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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 &parasympathetic 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