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The three distinct types of muscle tissue in the human body:
Skeletal muscle
Cardiac muscle
Smooth muscle
Skeletal muscles
Attach to the skeleton to provide strength and mobility to the body; the contractions of large skeletal muscles also function to generate heat
Cardiac muscles
In the heart provide the force necessary to pump blood throughout the body
Smooth muscles
Provide steady contraction within organs (and blood vessels) throughout the body
Muscle movements
Can be either voluntary or involuntary
Muscles
Both produce and resist movement
Muscle contractions
Resist movement when maintains posture (skeletal muscles) and maintaining the diameter of blood vessels (smooth muscles)
-contraction of skeletal muscles generate heat - shivering
Shivering
In which skeletal muscles alternatively and rapidly contract and relax, is used to generate heat in cold environments
Muscles are excitable by
Chemical and electrical signals
Excitation of muscles
Causes muscle contraction
Most skeletal muscles
Interact with the skeleton and are organized into groups
Skeletal muscles attach to bones
Via tendons
Skeletal muscle origin
Attaches to a relatively stationary bone
-proximal
The muscle insertion
Attaches to a bone across a joint
-distal
When skeletal muscles contract
Insertion is pulled towards the origin
Synergistic
Muscle groups that work together
Antagonistic
Muscle groups that oppose each other
Whole muscles
Are groups of muscle cells that share a common origin, insertion, and function
Fascicles
Are bundles of muscles cells sheathed in connective tissue (fascia)
Fasciae come together at
The ends of muscles to form the tendons
Muscles cells (fibres)
Are long, tube-shaped cells of variable length, are multinucleated, and are packed with myofibrils (organelles primarily made of actin and myosin)
muscle make-up order
whole muscle → muscle bundle (fascicle)→ single muscle cell (fiber)→ myofibril → sarcomeres → actin, myosin
contractile units
within myofibrils are segments (which extend between Z lines) called sarcomeres
sacromeres contain
thick filaments of myosin and thin filaments of actin
myosin
thick filaments
actin
thin filaments
parallel arrangement of the filaments
gives rise to striated appearance of skeletal muscle
muscle contractions occur
when the two filaments slide past each other and draw the two Z lines together
skeletal muscle cells are innervated by
nerves (motor neurons); there is one neuron per muscle cell, but multiple muscle cells per neuron
stimulation by a nerve (motor neurons)
increases the concentration of Ca2+ ions in the vicinity of the contractile proteins (myosin) in the sarcomeres
presence of Ca2+
permits the contraction of the fibre
absence of Ca2+
prevents contraction
when never stimulation stops
contraction stops
tetanus
caused by a bacterial infection, generally by Clostridium tetani
C. tetani produces
tetanospasmin, a neurotoxin that prevent inhibitory neurotransmitters that are necessary for muscle relaxation
- those inhibitory neurons typically function to limit the activity in CNS
during an infection with C. tetani
a lack of activity in inhibitory motor neurons can cause muscle spasms and spastic paralysis
how can infection by C. tetani be prevented
by immunization; treatment of an infection may include immunoglobulin therapy
motor neurons that innervate skeletal muscles secrete
the neurotransmitter acetylcholine into a neuromuscular junction
acetylcholine binds to
chemically-gated ion channels, which open (allowing Na+ to enter) to generate an electrical impulse in the muscle fibre
the electrical impulse is carried
into the interior of the cell via T tubules
T tubules
invaginations of the cell membrane
electrical impulse triggers
the release of Ca2+ ions from the sarcoplasmic reticulum (which stores Ca2+) into the scarcoplasm
sarcoplasm
specialized muscle fibre sarcoplasm
Ca2+ comes into
proximity of the myofibrils
Ca2+ initiates
the sliding filament mechanism responsible for the contraction (shortening) of the myofibril sarcomeres
contractions occur
when cross-bridges are formed between myosin and actin filaments (myosin heads bind to the actin)
in relaxed muscles
the myosin heads do not contact the actin filaments
after binding, the myosin heads
bend, which pulls the filaments toward the centre of the sarcomere causing shortening
Ca2+ ions must be present for
cross-bridges to form between the myosin and actin filaments
in the absence of Ca2+, a protein complex of
troponin-tropomyosin covers the myosin binding sites on the actin filaments
when Ca2+ binds to troponin
the protein complex shifts to expose the myosin binding sites on the actin filaments
primary source of energy in muscle cells
is ATP, but only a little ATP is stored in muscle cells
ATP
is required for both muscle contraction and muscle relaxation
ATP is used when
myosin heads bind to actin filaments, when those bound myosin heads detach, and when Ca2+ is transported back into the sarcoplasmic reticulum
ATP is replenished by
transferring a phosphate group from creatine phosphate to ADP, by breaking down stored glycogen into glucose for use in anaerobic metabolism, and by the aerobic metabolism of glucose and fatty acids circulating in the blood
cardiac and smooth muscles contract
involuntarily and can do so spontaneously, in the absence of stimulation by a nerve
cardiac muscle cells
are joined together at their ends by intercalcated discs, which contain gap junctions that permit electrical impulses to flow between connected cells
smooth muscle cells
also contain gap junctions, and most can contract spontaneously, except for those in the trachea and iris
cardiac and smooth muscle cells are innervated by
the autonomic nervous system, which can modify the degree of contraction
cardiac muscle cells also
contains actin and myosin filaments arranged in sarcomeres, which gives it the appearance of a striated muscle- similarly to skeletal muscles
cardiac pacemaker cells
contract with the fastest rhythm of all the cardiac muscle cells, which ultimately causes the other cardiac muscle cells to contract at the same pace
smooth muscle cells contain
actin and myosin filaments in bundles anchored to the cell membrane, which are arranged in a criss-cross pattern; gives the smooth appearance
interstitial cells of Cajal
serve as pacemaker cells in the smooth muscle layer (muscularis) of the intestine
skeletal muscle has
the fastest contraction speed, but those contractions are the least sustainable
cardiac muscle has
both a moderate contraction speed and contraction sustainability
smooth muscle cells have
the slowest contraction speed, but the highest contraction sustainability, generally, these muscles are constantly partially contraction (as in blood vessels)
slowest contraction speed
in smooth muscle cells ensures that ATP usage does not outpace ATP generation
muscles are largely derived from
the paraxial mesoderm
paraxial mesoderm
is divided into both head mesoderm and somitic mesoderm
head mesoderm
in the anterior part of the embryo, which will form the muscles of the face/skull
somitic mesoderm
in the posterior of the endoderm which will form the somites
somites
are transitory blocks of mesoderm divided into two regions:
-ventral somites
-dorsal somites
ventral somites
become sclerotome
dorsal somites
become dermomyotome
sclerotome
contributes to the axial skeleton and the tendons (via syndetome)
dermomyotome
gives rise to the musculature of the limbs, the back, and the rib cage (via mytome) and the dermis (via dermatome)- body’s muscles
somite pairs
periodically form along the dorsal embryo, as boundaries get created in the paraxial mesoderm
rate of somitogenesis
is different in every species, but progresses by the same mechanism, according to the clock-wavefront model
humans have
between 38-45 pairs of somites
individual somite identities (i.e. some somites will form cervical vertebrae with no ribs, while others will form thoracic vertebrae with ribs)
is established by the collinearity of Hox gene expression
the syndetome
is the dorsal-most region of the sclerotome
-is specified by neighboring myotome
responsible for tendon formation
syndetome
dorsomedial lip forms
the primaxial muscle ( the deep muscles of the back and intercostal muscles_
the ventrolip forms
abaxial muscle (the muscles of the ventral body wall and the limbs)