Synaptic Transmission: Difference between revisions

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#* Chemical: Communication via neurotransmitter release.
#* Chemical: Communication via neurotransmitter release.


== Chemical Synapses and Neurotransmitters ==
* Over 100 different neurotransmitters identified.
* Communication process: Synthesis, packaging, release, and binding of neurotransmitters, followed by rapid removal or degradation.
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* Acts through specialized receptors on postsynaptic cell
* Acts through specialized receptors on postsynaptic cell
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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.

  1. Electrical synapses use connexons for direct current flow.
    • Direct, passive flow of electrical current.
  2. Chemical synapses use neurotransmitters for cell-to-cell communication.
    • Chemical: Communication via neurotransmitter release.
Feature Electrical Synapses Chemical Synapses
Structure
  • Gap junctions
  • Connexons enable close neuron-to-neuron links
  • Larger synaptic cleft between neurons
  • Synaptic vesicles in presynaptic terminal
Function
  • Direct flow of electrical current
  • Current sourced from local potential difference
  • Neurotransmitters facilitate communication as chemical messengers
Key Characteristics
  • Permits passive electrical current flow
  • Influenced by presynaptic action potential
  • Presence of neurotransmitters in synaptic vesicles
  • Acts through specialized receptors on postsynaptic cell

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

  1. Sequence of events involved in transmission at a typical chemical synapse
    Synaptic Vesicle Preparation → ormation and filling of synaptic vesicles with neurotransmitter.
  2. Action Potential Arrival - Invades presynaptic terminal → Opens voltage-gated Ca2+ channels.
  3. 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

  1. Exocytosis
    • Ca2+ elevation → Synaptic vesicles fuse with presynaptic membrane.
    • Neurotransmitters released into synaptic cleft.
  2. Neurotransmitter Binding
    • Diffuses across cleft → Binds to postsynaptic receptors.
    • Opens/closes channels in postsynaptic membrane, altering ion flow.
  3. 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)

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

  1. Action Potential Arrival: Depolarizes presynaptic membrane → opens voltage-gated Ca2+ channels.
  2. Ca2+ Influx: Triggers release of Ach.
  3. Ach Release and Binding: Binds to nicotinic receptor on muscle membrane → depolarization (EPP).
  4. Muscle Action Potential: Triggered by EPP → muscle contraction.
  5. 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).