What neurotransmitter is released by inhibitory fibers that bind to GABA-A receptors? A) Glutamate B) Serotonin C) GABA D) Dopamine E) Acetylcholine
C) GABA Explanation: Inhibitory fibers release GABA (gamma-aminobutyric acid), which binds to GABA-A receptors, playing a crucial role in inhibitory neurotransmission.
How does a strong stimulus affect action potential firing? A) It decreases the firing rate B) It causes no change in firing rate C) It leads to high frequency action potential firing D) It leads to irregular firing E) It stops action potential firing
C) It leads to high frequency action potential firing Explanation: A strong stimulus results in high frequency action potential firing, demonstrating that the intensity of the stimulus correlates with the frequency of action potentials produced.
1/123
p.18
Neurotransmitter Types and Their Functions

What neurotransmitter is released by inhibitory fibers that bind to GABA-A receptors?
A) Glutamate
B) Serotonin
C) GABA
D) Dopamine
E) Acetylcholine

C) GABA
Explanation: Inhibitory fibers release GABA (gamma-aminobutyric acid), which binds to GABA-A receptors, playing a crucial role in inhibitory neurotransmission.

p.10
Action Potentials and Electrical Signals

How does a strong stimulus affect action potential firing?
A) It decreases the firing rate
B) It causes no change in firing rate
C) It leads to high frequency action potential firing
D) It leads to irregular firing
E) It stops action potential firing

C) It leads to high frequency action potential firing
Explanation: A strong stimulus results in high frequency action potential firing, demonstrating that the intensity of the stimulus correlates with the frequency of action potentials produced.

p.22
Neurotransmitter Types and Their Functions

Which receptors are associated with Acetylcholine?
A) Dopaminergic & Serotonergic
B) Muscarinic & Nicotinic
C) GABAergic & Glycinergic
D) Noradrenergic & Adrenergic
E) Purinergic & Glutamatergic

B) Muscarinic & Nicotinic
Explanation: Acetylcholine is known to bind to two types of receptors: muscarinic and nicotinic, which play crucial roles in various physiological functions.

p.14
Mechanism of Neurotransmitter Release

What initiates the opening of voltage-gated calcium channels in the axon terminal?
A) Influx of potassium ions
B) Arrival of action potential
C) Release of neurotransmitters
D) Binding of neurotransmitters
E) Hyperpolarization of the membrane

B) Arrival of action potential
Explanation: The arrival of an action potential at the axon terminal leads to the opening of voltage-gated calcium channels, allowing calcium ions to enter the terminal and trigger neurotransmitter release.

p.6
Structure and Function of Neurons

What is the characteristic of C fibers?
A) Myelinated and fast
B) Unmyelinated and slow
C) Myelinated and slow
D) Unmyelinated and fast
E) None of the above

B) Unmyelinated and slow
Explanation: C fibers are characterized as the slowest nerve fibers and are unmyelinated, which contributes to their slower conduction velocity.

p.18
Excitatory and Inhibitory Postsynaptic Potentials

What is the result of a small amount of glutamate being released in the stimulation of A fiber?
A) Hyperpolarization
B) Action potential
C) EPSP
D) IPSP
E) No effect

C) EPSP
Explanation: The small amount of glutamate released leads to the opening of AMPA receptors, causing a small depolarization, which is classified as an excitatory postsynaptic potential (EPSP).

p.16
Mechanism of Neurotransmitter Release

What additional requirement is needed for NMDA receptor activation besides glutamate binding?
A) Hyperpolarization
B) Calcium influx
C) Depolarization
D) Chloride influx
E) Potassium efflux

C) Depolarization
Explanation: NMDA receptors require both the binding of glutamate and depolarization of the postsynaptic membrane to open, allowing sodium and calcium to enter the neuron.

p.12
Types of Synapses: Electrical vs. Chemical

How does current flow in electrical synapses?
A) Only in one direction
B) Through neurotransmitter release
C) Through the lumen of gap junctions
D) Via synaptic vesicles
E) By diffusion through the membrane

C) Through the lumen of gap junctions
Explanation: In electrical synapses, the current flows through the lumen of gap junctions, allowing for bidirectional transmission without delays.

p.3
Action Potentials and Electrical Signals

How does an action potential propagate along a neuron?
A) It decreases in amplitude with distance
B) It spreads without decrement
C) It only travels in one direction
D) It requires external energy
E) It is dependent on the presence of neurotransmitters

B) It spreads without decrement
Explanation: An action potential propagates without decrement, meaning its amplitude remains constant as it travels along the neuron, allowing for effective signal transmission.

p.2
Structure and Function of Neurons

What structures are primarily produced in the cell body of a neuron?
A) Synaptic vesicles and neurotransmitters
B) Dendrites and axons
C) Transmembrane proteins and phospholipid bilayers
D) Action potentials and electrotonic potentials
E) Ion channels and receptors

C) Transmembrane proteins and phospholipid bilayers
Explanation: The cell body contains organelles like the ER and Golgi apparatus, which are responsible for producing transmembrane proteins and phospholipid bilayers, including those found in synaptic vesicles.

p.16
Types of Synapses: Electrical vs. Chemical

What type of receptors are AMPA and NMDA classified as?
A) Metabotropic receptors
B) Ionotropic receptors
C) G-protein coupled receptors
D) Voltage-gated receptors
E) Enzyme-linked receptors

B) Ionotropic receptors
Explanation: AMPA and NMDA receptors are classified as ionotropic receptors, which are ligand-gated ion channels that respond to the binding of glutamate.

p.21
Mechanism of Neurotransmitter Release

What is the primary function of the V-type proton pump in neurotransmitter release?
A) To synthesize neurotransmitters
B) To pump protons into the vesicle lumen
C) To degrade neurotransmitters
D) To transport neurotransmitters across the synaptic cleft
E) To inhibit neurotransmitter release

B) To pump protons into the vesicle lumen
Explanation: The V-type proton pump uses ATP to pump protons into the lumen of the vesicle, acidifying it and creating a high concentration of H+, which is crucial for the uptake of neurotransmitters through secondary active transport.

p.7
Action Potentials and Electrical Signals

Why must the receptor potential evoke an action potential to reach the CNS?
A) Because receptor potentials are always strong
B) Because receptor potentials decay and do not reach the CNS
C) Because action potentials are not graded
D) Because all sensory signals are inhibitory
E) Because receptor potentials are too fast

B) Because receptor potentials decay and do not reach the CNS
Explanation: Receptor potentials decay over distance and time, so they must evoke an action potential to ensure that the signal can effectively reach the central nervous system.

p.9
Action Potentials and Electrical Signals

What causes hyperpolarization during the action potential process?
A) Opening of mechanosensitive channels
B) Opening of voltage-gated K+ potassium channels
C) Inactivation of sodium channels
D) Closure of sodium channels
E) Continuous sodium influx

B) Opening of voltage-gated K+ potassium channels
Explanation: The opening of voltage-gated K+ potassium channels leads to hyperpolarization, which occurs after the large depolarization phase of the action potential.

p.12
Types of Synapses: Electrical vs. Chemical

What are the two main types of synapses?
A) Electrical and Thermal
B) Chemical and Mechanical
C) Electrical and Chemical
D) Chemical and Magnetic
E) Electrical and Optical

C) Electrical and Chemical
Explanation: The two main types of synapses are electrical and chemical, each with distinct mechanisms and characteristics that facilitate neuronal communication.

p.7
Sensory Receptors and Detection of Stimuli

What happens to the receptor potential when a small mechanical stimulus is applied?
A) It causes hyperpolarization
B) It results in a large depolarization
C) It leads to a small depolarization
D) It has no effect
E) It causes an action potential immediately

C) It leads to a small depolarization
Explanation: A small mechanical stimulus results in a small depolarization of the receptor potential, demonstrating the graded nature of the electrotonic potential in sensory receptors.

p.22
Excitatory and Inhibitory Postsynaptic Potentials

What is the function of glycine in the spinal cord?
A) Opens EPSP
B) Inhibits neurotransmission
C) Opens IPSP
D) Stimulates muscle contraction
E) Enhances pain perception

C) Opens IPSP
Explanation: Glycine functions to open inhibitory postsynaptic potentials (IPSP), similar to GABA, and is primarily found in the spinal cord, contributing to inhibitory neurotransmission.

p.16
Excitatory and Inhibitory Postsynaptic Potentials

What is the primary ion that enters the postsynaptic neuron through AMPA receptors?
A) Calcium
B) Potassium
C) Chloride
D) Sodium
E) Magnesium

D) Sodium
Explanation: AMPA receptors are permeable to 'one-charge' cations, primarily allowing sodium ions to influx into the postsynaptic neuron.

p.22
Mechanism of Neurotransmitter Release

What is a common method for terminating the effect of neurotransmitters?
A) Reuptake by presynaptic neurons
B) Diffusion into the bloodstream
C) Conversion to hormones
D) Binding to receptors
E) Activation of glial cells

A) Reuptake by presynaptic neurons
Explanation: One common method for terminating the effect of neurotransmitters is through reuptake by presynaptic neurons, which helps to clear neurotransmitters from the synaptic cleft and terminate their action.

p.9
Action Potentials and Electrical Signals

What happens after the initial depolarization during an action potential?
A) Voltage-gated potassium channels close
B) Voltage-gated sodium channels open
C) Membrane potential returns to resting level
D) Sodium influx stops
E) Hyperpolarization occurs

B) Voltage-gated sodium channels open
Explanation: Following the initial depolarization, voltage-gated sodium channels open, leading to the rapid rise of the action potential.

p.18
Excitatory and Inhibitory Postsynaptic Potentials

What occurs when two action potentials arrive rapidly one after another in fiber A?
A) Decreased EPSP
B) Temporal summation
C) Hyperpolarization
D) Spatial summation
E) No change

B) Temporal summation
Explanation: When two action potentials arrive rapidly in fiber A, they lead to temporal summation, resulting in a higher amplitude of EPSP as the second potential rides on the back of the first.

p.22
Neurotransmitter Types and Their Functions

Which neurotransmitter is associated with purinergic receptors?
A) Acetylcholine
B) Glycine
C) ATP
D) Norepinephrine
E) Serotonin

C) ATP
Explanation: ATP is known to interact with purinergic receptors, which can respond to ATP and play roles in various physiological processes.

p.14
Mechanism of Neurotransmitter Release

What process describes the release of neurotransmitters into the synaptic cleft?
A) Endocytosis
B) Exocytosis
C) Phagocytosis
D) Osmosis
E) Diffusion

B) Exocytosis
Explanation: The rapid release of neurotransmitters into the synaptic cleft occurs through exocytosis, where vesicles fuse with the plasma membrane to release their contents.

p.14
Mechanism of Neurotransmitter Release

What happens to the vesicle membrane after neurotransmitter release?
A) It is permanently destroyed
B) It becomes part of the plasma membrane
C) It is recycled immediately
D) It remains unchanged
E) It is converted into a different structure

B) It becomes part of the plasma membrane
Explanation: After neurotransmitter release, the vesicle membrane may become part of the plasma membrane, but through the Kiss & Run mechanism, the vesicle can close again and be refilled with neurotransmitter.

p.14
Excitatory and Inhibitory Postsynaptic Potentials

What type of receptor is activated by neurotransmitters on the postsynaptic membrane?
A) Voltage-gated channel
B) Ligand-gated channel
C) Mechanically-gated channel
D) Leak channel
E) Sodium-potassium pump

B) Ligand-gated channel
Explanation: The receptors on the postsynaptic membrane are ligand-gated channels that open in response to the binding of neurotransmitters, allowing ions to flow into the cell.

p.17
Neurotransmitter Types and Their Functions

What is the primary inhibitory neurotransmitter mentioned in the text?
A) Glutamate
B) Serotonin
C) GABA
D) Dopamine
E) Acetylcholine

C) GABA
Explanation: GABA (gamma amino-butyric acid) is identified as the frequent inhibitory neurotransmitter, playing a crucial role in inhibitory synaptic transmission.

p.12
Types of Synapses: Electrical vs. Chemical

What is a key feature of electrical synapses?
A) Presence of neurotransmitters
B) Unidirectional transmission
C) Gap junctions between neighboring neurons
D) Slow transmission speed
E) Involvement of synaptic vesicles

C) Gap junctions between neighboring neurons
Explanation: Electrical synapses are characterized by gap junctions that interconnect the cytoplasm of two neurons, allowing for direct electrical conduction.

p.22
Neurotransmitter Types and Their Functions

What type of receptors do catecholamines interact with?
A) Muscarinic
B) Purinergic
C) Noradrenergic
D) Glycinergic
E) Dopaminergic

C) Noradrenergic
Explanation: Catecholamines, such as norepinephrine, primarily interact with noradrenergic receptors, which are involved in the body's response to stress and other functions.

p.1
Sensory Receptors and Detection of Stimuli

What is the primary function of sensory receptors?
A) To produce hormones
B) To detect stimuli
C) To transmit electrical signals to muscles
D) To form synapses
E) To protect nerve cells

B) To detect stimuli
Explanation: Sensory receptors are specialized nerve endings that are designed specifically for the detection of different stimuli, playing a crucial role in the sensory system.

p.23
Mechanism of Neurotransmitter Release

What is one way neurotransmitters can be eliminated from the synaptic cleft?
A) They can be absorbed by the postsynaptic neuron
B) They can diffuse away
C) They can be converted into energy
D) They can be stored in vesicles
E) They can be transformed into hormones

B) They can diffuse away
Explanation: One of the methods for neurotransmitter elimination from the synaptic cleft is diffusion away from the synapse, allowing them to disperse into the surrounding area.

p.4
Action Potentials and Electrical Signals

In thick fibers, what happens to the percentage of current that enters the axon?
A) It decreases significantly
B) It remains constant
C) A higher percentage enters
D) A lower percentage enters
E) It is negligible

C) A higher percentage enters
Explanation: In thick fibers, a higher percentage of current enters the axis of the axon, which contributes to the propagation of electrical signals.

p.23
Mechanism of Neurotransmitter Release

How can cocaine affect neurotransmitter levels in the synaptic cleft?
A) It decreases neurotransmitter release
B) It prevents neurotransmitter binding
C) It increases the amount of epinephrine remaining in the synaptic cleft
D) It enhances enzymatic breakdown of neurotransmitters
E) It promotes the uptake of neurotransmitters

C) It increases the amount of epinephrine remaining in the synaptic cleft
Explanation: Cocaine can inhibit the reuptake of neurotransmitters like epinephrine, leading to an accumulation of these substances in the synaptic cleft.

p.4
Action Potentials and Electrical Signals

What is the space constant in thick fibers compared to thin fibers?
A) Smaller
B) Larger
C) The same
D) Variable
E) Non-existent

B) Larger
Explanation: The space constant is larger in thick fibers, meaning that the electrotonic potential decays slower, allowing for more effective signal propagation.

p.20
Axonal Transport and Synaptic Vesicle Dynamics

What is retrograde transport in axonal transport?
A) Transport from axon terminal to cell body
B) Transport from cell body to axon terminal
C) Transport of neurotransmitters into vesicles
D) Transport of ions across the membrane
E) Transport of proteins to the nucleus

A) Transport from axon terminal to cell body
Explanation: Retrograde transport refers to the movement of materials from the axon terminal back to the cell body, which is essential for recycling and signaling.

p.8
Action Potentials and Electrical Signals

What initiates electrotonic depolarization in sensory receptors?
A) Opening of voltage-gated sodium channels
B) Opening of mechanosensitive channels
C) Release of neurotransmitters
D) Inhibition of potassium channels
E) Activation of GABA receptors

B) Opening of mechanosensitive channels
Explanation: Electrotonic depolarization is initiated by the opening of mechanosensitive channels, which allows ions to flow and cause a change in membrane potential.

p.6
Action Potentials and Electrical Signals

What occurs when the mechanosensitive ion channel opens?
A) Potassium flows out
B) Chloride flows in
C) Non-selective cation channel opens, mostly sodium flows in
D) Calcium flows out
E) Magnesium flows in

C) Non-selective cation channel opens, mostly sodium flows in
Explanation: When the mechanosensitive ion channel opens, it allows sodium ions to flow into the nerve ending, leading to a small depolarization.

p.5
Action Potentials and Electrical Signals

What does 'loss-free' conduction of action potentials mean?
A) Action potentials can be lost during transmission
B) Action potentials will always reach the other end without being lost
C) Action potentials can reverse direction
D) Action potentials can change their pattern
E) Action potentials can be distorted

B) Action potentials will always reach the other end without being lost
Explanation: 'Loss-free' conduction means that once an action potential is generated, it will always reach the other end of the axon without being lost.

p.13
Types of Synapses: Electrical vs. Chemical

What structure forms the gap junction between two neurons?
A) Synaptic cleft
B) Connexons
C) Synaptic vesicles
D) Neurotransmitters
E) Axon terminals

B) Connexons
Explanation: Connexons, formed by connexin subunits, create the gap junctions that interconnect the cytoplasms of two neurons, allowing for direct electrical communication.

p.10
Action Potentials and Electrical Signals

What is the effect of a weak suprathreshold stimulus on action potential firing?
A) High frequency action potential firing
B) No action potential firing
C) Low frequency action potential firing
D) Irregular action potential firing
E) Constant action potential firing

C) Low frequency action potential firing
Explanation: A weak suprathreshold stimulus results in low frequency action potential firing, indicating that the intensity of the stimulus is encoded in the frequency of action potentials.

p.3
Action Potentials and Electrical Signals

What is the typical amplitude range of an action potential?
A) 1-5 mV
B) 10-20 mV
C) Several times 10 mV, around +20 to +30 mV
D) 50-100 mV
E) 0-1 mV

C) Several times 10 mV, around +20 to +30 mV
Explanation: The action potential has a high amplitude, typically several times 10 mV, reaching around +20 to +30 mV, which is crucial for its propagation.

p.7
Sensory Receptors and Detection of Stimuli

What occurs to the receptor potential when the mechanical stimulus is removed?
A) It remains constant
B) It immediately returns to resting potential
C) It decays over time
D) It becomes hyperpolarized
E) It triggers an action potential

C) It decays over time
Explanation: When the mechanical stimulus is removed, the receptor potential undergoes a gradual decay in time, indicating that the potential is not permanent and diminishes after the stimulus is no longer present.

p.18
Excitatory and Inhibitory Postsynaptic Potentials

What is the effect of stimulating both excitatory fiber A and inhibitory fiber C?
A) Only EPSP
B) Only IPSP
C) No effect
D) EPSP + IPSP
E) Action potential

D) EPSP + IPSP
Explanation: Stimulating both excitatory fiber A (producing EPSP) and inhibitory fiber C (producing IPSP) results in the cancellation of their effects, leading to a summed postsynaptic potential that may or may not reach the threshold.

p.23
Mechanism of Neurotransmitter Release

What role does acetylcholinesterase play in neurotransmitter elimination?
A) It enhances neurotransmitter release
B) It breaks down Acetylcholine in the synaptic cleft
C) It transports neurotransmitters back to the presynaptic terminal
D) It binds to postsynaptic receptors
E) It prevents neurotransmitter diffusion

B) It breaks down Acetylcholine in the synaptic cleft
Explanation: Acetylcholinesterase is an enzyme located in the synaptic cleft that specifically breaks down Acetylcholine, facilitating the termination of its action.

p.4
Myelination and Action Potentials

What is the effect of myelin sheath on the velocity of action potential propagation?
A) It decreases the velocity
B) It has no effect
C) It increases the velocity
D) It makes propagation erratic
E) It only affects thin fibers

C) It increases the velocity
Explanation: The myelin sheath acts as an electrical insulator, resulting in very rapid propagation of action potentials and significantly increasing the velocity of propagation.

p.2
Structure and Function of Neurons

What are axon terminals responsible for?
A) Receiving incoming signals
B) Manufacturing proteins
C) Forming synapses with other neurons
D) Producing electrical signals
E) Recycling cellular materials

C) Forming synapses with other neurons
Explanation: Axon terminals are responsible for forming synapses, where outgoing signals are transmitted to the dendrites of other neurons.

p.4
Action Potentials and Electrical Signals

How do voltage-gated sodium channels in thick fibers affect the velocity of propagation?
A) They decrease the velocity
B) They have no effect
C) They allow for a larger range, increasing velocity
D) They only function in thin fibers
E) They block propagation

C) They allow for a larger range, increasing velocity
Explanation: Voltage-gated sodium channels in thick fibers provide a larger range for action potentials, which contributes to a larger velocity of propagation compared to thin fibers.

p.6
Mechanism of Neurotransmitter Release

What happens to the mechanosensitive ion channel under resting conditions?
A) It is open
B) It is partially open
C) It is closed
D) It is inactive
E) It is blocked

C) It is closed
Explanation: Under resting conditions, the mechanosensitive ion channel is closed, meaning that there is no mechanical stimulus to trigger its opening.

p.17
Mechanism of Neurotransmitter Release

What is the role of the GABA B receptor?
A) It is a ligand-gated channel
B) It is coupled to a Gi protein
C) It opens sodium channels
D) It directly releases neurotransmitters
E) It is a voltage-gated channel

B) It is coupled to a Gi protein
Explanation: The GABA B receptor is described as a 7 TM receptor that is coupled to a Gi protein, which is involved in inhibitory signaling.

p.8
Action Potentials and Electrical Signals

What occurs if depolarization reaches the threshold of voltage-gated sodium channels?
A) Hyperpolarization occurs
B) The channel opens
C) The channel closes
D) No action potential is generated
E) The membrane becomes impermeable

B) The channel opens
Explanation: If depolarization reaches the threshold of voltage-gated sodium channels, the channels open, leading to the generation of an action potential.

p.15
Neurotransmitter Types and Their Functions

What characterizes the release of peptide transmitters from electrodense vesicles?
A) Rapid signaling
B) Immediate effect
C) Slow change in postsynaptic cell
D) High calcium concentration
E) Direct binding to receptors

C) Slow change in postsynaptic cell
Explanation: Peptide transmitters released from electrodense vesicles result in a slow change in the postsynaptic cell, often referred to as a neuromodulator effect, rather than rapid signaling.

p.3
Action Potentials and Electrical Signals

What does the term 'all or none response' refer to in action potentials?
A) It can vary in intensity
B) It either fully develops or does not develop at all
C) It can only occur in myelinated axons
D) It is dependent on the length of the axon
E) It can be partially blocked

B) It either fully develops or does not develop at all
Explanation: The 'all or none response' indicates that an action potential either occurs fully or not at all, emphasizing the binary nature of action potential generation.

p.2
Structure and Function of Neurons

What is the primary function of the cell body in a neuron?
A) Transmitting signals
B) Receiving incoming signals
C) Metabolic control center for manufacturing and recycling
D) Forming synapses
E) Producing electrical signals

C) Metabolic control center for manufacturing and recycling
Explanation: The cell body is considered the metabolic control center of the neuron, responsible for synthesizing proteins and recycling materials necessary for neuronal function.

p.12
Types of Synapses: Electrical vs. Chemical

What direction does information flow in a typical chemical synapse?
A) Bidirectional
B) Retrograde
C) Unidirectional from presynaptic to postsynaptic
D) Random
E) Only from postsynaptic to presynaptic

C) Unidirectional from presynaptic to postsynaptic
Explanation: In chemical synapses, the flow of information is typically unidirectional, moving from the presynaptic neuron to the postsynaptic neuron.

p.10
Action Potentials and Electrical Signals

What happens to the voltage-gated potassium channels after a mechanical stimulus is maintained?
A) They remain open indefinitely
B) They close immediately
C) They gradually close
D) They open wider
E) They become inactive

C) They gradually close
Explanation: After a mechanical stimulus is maintained, the voltage-gated potassium channels gradually close since there is no further depolarization to trigger their opening, affecting the action potential firing rate.

p.3
Action Potentials and Electrical Signals

Why do thick fibers have a larger velocity of action potential propagation compared to thin fibers?
A) They have more sodium channels
B) They allow current to spread more efficiently
C) They have a thicker myelin sheath
D) They retain current better than thin fibers
E) They have a higher resting potential

B) They allow current to spread more efficiently
Explanation: Thick fibers allow the current coming in through voltage-gated sodium channels to spread more efficiently, resulting in a larger velocity of propagation compared to thin fibers.

p.16
Excitatory and Inhibitory Postsynaptic Potentials

What effect do metabotropic receptors have on the postsynaptic membrane potential?
A) They cause depolarization
B) They stabilize the membrane potential at negative values
C) They always lead to action potentials
D) They cause large hyperpolarization
E) They have no effect on membrane potential

B) They stabilize the membrane potential at negative values
Explanation: Metabotropic receptors cause small hyperpolarizations (IPSPs) that stabilize the membrane potential at negative values without significantly changing it.

p.23
Excitatory and Inhibitory Postsynaptic Potentials

What happens when a neurotransmitter binds to a postsynaptic receptor?
A) It permanently binds to the receptor
B) It is immediately broken down
C) It dissociates from the receptor after a while
D) It causes the receptor to become inactive
E) It prevents further binding of neurotransmitters

C) It dissociates from the receptor after a while
Explanation: When a neurotransmitter binds to a postsynaptic receptor, it does not permanently bind; instead, it eventually dissociates, allowing for the possibility of further signaling.

p.5
Action Potentials and Electrical Signals

What is the primary mechanism that allows action potentials to jump from one node of Ranvier to the next?
A) Continuous conduction
B) Electrotonic potential
C) Saltatory conduction
D) Passive conduction
E) Retrograde conduction

C) Saltatory conduction
Explanation: The jumping of action potentials from one node of Ranvier to the next is known as saltatory conduction, which increases the speed of propagation significantly compared to continuous conduction.

p.20
Mechanism of Neurotransmitter Release

What role do V-type proton pumps play in neurotransmitter uptake?
A) They synthesize neurotransmitters
B) They facilitate the release of neurotransmitters
C) They are responsible for the uptake of neurotransmitters into synaptic vesicles
D) They transport ions across the membrane
E) They generate action potentials

C) They are responsible for the uptake of neurotransmitters into synaptic vesicles
Explanation: V-type proton pumps are involved in the uptake of neurotransmitters into synaptic vesicles, helping to maintain the necessary concentration for effective synaptic transmission.

p.17
Synaptic Transmission in CNS

What neurotransmitter do excitatory fibers release to bind to AMPA receptors?
A) GABA
B) Glycine
C) Serotonin
D) Glutamate
E) Norepinephrine

D) Glutamate
Explanation: Excitatory fibers release glutamate, which binds to AMPA receptors, facilitating excitatory synaptic transmission.

p.10
Action Potentials and Electrical Signals

What is the maximum number of action potentials a neuron can produce per second?
A) 100 APs
B) 250 APs
C) 500 APs
D) 1000 APs
E) 1500 APs

C) 500 APs
Explanation: A neuron can produce up to 500 action potentials per second, which highlights the neuron's capacity for rapid signaling in response to stimuli.

p.10
Action Potentials and Electrical Signals

What role do voltage-gated potassium channels play during action potential firing?
A) They cause depolarization
B) They have no effect
C) They cause hyperpolarization
D) They increase sodium influx
E) They trigger action potentials

C) They cause hyperpolarization
Explanation: Voltage-gated potassium channels open during the action potential, allowing K+ to flow outward, which hyperpolarizes the membrane potential following depolarization.

p.3
Action Potentials and Electrical Signals

What initiates the action potential in a neuron?
A) Activation of voltage-gated potassium channels
B) Activation of voltage-gated sodium channels
C) Release of neurotransmitters
D) Increase in calcium ions
E) Decrease in membrane potential

B) Activation of voltage-gated sodium channels
Explanation: The action potential is initiated by the activation of voltage-gated sodium channels, leading to a large influx of sodium ions and subsequent depolarization.

p.21
Mechanism of Neurotransmitter Release

What drives the uptake of neurotransmitters into vesicles?
A) Passive diffusion
B) Electrochemical gradient of H+
C) Active transport of neurotransmitters
D) Osmosis
E) Protein synthesis

B) Electrochemical gradient of H+
Explanation: The electrochemical gradient created by the high concentration of H+ ions drives the uptake of neurotransmitters into vesicles as a secondary active transport process.

p.20
Axonal Transport and Synaptic Vesicle Dynamics

What is the primary function of axonal transport in neurons?
A) To synthesize neurotransmitters
B) To transport materials from the cell body to the axon terminal
C) To generate action potentials
D) To maintain resting membrane potential
E) To facilitate synaptic transmission

B) To transport materials from the cell body to the axon terminal
Explanation: Axonal transport is crucial for moving synthesized materials, such as neurotransmitters, from the cell body to the axon terminal, ensuring proper neuronal function.

p.20
Axonal Transport and Synaptic Vesicle Dynamics

Which motor protein is responsible for anterograde transport in axonal transport?
A) Dynein
B) Kinesin
C) Myosin
D) Actin
E) Tubulin

B) Kinesin
Explanation: Kinesin is the motor protein that facilitates anterograde transport, moving materials from the cell body to the axon terminal at speeds of 50-400 mm/day.

p.19
Excitatory and Inhibitory Postsynaptic Potentials

What effect does a large maintained EPSP have on action potential frequency?
A) It decreases AP frequency
B) It has no effect on AP frequency
C) It increases AP frequency
D) It causes irregular AP firing
E) It leads to immediate repolarization

C) It increases AP frequency
Explanation: A large maintained EPSP results in a high frequency of action potentials, demonstrating that stronger excitatory signals can lead to increased neuronal firing rates.

p.14
Excitatory and Inhibitory Postsynaptic Potentials

What occurs when a chloride channel opens in response to neurotransmitter binding?
A) Sodium influx
B) Calcium influx
C) Hyperpolarization
D) Depolarization
E) No change in membrane potential

C) Hyperpolarization
Explanation: When a chloride channel opens, chloride ions move into the cell, making the inside of the postsynaptic cell more negative, resulting in hyperpolarization and an inhibitory postsynaptic potential (IPSP).

p.17
Neurotransmitter Types and Their Functions

What is the primary function of benzodiazepines and barbiturates in relation to GABA A receptors?
A) They inhibit GABA release
B) They activate GABA A receptors
C) They block chloride channels
D) They enhance excitatory neurotransmission
E) They increase sodium influx

B) They activate GABA A receptors
Explanation: Benzodiazepines and barbiturates are activators of GABA A receptors, leading to increased chloride influx and resulting in sedative effects such as relaxation and sleepiness.

p.11
Types of Synapses: Electrical vs. Chemical

What type of synapse involves the axon terminal attaching to the dendrites of another neuron?
A) Axosomatic
B) Axoaxonic
C) Axodendritic
D) Dendrodendritic
E) Somatosomatic

C) Axodendritic
Explanation: An axodendritic synapse is characterized by the axon terminal of one neuron attaching to the dendrites of another neuron, facilitating communication between the two.

p.18
Action Potentials and Electrical Signals

What is required for a postsynaptic neuron to fire an action potential?
A) A single EPSP
B) A threshold of -60 mV
C) Hyperpolarization
D) Inhibition from GABA
E) A single IPSP

B) A threshold of -60 mV
Explanation: The postsynaptic neuron needs to reach a threshold of -60 mV to evoke an action potential, which is not achieved by a single EPSP.

p.2
Structure and Function of Neurons

How many axons does a typical neuron have?
A) None
B) One
C) Two
D) Several
E) Many

B) One
Explanation: A typical neuron has one axon, which is responsible for transmitting outgoing signals to axon terminals.

p.1
Structure and Function of Neurons

What is the idealized structure of a neuron composed of?
A) Only axons
B) Cell body, dendrites, and axon
C) Dendrites and axon terminals only
D) Cell body and myelin sheath
E) Axon and synaptic cleft

B) Cell body, dendrites, and axon
Explanation: An idealized neuron consists of four basic regions: the cell body (soma), dendrites for receiving information, a single axon (which may be myelinated or unmyelinated), and axon terminals for forming synapses.

p.14
Excitatory and Inhibitory Postsynaptic Potentials

What is the result of sodium influx through ligand-gated channels in the postsynaptic cell?
A) Hyperpolarization
B) No change in membrane potential
C) Depolarization
D) Decrease in action potential
E) Inhibition of neurotransmitter release

C) Depolarization
Explanation: The influx of sodium ions through ligand-gated channels causes a small depolarization of the postsynaptic cell, leading to an excitatory postsynaptic potential (EPSP).

p.5
Action Potentials and Electrical Signals

What ensures that action potentials are conducted in a unidirectional manner?
A) Activation of sodium channels
B) Inactive voltage-gated sodium channels
C) Presence of potassium channels
D) Electrotonic potential
E) Myelination of the axon

B) Inactive voltage-gated sodium channels
Explanation: Action potentials are unidirectional because the region where the action potential originated has inactive voltage-gated sodium channels, preventing it from reversing direction.

p.8
Mechanism of Neurotransmitter Release

What effect does lidocaine have on action potential generation?
A) It enhances action potential generation
B) It blocks action potential generation
C) It has no effect on action potentials
D) It increases the threshold for action potentials
E) It only affects potassium channels

B) It blocks action potential generation
Explanation: Lidocaine blocks voltage-gated sodium channels, preventing the generation of action potentials and thus blocking pain sensation.

p.13
Mechanism of Neurotransmitter Release

What is the role of synapsin I in chemical synapses?
A) To release neurotransmitters
B) To attach synaptic vesicles to the actin cytoskeleton
C) To form gap junctions
D) To depolarize the postsynaptic membrane
E) To create the synaptic cleft

B) To attach synaptic vesicles to the actin cytoskeleton
Explanation: Synapsin I is involved in the attachment of synaptic vesicles to the actin cytoskeleton, facilitating their movement and release during neurotransmission.

p.11
Types of Synapses: Electrical vs. Chemical

What type of synapse occurs between the axon of one neuron and the axon of another neuron?
A) Axodendritic
B) Axosomatic
C) Axoaxonic
D) Dendrodendritic
E) Somatosomatic

C) Axoaxonic
Explanation: An axoaxonic synapse occurs when the axon of one neuron connects with the axon of another neuron, influencing the transmission of signals between them.

p.12
Types of Synapses: Electrical vs. Chemical

What is the primary mechanism of chemical synapses?
A) Electric conduction
B) Direct cytoplasmic connection
C) Neurotransmitter release
D) Ion channel opening
E) Gap junction formation

C) Neurotransmitter release
Explanation: Chemical synapses operate primarily through the release of neurotransmitters from the presynaptic neuron, which then evoke effects on the postsynaptic membrane.

p.4
Axonal Transport and Synaptic Vesicle Dynamics

What is the primary characteristic of axoplasm regarding electrical resistance?
A) Low resistance
B) High resistance
C) No resistance
D) Variable resistance
E) Infinite resistance

B) High resistance
Explanation: Axoplasm is characterized by high resistance, which affects the flow of electrical current within the axon.

p.7
Sensory Receptors and Detection of Stimuli

What is the effect of distance from the channel on the amplitude of the receptor potential signal?
A) It increases the amplitude
B) It has no effect
C) It decreases the amplitude
D) It causes a phase shift
E) It inverts the signal

C) It decreases the amplitude
Explanation: The amplitude of the receptor potential signal decreases with distance from the channel, leading to a decay in space, which affects how the signal is transmitted to the central nervous system.

p.1
Structure and Function of Neurons

Which part of the neuron is responsible for receiving information?
A) Axon
B) Axon terminals
C) Dendrites
D) Cell body
E) Myelin sheath

C) Dendrites
Explanation: Dendrites are the parts of the neuron that receive information from other neurons or sensory receptors, making them crucial for signal reception.

p.1
Types of Synapses: Electrical vs. Chemical

What type of synapse connects an axon terminal to the cell body of another neuron?
A) Axodendritic synapse
B) Axosomatic synapse
C) Axoaxonic synapse
D) Dendrodendritic synapse
E) Myelinated synapse

B) Axosomatic synapse
Explanation: An axosomatic synapse is formed when an axon terminal connects directly to the cell body (soma) of another neuron, facilitating communication between neurons.

p.9
Action Potentials and Electrical Signals

What occurs when the mechanical stimulus is removed?
A) Continuous depolarization
B) No further depolarization
C) Opening of sodium channels
D) Immediate hyperpolarization
E) Activation of potassium channels

B) No further depolarization
Explanation: When the mechanical stimulus is finished, there is no further depolarization, leading to the closure of voltage-gated potassium channels and a return to the resting membrane potential.

p.5
Action Potentials and Electrical Signals

What is the maximum speed of action potential conduction in myelinated fibers?
A) 50 m/s
B) 75 m/s
C) 100-120 m/s
D) 150 m/s
E) 200 m/s

C) 100-120 m/s
Explanation: The conduction speed of action potentials in myelinated fibers can reach a maximum of 100-120 m/s, making it very rapid compared to unmyelinated fibers.

p.8
Action Potentials and Electrical Signals

What happens to the receptor potential as it spreads?
A) It increases in amplitude
B) It spreads without decrement
C) It spreads with decrement
D) It remains constant
E) It becomes hyperpolarized

C) It spreads with decrement
Explanation: The receptor potential spreads with decrement, meaning that its amplitude decreases as it moves away from the site of depolarization.

p.8
Excitatory and Inhibitory Postsynaptic Potentials

What is the result of a subthreshold mechanical stimulus?
A) It generates a strong action potential
B) It produces a small receptor potential that decays
C) It causes hyperpolarization
D) It activates all mechanosensitive channels
E) It leads to a sustained action potential

B) It produces a small receptor potential that decays
Explanation: A subthreshold mechanical stimulus results in a small receptor potential that does not reach the threshold for action potential generation, leading to decay without signal transmission.

p.11
Action Potentials and Electrical Signals

What does the frequency of action potentials depend on?
A) The size of the neuron
B) The amplitude of electrotonic depolarization
C) The type of neurotransmitter
D) The length of the axon
E) The number of synapses

B) The amplitude of electrotonic depolarization
Explanation: The frequency of action potentials is influenced by the amplitude of electrotonic depolarization, meaning that a larger depolarization can lead to a higher frequency of action potentials.

p.7
Sensory Receptors and Detection of Stimuli

What is the relationship between the size of the mechanical stimulus and the receptor potential?
A) Larger stimuli always cause hyperpolarization
B) Larger stimuli cause smaller depolarization
C) Larger stimuli cause larger depolarization
D) There is no relationship
E) All stimuli cause the same depolarization

C) Larger stimuli cause larger depolarization
Explanation: The receptor potential is graded, meaning that a larger mechanical stimulus results in a larger depolarization, reflecting the strength of the stimulus.

p.1
Action Potentials and Electrical Signals

What is the role of action potentials in the nervous system?
A) To provide structural support to neurons
B) To propagate electrical signals rapidly to the CNS
C) To store neurotransmitters
D) To connect neurons at synapses
E) To detect environmental stimuli

B) To propagate electrical signals rapidly to the CNS
Explanation: Action potentials are essential for the rapid propagation of electrical signals along nerve fibers to the central nervous system (CNS) for processing.

p.9
Action Potentials and Electrical Signals

What initiates the depolarization in the action potential process?
A) Opening of voltage-gated potassium channels
B) Opening of mechanosensitive channels and Na+ influx
C) Closure of sodium channels
D) Inactivation of potassium channels
E) Mechanical stimulus cessation

B) Opening of mechanosensitive channels and Na+ influx
Explanation: The process begins with the opening of mechanosensitive channels, allowing Na+ sodium influx, which leads to depolarization and potentially a suprathreshold depolarization.

p.6
Structure and Function of Neurons

Which type of nerve fiber is the fastest?
A) C fibers
B) A-beta fibers
C) A-alpha fibers
D) B fibers
E) D fibers

C) A-alpha fibers
Explanation: A-alpha fibers are identified as the fastest nerve fibers, which are crucial for rapid signal transmission in the nervous system.

p.16
Excitatory and Inhibitory Postsynaptic Potentials

What ion channels are primarily involved in generating IPSPs?
A) Sodium channels
B) Calcium channels
C) Chloride channels
D) Potassium channels
E) Magnesium channels

C) Chloride channels
Explanation: IPSPs are primarily caused by the opening of ligand-gated chloride channels, which allow chloride ions to enter the postsynaptic cell, leading to small hyperpolarization.

p.23
Mechanism of Neurotransmitter Release

Which of the following is NOT a major pathway for neurotransmitter elimination?
A) Diffusion away from the synaptic cleft
B) Enzymatic breakdown
C) Binding to postsynaptic receptors
D) Reuptake by the presynaptic terminal
E) Uptake by surrounding glial cells

C) Binding to postsynaptic receptors
Explanation: While binding to postsynaptic receptors occurs, it is not considered a major pathway for neurotransmitter elimination, as the neurotransmitter will eventually dissociate from the receptor.

p.8
Structure and Function of Neurons

Where do voltage-gated sodium channels have the highest density?
A) At the axon terminal
B) In the cell body
C) Around the first myelin sheath
D) At the synapse
E) In the dendrites

C) Around the first myelin sheath
Explanation: The region with the highest density of voltage-gated sodium channels is located around the first myelin sheath, which is crucial for the generation of action potentials.

p.13
Synaptic Transmission in CNS

What is the typical synaptic delay for neurotransmitter release?
A) 0.1-0.5 ms
B) 1-5 ms
C) 10-20 ms
D) 50-100 ms
E) 100-200 ms

B) 1-5 ms
Explanation: The synaptic delay, which is the time it takes for the release of neurotransmitters to affect the postsynaptic membrane, typically ranges from 1 to 5 milliseconds.

p.2
Structure and Function of Neurons

What is the role of dendrites in a neuron?
A) Transmit outgoing signals
B) Form synapses
C) Receive incoming signals from other neurons
D) Produce electrical signals
E) Control metabolic functions

C) Receive incoming signals from other neurons
Explanation: Dendrites are specialized structures that receive incoming signals from other neurons, allowing for communication within the nervous system.

p.21
Mechanism of Neurotransmitter Release

What happens when a vesicle fuses with the plasma membrane?
A) Neurotransmitter is synthesized
B) Neurotransmitter is released rapidly
C) Neurotransmitter is degraded
D) Vesicle is recycled
E) Vesicle is destroyed

B) Neurotransmitter is released rapidly
Explanation: When the vesicle fuses with the plasma membrane, the neurotransmitter is released rapidly into the synaptic cleft, primarily through diffusion due to the high concentration in the vesicle.

p.19
Excitatory and Inhibitory Postsynaptic Potentials

What is the relationship between the size of the EPSP and action potential frequency?
A) Small EPSP leads to high AP frequency
B) Large EPSP leads to low AP frequency
C) Small EPSP leads to low AP frequency
D) EPSP size does not affect AP frequency
E) Large EPSP has no effect on AP frequency

C) Small EPSP leads to low AP frequency
Explanation: A small maintained excitatory postsynaptic potential (EPSP) results in a low frequency of action potentials (AP), indicating that the strength of the EPSP directly influences the firing rate of the neuron.

p.6
Sensory Receptors and Detection of Stimuli

What type of neuron is described as mechano-sensitive?
A) Motor neuron
B) Pseudounipolar sensory neuron
C) Interneuron
D) Bipolar neuron
E) Multipolar neuron

B) Pseudounipolar sensory neuron
Explanation: Pseudounipolar sensory neurons are described as mechano-sensitive, as they respond to mechanical stimuli through their peripheral axons that run to the skin.

p.17
Types of Synapses: Electrical vs. Chemical

Which GABA receptor types are ligand-gated chloride channels?
A) GABA B
B) GABA A and C
C) GABA A only
D) GABA C only
E) GABA A and B

B) GABA A and C
Explanation: GABA A and C receptors are specified as ligand-gated chloride channels, which facilitate the flow of chloride ions into the postsynaptic cell, leading to hyperpolarization.

p.15
Action Potentials and Electrical Signals

What happens during depolarization at the axon terminal?
A) Sodium channels close
B) N/P type calcium channels open
C) Potassium channels open
D) Neurotransmitter is released
E) Mitochondria produce ATP

B) N/P type calcium channels open
Explanation: During depolarization, N/P type calcium channels open, allowing calcium ions to enter the axon terminal, which is crucial for neurotransmitter release.

p.13
Types of Synapses: Electrical vs. Chemical

What is the primary function of electrical synapses?
A) To release neurotransmitters
B) To synchronize the depolarization of connected neurons
C) To create a synaptic cleft
D) To store neurotransmitters
E) To inhibit neuronal firing

B) To synchronize the depolarization of connected neurons
Explanation: Electrical synapses allow for rapid communication between neurons, enabling synchronization of depolarization when multiple neurons need to activate simultaneously.

p.11
Structure and Function of Neurons

What are dendritic spines?
A) Large compartments on the axon
B) Small compartments on dendrites
C) The cell body of a neuron
D) The axon terminal of a neuron
E) The synaptic cleft

B) Small compartments on dendrites
Explanation: Dendritic spines are small compartments found on dendrites that can form synapses, specifically referred to as axospinous synapses, enhancing synaptic connectivity.

p.21
Excitatory and Inhibitory Postsynaptic Potentials

Which of the following is NOT a criterion for a substance to be classified as a neurotransmitter?
A) It must be synthesized in the presynaptic neuron
B) It must evoke an effect on the postsynaptic neuron
C) It must be present in the postsynaptic neuron
D) Presynaptic depolarization should result in its release
E) There should be a specific receptor on the postsynaptic cell

C) It must be present in the postsynaptic neuron
Explanation: While a neurotransmitter must bind to a specific receptor on the postsynaptic cell to evoke an effect, it does not need to be present in the postsynaptic neuron itself; rather, it must be released from the presynaptic neuron.

p.2
Action Potentials and Electrical Signals

What are the two categories of electrical signals in neurons?
A) Graded and action potential
B) Electrotonic and action potential
C) Receptor and synaptic potentials
D) Excitatory and inhibitory potentials
E) Localized and decaying potentials

B) Electrotonic and action potential
Explanation: Electrical signals in neurons can be categorized into electrotonic potentials and action potentials, each with distinct properties and functions.

p.19
Action Potentials and Electrical Signals

What is the role of the repolarizing effect in action potentials?
A) It increases the duration of the action potential
B) It prevents the neuron from firing
C) It helps return the membrane potential to resting state
D) It enhances the EPSP
E) It causes depolarization

C) It helps return the membrane potential to resting state
Explanation: The repolarizing effect is crucial for returning the membrane potential to its resting state after an action potential, allowing the neuron to be ready for subsequent firing.

p.17
Excitatory and Inhibitory Postsynaptic Potentials

What effect does the activation of GABA A receptors have on neurons?
A) Increases action potential generation
B) Causes hyperpolarization and inhibition
C) Stimulates neurotransmitter release
D) Enhances excitatory signals
E) Decreases chloride influx

B) Causes hyperpolarization and inhibition
Explanation: Activation of GABA A receptors leads to the opening of chloride channels, resulting in chloride influx, hyperpolarization, and inhibition of neuronal activity.

p.8
Action Potentials and Electrical Signals

What happens with a suprathreshold stimulus?
A) It causes hyperpolarization
B) It generates an electrotonic potential only
C) It leads to a series of action potentials
D) It has no effect on action potentials
E) It only activates a few mechanosensitive channels

C) It leads to a series of action potentials
Explanation: A suprathreshold stimulus generates an electrotonic depolarization that reaches the threshold for voltage-gated sodium channels, resulting in a series of action potentials if the mechanical stimulus is maintained.

p.6
Structure and Function of Neurons

Where are the cell bodies of primary sensory neurons located?
A) In the spinal cord
B) In the dorsal root ganglion or trigeminal ganglion
C) In the brainstem
D) In the peripheral nervous system
E) In the cerebellum

B) In the dorsal root ganglion or trigeminal ganglion
Explanation: The cell bodies of primary sensory neurons are located in the dorsal root ganglion or trigeminal ganglion, which is essential for sensory signal processing.

p.9
Action Potentials and Electrical Signals

What allows for the generation of another action potential after the first one?
A) Closure of K+ channels
B) Return of sodium channels to closed state
C) Continuous mechanical stimulus maintaining sodium influx
D) Inactivation of potassium channels
E) Absence of depolarizing current

C) Continuous mechanical stimulus maintaining sodium influx
Explanation: As long as the mechanical stimulus is maintained, the membrane potential can depolarize again to the threshold of voltage-gated sodium channels, allowing for the generation of another action potential.

p.19
Mechanism of Neurotransmitter Release

What are synaptic vesicles primarily responsible for?
A) Storing neurotransmitters
B) Generating action potentials
C) Conducting electrical signals
D) Maintaining resting membrane potential
E) Facilitating repolarization

A) Storing neurotransmitters
Explanation: Synaptic vesicles are responsible for storing neurotransmitters, which are released into the synaptic cleft to transmit signals between neurons.

p.5
Action Potentials and Electrical Signals

Which type of axon conducts action potentials faster?
A) Thin unmyelinated axon
B) Thick unmyelinated axon
C) Thin myelinated axon
D) Thick myelinated axon
E) All axons conduct at the same speed

D) Thick myelinated axon
Explanation: Thick myelinated axons conduct action potentials faster than thin or unmyelinated axons due to the presence of saltatory conduction.

p.15
Structure and Function of Neurons

What is the role of mitochondria in the axon terminal?
A) To release neurotransmitters
B) To produce ATP for energy
C) To store calcium ions
D) To facilitate action potentials
E) To bind neurotransmitters

B) To produce ATP for energy
Explanation: Mitochondria in the axon terminal produce ATP, which is necessary for various energy-dependent processes, including pumping out calcium and filling synaptic vesicles with neurotransmitters.

p.13
Mechanism of Neurotransmitter Release

What triggers the fusion of synaptic vesicles with the presynaptic membrane?
A) Sodium influx
B) Potassium efflux
C) Calcium signal (Ca2+)
D) Chloride influx
E) Magnesium efflux

C) Calcium signal (Ca2+)
Explanation: The influx of calcium ions (Ca2+) is crucial for the docking proteins to fuse the synaptic vesicles with the presynaptic membrane, allowing for rapid neurotransmitter release.

p.21
Excitatory and Inhibitory Postsynaptic Potentials

What effect does binding of a neurotransmitter have on the postsynaptic neuron?
A) It always causes depolarization
B) It can evoke either EPSP or IPSP
C) It prevents neurotransmitter release
D) It causes neurotransmitter synthesis
E) It leads to vesicle recycling

B) It can evoke either EPSP or IPSP
Explanation: The binding of a neurotransmitter to its receptor on the postsynaptic neuron can lead to either excitatory postsynaptic potentials (EPSP) or inhibitory postsynaptic potentials (IPSP), depending on the nature of the neurotransmitter and the receptor.

p.2
Action Potentials and Electrical Signals

Which of the following is a property of electrotonic potentials?
A) They are all-or-nothing signals
B) They have a high amplitude
C) They decay in space and time
D) They are produced in the axon terminals
E) They are only excitatory

C) They decay in space and time
Explanation: Electrotonic potentials are characterized by their graded nature, low amplitude, and the fact that they decay both in space and time when the current ceases.

p.15
Mechanism of Neurotransmitter Release

What initiates the release of neurotransmitters at the axon terminal?
A) Action potential arrives
B) Sodium influx
C) Potassium efflux
D) Neurotransmitter binding
E) Calcium efflux

A) Action potential arrives
Explanation: The arrival of an action potential at the axon terminal triggers the opening of calcium channels, leading to the influx of calcium ions and subsequent exocytosis of neurotransmitters.

p.15
Excitatory and Inhibitory Postsynaptic Potentials

What type of potential is generated in the postsynaptic cell when neurotransmitters bind to receptors?
A) Action potential
B) Inhibitory postsynaptic potential (IPSP)
C) Excitatory postsynaptic potential (EPSP)
D) Resting membrane potential
E) Graded potential

C) Excitatory postsynaptic potential (EPSP)
Explanation: When neurotransmitters bind to ligand-gated channels, they can generate an excitatory postsynaptic potential (EPSP), which is a small depolarization that occurs for milliseconds.

p.11
Synaptic Transmission in CNS

How does a neuron decide whether to fire an action potential?
A) Based on its size
B) Based on incoming action potentials
C) Based on the type of neurotransmitter
D) Based on the number of synapses
E) Based on the age of the neuron

B) Based on incoming action potentials
Explanation: A neuron decides to fire an action potential based on the incoming action potentials that propagate along the fiber, which may or may not lead to the generation of an action potential.

p.20
Axonal Transport and Synaptic Vesicle Dynamics

What is the speed range for fast anterograde transport in axonal transport?
A) 10-50 mm/day
B) 50-400 mm/day
C) 400-800 mm/day
D) 1-5 mm/day
E) 5-10 mm/day

B) 50-400 mm/day
Explanation: Fast anterograde transport occurs at speeds ranging from 50 to 400 mm/day, allowing synaptic vesicles to travel significant distances to reach the axon terminal.

p.17
Action Potentials and Electrical Signals

Where is the highest number of voltage-gated sodium channels located in a neuron?
A) Dendrites
B) Axon terminal
C) Axon hillock
D) Soma
E) Synaptic cleft

C) Axon hillock
Explanation: The axon hillock is noted for having the highest concentration of voltage-gated sodium channels, making it the site where action potentials are typically generated.

p.11
Action Potentials and Electrical Signals

What happens to the membrane potential when the receptor potential is larger?
A) It decreases significantly
B) It remains constant
C) It reaches the threshold earlier
D) It becomes negative
E) It stabilizes at resting potential

C) It reaches the threshold earlier
Explanation: A larger receptor potential, resulting from more mechanosensitive channels being opened, allows the membrane potential to reach the threshold sooner, leading to a shorter time period between action potentials.

Study Smarter, Not Harder
Study Smarter, Not Harder