In this chapter, students will be able to understand: Define synapse, distinguish between electrical and chemical synapses by structure and by the way they transmit information, distinguish between excitatory and inhibitory postsynaptic potentials, describe how synaptic events are integrated and modified,...
Trang 1PowerPoint ® Lecture Slides
prepared by Janice Meeking, Mount Royal College
Nervous Tissue: Part C
Trang 2Copyright © 2010 Pearson Education, Inc.
The Synapse
from one neuron:
• To another neuron, or
• To an effector cell
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The Synapse
toward the synapse
away from the synapse
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Types of Synapses
neuron and the dendrite of another
neuron and the soma of another
• Axoaxonic (axon to axon)
• Dendrodendritic (dendrite to dendrite)
• Dendrosomatic (dendrite to soma)
Trang 5Copyright © 2010 Pearson Education, Inc. Figure 11.16
Dendrites Cell body
Axon
Axodendritic synapses
Axosomatic synapses
Cell body (soma) of postsynaptic neuron
Axon
(b)
Axoaxonic synapses
Axosomatic synapses
(a)
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Electrical Synapses
• Neurons are electrically coupled (joined by gap junctions)
• Communication is very rapid, and may be
unidirectional or bidirectional
• Are important in:
• Embryonic nervous tissue
• Some brain regions
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Chemical Synapses
neurotransmitters
• Axon terminal of the presynaptic neuron, which contains synaptic vesicles
• Receptor region on the postsynaptic neuron
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Synaptic Cleft
and postsynaptic neurons
from one neuron to the next
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Synaptic Cleft
• Is a chemical event (as opposed to an
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Information Transfer
channels
promotes fusion of synaptic vesicles with
axon membrane
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Information Transfer
receptors (often chemically gated ion channels) on the postsynaptic neuron
excitatory or inhibitory event (graded potential)
Trang 12Copyright © 2010 Pearson Education, Inc. Figure 11.17
Action potential arrives at axon terminal.
Voltage-gated Ca 2+
channels open and Ca 2+
enters the axon terminal.
Ca 2+ entry causes neurotransmitter- containing synaptic vesicles to release their contents by exocytosis.
Chemical synapses transmit signals from one neuron to another using neurotransmitters.
Ca 2+
Synaptic vesicles
Axon terminal
Mitochondrion
Postsynaptic neuron
Presynaptic neuron
Presynaptic neuron
Synaptic cleft
Ca 2+
Ca 2+
Ca 2+
Neurotransmitter diffuses across the synaptic cleft and binds to specific receptors on the
postsynaptic membrane.
Binding of neurotransmitter opens ion channels, resulting in graded potentials.
Neurotransmitter effects are terminated by reuptake through transport proteins, enzymatic degradation, or diffusion away from the synapse.
Ion movement Graded potential
Reuptake
Enzymatic degradation
Diffusion away from synapse
Postsynaptic neuron
1 2
3
4
5
6
Trang 13Copyright © 2010 Pearson Education, Inc. Figure 11.17, step 1
Action potential arrives at axon terminal.
Chemical synapses transmit signals from one neuron to another using neurotransmitters.
Ca 2+
Synaptic vesicles
Axon terminal
Mitochondrion
Postsynaptic neuron
Presynaptic neuron
Presynaptic neuron
Synaptic cleft
Ca 2+
Ca 2+
Ca 2+
Postsynaptic neuron
1
Trang 14Copyright © 2010 Pearson Education, Inc. Figure 11.17, step 2
Action potential arrives at axon terminal.
Voltage-gated Ca 2+
channels open and Ca 2+
enters the axon terminal.
Chemical synapses transmit signals from one neuron to another using neurotransmitters.
Ca 2+
Synaptic vesicles
Axon terminal
Mitochondrion
Postsynaptic neuron
Presynaptic neuron
Presynaptic neuron
Synaptic cleft
Ca 2+
Ca 2+
Ca 2+
Postsynaptic neuron
1 2
Trang 15Copyright © 2010 Pearson Education, Inc. Figure 11.17, step 3
Action potential arrives at axon terminal.
Voltage-gated Ca 2+
channels open and Ca 2+
enters the axon terminal.
Ca 2+ entry causes neurotransmitter- containing synaptic vesicles to release their contents by exocytosis.
Chemical synapses transmit signals from one neuron to another using neurotransmitters.
Ca 2+
Synaptic vesicles
Axon terminal
Mitochondrion
Postsynaptic neuron
Presynaptic neuron
Presynaptic neuron
Synaptic cleft
Ca 2+
Ca 2+
Ca 2+
Postsynaptic neuron
1 2
3
Trang 16Copyright © 2010 Pearson Education, Inc. Figure 11.17, step 4
Action potential arrives at axon terminal.
Voltage-gated Ca 2+
channels open and Ca 2+
enters the axon terminal.
Ca 2+ entry causes neurotransmitter- containing synaptic vesicles to release their contents by exocytosis.
Chemical synapses transmit signals from one neuron to another using neurotransmitters.
Ca 2+
Synaptic vesicles
Axon terminal
Mitochondrion
Postsynaptic neuron
Presynaptic neuron
Presynaptic neuron
Synaptic cleft
Ca 2+
Ca 2+
Ca 2+
Neurotransmitter diffuses across the synaptic cleft and binds to specific receptors on the
postsynaptic membrane.
Postsynaptic neuron
1 2
3
4
Trang 17Copyright © 2010 Pearson Education, Inc. Figure 11.17, step 5
Trang 18Copyright © 2010 Pearson Education, Inc. Figure 11.17, step 6
Reuptake
Enzymatic degradation
Diffusion away from synapse
Neurotransmitter effects are terminated
by reuptake through transport proteins, enzymatic degradation, or diffusion away from the synapse.
6
Trang 19Copyright © 2010 Pearson Education, Inc. Figure 11.17
Action potential arrives at axon terminal.
Voltage-gated Ca 2+
channels open and Ca 2+
enters the axon terminal.
Ca 2+ entry causes neurotransmitter- containing synaptic vesicles to release their contents by exocytosis.
Chemical synapses transmit signals from one neuron to another using neurotransmitters.
Ca 2+
Synaptic vesicles
Axon terminal
Mitochondrion
Postsynaptic neuron
Presynaptic neuron
Presynaptic neuron
Synaptic cleft
Ca 2+
Ca 2+
Ca 2+
Neurotransmitter diffuses across the synaptic cleft and binds to specific receptors on the
postsynaptic membrane.
Binding of neurotransmitter opens ion channels, resulting in graded potentials.
Neurotransmitter effects are terminated by reuptake through transport proteins, enzymatic degradation, or diffusion away from the synapse.
Ion movement Graded potential
Reuptake
Enzymatic degradation
Diffusion away from synapse
Postsynaptic neuron
1 2
3
4
5
6
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Termination of Neurotransmitter Effects
neurotransmitter effect is terminated
• Degradation by enzymes
• Reuptake by astrocytes or axon terminal
• Diffusion away from the synaptic cleft
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Synaptic Delay
across the synapse, and bind to receptors
5.0 ms)
neural transmission
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Postsynaptic Potentials
• Amount of neurotransmitter released
• Time the neurotransmitter is in the area
1 EPSP—excitatory postsynaptic potentials
2 IPSP—inhibitory postsynaptic potentials
Trang 23Copyright © 2010 Pearson Education, Inc. Table 11.2 (1 of 4)
Trang 24Copyright © 2010 Pearson Education, Inc. Table 11.2 (2 of 4)
Trang 25Copyright © 2010 Pearson Education, Inc. Table 11.2 (3 of 4)
Trang 26Copyright © 2010 Pearson Education, Inc. Table 11.2 (4 of 4)
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Excitatory Synapses and EPSPs
chemically gated channels that allow
directions
net depolarization
is of threshold strength and opens the
voltage-gated channels
Trang 28Copyright © 2010 Pearson Education, Inc. Figure 11.18a
An EPSP is a local depolarization of the postsynaptic membrane that brings the neuron closer to AP threshold
Neurotransmitter binding opens chemically gated ion channels, allowing the simultaneous pas- sage of Na + and K +
Time (ms) (a) Excitatory postsynaptic potential (EPSP)
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Inhibitory Synapses and IPSPs
of membrane becomes more negative)
produce an action potential
Trang 30Copyright © 2010 Pearson Education, Inc. Figure 11.18b
An IPSP is a local hyperpolarization of the postsynaptic membrane and drives the neuron away from AP threshold
Neurotransmitter binding opens K + or Cl – channels.
Time (ms) (b) Inhibitory postsynaptic potential (IPSP)
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Integration: Summation
potential
canceling each other out
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Trang 33Copyright © 2010 Pearson Education, Inc. Figure 11.19a, b
Threshold of axon of postsynaptic neuron
Excitatory synapse 1 (E 1 ) Excitatory synapse 2 (E 2 ) Inhibitory synapse (I 1 )
(b) Temporal summation:
2 excitatory stimuli close
in time cause EPSPs that add together.
Trang 34Copyright © 2010 Pearson Education, Inc. Figure 11.19c, d
(d) Spatial summation of EPSPs and IPSPs:
Changes in membane potential can cancel each other out.
(c) Spatial summation:
2 simultaneous stimuli at different locations cause EPSPs that add together.
E 1
E 1
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Integration: Synaptic Potentiation
• Repeated use increases the efficiency of
• Ca 2+ activates kinase enzymes that promote more
effective responses to subsequent stimuli
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Integration: Presynaptic Inhibition
neuron may be inhibited by the activity of
another neuron via an axoaxonic synapse
EPSPs are formed
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Neurotransmitters
neurotransmitters, which are released at different stimulation frequencies
identified
function
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Chemical Classes of Neurotransmitters
• Released at neuromuscular junctions and
some ANS neurons
• Synthesized by enzyme choline
acetyltransferase
• Degraded by the enzyme acetylcholinesterase (AChE)
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Chemical Classes of Neurotransmitters
• Catecholamines
• Dopamine, norepinephrine (NE), and epinephrine
• Indolamines
• Serotonin and histamine
biological clock
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Chemical Classes of Neurotransmitters
• GABA—Gamma ( )-aminobutyric acid
• Glycine
• Aspartate
• Glutamate
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Chemical Classes of Neurotransmitters
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Chemical Classes of Neurotransmitters
• Act in both the CNS and PNS
• Produce fast or slow responses
• Induce Ca2+ influx in astrocytes
• Provoke pain sensation
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Chemical Classes of Neurotransmitters
• Nitric oxide (NO)
• Synthesized on demand
• Activates the intracellular receptor guanylyl cyclase to cyclic GMP
• Involved in learning and memory
• Carbon monoxide (CO) is a regulator of cGMP
in the brain
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Chemical Classes of Neurotransmitters
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Functional Classification of
Neurotransmitters
• Neurotransmitter effects may be excitatory
(depolarizing) and/or inhibitory (hyperpolarizing)
• Determined by the receptor type of the postsynaptic neuron
• GABA and glycine are usually inhibitory
• Glutamate is usually excitatory
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Neurotransmitter Actions
• Neurotransmitter binds to channel-linked receptor and opens ion channels
• Promotes rapid responses
• Examples: ACh and amino acids
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• Promotes long-lasting effects
• Examples: biogenic amines, neuropeptides, and dissolved gases
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Neurotransmitter Receptors
1 Channel-linked receptors
2 G protein-linked receptors
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Channel-Linked (Ionotropic) Receptors
cations
that causes hyperpolarization
Trang 50Copyright © 2010 Pearson Education, Inc. Figure 11.20a
Ion flow blocked
Closed ion channel
(a) Channel-linked receptors open in response to binding
of ligand (ACh in this case).
Ions flow Ligand
Open ion channel
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G Protein-Linked (Metabotropic) Receptors
often prolonged and widespread
those that bind biogenic amines and
neuropeptides
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G Protein-Linked Receptors: Mechanism
receptor
second messengers, e.g., cyclic AMP, cyclic
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G Protein-Linked Receptors: Mechanism
• Open or close ion channels
• Activate kinase enzymes
• Phosphorylate channel proteins
• Activate genes and induce protein synthesis
Trang 54Copyright © 2010 Pearson Education, Inc. Figure 11.17b
2
Receptor activates G protein.
3
G protein activates adenylate cyclase.
4
Adenylate cyclase converts ATP to cAMP (2nd messenger).
cAMP changes membrane permeability
by opening or closing ion channels.
5b
cAMP activates enzymes.
5c
cAMP activates specific genes.
Active enzyme GDP
5a
(b) G-protein linked receptors cause formation of an intracellular second messenger (cyclic
AMP in this case) that brings about the cell’s response.
Nucleus
Trang 55Copyright © 2010 Pearson Education, Inc. Figure 11.17b, step 1
(b) G-protein linked receptors cause formation of an intracellular second messenger (cyclic
AMP in this case) that brings about the cell’s response.
Trang 56Copyright © 2010 Pearson Education, Inc. Figure 11.17b, step 2
(b) G-protein linked receptors cause formation of an intracellular second messenger (cyclic
AMP in this case) that brings about the cell’s response.
Nucleus
1
2
Trang 57Copyright © 2010 Pearson Education, Inc. Figure 11.17b, step 3
(b) G-protein linked receptors cause formation of an intracellular second messenger (cyclic
AMP in this case) that brings about the cell’s response.
G protein activates adenylate
1
2 3
Trang 58Copyright © 2010 Pearson Education, Inc. Figure 11.17b, step 4
(b) G-protein linked receptors cause formation of an intracellular second messenger (cyclic
AMP in this case) that brings about the cell’s response.
Neurotransmitter
(1st messenger) binds
and activates receptor.
Receptor activates G protein.
G protein activates adenylate cyclase.
Adenylate cyclase converts ATP to cAMP
1
2 3 4
Trang 59Copyright © 2010 Pearson Education, Inc. Figure 11.17b, step 5a
(b) G-protein linked receptors cause formation of an intracellular second messenger (cyclic
AMP in this case) that brings about the cell’s response.
Neurotransmitter
(1st messenger) binds
and activates receptor.
Receptor activates G protein.
G protein activates adenylate cyclase.
Adenylate cyclase converts ATP to cAMP (2nd messenger).
cAMP changes membrane permeability by opening and closing ion channels.
Nucleus
1
2 3 4
5a
Trang 60Copyright © 2010 Pearson Education, Inc. Figure 11.17b, step 5b
(b) G-protein linked receptors cause formation of an intracellular second messenger (cyclic
AMP in this case) that brings about the cell’s response.
Neurotransmitter
(1st messenger) binds
and activates receptor.
Receptor activates G protein.
G protein activates adenylate cyclase.
Adenylate cyclase converts ATP to cAMP (2nd messenger).
cAMP changes membrane permeability by opening and closing ion channels.
cAMP activates enzymes.
Trang 61Copyright © 2010 Pearson Education, Inc. Figure 11.17b, step 5c
(b) G-protein linked receptors cause formation of an intracellular second messenger (cyclic
AMP in this case) that brings about the cell’s response.
Neurotransmitter
(1st messenger) binds
and activates receptor.
Receptor activates G protein.
G protein activates adenylate cyclase.
Adenylate cyclase converts ATP to cAMP (2nd messenger).
cAMP changes membrane permeability by opening and closing ion channels.
cAMP activates enzymes.
cAMP activates specific genes.