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Questions and Answers
What is the approximate width of the synaptic cleft in a chemical synapse?
What is the approximate width of the synaptic cleft in a chemical synapse?
- 2 nm
- 2000 nm
- 200 nm (correct)
- 20 nm
Which characteristic distinguishes electrical synapses from chemical synapses?
Which characteristic distinguishes electrical synapses from chemical synapses?
- Dependence on neurotransmitter release
- Faster transmission speed (correct)
- Presence of ligand-gated channels
- Involvement of post-synaptic receptors
At the neuromuscular junction (NMJ), which neurotransmitter is primarily responsible for signal transmission?
At the neuromuscular junction (NMJ), which neurotransmitter is primarily responsible for signal transmission?
- Acetylcholine (Ach) (correct)
- GABA
- Serotonin
- Glutamate
In the central nervous system (CNS) type I synapses, which neurotransmitter is predominantly utilized for excitatory neurotransmission?
In the central nervous system (CNS) type I synapses, which neurotransmitter is predominantly utilized for excitatory neurotransmission?
Which neurotransmitter is primarily associated with inhibitory neurotransmission in CNS type II synapses?
Which neurotransmitter is primarily associated with inhibitory neurotransmission in CNS type II synapses?
Spider toxin, used in immunochemistry studies of the neuromuscular junction (NMJ), targets which specific structure?
Spider toxin, used in immunochemistry studies of the neuromuscular junction (NMJ), targets which specific structure?
The 'omega figure' observed in transmission electron microscopy (TEM) provides morphological evidence for which process during neurotransmission?
The 'omega figure' observed in transmission electron microscopy (TEM) provides morphological evidence for which process during neurotransmission?
Which microscopy technique is most suitable for observing the morphological evidence of exocytosis, such as omega figures, in stimulated nerve terminals?
Which microscopy technique is most suitable for observing the morphological evidence of exocytosis, such as omega figures, in stimulated nerve terminals?
What is the primary function of calcium ions (Ca++) in the process of neurotransmitter release at the synapse?
What is the primary function of calcium ions (Ca++) in the process of neurotransmitter release at the synapse?
In studies of synaptic transmission, how is the physiological measure of capacitance used to understand exocytosis and endocytosis?
In studies of synaptic transmission, how is the physiological measure of capacitance used to understand exocytosis and endocytosis?
Which of the following is NOT explicitly mentioned in the provided content as a key protein involved in regulating neurotransmitter release?
Which of the following is NOT explicitly mentioned in the provided content as a key protein involved in regulating neurotransmitter release?
Lambert-Eaton myasthenic syndrome (LEMS) is described as an autoimmune disorder affecting chemical synaptic transmission. Which specific component is targeted in LEMS?
Lambert-Eaton myasthenic syndrome (LEMS) is described as an autoimmune disorder affecting chemical synaptic transmission. Which specific component is targeted in LEMS?
What is the immediate consequence of the arrival of a pre-synaptic action potential at the axon terminal in chemical synaptic transmission?
What is the immediate consequence of the arrival of a pre-synaptic action potential at the axon terminal in chemical synaptic transmission?
Miniature end-plate potentials (mEPPs) observed at the frog neuromuscular junction in the absence of presynaptic action potentials are best described as:
Miniature end-plate potentials (mEPPs) observed at the frog neuromuscular junction in the absence of presynaptic action potentials are best described as:
Experiments using jellyfish aequorin protein at the squid giant synapse demonstrated that:
Experiments using jellyfish aequorin protein at the squid giant synapse demonstrated that:
How do end-plate potentials (EPPs) differ from miniature end-plate potentials (mEPPs) at the neuromuscular junction?
How do end-plate potentials (EPPs) differ from miniature end-plate potentials (mEPPs) at the neuromuscular junction?
Voltage-gated calcium channels (CaV++) are crucial for neurotransmitter release because:
Voltage-gated calcium channels (CaV++) are crucial for neurotransmitter release because:
The switch from primarily considering sodium (Na+) and potassium (K+) currents during action potentials to focusing on calcium (Ca++) current (ICa) in the presynaptic terminal is significant because:
The switch from primarily considering sodium (Na+) and potassium (K+) currents during action potentials to focusing on calcium (Ca++) current (ICa) in the presynaptic terminal is significant because:
What is the primary mechanism by which ionotropic receptors mediate fast chemical neurotransmission?
What is the primary mechanism by which ionotropic receptors mediate fast chemical neurotransmission?
Which of the following best describes the ionic basis of an inhibitory postsynaptic potential (IPSP)?
Which of the following best describes the ionic basis of an inhibitory postsynaptic potential (IPSP)?
What are the roles of choline acetyltransferase (ChaT) and acetylcholinesterase (AchE) in cholinergic neurotransmission?
What are the roles of choline acetyltransferase (ChaT) and acetylcholinesterase (AchE) in cholinergic neurotransmission?
How many molecules of acetylcholine (Ach) are required to gate the nicotinic acetylcholine receptor (AchR) channel?
How many molecules of acetylcholine (Ach) are required to gate the nicotinic acetylcholine receptor (AchR) channel?
What distinguishes the NMDA receptor from the AMPA/kainate receptor in glutamatergic neurotransmission?
What distinguishes the NMDA receptor from the AMPA/kainate receptor in glutamatergic neurotransmission?
Which of the following neurotransmitters is primarily responsible for mediating inhibitory neurotransmission in the central nervous system (CNS)?
Which of the following neurotransmitters is primarily responsible for mediating inhibitory neurotransmission in the central nervous system (CNS)?
Activation of GABA receptors typically leads to an influx of which ion, resulting in an inhibitory postsynaptic potential (IPSP)?
Activation of GABA receptors typically leads to an influx of which ion, resulting in an inhibitory postsynaptic potential (IPSP)?
Acetylcholinesterase (AchE) and GABA receptors are targets for which of the following, respectively?
Acetylcholinesterase (AchE) and GABA receptors are targets for which of the following, respectively?
What is the primary mechanism by which chloride (Cl-) channels contribute to inhibitory postsynaptic potentials?
What is the primary mechanism by which chloride (Cl-) channels contribute to inhibitory postsynaptic potentials?
Neuropeptides, in contrast to classical neurotransmitters, are primarily synthesized in which neuronal compartment?
Neuropeptides, in contrast to classical neurotransmitters, are primarily synthesized in which neuronal compartment?
Serotonin (5-HT) is categorized under which class of biogenic amines, based on its precursor amino acid?
Serotonin (5-HT) is categorized under which class of biogenic amines, based on its precursor amino acid?
Selective Serotonin Reuptake Inhibitors (SSRIs) primarily exert their therapeutic effects by targeting which process in neurotransmission?
Selective Serotonin Reuptake Inhibitors (SSRIs) primarily exert their therapeutic effects by targeting which process in neurotransmission?
Monoamine oxidase inhibitors (MAOIs) impact neurotransmitter levels by interfering with which mechanism of signal termination?
Monoamine oxidase inhibitors (MAOIs) impact neurotransmitter levels by interfering with which mechanism of signal termination?
Flashcards
Role of Ca++ in Exocytosis
Role of Ca++ in Exocytosis
Calcium ions (Ca++) are crucial for triggering exocytosis, the process of releasing neurotransmitters from the presynaptic terminal.
Ca++ Concentration and Synaptic Strength
Ca++ Concentration and Synaptic Strength
The amount of calcium ions (Ca++) entering the presynaptic terminal determines the strength of the signal.
SNARE Complex
SNARE Complex
A protein complex that helps fuse synaptic vesicles (containing neurotransmitters) with the presynaptic membrane.
Exocytosis
Exocytosis
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Proteins Regulating Neurotransmitter Release
Proteins Regulating Neurotransmitter Release
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Miniature End Plate Potential (mEPP)
Miniature End Plate Potential (mEPP)
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Presynaptic Calcium Influx
Presynaptic Calcium Influx
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Voltage-Gated Calcium Channels
Voltage-Gated Calcium Channels
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Vesicular Hypothesis
Vesicular Hypothesis
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Chemical Synapse
Chemical Synapse
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Electrical Synapse
Electrical Synapse
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Synaptic Cleft
Synaptic Cleft
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Post-synaptic Receptors
Post-synaptic Receptors
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Ligand-Gated Ion Channel
Ligand-Gated Ion Channel
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Transmission Electron Microscopy (TEM)
Transmission Electron Microscopy (TEM)
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Scanning Electron Microscopy (SEM)
Scanning Electron Microscopy (SEM)
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Ionotropic Receptor
Ionotropic Receptor
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Excitatory Postsynaptic Potential (EPSP)
Excitatory Postsynaptic Potential (EPSP)
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Inhibitory Postsynaptic Potential (IPSP)
Inhibitory Postsynaptic Potential (IPSP)
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Acetylcholine (Ach)
Acetylcholine (Ach)
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Acetylcholinesterase (AchE)
Acetylcholinesterase (AchE)
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Glutamate
Glutamate
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GABA
GABA
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Glycine
Glycine
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Cl- Channels: Inhibitory Effect
Cl- Channels: Inhibitory Effect
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GABA and Glycine: Inhibitory Neurotransmitters
GABA and Glycine: Inhibitory Neurotransmitters
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Inhibitory Neurotransmitters: Opposing Excitation
Inhibitory Neurotransmitters: Opposing Excitation
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Inhibitory Neurotransmitters: Shunting
Inhibitory Neurotransmitters: Shunting
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Neuropeptides: Short Proteins as Messengers
Neuropeptides: Short Proteins as Messengers
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Study Notes
Synaptic Transmission
- Synaptic transmission involves both chemical and electrical processes.
- Morphological studies examine the structure of synapses.
- Physiological studies investigate the function of synapses.
Neurotransmitters
- Acetylcholine (ACh), amino acids, amines, and peptides are neurotransmitters.
- Neurotransmitters like ACh, glutamate and GABA play roles in excitatory or inhibitory processes
- Uptake and termination of neurotransmitters influence their effects.
- Pharmacology studies the effects of drugs on neurotransmitters.
Chemical Synapses
- Chemical synapses are common, with a 200 nm gap between pre and post-synaptic cells.
- They require neurotransmitters to carry signals across the gap.
- The types of neurotransmitters and their functions vary (excitatory or inhibitory)
- Ionotropic receptors (ligand-gated channels) are important post-synaptic receptors.
Electrical Synapses
- Electrical synapses are rare, with a 20 nm gap.
- They allow direct electrical signal transmission.
- They use protein complexes called connexons.
Synaptic Morphology - Neuromuscular Junction (NMJ)
- Immunochemistry is used to identify pre- and post-synaptic proteins in the NMJ (neuromuscular junction).
- The NMJ is a synapse between a motor neuron and muscle fiber.
- Components like spider and cobra toxins affect pre- and post-synaptic functions of the NMJ.
Exocytosis During Neurotransmission
- Morphological evidence (TEM and SEM) shows vesicle fusion during stimulation/exocytosis.
- The freeze-fracture technique helps in observing the membranes of vesicles.
- Studying exocytosis is crucial to understanding synaptic transmission.
Physiological View of Exocytosis
- Miniature end-plate potentials (mEPPs) are graded potentials at the end-plate.
- mEPPs represent responses from single neurotransmitter vesicles.
- End-plate potentials (EPPs) are the sum of many mEPPs.
Jellyfish Aequorin Protein
- Aequorin is a calcium-sensitive protein that is luminescent.
- Studying its activity provides insights into calcium levels during synaptic depolarization.
- Measuring calcium levels is important in understanding the neurotransmitter release process.
Ca²⁺ Channels and NT Release
- Calcium channels open when sodium and potassium channels are activated during the action potential.
- Calcium ions play a crucial role in releasing neurotransmitters.
Exocytosis and Endocytosis
- Exocytosis increases membrane capacitance as membrane area increases
- Endocytosis decreases membrane capacitance as membrane area decreases.
- Types of exocytosis (classical and kiss and run types), and endocytosis are studied using capacitance measurements to study neural membrane function
SNARE Complex
- SNARE proteins are involved in vesicle fusion for neurotransmitter release.
- The proteins include calcium channel, calcium binding, and membrane fusion proteins facilitating NT release.
Toxins Affecting Ca Mechanism
- Botulinum toxin and tetanus toxin interfere with SNARE proteins and calcium channels.
Neurotransmitters 1. Acetylcholine
- Choline acetyltransferase (ChAT) synthesizes acetylcholine (ACh).
- Acetylcholinesterase (AChE) breaks down ACh.
- ACh uptake system is important for recycled reuse.
Glutamate and Amino Acid Transmitters
- Glutamate is a major excitatory neurotransmitter in the CNS.
- AMPA/kainate and NMDA receptors are glutamate receptors.
- Glycine and GABA are inhibitory neurotransmitters.
GABA Transmitters
- GABA is a major inhibitory neurotransmitter.
- GABA receptors control chloride channel activity.
Neuropeptides
- Neuropeptides are short proteins that regulate synaptic transmission.
- Amines or neuropeptides may be released alongside classical neurotransmitters for slow-acting modulation.
Biogenic Amines
- Biogenic amines are derived from amino acids, playing important roles as neuromodulators or transmitters.
Uptake and Synthesis of Neurotransmitters
- Glial cells and neurons are involved in the uptake and recycling of neurotransmitters.
Enzymatic Breakdown of Amines
- Monoamine oxidase (MAO) and catechol-O-methyl transferase (COMT) break down biogenic amines.
Pharmacological Intervention at Aminic Synapses
- Drugs that target various parts of the process affect neurotransmitter function, affecting behavior.
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