Synaptic Signalling Study Notes
Overview of Synaptic Signalling
References Used
Bear, Connors, Paradiso: 'Neuroscience- Exploring the Brain'
Berne & Levy: 'Principles of Physiology'
Haines: 'Fundamental Neuroscience'
Kandel, Schwartz, Jessell: 'Principles of Neural Science'
Dr. Kevin Whitehead's contact: k.j.whitehead@bham.ac.uk
Key Concepts
Synaptic Diversity: Various types of synapses can influence neural communication and behavioral outcomes.
Receptor-mediated Effects on Excitability:
Ionotropic Receptors: These are receptor-operated/ligand-gated channels that mediate rapid responses.
Metabotropic Receptors: These are G-protein coupled receptors that mediate slower but longer-lasting effects.
Synaptic Integration of Information
Spatial Summation: This refers to the summation of post-synaptic potentials occurring at multiple synapses simultaneously.
Temporal Summation: This pertains to the summation of post-synaptic potentials that occur at the same synapse in rapid succession.
Frequency Coding of Synaptic Signalling
Action potentials communicate information through the frequency rather than amplitude. The more frequent the action potentials, the greater the stimulus intensity.
The Chemical Synapse
Structure:
Presynaptic Active Zone: Site for vesicle docking and exocytosis.
Postsynaptic Density: Location for receptor expression and the intracellular signalling machinery.
Synaptic Arrangements in the CNS
Types of Synapses:
Axodendritic: Synapse between an axon and a dendrite.
Axosomatic: Synapse between an axon and a soma, often more influential due to proximity.
Axoaxonic: Synapse between two axons.
Influence of Point of Synaptic Contact
Proximity to Axon Hillock:
Synapses closer to the axon hillock exert a greater influence on action potential generation.
Inhibitory synapses are often found on the soma and near the axon hillock, providing a crucial mechanism for controlling neuron excitability.
A typical neuron may have between 1,000 to 10,000 synapses influencing its activity.
Receptor Signalling Mechanisms
Ionotropic Receptors:
When a transmitter binds, it causes a conformational change that opens the channel, allowing ion movement.
A typical activation might involve an excitatory post-synaptic potential (EPSP).
Metabotropic Receptors:
Transmitter binding leads to a conformational change, activating a G-protein that subsequently activates effector systems, leading to indirect effects such as opening or closing ion channels or stimulating/inhibiting enzymes and secondary messenger systems.
Electrical Effects of Receptor Activation
Post-Synaptic Membrane Potential:
Recording shows a resting membrane potential around -70 mV.
Following activation, small EPSPs and IPSPs can occur, altering the electrical state of the neuron.
Action Potential Generation
Threshold Potential: For an action potential to occur, the neuron must reach a threshold where voltage-dependent Na+ channels open.
The action potential is characterized as an all-or-nothing event, meaning its amplitude does not vary with stimulus strength.
Refractory Periods:
Absolute Refractory Period (ARP): Time frame during which no new action potential can be generated regardless of stimulus strength.
Relative Refractory Period (RRP): A period in which a stronger-than-usual stimulus is necessary to generate an action potential.
Summation Mechanisms
Spatial Summation
EPSPs from multiple synaptic inputs combine to increase overall membrane potential, enhancing the chance of generating an action potential.
Best co-operation of inputs happens when the coinciding EPSPs are close enough in time and space.
Temporal Summation
Rapid successive activation of the same synapse allows for increased local potential, which can serve to push the neuron over the threshold for firing.
Communication of Neurons
Neuronal communication results from integrating all input signals to send a frequency-encoded message:
The frequency of action potentials relates directly to the intensity of the stimulus, rather than using amplitude modulation.
Maximum firing rates can reach up to 200–300 Hz, primarily limited by the durations of the ARP and RRP.
Main Points Recapped
The influence of synapses varies depending on location: axodendritic versus axosomatic connections.
Different receptor types (ionotropic vs metabotropic) result in different signaling speeds and durations.
Ion fluxes, like Na+ for depolarization and Cl- for hyperpolarization, are critical for controlling membrane polarization and cell excitability.
Information integration occurs through spatial and temporal summation, leading to action potentials that encode signals through frequency modulation.