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Skeletal muscle is
Voluntary, striated, single long cylindrical cells, multiple peripheral nuclei
How long can muscle fibres get?
Up to 35cm
Muscle cell / fibre is made up of
myofibrils
Myofibrils are made up of
contractile units called sarcomeres
z disc
edge of sarcomere where thin filaments join together
A band
Length of thick filaments
I band
Area with only thin filaments
H zone
Area with only thick filaments
M line
Middle of H zone
Where are T tubules
around every end of A band (2 per sarcomere)
What do T Tubules do?
Allow Action potentials to be carried deep into the muscle
Sarcoplasmic reticulum (SR)
calcium storage, close to T tubules to allow fast reaction, specialised ER
Myosin has
A head and tail, tail holds and head binds to actin, polarised fashion because heads at end tails in middle
A myosin head move via
the hydrolysis of ATP into ADP and inorganic phosphate
What does titin do?
Anchors thick filament to the Z line
Actin has
myson binding sites attached, with tropomyosin looped around and troponin attached
First step in cross bridge cycle
Cross bridge formation
Second step in cross bridge cycle
Power stroke
Third step of cross bridge cycle
detachment
fourth step of cross bridge cycle
energisation of myosin head
Formation of cross bridge
Myosin head in activated state binds to actin (only when Ca has binded to troponin causing tropomyosin to move)
Powerstroke
ADP is released from myosin head, changing it from high energy state to low energy state and pulling actin over (shortening of sarcomere)
Detachment
New ATP molecule binds to myosin head, the actin to myosin bond is weakened and myosin detaches
Energisation of myosin head
ATP molecule is hydrolysed into ADP and P
How is calcium released from the SR?
An action potential, calcium leaves through calcium channels
How does calcium return to the SR?
Ca2+/ATPase uses active transport for Ca to return, constantly working
What happens to Ca when there is no muscle contraction from an action potential?
The concentration of Ca in cytoplasm decreases as none is being released, but it is all being reabsorbed by SR
Isotonic movement
Shortening, constant tension, velocity variable
Isometric movement
No shortening, length constant, tension variable
A stretched muscle has less
tension
Maximum active force is dependant on the degree of actin and. myosin overlap. At the optimum overlap of myosin, there is:
Maximum tension
A longer stretched muscle has less
cross bridging because myosin heads cant reach
An understretched muscle has
interferring and overlapping
Total tension=
Active + passive force
Passive force increases as
muscle stretches
Active force developed via
cross bridge cycling, dependant on actin-myosin overlap
At a muscles optiumum length, what kind of tension is present?
Only active force
What is the name of this step (in Excitation-contraction coupling):
AP travels down a motor neuron to the axon terminal, where voltage gated Ca channels open, allowing Ca to enter. The vesicles holding ACh are triggered and fuse with the terminal membrane, releasing ACh into the neuromuscular junction (synaptic cleft)
ACh released into neuromuscular junction
What is the name of this step (in Excitation-contraction coupling):
The binding of ACh to the receptors on the muscle end plate causes the opening of the ligand gated ion channels, which allow movement of ions into the muscle (mostly Na) making it less negative (End Plate Potential)
Activation of ACh receptors
What is the name of this step (in Excitation-contraction coupling):
If sufficient number of ligand gated ion channels are opened, the end plate potential reaches threshold and the voltage gated Na channels open, an AP is triggered then propagated along the sarcolemma into the T-tubule system
Muscle Action potential is triggered
What is the name of this step (in Excitation-contraction coupling):
AP is conducted down the T-Tubules coming in close contact with SR, results in voltage gated Ca channels in the SR opening up, Ca is released into the cytosol.
calcium is released from SR
What is the fifth step of Excitation-contraction coupling after calcium is released form the SR?
Ca binds to troponin, then cross bridge cycle happens
When does a contraction end
When Ca levels fall as it is actively pumped back into SR by Ca/ATPase pumps, tropomyosin moves back over myosin binding sites
Three sources of ATP for muscle metabolism
Creatine phosphate, anaerobic glycolysis, Aerobic metabolism
Creatine phosphate
Breif, no O needed, creatine phosphate + ADP = 1 ATP, acts as an ATP store
Anaerobic glycolysis
no O, fast but inefficient (2ATP), energy from glucose, build up of H+ limits to 120s of use, about 10-30s maximum effort
Aerobic metabolism
Endurance, efficient but slow (32ATP), requires Oxygen and therefore needs good blood flow, energy source from glucose, pyruvic acid, fatty acids, amino acids
Regulation of force is dependant on:
Rate of stimulation, number of motor units stimulated
Motor unit
a motor neuron + all the muscle fibers it innervates
Rate of stimulation
A single stimulus = twitch, high stimulation the twitches move together = fused tetanus, temporal summation = unfused tetnaus
Recruitment of motor units
Everyday activities require only type 1 motor units, any further more motor units recruited and tension increases, more efficient to use smaller less fatigued motor units first
Blood starts in the ——-, then moves to the ———-
right atrium, right ventricle
After the right ventricle, blood flows outwards to the lungs via the —— and then back in by the ——
Pulmonary artery, pulmonary veins
After the blood is brough back from the lungs by the pulmonary veins, it travels to the ——- then the ———- then out through aorta
left atrium, left ventricle
Majority of cardiac muscle is found in the ——- because it has to ovecome resistance to pump blood around body
left ventricle
Heartbeat initiates at
right atrium
Ventricular muscle cells are branched, with many —— junctions to form sheets
gap
Ventricular muscle has 1 t tubule placed on ————, and has a more developed —— than skeletal muscle
the z line, SR
Ventricular muscle has ———— which act as the glue between two cells
intercalated discs
Intercalated discs contain ——- which prevent cells from separating during contraction, and —— junctions which allow the action potential to be carried from one cell to the next quickly.
desmosomes, gap
Intercalated discs in muscle cells allow ——— contraction, unlike skeletal muscle where fibres are recruited via the motor nerves
coordinated
Cardiac muscle is myogenic, meaning
contraction starts within the muscle
RMP of cardiac muscle
-90mV, more negative than skeletal muscle
Ventricular muscle Action potentials have a fast —— caused by voltage gated Na channels opening
depolarisation
Plateau phase
during a ventricular muscle AP, voltage gated Calcium channels (extra) slowly open and slowly close, allowing longer AP
Action potentials in ventricular muscle are less likely to —- than skeletal muscle?
join together (tetanus) due to the long refractory period inhibiting release of new APs
Where is LTCC = L-type voltage gated calcium channel (I CaL) found?
T-tubule of cardiac muscle, allows calcium into cytoplasm between T tubule and SR
Where is RyR = ryanodine receptor (Calcium ligand gated channel) found?
In SR of cardiac muscle, allows Ca to bind and release Ca into the cytoplasm
What is the importance of Na/Ca exchanger in the cardiac muscle?
Uses the gradient of Na to remove Ca from cytoplasm into T tubule
Cardiac Muscle: excitation-contraction coupling
AP opens voltage gated type-L calcium channel in t tubule, releasing Ca into cytoplasm towards SR, triggering opening of (RyRa) ligand gated calcium induced calcium release into cytoplasm
How is calcium removed in cardiac muscle?
SR Ca2+-ATPase, or sarcolemmal Na+/Ca2+ exchange
Trigger for Ca2+ release from SR in skeletal muscle?
Voltage gated Na+ channel
Trigger for Ca2+ release from SR in cardiac muscle
ligand gated calcium induced calcium release
How to create a graded contraction in skeletal vs cardiac muscle?
recruitment of more fibres in skeletal, increase Ca in cardiac
Regulation of Cardiac Output (CO) =
SV x HR
Heart Rate (HR) is set by
the pacemaker cells in the sinoatrial node, can be modified by neurotransmitters
pacemaker cells have an unstable
RMP, spontaneously firing
Sympathetic nervous system
increases heart rate (force of contraction) by noradrenaline
Parasympathetic nerves
decrease heart rate by releasing ACh
SV can be increased by
noradrenaline, increased rate of firing, increased stretch of ventricles
Single unit smooth muscle
primarily found in the walls of hollow organs and viscera, sheets of cells that are electrically coupled and act in unison
Multiunit smooth muscle
Tissues made of discrete bundles of independant cells, innervated, contract in response to nerve, eye
What do smooth muscle cells have instead of T tubules?
Caveolae, wrinkles to increase surface area
Dense bodies in smooth muscle anchor ?
actin to sarcolemma
Contractile proteins in smooth muscle
actin and myosin filament
Initiation of contraction in smooth muscle
primarily due to voltage gated Ca2+ channels allowing Ca into cell, less reliant on SR stores
Calcium regulation in smooth muscle
Comes from outside cell, regulation via hormones, neurotransmitters and ions
Calmodulin
floats in cell until its activated by Ca, then binds to MLCK which activates and turns on myosin heads
Contraction in smooth muscle ends when
MLCP dephosphorylates the myosin light chain
Innervation of smooth muscle fibers
autonomic nerve fibers branch and form diffuse junctions with underlying smooth muscle fibers
Smooth muscle response to stretch
counteracts / contracts due to stretch activated calcium channels, overtime slowly adapts to change in length via calcium dependant K+ channels hyperpolarising membrane potential
Calcium source in smooth muscle
Outside cell and SR via IP3