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(1)

Chapter 48

(2)

Concept 48.1: Neuron organization and structure reflect function in information transfer

Neurons are nerve cells that transfer information within the body

• Neurons use two types of signals to

communicate: electrical signals (long-distance) and chemical signals (short-distance)

(3)

• Sensors detect external stimuli and internal conditions and transmit information along sensory neurons

• Sensory information is sent to the brain or ganglia, where interneurons integrate the information

• Motor output leaves the brain or ganglia via

motor neurons, which trigger muscle or gland activity

(4)

Figure 48.3

Sensor

Effector

Sensory input

Motor output

Integration

Peripheral nervous system (PNS)

(5)

• Many animals have a complex nervous system that consists of

– A central nervous system (CNS) where

integration takes place; this includes the brain and a nerve cord

– A peripheral nervous system (PNS), which carries information into and out of the CNS – The neurons of the PNS, when bundled

together, form nerves

(6)

Neuron Structure and Function

• Most of a neuron’s organelles are in the cell body

• 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 • The cone-shaped base of an axon is called the

axon hillock

(7)
(8)

• The synaptic terminal of one axon passes information across the synapse in the form of chemical messengers called neurotransmitters • *A synapse is a junction between an axon and

another cell

(9)

Concept 48.2: Ion pumps and ion channels establish the resting potential of a neuron

• Every cell has a voltage (difference in electrical charge) across its plasma membrane called a membrane potential

• The resting potential is the membrane potential of a neuron not sending signals

• Changes in membrane potential act as signals, transmitting and processing information

(10)

Formation of the Resting Potential

• In a mammalian neuron at resting potential, the

concentration of K+ is highest inside the cell, while

the concentration of Na+ is highest outside the cell

• *Sodium-potassium pumps use the energy of ATP

to maintain these K+ and Na+ gradients across the

plasma membrane

• *Operation of sodium-potassium pump moves:

– Sodium ions out of the cell – Potassium ions into the cell

(11)

• The opening of ion channels in the plasma

membrane converts chemical potential to electrical potential

• A neuron at resting potential contains many open K+ channels and fewer open Na+ channels; K+

diffuses out of the cell

• The resulting buildup of negative charge within the neuron is the major source of membrane potential

(12)

Key

NaK

Sodium-potassium pump

Potassium channel

Sodium channel

OUTSIDE OF CELL

(13)

Concept 48.3: Action potentials are the signals conducted by axons

• Changes in membrane potential occur because neurons contain gated ion channels that open or close in response to stimuli

(14)

• When gated K+ channels open, K+ diffuses out, making the inside of the cell more negative

• This is hyperpolarization, an increase in magnitude of the membrane potential

© 2011 Pearson Education, Inc.

(15)

• Opening other types of ion channels triggers a depolarization, a reduction in the magnitude of the membrane potential

• For example, depolarization occurs if gated Na+ channels open and Na+ diffuses into the cell

(16)

Graded potentials are changes in polarization where the magnitude of the change varies with the strength of the stimulus

• These are not the nerve signals that travel along axons, but they do have an effect on the

generation of nerve signals

© 2011 Pearson Education, Inc.

(17)

• *If a depolarization shifts the membrane potential sufficiently, it results in a massive change in

membrane voltage called an action potential

• Action potentials have a constant magnitude, are all-or-none, and transmit signals over long

distances

• *Action potentials are self-propagating

• They arise because some ion channels are

voltage-gated, opening or closing when the

membrane potential passes a certain level

(18)

Action potential M em b ra n e p o te n ti a l ( m V ) Falling phase Rising phase

Threshold (55)

Depolarization Undershoot Resting potential Time (msec)50 050

10070

0 1 2 3 4 5 6

(19)

Generation of Action Potentials: A Closer Look

• An action potential can be considered as a series of stages

• At resting potential

1. Most voltage-gated sodium (Na+) channels are

closed; most of the voltage-gated potassium (K+) channels are also closed

(20)

OUTSIDE OF CELL

INSIDE OF CELL Inactivation loop

Sodium

channel Potassiumchannel

Action potential Threshold Resting potential Time M em b ra n e p o te n ti al (m V )5010050 0 NaKKey 2 1 3 4 5 1 2 3 4 5 1

Resting state Undershoot

Depolarization

Rising phase of the action potential

Falling phase of the action potential

(21)

• When an action potential is generated

2. Voltage-gated Na+ channels open first and Na+

flows into the cell

3. During the rising phase, the threshold is

crossed, and the membrane potential increases 4. During the falling phase, voltage-gated Na+

channels become inactivated; voltage-gated K+

channels open, and K+ flows out of the cell

(22)

5. During the undershoot, membrane

permeability to K+ is at first higher than at rest,

then voltage-gated K+ channels close and

resting potential is restored

(23)

• *During the refractory period after an action potential, a second action potential cannot be initiated

• The refractory period is a result of a temporary inactivation of the Na+ channels

(24)

Conduction of Action Potentials

• At the site where the action potential is

generated, usually the axon hillock, an electrical current depolarizes the neighboring region of the axon membrane

• Action potentials travel in only one direction: toward the synaptic terminals

(25)
(26)

Evolutionary Adaptation of Axon Structure

• The speed of an action potential increases with the axon’s diameter

• In vertebrates, axons are insulated by a myelin sheath, which causes an action potential’s

speed to increase

• Myelin sheaths are made by glia—

oligodendrocytes in the CNS and Schwann cells in the PNS

(27)

Axon Myelin sheath

Schwann cell

Nodes of Ranvier

Node of Ranvier

Layers of myelin Axon

Schwann cell

Nucleus of Schwann cell

(28)

• Action potentials are formed only at nodes of Ranvier, gaps in the myelin sheath where

voltage-gated Na+ channels are found

• Action potentials in myelinated axons jump between the nodes of Ranvier in a process called saltatory conduction

(29)

Cell body

Schwann cell

Depolarized region (node of Ranvier)

(30)

Concept 48.4: Neurons communicate with other cells at synapses

• At electrical synapses, the electrical current flows from one neuron to another

• At chemical synapses, a chemical

neurotransmitter carries information across the gap junction

• Most synapses are chemical synapses

(31)

• The presynaptic neuron synthesizes and packages the neurotransmitter in synaptic vesicles located in the synaptic terminal

• The action potential causes the release of the neurotransmitter

• The neurotransmitter diffuses across the synaptic cleft and is received by the

postsynaptic cell

(32)

*

Stages in transmission at a Chemical

Synapse

1. An Action Potential depolarizes the

membrane of the axon terminal.

2. Calcium ions rush into neuron’s cytoplasm.

3. The synaptic vesicles release

neurotransmitter into the synaptic cleft.

4. Neurotransmitter binds with receptors

(33)

Presynaptic

cell Postsynaptic cell

Axon

Presynaptic membrane

Synaptic vesicle containing

neurotransmitter Postsynapticmembrane Synaptic

cleft

Voltage-gated

Ca2 channel Ligand-gatedion channels Ca2

(34)

Generation of Postsynaptic Potentials

• Direct synaptic transmission involves binding of neurotransmitters to ligand-gated ion channels in the postsynaptic cell

• Neurotransmitter binding causes ion channels to open, generating a postsynaptic potential

(35)

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

are depolarizations that bring the membrane potential toward threshold

Inhibitory postsynaptic potentials (IPSPs) are hyperpolarizations that move the membrane

potential farther from threshold

(36)

Neurotransmitters

• There are more than 100 neurotransmitters, belonging to five groups: acetylcholine, biogenic amines, amino acids,

neuropeptides, and gases

• A single neurotransmitter may have more than a dozen different receptors

• *Cause a response at chemically-gated/ligand-gated ion channels found at synapse

(37)

Acetylcholine

Acetylcholine is a common neurotransmitter in vertebrates and invertebrates

• It is involved in muscle stimulation, memory formation, and learning

• Vertebrates have two major classes of

acetylcholine receptor, one that is ligand gated and one that is metabotropic

(38)

Concept 50.5: The physical interaction of protein filaments is required for muscle function

• Muscle activity is a response to input from the nervous system

• The action of a muscle is always to contract; extension is passive

(39)

Vertebrate Skeletal Muscle

• Vertebrate skeletal muscle moves bones and the body and is characterized by a hierarchy of

smaller and smaller units

• A skeletal muscle consists of a bundle of long fibers, each a single cell, running parallel to the length of the muscle

• Each muscle fiber is itself a bundle of smaller myofibrils arranged longitudinally

(40)

• The myofibrils are composed of two kinds of myofilaments

Thin filaments consist of two strands of actin and two strands of a regulatory protein

Thick filaments are staggered arrays of myosin molecules

(41)

• Skeletal muscle is also called striated muscle

because the regular arrangement of myofilaments creates a pattern of light and dark bands

• The functional unit of a muscle is called a sarcomere and is bordered by Z lines

• *Sarcomere combine to make myofibrils

(42)

The Sliding-Filament Model of Muscle Contraction

• According to the sliding-filament model,

filaments slide past each other longitudinally, producing more overlap between thin and thick filaments

(43)

Figure 50.27

Sarcomere 0.5 m

Z M Z

Relaxed muscle

Contracting muscle

Fully contracted muscle

(44)

Figure 50.30 Synaptic terminal Axon of motor neuron T tubule Sarcoplasmic reticulum (SR) Myofibril Plasma membrane of muscle fiber

Sarcomere Ca2 released from SR Mitochondrion 2 1 3 4 5 6 7

Synaptic terminal of motor neuron Synaptic cleft T tubule

Sarcoplasmic reticulum (SR)

Plasma membrane ACh

Ca2 pump

Ca2

Ca2

CYTOSOL

(45)

• Action potentials travel to the interior of the muscle fiber along transverse (T) tubules

• The action potential along T tubules causes the

sarcoplasmic reticulum (SR) to release Ca2+

• *The Ca2+ binds to the troponin complex on the thin

filaments

• This binding exposes myosin-binding sites and allows the cross-bridge cycle to proceed

• Myosin heads perform a power stroke

(46)

• When motor neuron input stops, the muscle cell relaxes

• Transport proteins in the SR pump Ca2+ out of the cytosol

• Regulatory proteins bound to thin filaments shift back to the myosin-binding sites

(47)

• Amyotrophic lateral sclerosis (ALS), formerly called Lou Gehrig’s disease, interferes with the

excitation of skeletal muscle fibers; this disease is usually fatal

• Myasthenia gravis is an autoimmune disease that attacks acetylcholine receptors on muscle fibers; treatments exist for this disease

(48)

Nervous Control of Muscle Tension

• Contraction of a whole muscle is graded, which means that the extent and strength of its

contraction can be voluntarily altered

• There are two basic mechanisms by which the nervous system produces graded contractions

– Varying the number of fibers that contract

– Varying the rate at which fibers are stimulated

(49)

• In vertebrates, each motor neuron may synapse with multiple muscle fibers, although each fiber is controlled by only one motor neuron

• A motor unit consists of a single motor neuron and all the muscle fibers it controls

(50)

Figure 50.31

Spinal cord Motor unit 1

Motor unit 2

Synaptic terminals

Nerve

Motor neuron cell body

Motor neuron axon

Muscle

Tendon

(51)

• Recruitment of multiple motor neurons results in stronger contractions

• A twitch results from a single action potential in a motor neuron

• More rapidly delivered action potentials produce a graded contraction by summation

(52)

Figure 50.32 Tetanus Summation of two twitches Single twitch Action

potential Pair of action potentials

(53)

Tetanus is a state of smooth and sustained

contraction produced when motor neurons deliver a volley of action potentials

(54)

Types of Skeletal Muscle Fibers

• There are several distinct types of skeletal

muscles, each of which is adapted to a particular function

• They are classified by the source of ATP powering the muscle activity or by the speed of muscle

contraction

(55)

Oxidative and Glycolytic Fibers

• Oxidative fibers rely mostly on aerobic respiration to generate ATP

• These fibers have many mitochondria, a rich blood supply, and a large amount of myoglobin

• Myoglobin is a protein that binds oxygen more tightly than hemoglobin does

(56)

• Glycolytic fibers use glycolysis as their primary source of ATP

• Glycolytic fibers have less myoglobin than oxidative fibers and tire more easily

• In poultry and fish, light meat is composed of

glycolytic fibers, while dark meat is composed of oxidative fibers

(57)

Fast-Twitch and Slow-Twitch Fibers

Slow-twitch fibers contract more slowly but sustain longer contractions

• All slow-twitch fibers are oxidative

Fast-twitch fibers contract more rapidly but sustain shorter contractions

• Fast-twitch fibers can be either glycolytic or oxidative

– *Through conditioning fast glycolytic fibers can become fast oxidative fibers

(58)

Concept 50.6: Skeletal systems transform muscle contraction into locomotion

• Skeletal muscles are attached in antagonistic

pairs, the actions of which are coordinated by the nervous system

• The skeleton provides a rigid structure to which muscles attach

• *Skeletons function in support, protection, movement, and blood production

(59)
(60)

Nervous Systems

Different regions of the brain have different

functions.

Structures and associated function for animal

brains are products of

Evolution

Brain increasing complexity follows

(61)

Vertebrate Brain is Regionally Specialized

Forebrain

Cerebrum Thalamus

Hypothalamus

Pituitary gland

Pons Medulla oblongata Cerebellum

Spinal cord Midbrain

(62)

Figure 49.16

Motor cortex (control of

skeletal muscles) Somatosensory cortex

(sense of touch)

Sensory association cortex (integration

of sensory information)

Frontal lobe Temporal lobe Parietal lobe Occipital lobe Prefrontal cortex (decision making, planning) Broca’s area (forming speech) Auditory cortex (hearing) Cerebellum Visual association cortex (combining images and object recognition)

Visual cortex

(processing visual stimuli and pattern recognition)

(63)

Sensory and Motor Mechanisms

Chapter 50

Chapter 50

(64)

Overview: Sensing and Acting

• Sensory processes convey information about an animal’s environment to its brain, and muscles and skeletons carry out movements as instructed by

the brain

(65)

Concept 50.1: Sensory receptors transduce stimulus

energy and transmit signals to the central nervous system

• All stimuli represent forms of energy

• Sensation involves converting energy into a change in the membrane potential of sensory receptors

• When a stimulus’s input to the nervous system is processed a motor response may be generated

• This may involve a simple reflex or more elaborate processing

(66)

Sensory Pathways

• Sensory pathways have four basic functions in common

– Sensory reception – Tranduction

– Transmission – Integration

(67)

Sensory Reception and Transduction

• Sensations and perceptions begin with sensory reception, detection of stimuli by sensory

receptors

Sensory receptors interact directly with stimuli, both inside and outside the body

(68)

Sensory transduction is the conversion of

stimulus energy into a change in the membrane potential of a sensory receptor

• This change in membrane potential is called a receptor potential

• Receptor potentials are graded potentials; their magnitude varies with the strength of the stimulus

(69)

Transmission

• After energy has been transduced into a receptor potential, some sensory cells generate the

transmission of action potentials to the CNS

• Some sensory receptors are specialized neurons while others are specialized cells that regulate

neurons

• Sensory neurons produce action potentials and their axons extend into the CNS

(70)

• The response of a sensory receptor varies with intensity of stimuli

• If the receptor is a neuron, a larger receptor

potential results in more frequent action potentials • If the receptor is not a neuron, a larger receptor

potential causes more neurotransmitters to be released

(71)

Figure 50.4

(a) Single sensory receptor activated Gentle pressure

Sensory receptor

More pressure

Low frequency of

action potentials per receptor

High frequency of

action potentials per receptor

(b) Multiple receptors activated

Sensory receptor Gentle pressure

(72)

Types of Sensory Receptors

• Based on energy transduced, sensory receptors fall into five categories

– Mechanoreceptors – Chemoreceptors

– Electromagnetic receptors – Thermoreceptors

– Pain receptors

(73)

Mechanoreceptors

Mechanoreceptors sense physical deformation caused by stimuli such as pressure, stretch,

motion, and sound

• The knee-jerk response is triggered by the

vertebrate stretch receptor, a mechanoreceptor that detects muscle movement

• The mammalian sense of touch relies on

mechanoreceptors that are dendrites of sensory neurons

(74)

Concept 50.2: The mechanoreceptors responsible for hearing and equilibrium detect moving fluid or settling

particles

• Hearing and perception of body equilibrium are related in most animals

• For both senses, settling particles or moving fluid is detected by mechanoreceptors

(75)

Outer ear Middle ear Inner ear Skull bone Malleus Incus Stapes Semicircular canals Auditory nerve to brain Cochlea Eustachian tube Round window Oval window Tympanic membrane Auditory canal Pinna 1 m

Bundled hairs projecting from a hair cell

Cochlear duct Bone Auditory nerve Vestibular canal Tympanic canal Organ of Corti Tectorial membrane Basilar membrane

Hair cells Axons of sensory neurons

To auditory nerve

(76)

Hearing

• Vibrating objects create percussion waves in the air that cause the tympanic membrane to vibrate • The three bones of the middle ear transmit the

vibrations of moving air to the oval window on the cochlea

• These vibrations create pressure waves in the fluid in the cochlea that travel through the

vestibular canal

(77)

• *Pressure waves in the canal cause the basilar

membrane to vibrate, bending its hair cells called sterocilia

• This bending of hair cells depolarizes the

membranes of mechanoreceptors and sends

action potentials to the brain via the auditory nerve

– *Cause ion channels to open or close

(78)

Concept 50.3: Visual receptors on diverse animals depend on light-absorbing pigments

• Animals use a diverse set of organs for vision, but the underlying mechanism for capturing light is the same, suggesting a common evolutionary origin

(79)

Evolution of Visual Perception

• Light detectors in the animal kingdom range from simple clusters of cells that detect direction and intensity of light to complex organs that form

images

• Light detectors all contain photoreceptors, cells that contain light-absorbing pigment molecules

(80)

The Vertebrate Visual System

• In vertebrates the eye detects color and light, but the brain assembles the information and perceives the image

(81)

Figure 50.17a Sclera Suspensory ligament Cornea Iris Pupil Aqueous humor Lens

Vitreous humor Optic disk

(82)

Sensory Transduction in the Eye

• Transduction of visual information to the nervous system begins when light induces the conversion of cis-retinal to trans-retinal

Trans-retinal activates rhodopsin, which activates

a G protein, eventually leading to hydrolysis of cyclic GMP

(83)

• When cyclic GMP breaks down, Na channels

close

• This hyperpolarizes the cell

• The signal transduction pathway usually shuts off again as enzymes convert retinal back to the cis

form

(84)

Figure 50.18 Light Inactive rhodopsin Active rhodopsin Transducin Phosphodiesterase

Figure

Figure 48.3 Sensor Effector Sensory inputMotor output Integration Peripheral nervous system (PNS) Central nervoussystem (CNS)
Figure 48.4 Nucleus Dendrites Stimulus Axon hillock Cell body Presynaptic cell Signal direction Axon Synapse Neurotransmitter Synaptic terminalsPostsynaptic cell Synaptic terminals
Figure 48.12-3 K  K  K K Na NaNaActionpotential Axon Plasma  membraneCytosolActionpotentialActionpotential213
Figure 50.27 Sarcomere 0.5 m Z M Z Relaxed muscle Contracting muscle Fully contracted muscle Contracted sarcomere
+5

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