2.10 Animal Support-MNR
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Transcript of 2.10 Animal Support-MNR
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Support
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Animal skeletons function in support, protection,
and movement
•The various types of animal movements – All result from muscles working against some type
of skeleton
• The three main functions of a skeleton are
– Support, protection, and movement
• The three main types of skeletons are
– Hydrostatic skeletons, exoskeletons, and
endoskeletons
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Hydrostatic Skeletons
• A hydrostatic skeleton – Consists of fluid held under pressure in a closed
ody compartment
• This is the main type of skeleton – !n most cnidarians, flatworms, nematodes, and
annelids
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• Annelids use their hydrostatic skeleton for
peristalsis
– A type of movement on land produced yrhythmic waves of muscle contractions
Figure 49.25a–c
(a) "ody segments at the head and #ust in front
of the rear are short and thick $longitudinalmuscles contracted% circular muscles
relaxed& and anchored to the ground y
ristles' The other segments are thin and
elongated $circular muscles contracted%longitudinal muscles relaxed'&
(b) The head has moved forward ecausecircular muscles in the head segments have
contracted' Segments ehind the head and
at the rear are now thick and anchored, thus
preventing the worm from slipping ackward'
(c) The head segments are thick again and
anchored in their new positions' The rear
segments have released their hold on theground and have een pulled forward'
(ongitudinal
muscle relaxed
$extended&
Circular muscle
contracted
Circular
muscle
relaxed
(ongitudinal
muscle
contracted
Head"ristles
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Exoskeleton• An exoskeleton is a hard encasement
– )eposited on the surface of an animal• *xoskeletons
– Are found in most molluscs and arthropods
Endoskeleton• An endoskeleton consists of hard supporting
elements
– Such as ones, uried within the soft tissue of an
animal
• *ndoskeletons
– Are found in sponges, echinoderms, and chordates
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• The human skeleton
Figure 49.26
1 Ball-and-socket oints! where the humerus contacts
the shoulder girdle and where the femur contacts the
pelvic girdle, enale us to rotate our arms and
legs and move them in several planes'
2 "inge oints! such as etween the humerus and
the head of the ulna, restrict movement to a singleplane'
# $i%ot oints allow us to rotate our forearm at the
elow and to move our head from side to side'
ke&
Axial skeleton
Appendicular
skeleton
Skull
Shoulder
girdle
Clavicle
Scapula
Sternum
+i
Humerus
ertera
+adius-lna.elvic
girdle
Carpals
.halanges
/etacarpals
0emur
.atella
Tiia
0iula
Tarsals/etatarsals.halanges
1
Exa'les
o oints
2
#
Head of
humerus
Scapula
Humerus
-lna
-lna+adius
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.hysical Support on (and
• !n addition to the skeleton – /uscles and tendons help support large land
verterates
•Concept1 /uscles move skeletal parts ycontracting
• The action of a muscle
– *s al+a&s to contract
• Skeletal muscles are attached to the skeletonin antagonistic pairs – 2ith each memer of the pair working against each
other
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Figure 49.2,
"u'an rassoer
"iceps
contracts
Triceps
relaxes0orearm
flexes
"iceps
relaxes
Triceps
contracts
0orearm
extends
*xtensor
muscle
relaxes
0lexor
muscle
contracts
Tiiaflexes
*xtensor
muscle
contracts
0lexor
muscle
relaxes
Tiia
extends
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erterate Skeletal /uscle• erterate skeletal muscle
– !s characteri3ed y a hierarchy of smaller andsmaller units
Figure 49.2/
/uscle
"undle of
muscle fiers
Single muscle fier
$cell&
.lasma memrane
/yofiril
(ight
and )ark and
4 line
Sarcomere
T*/ 5'6 µm
I and A and I and
/ line
Thick
filaments
$myosin&
Thin
filaments
$actin&
H 3one
Sarcomere4 line4 line
7uclei
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• A skeletal muscle consists of a undle of long fiers – +unning parallel to the length of the muscle
• A muscle fier
– !s itself a undle of smaller myofirils arranged longitudinally• The myofirils are composed to two kinds of
myofilaments – Thin filaments, consisting of two strands of actin and one
strand of regulatory protein – Thick filaments, staggered arrays of myosin molecules
• Skeletal muscle is also called striated muscle – "ecause the regular arrangement of the myofilaments
creates a pattern of light and dark ands – *ach repeating unit is a sarcomere
– "ordered y 4 lines
– The areas that contain the myofilments
– Are the ! and, A and, and H 3one
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The Sliding-Filament Model of
Muscle Contraction• According to the sliding8filament model of muscle
contraction
– The filaments slide past each other longitudinally, producing
more overlap etween the thin and thick filaments
• The sliding of filaments is ased on
– The interaction etween the actin and myosin molecules of
the thick and thin filaments
• The 9head: of a myosin molecule inds to an actinfilament
– 0orming a cross8ridge and pulling the thin filament toward
the center of the sarcomere
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• As a result of this sliding
– The ! and and the H 3one shrink
Figure 49.29a–c
(a) 0elaxed 'uscle iber. !n a relaxed muscle fier, the I andsand H 3one are relatively wide'
(b) ontracting 'uscle iber. )uring contraction, the thick and
thin filaments slide past each other, reducing the width of the
I ands and H 3one and shortening the sarcomere'
(c) Full& contracted 'uscle iber. !n a fully contracted muscle
fier, the sarcomere is shorter still' The thin filaments overlap,
eliminating the H 3one' The I ands disappear as the ends of
the thick filaments contact the 4 lines'
5'6 µm
4 H A
Sarcomere
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• /yosin8actin interactions underlying
muscle fier contraction
Figure 49.#
Thick filament
Thin filaments
Thin filament
AT.
AT.
A). A).
A).
.i . i
.i
Cross8ridge
/yosin head $low8
energy configuration&
/yosin head $high8
energy configuration&
;
/yosin head $low8energy configuration&
Thin filament moves
toward center of sarcomere'
Thick
filament Actin
Cross8ridge
inding site
< Starting here, the myosin head is
ound to AT. and is in its low8
energy confinguration'
= The myosin head hydroly3es AT. to A). and inorganic
phosphate $ ! & and is in its
high8energy configuration'
.
< The myosin head inds to
actin, forming a cross8
ridge'
>
? +eleasing A). and $ i&, myosin
relaxes to its low8energy configuration,
sliding the thin filament'
.
6 "inding of a new mole8
cule of AT. releases the
myosin head from actin,
and a new cycle egins'
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The Role of Calcium and Regulatory
Proteins• A skeletal muscle fier contracts
– @nly when stimulated y a motor neuron
• 2hen a muscle is at rest
– The myosin8inding sites on the thin filament are
locked y the regulatory protein tropomyosin
Actin
Tropomyosin Ca=;8inding sites
Troponin complex
(a) 3&osin-binding sites blocked
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• 0or a muscle fier to contract
– The myosin8inding sites must e uncovered• This occurs when calcium ions $Ca=;&
– "ind to another set of regulatory proteins, the
troponin complex
Figure 49.#1b
Ca=;
/yosin8
inding site
(b) 3&osin-binding sites exosed
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• The stimulus leading to the contraction of
a skeletal muscle fier
– !s an action potential in a motor neuron thatmakes a synapse with the muscle fier
Figure 49.#2
/otor
neuron axon/itochondrion
Synaptic
terminal
T tuule
Sarcoplasmic
reticulum
/yofiril
.lasma memrane
of muscle fier
Sarcomere
Ca=; released
from sarcoplasmic
reticulum
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• The synaptic terminal of the motor neuron
– +eleases the neurotransmitter acetylcholine,
depolari3ing the muscle and causing it to
produce an action potential
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• Action potentials travel to the interior of the
muscle fier – Along infoldings of the plasma memrane calledtransverse $T& tuules
• The action potential along the T tuules
– Causes the sarcoplasmic reticulum to releaseCa=;
• The Ca=; inds to the troponin8tropomyosin
complex on the thin filaments – *xposing the myosin8inding sites and allowingthe cross8ridge cycle to proceed
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ACh
Synaptic
terminal
of motor neuron
Synaptic cleft T T-"-(*.(AS/A /*/"+A7*
S+
A).
CT@S@(
Ca=+
Ca=+
.=
Cytosolic Ca=; is
removed y active
transport intoS+ after action
potential ends'
6
• +eview of contraction in a skeletal muscle fier
Figure 49.##
Acetylcholine $ACh& released y synaptic terminal diffuses across synaptic
cleft and inds to receptor proteins on muscle fierBs plasma memrane,
triggering an action potential in muscle fier'
1
Action potential is propa8
gated along plasma
memrane and down
T tuules'
2
Action potentialtriggers Ca=;
release from sarco8
plasmic reticulum$S+&'
#
/yosin cross8ridges alternately attach
to actin and detach, pulling actin
filaments toward center of sarcomere%
AT. powers sliding of filaments'
5
Calcium ions ind to troponin%
troponin changes shape,removing locking action
of tropomyosin% myosin8inding
sites exposed'
4
Tropomyosin lockage of myosin8inding sites is restored% contraction
ends, and muscle fier relaxes'
,
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Neural Control of Muscle
Tension• Contraction of a whole muscle is graded
– 2hich means that we can voluntarily alter the extent andstrength of its contraction
• There are two asic mechanisms y which the nervoussystem produces graded contractions of whole muscles – "y varying the numer of fiers that contract
– "y varying the rate at which muscle fiers are stimulated
A t it
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• A motor unit – Consists of a single motor neuron and all the muscle fiers it controls
• +ecruitment of multiple motor neurons – +esults in stronger contractions
• A twitch
– +esults from a single action potential in a motor neuron• /ore rapidly delivered action potentials
– .roduce a graded contraction y summation
• Tetanus is a state of smooth and sustained contraction – .roduced when motor neurons deliver a volley of action potentials
Action
potential .air of
action
potentials
Series of action
potentials at
high freuency
Time
T e n s i o n
Singletwitch
Summation of
two twitches
Tetanus
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@ther Types of /uscle
• Cardiac muscle, found only in the heart
– Consists of striated cells that are electrically connected
y intercalated discs
– Can generate action potentials without neural input• !n smooth muscle, found mainly in the walls of
hollow organs
– The contractions are relatively slow and may e
initiated y the muscles themselves
• !n addition, contractions may e caused y
– Stimulation from neurons in the autonomic nervous
system