Inhibitory Neurotransmitters Flashcards
What is synaptic inhibition?
Lecture 4, slide 2
-it decreases the probability that there will be an action potential in the post synaptic neuron
Discuss how the equilibrium potentials of ions is related to the membrane potential during action potentials
Lecture 4, slide 2.5.-3
How is synaptic inhibition normally recruited? What are the different types of synaptic inhibition circuits?
Lecture 4, slide 3.5.-4
What happens when there is excitation without matched inhibition?
Lecture 4, slide 4.5
What type of synapses are inhibitory synapses?
Lecture 4, slide 5.5
Give examples of receptors mediating excitation and receptors mediating inhibition.
Lecture 4, slide 6
What are the main inhibitory neurotransmitters?
Lecture 4, slide 6.5
Discuss the structure of GABA-A receptors
Lecture 4, slide 7
What is the role of the GABA-A receptors?
Lecture 4, slide 7.5
How is the GABA-A receptor driving force established? Compare the chloride equilibrium potential in normal mature neurons compared to developing or hyperactive neurons.
Lecture 4, slide 8-8.5
What is postsynaptic shunting inhibition?
Lecture 4, slide 9-10.5
What are the two mechanism of postsynaptic inhibition via GABA-A receptors?
Lecture 4, slide 11
How are GABA-A receptors localised?
Lecture 4, slide 11.5
Discuss phasic and tonic GABAergic inhibition.
Lecture 4, slide 12-12.5
- phasic can be spontaneous or evoked. Either way it is transient
- tonic is background activity
What is the role of GABA-B receptors in phasic inhibition?
Lecture 4, slide 13-14
What effects do GABA-B receptors have on cation channels?
Lecture 4, slide 14.5-15.5
What are the different classes of GABA releasing interneuron? What do they target and what type of inhibition are they involved in?
Lecture 4, slide 16.5-17
What are the differences between the function of somatic and dendritic inhibition?
Lecture 4, slide 17.5
Give entrainment as an example of a specialised function of GABA-releasing neurons.
Lecture 4, slide 18
Discuss the pharmacological modification of GABA-A receptors (agonists, antagonists and modulators). Give examples
Lecture 4, slide 19.5
How can the lifetime of an inhibitory neurotransmitter in the synaptic cleft be pharmacologically targeted?
Lecture 4, slide 20
-by targeting GABA transporters
What does pharmacological blockade of GABA uptake cause?
Lecture 4, slide 20.5
How can we modulate GABA release from specific interneurons? Give examples.
Lecture 4, slide 21
Give examples of some commercial drugs that target the GABAergic system. What type of drug are they, what is their function and what are they used to treat?
Lecture 4, slide 21.5
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