HUF 2-42 Synaptic integration, neural circuits and plasticity Flashcards
1
Q
Generation of post-synaptic potentials
A
- EPSP: Na+ influx
- IPSP: K+ efflux
- Cl-: eqm. potential equal to or more -ve. than RMP
=> IPSP or shunting inhibition
(Cl- channel opens => ↑ postsynaptic resistance)
2
Q
Spatiotemporal summation of synaptic potentials
A
- Real-time integration of all synaptic inputs to decide timing of AP
- Dendritic spines: major sites of synaptic inputs
- Aberrations in dendritic spines structure and functions
=> brain disorders e.g. dementia in Alzheimer’s disease
3
Q
Microcircuits
A
- Building blocks for complex neuronal circuits
- Feedforward excitation
- Feedforward inhibition
- Convergence / Divergence
- Lateral inhibition
- Feedback / Recurrent inhibition
- Feedback / Recurrent excitation
4
Q
Feedforward excitation / inhibition
A
Stretch reflex
- maintain ms. length
- sensory neuron synaptically connected with motor neuron
- feedforward excitation to flexor
- feedforward inhibition to extensor
5
Q
Convergence / Divergence
A
- many-to-1 vs. 1-to-many
- integrate functions of multiple sensory receptors and multiple ms.
6
Q
Lateral inhibition
A
- enhance perception of contrast
- enable visual system to detect contours more easily (↑ signal-to-noise ratio)
- not limited to visual functions
7
Q
Feedback inhibition
A
- prevents over-excitation of neuron
- allows generation of rhythmic activities
- reciprocal inhibition (e.g. walking)
8
Q
Neuroplasticity
A
- Brain growth and development
- Regain functionality
- Learning and memory
- Changes in synaptic strength (esp. long term)
=> develop, learn, adapt - Aberrant synaptic plasticity
=> brain disorders (e.g. chronic pain, OCD) - Intense activities (i.e. use-dependent)
=> ↑ connection strength
=> bigger EPSP amplitude
=> Short-term potentiation (transient) OR LTP
9
Q
Long term potentiation (LTP)
A
- Early phase: protein synthesis-independent
=> short term memory - Late phase: protein synthesis-dependent
=> long term memory - Bidirectional change under stimulation:
high-freq. (50-100Hz) => LTP
low-freq. (1-3 Hz) => LTD (long term depression)
10
Q
Studying LTP in hippocampus
A
- Field potentials: reflect synaptic activity of thousands of neurons
- Bigger the amplitude, stronger the connection
- High-freq. stimulation to incoming pathways
=> ↑ amplitude of field EPSP (long-lasting: > 1 hr)
11
Q
Mechanism of LTP
A
- Intense presynaptic activity => ↑ glutamate release => bind to AMPA receptors => depolarisation (Na+ influx) => unblocking of NMDA receptor channels (Mg2+) => Ca2+ influx => LTP induction (↑ synaptic strength)
- Conditional deletion of NMDA receptor in CA1 => X LTP
- Smart mice: genetically engineered with extra copies of NMDA receptor genes
12
Q
Role of AMPA receptors in synaptic plasticity
A
AMPA receptors:
- upon GLU binding => Na+ influx
- dynamic eqm. between cell surface and intracellular recycling vesicles
- High-freq stimulation
=> rapid and big rise in Ca2+
=> phosphorylation of AMPA receptor subunits
=> stabilise AMPA receptors at postsynaptic membrane (and more are inserted)
=> LTP
- Low-freq stimulation => small and slow Ca2+ rise => dephosphorylation of AMPA receptor subunit => endocytosis of AMPA receptors => less responsive to GLU => LTD