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Chapter 48

Nervous Systems

PowerPoint Lectures for Biology, Seventh Edition


Neil Campbell and Jane Reece

Lectures by Chris Romero


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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 Ventral nerve cord Segmental ganglion

Segmental ganglia

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

Spinal cord (dorsal nerve cord)

Sensory ganglion

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

Sensor

Integration

Motor output

Effector
Figure 48.3

Peripheral nervous system (PNS)

Central nervous 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 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 White matter 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.

Hamstring muscle

Spinal cord (cross section) Sensory neuron Motor neuron 1 The reflex is initiated by tapping the tendon connected to the quadriceps (extensor) muscle. 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.

Figure 48.4

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Neuron Structure Most of a neurons organelles


Are located in the cell body
Dendrites Cell body

Nucleus Signal Axon direction Axon hillock

Synapse

Presynaptic cell Myelin sheath

Postsynaptic cell

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


Provide structural support for neurons and regulate the extracellular concentrations of ions and neurotransmitters

Figure 48.7
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50 m

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 Figure 48.8
Myelin sheath

Nodes of Ranvier

Schwann cell Nucleus of Schwann cell


0.1 m

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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 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 Reference electrode

Figure 48.9

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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+] 15 mM
[K+] 150 mM

[Na+] 150 mM [K+] 5 mM

+ +

[Cl] 10 mM [A] 100 mM

[Cl] + 120 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 chamber 92 mV Outer chamber Inner chamber +62 mV Outer chamber + 150 mM KCL + Potassium channel 150 mM NaCl

5 mM KCL

15 mM NaCl
Cl

+
Na+ Sodium + channel

K+ +

Cl

Artificial membrane

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


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(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
+50 Membrane potential (mV)

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
+50
Membrane potential (mV)

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 Stronger depolarizing stimulus action potential
+50 Membrane potential (mV)

Action potential
0

50

Threshold

Resting potential 100 0 1 2 3 4 5 6 Time (msec) (c) Action potential triggered by a depolarization that reaches the threshold.

Figure 48.12c

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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+ 3 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+ + + + + + + Na+ + + + + + + K+ 4 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. Na+ + + + + Na+ + +

+50 Membrane potential (mV)

Action potential 3 2 Threshold 1 Resting potential Time 5 1 4

K+

50

100 2 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+ + + + + + + + + Plasma membrane Cytosol Sodium channel K+ Potassium channel + +

Na+ Activation gates + + + + K+ Inactivation gate 5 + + + +

Na+ + + + +

Figure 48.13

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

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.

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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
+ ++ Na + +

+ +

+ +

+ +

+ +

+ +

+ + 1

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

K+ + + + + K+

Action potential
+

2 + + + + + + + +

+ +

Na

+ +

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.

Figure 48.14

+ +

+
+

K+ + + + + K+

Action potential
+ + + Na + +

3 + +

+ +

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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

Figure 48.16
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5 m

When an action potential reaches a terminal


The final result is the release of neurotransmitters into the synaptic cleft
Presynaptic cell Postsynaptic cell

Synaptic vesicles containing neurotransmitter

5 Presynaptic membrane

Na+ K+

Neurotransmitter Postsynaptic membrane Ligandgated ion channel

Voltage-gated Ca2+ channel 1 Ca2+ 2 Synaptic cleft 3 4 Postsynaptic membrane 6

Figure 48.17

Ligand-gated 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

Membrane potential (mV)

Threshold of axon of postsynaptic neuron Resting potential

70 E1 E1

Figure 48.18a

(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
1

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

E1 + I

Figure 48.18d

(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

Parasympathetic division

Enteric 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: Location of preganglionic neurons: brainstem and sacral segments of spinal cord Constricts pupil of eye Stimulates salivary gland secretion Constricts bronchi in lungs Slows heart Sympathetic ganglia Cervical Sympathetic division

Action on target organs:


Dilates pupil of eye Inhibits salivary gland secretion Relaxes bronchi in lungs Accelerates heart Location of preganglionic neurons: thoracic and lumbar segments of spinal cord

Neurotransmitter released by preganglionic neurons: acetylcholine

Neurotransmitter released by preganglionic neurons: acetylcholine

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

Stimulates activity of stomach and intestines Stimulates activity of pancreas

Thoracic

Inhibits activity of stomach and intestines Inhibits activity of pancreas Stimulates glucose release from liver; inhibits gallbladder 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: acetylcholine

Stimulates gallbladder

Lumbar Stimulates adrenal medulla Neurotransmitter released by postganglionic neurons: norepinephrine

Promotes emptying of bladder Promotes erection of genitalia

Inhibits emptying of bladder Promotes ejaculation and vaginal contractions

Figure 48.22

Synapse

Sacral

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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 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 Medulla oblongata

Pituitary gland Spinal cord Cerebellum

Central canal

Figure 48.23c

(c) Adult

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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 Reticular formation Input from touch, pain, and temperature receptors

Input from ears

Figure 48.24

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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 Light 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 Light Dark

Dark

1
Days of experiment 5

10

15

20

Figure 48.25

12

16

20

24

12

12

16

20

24

12

Time of day (hr)

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. Copyright 2005 Pearson Education, Inc. publishing as Benjamin Cummings

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 Corpus callosum Neocortex Right cerebral hemisphere

Basal nuclei

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

Frontal association area Speech Smell

Speech Taste Hearing Auditory association area

Somatosensory association area Reading Visual 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

Toes

Genitalia

Lips Jaw Tongue Primary motor cortex

Tongue Pharynx Abdominal organs Primary somatosensory 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 words

Seeing words

Min
Figure 48.29

Speaking words

Generating words

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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.

Gill withdrawal pathway Touching the siphon

Siphon sensory neuron Sensitization pathway

Gill motor neuron

Gill

Shocking the tail

Interneuron Tail sensory neuron

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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.

PRESYNAPTIC NEURON

7 NO diffuses into the presynaptic neuron, causing it to release more glutamate.

2 Glutamate binds to AMPA receptors, opening the AMPAreceptor channel and depolarizing the postsynaptic membrane.

NO

6 Ca2+ stimulates the postsynaptic neuron to produce nitric oxide (NO).

Glutamate AMPA receptor NO P Ca2+

NMDA receptor

3 Glutamate also binds to NMDA receptors. If the postsynaptic membrane is simultaneously depolarized, the NMDA-receptor channel opens.

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.

Signal transduction pathways POSTSYNAPTIC NEURON

4 Ca2+ diffuses into the 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

Copyright 2005 Pearson Education, Inc. publishing as Benjamin Cummings

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 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. 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 receptor 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. Slit Netrin-1 Slit

Growth cone

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.

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

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 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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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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