midterm Flashcards
(95 cards)
muscle tissue types (how they differentiated)
excitability
contractibility
extensibility
elasticity
differentiated by: fiber shape
location/number of nuceli, appearance stariated smooth
nature of control (voluntary/involuntary)
3 major muscle types
smooth: spindle shaped, non striated, walls of internal organs
involuntary
cardiac: involuntary, striated, branched, uninucleated fibers, occurs in walls of heart
skeletal: voluntary, striated, attached to skeleton
skeletal muscle- macro structure
epimysium: surrounds all the muscle fiber bundles to form the entire muscle
perimysium: surrounds several muscle fibers and forms fasciculi
fasciculus: bundles of muscle fibers
endomysium: connective tissue that wraps each muscle fiber
the weight of a muscle fiber consist of..
75% water
20% protein
5% other - minerals
structure of muscle (sacrolemma, satelite cells, sacroplasm, SR)
sacrolemma: muscle cell membrane surrounding muscle fiber
satelite cells: located within the sacrolemma, help regenerate cell growth, play a role in hypertrophy
sacroplasm: protoplasm, nuceli
Sacroplasmic reticulum (SR)
network of tubules and vesicles (traids)
located around myofibrils
role: stores, releases, and absorbs calcium
muscle—> fasicle—> muscle cell—-> myofibril—>myofilaments
myofilaments include
myosin (thick myofilament)
actin (thin myofilament)
actin and myosin are contractile proteins
within the actin (the regulatory proteins)
troponin (thin)
tropomyosin (thick)
both are regulatory proteins
sacomere
an arrangement of actins and myosins borded by z discs
Z discs: the thick structures that are perpendicular to and anchor proteins
I band, A band, H zone
I band a light area that contains only actin
A band a dark area that contians actin and myosin
H zone a light area that contains only myodin
tropomyosin, troponin
regulatory proteins
tropomyosin: lies along actin like a cord, inhibits actin-myosin interaction
troponin: embedded at regular intervals along actin
interacts binds with Ca
removes inhibition
globular head
actin binding site
ATP binding site
myosin (heads)
myosin has 2 heads
each head has 1 heavy chain
heavy chain determines the ATPase activity
3 predominant types of MHC:
type 1 MHC: slowest contracting
type 2a MHC: moderatley fast contracting
type 2x MHC: fast contracting
M band and M bridges
M band: ensures myosin filaments stay in correct position within the sacromere
M bridges: hexagonal pattern (connect with 6 myosin filaments)
myosin and actin filaments lie in a hexagonal pattern around each other
muscle action (2 components mechanical/chemical)
mechancial- sliding filament theory
chemical - enewrgy-via ATP hyrdolysis
sliding filament theory
myosin cross bridges attach to actin filament
cross bridges rotate
cross bridges detach
REPESAT
only about 50% of cross bridges attached at any one time
rearrangement of actin and myosin at rest and during muscle shortening
during contraction (concentric)
the length of the thick and thin filaments do not change
the length of the sacromere decreases as actin is pulled over myosin
i band a h zone during contraction
H zone disappears
I band becomes very narrow
ATP hyrdrolysis
Main molecule used for energy in muscle contraction is from ATP hydrolysis
ATP
ATP is broken down by an enzyme ATPase
broken donw into ADP+ PI+ energy
PI= inorganic phosphate
sliding filament steps
ATP bounds to myosin
ATP hyrdolysis, energy stored in globular head
loose binding between myosin and actin
ATP—> ADP+Pi+ energy (remains attached to globular head)
Pi released- tightens binding
conformational change of myosin head (reposition angle of attachemnt of myosin and actin)
elicits pulling of actin towards m line (cross bridge movement)
myosin drops ADP as it moves
New ATP binds to myosin
release of myosin head from actin (cross bridge disaasociates)
when does myosin detachment from actin occur
when new ATP joins the actomyosin complex completing the sliding motion, cross birdgesridges disassociate
the 7 main steps of sliding filament theory
ATP bound to myosin head
ATP hydrolysis
loose binding of actin and myosin
release of Pi cause tightening
cross bridge begins movement to start the sliding filament theory
ADP is released
Myosin binds with new ATP
Excitation-contraction steps
electrical discharge at muscle initiates chemical events at cell surface
cell (SR) releases intracellular Ca
Ca combines to troponin-tropomyosin in actin filament
troponin pulls tropomyosin off actin active sites (removes inhibitory action)
allows actin to combine with myosin
removal of Ca restores the inhibitory action of troponin-tropomyosin
EC coupling and sliding filament model
depolarization of T-tubule system causes Ca release from lateral sacs of sacroplamsic reticulum
Ca binds to troponin-tropomyosin in actin filaments, releasing the inhibition that prevents actin from combining with myosin
actin combines with myosin (ADP,PI, and energy)-actomyosin complex
energy produces myosin crossbridge movement (myosin tightens bond with actin) and creates tension
New ATP binds to myosin crossbridge, which breaks actin-myosin bond, allowing cross bridge disassociation and sliding of thick and thin filaments
cross-bridge activation continues when Ca concentration remains high enough to inhibit troponin-tropomyosin system
when muscle stimulation ceases, intracellular Ca concentration rapidly decreases as Ca moves back into lateral sacs of SR through active transport, requires ATP hyrdrolysis
Ca removal restores inhibitory action of troponin-tropomyosin
in presence of ATP, actin and myosin remain in dissociated, relaxed state