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Chapter 48

Nervous Systems

PowerPoint Lectures for


Biology, Seventh Edition
Neil Campbell and Jane Reece

Lectures by Chris Romero


Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings
• Overview: Command and Control Center

• The human brain


– Contains an estimated 100 billion nerve cells,
or neurons

• Each neuron
– May communicate with thousands of other
neurons

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• Functional magnetic resonance imaging
– Is a technology that can reconstruct a three-
dimensional map of brain activity

Figure 48.1

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• The results of brain imaging and other research
methods
– Reveal that groups of neurons function in
specialized circuits dedicated to different tasks

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• Concept 48.1: Nervous systems consist of
circuits of neurons and supporting cells
• All animals except sponges
– Have some type of nervous system

• What distinguishes the nervous systems of


different animal groups
– Is how the neurons are organized into circuits

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Organization of Nervous Systems
• The simplest animals with nervous systems,
the cnidarians
– Have neurons arranged in nerve nets

Nerve net

Figure 48.2a (a) Hydra (cnidarian)

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• Sea stars have a nerve net in each arm
– Connected by radial nerves to a central nerve
ring

Radial
nerve

Nerve
ring

Figure 48.2b (b) Sea star (echinoderm)

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• In relatively simple cephalized animals, such
as flatworms
– A central nervous system (CNS) is evident
Eyespot

Brain

Nerve
cord

Transverse
nerve

Figure 48.2c (c) Planarian (flatworm)

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• Annelids and arthropods
– Have segmentally arranged clusters of
neurons called ganglia

• These ganglia connect to the CNS


– And make up a peripheral nervous system
(PNS)
Brain Brain
Ventral
nerve cord
Ventral
nerve
cord
Segmental
Segmental ganglia
ganglion

Figure 48.2d, e (d) Leech (annelid) (e) Insect (arthropod)

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• Nervous systems in molluscs
– Correlate with the animals’ lifestyles

• Sessile molluscs have simple systems


– While more complex molluscs have more
sophisticated systems
Anterior
nerve ring Ganglia

Brain

Longitudinal
nerve cords Ganglia

Figure 48.2f, g (f) Chiton (mollusc) (g) Squid (mollusc)

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• In vertebrates
– The central nervous system consists of a brain
and dorsal spinal cord
– The PNS connects to the CNS

Brain

Sensory
Spinal
ganglion
cord
(dorsal
nerve
cord)

Figure 48.2h (h) Salamander (chordate)

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Information Processing
• Nervous systems process information in three
stages
– Sensory input, integration, and motor output

Sensory input

Integration
Sensor

Motor output

Effector
Figure 48.3 Peripheral nervous Central nervous
system (PNS) system (CNS)
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• Sensory neurons transmit information from
sensors
– That detect external stimuli and internal
conditions

• Sensory information is sent to the CNS


– Where interneurons integrate the information

• Motor output leaves the CNS via motor


neurons
– Which communicate with effector cells
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• The three stages of information processing
– Are illustrated in the knee-jerk reflex
2 Sensors detect 3 Sensory neurons 4 The sensory neurons communicate with
a sudden stretch in convey the information motor neurons that supply the quadriceps. The
the quadriceps. to the spinal cord. motor neurons convey signals to the quadriceps,
Cell body of causing it to contract and jerking the lower leg forward.
sensory neuron
in dorsal Gray matter
root ganglion 5 Sensory neurons
Quadriceps from the quadriceps
muscle also communicate
White with interneurons
matter in the spinal cord.

Hamstring
muscle 6 The interneurons
inhibit motor neurons
that supply the
Spinal cord hamstring (flexor)
(cross section) muscle. This inhibition
prevents the hamstring
Sensory neuron from contracting,
Motor neuron which would resist
1 The reflex is the action of
Interneuron
initiated by tapping the quadriceps.
the tendon connected
to the quadriceps
Figure 48.4 (extensor) muscle.

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Neuron Structure
• Most of a neuron’s organelles
– Are located in the cell body
Dendrites

Cell body

Nucleus
Synapse
Signal
Axon direction
Axon hillock

Presynaptic cell Postsynaptic cell


Myelin sheath

Synaptic
Figure 48.5
terminals
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• Most neurons have dendrites
– Highly branched extensions that receive
signals from other neurons

• The axon is typically a much longer extension


– That transmits signals to other cells at
synapses
– That may be covered with a myelin sheath

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• Neurons have a wide variety of shapes
– That reflect their input and output interactions
Dendrites

Axon

Cell
body

Figure 48.6a–c (a) Sensory neuron (b) Interneurons (c) Motor neuron
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Supporting Cells (Glia)
• Glia are supporting cells
– That are essential for the structural integrity of
the nervous system and for the normal
functioning of neurons

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• In the CNS, astrocytes
– Provide structural support for neurons and
regulate the extracellular concentrations of
ions and neurotransmitters

50 µm
Figure 48.7
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• Oligodendrocytes (in the CNS) and Schwann
cells (in the PNS)
– Are glia that form the myelin sheaths around
the axons of many vertebrate neurons

Node of Ranvier
Layers of myelin
Axon
Schwann
cell Schwann
cell
Nodes of Nucleus of
Axon Myelin sheath
Ranvier Schwann cell
Figure 48.8
0.1 µm

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• Concept 48.2: Ion pumps and ion channels
maintain the resting potential of a neuron
• Across its plasma membrane, every cell has a
voltage
– Called a membrane potential

• The inside of a cell is negative


– Relative to the outside

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• The membrane potential of a cell can be
measured
APPLICATION Electrophysiologists use intracellular recording to measure the membrane potential of
neurons and other cells.

TECHNIQUE A microelectrode is made from a glass capillary tube filled with an electrically conductive
salt solution. One end of the tube tapers to an extremely fine tip (diameter < 1 µm). While looking through a
microscope, the experimenter uses a micropositioner to insert the tip of the microelectrode into a cell. A
voltage recorder (usually an oscilloscope or a computer-based system) measures the voltage between the
microelectrode tip inside the cell and a reference electrode placed in the solution outside the cell.

Microelectrode
–70 mV

Voltage
recorder

Reference
Figure 48.9 electrode
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The Resting Potential
• The resting potential
– Is the membrane potential of a neuron that is
not transmitting signals

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• In all neurons, the resting potential
– Depends on the ionic gradients that exist
across the plasma membrane
CYTOSOL EXTRACELLULAR
FLUID

[Na+] – + [Na+]
15 mM 150 mM

[K+] – + [K+]
150 mM 5 mM
– +
[Cl–] [Cl–]
10 mM – + 120 mM

[A–]
100 mM – +

Plasma
membrane

Figure 48.10
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• The concentration of Na+ is higher in the
extracellular fluid than in the cytosol
– While the opposite is true for K+

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• By modeling a mammalian neuron with an
artificial membrane
– We can gain a better understanding of the
resting potential of a neuron
Inner Outer
chamber –92 mV chamber Inner +62 mV Outer
chamber chamber

– +
+ –
150 mM 5 mM 15 mM 150 mM
KCL KCL NaCl NaCl

Cl–
– +
+ –

K+ Na+
– + Cl–
Potassium Sodium + –
Artificial
channel channel
membrane

Figure 48.11a, b (a) Membrane selectively permeable to K+ (b) Membrane selectively permeable to Na+
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• A neuron that is not transmitting signals
– Contains many open K+ channels and fewer
open Na+ channels in its plasma membrane

• The diffusion of K+ and Na+ through these


channels
– Leads to a separation of charges across the
membrane, producing the resting potential

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Gated Ion Channels
• Gated ion channels open or close
– In response to membrane stretch or the
binding of a specific ligand
– In response to a change in the membrane
potential

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• Concept 48.3: Action potentials are the signals
conducted by axons
• If a cell has gated ion channels
– Its membrane potential may change in
response to stimuli that open or close those
channels

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• Some stimuli trigger a hyperpolarization
– An increase in the magnitude of the membrane
potential Stimuli
+50

Membrane potential (mV)


0

–50 Threshold

Resting
potential Hyperpolarizations
–100
0 1 2 3 4 5
Time (msec)
(a) Graded hyperpolarizations
produced by two stimuli that
increase membrane permeability
to K+. The larger stimulus produces
Figure 48.12a a larger hyperpolarization.
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• Other stimuli trigger a depolarization
– A reduction in the magnitude of the membrane
potential Stimuli
+50

Membrane potential (mV)


0

–50 Threshold

Resting Depolarizations
potential
–100
0 1 2 3 4 5
Time (msec)
(b) Graded depolarizations produced
by two stimuli that increase
membrane permeability to Na+.
The larger stimulus produces a
Figure 48.12b larger depolarization.
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• Hyperpolarization and depolarization
– Are both called graded potentials because the
magnitude of the change in membrane
potential varies with the strength of the
stimulus

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Production of Action Potentials
• In most neurons, depolarizations
– Are graded only up to a certain membrane
voltage, called the threshold

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• A stimulus strong enough to produce a
depolarization that reaches the threshold
– Triggers a different type of response, called an
action potential +50
Stronger depolarizing stimulus

Action

Membrane potential (mV)


potential

Threshold
–50

Resting
potential
–100
0 1 2 3 4 5 6
Time (msec)
(c) Action potential triggered by a
depolarization that reaches the
Figure 48.12c threshold.
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• An action potential
– Is a brief all-or-none depolarization of a
neuron’s plasma membrane
– Is the type of signal that carries information
along axons

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• Both voltage-gated Na+ channels and voltage-
gated K+ channels
– Are involved in the production of an action
potential

• When a stimulus depolarizes the membrane


– Na+ channels open, allowing Na+ to diffuse into
the cell

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• As the action potential subsides
– K+ channels open, and K+ flows out of the cell

• A refractory period follows the action potential


– During which a second action potential cannot
be initiated

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• The generation of an action potential
Na+ Na+

– – – – – – – – Na+ Na+

+ + + + + + + +
+ + + + + + + +

K+ – – – – – – – –

3 Rising phase of the action potential K+


Depolarization opens the activation
gates on most Na+ channels, while the 4 Falling phase of the action potential
K+ channels’ activation gates remain The inactivation gates on
closed. Na+ influx makes the inside of most Na+ channels close,
the membrane positive with respect blocking Na+ influx. The
to the outside. activation gates on most
+50
Action K+ channels open,

Membrane potential
Na+ Na+ potential permitting K+ efflux
3 which again makes
+ + + + + + + + 0
the inside of the cell

(mV)
2 4 negative.
Threshold
– – – – – – – – –50
1 5 1
K+
Resting potential
–100
2 Depolarization A stimulus opens the Time
activation gates on some Na+ channels. Na+
influx through those channels depolarizes the
membrane. If the depolarization reaches the Na+ Na+
threshold, it triggers an action potential.
+ + + + + + + +
Extracellular fluid Activation
Potassium gates
Na+
channel
– – – – – – – –
+ + + + + + + + + + + + + +
K+
Plasma membrane
– – – – – – – – – – – – – – Undershoot
5 Both gates of the Na+ channels
Cytosol are closed, but the activation gates on some K+
Sodium K+ Inactivation
channels are still open. As these gates close on
channel gate
most K+ channels, and the inactivation gates
1 Resting state The activation gates on the Na+ and K+ channels open on Na+ channels, the membrane returns to
Figure 48.13 are closed, and the membrane’s resting potential is maintained. its resting state.

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Conduction of Action Potentials
• An action potential can travel long distances
– By regenerating itself along the axon

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• At the site where the action potential is
generated, usually the axon hillock
– An electrical current depolarizes the
neighboring region of the axon membrane
Axon

Action
potential
– – + + + + + +
+ ++ – – – – – –
1 An action potential is generated
Na
+ + – – – – – – as Na+ flows inward across the
– – + + + + + + membrane at one location.

Action 2 The depolarization of the action


K+ potential
+ + – – + + + + potential spreads to the neighboring
– – +
Na +
+ – – – – region of the membrane, re-initiating
– – + + – – – –
the action potential there. To the left
+ + – – + + + +
K+ of this region, the membrane is
repolarizing as K+ flows outward.
Action The depolarization-repolarization process is
3
K+ potential
+ + + + – – – – repeated in the next region of the
– – – – + ++ + + membrane. In this way, local currents
– – – – Na + +
+ + of ions across the plasma membrane
+ + – – – –
Figure 48.14 + +
K+
cause the action potential to be propagated
along the length of the axon.

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Conduction Speed
• The speed of an action potential
– Increases with the diameter of an axon

• In vertebrates, axons are myelinated


– Also causing the speed of an action potential
to increase

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• Action potentials in myelinated axons
– Jump between the nodes of Ranvier in a
process called saltatory conduction
Schwann cell

Depolarized region
(node of Ranvier)
Myelin
sheath

––

––
+ –
Cell body ++ +
+ +
++
Axon
–– +
– ++
––

Figure 48.15

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• Concept 48.4: Neurons communicate with
other cells at synapses
• In an electrical synapse
– Electrical current flows directly from one cell to
another via a gap junction

• The vast majority of synapses


– Are chemical synapses

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• In a chemical synapse, a presynaptic neuron
– Releases chemical neurotransmitters, which
are stored in the synaptic terminal
Postsynaptic
neuron

Synaptic
terminal
of presynaptic
neurons

5 µm
Figure 48.16
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• When an action potential reaches a terminal
– The final result is the release of
neurotransmitters into the synaptic cleft
Postsynaptic cell
Presynaptic
cell

5 Na+
Synaptic vesicles Neuro-
K+
containing transmitter
Presynaptic
neurotransmitter
membrane
Postsynaptic
membrane

Ligand-
gated
Voltage-gated ion channel
Ca2+ channel
1 Ca2+
4 Postsynaptic
2 6
membrane

Synaptic cleft 3

Ligand-gated
Figure 48.17 ion channels

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Direct Synaptic Transmission
• The process of direct synaptic transmission
– Involves the binding of neurotransmitters to
ligand-gated ion channels

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• Neurotransmitter binding
– Causes the ion channels to open, generating a
postsynaptic potential

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• Postsynaptic potentials fall into two categories
– Excitatory postsynaptic potentials (EPSPs)

– Inhibitory postsynaptic potentials (IPSPs)

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• After its release, the neurotransmitter
– Diffuses out of the synaptic cleft

– May be taken up by surrounding cells and


degraded by enzymes

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Summation of Postsynaptic Potentials
• Unlike action potentials
– Postsynaptic potentials are graded and do not
regenerate themselves

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• Since most neurons have many synapses on
their dendrites and cell body
– A single EPSP is usually too small to trigger an
action potential in a postsynaptic neuron
Terminal branch of
presynaptic neuron

Postsynaptic
neuron E1

Threshold of axon of
Membrane potential (mV)

0 postsynaptic neuron

Resting
potential

–70
E1 E1

(a) Subthreshold, no
summation
Figure 48.18a
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• If two EPSPs are produced in rapid succession
– An effect called temporal summation occurs

E1

Axon
hillock

Action
potential

E1 E1

(b) Temporal summation

Figure 48.18b

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• In spatial summation
– EPSPs produced nearly simultaneously by
different synapses on the same postsynaptic
neuron add together E 1
E2

Action
potential

E1 + E2

(c) Spatial summation


Figure 48.18c
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• Through summation
– An IPSP can counter the effect of an EPSP
E1

E1 I E1 + I
(d) Spatial summation
of EPSP and IPSP
Figure 48.18d

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Indirect Synaptic Transmission
• In indirect synaptic transmission
– A neurotransmitter binds to a receptor that is
not part of an ion channel

• This binding activates a signal transduction


pathway
– Involving a second messenger in the
postsynaptic cell, producing a slowly
developing but long-lasting effect

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Neurotransmitters
• The same neurotransmitter
– Can produce different effects in different types
of cells

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• Major neurotransmitters

Table 48.1

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Acetylcholine
• Acetylcholine
– Is one of the most common neurotransmitters
in both vertebrates and invertebrates
– Can be inhibitory or excitatory

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Biogenic Amines
• Biogenic amines
– Include epinephrine, norepinephrine,
dopamine, and serotonin
– Are active in the CNS and PNS

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Amino Acids and Peptides
• Various amino acids and peptides
– Are active in the brain

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Gases
• Gases such as nitric oxide and carbon
monoxide
– Are local regulators in the PNS

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• Concept 48.5: The vertebrate nervous system
is regionally specialized
• In all vertebrates, the nervous system
– Shows a high degree of cephalization and
distinct CNS and PNS components Central nervous
Peripheral nervous
system (CNS)
system (PNS)
Brain Cranial
Spinal cord nerves
Ganglia
outside
CNS
Spinal
nerves

Figure 48.19
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• The brain provides the integrative power
– That underlies the complex behavior of
vertebrates

• The spinal cord integrates simple responses to


certain kinds of stimuli
– And conveys information to and from the brain

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• The central canal of the spinal cord and the
four ventricles of the brain
– Are hollow, since they are derived from the
dorsal embryonic nerve cord

Gray matter
White
matter

Ventricles

Figure 48.20

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The Peripheral Nervous System
• The PNS transmits information to and from the
CNS
– And plays a large role in regulating a
vertebrate’s movement and internal
environment

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• The cranial nerves originate in the brain
– And terminate mostly in organs of the head
and upper body

• The spinal nerves originate in the spinal cord


– And extend to parts of the body below the
head

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• The PNS can be divided into two functional
components
– The somatic nervous system and the
autonomic nervous system
Peripheral
nervous system

Somatic Autonomic
nervous nervous
system system

Sympathetic Parasympathetic Enteric


division division division

Figure 48.21

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• The somatic nervous system
– Carries signals to skeletal muscles

• The autonomic nervous system


– Regulates the internal environment, in an
involuntary manner
– Is divided into the sympathetic,
parasympathetic, and enteric divisions

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• The sympathetic and parasympathetic
divisions
– Have antagonistic effects on target organs
Parasympathetic division
Action on target organs:
Sympathetic division

Action on target organs:

Constricts pupil Dilates pupil


Location of of eye Location of
preganglionic neurons: of eye
preganglionic neurons:
brainstem and sacral thoracic and lumbar
segments of spinal cord Stimulates salivary Inhibits salivary
gland secretion segments of spinal cord
gland secretion
Sympathetic
Neurotransmitter Constricts ganglia Relaxes bronchi Neurotransmitter
released by bronchi in lungs Cervical in lungs released by
preganglionic neurons:
preganglionic neurons:
acetylcholine
Slows heart Accelerates heart acetylcholine

Inhibits activity of
stomach and intestines
Location of Stimulates activity Thoracic Location of
postganglionic neurons: of stomach and postganglionic neurons:
in ganglia close to or intestines Inhibits activity
some in ganglia close to
within target organs of pancreas
target organs; others in
Stimulates activity a chain of ganglia near
of pancreas Stimulates glucose spinal cord
release from liver;
inhibits gallbladder
Stimulates Lumbar
Neurotransmitter
gallbladder
released by Stimulates Neurotransmitter
postganglionic neurons: adrenal medulla released by
acetylcholine postganglionic neurons:
Promotes emptying norepinephrine
Inhibits emptying
of bladder
of bladder

Promotes erection Promotes ejaculation and


of genitalia Sacral
Figure 48.22 Synapse vaginal contractions

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• The sympathetic division
– Correlates with the “fight-or-flight” response

• The parasympathetic division


– Promotes a return to self-maintenance
functions

• The enteric division


– Controls the activity of the digestive tract,
pancreas, and gallbladder

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Embryonic Development of the Brain
• In all vertebrates
– The brain develops from three embryonic
regions: the forebrain, the midbrain, and the
Embryonic brain regions

hindbrain
Forebrain

Midbrain

Hindbrain

Midbrain Hindbrain

Forebrain

(a) Embryo at one month


Figure 48.23a
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• By the fifth week of human embryonic
development
– Five brain regions have formed from the three Embryonic brain regions

embryonic regions
Telencephalon

Diencephalon

Mesencephalon

Metencephalon

Myelencephalon

Mesencephalon
Metencephalon
Diencephalon
Myelencephalon

Spinal cord
Telencephalon

Figure 48.23b (b) Embryo at five weeks

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• As a human brain develops further
– The most profound change occurs in the
forebrain, which gives rise to the cerebrum
Brain structures present in adult

Cerebrum (cerebral hemispheres; includes cerebral


cortex, white matter, basal nuclei)

Diencephalon (thalamus, hypothalamus, epithalamus)

Midbrain (part of brainstem)

Pons (part of brainstem), cerebellum

Medulla oblongata (part of brainstem)

Diencephalon:
Cerebral hemisphere Hypothalamus
Thalamus
Pineal gland
(part of epithalamus)

Brainstem:

Midbrain
Pons
Pituitary
gland Medulla
oblongata
Spinal cord Cerebellum
Central canal
(c) Adult
Figure 48.23c
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The Brainstem
• The brainstem consists of three parts
– The medulla oblongata, the pons, and the
midbrain

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• The medulla oblongata
– Contains centers that control several visceral
functions

• The pons
– Also participates in visceral functions

• The midbrain
– Contains centers for the receipt and integration
of several types of sensory information

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Arousal and Sleep
• A diffuse network of neurons called the
reticular formation
– Is present in the core of the brainstem

Eye
Input from ears
Reticular formation
Input from touch,
pain, and temperature
Figure 48.24 receptors

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• A part of the reticular formation, the reticular
activating system (RAS)
– Regulates sleep and arousal

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The Cerebellum
• The cerebellum
– Is important for coordination and error
checking during motor, perceptual, and
cognitive functions

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• The cerebellum
– Is also involved in learning and remembering
motor skills

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The Diencephalon
• The embryonic diencephalon develops into
three adult brain regions
– The epithalamus, thalamus, and hypothalamus

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• The epithalamus
– Includes the pineal gland and the choroid
plexus

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• The thalamus
– Is the main input center for sensory information
going to the cerebrum and the main output
center for motor information leaving the
cerebrum

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• The hypothalamus regulates
– Homeostasis

– Basic survival behaviors such as feeding,


fighting, fleeing, and reproducing

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Circadian Rhythms
• The hypothalamus also regulates circadian
rhythms
– Such as the sleep/wake cycle

• Animals usually have a biological clock


– Which is a pair of suprachiasmatic nuclei
(SCN) found in the hypothalamus

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• Biological clocks usually require external cues
– To remain synchronized with environmental cycles
EXPERIMENT In the northern flying squirrel (Glaucomys sabrinus), activity normally begins with the onset of darkness and ends
at dawn, which suggests that light is an important external cue for the squirrel. To test this idea, researchers monitored the activity of captive
squirrels for 23 days under two sets of conditions: (a) a regular cycle of 12 hours of light and 12 hours of darkness and (b) constant darkness.
The squirrels were given free access to an exercise wheel and a rest cage. A recorder automatically noted when the wheel was rotating and
when it was still.
(a) 12 hr light-12 hr dark cycle (b) Constant darkness
Light Dark Light Dark

RESULTS 1
When the squirrels
were exposed to a regular light/dark
cycle, their wheel-turning activity 5
Days of experiment

(indicated by the dark bars) occurred


at roughly the same time every day.
However, when they were kept in 10
constant darkness, their activity phase
began about 21 minutes later each day.
15

20

12 16 20 24 4 8 12 12 16 20 24 4 8 12
Figure 48.25
Time of day (hr) Time of day (hr)

CONCLUSION The northern flying squirrel’s internal clock can run in constant darkness, but it does so on
its own cycle, which lasts about 24 hours and 21 minutes. External (light) cues keep the clock running on a 24-hour cycle.
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The Cerebrum
• The cerebrum
– Develops from the embryonic telencephalon

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• The cerebrum has right and left cerebral
hemispheres
– That each consist of cerebral cortex overlying
white matter and basal nuclei
Left cerebral Right cerebral
hemisphere hemisphere

Corpus
callosum
Basal
nuclei
Neocortex

Figure 48.26

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• The basal nuclei
– Are important centers for planning and learning
movement sequences

• In mammals
– The cerebral cortex has a convoluted surface
called the neocortex

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• In humans, the largest and most complex part
of the brain
– Is the cerebral cortex, where sensory
information is analyzed, motor commands are
issued, and language is generated

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• A thick band of axons, the corpus callosum
– Provides communication between the right and
left cerebral cortices

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• Concept 48.6: The cerebral cortex controls
voluntary movement and cognitive functions
• Each side of the cerebral cortex has four lobes
– Frontal, parietal, temporal, and occipital
Frontal lobe Parietal lobe

x
rte
x
rte

co
co

ry
so
tor
Somatosensory

en
Mo
Frontal Speech association

tos
association area

ma
Taste
area So
Reading
Speech
Hearing
Visual
Smell association
Auditory area
association
area
Vision

Figure 48.27 Temporal lobe Occipital lobe

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• Each of the lobes
– Contains primary sensory areas and
association areas

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Information Processing in the Cerebral Cortex
• Specific types of sensory input
– Enter the primary sensory areas

• Adjacent association areas


– Process particular features in the sensory input
and integrate information from different
sensory areas

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• In the somatosensory cortex and motor cortex
– Neurons are distributed according to the part
of the body that generates sensory input or
receives motor input
Frontal lobe Parietal lobe

Uppe
Shou
Elb
For

Head
Trunk

Knee

Trunk
Neck
Hip
ow

Leg
ear

r arm
lder

Elb
W

Hip
For
m
ris
Ha

ow
ear
Fin
t
nd

ge

Ha
rs

m
Fin

nd
ge
Th Th rs
um um
Ne b Ey b
Br c k e
ow No
Ey Fa s e
e c
Fac Lip e Genitalia
e Toes T s
ee
Gu th
m
Jaw s
Lips
Jaw Tongue
Tongue
Pharynx
Primary Primary
motor cortex Abdominal somatosensory
organs cortex
Figure 48.28

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Lateralization of Cortical Function
• During brain development, in a process called
lateralization
– Competing functions segregate and displace
each other in the cortex of the left and right
cerebral hemispheres

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• The left hemisphere
– Becomes more adept at language, math,
logical operations, and the processing of serial
sequences

• The right hemisphere


– Is stronger at pattern recognition, nonverbal
thinking, and emotional processing

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Language and Speech
• Studies of brain activity
– Have mapped specific areas of the brain
responsible for language and speech
Max

Hearing Seeing
words words

Min
Speaking Generating
words words
Figure 48.29
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• Portions of the frontal lobe, Broca’s area and
Wernicke’s area
– Are essential for the generation and
understanding of language

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Emotions
• The limbic system
– Is a ring of structures around the brainstem
Thalamus
Hypothalamus

Prefrontal cortex

Olfactory
bulb
Amygdala Hippocampus

Figure 48.30
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• This limbic system includes three parts of the
cerebral cortex
– The amygdala, hippocampus, and olfactory
bulb

• These structures interact with the neocortex to


mediate primary emotions
– And attach emotional “feelings” to survival-
related functions

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• Structures of the limbic system form in early
development
– And provide a foundation for emotional
memory, associating emotions with particular
events or experiences

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Memory and Learning
• The frontal lobes
– Are a site of short-term memory

– Interact with the hippocampus and amygdala


to consolidate long-term memory

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• Many sensory and motor association areas of
the cerebral cortex
– Are involved in storing and retrieving words
and images

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Cellular Mechanisms of Learning
• Experiments on invertebrates
– Have revealed the cellular basis of some types
of learning
(a) Touching the siphon triggers a reflex that
causes the gill to withdraw. If the tail is Siphon
shocked just before the siphon is touched,
the withdrawal reflex is stronger. This Mantle
strengthening of the reflex is a simple form
of learning called sensitization. Gill

Tail

Head

(b) Sensitization involves interneurons that


make synapses on the synaptic terminals of
Gill withdrawal pathway
the siphon sensory neurons. When the tail
is shocked, the interneurons release
serotonin, which activates a signal Touching
Siphon sensory Gill motor
transduction pathway that closes K+ the siphon
neuron neuron
channels in the synaptic terminals of Gill
the siphon sensory neurons. As a result, Sensitization pathway
action potentials in the siphon sensory
neurons produce a prolonged Interneuron
Shocking
depolarization of the terminals. That allows
the tail Tail sensory
more Ca2+ to diffuse into the terminals,
which causes the terminals to release more neuron
of their excitatory neurotransmitter onto the gill
motor neurons. In response, the motor neurons
generate action potentials at a higher frequency,
Figure 48.31a, b producing a more forceful gill withdrawal.

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• In the vertebrate brain, a form of learning called
long-term potentiation (LTP)
– Involves an increase in the strength of synaptic
transmission 1 The presynaptic
neuron releases glutamate.

2 Glutamate binds to AMPA


PRESYNAPTIC NEURON receptors, opening the AMPA-
receptor channel and depolarizing
the postsynaptic membrane.
7 NO diffuses into the
presynaptic neuron, causing
it to release more glutamate. NO

6 Ca2+ stimulates the NMDA 3 Glutamate also binds to NMDA


receptor receptors. If the postsynaptic
postsynaptic neuron to Glutamate
produce nitric oxide (NO). membrane is simultaneously
AMPA receptor
depolarized, the NMDA-receptor
channel opens.
NO P
5 Ca2+ initiates the phos-
Ca2+
phorylation of AMPA receptors,
making them more responsive.
Ca2+ also causes more AMPA
Signal transduction pathways
receptors to appear in the 4 Ca2+ diffuses into the
Figure 48.32 postsynaptic membrane.
POSTSYNAPTIC NEURON
postsynaptic neuron.

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Consciousness
• Modern brain-imaging techniques
– Suggest that consciousness may be an
emergent property of the brain that is based on
activity in many areas of the cortex

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• Concept 48.7: CNS injuries and diseases are
the focus of much research
• Unlike the PNS, the mammalian CNS
– Cannot repair itself when damaged or
assaulted by disease

• Current research on nerve cell development


and stem cells
– May one day make it possible for physicians to
repair or replace damaged neurons

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Nerve Cell Development
• Signal molecules direct an axon’s growth
– By binding to receptors on the plasma
membrane of the growth cone

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• This receptor binding triggers a signal
transduction pathway
– Which may cause an axon to grow toward or
away from the source of the signal
Midline of
spinal cord
Developing axon
of interneuron

Developing axon
Growth of motor neuron
cone
Netrin-1
receptor
Netrin-1
receptor

Slit
receptor
Netrin-1
Slit
Cell Netrin-1
Floor Slit
plate adhesion
Slit receptor
molecules
1 Growth toward the floor plate. 2 Growth across the mid-line. 3 No turning back. Netrin-1 and Slit, produced by cells
Cells in the floor plate of the Once the axon reaches the Now the axon synthesizes of the floor plate, bind to receptors
spinal cord release Netrin-1, which floor plate, cell adhesion molecules receptors that bind to Slit, on the axons of motor neurons. In
diffuses away from the floor plate on the axon bind to complementary a repulsion protein re- this case, both proteins act to repel
and binds to receptors on the molecules on floor plate cells, leased by floor plate cells. the axon, directing the motor neuron
growth cone of a developing directing the growth of the axon This prevents the axon to grow away from the spinal cord.
interneuron axon. Binding stimulates across the midline. from growing back across
axon growth toward the floor plate. the midline.

Figure 48.33a, b (a) Growth of an interneuron axon toward and across the midline of the spinal cord
(diagrammed here in cross section)
(b) Growth of a motor neuron axon away
from the midline of the spinal cord

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• The genes and basic events involved in axon
guidance
– Are similar in invertebrates and vertebrates

• Knowledge of these events may be applied one


day
– To stimulate axonal regrowth following CNS
damage

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Neural Stem Cells
• The adult human brain
– Contains stem cells that can differentiate into
mature neurons

10 µm
Figure 48.34
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• The induction of stem cell differentiation and
the transplantation of cultured stem cells
– Are potential methods for replacing neurons
lost to trauma or disease

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Diseases and Disorders of the Nervous System
• Mental illnesses and neurological disorders
– Take an enormous toll on society, in both the
patient’s loss of a productive life and the high
cost of long-term health care

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Schizophrenia
• About 1% of the world’s population
– Suffers from schizophrenia

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• Schizophrenia is characterized by
– Hallucinations, delusions, blunted emotions,
and many other symptoms

• Available treatments have focused on


– Brain pathways that use dopamine as a
neurotransmitter

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Depression
• Two broad forms of depressive illness are
known
– Bipolar disorder and major depression

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• Bipolar disorder is characterized by
– Manic (high-mood) and depressive (low-mood)
phases

• In major depression
– Patients have a persistent low mood

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• Treatments for these types of depression
include
– A variety of drugs such as Prozac and lithium

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Alzheimer’s Disease
• Alzheimer’s disease (AD)
– Is a mental deterioration characterized by
confusion, memory loss, and other symptoms

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• AD is caused by the formation of
– Neurofibrillary tangles and senile plaques in
the brain 20 µm
Senile plaque Neurofibrillary tangle

Figure 48.35
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• A successful treatment for AD in humans
– May hinge on early detection of senile plaques

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Parkinson’s Disease
• Parkinson’s disease is a motor disorder
– Caused by the death of dopamine-secreting
neurons in the substantia nigra
– Characterized by difficulty in initiating
movements, slowness of movement, and
rigidity

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• There is no cure for Parkinson’s disease
– Although various approaches are used to
manage the symptoms

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