Ch 4 Neural Conduction and Synaptic Transmission Flashcards

1
Q

resting membrane potention

A

polarized (not 0)
-70mV

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2
Q

at rest, which ions are more prominent inside and outside of cell membrane

A

Na+ and Cl- outside, K+ inside and negative proteins

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3
Q

what causes pressure for Na+ to come into cell

A

electrostatic pressure

random motion 9wants to move down gradient)

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4
Q

at rest, which channels are closed and open

A

Na+ closed
K+ open (dont move too much due to wanting inside cell to be negative

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5
Q

how does resting membrane stayed fixed

A

sodium potassium pump
3Na out for each 2K in

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6
Q

what are postsynaptic potentials

A

Disturbances of the resting membrane potential from input from other cells across the synapse

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7
Q

post synaptic potentials from neurotransmitters are either

A

excitatory post-synaptic potentials (depolarize)

inhibitory post-synaptic potentials (hyperpolarize)

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8
Q

all PSPs are graded potentials which means

A

Amplitudes are proportional to the intensity of the signals that elicit them
Instantaneous

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9
Q

the two important characteristics of PSP transmission

A

rapid (instant regardless of duration)

decremental (decrease in amplitude as they go through the neuron)

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10
Q

describe how PSPs impact if there is an Action Potential

A

firing depends on the balance of EPSPs and IPSPs

if the sum of potentials that reaches the axon initial segment is enough to depolarize to threshold of excitation (65mV) an AP is generated

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11
Q

summation of PSPs can be described over space and time, explain both

A

Spatial summation
Sum to form greater PSPs when multiple are present, E and I cancel each other out

Temporal summation
Rapid succession of PSPs builds their strength

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12
Q

purpose of the refractory period

A

APs travel in one direction along the axon

Rate of neuronal firing is related to the intensity of the stimulation

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13
Q

refractory period (and its types)

A

Brief period after an AP where it is impossible to send another AP
The absolute refractory period

Followed by the relative refractor period (possible to fire again but only with higher-than-normal stimulation)

End of the period is when stimulation required returns to baseline

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14
Q

how does axon conduction and PSPs differ

A

axon conduction is nondecrememental, intensity of each fire is the same along the axon as the influxes of sodium along the axon recharge it

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15
Q

an AP that travels along the axon back to the cell body is called ___ conduction, and an AP that goes down the axon to the terminal buttons is called ___ conduction

A

antidromic

orthodromic

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16
Q

what direction does dendrodentritic synapses go in

A

either direction!

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16
Q

Conduction in Neurons without Axons

A

Interneurons use graded potentials, and normally do not have APs

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16
Q

what is special about axoaxonic synapses

A

Mediate presynaptic facilitation and inhibition - selectively impact the effects of that button on the postsynaptic neuron

Advantage is that they can selectively influence one particular synapse rather than the entire presynaptic neuron

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17
Q

most synapses in the brain form what kind of synapse

A

tripartite

two neurons and an astroglial cell

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18
Q

directed vs non directed synapse

A

Directed synapse
Site of neurotransmitter release and the site of neurotransmitter reception are in close proximity

Nondirected synapse
Site of release is at some distance from the site of reception
§ Ex. NTs released from varicosities (bulges/swellings) in the axon branches and are thus widely spread to targets
□ String of beads synapses

19
Q

describe how exocytosis releases NT

A

NT congregate near Ca2+ channels in the presynaptic neuron

Channels are stimulated by AP and open, Ca2+ floods in

this triggers a chain reaction where NT vesicles fuse with presynaptic neuron and empty into the synapse

20
Q

neurotransmitters vs neuropeptides

A

NTs
released in pulses each time AP triggers influx of calcium

NPs
released gradually in response to general increase of intracellular calcium

21
Q

any molecule that binds to another is called a

22
Q

what are receptor subtypes and why are they advantageous

A

The different types of receptors to which a particular NT can bind are called the receptor subtypes for that NT
§ Typically located in different brain areas, and respond in different ways
□ Advantage: one NT can have multiple effects

23
what are ionotropic receptors and metabotropic receptors associated with
Ionotropic receptors are associated with ligan-activated ion channels Metabotropic receptors are associated with signal proteins and G proteins
24
Differentiate between ionotropic and metabotropic receptors:
Ionotropic receptors are faster, as they open/close ion channels directly, leading to immediate postsynaptic potentials (PSPs) like EPSPs and IPSPs. Metabotropic receptors are slower and more complex, often triggering secondary messengers that can cause longer-lasting changes in the neuron.
25
NT binds to metabotropic receptor, what are the two things that can happen
Subunit of G breaks away and either binds to ion channel (PSP) Triggers synthesis of a second messanger (longer)
26
two ways to stop NTs from being in synapse
reuptake degradation
27
gap junctions are important for what kind of synapse
electrical
28
what glial cell is particularily important for synaptic communication in the brain
astrocytes
29
3 types of membrane transporters
pumps co-transporters exchangers
30
neurotoxins from environment
palytoxin: from corals, affects sodium potassium pump and is lethal tetrodotoxin: pufferfish, stops depolarization and muscles stop working
31
basis of electroencephalography
neurons create a field of neurons in which we can record their activity gives high temporal resolution
32
the 3 classes of small-molecule NTs
amino acids monoamines acetylcholine
32
what are some animo acids and what do amino acids do
they are fast acting, working in directed synpases of CNS glutamate: excitatory GABA: inhibitory aspartate glycine
33
monoamines
more diffuse effects and larger than amino acids dopamine, epinephrine, norepiniephrine, serotonin
34
the 2 groups that monoamines are in
Catecholamines: synthesized from the amino acid tyrosine (converted into L-dopa which converts into them) □ Dopamine □ Norepinephrine ® Neurons that release this have an extra enzyme which converts dopamine into them ◊ Neurons are noradrenergic □ Epinephrine ® Neurons that release this are called adrenergic Indolamines □ Serotonin ® Synthesized from the amino acid tryptophan
35
acetylcholine
NT at neuromuscular junctions, at many synapses in the autonomic nervous system and at synapses in several parts of the central nervous system Neurons that release this are cholinergic
36
unconventional NTs
soluble-gas (nitric oxide and carbon monoxide) diffuse through and stimulate a second messenger retrograde transmission (post->presynaptic neuron) endocannabinoids synthesized by fatty compounds released by dendrites affect presynaptic neurons/their transmission
37
Neuropeptides:
Larger molecules that include: Pituitary peptides, hypothalamic peptides, brain-gut peptides, and opioid peptides. Neuropeptides can act on a variety of brain functions and behavioral processes.
38
agonist
facilitate effects
39
steps of NT action
1. synthesize them 2. put them in vesicles 3. those that leak are degraded 4. AP causes vesicles to fuse to presynaptic membrane and release NTs 5. Inhibitory feedback: bind to autoreceptors to prevent more NTs from being releases 6. NTs bind to postsynaptic membrane 7. Nts deactivated or reuptake
40
antagonists
block/reduce/inhibit
40
are endogenous opioids NTs or NPs
NPs, there are metabotropic
41
what makes an NT an NT
presence in presynaptic neuron AP dependent release or Ca2+ dependent release action at postsynaptic neurons
42
diff between NT and neuromodulator
NT released from axon terminal that excites or inhibits postsynaptic neuron neuromodulator released from neuron and affects a population of neurons released into ECF alter strength of neural activity across a population of neurons rather than excite/inhibit one specific neuron
43
if a drug is an allosteric modulator, what does it do
Can bind to specialized sites on the receptor to affect its ability to attract agonists/NTs
44
acetylcholine and cholinesterase have shown what benefit to memory
spatial learning