muscle physiology. homeostasis skeletal muscles contribute to homeostasis by playing a major role in...
TRANSCRIPT
Muscle physiology
homeostasis
• skeletal muscles contribute to homeostasis by playing a major role in the procurement of food, breathing,heat generation for maintenance of body temperature, and movement away from harm.
Introduction Skeletal muscle
Cardiac muscle
Smooth muscle
Striated muscle
Unstriated muscle
Involuntary muscle
voluntary muscle
A
B
A: depending on whether alternating dark and light bands can be seen under LM
B: depending on whether they are innervated by the somatic nervous system and are subject to voluntary control
The structure of skeletal muscle
• Skeletal muscle are stimulated to contract via release of Ach at neuromuscular junctions between motor neuron terminals and muscle cells
• To understand how the muscle Ap initiated by Ach bring about contraction , firstly you must know the structural components of a skeletal muscle fiber
• The levels of organization in a skeletal muscle can be summarized as follows:
The structure of skeletal muscle
Whole muscle
An organ
Muscle fiber
A cell
myofibril
A specialized intracellular structure
Thick and thin filaments
Cytoskeletal elements
Myosin and actin
proteins
The structure of skeletal muscle
Levels of organization in a skeletal muscle
Enlargement of a cross section of a whole muscle
The structure of skeletal muscle
Seen under light microscope
Enlargement of a myofibril within a muscle fiber
A myofibril displays alternating dark band (the A bands ) and light bands (the I bands) the bands of all the myofibrils lined up parallel to each other lead to the striated appearance
The structure of skeletal muscle
Cytoskeletal components of a myofibril Alternate stacked sets of thick and thin filaments that slightly overlap each other are responsible for the A and I bands
A band : a stacked set of thick filaments along with the portions of the thin filaments that overlap on both ends of the thick filaments
H zone : lighter area within the middle of the A band
I band: the remaining portion of the thin filaments that do not project into the A band (only thin filaments)
Z line : in the middle of each I band, hold the Sarcomere together
Sarcomere: the area between two Z lines ,
the functional unit of skeletal muscle
M line : in the middle of each A band, within the center of the H zone
The structure of skeletal muscle
Protein components of thick and thin filaments
Structure of thick filaments
Structure of myosin molecules and their organization within a thick filament
The head of myosin form cross bridge (actin binding site and a myosin ATPase site—ATP splitting site)
Structure of thin filaments
Composition of a thin filament
Three protein:
Actin: binding of actin and myosin molecules at the cross bridges results in energy-consuming contraction of the muscle fiber
Tropomyosin: covers the actin sites that bind with the cross bridges
Troponin : has three units – one binds to tropomyosin , one binds to actin and one bind with Ca2+
Molecular basis of skeletal muscle contraction—sliding-filament mechanism
• During contraction, cycles of cross-bridge binding and bending pull the thin filaments inward and closer together between the stationary thick filaments, causing shortening of the sarcomere
Changes in banding pattern during shortening. there is no thin filament or thick filament shortening
Role of Ca2+ in turning on cross bridges
Muscle fiber relaxed: no cross-bridges binding– its binding site on actins is covered by the troponin- tropomyosin complex
Muscle fiber excited: released Ca2+ binds with troponin, pulling the complex aside to expose the binding site; cross-bridges binding actins occurs
Binding of actin and myosin cross bridge triggers power stroke that pulls thin filament inward during contraction
excitation --?-- contraction
• Calcium is the link between excitation and contraction (excitation-contraction coupling)
• excitation-contraction coupling refers to the series of events linking muscle excitation (Ap) to muscle contraction (sarcomere shortening)
The structure basis of excitation-contraction coupling
The T tubules and sarcoplasmic reticulum in relationship to the myofibrils
The T tubules dip deep into the muscle fiber at the junctions between the A and I bands of the myofibrils
The sarcoplasmic reticulum is a membranous network runs longitudinally and surrounds each myofibril.
The ends of each segment are expanded to form lateral sacs (terminal cisternae)—Ca2+ store
• How is a change in T tubule potential linked with the release of Ca2+ from the lateral sacs?
Excitation-contraction coupling
Step 1. Ach released from the terminal of motor neuron cross the cleft and bind to receptors/channels on motor end plate – end plated potential occurs
Excitation-contraction coupling
Step 2. Ap generated and propagated across surface membrane and down T tubules
Step 3. Ap triggers Ca2+ release from sarcoplasmic reticulum– ca2+ store
SR foot protein( ryanodine receptors )---di
hydropyridine receptros(T tubule votage-gated sensors.)
Excitation-contraction coupling
Step 5. myosin cross bridges attach to actin and bend –sarcomere shortened, powered by energy provided by ATP
actin binding site and
an ATPase site.—enzymatic site (split ATP into ADP and Pi)
Excitation-contraction coupling---relaxation
Step 6. Ca2+ actively taken up by sarcoplasmic reticulum when there is no Ap
Ca2+ -ATPase pump
Excitation-contraction coupling
Step 7. when Ca2+ no longer bind to troponin , tropomyosin slips back to its blocking position over binding sites on actin. (need ATP) Contract ends; actin slides back to original resting position
The relationship of an Ap to the resultant muscle contraction
The contraction activity far outlasts the electrical activity that initiated it
• A single Ap in skeletal muscle fiber lasts only 1 to 2 m sec
• The duration of the contraction is 100 m sec (contraction time 50 m sec and relaxation time 50m sec)
The relationship of an Ap to the resultant muscle twitch
The duration of the Ap is not draw to scale but is exaggerated
Contractions of a whole muscle can be of varying strength
Whole muscle tension depends on:• The number of muscle fiber contracting • The frequency of stimulation• The length of the fiber at the onset of
contraction• the extent of fatigue• The thickness of the fiber
Single twitch
If a muscle fiber is restimulated after it has completely relaxed, the second twitch is the same magnitude as the first twitch (single twitch)
Twitch summation
If a muscle fiber is restimulated before it has completely relaxed, the second twitch is added on to the first twitch, resulting in summation . (twitch summation)
tetanus
If a muscle fiber is restimulated so rapidly that it does not have an opportunity to relaxed at all, a maximal sustained contraction known as tetanus take place .(tetanus)
The frequency of stimulation can influence the tension developed by each muscle fiber
the single twitch is not of maximal strength, and the tetanus cause maximal strength
Why the twitch summation is possible and Ap summation is not ?
--- For twitch summation: the duration of the twitch (100 msec) is much longer than the du
ration of Ap (1to2 msec) . When the previous twitch is not complete, the muscle can receive another stimulus
--- For Ap: once the Ap is initiated , there is a brief refractory period occurs
during which another Ap cannot be initiated
What is the mechanism of twitch summation and tetanus at the cellular level?
Why the single twitch is not of maximal strength? During the single twitch not all of the cross bridges find a binding sites. (pulling the thin fil
ament to the thick filament) . All the released Ca2+ from the first contractile response to be pumped back an identical twitch response will occur
The mechanism of twitch summation The first contractile activity is still present when the second Ap takes place . There is anothe
r spurt of Ca2+ release ,the magnitude of cross-bridge cycling and tension increase
The mechanism of tetanus As the frequency of Ap increases, the duration of elevated cytosolic Ca2+ concentration incr
eases, an contractile activity likewise increases until a maximum tetanic contraction is reached. With tetanus , the maximum number of cross-bridge cycling, and tension are at their peak
The length of the fiber at the onset of contraction influence the muscle tension
• There is an optimal muscle length at which maximal tension can be developed upon a subsequent contraction—optimal length(lo)
Length-tension relation
Maximal tetanic contraction can be achieved when a muscle fiber is at its optimal length (A)
The percentage of maximal tetanic contraction will be decrease when the muscle fiber is longer or shorter than (B,C,D)
In the body, the resting muscle length is at optimal length. Muscles cannot vary beyond 30% of the optimal length
The two primary types of contraction are isotonic and isometric
• Isotonic contraction: muscle tension remains constant as the muscle changes length
• Isometric contraction: tension develops at constant muscle length
The category of the two types of contraction depend on the relationship between muscle tension and the load
Isotonic contraction (tension is less than the load)
• e.g. you are going to lift an object:
• The tension in biceps developing and enough to overcome the weight of an subject, then you lift the object and the muscle shortening. The weight of the object does not changes so the tension remains constant during the muscle shortening
• Significance : body movement and moving an external object
• e.g. an object is too heavy for you.
• the tension develop in your muscle is less than that required to lift the load, the muscle cannot shorten and lift the object, the
muscle remains at constant length and tension develop
• Significance : maintaining posture and supporting objects in a fixed position
Isometric contraction
(the tension exceeds the load)
During a given movement , a muscle may shift between the two type . e.g. pick up a book to read (isotonic), as you stop to hold the book in front of you (isometric)
Load- velocity relationship
The velocity of shortening decreases as the load increases
Isotonic contraction: The greater the load , the lower the velocity of shortening a muscle. When the load is maximum the velocity is zero-- Isometric contraction