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- Consider the circuit from Q5 (above). We want to add another inhibitory neuron to this circuit to increase the likelihood that neuron D will have an action potential. With which cell (A, B, C or D) should our new inhibitory neuron make a synapse to make it more likely that the post - synaptic neuron will have anaction potential?The diagram below shows a simple neural circuit with three pre - synaptic cells labelled 'A', 'B' and 'C', and a post - synaptic cell labelled 'D ' (see image below). Assume neurons A and B each have outputs of +2 and neuron C has output of -1.1.1 What would be the effect of blocking neurotransmitter degradation on neurotransmitter concentration at the synapse? 1.2You are studying an excitatory synapse that is not strong enough to evoke a postsynaptic action potential. Would the probability of a postsynaptic potential increase or decrease after blocking neurotransmitter degradation? 1.3 ) You are studying an excitatory synapse that evokes a postsynaptic action potential. Would the probability of a postsynaptic potential increase or decrease after blocking presynaptic voltage-gated calcium channels?1.show that the Mcculloch_Pitts formal model of a neuron may be approximated by a sigmoidal neuron(I. ا, neuron using a sigmoid activation function with large synaptic weights 2.Show that a linear neuron may be approximated by a sigmoidal neuron with small synaptic weights.
- What is inhibitory synapse ? Prepare the figure of excitatorysynapse ?What is long-term potentiation (LTP) and how does it occur? What changes in the cell should we expect to observe when a synapse is in a "potentiated" state?What effect would you expect an antagonist that targets the voltage sensing domain of perisynaptic calcium channels of an inhibitory interneuron have on the firing frequency of a finically active neuron that interneuron synapses onto? Explain in details
- If TTX (tetrodotoxin) selectively binds voltage gated Na+ channels, and you tag TTX with a fluorescent marker and then you use it as a probe to label voltage-gated Na+ channels in various neurons in the CNS, would you expect the pattern of fluorescence to be different between myelinated and nonmyelinated axons? If so, how? If not, why not?If an axon ([Na+]in = 200 mM) is bathed in solution consisting of [Na+]out = 10 mM, will there be an action potential if a supra-threshold stimulus (changed Vm to -20 mV with opening of Na channels) is injected into the axon?explain the simplified version of the synaptic process resulting in long-term potentiationand explain the roles of AMPA and NMDA receptors; glutamate; sodium, calcium, and magnesium ions in strengthening a synapse.
- What is a typical value for an inhibitory post synaptic potential? Why is it inhibitory?The correlation between neurons can explain the basis of the synaptic modification, that is, how much they can connect to each other or if they are not synchronized, how much they can lose or weaken their connections. • Draw a picture of an excitatory synapse such as glutamatergic with its receptors between the pre- and postsynaptic neuron. • Briefly explain what mechanisms involve neuronal plasticity and why synapses are enhanced or weakened.Sequence the following list of events of a neuronal action potential by placing 1 next to the first event, 2 next to the second event, and so on. a. _____ The activation gates of voltage-gated Na+ channels open, Na+ flood the cytoplasm, and depolarization occurs. b. _____ K+ continue to flow out of the axon until the membrane is hyperpolarized. c. _____ Local potentials cause the membrane to depolarize to threshold. d. _____ The inactivation gates of voltage-gated Na+ channels close as voltage-gated K+ channels open, K+ begin to exit the axon, and repolarization begins. e. _____ Repolarization continues and Na+ channels return to resting