Chapter 12 Central Nervous System Flashcards

1
Q

The nervous system

A

Brain and spinal cord
Receptors of sense organs (eyes, ears, etc.)
Nerves that connect to other systems

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2
Q

Nervous tissue contains two kinds of cells

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Neurons for intercellular communication
Neuroglia (glial cells)

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3
Q

Neuroglia (glial cells)

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Essential to survival and function of neurons
Preserve structure of nervous tissue

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4
Q

Anatomical divisions of the nervous system

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Central nervous system
Peripheral nervous system

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5
Q

Central nervous system (CNS)

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Brain and spinal cord
Consists of nervous tissue, connective tissue, and blood vessels
Functions to process and coordinate sensory data from inside and outside body
Motor commands control activities of peripheral organs (e.g., skeletal muscles)
Higher functions of brain include intelligence, memory, learning, and emotion

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6
Q

Special Sensory Receptors Path

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Smell, Taste, Vision, Balance, Hearing - to Afferent Div of the PNS then to brain (CNS)

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7
Q

Visceral Sensory Receptors Path

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Monitors internal organs, to Afferent Div of the PNS then to brain

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8
Q

Somatic Sensory Receptors Path

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Skeletal, Muscle, Joints, Skin, (External Senses) to Afferent Div of PNS and then to brain

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9
Q

From Brain (CNS) to Skeletal Syst

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Brain to Efferent Motor Command then to Somatic Nervous Syst (SNS), to Skeletal syst.

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10
Q

From Brain to Parasympathetic System

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Brain, To Efferent Syst, Motor Commands, Autonomic Nervous Syst (ANS), Parasympathetic Syst to Smooth Muscle, Cardiac Muscle and Glands

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11
Q

From Brain to Sympathetic Nervous Syst

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Brain, to Efferent Motor Commands, Autonomic Nervous Syst (ANS), Sympathetic Syst. to Smooth Muscle, Cardiac Muscle, Glands and Adipose Tissue

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12
Q

Neurons

A

Basic functional units of the nervous system
Send and receive signals
Function in communication, information processing, and control

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13
Q

Neurons – Cell body (soma)

A

Large nucleus and nucleolus
Perikaryon (cytoplasm)
Mitochondria (produce energy)
RER (Rough Endoplasmic Reticulum) and ribosomes (synthesize proteins)

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14
Q

Cytoskeleton of perikaryon

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Neurofilaments and neurotubules
Similar to intermediate filaments and microtubules
Neurofibrils
Bundles of neurofilaments that provide support for dendrites and axon

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15
Q

Nissl bodies

A

Dense areas of RER and ribosomes in perikaryon
Make nervous tissue appear gray (gray matter)

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16
Q

Dendrites

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Short and highly branched processes extending from cell body

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17
Q

Dendritic spines

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Fine processes on dendrites
Receive information from other neurons
80–90 percent of neuron surface area

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18
Q

Axon

A

Single, long cytoplasmic process
Propagates electrical signals (action potentials)

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19
Q

Axoplasm

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Cytoplasm of axon
Contains neurofibrils, neurotubules, enzymes, and organelles

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20
Q

Structures of the axon

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Axolemma - Plasma membrane of the axon and Covers the axoplasm

Initial segment - Base of axon

Axon hillock - Thick region that attaches initial segment to cell body

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21
Q

Structures of the axon pt 2

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Collaterals
Branches of the axon
Telodendria
Fine extensions of distal axon
Axon terminals (synaptic terminals)
Tips of telodendria

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22
Q

Neurons - Axonal (axoplasmic) transport

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Movement of materials between cell body and axon terminals
Materials move along neurotubules within axon
Powered by mitochondria, kinesin, and dynein

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23
Q

Structural classification of neurons

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Anaxonic neurons - May have more than 2 processes
Small and may all be Dendrites
All cell processes look similar, Axons not Obvious
Found in brain and special sense organs
Bipolar neurons - 2 processes, Seperated by Cell Body
Small and rare
One dendrite and one axon
Found in special sense organs (sight, smell, hearing)

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24
Q

Structural classification of neurons pt 2

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Unipolar neurons (pseudounipolar neurons)
Single Elongated Process off to the side
Axon and dendrites are fused
Cell body to one side
Most sensory neurons of PNS
Multipolar neurons - have more than 2 processes
Has single long axon and multiple dendrites
Common in the CNS
All motor neurons that control skeletal muscles

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25
Sensory neurons (afferent neurons)
Unipolar Cell bodies grouped in sensory ganglia Processes (afferent fibers) extend from sensory receptors to CNS
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Somatic sensory neurons
Monitor external environment
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Visceral sensory neurons
Monitor internal environment
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Ganglia
Nerve cell cluster or a group of nerve cell bodies located in the autonomic nervous system and sensory system ganglia house the cells bodies of afferent nerves and efferent nerves
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Sensory receptors
Interoceptors Monitor internal systems (e.g., digestive, urinary) Internal senses (stretch, deep pressure, pain) Exteroceptors Monitor external environment (e.g., temperature) Complex senses (e.g., sight, smell, hearing) Proprioceptors Monitor position and movement of skeletal muscles and joints
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Types of sensory receptors pt 2
Proprioceptors (cont) Carry instructions from CNS to peripheral effectors Via efferent fibers (axons) Somatic motor neurons of SNS Innervate skeletal muscles Visceral motor neurons of ANS Innervate all other peripheral effectors Smooth and cardiac muscle, glands, adipose tissue
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Motor neurons
Signals from CNS to visceral effectors cross autonomic ganglia that divide axons into Preganglionic fibers Postganglionic fibers
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Interneurons
Most are in brain and spinal cord Some in autonomic ganglia Located between sensory and motor neurons Responsible for Distribution of sensory information Coordination of motor activity Involved in higher functions Memory, planning, learning
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Neuroglia
Support and protect neurons Make up half the volume of the nervous system Many types in CNS and PNS
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Neuroglia
Types of NEUROGLIA Astrocytes Ependymal Oligodendrites Microgila
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Astrocytes (Brain) Star Shaped, anchor to capillaries
Blood Brain Barrier, structural support, regulate ion, neutrient, gas concentrations, absorb recycle neurotransmitters, scar tissue after injury Have large cell bodies with many processes Function to Maintain blood brain barrier (BBB) Create three-dimensional framework for CNS Repair damaged nervous tissue Guide neuron development Control interstitial environment
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Ependymals (Brain) - simple cuboidal epithelial cells that line fluid- filled passageways within the brain and spinal cord
line the ventricles + central canal (spinal cord), assist with cerebrospinal fluid Form epithelium that lines central canal of spinal cord and ventricles of brain Produce and monitor cerebrospinal fluid (CSF) Have cilia that help circulate CSF
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Oligodendrites (Brain)
structural framework, myelinate sheet like process that surrounds CNS Axons, increases speed of action potentials. Nerves appear white. Internodes—myelinated segments of axon Nodes (nodes of Ranvier) lie between internodes Where axons may branch White matter Regions of CNS with many myelinated axons Gray matter of CNS Contains unmyelinated axons, neuron cell bodies, and dendrites
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Microgila (Brain) - are phagocytes
Smallest and least numerous neuroglia Have many fine-branched processes Migrate through nervous tissue Clean up cellular debris, wastes, and pathogens by phagocytosis
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Neural responses to injuries
Wallerian degeneration Axon distal to injury degenerates Schwann cells Form path for new growth Wrap around new axon
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Nerve regeneration in CNS
Limited by astrocytes, which Produce scar tissue Release chemicals that block regrowth
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All plasma (cell) membranes produce electrical signals by ion movements
Membrane potential is particularly important to neurons
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Resting membrane potential
Three important concepts The extracellular fluid (ECF) and intracellular fluid (cytosol) differ greatly in ionic composition Extracellular fluid contains high concentrations of Na+ and Cl– Cytosol contains high concentrations of K+ and negatively charged proteins Cells have selectively permeable membranes Membrane permeability varies by ion
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Graded potential
Temporary, localized change in resting potential Caused by a stimulus
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Action potential (nerve impulses) All-or-none principle Any stimulus that changes the membrane potential to threshold Will cause an action potential All action potentials are the same No matter how large the stimulus An action potential is either triggered or not
Is an electrical impulse Produced by graded potential Propagates along surface of axon to synapse Propagated changes in membrane potential Affect an entire excitable membrane Begin at initial segment of axon Do not diminish as they move away from source Stimulated by a graded potential that depolarizes the axolemma to threshold Threshold for an axon is –60 to –55 mV
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Passive processes acting across cell membrane
Current Movement of charges to eliminate a potential difference Resistance How much the membrane restricts ion movement If resistance is high, current is small
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Passive processes acting across cell membrane
Chemical gradients Concentration gradients of ions (Na+, K+) Electrical gradients Charges are separated by cell membrane Cytosol is negative relative to extracellular fluid
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Electrochemical gradient
Sum of chemical and electrical forces acting on an ion across the membrane A form of potential energy
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Equilibrium potential
Membrane potential at which there is no net movement of a particular ion across cell membrane K+ = –90 mV Na+ = +66 mV Plasma membrane is highly permeable to K+ Explains similarity of equilibrium potential for K+ and resting membrane potential (–70 mV) Resting membrane’s permeability to Na+ is very low So Na+ has a small effect on resting potential
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Resting membrane potential exists because: Cytosol differs from extracellular fluid in chemical and ionic composition Plasma membrane is selectively permeable
Membrane potential changes in response to temporary changes in membrane permeability Results from opening or closing of specific membrane channels In response to stimuli
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Na+ and K+ are the primary determinants of membrane potential
Passive ion channels (leak channels) Are always open Permeability changes with conditions Active ion channels (gated ion channels) Open and close in response to stimuli At resting membrane potential, most are closed
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Chemically Gated Ion Channel - (Active Channel)
Called Ligand - Gated Ion Channel. Opens when it binds to specific Chems (ie ACh) Found on cell bodies and dendrites of neurons
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Voltage-gated ion channels
Respond to changes in membrane potential Found in axons of neurons and sarcolemma of skeletal and cardiac muscle cells Activation gate opens when stimulated Inactivation gate closes to stop ion movement Three possible states Closed but capable of opening Open (activated) Closed and incapable of opening (inactivated)
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Mechanically gated ion channels
Respond to membrane distortion Found in sensory receptors that respond to touch, pressure, or vibration
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Graded potentials (local potentials) - Characteristics Membrane potential is most changed at site of stimulation; effect decreases with distance Effect spreads passively, due to local currents Graded change in membrane potential may involve depolarization or hyperpolarization Stronger stimuli produce greater changes in membrane potential and affect a larger area
Changes in membrane potential That cannot spread far from site of stimulation Produced by any stimulus that opens gated channels Example: a resting membrane is exposed to a chemical Chemically gated Na+ channels open Sodium ions enter cell Membrane potential rises (depolarization)
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Graded potentials - Repolarization When the stimulus is removed, membrane potential returns to normal Hyperpolarization Results from opening potassium ion channels Positive ions move out, not into cell Opposite effect of opening sodium ion channels Increases the negativity of the resting potential
Sodium ions move parallel to plasma membrane Producing local current Which depolarizes nearby regions of plasma membrane (graded potential) Change in potential is proportional to stimulus Often trigger specific cell functions Example: exocytosis of glandular secretions ACh causes graded potential at motor end plate at neuromuscular junction
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Resting membrane with closed chemically gated sodium ion channels
-70mv
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Membrane exposed to chemical that opens the sodium ion channels
-65mv
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Generation of action potentials Step 1: Depolarization to threshold Step 2: Activation of voltage-gated Na channels Na+ rushes into cytosol Inner membrane surface changes from negative to positive Results in rapid depolarization
Generation of action potentials Step 3: Inactivation of Na channels and activation of K+ channels At +30 mV, inactivation gates of voltage-gated Na+ channels close Voltage-gated K+ channels open K+ moves out of cytosol Repolarization begins
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Characteristics of graded potentials (Action Potentials) Membrane potential is most changed at site of stimulation; effect decreases with distance Effect spreads passively, due to local currents Graded change in membrane potential may involve depolarization or hyperpolarization Stronger stimuli produce greater changes in membrane potential and affect a larger area
Generation of action potentials Step 1: Depolarization to threshold Step 2: Activation of voltage-gated Na channels Na+ rushes into cytosol Inner membrane surface changes from negative to positive Results in rapid depolarization
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Depolarization to Threshold (-60mv)
The stimulus that initiates an action potential is a graded depolarization large enough to open voltage-gated sodium channels. The opening of the channels occurs at a membrane potential known as the threshold.
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Activation of Sodium Ion Channels and Rapid Depolarization (+10mv)
When the sodium channel activation gates open, the plasma membrane becomes much more permeable to Na+. Driven by the large electrochemical gradient, sodium ions rush into the cytosol, and rapid depolarization occurs. The inner membrane surface now has more positive ions than negative ones, and the membrane potential has changed from −60 mV to a positive value.
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Generation of action potentials Step 3: Inactivation of Na channels and activation of K+ channels At +30 mV, inactivation gates of voltage-gated Na+ channels close Voltage-gated K+ channels open K+ moves out of cytosol Repolarization begins
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Inactivation of Sodium Ion Channels and Activation of Potassium Ion Channels Starts Repolarization
As the membrane potential approaches +30 mV, the inactivation gates of the voltage-gated sodium channels close. This step is known as sodium channel inactivation, and it coincides with the opening of voltage-gated potassium channels. Positively charged potassium ions move out of the cytosol, shifting the membrane potential back toward the resting level. Repolarization now begins
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Generation of action potentials Step 4: Return to resting membrane potential Voltage-gated K+ channels begin to close As membrane reaches normal resting potential K+ continues to leave cell Membrane is briefly hyperpolarized to –90 mV After all voltage-gated K+ channels finish closing Resting membrane potential is restored Action potential is over
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Time Lag in Closing All Potassium Ion Channels Leads to Temporary Hyperpolarization
The voltage-gated sodium channels remain inactivated until the membrane has repolarized to near threshold level. At this time, they regain their normal status: closed but capable of opening. The voltage-gated potassium channels begin closing as the membrane reaches the normal resting membrane potential (about −70 mV). Until all of these potassium channels have closed, potassium ions continue to leave the cell. This produces a brief hyperpolarization.
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After all the voltage-gated potassium channels close, the membrane potential returns to the normal resting level. The action potential is now over, and the membrane is once again at the resting membrane potential.
Refractory period From beginning of action potential To return to resting state During which the membrane will not respond normally to additional stimuli
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Absolute refractory period All voltage-gated Na+ channels are already open or inactivated Membrane cannot respond to further stimulation
Relative refractory period Begins when Na+ channels regain resting condition Continues until membrane potential stabilizes Only a strong stimulus can initiate another action potential
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Depolarization results from influx of Na+ Repolarization involves loss of K+ Sodium–potassium exchange pump Returns concentrations to prestimulation levels Maintains concentration gradients of Na+ and K+ over time Uses one ATP for each exchange of two extracellular K+ for three intracell ular Na+
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Propagation Moves an action potential along an axon in a series of steps
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Continuous propagation of action potentials
Occurs in unmyelinated axons Affects one segment of an axon at a time Step 1: Action potential develops at initial segment Depolarizes membrane to +30 mV Step 2: Local current develops Depolarizes second segment to threshold
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1) As an action potential develops at the initial segment, the membrane potential at this site depolarizes to +30 mV
2) A local current then develops as the sodium ions entering at 1 spread away from the open voltage-gated channels. A graded depolarization quickly brings the axon membrane (axolemma) in segment 2 to threshold.
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Continuous propagation Step 3: Action potential occurs in second segment Initial segment begins repolarization Step 4: Local current depolarizes next segment Cycle repeats Action potential travels in one direction (1 m/sec)
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Saltatory propagation of action potentials Occurs in myelinated axons Faster than continuous propagation Requires less energy Myelin prevents continuous propagation Local current “jumps” from node to node Depolarization occurs only at nodes
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Axon diameter affects propagation speed of action potentials
The larger the diameter, the lower the resistance and faster the speed
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Types of axons based on diameter, myelination, and propagation speed
Type A fibers Type B fibers Type C fibers
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Type A fibers Myelinated Large diameter Transmit information to and from CNS rapidly (120 m/sec), for example Sensory information such as position and balance Motor impulses to skeletal muscles
Type B fibers Myelinated Medium diameter Transmit information at intermediate speeds (18 m/sec) Type C fibers Unmyelinated Small diameter Transmit information slowly (1 m/sec) Example: most sensory information
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Messages carried by nerves are routed according to priority Critical information is transmitted through Type A fibers, for example
Sensory information about things that threaten survival Motor commands that prevent injury
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Synapse Specialized site where a neuron communicates with another cell
Presynaptic neuron Sends the message Postsynaptic neuron Receives message
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Types of synapses
Electrical synapses Direct physical contact between cells Presynaptic and postsynaptic membranes are locked together at gap junctions Ions pass between cells through pores Local current affects both cells Action potentials are propagated quickly Found in some areas of brain, the eye, and ciliary ganglia Chemical synapses Signal transmitted across a gap by neurotransmitters
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Chemical synapses
Most common type of synapse between neurons Only type of synapse between neurons and other cells Cells are separated by synaptic cleft Presynaptic cell sends the message Postsynaptic cell receives the message
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Types of chemical synapses
Neuromuscular junction Synapse between neuron and skeletal muscle cell Neuroglandular junction Synapse between neuron and gland cell
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Neurotransmitters
Chemical messengers contained within synaptic vesicles in axon terminal of presynaptic cell Released into synaptic cleft Affect receptors of postsynaptic membrane Broken down by enzymes Reabsorbed and reassembled by axon terminal
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Function of chemical synapses
Axon terminal releases neurotransmitters that bind to postsynaptic plasma membrane Produces localized change in permeability and graded potentials Action potential may or may not be generated in postsynaptic cell, depending on Amount of neurotransmitter released Sensitivity of postsynaptic cell
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Cholinergic synapses Release acetylcholine (ACh) at All neuromuscular junctions involving skeletal muscle fibers Many synapses in CNS All neuron-to-neuron synapses in PNS All neuromuscular and neuroglandular junctions in parasympathetic division of ANS
Release acetylcholine (ACh) at All neuromuscular junctions involving skeletal muscle fibers Many synapses in CNS All neuron-to-neuron synapses in PNS All neuromuscular and neuroglandular junctions in parasympathetic division of ANS
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Events at a cholinergic synapse
Action potential arrives at axon terminal and depolarizes membrane Extracellular calcium ions enter axon terminal and trigger exocytosis of ACh ACh binds to receptors on postsynaptic membrane and depolarize it ACh is removed from synaptic cleft by acetylcholinesterase (AChE) AChE breaks ACh into acetate and choline
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Synaptic delay
A synaptic delay of 0.2–0.5 msec occurs between Arrival of action potential at axon terminal And effect on postsynaptic membrane Mostly due to time required for calcium ion influx and neurotransmitter release Fewer synapses lead to faster responses Some reflexes involve only one synapse
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Synaptic fatigue
Occurs when neurotransmitter cannot be recycled fast enough to meet demands of intense stimuli Response of synapse weakens until ACh is replenished
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Classes of neurotransmitters
Excitatory neurotransmitters Cause depolarization of postsynaptic membranes Promote action potentials Inhibitory neurotransmitters Cause hyperpolarization of postsynaptic membranes Suppress action potentials
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The effect of a neurotransmitter on postsynaptic membrane Depends on the properties of the receptor Not on the nature of the neurotransmitter
Major classes of neurotransmitters include Biogenic amines Amino acids Neuropeptides Dissolved gases
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Biogenic amines
Norepinephrine (NE) Released by adrenergic synapses Excitatory and depolarizing effect Widely distributed in brain and portions of ANS Dopamine A CNS neurotransmitter May be excitatory or inhibitory Involved in Parkinson’s disease and cocaine use
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Biogenic amines
Serotonin CNS neurotransmitter Affects attention and emotional states Gamma-aminobutyric acid (GABA) Inhibitory effect Functions in CNS are not well understood
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Neuromodulators
Chemicals released by axon terminals that alter Rate of neurotransmitter release Or response by postsynaptic cell Effects are long term and slow to appear Responses involve multiple steps and intermediary compounds Affect presynaptic membrane, postsynaptic membrane, or both Released alone or with a neurotransmitter
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Dissolved gases Are important neurotransmitters
Nitric oxide (NO) Carbon monoxide (CO)
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Neurotransmitters and neuromodulators may have A direct effect on membrane potential By opening or closing chemically gated ion channels Example: ACh, glutamate, aspartate An indirect effect through G proteins Example: E, NE, dopamine, serotonin, histamine, GABA An indirect effect via intracellular enzymes Example: lipid-soluble gases (NO, CO)
Indirect effects by second messengers G protein links First messenger (neurotransmitter) And second messengers (ions or molecules in cell) G proteins include an enzyme that is activated when an extracellular compound binds Example: adenylate cyclase Produces the second messenger cyclic-AMP (cAMP)
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Indirect effects by intracellular enzymes
Lipid-soluble gases (NO, CO) Diffuse through lipid membranes Bind to enzymes inside of brain cells
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Information processing
Response of postsynaptic cell (integration of stimuli) At the simplest level (individual neurons) Many dendrites receive neurotransmitter messages simultaneously Some excitatory, some inhibitory Net effect on axon hillock determines if action potential is produced
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Indirect effects by intracellular enzymes Lipid-soluble gases (NO, CO) Diffuse through lipid membranes Bind to enzymes inside of brain cells
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Postsynaptic potentials
Graded potentials developed in a postsynaptic cell In response to neurotransmitters Types of postsynaptic potentials Excitatory postsynaptic potential (EPSP) Graded depolarization of postsynaptic membrane Inhibitory postsynaptic potential (IPSP) Graded hyperpolarization of postsynaptic membrane
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Information Processing
A neuron that receives many IPSPs Is inhibited from producing an action potential Because the stimulation needed to reach threshold is increased To trigger an action potential One EPSP is not enough EPSPs (and IPSPs) combine through summation Temporal summation Spatial summation
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Temporal summation Rapid, repeated stimuli at a single synapse
Spatial summation Simultaneous stimuli arrive at multiple synapses
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A neuron becomes facilitated As EPSPs accumulate And raise membrane potential closer to threshold Until a small stimulus can trigger action potential Summation of EPSPs and IPSPs Neuromodulators and hormones Can change membrane sensitivity to neurotransmitters Shifting balance between EPSPs and IPSPs
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Axoaxonic synapses
Synapses between axons of two neurons Presynaptic inhibition Decreases the rate of neurotransmitter release at presynaptic membrane Presynaptic facilitation Increases the rate of neurotransmitter release at presynaptic membrane
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Information Processing -
Information may be conveyed simply by the frequency of action potentials received Depends on degree of depolarization above threshold Holding membrane potential above threshold Has the same effect as a second, large stimulus Maximum rate of action potentials is reached when relative refractory period is eliminated
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Summary Information is relayed in the form of action potentials Neurotransmitters released at a synapse may have excitatory or inhibitory effects Neuromodulators can alter rate of neurotransmitter release or response of a postsynaptic neuron Neurons may be facilitated or inhibited by chemicals other than neurotransmitters or neuromodulators
Summary Response of postsynaptic neuron can be altered by Neuromodulators or other chemicals that cause facilitation or inhibition Activity under way at other synapses Modification of rate of neurotransmitter release through facilitation or inhibition