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CHAPTER 12NERVOUS SYSTEM
12.1 The nervous system
12.2 The transmission of impulse
12.3 The synapse
12.4 Neuromuscular junction
12.4.1 Structure of the neuromuscular junction
12.4.2 Structure of the skeletal muscle
12.4.3 The sliding-filament theory
12.4.4 Mechanism of the muscle contraction
12.4.5 The autonomic nervous system
12.5 Drug abuse
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OBJECTIVESAt the end of the lesson, students should be able to :
1) Build the organization chart of the humannervous system
2) Explain the rising of a resting potential inneurons
3) List down the characteristics of impulse
4) Explain the propagation of impulse along theaxon
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NERVOUS SYSTEM
To synchronize the activities of the inner bodyparts (by cooperating with the endocrine /
enzymatic systems) towards general balance.
Performs the three overlapping functions ofsensory input, integration & motor output.
Impulse is transmitted from one receptor to aneffector specifically.
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Sensory input
Brain & spinal cord
Motor input
Sensory receptor
EffectorPeripheral nervous
system (PNS)
Central nervous
system (CNS)
THE RELATIONSHIP BETWEEN THE SENSORY INPUT, INTEGRATION &
MOTOR OUTPUT
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ORGANIZATION
NERVOUS SYSTEM
CENTRALNERVOUS SYSTEM
PERIPHERALNERVOUS SYSTEM
BRAIN SPINAL CORD SENSORYMOTOR
(EFFERENT DIV)
SOMATIC
AUTONOMIC
PARASYMPATHETIC
SYMPATHETIC
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CENTRAL NERVOUS
SYSTEM
Comprises of :1) the brain
2) the spinal cord
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PERIPHERAL NERVOUS SYSTEM
consists of neurons that interconnect the brain to all partsof the body ;
a) the body muscle
b) the sensory organs
c) the organ built systems
the neurons are :
a) motor neurons somatic & autonomicb) sensory neurons
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MOTOR NEURONSSOMATIC
Controls thevoluntarily responseswhich involves the
skeletal muscles
AUTONOMIC
Regulates the internal environmentby controlling smooth & cardiacmuscles
Controls the involuntarily responsesof all the internal organs & glands
Actions are controlled in themedulla & hypothalamus
Consists ofsympathetic ¶sympathetic division.
Both act on the same target but very
often antagonistic in the effect theybring.
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Neuronbasic unit of nervous system
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Neuron
Functions :
a) receive information from the inner/ outerenvironment ; and/or from other neurons.
b) integrates information received &produces the
appropriate output signals.
c) guiding the signals until it reaches the farend/terminal of a neuron.
d) sending signals to other nerve cells, glands or
muscles.
Comprises of plasma membrane
The selective permeability of the membrane ensures theinformation from the environment reaches the desired target
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RESTING POTENTIAL & THE GENERATION
OF THE ACTION POTENTIAL
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Unstimulated neuronmaintains a different chargecondition across the
membranes.
The different chargesdevelops a localizedelectrical gradient, which iscalled the resting potential.
The resting potentialdevelops when the charge ismore negative within thecell than from the outside
(which is more positive).
The voltage measuredacross the plasma membrane(the membrane potential) is
about -70 mV.
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RESTING POTENTIAL
The intracellular & extracellular fluid of a neuron contains allkinds of solutes; including ions (cations &anions)
The fluid within the neurons contains mostlypotassium ions (K+)& a lower concentration of sodium ions (Na+)
In contrast, the extracellular fluid contains a higher concentrationof sodium ions.
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In its unstimulated stage, the membrane of the neuron is highly
permeable to K+ ions which passively diffuse across the membrane
according to the concentration gradient (from the inside, out of themembrane)
A slow diffusion of Na+ ions occur across the membrane because the
permeability to these ions is lower than to the K
+
ions.
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These diffusions do not achieve an equilibrium since the
sodium-potassium pump transports these ions againsttheir concentration gradient.
This results in the resting potential condition or the
polarization stage.
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THE ACHIEVEMENT OF RESTING (POLARIZED) STAGE
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THE RISING OF ACTION POTENTIAL
The neuron is stimulated by
the change in theenvironment (inner / outer).
The electrical potential across
the membrane will change
form its resting stage; the
charge within the cell
becomes more positive
because :
the sodium-potassium pumpsstop functioning
Na+ ions rush into the cell,
changing the membrane
potential to a more positive
state
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The change in theelectrical potential iscalled depolarization.
If graded potentials sum to 55mv, a thresholdpotential is achieved. This
triggers an action potential(impulse).
At the peak of the actionpotential, the sodium-
potassium pumps continuefunctioning; theconductivity of the Na+
ions decreases while theconductivity of the K+
ions increases again
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The K+ ions diffuse
out passively from thecell; resulting a more
negative state within
the cell.
The neuron is said to
undergo repolarization
which ultimatelyreaches the resting
stage.
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CHANGES IN THE MEMBRANE POTENTIAL :
DEPOLARIZATION, ACTION POTENTIAL, REPOLARIZATION
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In the resting state, both the sodium channel
and potassium channel are closed, and the
membranes resting potential is maintained.
During the depolarizing phase, the action
potential is generated as activation gates of
the sodium channels open, and thepotassium channel remains closed.
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THE TRANSMISSION OFIMPULSE
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THE TRANSMISSION OF IMPULSE
Is an electrical phenomena
that occurs through thedendrite, dendron & theaxon.
Involves 2 important
phases :1) the resting stage
2) the action potential
The features of actionpotentials / impulse are :
1) stimulation
2) all-or-nothing event
3) refractory period
4) speed of conduction
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STIMULATION
There are 2 kinds of stimulation that affect the nerves:
1) common stimulation
- involves the stimulation of the receptor organs
- e.g light, sound, taste, smell
2) situational stimulation
- all the stimulation that are capable of depolarizing
the axons.
- e.g mechanical, chemical, heat, pressure, electrical
stimulations.
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ALL-OR-NOTHING EVENT
The size of a nerve impulse is not determined by the size of the
stimulation received.The action potential is triggered only if the depolarization of the
membrane is above the threshold level.
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Below the threshold level, the stimulation is not sufficient todepolarize the membrane & thus triggering the action potential.
If an action potential is achieved, a stronger intensity of astimulus wont increase the size of it.
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THE ALL-OR-NOTHING EVENT
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REFRACTORY PERIOD
Impulse travels one-way along theaxon from the excitable region to the
resting region next to it.
The previously active regionundergoes a recovery phase which is
known as the refractory period.
Two phases are involved in this very
short period of about 5-10ms :
1) absolute refractory period
2) relative refractory period
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Absolute refractory period
the previously active region
undergoes a recovery phaseduring which the axon cannotrespond to a depolarizationeven if the stimulus intensityis increased.
during this period the axonmembrane goes throughhiperpolarization; themembranes permeability toK+ ions increasesdramatically.
these ions diffuse out veryhighly making the chargewithin the neuron becomestoo negative.
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Relative refractory perioda phase following the
absolute refractoryperiod where a high-intensity stimulusmay produce adepolarization.
the axon membranereaching its normal
permeability state,
allowing the Na+
ionsinto the cell; thecharge within the cellslowly becomes lessnegative; nearing its
resting state.
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SPEED OF CONDUCTIONDepends on :
a) the presence ofmyelin
sheath
act as an electrical insulator
depolarization only occurs atthe nodes of Ranvier whereno myelin sheath is present.
local circuits are set up atthese points & current flowsacross the axon membranegenerating the next action
potential.
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in effect, the actionpotential jumps fromnode to node & passesalong the myelinatedaxon faster.
this type of conductionis called saltatory.
the conduction
velocities is increasedup to 50x as comparedto in the unmyelinatedaxon.
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b) The axon diameter
the bigger the diameter,the higher the velocity of
the propagated actionpotential.
the resistance is reducedwhen the diameter of the
axon is big
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THE SALTATORY CONDUCTION ALONG THE MYELINATED AXON
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GENERATION & PROPAGATION OF IMPULSE
The action potential is produced
locally in axon; the membrane is
depolarized at a specific area in the
axon.
The action potential flows along the
axon because it is self-propagated.
An action potential achieved at one
region of the membrane is sufficient to
depolarized a neighboring regionabove threshold because the
depolarized area has a different charge
from the inactive area next to it; thus a
local circuit is produced.
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The current flow from one
activated region to theinactivated area enables
depolarization to occur, thus
produces the action potential.
The continuous occurrence of
depolarization from one area
to the one next to it, ensures
the transmission of impulse
even in a great distance.
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THE PROPAGATION OF IMPULSE ALONG THE AXON
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SYNAPSE
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Objectives
At the end of the lesson, students should be able to:
Draw out and label a picture of a synapse
Explain the mechanism of the impulse transmissionacross the synapse
Compare the transmission of impulse across thesynapse with the transmission along the axon
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Synapse
An area of functional
between neurons for
transferring information.
Found between fineterminal branches (axon),
dendrites or cell body.
2 types of synapsesa) electrical
b) chemical
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Structure of the chemical synapse
Commonly found in
vertebrates
Consist a bulbous
expansion of a nerve
terminal called synaptic
knob
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The membrane of the
synaptic knob is thickened
and form the presynapticmembrane
The thickened membrane
of the dendrite is termed
the postsynaptic membrane
The two membranes areseparated by a gap called
synaptic cleft (20nm)
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Structure of the chemical synapse
The cytoplasm of thesynaptic knotcontainsmitochondria,smooth
endoplasmicreticulum,microfilaments,andnumerous synapticvesicles
Each vesiclecontains a chemicalneurotransmitter
substance
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Two main neurotransmittersubstances are
a) acetylcholine
- secreted by parasympathetic
b) noradrenaline
- secreted by sympathetic
nerves
Protein channels are found onthe postsynaptic membrane andthey have receptors for theneurotransmitter substance
These channels allow themovement of ions into the
postsynaptic neurons
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Mechanism of synaptictransmission
M h i f i i i
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Mechanism of synaptic transmission
The arrival of nerve
impulses at thesynaptic knob
depolarizes the
presynaptic
membrane.
The permeability of
the membrane toCa2+ ions is
increased, and they
easily enter the knob.
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The entrance of those ions
causes the synaptic
vesicles to fuse with thepresynaptic membrane and
rupture; discharging their
contents into the synaptic
cleft.
The vesicles then return to
the cytoplasm where they
are refilled with
neurotransmitter
substance.
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The neurotransmitter
substance diffuses across the
synaptic cleft and attaches to
a specific receptor site on thepostsynaptic membrane;
causing the opening of the
protein channels.
Na+ ions enter thepostsynaptic neurons,
followed by the leaving of
K+ ions down their
respective concentration
gradient.
This leads to a depolarization
of the postsynaptic
membrane.
The depolari ation
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The depolarizationresponse is known as anexcitatory postsynapticpotential (EPSP)
Having produced a changein the permeability of the
postsynaptic membrane,the neurotransmittersubstance is thenhydrolyzed by a specificenzyme
acetylcholine ishydrolyzed byacetylcholinesterase
noradrenalin ishydrolyzed by
monoaminoxidase
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The depolarizing effect of the EPSP is additive, a phenomenon calledsummation:
two or more EPSP arising simultaneously at different regions on the sameneuron may produce collectively sufficient depolarization (spatialsummation).
rapid release of transmitter substance from several synaptic vesicles by thesame synaptic knob produces individual EPSP close together, they summate
and give rise to action potential in postsynaptic neuron (temporalsummation).
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Fig 12.11 : The relationship between EPSP with the achievement of action potential
The action potential produced is then transmitted along the postsynaptic axon by the
flow of an electric current.
The summation effect of EPSP delays the transmission of impulse in neurons; but it
ensures the flow of impulse is unidirectional.Because: the synaptic vesicles only exist in the presynaptic membrane side.
C i f i l t i i th d
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Comparison of impulse transmission : across the synapse and
along the axon
Synapse Axon1. Impulse is chemically transmitted. 1. Impulse is electrically transmitted.
2. Involves the neurotransmitter substances. 2. No neurotransmitter substances are
involved.
3. Impulse transmission is slower because :
-the neurotransmitter need to diffuse
across the synaptic cleft
-the summation of EPSP is needed to
reach the threshold level
3. Impulse transmission is very fast.
4. Involves the diffusion of Ca+ ions into
the synaptic knob to activate the vesicles.
4. Ca+ ions are not involved.
5. The diffusion of Na across the membrane
is needed.
5. The diffusion of Na across the membrane
is needed.
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NEUROMUSCULAR JUNCTION
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OBJECTIVES
At the end of the lesson, students should be able to:
draw out a label picture of a neuromuscular junction
completely explain the rising of end-plate potential
explain the fine structure of the skeletal muscle which
consists of myofibril, actin, myosin and sarcomere.
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STRUCTURE OF THE NEUROMUSCULAR JUNCTION
1. SPECIALIZED FORM OF SINAPSE FOUND BETWEENNERVE TERMINALS & MUSCLE FIBRES
2. THE CYTOPLASM OF THE MOTOR NEURONTERMINAL RELEASES ACETYLCHOLINE ONSTIMULATION
3. THE REGION WHERE THE THE AXON OF THE MOTORNEURON DIVIDES & FORM NON-MYELINATED
BRANCHES ON THE MEMBRANE CELL SURFACE ISCALLED THE THE MOTOR END- PLATE
4. POSTSYNAPTIC MEMBRANE (MUSCLE MEMBRANE )CALLED SARCOLEMMA HAS MANY FOLDS CALLEDJUNCTIONAL FOLDS
5. A LOCAL DEPOLARIZATION AT EACH MOTOR ENDPLATE PRODUCES END-PLATE POTENTIAL (EPP)
6. EPP IS SUFFICIENT TO LEAD TO A PROPAGATEDACTION POTENTIAL ALONG SARCOLEMMA DOWNINTO THE MUSCLE FIBRE VIA TRANSVERSE TUBULESYSTEM (T-SYSTEM)
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STRUCTURE OF THE SKELETAL MUSCLE
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STRUCTURE OF THE SKELETAL MUSCLE
The major components are the
cylindrical muscle fibres; whichmeasure about 10 100 m in
diameter and 1 40 mm in
length
Within the muscle fibres are
numerous thin myofibrils
Each myofibril is composed of
two types of proteinaceousmyofilaments, actin (thin
filaments) and myosin (thick
filaments)
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The cytoplasm of the
myofibril is called
sarcoplasm and containsa network of internal
membranes termed the
sarcoplasmic reticulum
The skeletal muscle is
observed to be striated; a
regular alternation of light
and dark bands
The light and the dark
bands are called the I and
A bands respectively
The bands are due to the regular
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e b ds e due o e eguarrangement of actin andmyosin
Traversing the middle of each Iband is a dark line called the Zline
The section of a myofibril
between two Z line is called asarcomere; the functional unitof muscle contraction
In certain regions of thesarcomere, actin and myosinfilaments overlap
Myosin and actin filamentsconstitute the A band, whilstactin filament alone constitute
the I band
The centre of the A band is lighter
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The centre of the A band is lighter
than its other regions because it
constitutes only the filament
myosin, and is called the H band
The H band is bisected by a dark
line, the M line; which joins
adjacent myosin filaments together
at a point halfway along their length
Running transversely across the
fibre and between fibrils is a system
of tubules known as the T system
The T system is in contact with the
surface of the sarcolemma
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At certain points the T tubules
pass between the pairs of
vesicles which are components
of the sarcoplasmic reticulum
The vesicles are involved in the
uptake and release of Ca2+ ions
which controls the contractile
behaviour of the muscle fibre
MECHANISM OF MUSCLE CONTRACTION
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MECHANISM OF MUSCLE CONTRACTION
AT REST, TROPOMYOSIN BLOCKS THEMYOSIN ATTACHMENT TO ACTIN
UPON STIMULATION BY NERVEIMPULSE, Ca2+ IONS ARE RELEASEDINTO THE SARCOPLASM
THE IONS BIND TO THE TROPONINCOMPLEX
TROPONIN COMPLEX CHANGES ITSCONFORMATION
NOW THE MYOSIN BINDING SITESARE EXPOSED
MYOSIN HEADS ATTACHED TO THEACTIN FILAMENT
CROSS BRIDGES ARE FORMED
MUSCLE CONTRACTS
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IN SOME MUSCLES Ca2+ ALSOSTIMULATES THE MYOSINATPASE ACTIVITY.
THE ATPASE HYDROLIZES THEATP & CHANGE THE MYOSINHEAD TO A HIGH ENERGYCONFIGURATION.
THIS ALLOWS THE FORMATIONOF CROSS BRIDGES.
WHEN THE EXCITATION OF THESARCOMERES CEASES, Ca2+ ARE
PUMPED BACK INTO THEVESICLES.
SARCOMERES RELAXES
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THE MECHANISM OF MUSCLE CONTRACTION
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The Sliding Filament Theory
The Sliding Filament Theory
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The Sliding Filament TheoryProposed by Huxley and
Hanson in 1954.
They suggested that the muscle
contracts when the thin filament
(actin) and the thick filament
(myosin) slide past each other.
During contraction the actin
filament move inwards towards
the centre of the sarcomere,making it (the sarcomere)looks
shorter without changing the
length of the A band.
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The myosin head is the centre ofbioenergetic reactions that powermuscle contraction.
The high energy configurationheads of the myosin filamentoperate like a hook attaching tothe specific sites on actin in a
particular way to form crossbridges.
The high energy configurationstate is achieved when the ATP
molecules bound to the headsbeen hydrolyzed into ADP andinorganic phosphate, andreleasing high energy used tochange the configuration.
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The myosin heads then
change their relative
configuration such that the
actin molecules are pulled
further into the A band.
After the process is
completed, the myosin
heads, bound to another
ATP molecules, detachfrom the actin.
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They then split the new ATP
molecules to revert to the high
energy configuration and attach to
another sites further along the actinfilament.
The cross bridge
attachment/detachment cycles
could be repeated many timesdepending on the speed of
shortening.
The pulling of the actin filament
repeatedly towards the centre isunidirectional in a mechanism
called the ratchet mechanism.
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AUTONOMIC
NERVOUS SYSTEM
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OBJECTIVES
At the end of the lesson, students should be
able to :
Explain the structure and the functions of the
sympathetic and parasympathetic systems
Compare both the sympathetic and the
parasympathetic system
MAMALIAN AUTONOMIC NERVOUS SYSTEM (ANS)
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( )
A part of peripheral nervous system controlling the involuntaryactivities of internal environment ;eg: heart rate, peristalsis, sweating
Consist of motor neuron passing to the smooth muscles of internalorgan and cardiac muscle
Most activities of ANS is integrated locally within the spinal cord orbrain by visceral reflexes
ANS composed 2 types of neurons :
Preganglionic neuron (mylienated) emerges from CNS
Postganglionic neuron (unmylienated) leading the effectors
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2 division of ANS :
Symphatetic nervous system
Parasymphatetic nervous system
The two systems differ primarily in the structural
organization of their neurons
SYMPATHETIC NERVOUS SYSTEM (SNS)
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SYMPATHETIC NERVOUS SYSTEM (SNS)
Neurons are originated from spinal cord( the thoracic + lumbarregion)
Synapses + cell bodies of postganglionic neurons in the trunk regionare situated in ganglia close to spinal cord
Adjacent segmental symphatetic ganglia on each side of spinal cordare linked together by the sympathetic nerve tract
They form chain of symphatetic ganglia running alongside the spinalcord
Its preganglionic neurons are shorter than postganglionic neurons
The chemical transmitter substance released at postganglionic effectorsynapses in noradrenalin (Ad)
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The effect s spread to all part of the body and
takes time to decease
The symphatetic nervous system is especially
dominant under stress or at time danger
Eg.of its effects :Dilates pupil
Increase amplitude and rate of heart beatIncrease ventilation rate
Constricts arterioles to gut and smooth muscle
PARASYMPHATETIC NERVOUS SYSTEM (PNS)
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PARASYMPHATETIC NERVOUS SYSTEM (PNS)
Neurons originated from the cranial and the sacral region of the CNS
The ganglia of PNS situated close to or within the effector organ
Its preganglionic neurons longer than its postganglionic neurons
Chemical transmitter substance secreted at the postganglionic
synapses is AceKoa
Its effect locally and short
PNS controls the routine activities of the body at rest ; a compensationfor the symphatetic effect
Eg :decrease the amplitude + rate of heart beat,ventilation rate
Maintains steady muscle tone in atrioles to gut,smooth muscle,brain and skeletal
muscle
Diff b h i & h i
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Differences between symphatetic & parasymphatetic nervous system
Feature Symphatetic Parasymphatetic
Origin of neuron Emerges from thoracic and
lumbar regions of CNS
Emerges from cranial +
sacral regions of CNS
Position of ganglion Close to spinal cord Close to effector
Length of fibres Short preganglionic , long
postganglionic fibers
Long preganglionic
fibers,short postganlionic
fibers
Numbers of fibers Numerous postganglionic fibres Few ganglionic fibers
Distribution of fibers Preganglionic fibers innervate a
wide area
Preganglionic fibers
innervate a restricted region
Area of influence Effect difuse Effect localized
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Feature Symphatetic Parasymphatetic
Transmitter substance Noradrenalin released ateffector
AceKoa released ateffector
General effects Increase metabolite
Lowers sensory threshold
Restores sensory
threshold to normal level
Decrease metabolite level
Overall effect Excitatory homeostatic
effects
Inhibitory homeostatic
effect
Condition when active Dominant duringdanger,stress + activity
Dominant during rest
Controls routine body
activities
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DRUG ABUSE
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OBJECTIVES
At the end of the lesson the students should be able to :
Give the definition of drugs
List and give explanations of the 5 types of drugs
Explain the effect of cocaine on the synapses andneuromuscular junction
DRUGS
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DRUGSDefinition
Any chemical substance that alters the physiological state of a living organisms
Also known as psychoactive substance which could lead to addiction ifabused
giving harmful effect to mental & physical activities
Addiction
Chemically dependent on drugs resulting from the body tolerancemore dosage is needed to get the same effect
Individual is said to be addicted when the drugs has taken over the importantrole in his biochemical reaction
Most drugs interfere with the impulse transmission by : Changing
Hindering synthesis the neurotransmitter substance
Releasing and absorbing
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TYPES OF DRUGS
DEPRESSANTSTIMULANT
HALLUCINOGEN
ANTI-DEPRESSANT
INHALANT
STIMULANT
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STIMULANT
Small dosage - activities of CNS (feeling more energetic)
High dosage/prolong consumption lead to depression
Eg :
1. Caffeine prevents the hydrolyses of neurotransmitter substances continuous depolarization occurs at the postsynapse membrane
Small dosage stimulates the cerebrum cortex-increase alertness
High dosage influence medulla oblongata interfering motor andintellectual coordination
2. Nicotine mimics the effect of AceKoa on receptor and stimulates thesensory receptors
- short term use change in heart beat rate and blood pressure
3. Amphetamines and cocaine
Block the reabsorption of neurotransmitters from the postsynapsesmembrane continuous depolarization of the postsynapsemembranes in long period
DEPRESSANT
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SS N
Lowering activities in CNS lowering body activities as a
whole
Eg : Barbiturates
Gives different based on dosage consumed
Low dosage
stimulate synaptic activities, so persons would in state of euphoria/excited
High dosage
synaptic action is hindered ( a feeling of depression is experienced by the
individual)
HALLUCINOGEN
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HALLUCINOGEN
Change the perception of the senses especially sight and
hearing
Some acts by imitating/inhibiting the action ofneurotransmitter substance
Most involve in causing disorientation and hallucinating not fatal
Eg: LSD (Lysergic acid diethylamide) Marijuana
ANTI-DEPRESSANT
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(TRANQUILIZERS)
Use as pain killer & to lessen anxiety
Mimic the action ofendorphin and enkephalins which areneuromodulators that assist the action of the neurotransmittersubstances
Endorphin + enkephalins inhibit the transmission of pain signals to brain
Eg :Narcotics ( heroin, morphine)
Prolong consumption of narcotics increase the receptors for enkephalins bind to the receptor used
by enkephalins therefore, pain signals are prevented fromreaching brain
P l i f i
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Prolong consumption of narcotics
increase the receptors for enkephalins bind to thereceptor used by enkephalins therefore, pain signals
are prevented from reaching brain
High dosage needed when body becomes tolerant tothe drug
When drug withdrawn from body pain pathwayneurons become extremely sensitive
Because number of enkephalins receptor has beenincreased, more receptors are left unbound by
enkephalins and pain impulses are not blocked
The withdrawing addict experiences greater pain thannormal until the number of receptors reaches its
preaddiction level
INHALANT
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INHALANT
Drugs that taken by means of inhaling
Eg:
Organics solvent
Ether
Chloroform
Organic based adhesive substance
Causes :
Hallucination
Higher heart beat rate
Anaesthetize condition
A near fainted feelings
COCAINE :
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THE MECHANISM OF ACTION
As stimulant, cocaine effects the brains limbicsystem (the bodys pleasure centre) by imitatinga neuromodulator that blocks the reabsorption ofdopamine (neurotransmitter substance) back into
the presynapse membranes
Result of blockage
dopamine stays in synaptic clefts and continually binds tothe receptors in postsynaptic membrane
Depolarization occurs repeatedly which result incontinuous impulse transmission causes????????
Causes :
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intense pleasure, increase energy and feeling of power
Neuron respond to continual stimulation by reducing thenumber of dopamine receptor in postsynaptic membranes
Thus, more and more drug is needed for the addict toexperience the pleasurable effects that the dopamine bindingelicits
Addiction build, cocaine addicts find that their pleasure centrescant function at all without the stimulation of drugs
The drugs effect wear off and the addicts begins to suffer deepdepression
When drug again introduced into the body, the mood ofdepression swings to euphoria (intense feeling of happinessand pleasant excitement)
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Thats all for this topic