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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 threedimensional 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
Segmental
ganglion

Figure 48.2d, e

Ventral
nerve cord

Segmental
ganglia

(d) Leech (annelid)

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(e) Insect (arthropod)

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

Figure 48.2f, g

(f) Chiton (mollusc)

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Ganglia

(g) Squid (mollusc)

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

Spinal
cord
(dorsal
nerve
cord)

Figure 48.2h

Sensory
ganglion

(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
system (PNS)

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Central nervous
system (CNS)

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
a sudden stretch in
the quadriceps.

3 Sensory neurons
convey the information
to the spinal cord.
Cell body of
sensory neuron
in dorsal
root ganglion

Quadriceps
muscle

4 The sensory neurons communicate with


motor neurons that supply the quadriceps. The
motor neurons convey signals to the quadriceps,
causing it to contract and jerking the lower leg forward.
Gray matter
5 Sensory neurons
from the quadriceps
also communicate
with interneurons
in the spinal cord.

White
matter

Hamstring
muscle
Spinal cord
(cross section)

Figure 48.4

1 The reflex is
initiated by tapping
the tendon connected
to the quadriceps
(extensor) muscle.

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Sensory neuron
Motor neuron
Interneuron

6 The interneurons
inhibit motor neurons
that supply the
hamstring (flexor)
muscle. This inhibition
prevents the hamstring
from contracting,
which would resist
the action of
the quadriceps.

Neuron Structure
Most of a neurons organelles
Are located in the cell body
Dendrites
Cell body

Nucleus

Synapse

Signal
Axon direction
Axon hillock

Presynaptic cell

Postsynaptic cell
Myelin sheath

Figure 48.5
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Synaptic
terminals

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 48.6ac (a) Sensory neuron


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(b) Interneurons

(c) Motor neuron

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

Figure 48.7
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50 m

Provide structural support for neurons and


regulate the extracellular concentrations of
ions and neurotransmitters

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
Axon

Myelin sheath

Nodes of
Ranvier

Schwann
cell
Nucleus of
Schwann cell

Figure 48.8

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0.1 m

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 m). 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

Figure 48.9

Reference
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
EXTRACELLULAR
FLUID

CYTOSOL
[Na+]
15 mM

[Na+]
150 mM

[K+]
150 mM

[K+]
5 mM

[Cl]
10 mM

[Cl]
+ 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
Outer
chamber

92 mV

150 mM
KCL

5 mM
KCL

Sodium +
channel

15 mM
NaCl

+
Cl

Artificial
membrane

Figure 48.11a, b (a) Membrane selectively permeable to K+


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+62 mV

Cl
K+

Potassium
channel

Inner
chamber

Inner
chamber

Outer
chamber

150 mM
NaCl

Na+

(b) Membrane selectively permeable to Na +

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
Stimuli
potential
Membrane potential (mV)

+50

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
Stimuli
potential
Membrane potential (mV)

+50

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

Membrane potential (mV)

Triggers a different type of response, called an


Stronger depolarizing stimulus
action potential
+50
Action
potential
0

50

Threshold

Resting
potential
100

Figure 48.12c

0 1 2 3 4 5 6
Time (msec)
(c) Action potential triggered by a
depolarization that reaches the
threshold.

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An action potential
Is a brief all-or-none depolarization of a
neurons plasma membrane
Is the type of signal that carries information
along axons

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Both voltage-gated Na+ channels and voltagegated 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+

+ +

+ +

+ +

+ +

K+
Rising phase of the action potential
Depolarization opens the activation
gates on most Na+ channels, while the
K+ channels activation gates remain
closed. Na+ influx makes the inside of
the membrane positive with respect
to the outside.
Na+
+ +

+ +

+50

+ +


K+

50

Depolarization A stimulus opens the


activation gates on some Na+ channels. Na+
influx through those channels depolarizes the
membrane. If the depolarization reaches the
threshold, it triggers an action potential.
Extracellular fluid

Na+

+ + + + + + + +

Action
potential
3

100
2

+ +

Na+
+ +

+ +

Sodium
channel

Figure 48.13

+ +

Falling phase of the action potential


The inactivation gates on
most Na+ channels close,
blocking Na+ influx. The
activation gates on most
K+ channels open,
permitting K+ efflux
which again makes
the inside of the cell
negative.

Threshold
5

Resting potential
Time

Na+

Potassium
channel

Activation
gates

+ +

+ +

+ +

K+

Inactivation
gate

Resting state
The activation gates on the Na+ and K+ channels
are closed, and the membranes resting potential is maintained.

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Na+

+ +

+ +

+ +

+ +

K+

Plasma membrane

Cytosol

+ +

K+

Membrane potential
(mV)

Na+

Na+

Undershoot
Both gates of the Na+ channels
are closed, but the activation gates on some K+
channels are still open. As these gates close on
most K+ channels, and the inactivation gates
open on Na+ channels, the membrane returns to
its resting state.

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

+ ++
Na
+ +

K+
+ +


+ +
K+

Figure 48.14

Action
potential

Na

+
+

+ +

K+
+ +


+ +
K+

Action
potential

+ ++
Na
+ +

+
+

An action potential is generated


as Na+ flows inward across the
membrane at one location.

The depolarization of the action


potential spreads to the neighboring
region of the membrane, re-initiating
the action potential there. To the left
of this region, the membrane is
repolarizing as K+ flows outward.

The depolarization-repolarization process is


repeated in the next region of the
membrane. In this way, local currents
of ions across the plasma membrane
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

5 m

Synaptic
terminal
of presynaptic
neurons

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

Synaptic vesicles
containing
neurotransmitter

5
Presynaptic
membrane

Neurotransmitter
Postsynaptic
membrane
Ligandgated
ion channel

Voltage-gated
Ca2+ channel
1 Ca2+

2
3

Synaptic cleft

Figure 48.17

Na+
K+

Ligand-gated
ion channels

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Postsynaptic
membrane

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

Membrane potential (mV)

Postsynaptic
neuron

Figure 48.18a

E1

Threshold of axon of
postsynaptic neuron

Resting
potential

70
E1

E1

(a) Subthreshold, no
summation

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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
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

Figure 48.18d

E1 + I

(d) Spatial summation


of EPSP and IPSP

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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
system (CNS)

Brain
Spinal cord

Peripheral nervous
system (PNS)
Cranial
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
vertebrates 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
nervous
system

Autonomic
nervous
system

Sympathetic
division

Figure 48.21
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Parasympathetic
division

Enteric
division

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

Sympathetic division

Action on target organs:


Location of
preganglionic neurons:
brainstem and sacral
segments of spinal cord

Neurotransmitter
released by
preganglionic neurons:
acetylcholine

Location of
postganglionic neurons:
in ganglia close to or
within target organs

Action on target organs:


Dilates pupil
of eye

Constricts pupil
of eye

Inhibits salivary
gland secretion

Stimulates salivary
gland secretion
Constricts
bronchi in lungs

Sympathetic
ganglia
Cervical

Accelerates heart

Slows heart

Stimulates activity
of stomach and
intestines

Inhibits activity of
stomach and intestines

Thoracic

Inhibits activity
of pancreas

Stimulates activity
of pancreas

Neurotransmitter
released by
postganglionic neurons:
acetylcholine

Stimulates
gallbladder

Stimulates glucose
release from liver;
inhibits gallbladder

Lumbar

Stimulates
adrenal medulla

Promotes emptying
of bladder

Figure 48.22

Promotes erection
of genitalia

Relaxes bronchi
in lungs

Inhibits emptying
of bladder

Synapse

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Sacral

Promotes ejaculation and


vaginal contractions

Location of
preganglionic neurons:
thoracic and lumbar
segments of spinal cord

Neurotransmitter
released by
preganglionic neurons:
acetylcholine

Location of
postganglionic neurons:
some in ganglia close to
target organs; others in
a chain of ganglia near
spinal cord

Neurotransmitter
released by
postganglionic neurons:
norepinephrine

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
hindbrain
Embryonic brain regions

Forebrain

Midbrain

Hindbrain

Midbrain

Hindbrain

Forebrain

Figure 48.23a
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(a) Embryo at one month

By the fifth week of human embryonic


development
Five brain regions have formed from the three
embryonic regions
Embryonic brain regions

Telencephalon
Diencephalon
Mesencephalon
Metencephalon
Myelencephalon

Mesencephalon
Metencephalon
Diencephalon

Myelencephalon

Spinal cord
Telencephalon

Figure 48.23b
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(b) Embryo at five weeks

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)


Cerebral hemisphere

Diencephalon:
Hypothalamus
Thalamus
Pineal gland
(part of epithalamus)
Brainstem:
Midbrain
Pons

Pituitary
gland
Spinal cord

Figure 48.23c

(c) Adult

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Cerebellum

Central canal

Medulla
oblongata

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
Reticular formation

Figure 48.24

Input from touch,


pain, and temperature
receptors

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Input from ears

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
Light

Dark

Light

Dark

1
Days of experiment

RESULTS

When the squirrels


were exposed to a regular light/dark
cycle, their wheel-turning activity
(indicated by the dark bars) occurred
at roughly the same time every day.
However, when they were kept in
constant darkness, their activity phase
began about 21 minutes later each day.

(b) Constant darkness

10

15

20

Figure 48.25

12

16

20

24

Time of day (hr)

12

12

16

20

24

Time of day (hr)

CONCLUSION
The northern flying squirrels 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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12

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
hemisphere

Right cerebral
hemisphere

Corpus
callosum
Neocortex

Figure 48.26

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Basal
nuclei

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

Speech
Smell

Figure 48.27

Temporal lobe

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Parietal lobe

co
rte
x

So
ma
tos

Frontal
association
area

en
so
ry

Mo
tor

co
rte
x

Frontal lobe

Speech

Taste

Somatosensory
association
area
Reading

Hearing
Auditory
association
area

Visual
association
area
Vision
Occipital lobe

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

Lips
Jaw
Tongue

Genitalia

Tongue
Pharynx
Primary
motor cortex

Figure 48.28
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Abdominal
organs

Primary
somatosensory
cortex

Leg

Hip

Fac

Trunk
Neck

Fin
ge
rs
Th
um
b
Ey
e
No
Fa s e
c
Lip e
s
Toes T
ee
Gu th
m
J aw s

Th
um
b
Ne
Bro ck
Ey w
e

Head

r arm
Uppe
ow
Elb
rm
rea
Fo
nd
Ha

Knee

Hip

t
ris
nd
Ha

Trunk
lder
Shou
ow
Elb
rm
rea
Fo

Fin
ge
rs

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
words

Seeing
words

Min
Figure 48.29

Speaking
words

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Generating
words

Portions of the frontal lobe, Brocas area and


Wernickes 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
Figure 48.30
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Hippocampus

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 survivalrelated 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
shocked just before the siphon is touched,
the withdrawal reflex is stronger. This
strengthening of the reflex is a simple form
of learning called sensitization.

Siphon
Mantle
Gill

Tail
Head

Figure 48.31a, b

(b) Sensitization involves interneurons that


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

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Gill withdrawal pathway


Touching
the siphon

Siphon sensory
neuron

Gill motor
neuron

Sensitization pathway
Shocking
the tail

Interneuron
Tail sensory
neuron

Gill

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


receptors, opening the AMPAreceptor channel and depolarizing
the postsynaptic membrane.

PRESYNAPTIC NEURON

7 NO diffuses into the


presynaptic neuron, causing
it to release more glutamate.

NO

6 Ca2+ stimulates the


postsynaptic neuron to
produce nitric oxide (NO).

Glutamate
AMPA receptor
NO

Figure 48.32

5 Ca2+ initiates the phosphorylation of AMPA receptors,


making them more responsive.
Ca2+ also causes more AMPA
receptors to appear in the
postsynaptic membrane.

NMDA
receptor

3 Glutamate also binds to NMDA


receptors. If the postsynaptic
membrane is simultaneously
depolarized, the NMDA-receptor
channel opens.

P
Ca2+

Signal transduction pathways


POSTSYNAPTIC NEURON

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4 Ca2+ diffuses into the


postsynaptic neuron.

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 axons 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
of motor neuron

Growth
cone

Netrin-1
receptor
Netrin-1
receptor
Slit
receptor
Netrin-1
Floor
plate
1 Growth toward the floor plate.
2
Cells in the floor plate of the
spinal cord release Netrin-1, which
diffuses away from the floor plate
and binds to receptors on the
growth cone of a developing
interneuron axon. Binding stimulates
axon growth toward the floor plate.

Figure 48.33a, b

Cell
adhesion
molecules
Growth across the mid-line.
3
Once the axon reaches the
floor plate, cell adhesion molecules
on the axon bind to complementary
molecules on floor plate cells,
directing the growth of the axon
across the midline.

Slit

No turning back.
Now the axon synthesizes
receptors that bind to Slit,
a repulsion protein released by floor plate cells.
This prevents the axon
from growing back across
the midline.

(a) Growth of an interneuron axon toward and across the midline of the spinal cord
(diagrammed here in cross section)

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Slit
receptor

Slit
Netrin-1

Netrin-1 and Slit, produced by cells


of the floor plate, bind to receptors
on the axons of motor neurons. In
this case, both proteins act to repel
the axon, directing the motor neuron
to grow away from the spinal cord.

(b) Growth of a motor neuron axon away


from the midline of the spinal cord

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

10 m

Contains stem cells that can differentiate into


mature neurons

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
patients loss of a productive life and the high
cost of long-term health care

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Schizophrenia
About 1% of the worlds 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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Alzheimers Disease
Alzheimers 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 m
Senile plaque

Figure 48.35
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Neurofibrillary tangle

A successful treatment for AD in humans


May hinge on early detection of senile plaques

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Parkinsons Disease
Parkinsons 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 Parkinsons disease


Although various approaches are used to
manage the symptoms

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