Neurons, Synapses, and Signaling

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Chapter 48 Neurons, Synapses, and Signaling PowerPoint Lecture Presentations for Biology Eighth Edition Neil Campbell and Jane Reece Lectures by Chris Romero, updated by Erin Barley with contributions from Joan Sharp Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Overview: Lines of Communication The cone snail kills prey with venom that disables neurons 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) Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-1

The transmission of information depends on the path of neurons along which a signal travels Processing of information takes place in simple clusters of neurons called ganglia or a more complex organization of neurons called a brain Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Concept 48.1: Neuron organization and structure reflect function in information transfer The squid possesses extremely large nerve cells and is a good model for studying neuron function Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Introduction to Information Processing Nervous systems process information in three stages: sensory input, integration, and motor output Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-2 Ganglia Nerves with giant axons Brain Arm Nerve Eye Mantle

Fig. 48-2a

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 Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Many animals have a complex nervous system which 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 brings information into and out of the CNS Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-3 Sensory input Sensor Integration Motor output Effector Peripheral nervous system (PNS) Central nervous system (CNS)

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 An axon joins the cell body at the axon hillock Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-4 Dendrites Stimulus Nucleus Cell body Axon hillock Presynaptic cell Axon Synapse Synaptic terminals Neurotransmitter Postsynaptic cell

Fig. 48-4a Synapse Synaptic terminals Neurotransmitter Postsynaptic cell

A synapse is a junction between an axon and another cell The synaptic terminal of one axon passes information across the synapse in the form of chemical messengers called neurotransmitters Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Information is transmitted from a presynaptic cell (a neuron) to a postsynaptic cell (a neuron, muscle, or gland cell) Most neurons are nourished or insulated by cells called glia Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-5 Dendrites Axon Cell body Portion of axon 80 µm Cell bodies of overlapping neurons Sensory neuron Interneurons Motor neuron

Fig. 48-5a Dendrites Axon Cell body Sensory neuron

Fig. 48-5b Portion of axon 80 µm Cell bodies of overlapping neurons Interneurons

Fig. 48-5c 80 µm Cell bodies of overlapping neurons

Fig. 48-5d Motor neuron

Concept 48.2: Ion pumps and ion channels maintain the resting potential of a neuron Every cell has a voltage (difference in electrical charge) across its plasma membrane called a membrane potential Messages are transmitted as changes in membrane potential The resting potential is the membrane potential of a neuron not sending signals Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Formation of the Resting Potential In a mammalian neuron at resting potential, the concentration of K + is greater inside the cell, while the concentration of Na + is greater outside the cell Sodium-potassium pumps use the energy of ATP to maintain these K + and Na + gradients across the plasma membrane These concentration gradients represent chemical potential energy Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

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 Anions trapped inside the cell contribute to the negative charge within the neuron Animation: Resting Potential Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-6 Key Na + K + Sodiumpotassium pump Potassium channel Sodium channel OUTSIDE CELL OUTSIDE CELL [K + ] 5 mm [Na + ] 150 mm [Cl ] 120 mm INSIDE CELL [K + ] 140 mm [Na + ] 15 mm [Cl ] 10 mm [A ] 100 mm INSIDE CELL (a) (b)

Fig. 48-6a OUTSIDE [K + ] CELL 5 mm [Na + ] 150 mm [Cl ] 120 mm INSIDE CELL [K + ] 140 mm [Na + ] 15 mm [Cl ] 10 mm [A ] 100 mm (a)

Fig. 48-6b Key Na + K + Sodiumpotassium pump Potassium channel Sodium channel OUTSIDE CELL INSIDE CELL (b)

Modeling of the Resting Potential Resting potential can be modeled by an artificial membrane that separates two chambers The concentration of KCl is higher in the inner chamber and lower in the outer chamber K + diffuses down its gradient to the outer chamber Negative charge builds up in the inner chamber At equilibrium, both the electrical and chemical gradients are balanced Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-7 Inner chamber 90 mv Outer chamber +62 mv 140 mm 5 mm KCI KCI 15 mm NaCI 150 mm NaCI Cl Potassium channel K + Cl Na + Sodium channel (a) Membrane selectively permeable to K + (b) Membrane selectively permeable to Na + E K = 62 mv(log 5 mm 150 mm = 90 mv E 140 mm) Na = 62 mv (log 15 mm ) = +62 mv

Fig. 48-7a Inner chamber 90 mv Outer chamber 140 mm 5 mm KCI KCI Potassium channel K + Cl (a) Membrane selectively permeable to K + E K = 62 mv(log 5 mm 140 mm) = 90 mv

The equilibrium potential (E ion ) is the membrane voltage for a particular ion at equilibrium and can be calculated using the Nernst equation: E ion = 62 mv (log[ion] outside /[ion] inside ) The equilibrium potential of K + (E K ) is negative, while the equilibrium potential of Na + (E Na ) is positive Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

In a resting neuron, the currents of K + and Na + are equal and opposite, and the resting potential across the membrane remains steady Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-7b +62 mv 15 mm NaCI 150 mm NaCI Cl Na + Sodium channel (b) Membrane selectively permeable to Na + E Na = 62 mv (log 150 mm 15 mm ) = +62 mv

Concept 48.3: Action potentials are the signals conducted by axons Neurons contain gated ion channels that open or close in response to stimuli Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-8 TECHNIQUE Microelectrode Voltage recorder Reference electrode

Membrane potential changes in response to opening or closing of these channels 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 Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-9 Stimuli Stimuli Strong depolarizing stimulus +50 +50 +50 Action potential Membrane potential (mv) 0 Membrane potential (mv) 50 Threshold 50 0 Threshold Membrane potential (mv) 0 50 Threshold Resting potential Hyperpolarizations 100 100 0 1 2 3 4 5 Time (msec) Resting potential Depolarizations 0 1 2 3 4 5 Time (msec) 100 Resting potential 0 1 2 3 4 5 6 Time (msec) (a) Graded hyperpolarizations (b) Graded depolarizations (c) Action potential

Fig. 48-9a +50 Stimuli Membrane potential (mv) 0 50 Threshold 100 Resting potential Hyperpolarizations 0 1 2 3 4 5 Time (msec) (a) Graded hyperpolarizations

Other stimuli trigger 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 Graded potentials are changes in polarization where the magnitude of the change varies with the strength of the stimulus Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-9b +50 Stimuli Membrane potential (mv) 0 50 Threshold 100 Resting potential Depolarizations 0 1 2 3 4 5 Time (msec) (b) Graded depolarizations

Production of Action Potentials Voltage-gated Na + and K + channels respond to a change in membrane potential When a stimulus depolarizes the membrane, Na + channels open, allowing Na + to diffuse into the cell The movement of Na + into the cell increases the depolarization and causes even more Na + channels to open A strong stimulus results in a massive change in membrane voltage called an action potential Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-9c Strong depolarizing stimulus +50 Action potential Membrane potential (mv) 0 50 Threshold Resting potential 100 (c) Action potential 0 1 2 3 4 5 Time (msec) 6

An action potential occurs if a stimulus causes the membrane voltage to cross a particular threshold An action potential is a brief all-or-none depolarization of a neuron s plasma membrane Action potentials are signals that carry information along axons Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Generation of Action Potentials: A Closer Look A neuron can produce hundreds of action potentials per second The frequency of action potentials can reflect the strength of a stimulus An action potential can be broken down into a series of stages Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-10-1 Key Na + K + Depolarization Membrane potential (mv) +50 0 50 Action potential 100 Time Threshold 1 2 3 Resting potential 4 5 1 Extracellular fluid Sodium channel Potassium channel Plasma membrane Cytosol Inactivation loop 1 Resting state

Fig. 48-10-2 Key Na + K + 2 Depolarization Membrane potential (mv) +50 0 50 Action potential 100 Time Threshold 1 2 3 Resting potential 4 5 1 Extracellular fluid Sodium channel Potassium channel Plasma membrane Cytosol Inactivation loop 1 Resting state

Fig. 48-10-3 Key Na + K + 3 Rising phase of the action potential 2 Depolarization Membrane potential (mv) +50 0 50 Action potential 100 Time Threshold 1 2 3 Resting potential 4 5 1 Extracellular fluid Sodium channel Potassium channel Plasma membrane Cytosol Inactivation loop 1 Resting state

Fig. 48-10-4 Key Na + K + Rising phase of the action potential 3 4 Falling phase of the action potential 2 Depolarization Membrane potential (mv) +50 0 50 Action potential 100 Time Threshold 1 2 3 Resting potential 4 5 1 Extracellular fluid Sodium channel Potassium channel Plasma membrane Cytosol Inactivation loop 1 Resting state

Fig. 48-10-5 Key Na + K + Rising phase of the action potential 3 4 Falling phase of the action potential 2 Depolarization Membrane potential (mv) +50 0 50 Action potential 100 Time Threshold 1 2 3 Resting potential 4 5 1 Extracellular fluid Sodium channel Potassium channel Plasma membrane Cytosol Inactivation loop 1 Resting state 5 Undershoot

At resting potential 1. Most voltage-gated Na + and K + channels are closed, but some K + channels (not voltagegated) are open Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

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 Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

5. During the undershoot, membrane permeability to K + is at first higher than at rest, then voltagegated K + channels close; resting potential is restored Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

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 BioFlix: : How Neurons Work Animation: Action Potential Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Conduction of Action Potentials An action potential can travel long distances by regenerating itself along the axon At the site where the action potential is generated, usually the axon hillock, an electrical current depolarizes the neighboring region of the axon membrane Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Inactivated Na + channels behind the zone of depolarization prevent the action potential from traveling backwards Action potentials travel in only one direction: toward the synaptic terminals Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-11-1 Axon Action potential Plasma membrane Na + Cytosol

Fig. 48-11-2 Axon Action potential Plasma membrane Na + Cytosol K + Action potential Na + K +

Fig. 48-11-3 Axon Action potential Plasma membrane Na + Cytosol K + Action potential Na + K + K + Action potential Na + K +

Conduction Speed 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 Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-12 Node of Ranvier Layers of myelin Axon Axon Myelin sheath Schwann cell Nodes of Ranvier Schwann cell Nucleus of Schwann cell 0.1 µm

Fig. 48-12a Node of Ranvier Layers of myelin Axon Axon Myelin sheath Schwann cell Nodes of Ranvier Schwann cell Nucleus of Schwann cell

Fig. 48-12b Myelinated axon (cross section) 0.1 µm

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 Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-13 Schwann cell Depolarized region (node of Ranvier) Cell body Myelin sheath Axon

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 Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-14 Postsynaptic neuron Synaptic terminals of presynaptic neurons 5 µm

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 Animation: Synapse Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-15 Synaptic vesicles containing neurotransmitter Presynaptic membrane 5 K + Na+ Voltage-gated Ca 2+ channel 1 Ca 2+ 2 4 Postsynaptic membrane 6 Synaptic cleft 3 Ligand-gated ion channels

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 Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

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 Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

After release, the neurotransmitter May diffuse out of the synaptic cleft May be taken up by surrounding cells May be degraded by enzymes Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Summation of Postsynaptic Potentials Unlike action potentials, postsynaptic potentials are graded and do not regenerate 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 If two EPSPs are produced in rapid succession, an effect called temporal summation occurs Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-16 E 1 Terminal branch of presynaptic neuron E 1 E 1 E 1 E 2 E 2 E 2 E 2 Postsynaptic neuron I I Axon hillock I I Membrane potential (mv) 0 70 Resting potential Threshold of axon of postsynaptic neuron E 1 E 1 E 1 E 1 Action potential E 1 + E 2 Action potential E 1 I E 1 + I (a) Subthreshold, no summation (b) Temporal summation (c) Spatial summation (d) Spatial summation of EPSP and IPSP

Fig. 48-16ab E 1 Terminal branch of presynaptic neuron E 1 E 2 E 2 Postsynaptic neuron I I Axon hillock Membrane potential (mv) 0 70 Resting potential E 1 Threshold of axon of postsynaptic neuron E 1 Action potential E 1 E 1 (a) Subthreshold, no summation (b) Temporal summation

In spatial summation, EPSPs produced nearly simultaneously by different synapses on the same postsynaptic neuron add together The combination of EPSPs through spatial and temporal summation can trigger an action potential Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-16cd E 1 E 1 E 2 E 2 I I Membrane potential (mv) 0 70 E 1 + E 2 Action potential E 1 I E 1 + I (c) Spatial summation (d) Spatial summation of EPSP and IPSP

Through summation, an IPSP can counter the effect of an EPSP The summed effect of EPSPs and IPSPs determines whether an axon hillock will reach threshold and generate an action potential Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Modulated 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 Effects of indirect synaptic transmission have a slower onset but last longer Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Neurotransmitters The same neurotransmitter can produce different effects in different types of cells There are five major classes of neurotransmitters: acetylcholine, biogenic amines, amino acids, neuropeptides, and gases Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Table 48-1

Table 48-1a

Table 48-1b

Acetylcholine Acetylcholine is a common neurotransmitter in vertebrates and invertebrates In vertebrates it is usually an excitatory transmitter Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Biogenic Amines Biogenic amines include epinephrine, norepinephrine, dopamine, and serotonin They are active in the CNS and PNS Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Amino Acids Two amino acids are known to function as major neurotransmitters in the CNS: gammaaminobutyric acid (GABA) and glutamate Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Neuropeptides Several neuropeptides, relatively short chains of amino acids, also function as neurotransmitters Neuropeptides include substance P and endorphins, which both affect our perception of pain Opiates bind to the same receptors as endorphins and can be used as painkillers Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-17 EXPERIMENT Radioactive naloxone Drug Protein mixture RESULTS Proteins trapped on filter Measure naloxone bound to proteins on each filter

Fig. 48-17a EXPERIMENT Radioactive naloxone Drug Protein mixture Proteins trapped on filter Measure naloxone bound to proteins on each filter

Fig. 48-17b RESULTS

Gases Gases such as nitric oxide and carbon monoxide are local regulators in the PNS Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Fig. 48-UN1 Action potential +50 Membrane potential (mv) 0 50 100 70 Rising phase Depolarization Falling phase Time (msec) Threshold ( 55) Undershoot Resting potential

Fig. 48-UN2 Electrode Squid axon

Fig. 48-UN3

You should now be able to: 1. Distinguish among the following sets of terms: sensory neurons, interneurons, and motor neurons; membrane potential and resting potential; ungated and gated ion channels; electrical synapse and chemical synapse; EPSP and IPSP; temporal and spatial summation 2. Explain the role of the sodium-potassium pump in maintaining the resting potential Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

3. Describe the stages of an action potential; explain the role of voltage-gated ion channels in this process 4. Explain why the action potential cannot travel back toward the cell body 5. Describe saltatory conduction 6. Describe the events that lead to the release of neurotransmitters into the synaptic cleft Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

7. Explain the statement: Unlike action potentials, which are all-or-none events, postsynaptic potentials are graded 8. Name and describe five categories of neurotransmitters Copyright 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings