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Seminar 1 - Introduction to Synaptic Physiology

William Chapman Synaptic Plasticity 3rd Year English 54 cards

trisynaptic loop?

Cards in this deck (54)

  1. 1what are the 3 pillars of neurophysiology?1) intrinsic excitability
    2) synaptic function
    3) network behaviours
  2. 2what does an axon do?'talking'
  3. 3dendrite?listening
  4. 4how many neurons and synapses are in the human CNS?100 billion neurons
    100 trillion synapses
  5. 52 types of synapses?chemical (most common) --> NT mediated
    electrical --> gap junction mediated
  6. 6which of GABAa-c are GPCR?GABAb
  7. 7what is PSD?post synaptic density
    darker area --> tells you where the receptors are expressed on the membrane/ where the synapse is
  8. 8imaging spines problems?only tells you the location and not the function
    not able to quantify the strength of each synapse
    only shows one dendrite --> doesn't show the complex network and other connections
    doesn't identify the specific synaptic strengthening when someone learns something
  9. 9what affects release probability?dynamic and changed by the frequency with which the synapses are activated, iconic conditions, temperature, activation of presynaptic
  10. 10why may an AP not cause NT release?maybe not enough vesicles/docked vesicles
    probability renders Ca2+ channels closed
  11. 11how to carry out in vitro and in vivo hippocampal recordings?in vitro - electrophysiological recordings on hippocampal slices
    in vivo - electronic diode placed on head and placed on hippocampus
  12. 12where is the human hippocampus situated?sits at the base of the temporal lobe --> one either side
    fornix carries info out of the other areas
    information from the cortex comes into the dentate gyrus (DG)
  13. 13trisynaptic loop?trisynaptic loop?
  14. 14what is the perforant pathway?axons of the cortical cells coming into the hippocampus
    forms synapses with the DG cells (granule cells)
  15. 15what is the MFP?mossy fibre pathway
    granule cell axons synapse with cells in the CA3 (pyramidal cells)
  16. 16what is the schaffer collateral commissural pathway?studied the most
    CA3 --> CA1 (pyramidal neurons)
    then sends information to the cortex and other brain regions
  17. 17what is the TAP?tempero- ammonic pathway
    cortex --> CA1
  18. 18what is the ACP?associational commissural pathway
    CA3 pyramidal cells synapse on other CA3 cells on both the same and opposite side of the brain
  19. 19what is synaptic plasticity?a change in the strength of functional coupling between discrete neuronal structures ( or neuron-effector ( gland/heart) systems)
    EVERY TIME A SYNAPSE IS ACTIVATED IT EXHIBITS PLASTICITY
  20. 20what is the time course for synaptic plasticity?what is the time course for synaptic plasticity?
  21. 21pathological plasticity?changed wiring in neuropathic pain/ epilepsy
  22. 22regenerative plasticity?rewiring after the trauma
  23. 23what is the plasticity protocol?use a test stimulus and a conditioning stimulus
    first, need to work out the baseline response --> stimulate and calculate synaptic response --> roughly the same
    stimulate at the SAME RATE --> frequency and intensity is always the same
  24. 24homosynaptic plasticity?when the plasticity occurs at the synapses you have conditioned
    only conditioned synapses express plasticity
  25. 25heterosynaptic plasticity?conditioned and some non-conditioned synapses express plasticity
  26. 26other?chemical plasticity
    chemicals that induce plasticity --> not every specific
  27. 27why does plasticity happen?memory
    sensory (chronic pain, vision, olfaction, touch)
    effector system (NMJ)
    addiction/ reward
    network computation
    network maintenance
    pathologies
  28. 28what presynaptic changes to synaptic function can arise??changes in Ca2+ ion channel density function
    changes in NT storage --> more/ less vesicles
    more/fewer vesicles released
    changes in membrane potential
  29. 29postsynaptic?receptor density ( +/- AMPA-Rs)
    receptor sensitivity
    in/decreased receptor efficiency (increased conductancy or probability of opening)
    changes to spine/active zone number
    changes in ionic gradients (Cl- and K+)
  30. 30trans-synaptic?changes in removal of NT
    change distance between synapses
    changes in extracellular pH
    changes in physiological properties of synaptic cleft
  31. 31how is long term synaptic plasticity induced in vivo?appropriate intrinsic presynaptic firing patterns
    neuronal synchrony
  32. 32induce LTP?100Hz
  33. 33induce LTD?1Hz x 900
  34. 34what is electrophysiology?recording electrical changes that occur from ions moving across a lipid membrane
  35. 35Nernst equation?Nernst equation?
  36. 36what is the reseting neuronal membrane most permeable to?potassium ions as it is closest to Ek
  37. 37how are signals in the NS encoded?voltage fluctuations
  38. 38what does the current clamp do?records the membrane potential of the cell --> currents is constant and voltage change is recorded
    neuron is allowed to do what it wants (depolarise and hyperpolarise)
    can inject current to depolarise or hyper polarise
    records what the cell does under physiological conditions
  39. 39voltage clamp?experimenter controls (clamps) the membrane voltage
    the amount of current required to maintain the cells at a given voltage is measured
  40. 40what type of preparations? in order of easiest first?1) dissociated neuronal cultures
    2) organotypic brain slices
    3) acute brain slices
    4) whole animal
  41. 41how do mEPSPs occur?occur spontaneously in the absence of AP firing
    channels spontaneously open and may allow Ca2+ in and cause NT release. Or a vesicle may spontaneously fuse with the presynaptic membrane
  42. 42what are sEPSCs?spontaneous synaptic transmission occurring as a result of spontaneous presynaptic action potentials
  43. 43what is quantal analysis?n = no. active synapses
    p = probability of release
    q = potency of neurotransmitter
  44. 44in terms of quantal analysis, a change in mEPSP frequency and amplitude means what?change in mEPSP frequency = suggests a change in P or N
    change in mEPSP amplitude = suggests a change in Q
  45. 45what is minimal stimulation?stimulating at a very low level that causes APs to fire in one fibre and transmitter only to be released from one synapse
  46. 46what is minimal stimulation used for?a way of measuring the probability of release
    if 5 stimulations only gets 1 response
    Pr= 0.2
    assumption = stimulation always evokes an action potential (Pap = 1)
  47. 47what does DHPG induce?increased failures --> form of chemical synaptic plasticity
  48. 48what is a disadvantage of whole cell patch clamp?space clamp
    neuron is very large and notable to clamp its voltage properly
    not able to clamp voltage precisely enough
    errors from large fast currents
  49. 49techniques to get around this limitation?dendritic patch clamp --> very difficult because dendrite is small (3cm)--> record synaptic currents much closer to the synapse
    patches to record fractions of large fast currents
    using outside-out patches to study AMPA-R currents
  50. 50give an example of a presynaptic recording from a giant bouton?Calyx of held - auditory pathway from ears to the brainstem
    need to record from terminals directly to understand them well --> size is a problem
  51. 51what is real time imaging?important neurophysiological method for studying neuronal function
  52. 52how is this done?Ca sensitive fluorescent dyes or proteins introduced into neurons to enable the monitoring of synaptic activity
    Ca is important in producing both long and short-term plasticity
    equipment is way more expensive than electrophysiology
  53. 53what will a Ca dye report?1) ca entry that triggers NT release in presynaptic vesicles
    2) ca entry into postsynaptic elements that have been activated
    3) action potential firing (as APs drive ca entry)
  54. 54give an example of a genetically encoded Ca indicatorGCaMP6

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3rd Year Synaptic Plasticity Flashcards on Seminar 1 - Introduction to Synaptic Physiology, created by William Chapman on 28/04/2017.
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