractions: Isotonic contractions & isometric contractions
  • 39.
  • 40. Motor unit  The actual group of muscle fibers in a muscle innervated by a single motor neuron*  Small motor unit is an arrangement where a single motor neuron supplies a small number of muscle fibers in a muscle**  Large motor unit is an arrangement where a single motor neuron supplies a large number of muscle fibers in a muscle***
  • 41. Motor unit. A motor unit consists of one somatic motor neuron and the muscle fibers sup-plied by its branches. Motor neuron Myelin sheath NMJ Muscle fibers
  • 42. Twitch  An single (isolated) contraction in the muscle fibers produced by the activation when a single action potential from a motor neuron.  A twitch can last for a few milliseconds or 100 milliseconds, depending on the muscle type.
  • 43. A Myogram of a Muscle Twitch
  • 44. Twitch  Significance:  A single twitch does not produce any significant muscle activity in a living body.  A series of action potentials to the muscle fibers is necessary to produce a muscle contraction that can produce work.
  • 45. The Frequency of Motor Neuron Stimulation
  • 46. Muscle tone  Constant low-level contractions that allow for posture and stability (joints)*  Hypotonia  The absence of low-level contractions that lead to muscle tone**  Hypertonia  Excessive muscle tone; present with muscle rigidity or spasticity***
  • 47. Types of muscle fibers 1. Slow oxidative (SO) fibers 2. Fast oxidative (FO) fibers 3. Fast glycolytic (FG) fibers
  • 48. Fast fibers vs. Slow fibers  Fast & Slow – speed of contraction: dependent on how quickly myosin’s ATPase hydrolyzes ATP to produce cross-bridge.  Fast fibers hydrolyze ATP approximately twice as quickly as slow fibers, resulting in much quicker cross- bridge cycling.
  • 49. Oxidative vs. Glycolytic  Oxidative fibers  Produce more ATP during each metabolic cycle, making it more resistant to fatigue.  Contain more mitochondria*  Glycolytic fibers  Produce less ATP per cycle; fatigue at a quicker rate.
  • 50. Slow oxidative (SO) fibers  Possess a large number of mitochondria  Capable of contracting for longer period*  Extensively supplied with blood capillaries**  Possess myoglobin (O2-carrying molecule)***  Useful to maintain posture, stabilize bones and joints, and make small movements that do not require large amounts of energy.
  • 51. Fast oxidative (FO) fibers  Produce ATP relatively quickly – produce higher amount of tension than SO fibers.  Do not possess significant myoglobin*  They produce more tension than SO fibers but they are more fatigue-resistant than FG fibers.  Used primarily: walking (require more energy than postural control but less energy than an explosive movement, such as sprinting)
  • 52. Fast glycolytic (FG) fibers  Use glycolysis as ATP source  Produce high levels of tension*  Produce rapid, forceful contractions to make quick, powerful movements.  Fatigue quickly, permitting them to only be used for short periods. The predominant fiber type in a muscle is determined by the primary function of the muscle.
  • 53. Terms (skeletal muscle)  Hypertrophy  An increase in muscle mass due to the additions of structural proteins*  Atrophy  The loss of muscle mass due to breakdown of structural proteins.  Sarcopenia  Age-related muscle atrophy.
  • 54. Marathoners. Long-distance runners have a large number of SO fibers and relatively few FO and FG fibers. (credit: “Tseo2”/Wikimedia Commons). SO fibers are capable to sustain low levels of muscle contractions for greater periods without fatiguing. Endurance Exercise
  • 55. Body builders have a large number of FG fibers and relatively few FO and SO fibers. (credit: Lin Mei/flickr) Resistance Exercise
  • 56.
  • 57. SMOOTH MUSCLE  Present in the walls of hollow organs like the urinary bladder, uterus, stomach, intestines, and in the walls of passageways, such as the arteries and veins and the tracts of the respiratory, urinary, and reproductive systems.
  • 58. Smooth muscle tissue is found around organs in the digestive, respiratory, reproductive tracts and the iris of the eye. LM × 1600. (Micrograph provided by the Regents of University of Michigan Medical School © 2012)
  • 59. Smooth muscle  Do not have striations, sarcomere & T tubules*  Dense body – analogous to the Z-discs of skeletal and cardiac muscle fibers (fastened to the sarcolemma); anchor the thin filaments.  Calveoli – membrane indentations that supplies calcium ions from ECF.  Limited SR**
  • 60. The dense bodies and intermediate filaments are networked through the sarcoplasm, which cause the muscle fiber to contract.
  • 61. Smooth muscle  Cross-bridge formation is regulated by the the regulatory protein calmodulin.  Ca++ bind to calmodulin.  Ca++-calmodulin complex activates myosin kinase, which, in turn, activates the myosin heads by phosphorylating them*  The heads can then attach to actin-binding sites and pull on the thin filaments.
  • 63. Latch-bridges  Subset of cross-bridges between myosin heads and actin that keep the thick and thin filaments linked together for a prolonged period without the need for ATP.  Allows for maintenance of muscle “tone” in SM with very little energy expenditure.
  • 64. Varicosity  Series of neurotransmitter-filled bulges of axons through smooth muscle; loosely forming motor units.  Releases neurotransmitters into the synaptic cleft.  Corresponds to the NMJ of the skeletal muscles.
  • 65. A series of axon-like swelling, called varicosities or “boutons,” from autonomic neurons form motor units through the smooth muscle.
  • 66. Types of smooth muscle 1. Single-unit or visceral 2. Multiunit
  • 67. Single unit muscle  Has its muscle fibers joined by gap junctions so that the muscle contracts as a single unit.  Found in the walls of all visceral organs except the heart, and so it is commonly called visceral muscle.  Exhibit stress-relaxation response*  Produces slow, steady contractions that allow substances, such as food, to move through the body (peristalsis)
  • 68. Multiunit muscle  Does not act as a single unit but instead is composed of may independent single-cell units.  Stimuli come from autonomic nerves or hormones but not from stretching.  Found around large blood vessels, in the respiratory airways, and in the eyes.
  • 69. Hyperplasia  Unlike other muscle, SM can divide to produce more cells, a process called hyperplasia.  Observed in the uterus at puberty, which responds to increased estrogen levels by producing more uterine smooth muscle fibers, and greatly increases the size of the myometrium.

Editor's Notes

  1. Muscle is one of the four primary tissue types of the body, and the body contains three types of muscle tissue: skeletal muscle, cardiac muscle, and smooth muscle. Most of the skeletal muscle produces movement by acting on the skeleton. Cardiac muscle is found in the wall of the heart and pumps blood through the circulatory system. Smooth muscle is found in the skin (hair follicles); walls of internal organs, blood vessels, and internal passageways, where it assists in moving materials.
  2. FUNCTIONS OF THE MUSCULAR SYSTEM Locomotion (skeletal) Vasoconstriction and vasodilatation- constriction and dilation of blood vessel walls are the results of smooth muscle contraction. Peristalsis – wavelike motion along the digestive tract is produced by the Smooth muscle. Cardiac motion Posture maintenance- contraction of skeletal muscles maintains body posture and muscle tone. Heat generation – about 75% of ATP energy used in muscle contraction is released as heat (skeletal).
  3. STRIATIONS: stripes; occurs due to the very regular arrangement of contractile proteins (actin and myosin) in the cytoplasm of striated muscles.
  4. EXCITABILITY: or irritable; skeletal mm can respond to regulatory mechanisms such as nerve signals. CONTRACTILITY: ability to contract or shorten, allows muscle to pull on bones and produce body movement. ELASTICITY: ability to recoil back to its original length due to elastic fibers. EXTENSIBILITY: ability to extend or stretch (skeletal).
  5. (a) skeletal muscle, (b) smooth muscle, and (c) cardiac muscle. From top, LM × 1600, LM × 1600, LM × 1600. (Micrographs)
  6. The best-known feature of skeletal muscle is its ability to contract and cause movement. Skeletal muscles act maintain posture. Muscles also prevent excess movement of the bones and joints, maintaining skeletal stability and preventing skeletal structure damage or deformation. Muscles work to keep joints stable. These muscles allow functions, such as swallowing, urination, and defecation, to be under voluntary control.
  7. EPIMYSIUM Inside each skeletal muscle, muscle fibers are organized into individual bundles, each called FASCICLE, covered by PERIMYSIUM. Inside each fascicle, each muscle fiber is encased the ENDOMYSIUM. The endomysium contains the extracellular fluid and nutrients to support the muscle fiber. These nutrients are supplied via blood to the muscle tissue.
  8. The muscle cell is also known as FIBERS because of their threadlike shape; long and cylindrical.
  9. Each skeletal muscle fiber is a single muscle cell. Muscle fibers are cylindrical cells with many nuclei . The cell membrane is called SARCOLEMMA; the cytoplasm is called SARCOPLASM. The sarcoplasm contains abundant, parallel thread like MYOFIBRILS, that run in parallel fashion.
  10. MYOFIBRIL: made up of still finer fibers, called THICK & THIN MYOFILAMENTS. The striated appearance of skeletal muscle fibers is due to the arrangement of the myofilaments of actin and myosin in sequential order from one end of the muscle fiber to the other.
  11. The SARCOMERE is the basic contractile unit of the muscle fiber. The sarcomere is bundled within the myofibril that runs the entire length of the muscle fiber. As myofibrils contract, the entire muscle cell contracts. Hundreds to thousands (each with thousands of sarcomeres) can be found inside one muscle fiber. Each sarcomere is approximately 2 μm in length with a three-dimensional cylinder-like arrangement. It is bordered by structures called Z-DISCS (also called Z-lines), to which the actin myofilaments are anchored; it is a landmark separating one sarcomere from the next. M LINE: it is where the thick filaments are held together & stabilized. Bands or zones of the sarcomere that define its regions: A BAND: the segment that runs the entire length of the thick filaments. I BAND: the segment that includes the Z line and the ends of the thin filament where they do not overlap with the thick filaments. H ZONE: the middle region of thick filaments where they do not overlap with the thin filaments. SARCOPLASMIC RETICULUM: specialized smooth endoplasmic reticulum, which stores, releases, and retrieves calcium ions (Ca++).
  12. MYOFILAMENTS It is a fact that thousands of thick and thin myofilaments lie side by side in each myofibril. There are four kinds of proteins that make up myofilaments: MYOSIN, ACTIN, TROPOMYOSIN, & TROPONIN.
  13. The THIN FILAMENT is made up of 3 proteins: TROPONIN, ACTIN, TROPOMYOSIN. Figure shows that globular ACTIN molecules are strung together like beads to form 2 fibrous strands that twist each other to form the bulk of the thin filament. The ACTIN molecule contains a BINDING SITE FOR MYOSIN. Actin & myosin have a chemical attraction for one another. At rest, the ACTIVE SITES ON ACTIN are covered by long TROPOMYOSIN molecules. The tropomyosin molecule seem to block the myosin from binding with actin; this position is held by TROPONIN, which are spaced at intervals along the thin filaments.
  14. PORTION OF THE THICK FILAMENT The thick filaments are made up of MYOSIN MOLECULES. The myosin molecules are shaped like GOLF CLUBS, with their LONG SHAFTS bundled to form a thick filament and their “HEADS” sticking out from the bundle. The myosin heads are chemically attracted to the actin molecules of the nearby thin filaments, so they angle toward the thin filaments.
  15. Excitation signals from the neuron are the only way to functionally activate the fiber to contract.
  16. NEUROMUSCULAR JUNCTION A motor neuron connects to the sarcolemma of a muscle fiber at a folded MOTOR ENDPLATE to form a junction called NMJ.
  17. A NMJ is a type of connection called a SYNAPSE, characterized by a narrow gap (SYNAPTIC CLEFT), across which NEUROTRANSMITTER transmit signals. When nerve impulses reach the end of a motor neuron fiber, small vesicles release a neurotransmitter (ACh) into the synaptic cleft. Acetylcholine molecules contact the sarcolemma; there they stimulate acetylcholine receptors and thereby initiate an electrical impulse in the sarcolemma. Once ACh binds, a channel in the ACh receptor opens and positively charged ions can pass through into the muscle fiber, causing it to depolarize, meaning that the membrane potential of the muscle fiber becomes less negative (closer to zero.)
  18. 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 Ca++ to diffuse out of the SR and into the sarcoplasm. It is the arrival of Ca++ in the sarcoplasm that initiates contraction of the muscle fiber by its contractile units, or sarcomeres.
  19. T TUBULES: extensions of the sarcolemma; periodic invaginations in the sarcolemma (“T” stands for “transverse”). 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 TRIAD. TRIAD: a triplet of adjacent tubules: a terminal sac of the SR, a T tubule, and another terminal sac of SR. The triad surrounds the cylindrical structure called a myofibril.
  20. *Troponin normally holds tropomyosin strands in a position that blocks the chemically active sites of actin.
  21. The impulse in the T tubules triggers the release of a flood of Ca++ ions from the SR.
  22. In the sarcoplasm, the calcium ions combine with troponin molecules in the thin filaments of the myofibrils. Recall that troponin normally holds tropomyosin strands in a position that blocks the chemically active sites of actin. Binding of calcium to troponin shifts tropomyosin to expose active sites on the actin molecul
  23. Once the active sites are exposed, energized myosin heads bind to actin molecules in the nearby thin filaments. The process whereby the myosin head attaches to the actin is known as the CROSS-BRIDGE FORMATION.
  24. (a) The active site on actin is exposed as calcium binds to troponin. (b) The myosin head is attracted to actin, and myosin binds actin at its actin-binding site, forming the cross-bridge.
  25. (c) During the POWER STROKE, the phosphate generated in the previous contraction cycle is released. This results in the myosin head pivoting toward the center of the sarcomere, after which the attached ADP and phosphate group are released.
  26. (d) A new molecule of ATP attaches to the myosin head, causing the cross-bridge to detach.
  27. (e) The myosin head hydrolyzes ATP to ADP and phosphate, which returns the myosin to the cocked position.
  28. ATP hydrolysis releases the inorganic phosphate and transferring the energy to the myosin head. When myosin binds to actin, the stored energy is released, and myosin head springs back to its original position. The energy transferred from ATP is used to do the work of pulling the thin filament during contraction.
  29. CREATINE PHOSPHATE is a molecule that can store energy in its phosphate bonds. In a RESTING MUSCLE, excess ATP transfers its energy to creatine, producing ADP and creatine phosphate. This acts as an energy reserve that can be used to quickly create more ATP. When the muscle starts to contract and needs energy, creatine phosphate transfers its phosphate back to ADP to form ATP and creatine. This reaction is catalyzed by the enzyme CREATINE KINASE and occurs very quickly; thus, creatine phosphate-derived ATP powers the first few seconds of muscle contraction. However, creatine phosphate can only provide approximately 15 seconds worth of energy, at which point another energy source has to be used
  30. Each glucose molecule produces two ATP and two molecules of pyruvic acid, which can be used in aerobic respiration or converted to lactic acid. If oxygen is not available, pyruvic acid is converted to lactic acid, which may contribute to muscle fatigue. This occurs during strenuous exercise when high amounts of energy are needed but oxygen cannot be sufficiently delivered to muscle.
  31. AEROBIC RESPIRATION is the breakdown of glucose in the presence of oxygen (O2) to produce carbon dioxide, water, and ATP. Approximately 95 percent of the ATP required for resting or moderately active muscles is provided by aerobic respiration, which takes place in mitochondria.
  32. A CONCENTRIC CONTRACTION involves the muscle shortening to move a load. An example of this is the biceps brachii muscle contracting when a hand weight is brought upward with increasing muscle tension. The angle of the elbow joint decreases as the forearm is brought toward the body. Here, the biceps brachii contracts as sarcomeres in its muscle fibers are shortening and cross-bridges form; the myosin heads pull the actin. An ECCENTRIC CONTRACTION occurs as the muscle tension diminishes and the muscle lengthens. In this case, the hand weight is lowered in a slow and controlled manner as the amount of cross-bridges being activated by nervous system stimulation decreases. In this case, as tension is released from the biceps brachii, the angle of the elbow joint increases. Eccentric contractions are also used for movement and balance of the body.
  33. An ISOMETRIC CONTRACTION occurs as the muscle produces tension without changing the angle of a skeletal joint. Isometric contractions involve sarcomere shortening and increasing muscle tension, but do not move a load, as the force produced cannot overcome the resistance provided by the load. For example, if one attempts to lift a hand weight that is too heavy, there will be sarcomere activation and shortening to a point, and ever-increasing muscle tension, but no change in the angle of the elbow joint. In everyday living, isometric contractions are active in maintaining posture and maintaining bone and joint stability.
  34. INTRO: every skeletal muscle fiber must be innervated by the axon terminal of a motor neuron in order to contract. Each muscle fiber is innervated by only one motor neuron. *The size of the motor unit is variable depending on the nature of the muscle. **SMALL MOTOR UNITS very fine motor control of the muscle. The best example in humans is the small motor units of the extraocular eye muscles that move the eyeballs. ***Large motor units are concerned with simple, or “gross,” movements, such as powerfully extending the knee joint. The best example is the large motor units of the thigh muscles or back muscles, where a single motor neuron will supply thousands of muscle fibers in a muscle
  35. The tension produced by a single twitch can be measured by a myogram, an instrument that measures the amount of tension produced over time ([link]).
  36. A single muscle twitch has a latent period, a contraction phase when tension increases, and a relaxation phase when tension decreases. During the LATENT PERIOD, the action potential is being propagated along the sarcolemma. During the CONTRACTION PHASE, Ca++ ions in the sarcoplasm bind to troponin, tropomyosin moves from actin-binding sites, cross-bridges form, and sarcomeres shorten. During the RELAXATION PHASE, tension decreases as Ca++ ions are pumped out of the sarcoplasm and cross-bridge cycling stops.
  37. Normal muscle contraction is more sustained, and it can be modified by input from the nervous system to produce varying amounts of force; this is called a graded muscle response. The frequency of action potentials (nerve impulses) from a motor neuron and the number of motor neurons transmitting action potentials both affect the tension produced in skeletal muscle.
  38. The rate at which a motor neuron fires action potentials affects the tension produced in the skeletal muscle. If the fibers are stimulated while a previous twitch is still occurring, the second twitch will be stronger. This response is called WAVE SUMMATION, because the excitation-contraction coupling effects of successive motor neuron signaling is summed, or added together. The bottom of each wave, the end of the relaxation phase, represents the point of stimulus. Summation results in greater contraction of the motor unit. If the stimulus frequency is so high that the relaxation phase disappears completely, contractions become continuous in a process called COMPLETE TETANUS. During tetanus, the concentration of Ca++ ions in the sarcoplasm allows virtually all of the sarcomeres to form cross-bridges and shorten, so that a contraction can continue uninterrupted (until the muscle fatigues and can no longer produce tension).
  39. *Even if a muscle is not producing movement, it is contracted in a small amount to maintain its contractile proteins. **Damage to parts of the CNS (cerebellum), loss of innervations to skeletal muscle (poliomyelitis). Hypotonic muscles have a flaccid appearance & a weak reflex. HYPERTONIA; accompanied by hyperreflexia; damage to upper motor neurons; muscle rigidity (Parkinson’s) or spasticity (a limb snap back from passive stretching, as seen some strokes).
  40. Two criteria to consider when classifying the types of muscle fibers are how fast some fibers contract relative to others, and how fibers produce ATP. SO fibers contract relatively slowly and use aerobic respiration (oxygen and glucose) to produce ATP. FO fibers have fast contractions and primarily use aerobic respiration, but because they may switch to anaerobic respiration (glycolysis), can fatigue more quickly than SO fibers. FG fibers have fast contractions and primarily use anaerobic glycolysis. The FG fibers fatigue more quickly than the others.
  41. METABOLIC PATHWAY If a fiber primarily produces ATP through aerobic pathways it is oxidative. More ATP can be produced during each metabolic cycle, making the fiber more resistant to fatigue. *The OXIDATIVE FIBERS contain many more mitochondria than the glycolytic fibers, because aerobic metabolism, which uses oxygen (O2) in the metabolic pathway, occurs in the mitochondria.
  42. *Because of the large amount of ATP they can produce, but they have a relatively small diameter and do not produce a large amount of tension. **To supply O2 from the red blood cells in the bloodstream. ***Similar to O2-carrying hemoglobin in the red blood cells. The myoglobin stores some of the needed O2 within the fibers themselves (and gives SO fibers their red color). All of these features allow SO fibers to produce large quantities of ATP, which can sustain muscle activity without fatiguing for long periods of time. They do not produce high tension, and thus they are not used for powerful, fast movements that require high amounts of energy and rapid cross-bridge cycling.
  43. INTRO: FO fibers are sometimes called intermediate fibers because they possess characteristics that are intermediate between fast fibers and slow fibers. They are oxidative because they produce ATP aerobically, possess high amounts of mitochondria, and do not fatigue quickly. *Giving them a lighter color than the red SO fibers.
  44. *They have a large diameter and possess high amounts of glycogen, which is used in glycolysis to generate ATP quickly to produce high levels of tension. Because they do not primarily use aerobic metabolism, they do not possess substantial numbers of mitochondria or significant amounts of myoglobin and therefore have a white color. FG fibers are used to produce rapid, forceful contractions to make quick, powerful movements. These fibers fatigue quickly, permitting them to only be used for short periods. Most muscles possess a mixture of each fiber type. The predominant fiber type in a muscle is determined by the primary function of the muscle.
  45. *Although muscle cells can change in size, new cells are not formed when muscles grow.
  46. EXAMPLE OF RELATIONSHIP BETWEEN THE PRIMARY TYPE OF MUSCLE UTILIZE ON THE KIND OF EXERCISE BY ATHLETES Slow fibers are predominantly used in endurance exercises that require little force but involve numerous repetitions. The aerobic metabolism used by slow-twitch fibers allows them to maintain contractions over long periods. Endurance training modifies these slow fibers to make them even more efficient by producing more mitochondria to enable more aerobic metabolism and more ATP production. Endurance exercise can also increase the amount of myoglobin in a cell, as increased aerobic respiration increases the need for oxygen. Myoglobin is found in the sarcoplasm and acts as an oxygen storage supply for the mitochondria. The training can trigger the formation of more extensive capillary networks around the fiber, a process called angiogenesis, to supply oxygen and remove metabolic waste. To allow these capillary networks to supply the deep portions of the muscle, muscle mass does not greatly increase in order to maintain a smaller area for the diffusion of nutrients and gases.
  47. Resistance exercises require large amounts of FG fibers to produce short, powerful movements that are not repeated over long periods. The high rates of ATP hydrolysis and cross-bridge formation in FG fibers result in powerful muscle contractions. Muscles used for power have a higher ratio of FG to SO/FO fibers, and trained athletes possess even higher levels of FG fibers in their muscles. Resistance exercise affects muscles by increasing the formation of myofibrils, thereby increasing the thickness of muscle fibers. This added structure causes hypertrophy, or the enlargement of muscles, exemplified by the large skeletal muscles seen in body builders and other athletes ([link]). Because this muscular enlargement is achieved by the addition of structural proteins, athletes trying to build muscle mass often ingest large amounts of protein.
  48. So-named because the cells do not have striations. Also present in the eyes, where it functions to change the size of the iris and alter the shape of the lens; in the skin where it causes hair to stand erect in response to cold temperature or fear.
  49. Smooth muscle fibers are spindle-shaped (wide in the middle and tapered at both ends) and have a single nucleus; they range from about 30 to 200 μm (thousands of times shorter than skeletal muscle fibers).
  50. Smooth muscle fibers do have actin and myosin contractile proteins, and thick and thin filaments. Calcium ions are supplied by the SR in the fibers and by sequestration from the extracellular fluid through membrane indentations called calveoli Smooth muscle fibers have a limited calcium-storing SR but have calcium channels in the sarcolemma (similar to cardiac muscle fibers) that open during the action potential along the sarcolemma *Small diameter **Most of the calcium required for contraction comes from the outside of the cell.
  51. Because smooth muscle cells do not contain troponin, cross-bridge formation is not regulated by the troponin-tropomyosin complex but instead by the regulatory protein calmodulin. In a smooth muscle fiber, external Ca++ ions passing through binding sites and pull on the thin filaments. PHOSPHORYLATING them (converting ATP to ADP and Pi, with the Pi attaching to the head)
  52. SMOOTH MUSCLE FIBER. A, Thin bundles of myofilaments span the diameter of a relaxed fiber. The scanning electron micrograph (right) shows that the surface of the cell is rather flat when the fiber is relaxed. B, During CONTRACTION, sliding of the myofilaments causes the fiber to shorten by “balling up.” The micrograph shows that the fiber becomes shorter and thicker, exhibiting “dimples” where the myofilament bundles
  53. Contractions can continue without using large amounts of energy.
  54. Also, visceral muscle in the walls of the hollow organs (except the heart) contains PACESETTER CELLS. A pacesetter cell can spontaneously trigger action potentials and contractions in the muscle.
  55. *BASED ON ORGANIZATION
  56. *This means that as the muscle of a hollow organ is stretched when it fills, the mechanical stress of the stretching will trigger contraction, but this is immediately followed by relaxation so that the organ does not empty its contents prematurely. This is important for hollow organs, such as the stomach or urinary bladder, which continuously expand as they fill. The smooth muscle around these organs also can maintain a muscle tone when the organ empties and shrinks, a feature that prevents “flabbiness” in the empty organ.
  57. Multiunit smooth muscle cells rarely possess gap junctions, and thus are not electrically coupled. As a result, contraction does not spread from one cell to the next, but is instead confined to the cell that was originally stimulated.
  58. Similar to skeletal and cardiac muscle cells, smooth muscle can undergo hypertrophy to increase in size.