Cards (8)

  • TYPES OF SYNAPSES
    • point in which two neurons form a connections
    • aim --> transmit singals from one neuron to another
    • presynaptic neuron --> before the synapse
    • postsynaptic neuron --> after the synapse
    • synaptic cleft --> gap between pre and post
    • pos-synaptic potential --> excitatory or inhibitory protentials 
    • one way transmission --.> rectifying 
    • two way transmission --> non-rectifying
  • ELECTRICAL SYNAPSES
    • formed where two neurons have a really close connection --> forms a gap junction --> joined together through connnecons
    • direct transfer of ions
    • non-rectifying
    • fast transmission
    • single often attenuated --> signal is smaller in second neuron
    • gap junction made up of 2 connexons  each connexon has 6 connexins
    • highly reliable --> useful in systems in escape reflex or coordinate large number of cells in a tissue (heart)
    • aren't flexible --> not as common
  • CHEMICAL SYNAPSE
    • very flexible 
    • synaptic delay  time taken for it to cross the synaptic cleft
    • vesicular release of neurotransmitter is released into the synaptic cleft
    1. snare proteins
    2. synaptobrevin --> on the vesicLes
    3. SNAP-25 --> on the nerve terminal membrane
    4. syntaxin --> on the nerve terminal membrane
    5. SNARE proteins interact and bind to each other, drawing the vesicle close to the membrane
    6. when calcium increase  vesicle fuses with the membrane release ach into the synapstic cleft
    7. calcium is sensed by synaptotagmin --> causes a conformational change in the snare proteins 
  • VESICLE RECYCLING
    • clathrin coat the outside of the vesicle  bind to the vesicle but form interactions with outher clathrin molecules
    • forms a cage like structure that coats the vesicle and drag it away form the membrane
    • size of the cage is defined by the size of clathrin  vesicles are usually abojut the same size  constant number of vesicle
    • maintains constant size of the terminal
  • ACTIVE ZONE
    • where neurotransmitters are being released
    • energy-consuming --> lots of mitochondria
    • signals need to be turned off:
    1. enzyme (ach) can break down the neurotransmitter
    2. there is an uptake system for neurotransmitters 
  • QUANTAL HYPOTHESIS
    • neurotransmitter release is quantal
    • miniture end plate potential vary in a step way manner  distribution of the amplitude vary in a integer multiplier
    • 1 quantum --> amount of transmitter per vesicle 
    • quantal content = epp / 1 quantum current 
    1. average zize of a full end plate potential
    • miniture postsynaptic potentials
    1. occur spontaneously even when no calcium is present
    2. have amplitudes that are multiples of a quantal unit
    3. sue to release of one or a few quanta 
  • QUANTAL HYPOTHESIS cont.
    • evoked release (epp)
    1. as extracellular calcium is lowered --> epsp amplitude decreases in a step-wise manner
    2. quantal analysis of ap-evoked epsps show that they involve release of up to 200 quanta per ap
    3. each quantum contains several thousands molecules of ach
  • TETANUS
    • caused by anaerobic bacterium --> clostridium tetani
    • toxin cleaves snare proteins  --> causes muscle spasm 
    • binds to and enters the presynaptic nerve terminal --> in the skeletal muscle meuromuscular junction --> released in the dendrietes and destroy snare proteins in inhibitory neurotransmitter --> stops the release of gaba or glycine