BIOSCI 107- MODULE 7 muscles

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Last updated 10:56 AM on 6/23/26
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92 Terms

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Skeletal muscle is

Voluntary, striated, single long cylindrical cells, multiple peripheral nuclei

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How long can muscle fibres get?

Up to 35cm

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Muscle cell / fibre is made up of

myofibrils

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Myofibrils are made up of

contractile units called sarcomeres

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z disc

edge of sarcomere where thin filaments join together

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A band

Length of thick filaments

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I band

Area with only thin filaments

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H zone

Area with only thick filaments

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M line

Middle of H zone

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Where are T tubules

around every end of A band (2 per sarcomere)

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What do T Tubules do?

Allow Action potentials to be carried deep into the muscle

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Sarcoplasmic reticulum (SR)

calcium storage, close to T tubules to allow fast reaction, specialised ER

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Myosin has

A head and tail, tail holds and head binds to actin, polarised fashion because heads at end tails in middle

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A myosin head move via

the hydrolysis of ATP into ADP and inorganic phosphate

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What does titin do?

Anchors thick filament to the Z line

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Actin has

myson binding sites attached, with tropomyosin looped around and troponin attached

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First step in cross bridge cycle

Cross bridge formation

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Second step in cross bridge cycle

Power stroke

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Third step of cross bridge cycle

detachment

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fourth step of cross bridge cycle

energisation of myosin head

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Formation of cross bridge

Myosin head in activated state binds to actin (only when Ca has binded to troponin causing tropomyosin to move)

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Powerstroke

ADP is released from myosin head, changing it from high energy state to low energy state and pulling actin over (shortening of sarcomere)

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Detachment

New ATP molecule binds to myosin head, the actin to myosin bond is weakened and myosin detaches

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Energisation of myosin head

ATP molecule is hydrolysed into ADP and P

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How is calcium released from the SR?

An action potential, calcium leaves through calcium channels

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How does calcium return to the SR?

Ca2+/ATPase uses active transport for Ca to return, constantly working

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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

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Isotonic movement

Shortening, constant tension, velocity variable

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Isometric movement

No shortening, length constant, tension variable

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A stretched muscle has less

tension

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Maximum active force is dependant on the degree of actin and. myosin overlap. At the optimum overlap of myosin, there is:

Maximum tension

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A longer stretched muscle has less

cross bridging because myosin heads cant reach

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An understretched muscle has

interferring and overlapping

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Total tension=

Active + passive force

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Passive force increases as

muscle stretches

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Active force developed via

cross bridge cycling, dependant on actin-myosin overlap

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At a muscles optiumum length, what kind of tension is present?

Only active force

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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)

  1. ACh released into neuromuscular junction


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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)

  1. Activation of ACh receptors


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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

  1. Muscle Action potential is triggered


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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.

  1. calcium is released from SR


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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

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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

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Three sources of ATP for muscle metabolism

Creatine phosphate, anaerobic glycolysis, Aerobic metabolism

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Creatine phosphate

Breif, no O needed, creatine phosphate + ADP = 1 ATP, acts as an ATP store

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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

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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

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Regulation of force is dependant on:

Rate of stimulation, number of motor units stimulated

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Motor unit

a motor neuron + all the muscle fibers it innervates

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Rate of stimulation

A single stimulus = twitch, high stimulation the twitches move together = fused tetanus, temporal summation = unfused tetnaus

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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

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Blood starts in the ——-, then moves to the ———-

right atrium, right ventricle

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After the right ventricle, blood flows outwards to the lungs via the —— and then back in by the ——

Pulmonary artery, pulmonary veins

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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

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Majority of cardiac muscle is found in the ——- because it has to ovecome resistance to pump blood around body

left ventricle

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Heartbeat initiates at

right atrium

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Ventricular muscle cells are branched, with many —— junctions to form sheets

gap

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Ventricular muscle has 1 t tubule placed on ————, and has a more developed —— than skeletal muscle

the z line, SR

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Ventricular muscle has ———— which act as the glue between two cells

intercalated discs

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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

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Intercalated discs in muscle cells allow ——— contraction, unlike skeletal muscle where fibres are recruited via the motor nerves

coordinated

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Cardiac muscle is myogenic, meaning

contraction starts within the muscle

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RMP of cardiac muscle

-90mV, more negative than skeletal muscle

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Ventricular muscle Action potentials have a fast —— caused by voltage gated Na channels opening

depolarisation

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Plateau phase

during a ventricular muscle AP, voltage gated Calcium channels (extra) slowly open and slowly close, allowing longer AP

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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

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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

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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

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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

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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

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How is calcium removed in cardiac muscle?

SR Ca2+-ATPase, or sarcolemmal Na+/Ca2+ exchange

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Trigger for Ca2+ release from SR in skeletal muscle?

Voltage gated Na+ channel

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Trigger for Ca2+ release from SR in cardiac muscle

ligand gated calcium induced calcium release

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How to create a graded contraction in skeletal vs cardiac muscle?

recruitment of more fibres in skeletal, increase Ca in cardiac

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Regulation of Cardiac Output (CO) =

SV x HR

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Heart Rate (HR) is set by

the pacemaker cells in the sinoatrial node, can be modified by neurotransmitters

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pacemaker cells have an unstable

RMP, spontaneously firing

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Sympathetic nervous system

increases heart rate (force of contraction) by noradrenaline

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Parasympathetic nerves

decrease heart rate by releasing ACh

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SV can be increased by

noradrenaline, increased rate of firing, increased stretch of ventricles

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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

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Multiunit smooth muscle

Tissues made of discrete bundles of independant cells, innervated, contract in response to nerve, eye

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What do smooth muscle cells have instead of T tubules?

Caveolae, wrinkles to increase surface area

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Dense bodies in smooth muscle anchor ?

actin to sarcolemma

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Contractile proteins in smooth muscle

actin and myosin filament

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Initiation of contraction in smooth muscle

primarily due to voltage gated Ca2+ channels allowing Ca into cell, less reliant on SR stores

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Calcium regulation in smooth muscle

Comes from outside cell, regulation via hormones, neurotransmitters and ions

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Calmodulin

floats in cell until its activated by Ca, then binds to MLCK which activates and turns on myosin heads

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Contraction in smooth muscle ends when

MLCP dephosphorylates the myosin light chain

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Innervation of smooth muscle fibers

autonomic nerve fibers branch and form diffuse junctions with underlying smooth muscle fibers

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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

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Calcium source in smooth muscle

Outside cell and SR via IP3