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Title: Natural Science


1
Natural Science
  • 04 Nerve Impulses

2
Some animations may have been used from
neurons.med.utoronto.ca/index.swf under the
conditions stated below
3
  • Nerve Conduction
  • Nerve conduction is when nerve impulses are made
    and move along our neurons.
  • None of our thoughts, or memories would be
    possible without nerve conduction.

4
  • Nerve conduction is an electrochemical process.
  • It uses electricity made with chemical molecules.
  • The electricity in the brain is not produced by
    electrons flowing like they do through an
    electrical wire.
  • Instead, the brains electricity is caused by the
    movements of electrically charged molecules
    through the neurons membranes.

5
  • The membrane of a neuron, like that of any other
    cell, contains tiny holes known as channels. It
    is through these channels that charged molecules
    pass through the neural membrane.
  • But the channels in neurons are so specialized
    that they can coordinate the movements of these
    charges across the membrane so as to conduct
    nerve impulses.

6
  • Here is a simplified sequence of events by which
    a nerve impulse is conducted.
  • (see figure one at this site)

7
  • In the resting state the channels in the neural
    membrane create an unequal distribution of
    charges.

8
  • The nerve impulses open and close ion channels.
    Ions move across the membrane and change the
    electrical potential across the membrane. For a
    short time the inside becomes more positive than
    the outside.

9
  • Other channels quickly re-establish the resting
    potential, but next to this area the potential is
    changed. http//thebrain.mcgill.ca/flash/d/d_01/d
    _01_m/d_01_m_fon/d_01_m_fon.html

10
  • Ion Channels and Nerve Impulses

11
  • Ion transport proteins have a special role in the
    nervous systems because voltage-gated ion
    channels and ion pumps are needed to form a nerve
    impulse.

12
  • Ion channels use energy to build and maintain a
    concentration gradient of ions between the
    extracellular fluid and the cells cytosol.

13
  • Channel proteins in the plasma membrane. Membrane
    channel proteins (or channel proteins), allow the
    movement of specific ions across the cell
    membrane.

14
  • The concentration gradient results in electrical
    potential energy building up across the membrane,
    the basis for the conduction of a nerve impulse.

15
  • This concentration gradient results in a net
    negative charge on the inside of the membrane and
    a positive charge on the outside.

16
  • Ion channels and ion pumps are very specific
    they allow only certain ions through the cell
    membrane.

17
  • For example, potassium channels will allow only
    potassium ions through, and the sodium-potassium
    pump acts only on sodium and potassium ions.

18
  • All cells have an electrical charge which is due
    to the concentration gradient of ions that exists
    across the membrane.

19
  • All cells have an electrical charge which is due
    to the concentration gradient of ions that exists
    across the membrane.

19
20
  • The number of positively charged ions outside the
    cell membrane is greater than the number of
    positively charged ions in the cytosol. This
    difference causes a voltage difference across the
    membrane.

20
21
  • The number of positively charged ions outside the
    cell membrane is greater than the number of
    positively charged ions in the cytosol. This
    difference causes a voltage difference across the
    membrane.

22
  • The number of ions outside is greater than the
    number of ions in the cytosol. This causes a
    voltage difference across the membrane.

22
23
  • Voltage is electrical potential energy that is
    caused by a separation of opposite charges, in
    this case across the membrane.
  • The voltage across a membrane is called membrane
    potential.

23
24
  • Voltage is electrical potential energy that is
    caused by a separation of opposite charges, in
    this case across the membrane.
  • The voltage across a membrane is called membrane
    potential.

25
  • Membrane potential is the basis for the
    conduction of nerve impulses along the cell
    membrane of neurons. Ions that are important in
    the formation of a nerve impulse include sodium
    (Na) and potassium (K).

25
26
  • Membrane potential is the basis for the
    conduction of nerve impulses along the cell
    membrane of neurons. Ions that are important in
    the formation of a nerve impulse include sodium
    (Na) and potassium (K).

27
  • How Diffusion Works
  • and quiz

27
28
  • How Facilitated Diffusion Works
  • And quiz

28
29
  • How the Sodium Potassium Pump Works
  • And quiz

29
30
  • Receptors Linked to a Channel Protein
  • And quiz

30
31
  • For review look at 3. Ions and Ion Transport

31
32
  • Resting Potential

33
  • When a neuron is not conducting a nerve impulse,
    it is said to be at rest. The resting potential
    is the resting state of the neuron, during which
    the neuron has an overall negative charge.

34
  • In neurons the resting potential is approximately
    -70 milliVolts (mV). The negative sign indicates
    the negative charge inside the cell relative to
    the outside.

35
  • The reasons for the overall negative charge of
    the cell include

36
  • The sodium-potassium pump removes Na ions from
    the cell by active transport. A net negative
    charge inside the cell is due to the higher
    concentration of Na ions outside the cell than
    inside the cell.

37
  • The sodium-potasium pump is also called the
    Na/K-ATPase (fully sodium-potassium adenosine
    triphosphatase, also known as the Na/K pump, or
    sodium pump, for short).
  • It is an enzyme (EC 3.6.3.9) located in the
    plasma membrane in all animals.
  • As its name suggests, it uses ATP in its action.

37
38
38
39
  • Animation of the sodium-potassium pump is at
  • http//highered.mcgraw-hill.com/sites/0072495855/s
    tudent_view0/chapter3/animation__sodium-potassium_
    exchange_pump__quiz_1_.html

40
  • Na, K-ATPase and other ion pumps must work all
    the time in our body. If they were to stop, our
    cells would swell up, and might even burst, and
    we would rapidly lose consciousness. A great deal
    of energy is needed to drive ion pumps - in
    humans, about 1/3 of the ATP that the body
    produces.

41
  • Since neurons purposely allow Na to flood into
    the cell and K to go out, we can assume that
    neurons use much more energy for pumping

42
  • Ion pumps are affected by chemical substances.
  • Digitalis plants contain a substance that
    inhibits Na, K-ATPase which results in an
    accumulation of sodium ions in cells.
  • Used as a pharmaceutical, it causes reinforced
    heart muscle activity.

43
  • Most cells have potassium-selective ion channel
    proteins that remain open all the time. The K
    ions move down the concentration gradient
    (passively) through these potassium channels and
    out of the cell, which results in a build-up of
    excess positive charge outside of the cell.

44
  • There are a number of large, negatively charged
    molecules, such as proteins, inside the cell.

45
  • For review click on 4. Resting Membrane Potential

45
46
  • Potassium (K), which is positively charged,
    passes most easily through a neural membrane in
    its resting state.
  • Sodium (Na) and chloride (Cl-), which has a
    negative charge, have more difficulty passing
    through the membrane.
  • Large, negatively charged molecules inside the
    neuron cannot get out but also influence the
    membranes electrical potential.
  • The calcium ion (Ca) also plays an important
    role, but in the process of synaptic
    transmission.

46
47
  • Membrane ion-channel and ion-pumping proteins.

47
48
  • Action Potential

49
  • An action potential is an electrical charge that
    travels along the membrane of a neuron. It is
    made when a neurons membrane potential is
    changed by chemical signals from a nearby cell.

50
  • In an action potential, the cell membrane
    potential changes quickly from negative to
    positive as sodium ions flow into and potassium
    ions flow out of the cell through ion channels.

51
  • The movement of an action potential down an axon.

51
52
  • The movement of an action potential down an axon.

53
  • A chemical message from another nerve causes the
    sodium ion channels at one point in the axon to
    open. Sodium ions rush across the membrane and
    cause the interior of the axon to become
    positively charged (depolarized) because the cell
    now contains more positive charges. Potassium ion
    channels then open and potassium ions flow out of
    the cell, which end the action potential. The
    action potential then moves down the axon
    membrane toward the synapse.

54
  • The cell becomes depolarized. An action potential
    works on an all-or-nothing basis. This means, the
    membrane potential has to reach a certain level
    of depolarization, called the threshold,
    otherwise an action potential will not start.

55
  • This threshold potential varies, but is generally
    about 15 millivolts (mV) more positive than the
    cell's resting membrane potential. If a membrane
    depolarization does not reach the threshold
    level, an action potential will not happen.

56
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58
  • The first channels to open are the sodium ion
    channels, which allow sodium ions to enter the
    cell. The resulting increase in positive charge
    inside the cell (up to about 40 mV) starts the
    action potential.

58
59
  • The first channels to open are the sodium ion
    channels, which allow sodium ions to enter the
    cell. The resulting increase in positive charge
    inside the cell (up to about 40 mV) starts the
    action potential.

60
  • Potassium ion-channels then open up, allowing
    potassium ions out of the cell, which ends the
    action potential.

60
61
  • Potassium ion-channels then open up, allowing
    potassium ions out of the cell, which ends the
    action potential.

62
  • Both of the ion channels then close, and the
    sodium- potassium pump restores the resting
    potential of -70 mV.

62
63
  • Both of the ion channels then close, and the
    sodium- potassium pump restores the resting
    potential of -70 mV.

64
  • The action potential will move down the axon
    toward the synapse like a wave.

64
65
  • The action potential will move down the axon
    toward the synapse like a wave.

66
  • Video
  • http//highered.mcgraw-hill.com/sites/0072495855/s
    tudent_view0/chapter14/animation__the_nerve_impuls
    e.html

67
  • Quiz 1
  • Quiz 4

68
  • In myelinated neurons, ion flows occur only at
    the nodes of Ranvier. As a result, the action
    potential signal is quickly pushed along the axon
    membrane, from node to node, rather than
    spreading smoothly along the membrane, as they do
    in axons that do not have a myelin sheath.

69
  • The quick pushing of the action potential signal
    along the axon membrane, from node to node, is
    called saltatory conduction.

69
70
  • Comparison
  • http//faculty.stcc.edu/AandP/AP/AP1pages/nervssys
    /unit11/saltator.htm


70
71
  • Saltatory conduction
  • Saltatory conduction is faster than smooth
    conduction. Some typical action potential
    velocities


Fiber Diameter AP Velocity
Unmyelinated 0.2-1.0 micron 0.2-2 m/sec
Myelinated 2-20 microns 12-120 m/sec
71
72
  • The action potential is increased at the Nodes of
    Ranvier. This is due to clustering of Na and K
    ion channels at the Nodes of Ranvier.

72
73
  • Unmyelinated axons do not have Nodes of Ranvier
    and ion channels in these axons are spread over
    the entire membrane surface.

74
  • Video-
  • The Schwann Cell and Action Potential
  • http//www.knowmia.com/watch/lesson/433

75
  • For review go to this page and click on 5. Action
    Potential

75
76
  • Communication Between Neurons

77
  • Neurons communicate with each other at
    specialized junctions called synapses. Synapses
    are also found at junctions between neurons and
    other cells, such as muscle cells.

78
  • Neuromuscular junction
  • Axon
  • Synaptical junction
  • Muscle fiber
  • Myofibrils

79
  • There are two types of synapses
  • - chemical synapses use chemical signaling
    molecules as messengers
  • - electrical synapses use ions as messengers
  • We will look at chemical synapses.

80
  • The axon terminal of one neuron usually does not
    touch the other cell at a chemical synapse.
    Between the axon terminal and the receiving cell
    is a gap called a synaptic cleft.

81
  • The transmitting cell is called the presynaptic
    neuron, and the receiving cell is called the
    postsynaptic cell or if it is another neuron, a
    postsynaptic neuron.

82
  • The brain has a huge number of synapses. Each of
    the 1012 (one trillion) neurons, including glial
    cells, has on average 7,000 synaptic connections
    to other neurons.

83
  • It has been estimated that the brain of a three
    year-old child has about 1016 synapses (10
    quadrillion). This number declines with age, and
    levels off by adulthood.

84
  • An adult has between 1015 and 5 x 1015 synapses
    (1 to 5 quadrillion).

85
  • Neurotransmitter Release

86
  • A neurotransmitter is a chemical message that is
    used to relay electrical signals between a neuron
    and another cell.

87
  • Neurotransmitter molecules are made inside the
    presynaptic neuron and stored in vesicles at the
    axon terminal.

88
  • Some neurons make only one type of
    neurotransmitter, but most neurons make two or
    more types of neurotransmitters.

89
  • When an action potential reaches the axon
    terminal, it causes the neurotransmitter vesicles
    to fuse with the terminal membrane, and the
    neurotransmitter is released into the synaptic
    cleft.

90
  • The neurotransmitters then diffuse across the
    synaptic cleft and bind to receptor proteins on
    the membrane of the postsynaptic cell.

91
  • The synaptic cleft. Neurotransmitter that is
    released into the synaptic cleft diffuses across
    the synaptic membrane and binds to its receptor
    protein on the post synaptic cell.

92
  • Neuromuscular junction
  • presynaptic terminal
  • sarcolemma
  • synaptic vesicles
  • Acetylcholine receptors
  • mitchondrion

93
  • At a synapse, neurotransmitters are released by
    the axon terminal. They bind with receptors on
    the other cell.

93
94
  • The location of synapses. Synapses are found at
    the end of the axons (called axon terminals) and
    help connect a single neuron to thousands of
    other neurons. Chemical messages called
    neurotransmitters are released at the synapse and
    pass the message onto the next neuron or other
    type of cell.

94
95
  • Neurotransmitter Action

96
  • Many types of neurotransmitters exist.
  • Neurotransmitters can have an excitatory or
    inhibitory effect on the postsynaptic cell.

97
  • Common Neurotransmitters and Their Receptors

Name Receptor Name and Type Ions Involved
Glutamate (glutamic acid) Glutamate receptors (ligand-gated ion channels and G protein-coupled receptors) Ca2, K, Na
Acetylcholine Acetylcholine receptors (ligand-gated ion channel) Na
Norepinephrine (noradrenaline) Adrenoceptors (G protein-coupled receptors) Ca2
Epinephrine (adrenaline) Adrenoceptors (G protein-coupled receptors) Ca2
Serotonin (5-hydroxytryptamine) 5-HT receptors 5-HT3 is a ligand-gated ion channel 5-HT1, 5-HT2, 5-HT4, 5-HT5A, 5-HT7 are G protein-coupled receptors K, Na
Gamma-aminobutyric acid (GABA) GABAA and GABAC (ligand-gated ion channels) GABAB (G protein-coupled receptors) Cl- K
Histamine Histamine receptors (H1, H2, H3, H4) (G protein-coupled receptors)
98
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99
  • An excitatory neurotransmitter initiates an
    action potential and an inhibitory
    neurotransmitter prevents one from starting.

100
  • Glutamate is the most common excitatory
    transmitter in the body while GABA and glycine
    are inhibitory neurotransmitters.

101
  • Acetycholine

102
  • The release of acetylcholine, an excitatory
    neurotransmitter causes an inflow of positively
    charged sodium ions (Na) into the postsynaptic
    neuron.

103
  • This inflow of positive charge causes a
    depolarization of the membrane at that point. The
    depolarization then spreads to the rest of the
    postsynaptic neuron.

104
  • The effect of a neurotransmitter also can depend
    on the receptor it binds to. So, a single
    neurotransmitter may be excitatory to the
    receiving neuron, or it may inhibit such an
    impulse by causing a change in the membrane
    potential of the cell.

105
  • Synapses too can be excitatory or inhibitory and
    will either increase or decrease activity in the
    target neuron, based on the opening or closing of
    ion channels.

106
  • Neurotransmitter receptors can be gated ion
    channels that open or close through
    neurotransmitter binding or they can be
    protein-linked receptors.

107
  • Protein-linked receptors are not ion channels
    instead they cause a signal transduction that
    involves enzymes and other molecules (called
    second messengers) in the postsynaptic cell.

108
  • Video-
  • http//highered.mcgraw-hill.com/sites/0072495855/s
    tudent_view0/chapter14/animation__transmission_acr
    oss_a_synapse.html

109
  • Quiz 3

110
  • Neurotransmitter Reuptake

111
  • Many neurotransmitters are removed from the
    synaptic cleft by neurotransmitter transporters
    in a process called reuptake. Reuptake is the
    removal of a neurotransmitter from the synapse by
    the pre-synaptic neuron.

112
  • Reuptake happens after the neurotransmitter has
    transmitted a nerve impulse.
  • Without reuptake, the neurotransmitter molecules
    might continue to stimulate or inhibit an action
    potential in the post-synaptic neuron.

113
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114
  • A synapse before and during reuptake.

115
  • Re-uptake is carried out by transporter proteins
    which bind to the released transmitter and
    actively transport it across the plasma membrane
    into the pre-synaptic neuron.

116
  • Video-
  • Synaptic Transmission
  • http//www.youtube.com/watch?v9vZI_XKca88feature
    related

116
117
  • Reuptake of neurotransmitter as a medical target.

118
  • The reuptake of neurotransmitter is the target of
    some types of medicine.
  • For example, serotonin is a neurotransmitter that
    is produced by neurons in the brain.

119
  • Serotonin is believed to play an important role
    in the regulation of mood, emotions, and
    appetite.

120
  • After release into the synaptic cleft, serotonin
    molecules either attach to the serotonin
    receptors (5-HT receptors) of the post-synaptic
    neuron, or they attach to receptors on the
    surface of the presynaptic neuron that produced
    the serotonin molecules, for reuptake.

121
  • Reuptake is a form of recycling because the
    neuron takes back the released neurotransmitter
    for later use.

122
  • Medicines called selective serotonin reuptake
    inhibitors (SSRIs) block the reuptake of the
    neurotransmitter serotonin.
  • This blocking action increases the amount of
    serotonin in the synaptic cleft, which prolongs
    the effect of the serotonin on the postsynaptic
    neuron.

123
  • Some scientists hypothesize that decreased levels
    of serotonin in the brain are linked to clinical
    depression and other mental illnesses.
  • So SSRI medications such as sertraline and
    fluoxetine are often prescribed for depression
    and anxiety disorders.

124
  • Another way that a neurotransmitter is removed
    from a synapse is digestion by an enzyme.

125
  • L-Monoamine oxidases (MAO) (EC 1.4.3.4) are a
    family of enzymes that catalyze the oxidation of
    monoamines
  • They are found bound to the outer membrane of
    mitochondria in most cell types in the body.
  • They belong to the protein family of
    flavin-containing amine oxidoreductases.

126
  • In humans there are two types of MAO MAO-A and
    MAO-B.
  • Both are found in neurons and astroglia.
  • Outside the central nervous system
  • MAO-A is also found in the liver,
    gastrointestinal tract, and placenta.
  • MAO-B is mostly found in blood platelets.

126
127
  • They are well known enzymes in pharmacology,
    since they are the substrate for the action of a
    number of monoamine oxidase inhibitor drugs.
  • Both MAOs are inactivate monoaminergic
    neurotransmitters, for which they display
    different specificities.

127
128
  • Serotonin, melatonin, norepinephrine, and
    epinephrine are mainly broken down by MAO-A.
  • Phenethylamine and benzylamine are mainly broken
    down by MAO-B.
  • Both forms break down dopamine, tyramine, and
    tryptamine equally

128
129
  • MAO dysfunction (too much or too little MAO
    activity) is thought to be responsible for a
    number of psychiatric and neurological disorders.

129
130
  • For example, unusually high or low levels of MAOs
    in the body have been associated with depression,
    schizophrenia, substance abuse, attention deficit
    disorder, migraines, and irregular sexual
    maturation.

130
131
  • Monoamine oxidase inhibitors are one of the major
    classes of drug prescribed for the treatment of
    depression.
  • MAO-A inhibitors act as antidepressant and
    antianxiety agents, whereas MAO-B inhibitors are
    used alone or in combination to treat Alzheimers
    and Parkinsons diseases.

131
132
  • MAO is also heavily depleted by use of tobacco
    cigarettes.

132
133
  • Neurotransmitters and Disease

133
134
  • Before we begin
  • We often think of disease (or the cause of
    disease) as a bad functioning of the cells or
    systems.
  • But the proper functioning may be the underlying
    cause of disease.

135
  • Before we begin
  • We often think of disease (or the cause of
    disease) as a bad functioning of the cells or
    systems.
  • But the proper functioning may be the underlying
    cause of disease.
  • When we look at diseases which are caused by
    compulsive or addiction related behaviors,
    remember that they may be based on the proper
    functioning of neurotransmitters or their
    receptors.

136
  • Diseases that affect nerve communication can have
    serious consequences.

136
137
  • A person with Parkinson's disease has a
    deficiency of the neurotransmitter dopamine.
  • Progressive death of brain cells that produce
    dopamine increases this deficit, which causes
    tremors, and a stiff, unstable posture.

137
138
  • L-dopa is a chemical related to dopamine that is
    given as a medicine to ease some of the symptoms
    of Parkinsons disease.
  • The L-dopa acts as a substitute neurotransmitter,
    but it cannot reverse the disease.

138
139
  • The soil bacterium Clostridium tetani produces a
    neurotoxin that causes the disease tetanus.
  • The bacteria usually get into the body through an
    injury caused by an object that is contaminated
    with C. tetani spores.

139
140
  • The C. tetani neurotoxin blocks the release of
    the neurotransmitter GABA, which causes skeletal
    muscles to relax after contraction.
  • When the release of GABA is blocked, the muscle
    tissue does not relax and remains contracted.

140
141
  • Tetanus can be fatal when it affects the muscles
    used in breathing.
  • Tetanus is treatable and can be prevented by
    vaccination.

141
142
  • Electrical Synapses

142
143
  • An electrical synapse is a link between two
    neighboring neurons that is formed at a narrow
    gap between the pre- and postsynaptic cells
    called a gap junction.

143
144
  • At gap junctions, cells are about 3.5 nm from
    each other, a much shorter distance than the 20
    to 40 nm distance that separates cells at
    chemical synapses.

144
145
  • Electrical synapses. The image at the bottom
    right shows the location of gap junctions between
    cells.

145
146
  • Each gap junction has many channels which cross
    the plasma membranes of both cells. Gap junction
    channels are wide enough to allow ions and even
    medium sized molecules like signaling molecules
    to flow from one cell to the next.

146
147
  • For example, when positive ions move through the
    channel into the next cell, the extra positive
    charges depolarize the postsynaptic cell.

147
148
  • Signaling at electrical synapses is faster than
    the chemical signaling that occurs across
    chemical synapses.

148
149
  • Ions directly depolarize the cell without the
    need for receptors to recognize chemical
    messengers, which occurs at chemical synapses.

149
150
  • Such fast communication between neurons may
    indicate that in some parts of the brain large
    groups of neurons can work as a single unit to
    process information.

150
151
  • Electrical synapses are numerous in the retina
    and cerebral cortex.

151
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