Synaptic Transmission: Difference between revisions
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== Chemical Synapses and Neurotransmitters == | |||
* Over 100 different neurotransmitters identified. | |||
* Communication process: Synthesis, packaging, release, and binding of neurotransmitters, followed by rapid removal or degradation. | |||
== Overview of Chemical Synapses == | |||
* Presynaptic terminal with synaptic vesicles. | |||
* Postsynaptic cell, separated by synaptic cleft. | |||
* Filamentous elements in pre- and postsynaptic processes. | |||
* Structures in synaptic cleft, including active zone and postsynaptic density. | |||
= Signaling Transmission Sequence at Chemical Synapses = | |||
# [[File:Sequence of events involved in transmission at a typical chemical synapse.jpg|thumb|Sequence of events involved in transmission at a typical chemical synapse ]]Synaptic Vesicle Preparation → ormation and filling of synaptic vesicles with neurotransmitter. | |||
# Action Potential Arrival - Invades presynaptic terminal → Opens voltage-gated Ca2+ channels. | |||
# Ca2+ Influx: | |||
#* Rapid influx due to concentration gradient (10–3 M external vs. 10–7 M internal). | |||
#* Elevates Ca2+ in presynaptic terminal. | |||
=== Exocytosis and Postsynaptic Response === | |||
# Exocytosis | |||
#* Ca2+ elevation → Synaptic vesicles fuse with presynaptic membrane. | |||
#* Neurotransmitters released into synaptic cleft. | |||
# Neurotransmitter Binding | |||
#* Diffuses across cleft → Binds to postsynaptic receptors. | |||
#* Opens/closes channels in postsynaptic membrane, altering ion flow. | |||
# Postsynaptic Neuron Response | |||
#* Alters conductance and membrane potential. | |||
#* Increases/decreases probability of firing an action potential. | |||
=== Termination of Signal === | |||
* Neurotransmitter Removal | |||
** Uptake into glial cells or enzymatic degradation. | |||
* Effect | |||
** Terminates neurotransmitter action. | |||
** Ensures transient information transmission from one neuron to another. | |||
=== Slide 14: Overview of Chemical Synapse Transmission === | |||
* Neurotransmitter Role: Chemical signals like acetylcholine play critical roles in transmitting information across neurons, as demonstrated by Otto Loewi in 1926. | |||
* Classification: Over 100 neurotransmitters identified, broadly categorized into small-molecule neurotransmitters and neuropeptides. | |||
=== Slide 15: Neurotransmitter Diversity and Regulation === | |||
* Diverse Functions: Neurotransmitters can excite or inhibit postsynaptic neurons, with small-molecule neurotransmitters facilitating rapid responses and neuropeptides modulating slower functions. | |||
* Co-Transmitters: Enable dynamic changes in signaling properties based on synaptic activity. | |||
* Synaptic Regulation: Synthesis, packaging, release, and removal/degradation of neurotransmitters are tightly controlled to maintain appropriate levels. | |||
=== Slide 16: Synaptic Vesicle Preparation and Action Potential === | |||
* Vesicle Formation: Synaptic vesicles are prepared by being filled with neurotransmitters, ready for release upon an action potential arrival. | |||
* Action Potential's Role: Triggers the opening of voltage-gated Ca2+ channels in the presynaptic terminal, leading to Ca2+ influx due to the concentration gradient. | |||
=== Slide 17: Exocytosis and Neurotransmitter Release === | |||
* Ca2+ Influx: Causes a rapid increase in presynaptic Ca2+ levels, facilitating the fusion of synaptic vesicles with the presynaptic membrane. | |||
* Exocytosis: Releases neurotransmitters into the synaptic cleft, where they diffuse across to bind to postsynaptic receptors. | |||
=== Slide 18: Postsynaptic Response and Signal Termination === | |||
* Neurotransmitter Binding: Alters postsynaptic ion flow by opening or closing channels, changing membrane potential and conductance. | |||
* Neuron Firing Probability: Influences the likelihood of the postsynaptic neuron firing an action potential. | |||
* Termination of Signal: Achieved through neurotransmitter uptake into glial cells or enzymatic degradation, ensuring the transient nature of the signal. | |||
= Synaptic Transmission at the Neuromuscular Junction (NMJ) = | |||
[[File:Neuromuscular Transmission and Nicotinic Synapses.jpg|thumb|Neuromuscular Transmission and Nicotinic Synapses ]] | |||
* NMJ: Connection between alpha-motor neuron axons and skeletal muscle fibers. | |||
* Mechanism: Cholinergic transmission using acetylcholine (Ach). | |||
* Relevance: Basics of neurotransmitter release applicable across all synapses. | |||
=== Sequence of Events in Synaptic Transmission === | |||
# Action Potential Arrival: Depolarizes presynaptic membrane → opens voltage-gated Ca2+ channels. | |||
# Ca2+ Influx: Triggers release of Ach. | |||
# Ach Release and Binding: Binds to nicotinic receptor on muscle membrane → depolarization (EPP). | |||
# Muscle Action Potential: Triggered by EPP → muscle contraction. | |||
# Ach Breakdown: Acetylcholinesterase (AchE) terminates Ach action → reuptake of choline. | |||
=== Other Cholinergic Synapses === | |||
* Neuronal Nicotinic (NN) Receptors: In autonomic ganglia, activated by presynaptic cholinergic neurons. | |||
* Muscarinic Receptors: In parasympathetic target tissues, G-protein coupled receptors. | |||
= Synapses Between Neurons = | |||
* Location: On the cell body and dendrites. | |||
* Influence: Closer synapses to the axon hillock have greater influence on action potential initiation. | |||
* EPSP vs. IPSP: EPSP increases excitability (more likely to fire), while IPSP decreases excitability (less likely to fire). | |||
* Key Receptors: EPSP (Nicotinic, Non-NMDA, NMDA), IPSP (GABAA&C, Glycine). | |||
=== EPSP and IPSP Explained === | |||
* EPSP: Increased Na+ conductance, similar to EPP at NMJ. | |||
* IPSP: Increased Cl- conductance, reducing neuron's excitability. | |||
* Important Receptors: | |||
** EPSP: Nicotinic, Non-NMDA, NMDA (ligands: Ach, glutamate, aspartate). | |||
** IPSP: GABAA&C, Glycine (ligands: GABA, glycine). |
Revision as of 05:50, 23 March 2024
Overview
- The human brain consists of 86 billion neurons.
- Communication among these neurons is facilitated by synapses.
Types of Synapses
Two main types: Electrical and Chemical Synapses.
- Electrical synapses use connexons for direct current flow.
- Direct, passive flow of electrical current.
- Chemical synapses use neurotransmitters for cell-to-cell communication.
- Chemical: Communication via neurotransmitter release.
Feature | Electrical Synapses | Chemical Synapses |
---|---|---|
Structure |
|
|
Function |
|
|
Key Characteristics |
|
|
Chemical Synapses and Neurotransmitters
- Over 100 different neurotransmitters identified.
- Communication process: Synthesis, packaging, release, and binding of neurotransmitters, followed by rapid removal or degradation.
Overview of Chemical Synapses
- Presynaptic terminal with synaptic vesicles.
- Postsynaptic cell, separated by synaptic cleft.
- Filamentous elements in pre- and postsynaptic processes.
- Structures in synaptic cleft, including active zone and postsynaptic density.
Signaling Transmission Sequence at Chemical Synapses
- Synaptic Vesicle Preparation → ormation and filling of synaptic vesicles with neurotransmitter.
- Action Potential Arrival - Invades presynaptic terminal → Opens voltage-gated Ca2+ channels.
- Ca2+ Influx:
- Rapid influx due to concentration gradient (10–3 M external vs. 10–7 M internal).
- Elevates Ca2+ in presynaptic terminal.
Exocytosis and Postsynaptic Response
- Exocytosis
- Ca2+ elevation → Synaptic vesicles fuse with presynaptic membrane.
- Neurotransmitters released into synaptic cleft.
- Neurotransmitter Binding
- Diffuses across cleft → Binds to postsynaptic receptors.
- Opens/closes channels in postsynaptic membrane, altering ion flow.
- Postsynaptic Neuron Response
- Alters conductance and membrane potential.
- Increases/decreases probability of firing an action potential.
Termination of Signal
- Neurotransmitter Removal
- Uptake into glial cells or enzymatic degradation.
- Effect
- Terminates neurotransmitter action.
- Ensures transient information transmission from one neuron to another.
Slide 14: Overview of Chemical Synapse Transmission
- Neurotransmitter Role: Chemical signals like acetylcholine play critical roles in transmitting information across neurons, as demonstrated by Otto Loewi in 1926.
- Classification: Over 100 neurotransmitters identified, broadly categorized into small-molecule neurotransmitters and neuropeptides.
Slide 15: Neurotransmitter Diversity and Regulation
- Diverse Functions: Neurotransmitters can excite or inhibit postsynaptic neurons, with small-molecule neurotransmitters facilitating rapid responses and neuropeptides modulating slower functions.
- Co-Transmitters: Enable dynamic changes in signaling properties based on synaptic activity.
- Synaptic Regulation: Synthesis, packaging, release, and removal/degradation of neurotransmitters are tightly controlled to maintain appropriate levels.
Slide 16: Synaptic Vesicle Preparation and Action Potential
- Vesicle Formation: Synaptic vesicles are prepared by being filled with neurotransmitters, ready for release upon an action potential arrival.
- Action Potential's Role: Triggers the opening of voltage-gated Ca2+ channels in the presynaptic terminal, leading to Ca2+ influx due to the concentration gradient.
Slide 17: Exocytosis and Neurotransmitter Release
- Ca2+ Influx: Causes a rapid increase in presynaptic Ca2+ levels, facilitating the fusion of synaptic vesicles with the presynaptic membrane.
- Exocytosis: Releases neurotransmitters into the synaptic cleft, where they diffuse across to bind to postsynaptic receptors.
Slide 18: Postsynaptic Response and Signal Termination
- Neurotransmitter Binding: Alters postsynaptic ion flow by opening or closing channels, changing membrane potential and conductance.
- Neuron Firing Probability: Influences the likelihood of the postsynaptic neuron firing an action potential.
- Termination of Signal: Achieved through neurotransmitter uptake into glial cells or enzymatic degradation, ensuring the transient nature of the signal.
Synaptic Transmission at the Neuromuscular Junction (NMJ)
- NMJ: Connection between alpha-motor neuron axons and skeletal muscle fibers.
- Mechanism: Cholinergic transmission using acetylcholine (Ach).
- Relevance: Basics of neurotransmitter release applicable across all synapses.
Sequence of Events in Synaptic Transmission
- Action Potential Arrival: Depolarizes presynaptic membrane → opens voltage-gated Ca2+ channels.
- Ca2+ Influx: Triggers release of Ach.
- Ach Release and Binding: Binds to nicotinic receptor on muscle membrane → depolarization (EPP).
- Muscle Action Potential: Triggered by EPP → muscle contraction.
- Ach Breakdown: Acetylcholinesterase (AchE) terminates Ach action → reuptake of choline.
Other Cholinergic Synapses
- Neuronal Nicotinic (NN) Receptors: In autonomic ganglia, activated by presynaptic cholinergic neurons.
- Muscarinic Receptors: In parasympathetic target tissues, G-protein coupled receptors.
Synapses Between Neurons
- Location: On the cell body and dendrites.
- Influence: Closer synapses to the axon hillock have greater influence on action potential initiation.
- EPSP vs. IPSP: EPSP increases excitability (more likely to fire), while IPSP decreases excitability (less likely to fire).
- Key Receptors: EPSP (Nicotinic, Non-NMDA, NMDA), IPSP (GABAA&C, Glycine).
EPSP and IPSP Explained
- EPSP: Increased Na+ conductance, similar to EPP at NMJ.
- IPSP: Increased Cl- conductance, reducing neuron's excitability.
- Important Receptors:
- EPSP: Nicotinic, Non-NMDA, NMDA (ligands: Ach, glutamate, aspartate).
- IPSP: GABAA&C, Glycine (ligands: GABA, glycine).