muscle tissue types
skeletal, smooth, cardiac
properties of muscle tissue
excitable
conductive
contractile
elasticity
extensibility
excitable
Responsive to a stimulus
conductive
transfers stimulus along the cell membrane
contractile
shorten their length to create tension
elasticity
return to rest after shortening or lengthening
extensibility
stretch beyond their resting length
primary function od muscle tissue
movement
support
posture
temperature regulations
communications
epimysium
surrounds entire muscle DICT
perimysium
surrounds fascicles DICT with BV and nerves
endomysium
surrounds and electrically insulates each muscle fiber ARC with reticular fibers
deep fisca
large sheet external to epimysium
superficial fascia
separate muscle from skin ARADCT
tendon
attaches a muscle to bone skin or other muscles
aponeurosis
this flattened connective tissue
sacrolemma
plasma membrane
sarcoplasm
cytoplasm
sarcoplasmic reticulum
smooth ER
Myofibrils
muscle fiber running the entire length
contraction = shorten
contain myofilaments
thick filaments
myosin
tail
thin filaments
• Actin
• Tropomyosin
• Troponin
sacromere
functional unit of muscle
smallest piece functions as a muscle
I band
contains thin filaments not thick
A band
contains thick filament
are dark
H zone
center of A band contains thick filaments not thin
M line
protein in center of H zone that attaches thick filaments
contraction of skeletal muscle
• Contracting muscles pull on tendons to produce movement.
• To
pull, muscles develop tensions as their sarcomeres shorten.
• For
sarcomeres to shorten, thick filaments attach to thin filaments
and
pull them toward the centers of the sarcomeres
• The
sliding filament theory explains muscle contraction
sliding filaments theory
Calcium ions bind to troponin on actin’s active site
Myosin binds actin to form a cross-bridge (“cocked” formation)
Phosphate is released, the myosin head
moves into
low-energy conformation and actin slides towards the M line
(“powerstroke”)
A new molecule of ATP replaces ADP
(cross-bridge detachment)
Cross-bridges break and the cycle repeats
NMJ
where the axon terminal of an alpha motor neuron and the membrane of a muscle fiber meet
Stimulation causes build-up of
intracellular Na+, exit of intracellular K
Graded potentials lead to
action potentials and Ca2+ release
Stimulation ends when
acetylcholinesterase degrades
Ach in synaptic cleft
synaptic knob
expanded tip of neuron axon
synaptic vesicles
Membrane sacs in synaptic knob, filled with acetylcholine (ACh)
synaptic cleft
Narrow space separating synaptic knob and motor end plate
motor end plate
Region of sarcolemma with many folds (increased surface area)
under
the synaptic knob
ACh receptors:
Proteins that bind Ach on the motor end plate
Acetylcholinesterase (AChE)
Enzyme in synaptic cleft that breaks down Ach (prevents continuous stimulation of muscle)
motor unit
a single motor neuron and the muscle fiber it controls
Muscle tension is ideal at a specific
muscle length
This is due to optimal placement
of actin and myosin for cross-bridge
formation
Muscle Atrophy
A wasting of muscle that reduces fiber size
Reduced stimulation results in reduced muscle size, tone, and power
Muscle hypertrophy
An increase in fast muscle fiber SIZE (not cells!)
Building
muscle increases fiber size not number of fibers
Number of
myofibrils per fiber increases
More mitochondria and more
glycogen stored in the cells
Results from repetitive, exhaustive
stimulation of muscle
Resting Muscle
• More ATP is produced than needed
• ATP transfers the energy to
create ADP
ATP + creatine → creatine phosphate + ADP
contracting muscle
The reverse reaction generates ATP from
creatine
phosphate
Creatine phosphate + ADP → ATP + creatine
• ATP is
continuously generated at the same
rate it is used
Fatigue-inducing situations
• Lactic acid build-up after high-intensity exercise
• Glycogen
depletion after medium-intensity exercise over long periods of time
muscle fatigue
Muscle cannot continue contractions even under nervous stimulation
smooth muscles
• Smaller than skeletal muscle cells
• Spindle-shaped
•
Have centrally-located nucleus
• No T-tubules or visible
sarcomeres
• Do not fuse during development
• Connected by
junctions
• Have membrane invaginations called caveolae
main function of smooth muscle
line walls of hollow organs
responsible for involuntary movements
contraction of organs
Excitation-Contraction Coupling
in Smooth Muscle Tissue
1. Ca2+ enters sarcoplasm; interacts with calmodulin
2. Myosin
light chain kinase (MLCK)
phosphorylates myosin
3. Myosin-actin cross-bridges form
4. Cross-bridges develop muscle tension
5. Relaxation: removal
of Ca2+ and
myosin dephosphorylation