Chapter 12 Nervous Tissue - Houston Community College

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Copyright 2009 John Wiley & Sons, Inc. 1 Chapter 12 Nervous Tissue

Transcript of Chapter 12 Nervous Tissue - Houston Community College

Page 1: Chapter 12 Nervous Tissue - Houston Community College

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Chapter 12

Nervous Tissue

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Overview of the Nervous System

The nervous system, along with the

endocrine system, helps to keep controlled

conditions within limits that maintain health

and helps to maintain homeostasis.

The nervous system is responsible for all our

behaviors, memories, and movements.

The branch of medical science that deals with

the normal functioning and disorders of the

nervous system is called neurology.

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The excitable characteristics of nervous

tissue allows for generation of nerve impulses

(action potentials).

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Major Structures of the Nervous System

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Overview of Major Structures Twelve pairs of cranial nerves.

Thirty-one pairs of spinal nerves emerge from the spinal cord.

Ganglia, located outside the brain and spinal cord, are small masses of nervous tissue, containing primarily cell bodies of neurons.

Enteric plexuses help regulate the digestive system.

Sensory receptors are either parts of neurons or specialized cells that monitor changes in the internal or external environment.

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Functions of Nervous System Sensory function: to sense changes in the internal and

external environment through sensory receptors.

Sensory (afferent) neurons serve this function.

Integrative function: to analyze the sensory

information, store some aspects, and make decisions

regarding appropriate behaviors

Association or interneurons serve this function.

Perception; the conscious awareness of sensory

stimuli.

Motor function is to respond to stimuli by initiating

action.

Motor (efferent) neurons serve this function.

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Nervous System Divisions

Central nervous system (CNS)

consists of the brain and spinal cord

Peripheral nervous system (PNS)

consists of cranial and spinal nerves that contain

both sensory and motor fibers

connects CNS to muscles, glands & all sensory

receptors.

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Histology of the Nervous System:

Neurons (nerve cells) Functional unit of nervous system

Have capacity to produce action potentials electrical excitability: the ability to respond to a stimulus

and convert it into an action potential (nerve impulse).

Nerve impulses travel at speeds ranging from 0.5 to 130 meters per second

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Parts of a neuron:

Cell body (soma, or perikaryon) single nucleus with prominent nucleolus

Nissl bodies (chromatophilic substance)

rough ER & free ribosomes for protein synthesis

neurofilaments give cell shape and support

microtubules move material inside cell

Lipofuscin: a product of neuronal lysosomes, pigment clumps (harmless aging)

Cell processes = dendrites & axons(extension)

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Structure of a Multipolar Neuron

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Structural Classification of Neurons

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Axonal Transport P.419

Cell body is location for most protein synthesis

neurotransmitters & repair proteins

Axonal transport system moves substances

slow axonal flow

movement in one direction only -- away from cell body

movement at 1-5 mm per day

fast axonal flow

moves organelles & materials along surface of microtubules

at 200-400 mm per day

transports in either direction

for use or for recycling in cell body

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Sensory receptors that are dendrites of

unipolar neurons

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CNS Neurons

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Functional classification: P.420

1. sensory or afferent: most are unipolar

2. motor or efferent: most are multipolar

3. interneurons or association neurons: most

multipolar.

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Neuroglia of the CNS

Astrocytes:

Oligodendrocytes:

Microglia:

Ependymal Cells:

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Neuroglia of the CNS: P.421 Astrocytes: support neurons, participate in the

formation of the blood-brain barrier, may play

role in learning and memory.

Oligodendrocytes: responsible for the formation

the myelin sheath (a multilayered lipid and

protein covering some axons and insulates

them0.

Microglia: function as phagocytes.

Ependymal: line the ventricles of the brain and

central canal of the spinal cord, produces CSF,

and form the blood-cerebrospinal fluid barrier

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Neuroglia of the PNS :P.422

Schwann cells encircling PNS axons

Each cell produces part of the myelin sheath

surrounding an axon in the PNS

Satellite cells surround the cell bodies (PNS)

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Myelinated and unmyelinated axons

Schwann cells myelinate (wrap around) axons in the PNS during fetal development

Schwann cell cytoplasm & nucleus forms outermost layer of neurolemma with inner portion being the myelin sheath

Tube guides growing axons that are repairing themselves

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Myelinated and unmyelinated axons

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Organization of the Nervous System

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Subdivisions of the PNS

Somatic (voluntary) nervous system (SNS) neurons from cutaneous and special sensory receptors to the

CNS

motor neurons to skeletal muscle tissue

Autonomic (involuntary) nervous systems sensory neurons from visceral organs to CNS

motor neurons to smooth & cardiac muscle and glands

sympathetic division (speeds up heart rate)

parasympathetic division (slow down heart rate)

Enteric nervous system (ENS) involuntary sensory & motor neurons control GI tract

neurons function independently of ANS & CNS

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Electrical Signals in Neurons

Neurons are electrically excitable due to the

voltage difference across their membrane

Communicate with 2 types of electric signals

action potentials that can travel long distances

graded potentials that are local membrane

changes only

In living cells, a flow of ions occurs through

ion channels in the cell membrane

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Overview of Nervous System Functions

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The production of graded potentials and

action potentials depends on: The resting membrane potential

The ion channels.

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Types of Ion Channels

Leakage (nongated) channels are always open nerve cells have more K+ than Na+ leakage channels

as a result, membrane permeability to K+ is higher

explains resting membrane potential of -70mV in nerve tissue

Ligand-gated channels open and close in response to a stimulus results in neuron excitability

Voltage-gated channels respond to a direct change in the membrane potential.

Mechanically gated ion channels respond to mechanical vibration or pressure.

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Ion channels in plasma membrane

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Resting Membrane Potential

Negative ions along inside of cell membrane &

positive ions along outside

potential energy difference at rest is -70 mV

cell is “polarized”

Resting potential exists because

concentration of ions different inside & outside

extracellular fluid rich in Na+ and Cl

cytosol full of K+, organic phosphate & amino acids

membrane permeability differs for Na+ and K+

50-100 greater permeability for K+

inward flow of Na+ can’t keep up with outward flow of K+

Na+/K+ pump removes Na+ as fast as it leaks in

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Resting Membrane Potential

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Factors that contribute to the RMP

Unequal distribution of ions in the ECF and

cytosol.

Inability of most anions to leave the cell.

Electrogenic nature of the Na+/K+ ATPases

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Factors that contribute to resting

membrane potential

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Graded Potentials

Small deviations from resting potential of -70mV

hyperpolarization = membrane has become more negative

depolarization = membrane has become more positive

The signals are graded, meaning they vary in

amplitude (size), depending on the strength of the

stimulus and localized.

Graded potentials occur most often in the dendrites

and cell body of a neuron.

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Hyperpolarized/Depolarized Graded

Potential

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Graded potentials in response to opening

mechanically-gated channels or ligand-

gated channels

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Stimulus strength and graded potentials

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Summation

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Generation of Action Potentials

An action potential (AP) or impulse is a sequence of

rapidly occurring events that decrease and

eventually reverse the membrane potential

(depolarization) and then restore it to the resting

state (repolarization).

During an action potential, voltage-gated Na+ and K+

channels open in sequence (

According to the all-or-none principle, if a stimulus reaches

threshold, the action potential is always the same.

A stronger stimulus will not cause a larger impulse.

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Action Potentials

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Stimulus strength and Action Potential

generation

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Changes in ion flow during depolarizing

and repolarizing phases of Action

Potential

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Depolarizing Phase

Chemical or mechanical stimulus caused a graded potential to reach at least (-55mV or threshold)

Voltage-gated Na+ channels open & Na+ rushes into cell

in resting membrane, inactivation gate of sodium channel is open & activation gate is closed (Na+ can not get in)

when threshold (-55mV) is reached, both open & Na+ enters

inactivation gate closes again in few ten-thousandths of second

only a total of 20,000 Na+ actually enter the cell, but they change the membrane potential considerably(up to +30mV)

Positive feedback process

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Repolarizing Phase

When threshold potential of -55mV is reached, voltage-gated K+ channels open

K+ channel opening is much slower than Na+ channel opening which caused depolarization

When K+ channels finally do open, the Na+ channels have already closed (Na+ inflow stops)

K+ outflow returns membrane potential to -70mV

If enough K+ leaves the cell, it will reach a -90mV membrane potential and enter the after-hyperpolarizing phase

K+ channels close and the membrane potential returns to the resting potential of -70mV

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Refractory period

Period of time during which neuron can not generate another action potential

Absolute refractory period even very strong stimulus will

not begin another AP

inactivated Na+ channels must return to the resting state before they can be reopened

large fibers have absolute refractory period of 0.4 msec and up to 1000 impulses per second are possible

Relative refractory period a suprathreshold stimulus will be able to start an AP

K+ channels are still open, but Na+ channels have closed

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Continuous versus Saltatory Conduction

Continuous conduction (unmyelinated fibers)

step-by-step depolarization of each portion of the

length of the axolemma

Saltatory conduction

depolarization only at nodes of Ranvier where

there is a high density of voltage-gated ion

channels

current carried by ions flows through extracellular

fluid from node to node

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Propagation of an Action Potential in a

neuron after it arises at the trigger zone

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Factors that affect speed of propagation

Amount of myelination

Axon diameter

Temperature

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Speed of impulse propagation

The propagation speed of a nerve impulse is not related to stimulus strength.

larger, myelinated fibers conduct impulses faster due to size & saltatory conduction

Fiber types

A fibers largest (5-20 microns & 130 m/sec)

myelinated somatic sensory & motor to skeletal muscle

B fibers medium (2-3 microns & 15 m/sec)

myelinated visceral sensory & autonomic preganglionic

C fibers smallest (.5-1.5 microns & 2 m/sec)

unmyelinated sensory & autonomic motor

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Signal Transmission at the Synapse

2 Types of synapses

electrical

ionic current spreads to next cell through gap junctions

faster, two-way transmission & capable of synchronizing

groups of neurons

chemical

one-way information transfer from a presynaptic neuron

to a postsynaptic neuron

axodendritic -- from axon to dendrite

axosomatic -- from axon to cell body

axoaxonic -- from axon to axon

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Signal transmission at the chemical

synapse

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Chemical Synapses

Action potential reaches end bulb and voltage-gated

Ca+ 2 channels open

Ca+2 flows inward triggering release of

neurotransmitter

Neurotransmitter crosses synaptic cleft & binding to

ligand-gated receptors

the more neurotransmitter released the greater the change

in potential of the postsynaptic cell

Synaptic delay is 0.5 msec

One-way information transfer

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Signal transmission at a chemical synapse

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Excitory and Inhibitory Postsynaptic

Potentials

The effect of a neurotransmitter can be either

excitatory or inhibitory

a depolarizing postsynaptic potential is called an EPSP

it results from the opening of ligand-gated Na+ channels

the postsynaptic cell is more likely to reach threshold

an inhibitory postsynaptic potential is called an IPSP

it results from the opening of ligand-gated Cl- or K+ channels

it causes the postsynaptic cell to become more negative or

hyperpolarized

the postsynaptic cell is less likely to reach threshold

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Ionotropic and Metatropic Receptors

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Removal of Neurotransmitter

Diffusion

move down concentration gradient

Enzymatic degradation

acetylcholinesterase

Uptake by neurons or glia cells

neurotransmitter transporters

Prozac = serotonin reuptake

inhibitor

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Three Possible Responses

Small EPSP occurs

potential reaches -56 mV only

An impulse is generated

threshold was reached

membrane potential of at least -55 mV

IPSP occurs

membrane hyperpolarized

potential drops below -70 mV

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Summation

If several presynaptic end bulbs release their

neurotransmitter at about the same time, the

combined effect may generate a nerve

impulse due to summation

Summation may be spatial or temporal.

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Spatial Summation

Summation of effects of

neurotransmitters

released from several

end bulbs onto one

neuron

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Temporal Summation

Summation of effect of

neurotransmitters

released from 2 or

more firings of the

same end bulb in rapid

succession onto a

second neuron

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Summation

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Neurotransmitters

Both excitatory and inhibitory

neurotransmitters are present in the CNS and

PNS; the same neurotransmitter may be

excitatory in some locations and inhibitory in

others.

Important neurotransmitters include

acetylcholine, glutamate, aspartate, gamma

aminobutyric acid, glycine, norepinephrine,

epinephrine, and dopamine.

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Neurotransmitters

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Neurotransmitter Effects

Neurotransmitter effects can be modified

synthesis can be stimulated or inhibited

release can be blocked or enhanced

removal can be stimulated or blocked

receptor site can be blocked or activated

Agonist

anything that enhances a transmitters effects

Antagonist

anything that blocks the action of a neurotranmitter

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Small-Molecule Neurotransmitters

Acetylcholine (ACh)

released by many PNS neurons & some CNS

excitatory on NMJ but inhibitory at others

inactivated by acetylcholinesterase

Amino Acids

glutamate released by nearly all excitatory neurons

in the brain ---- inactivated by glutamate specific

transporters

GABA is inhibitory neurotransmitter for 1/3 of all

brain synapses (Valium is a GABA agonist --

enhancing its inhibitory effect)

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Neural Circuits

A neuronal network may contain thousands or even millions of neurons.

Neuronal circuits are involved in many important activities

breathing

short-term memory

waking up

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Neural Circuits

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Regeneration & Repair

Plasticity maintained throughout life

sprouting of new dendrites

synthesis of new proteins

changes in synaptic contacts with other neurons

Limited ability for regeneration (repair)

PNS can repair damaged dendrites or axons

CNS no repairs are possible

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Damage and Repair in the Peripheral

Nervous System When there is damage to an axon, usually there are

changes, called chromatolysis, which occur in the cell body of the affected cell; this causes swelling of the cell body and peaks between 10 and 20 days after injury.

By the third to fifth day, degeneration of the distal portion of the neuronal process and myelin sheath (Wallerian degeneration) occurs; afterward, macrophages phagocytize the remains.

Retrograde degeneration of the proximal portion of the fiber extends only to the first neurofibral node.

Regeneration follows chromatolysis; synthesis of RNA and protein accelerates, favoring rebuilding of the axon and often taking several months.

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Repair within the PNS

Axons & dendrites may be

repaired if

neuron cell body remains

intact

schwann cells remain active

and form a tube

scar tissue does not form

too rapidly

Chromatolysis

24-48 hours after injury,

Nissl bodies break up into

fine granular masses

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Repair within the PNS

By 3-5 days,

wallerian degeneration occurs (breakdown of

axon & myelin sheath distal to injury)

retrograde degeneration occurs back one node

Within several months, regeneration occurs

neurolemma on each side of injury repairs tube

(schwann cell mitosis)

axonal buds grow down the tube to reconnect (1.5

mm per day)

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Neurogenesis in the CNS

Formation of new neurons from stem cells

was not thought to occur in humans

There is a lack of neurogenesis in other

regions of the brain and spinal cord.

Factors preventing neurogenesis in CNS

inhibition by neuroglial cells, absence of growth

stimulating factors, lack of neurolemmas, and

rapid formation of scar tissue

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End of Chapter 12