SlideShare a Scribd company logo
MuscularSystem
Principles of Anatomy and Physiology
Location Function Appearance Control
Skeletal
Skeletal Move bones Multinucleated
and striated
Voluntary
Cardiac
Heart Pump blood 1nucleus, striated,
and intercalated
discs
Involuntary
Visceral
(smooth muscle)
Various organs,
example:
GI tract
Various functions,
example:
peristalsis
1nucleus and
no striations
Involuntary
3 Types of Muscular Tissue
OpenStax College, Skeletal Smooth Cardiac, https://commons.wikimedia.org/wiki/File:414_Skeletal_Smooth_Cardiac.jpg, CC BY 3.0
Functions of Muscular Tissue
Producing body movements Stabilizing body positions
Generating heat
Storing and mobilizing
substances within the body
Electrical
excitability
Contractility Extensibility Elasticity
Properties of Muscular Tissue
Levels of Organization within a Skeletal Muscle
Skeletalmuscle
Skeletal muscle Epimysium
Muscle fascicle
Organ made up of fascicles that contain muscle
fibers (cells), blood vessels, and nerves; wrapped
in epimysium
Fascicle
Muscle fascicle Perimysium
Endomysium
Muscle fiber
Bundle of muscle fibers wrapped in perimysium
Levels of Organization within a Skeletal Muscle
Muscle fiber (cell)
Muscle fiber
Sarcolemma
Myofibrils
• Long, cylindrical cell covered by endomysium and
sarcolemma
• Contains sarcoplasm, myofibrils, peripherally located
nuclei, mitochondria, transverse tubules, sarcoplasmic
reticulum, and terminal cisterns
• Striated appearance
Myofibril
Sarcoplasmic Thin (actin) Sarcomere H zone Thick
reticulum filament (myosin)
filament
I band A band Z disc M line
• Threadlike contractile elements within the sarcoplasm
of muscle fiber that extend for the entire length of the
fiber
• Composed of filaments
Filaments (myofilaments
)
2 types of contractile proteins within myofibrils are:
• Thick filaments composed of myosin
• Thin filaments composed of actin, tropomyosin
and troponin
• Sliding of thin filaments past thick filaments produces
muscle shortening
Levels of Organization within a Skeletal Muscle
Myofibrils
Portion of a thick filament
Myosin head
Portion of a thin filament
Tropomyosin Actin Troponin
Muscle Myofibril
fiber
Microscopic Anatomy of a Muscle Fiber
Sarcomere Thick (myosin)
filament
Thin (actin)
filament
I band A band M line
Z disc
H zone
Sarcoplasmic
reticulum
Muscle Myofibril
fiber
Microscopic Anatomy of a Muscle Fiber
T
erminal cisterna
T tubule
Triad
Sarcoplasmic reticulum
Components of a Sarcomere
Z discs Narrow, plate-shaped regions of dense material that
separate one sarcomere
from the next
A band Dark, middle part of the sarcomere that extends for
the entire length of the thick filaments and includes
those parts of the thin filament that overlap them
I band Lighter, less dense area of the sarcomere that
contains the remainder of the thin filaments but no
thick ones. A Z disc passes through the center of
each I band.
H zone Narrow region in the center of each A band that
contains thick filaments but no thin filaments
M line Region in the center of the H zone that contains
proteins that hold thick filaments together at the
center of the sarcomere
Muscle Proteins Contractile
Myosin
Actin
Muscle Proteins Regulatory
Troponin Tropomyosin
Muscle Proteins Structural
Alpha-actinin
(structural protein
of Z disc)
Nebulin
(anchors thin
filaments to Z disc)
Dystrophin
(links thin filament
to integral
membrane
proteins)
Myomesin
(forms M line
proteins)
Titin
(connects Z disc
to M line)
Skeletal Muscle Fiber Proteins
Type Description
Contractile
proteins:
Proteins that generate force during muscle contractions
Myosin Contractile protein that makes up a thick filament; molecule consists of a tail and 2 myosin
heads, which bind to myosin-binding sites on actin molecules of a thin filament during muscle
contraction
Actin Contractile protein that is the main component of a thin filament; each actin molecule has a
myosin-binding site where the myosin head of a thick filament binds during muscle contraction
Regulatory
proteins:
Proteins that help switch the muscle contraction process on and off
Tropomyosin Regulatory protein that is a component of a thin filament; when skeletal muscle fiber is relaxed,
tropomyosin covers myosin-binding sites on actin molecules, thereby preventing myosin from
binding to actin
Troponin Regulatory protein that is a component of a thin filament; when calcium ions (Ca2+) bind to
troponin, it changes shape; this conformational change moves tropomyosin away from myosin-
binding sites on actin molecules, and muscle contraction subsequently begins as myosin binds
to actin
Skeletal Muscle Fiber Proteins
Type Description
Structural
proteins:
Proteins that keep thick and thin filaments of myofibrils in proper alignment, give myofibrils
elasticity and extensibility, and link myofibrils to the sarcolemma and the extracellular matrix
Titin Structural protein that connects the Z disc to the M line of a sarcomere, thereby helping to
stabilize the thick filament position; can stretch and then spring back unharmed, and thus
accounts for much of the elasticity and extensibility of myofibrils
-Actinin Structural protein of Z discs that attaches to actin molecules of a thin filament; helps anchor thin
filaments to Z discs and regulates the length of thin filaments during development
Myomesin Structural protein that wraps around the entire length of each thin filament; helps anchor thin
filaments to Z discs and regulates the length of the thin filaments during development
Nebulin Structural protein that wraps around entire length of each thin filament; helps anchor thin
filaments to Z discs and regulates length of thin filaments during development
Dystrophin Structural protein that links thin filaments of a sarcomere to integral membrane proteins in the
sarcolemma, which are attached in turn to proteins in the connective tissue matrix that surrounds
muscle fibers; thought to help reinforce the sarcolemma and help transmit tension generated by
sarcomeres to tendons
The Sliding Filament Mechanism
Myosin pulls on actin
Thin filament slides inward
Z discs move toward each
other, and the sarcomere
shortens
Muscle contraction
H
H
M
M
Z Z
Z Z
Cocking of
myosin head
The Contraction Cycle
Crossbridgedetachment
Calcium Actin
Thin
filament
Crossbridge
Thick
filament
Myosin
head
ATP attaches
and myosin
head detaches
Power
stroke
ADPand Pi
released
Thin
filament
Myosin head
Thick
filament
Troponin
Calcium binding
ADPand Pi
Excitation-contraction Coupling
Sarcoplasmic
reticulum
T tubule
+
+
+
+
+
Sarco/endoplasmic
reticulum Ca2+
ATPase (SERCA)
This concept connects the events of a muscle action
potential with the sliding filament mechanism.
Action potential
(depolarization)
Sarcoplasm
Voltage-gated
Ca2+ channel
(open)
Channel
sensor
Ca2+
Excitation-contraction Coupling
This concept connects the events of a muscle action
potential with the sliding filament mechanism.
Sarcoplasm
Sarcoplasmic
reticulum
+
+
+
+
T tubule +
Sarco/endoplasmic
reticulum Ca2+
ATPase (SERCA)
Repolarization
Channel
sensor
Ca2+
Voltage-gated
Ca2+ channel
(closed)
Length-tension Relationship
%Sarcomere length
Tension
(%of maximum)
The force of a muscle contraction depends on the length
of the sarcomeresin a muscle before contraction.
Optimal
Too
small
Overstretched
What Starts the Excitation Process?
Synaptic cleft
Nerve impulse (action potential)
Synaptic end bulb
Motor end-plate
Synaptic vesicle
containingACh*
Sarcolemma
Neuromuscular
junction
Sarcolemma
Myelin sheath surrounding
axon of motor neuron
muscle fiber
Sarcoplasm
Axon terminal
Synaptic end bulb
Myofibril of
What Starts the Excitation Process?
Na+
Calcium
Synaptic end bulb
Nerve impulse
(action potential)
Voltage-gated
calcium channels
Synaptic vesicle
containingACh*
Synaptic
cleft
Ligand-gated
sodium channel
Motor end-plate
Na+
Sarcoplasm
Sarcoplasmic
reticulum
T tubule
+
+
+
+
+
Action potential
(depolarization)
Voltage-gated
Ca2+ channel
(open)
Channel
sensor
Ca2+
What Starts the Excitation Process?
What Starts the Excitation Process?
Synaptic cleft
Acetylcholinesterase
• Breaks down ACh
Na-
Excitation-contraction Coupling
Ca2+
Depolarization
Muscle contracts
Sarcoplasm
Sarcoplasmic
reticulum
Synaptic
cleft
ACh
Excitation-contraction Coupling
Ca2+
Muscle contracts
Sarcoplasm
Sarcoplasmic
reticulum
Acetyl-
cholinesterase
Synaptic
cleft
Muscle Metabolism
Creation
of creatine
phosphate
How do muscles derive the ATP necessary
to power the contraction cycle?
Anaerobic
glycolysis
Cellular
respiration
Creation of Creatine Phosphate (CP)
Creatine kinase catalyzes the transfer of a phosphate group
from CP to ADP to rapidly yieldATP
.
Duration of energy provided: 15 seconds
Creatine Creatine phosphate
Creatine kinase
+
ADP
Restingmuscle
+
ATP
Energy for muscle
contraction
Active muscle
ATP
+
Creatine
When CP stores are depleted, glucose is converted into pyruvic acid to generate ATP.
Glycolysis
Anaerobic Glycolysis
Duration of energy provided: 2 minutes
ATP
ATP
Pyruvate
Pyruvate
Lactic acid
to blood
No oxygen
Blood
glucose
Muscle
glycogen
Glucose
Under aerobic conditions, pyruvic acid can
enter the mitochondria and undergo a series
of oxygen-requiring reactions to generate
large amounts of ATP
.
Cellular Respiration
Cellular Respiration
Duration of energy provided: minutes up to hours
Pyruvic
acid
Fatty
acids
Heat
CO2
H2O
Pyruvic acid can enter the mitochondria and undergo a series of oxygen-requiring
reactions to generate large amounts of ATP
.
O2
Blood
glucose
Cellular respiration
in mitochondria
28 34 ATPmolecules
Muscle fatigueis the inability to maintain the
force of contraction after prolonged activity.
Muscle Fatigue
The onset of fatigue is due to:
• Inadequate release of Ca2+ from SR
• Depletion of CP
, oxygen, and nutrients
• Build-up of lactic acid and ADP
• Insufficient release of ACh at the
neuromuscular junction (NMJ)
Muscle Fatigue
Central fatigue is the type of fatigue
associated with the concentration of
neurotransmitters within the central nervous
system,which affects muscle function.
Central Fatigue
oxygen debt
Oxygen Consumption after Exercise
Why do people continue to breathe heavily for
a time after stopping exercise?
The extra oxygen goes toward:
Oxygen Consumption after Exercise
Replenishing
CPstores
Converting lactate
into pyruvate
Reloading O2
onto myoglobin
Control of Muscle Tension
Somatic motor
neuron
Muscle fibers
Spinal cord
The strength of a muscle contraction depends on how many motor units are activated.
Weak muscle contraction
Activation of a few motor units
Strong muscle contraction
Activation of many motor units
Twitch Contraction
Latent
period
Contraction
period
Relaxation
period
Wave summation
→ results in a stronger
contraction
Frequency of Stimulation
Unfused tetanus Fused tetanus
Time Time Time
T
ension
Factors that Influence Tension
3. Sarcomere length
1. Size of motor unit 2. Recruitment of motor units
4. Frequency of stimulation
Even when at rest, a skeletal muscle exhibits a
small amount of tension, called tone. Tone is
established by the alternating, involuntary action
of small groups of motor units in a muscle.
Muscle Tone
Isotonic Isometric
Tension is constant while muscle length changes. A muscle contracts but
does not change in length.
Isotonic vs. Isometric Contractions
Concentric Eccentric
Structural Characteristics
Structural
characteristics
Slow oxidative
fibers (1)
Fast oxidative-
glycolytic
fibers (2)
Fast glycolytic
fibers (3)
Myoglobin
content
Large
amount
Large
amount
Small
amount
Mitochondria Many Many Few
Capillaries Many Many Few
Color Red Red-pink White (pale)
1
2
3
3
1
2
Functional Characteristics
Functional
characteristics
Slow oxidativefibers Fast oxidative-
glycolyticfibers
Fast glycolyticfibers
Capacity for
generating ATP
and method used
High, by aerobic
respiration
Intermediate,by both
aerobic respiration and
anaerobic glycolysis
Low, by anaerobic
glycolysis
Rate of ATP hydrolysis
by myosin ATPase
Slow Fast Fast
Contraction velocity Slow Fast Fast
Fatigue resistance High Intermediate Low
Creatine kinase Lowest amount Intermediate amount Highest amount
Glycogen stores Low Intermediate High
Primaryfunction of
fibers
Maintaining posture
and aerobic endurance
activities
Walking,sprinting Rapid,intense
movements of short
duration
Exercise and Skeletal Muscle Tissue
What fiber type does a marathonermost
heavily rely on?
Slow oxidativefibers
• Slow enough pace for cellular respiration to occur
• Needs a lot of energy
Exercise and Skeletal Muscle Tissue
What fiber type does a shot-putter most
heavily rely on?
Fast glycolyticfibers
• Needs short bursts of energy
Exercise and Skeletal Muscle Tissue
What fiber type does a soccer playermost
heavily rely on?
Fast oxidative-glycolyticfibers
• Has periods where more energy and periods of
rest are needed, with slower cellular respiration
Cardiac muscle has the same arrangement as skeletal muscle, but also has intercalateddiscs.
Cardiac Muscle
Intercalated discs
Cardiac
muscle fiber
Desmosome
Gap junction
Mitochondria
Nucleus
Cardiac muscle cells have more mitochondria,
and their contractions last 10 15 times longer
than skeletal muscle contractions.
Cardiac Muscle
Smooth muscle
Smooth Muscle
Skeletal muscle Cardiac muscle
Smooth Muscle
Skeletal muscle Cardiac muscle
Smooth muscle
• Found in most visceral organs
(e.g., intestines, stomach)
• Work automatically without
you being aware of them
• Involved in many
'housekeeping' functions
Smooth Muscle
Single-unit fibers Multi-unit fibers
Muscle
fibers
Autonomic
neurons
Gap junction
Nucleus
• Can shorten/stretch more than skeletal
and cardiac muscle
• Fibers shorten in response to stretch!
Smooth Muscle
Relaxed muscle cell
• Contracts slower and for longer than
skeletal and cardiac muscle
• No sarcomeres, troponin, or tropomyosin
• Proteins contract like a corkscrew, using
calmodulin and myosin light chain kinase
Contracted muscle cell
Major Features of the 3 Types of Muscle Tissue
Characteristic Skeletal muscle Cardiac muscle Smooth muscle
Microscopic appearance
and features
Long, cylindrical fiber with
many peripherally located
nuclei; unbranched; striated
Branched cylindrical fiber with 1
centrally located nucleus; intercalated
discs join neighboring fibers; striated
Fiber thickest in the middle, tapered
at each end, and with 1centrally
positioned nucleus; not striated
Location Most commonly attached by
tendon to bones
Heart Walls of hollow viscera, airways,
blood vessels, iris and ciliary body of
eye, arrector pili muscles of hair
follicles
Fiber diameter Very large (10 100 m) Large (19 20 m) Small (3 8 m)
Connective tissue
components
Endomysium, perimysium,
and epimysium
Endomysium and perimysium Endomysium
Contractile proteins
organized into sarcomeres
Yes Yes No
Transverse tubules present Yes, aligned with each Yes, aligned with each Z disc No
Major Features of the 3 Types of Muscle Tissue
Characteristic Skeletal muscle Cardiac muscle Smooth muscle
Sarcoplasmic reticulum Abundant Some Very little
Junctions between fibers None Intercalated discs contain gap
junctions and desmosomes
Gap junctions in visceral smooth
muscle; none in multi-unit smooth
muscle
Source of Ca2+ for
contraction
Sarcoplasmic reticulum Sarcoplasmic reticulum and interstitial
fluid
Sarcoplasmic reticulum and
interstitial fluid
Regulator proteins for
contraction
Troponin and tropomyosin Troponin and tropomyosin Calmodulin and myosin light-chain
kinase
Speed of contraction Fast Moderate Slow
Nervouscontrol Voluntary (somatic nervous
system)
Involuntary (autonomic nervous
system)
Involuntary (autonomic nervous
system)
Contraction regulation Acetylcholine released by
somatic motor neurons
Acetylcholine and norepinephrine
released by autonomic motor
neurons, several hormones
Acetylcholine and norepinephrine
released by autonomic motor
neurons; several hormones; local
chemical change; stretching
Capacity for regeneration Limited, via satellite cells Limited, under certain conditions Considerable (compared with other
muscle tissues, but limited compared
with epithelium), via pericytes
Mature skeletal muscle fibers cannot undergo mitosis.
Regeneration of Muscle Tissue
Hypertrophy Hyperplasia
Increase in cell size Increase in cell number
In a Nutshell
✓ The muscular system is made up of 3 types
of muscles: skeletal, cardiac, and smooth.
✓ Skeletal muscle cells are referred to as
muscle fibers and are multinucleated and
striated.
✓ Major functional properties of skeletal
muscle fibers include electrical excitability,
contractility, extensibility, and elasticity.
✓ The contractility of muscle fibers involves
the sliding of microfilaments in the skeletal
muscle fiber.
✓ Contraction is coupled with electrical
excitation of the skeletal muscle fiber.
In a Nutshell
✓ Impulses come from the nervous system to
the muscular system at the neuromuscular
junction (NMJ).
✓ Cardiac muscles differ from the skeletal
muscles because they are involuntary.
Although there are many similarities, cardiac
muscles also exhibit differences in structure
and function.
✓ Smooth muscles also differ from skeletal
muscles. They are also involuntary, and they
use different regulatory proteins during their
contractions.
End…

More Related Content

Similar to 09 The Muscular System.pdf

Structure of skeletal_muscle
Structure of skeletal_muscleStructure of skeletal_muscle
Structure of skeletal_muscle
Personal
 
Muscle funccellularlevel animal systems
Muscle funccellularlevel animal systemsMuscle funccellularlevel animal systems
Muscle funccellularlevel animal systems
Yukti Sharma
 
Lecture 2 muscle tissue cont
Lecture 2   muscle tissue contLecture 2   muscle tissue cont
Lecture 2 muscle tissue cont
missazyaziz
 
Movement I
Movement IMovement I
Movement I
vacagodx
 

Similar to 09 The Muscular System.pdf (20)

5.Muscle tissue.pptx cell and tissue organization
5.Muscle tissue.pptx cell and tissue organization5.Muscle tissue.pptx cell and tissue organization
5.Muscle tissue.pptx cell and tissue organization
 
Structure of skeletal_muscle
Structure of skeletal_muscleStructure of skeletal_muscle
Structure of skeletal_muscle
 
Muscles 2
Muscles 2Muscles 2
Muscles 2
 
Muscle funccellularlevel animal systems
Muscle funccellularlevel animal systemsMuscle funccellularlevel animal systems
Muscle funccellularlevel animal systems
 
Muscular system Physiology
Muscular system PhysiologyMuscular system Physiology
Muscular system Physiology
 
Chemical and molecular basis of muscle contraction
Chemical and molecular basis of muscle contractionChemical and molecular basis of muscle contraction
Chemical and molecular basis of muscle contraction
 
7.-The-Histology-and-Physiology-of-Muscles.ppt
7.-The-Histology-and-Physiology-of-Muscles.ppt7.-The-Histology-and-Physiology-of-Muscles.ppt
7.-The-Histology-and-Physiology-of-Muscles.ppt
 
Muscle-strcuture.pptx
Muscle-strcuture.pptxMuscle-strcuture.pptx
Muscle-strcuture.pptx
 
Lecture 2 muscle tissue cont
Lecture 2   muscle tissue contLecture 2   muscle tissue cont
Lecture 2 muscle tissue cont
 
A and P Mod5
A and P Mod5A and P Mod5
A and P Mod5
 
Muscle Ppt
Muscle PptMuscle Ppt
Muscle Ppt
 
Movement I
Movement IMovement I
Movement I
 
CONTRACTILE TISSUES. medical physiologyptx
CONTRACTILE TISSUES. medical physiologyptxCONTRACTILE TISSUES. medical physiologyptx
CONTRACTILE TISSUES. medical physiologyptx
 
10 muscular tissue
10 muscular tissue10 muscular tissue
10 muscular tissue
 
11.2 movement
11.2 movement11.2 movement
11.2 movement
 
Exercise physiology 1
Exercise physiology 1Exercise physiology 1
Exercise physiology 1
 
skeletal muscle.pdf
skeletal muscle.pdfskeletal muscle.pdf
skeletal muscle.pdf
 
Muscles and Muscle Tissue
Muscles and Muscle TissueMuscles and Muscle Tissue
Muscles and Muscle Tissue
 
General physiology lecture 3
General physiology lecture 3General physiology lecture 3
General physiology lecture 3
 
Muscle
MuscleMuscle
Muscle
 

More from RexBlancoNuez

pdfslide.net_-parts-of-the-skeletal-system-bones-skeleton-joints-cartilages.ppt
pdfslide.net_-parts-of-the-skeletal-system-bones-skeleton-joints-cartilages.pptpdfslide.net_-parts-of-the-skeletal-system-bones-skeleton-joints-cartilages.ppt
pdfslide.net_-parts-of-the-skeletal-system-bones-skeleton-joints-cartilages.ppt
RexBlancoNuez
 

More from RexBlancoNuez (13)

Red Orange Print Style Bayaning Pilipino PH Presentation.pptx
Red Orange Print Style Bayaning Pilipino PH Presentation.pptxRed Orange Print Style Bayaning Pilipino PH Presentation.pptx
Red Orange Print Style Bayaning Pilipino PH Presentation.pptx
 
Acute Respiratory Distress Syndrome - GROUP 3.pptx
Acute Respiratory Distress Syndrome - GROUP 3.pptxAcute Respiratory Distress Syndrome - GROUP 3.pptx
Acute Respiratory Distress Syndrome - GROUP 3.pptx
 
Identifying of Pre-referral Treatment.ppt
Identifying of Pre-referral Treatment.pptIdentifying of Pre-referral Treatment.ppt
Identifying of Pre-referral Treatment.ppt
 
laos police system, president,locationppt.pptx
laos police system, president,locationppt.pptxlaos police system, president,locationppt.pptx
laos police system, president,locationppt.pptx
 
POSITIONING-A-PATIENT-IN-BED.pptx
POSITIONING-A-PATIENT-IN-BED.pptxPOSITIONING-A-PATIENT-IN-BED.pptx
POSITIONING-A-PATIENT-IN-BED.pptx
 
Protein-Metabolism.pptx
Protein-Metabolism.pptxProtein-Metabolism.pptx
Protein-Metabolism.pptx
 
pdfslide.net_-parts-of-the-skeletal-system-bones-skeleton-joints-cartilages.ppt
pdfslide.net_-parts-of-the-skeletal-system-bones-skeleton-joints-cartilages.pptpdfslide.net_-parts-of-the-skeletal-system-bones-skeleton-joints-cartilages.ppt
pdfslide.net_-parts-of-the-skeletal-system-bones-skeleton-joints-cartilages.ppt
 
14.0 The Lymphatic System.pdf
14.0 The Lymphatic System.pdf14.0 The Lymphatic System.pdf
14.0 The Lymphatic System.pdf
 
Chapter_4__Enzymes_and_Vitamins__Enzymes_part_2_.pdf.pdf
Chapter_4__Enzymes_and_Vitamins__Enzymes_part_2_.pdf.pdfChapter_4__Enzymes_and_Vitamins__Enzymes_part_2_.pdf.pdf
Chapter_4__Enzymes_and_Vitamins__Enzymes_part_2_.pdf.pdf
 
05 The Skeletal System - Bone Tissue (1).pdf
05 The Skeletal System - Bone Tissue (1).pdf05 The Skeletal System - Bone Tissue (1).pdf
05 The Skeletal System - Bone Tissue (1).pdf
 
12.0 The Endocrine System.pdf
12.0 The Endocrine System.pdf12.0 The Endocrine System.pdf
12.0 The Endocrine System.pdf
 
07 The Skeletal System - Appendicular Skeleton.pdf
07 The Skeletal System - Appendicular Skeleton.pdf07 The Skeletal System - Appendicular Skeleton.pdf
07 The Skeletal System - Appendicular Skeleton.pdf
 
08 The Skeletal System - Joints (1).pdf
08 The Skeletal System - Joints (1).pdf08 The Skeletal System - Joints (1).pdf
08 The Skeletal System - Joints (1).pdf
 

Recently uploaded

Cell structure slideshare.pptx Unlocking the Secrets of Cells: Structure, Fun...
Cell structure slideshare.pptx Unlocking the Secrets of Cells: Structure, Fun...Cell structure slideshare.pptx Unlocking the Secrets of Cells: Structure, Fun...
Cell structure slideshare.pptx Unlocking the Secrets of Cells: Structure, Fun...
ananyagirishbabu1
 
Benefits of Dentulu's Salivary Testing.pptx
Benefits of Dentulu's Salivary Testing.pptxBenefits of Dentulu's Salivary Testing.pptx
Benefits of Dentulu's Salivary Testing.pptx
Dentulu Inc
 
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdfDemystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
SasikiranMarri
 

Recently uploaded (20)

Contact Now 89011**83002 Dehradun ℂall Girls By Full Service ℂall Girl In De...
Contact Now  89011**83002 Dehradun ℂall Girls By Full Service ℂall Girl In De...Contact Now  89011**83002 Dehradun ℂall Girls By Full Service ℂall Girl In De...
Contact Now 89011**83002 Dehradun ℂall Girls By Full Service ℂall Girl In De...
 
Notify ME 89O1183OO2 #cALL# #gIRLS# In Chhattisgarh By Chhattisgarh #ℂall #gI...
Notify ME 89O1183OO2 #cALL# #gIRLS# In Chhattisgarh By Chhattisgarh #ℂall #gI...Notify ME 89O1183OO2 #cALL# #gIRLS# In Chhattisgarh By Chhattisgarh #ℂall #gI...
Notify ME 89O1183OO2 #cALL# #gIRLS# In Chhattisgarh By Chhattisgarh #ℂall #gI...
 
HEAT WAVE presented by priya bhojwani..pptx
HEAT WAVE presented by priya bhojwani..pptxHEAT WAVE presented by priya bhojwani..pptx
HEAT WAVE presented by priya bhojwani..pptx
 
Master the Art of Yoga with Joga Yoga Training
Master the Art of Yoga with Joga Yoga TrainingMaster the Art of Yoga with Joga Yoga Training
Master the Art of Yoga with Joga Yoga Training
 
QA Paediatric dentistry department, Hospital Melaka 2020
QA Paediatric dentistry department, Hospital Melaka 2020QA Paediatric dentistry department, Hospital Melaka 2020
QA Paediatric dentistry department, Hospital Melaka 2020
 
Dehradun ❤CALL Girls 8901183002 ❤ℂall Girls IN Dehradun ESCORT SERVICE❤
Dehradun ❤CALL Girls  8901183002 ❤ℂall  Girls IN Dehradun ESCORT SERVICE❤Dehradun ❤CALL Girls  8901183002 ❤ℂall  Girls IN Dehradun ESCORT SERVICE❤
Dehradun ❤CALL Girls 8901183002 ❤ℂall Girls IN Dehradun ESCORT SERVICE❤
 
Deepfake Detection_Using Machine Learning .pptx
Deepfake Detection_Using Machine Learning .pptxDeepfake Detection_Using Machine Learning .pptx
Deepfake Detection_Using Machine Learning .pptx
 
Cell structure slideshare.pptx Unlocking the Secrets of Cells: Structure, Fun...
Cell structure slideshare.pptx Unlocking the Secrets of Cells: Structure, Fun...Cell structure slideshare.pptx Unlocking the Secrets of Cells: Structure, Fun...
Cell structure slideshare.pptx Unlocking the Secrets of Cells: Structure, Fun...
 
VVIP Dehradun Girls 9719300533 Heat-bake { Dehradun } Genteel ℂall Serviℂe By...
VVIP Dehradun Girls 9719300533 Heat-bake { Dehradun } Genteel ℂall Serviℂe By...VVIP Dehradun Girls 9719300533 Heat-bake { Dehradun } Genteel ℂall Serviℂe By...
VVIP Dehradun Girls 9719300533 Heat-bake { Dehradun } Genteel ℂall Serviℂe By...
 
Digital Healthcare: The Future of Medical Consultations
Digital Healthcare: The Future of Medical ConsultationsDigital Healthcare: The Future of Medical Consultations
Digital Healthcare: The Future of Medical Consultations
 
Overcome Your Phobias with Hypnotherapy.pptx
Overcome Your Phobias with Hypnotherapy.pptxOvercome Your Phobias with Hypnotherapy.pptx
Overcome Your Phobias with Hypnotherapy.pptx
 
Enhancing-Patient-Centric-Clinical-Trials.pdf
Enhancing-Patient-Centric-Clinical-Trials.pdfEnhancing-Patient-Centric-Clinical-Trials.pdf
Enhancing-Patient-Centric-Clinical-Trials.pdf
 
Chris Shade BS MEd MS LPC-Associate "Presume" (What Do I Do?)
Chris Shade BS MEd MS LPC-Associate "Presume" (What Do I Do?)Chris Shade BS MEd MS LPC-Associate "Presume" (What Do I Do?)
Chris Shade BS MEd MS LPC-Associate "Presume" (What Do I Do?)
 
The Docs PPG - 30.01.2024.pptx..........
The Docs PPG - 30.01.2024.pptx..........The Docs PPG - 30.01.2024.pptx..........
The Docs PPG - 30.01.2024.pptx..........
 
Contact mE 👙👨‍❤️‍👨 (89O1183OO2) 💘ℂall Girls In MOHALI By MOHALI 💘ESCORTS GIRL...
Contact mE 👙👨‍❤️‍👨 (89O1183OO2) 💘ℂall Girls In MOHALI By MOHALI 💘ESCORTS GIRL...Contact mE 👙👨‍❤️‍👨 (89O1183OO2) 💘ℂall Girls In MOHALI By MOHALI 💘ESCORTS GIRL...
Contact mE 👙👨‍❤️‍👨 (89O1183OO2) 💘ℂall Girls In MOHALI By MOHALI 💘ESCORTS GIRL...
 
Myopia Management & Control Strategies.pptx
Myopia Management & Control Strategies.pptxMyopia Management & Control Strategies.pptx
Myopia Management & Control Strategies.pptx
 
Benefits of Dentulu's Salivary Testing.pptx
Benefits of Dentulu's Salivary Testing.pptxBenefits of Dentulu's Salivary Testing.pptx
Benefits of Dentulu's Salivary Testing.pptx
 
What can we really do to give meaning and momentum to equality, diversity and...
What can we really do to give meaning and momentum to equality, diversity and...What can we really do to give meaning and momentum to equality, diversity and...
What can we really do to give meaning and momentum to equality, diversity and...
 
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdfDemystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
 
Storage_of _Bariquin_Components_in_Storage_Boxes.pptx
Storage_of _Bariquin_Components_in_Storage_Boxes.pptxStorage_of _Bariquin_Components_in_Storage_Boxes.pptx
Storage_of _Bariquin_Components_in_Storage_Boxes.pptx
 

09 The Muscular System.pdf

  • 2. Location Function Appearance Control Skeletal Skeletal Move bones Multinucleated and striated Voluntary Cardiac Heart Pump blood 1nucleus, striated, and intercalated discs Involuntary Visceral (smooth muscle) Various organs, example: GI tract Various functions, example: peristalsis 1nucleus and no striations Involuntary 3 Types of Muscular Tissue OpenStax College, Skeletal Smooth Cardiac, https://commons.wikimedia.org/wiki/File:414_Skeletal_Smooth_Cardiac.jpg, CC BY 3.0
  • 3. Functions of Muscular Tissue Producing body movements Stabilizing body positions Generating heat Storing and mobilizing substances within the body
  • 5. Levels of Organization within a Skeletal Muscle Skeletalmuscle Skeletal muscle Epimysium Muscle fascicle Organ made up of fascicles that contain muscle fibers (cells), blood vessels, and nerves; wrapped in epimysium Fascicle Muscle fascicle Perimysium Endomysium Muscle fiber Bundle of muscle fibers wrapped in perimysium
  • 6. Levels of Organization within a Skeletal Muscle Muscle fiber (cell) Muscle fiber Sarcolemma Myofibrils • Long, cylindrical cell covered by endomysium and sarcolemma • Contains sarcoplasm, myofibrils, peripherally located nuclei, mitochondria, transverse tubules, sarcoplasmic reticulum, and terminal cisterns • Striated appearance Myofibril Sarcoplasmic Thin (actin) Sarcomere H zone Thick reticulum filament (myosin) filament I band A band Z disc M line • Threadlike contractile elements within the sarcoplasm of muscle fiber that extend for the entire length of the fiber • Composed of filaments
  • 7. Filaments (myofilaments ) 2 types of contractile proteins within myofibrils are: • Thick filaments composed of myosin • Thin filaments composed of actin, tropomyosin and troponin • Sliding of thin filaments past thick filaments produces muscle shortening Levels of Organization within a Skeletal Muscle Myofibrils Portion of a thick filament Myosin head Portion of a thin filament Tropomyosin Actin Troponin
  • 8. Muscle Myofibril fiber Microscopic Anatomy of a Muscle Fiber Sarcomere Thick (myosin) filament Thin (actin) filament I band A band M line Z disc H zone Sarcoplasmic reticulum
  • 9. Muscle Myofibril fiber Microscopic Anatomy of a Muscle Fiber T erminal cisterna T tubule Triad Sarcoplasmic reticulum
  • 10. Components of a Sarcomere Z discs Narrow, plate-shaped regions of dense material that separate one sarcomere from the next A band Dark, middle part of the sarcomere that extends for the entire length of the thick filaments and includes those parts of the thin filament that overlap them I band Lighter, less dense area of the sarcomere that contains the remainder of the thin filaments but no thick ones. A Z disc passes through the center of each I band. H zone Narrow region in the center of each A band that contains thick filaments but no thin filaments M line Region in the center of the H zone that contains proteins that hold thick filaments together at the center of the sarcomere
  • 13. Muscle Proteins Structural Alpha-actinin (structural protein of Z disc) Nebulin (anchors thin filaments to Z disc) Dystrophin (links thin filament to integral membrane proteins) Myomesin (forms M line proteins) Titin (connects Z disc to M line)
  • 14. Skeletal Muscle Fiber Proteins Type Description Contractile proteins: Proteins that generate force during muscle contractions Myosin Contractile protein that makes up a thick filament; molecule consists of a tail and 2 myosin heads, which bind to myosin-binding sites on actin molecules of a thin filament during muscle contraction Actin Contractile protein that is the main component of a thin filament; each actin molecule has a myosin-binding site where the myosin head of a thick filament binds during muscle contraction Regulatory proteins: Proteins that help switch the muscle contraction process on and off Tropomyosin Regulatory protein that is a component of a thin filament; when skeletal muscle fiber is relaxed, tropomyosin covers myosin-binding sites on actin molecules, thereby preventing myosin from binding to actin Troponin Regulatory protein that is a component of a thin filament; when calcium ions (Ca2+) bind to troponin, it changes shape; this conformational change moves tropomyosin away from myosin- binding sites on actin molecules, and muscle contraction subsequently begins as myosin binds to actin
  • 15. Skeletal Muscle Fiber Proteins Type Description Structural proteins: Proteins that keep thick and thin filaments of myofibrils in proper alignment, give myofibrils elasticity and extensibility, and link myofibrils to the sarcolemma and the extracellular matrix Titin Structural protein that connects the Z disc to the M line of a sarcomere, thereby helping to stabilize the thick filament position; can stretch and then spring back unharmed, and thus accounts for much of the elasticity and extensibility of myofibrils -Actinin Structural protein of Z discs that attaches to actin molecules of a thin filament; helps anchor thin filaments to Z discs and regulates the length of thin filaments during development Myomesin Structural protein that wraps around the entire length of each thin filament; helps anchor thin filaments to Z discs and regulates the length of the thin filaments during development Nebulin Structural protein that wraps around entire length of each thin filament; helps anchor thin filaments to Z discs and regulates length of thin filaments during development Dystrophin Structural protein that links thin filaments of a sarcomere to integral membrane proteins in the sarcolemma, which are attached in turn to proteins in the connective tissue matrix that surrounds muscle fibers; thought to help reinforce the sarcolemma and help transmit tension generated by sarcomeres to tendons
  • 16. The Sliding Filament Mechanism Myosin pulls on actin Thin filament slides inward Z discs move toward each other, and the sarcomere shortens Muscle contraction H H M M Z Z Z Z
  • 17. Cocking of myosin head The Contraction Cycle Crossbridgedetachment Calcium Actin Thin filament Crossbridge Thick filament Myosin head ATP attaches and myosin head detaches Power stroke ADPand Pi released Thin filament Myosin head Thick filament Troponin Calcium binding ADPand Pi
  • 18. Excitation-contraction Coupling Sarcoplasmic reticulum T tubule + + + + + Sarco/endoplasmic reticulum Ca2+ ATPase (SERCA) This concept connects the events of a muscle action potential with the sliding filament mechanism. Action potential (depolarization) Sarcoplasm Voltage-gated Ca2+ channel (open) Channel sensor Ca2+
  • 19. Excitation-contraction Coupling This concept connects the events of a muscle action potential with the sliding filament mechanism. Sarcoplasm Sarcoplasmic reticulum + + + + T tubule + Sarco/endoplasmic reticulum Ca2+ ATPase (SERCA) Repolarization Channel sensor Ca2+ Voltage-gated Ca2+ channel (closed)
  • 20. Length-tension Relationship %Sarcomere length Tension (%of maximum) The force of a muscle contraction depends on the length of the sarcomeresin a muscle before contraction. Optimal Too small Overstretched
  • 21. What Starts the Excitation Process? Synaptic cleft Nerve impulse (action potential) Synaptic end bulb Motor end-plate Synaptic vesicle containingACh* Sarcolemma Neuromuscular junction Sarcolemma Myelin sheath surrounding axon of motor neuron muscle fiber Sarcoplasm Axon terminal Synaptic end bulb Myofibril of
  • 22. What Starts the Excitation Process? Na+ Calcium Synaptic end bulb Nerve impulse (action potential) Voltage-gated calcium channels Synaptic vesicle containingACh* Synaptic cleft Ligand-gated sodium channel Motor end-plate Na+
  • 23. Sarcoplasm Sarcoplasmic reticulum T tubule + + + + + Action potential (depolarization) Voltage-gated Ca2+ channel (open) Channel sensor Ca2+ What Starts the Excitation Process?
  • 24. What Starts the Excitation Process? Synaptic cleft Acetylcholinesterase • Breaks down ACh Na-
  • 27. Muscle Metabolism Creation of creatine phosphate How do muscles derive the ATP necessary to power the contraction cycle? Anaerobic glycolysis Cellular respiration
  • 28. Creation of Creatine Phosphate (CP) Creatine kinase catalyzes the transfer of a phosphate group from CP to ADP to rapidly yieldATP . Duration of energy provided: 15 seconds Creatine Creatine phosphate Creatine kinase + ADP Restingmuscle + ATP Energy for muscle contraction Active muscle ATP + Creatine
  • 29. When CP stores are depleted, glucose is converted into pyruvic acid to generate ATP. Glycolysis Anaerobic Glycolysis Duration of energy provided: 2 minutes ATP ATP Pyruvate Pyruvate Lactic acid to blood No oxygen Blood glucose Muscle glycogen Glucose
  • 30. Under aerobic conditions, pyruvic acid can enter the mitochondria and undergo a series of oxygen-requiring reactions to generate large amounts of ATP . Cellular Respiration
  • 31. Cellular Respiration Duration of energy provided: minutes up to hours Pyruvic acid Fatty acids Heat CO2 H2O Pyruvic acid can enter the mitochondria and undergo a series of oxygen-requiring reactions to generate large amounts of ATP . O2 Blood glucose Cellular respiration in mitochondria 28 34 ATPmolecules
  • 32. Muscle fatigueis the inability to maintain the force of contraction after prolonged activity. Muscle Fatigue
  • 33. The onset of fatigue is due to: • Inadequate release of Ca2+ from SR • Depletion of CP , oxygen, and nutrients • Build-up of lactic acid and ADP • Insufficient release of ACh at the neuromuscular junction (NMJ) Muscle Fatigue
  • 34. Central fatigue is the type of fatigue associated with the concentration of neurotransmitters within the central nervous system,which affects muscle function. Central Fatigue
  • 35. oxygen debt Oxygen Consumption after Exercise Why do people continue to breathe heavily for a time after stopping exercise?
  • 36. The extra oxygen goes toward: Oxygen Consumption after Exercise Replenishing CPstores Converting lactate into pyruvate Reloading O2 onto myoglobin
  • 37. Control of Muscle Tension Somatic motor neuron Muscle fibers Spinal cord The strength of a muscle contraction depends on how many motor units are activated. Weak muscle contraction Activation of a few motor units Strong muscle contraction Activation of many motor units
  • 39. Wave summation → results in a stronger contraction Frequency of Stimulation Unfused tetanus Fused tetanus Time Time Time T ension
  • 40. Factors that Influence Tension 3. Sarcomere length 1. Size of motor unit 2. Recruitment of motor units 4. Frequency of stimulation
  • 41. Even when at rest, a skeletal muscle exhibits a small amount of tension, called tone. Tone is established by the alternating, involuntary action of small groups of motor units in a muscle. Muscle Tone
  • 42. Isotonic Isometric Tension is constant while muscle length changes. A muscle contracts but does not change in length. Isotonic vs. Isometric Contractions Concentric Eccentric
  • 43. Structural Characteristics Structural characteristics Slow oxidative fibers (1) Fast oxidative- glycolytic fibers (2) Fast glycolytic fibers (3) Myoglobin content Large amount Large amount Small amount Mitochondria Many Many Few Capillaries Many Many Few Color Red Red-pink White (pale) 1 2 3 3 1 2
  • 44. Functional Characteristics Functional characteristics Slow oxidativefibers Fast oxidative- glycolyticfibers Fast glycolyticfibers Capacity for generating ATP and method used High, by aerobic respiration Intermediate,by both aerobic respiration and anaerobic glycolysis Low, by anaerobic glycolysis Rate of ATP hydrolysis by myosin ATPase Slow Fast Fast Contraction velocity Slow Fast Fast Fatigue resistance High Intermediate Low Creatine kinase Lowest amount Intermediate amount Highest amount Glycogen stores Low Intermediate High Primaryfunction of fibers Maintaining posture and aerobic endurance activities Walking,sprinting Rapid,intense movements of short duration
  • 45. Exercise and Skeletal Muscle Tissue What fiber type does a marathonermost heavily rely on? Slow oxidativefibers • Slow enough pace for cellular respiration to occur • Needs a lot of energy
  • 46. Exercise and Skeletal Muscle Tissue What fiber type does a shot-putter most heavily rely on? Fast glycolyticfibers • Needs short bursts of energy
  • 47. Exercise and Skeletal Muscle Tissue What fiber type does a soccer playermost heavily rely on? Fast oxidative-glycolyticfibers • Has periods where more energy and periods of rest are needed, with slower cellular respiration
  • 48. Cardiac muscle has the same arrangement as skeletal muscle, but also has intercalateddiscs. Cardiac Muscle Intercalated discs Cardiac muscle fiber Desmosome Gap junction Mitochondria Nucleus
  • 49. Cardiac muscle cells have more mitochondria, and their contractions last 10 15 times longer than skeletal muscle contractions. Cardiac Muscle
  • 50. Smooth muscle Smooth Muscle Skeletal muscle Cardiac muscle
  • 51. Smooth Muscle Skeletal muscle Cardiac muscle Smooth muscle • Found in most visceral organs (e.g., intestines, stomach) • Work automatically without you being aware of them • Involved in many 'housekeeping' functions
  • 52. Smooth Muscle Single-unit fibers Multi-unit fibers Muscle fibers Autonomic neurons Gap junction Nucleus
  • 53. • Can shorten/stretch more than skeletal and cardiac muscle • Fibers shorten in response to stretch! Smooth Muscle Relaxed muscle cell • Contracts slower and for longer than skeletal and cardiac muscle • No sarcomeres, troponin, or tropomyosin • Proteins contract like a corkscrew, using calmodulin and myosin light chain kinase Contracted muscle cell
  • 54. Major Features of the 3 Types of Muscle Tissue Characteristic Skeletal muscle Cardiac muscle Smooth muscle Microscopic appearance and features Long, cylindrical fiber with many peripherally located nuclei; unbranched; striated Branched cylindrical fiber with 1 centrally located nucleus; intercalated discs join neighboring fibers; striated Fiber thickest in the middle, tapered at each end, and with 1centrally positioned nucleus; not striated Location Most commonly attached by tendon to bones Heart Walls of hollow viscera, airways, blood vessels, iris and ciliary body of eye, arrector pili muscles of hair follicles Fiber diameter Very large (10 100 m) Large (19 20 m) Small (3 8 m) Connective tissue components Endomysium, perimysium, and epimysium Endomysium and perimysium Endomysium Contractile proteins organized into sarcomeres Yes Yes No Transverse tubules present Yes, aligned with each Yes, aligned with each Z disc No
  • 55. Major Features of the 3 Types of Muscle Tissue Characteristic Skeletal muscle Cardiac muscle Smooth muscle Sarcoplasmic reticulum Abundant Some Very little Junctions between fibers None Intercalated discs contain gap junctions and desmosomes Gap junctions in visceral smooth muscle; none in multi-unit smooth muscle Source of Ca2+ for contraction Sarcoplasmic reticulum Sarcoplasmic reticulum and interstitial fluid Sarcoplasmic reticulum and interstitial fluid Regulator proteins for contraction Troponin and tropomyosin Troponin and tropomyosin Calmodulin and myosin light-chain kinase Speed of contraction Fast Moderate Slow Nervouscontrol Voluntary (somatic nervous system) Involuntary (autonomic nervous system) Involuntary (autonomic nervous system) Contraction regulation Acetylcholine released by somatic motor neurons Acetylcholine and norepinephrine released by autonomic motor neurons, several hormones Acetylcholine and norepinephrine released by autonomic motor neurons; several hormones; local chemical change; stretching Capacity for regeneration Limited, via satellite cells Limited, under certain conditions Considerable (compared with other muscle tissues, but limited compared with epithelium), via pericytes
  • 56. Mature skeletal muscle fibers cannot undergo mitosis. Regeneration of Muscle Tissue Hypertrophy Hyperplasia Increase in cell size Increase in cell number
  • 57. In a Nutshell ✓ The muscular system is made up of 3 types of muscles: skeletal, cardiac, and smooth. ✓ Skeletal muscle cells are referred to as muscle fibers and are multinucleated and striated. ✓ Major functional properties of skeletal muscle fibers include electrical excitability, contractility, extensibility, and elasticity. ✓ The contractility of muscle fibers involves the sliding of microfilaments in the skeletal muscle fiber. ✓ Contraction is coupled with electrical excitation of the skeletal muscle fiber.
  • 58. In a Nutshell ✓ Impulses come from the nervous system to the muscular system at the neuromuscular junction (NMJ). ✓ Cardiac muscles differ from the skeletal muscles because they are involuntary. Although there are many similarities, cardiac muscles also exhibit differences in structure and function. ✓ Smooth muscles also differ from skeletal muscles. They are also involuntary, and they use different regulatory proteins during their contractions.