week 3 Flashcards

Name and describe the phases of communication within the neuron. Explain conduction of an action potential. Describe and explain synaptic communication between neurons. Identify and describe various neurotransmitters in the brain. Describe non-chemical communication.

1
Q

When cells communicate where does the info come through?

A

Communication between cell is directional
Info comes through dendrites and soma
Then transmits down the axon outwards other neurons

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2
Q

What triggers an electrical signal(action potential)?

A

The electrical change that occur in the cell which would trigger an electrical signal called the action potential which moves down the axon all the way to the terminal buttons

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3
Q

How does communication with the cell begin?

A

Communication begins by disturbing the resting potential of a cell.
Disturb by depolarizing (+++) or hyperpolarizing (—) the cell

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4
Q

What is Membrane Potential?

A

The electrical charge across a cell membrane (voltage unit = mV)

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5
Q

What is Resting membrane potential?

A

The potential of a neuron when it is not being altered by excitatory or inhibitory innervation;
Voltage is more negative inside relative to outside; -40 to -90 mV (-70mV)
When at rest the cell is maintaining polarization, that difference between the intracellular and extracellular spaces

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6
Q

What is Intracellular and extracellular?

A

Intracellular(inside of cell) is always more negative than extracellular(outside of cell) when at rest

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7
Q

What are Cations and Anions?

A

Ions: charged molecules
Cations (K+, Na+, Ca2+); positive charged ions
Anions (Cl-); negative charged ions

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8
Q

What is Diffusion?

A

Movement of molecules from regions of high concentration to regions of low concentration = Concentration Gradient

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9
Q

What is Electrostatic Pressure?

A

Opposites attract; Similarity repulse = Electrical Gradient (polarization)

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10
Q

What are 2 forces working on ions?

A

Diffusion

Electrostatic Pressure

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11
Q

How do you maintain polarization?

A

Voltage-gated Ion channel (passive transport pump)

Sodium-Potassium pump (active transport pump)

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12
Q

Desribe the Voltage-gated Ion channel

A

An ion channel that opens or closes according to the value of the membrane potential (how pos. or neg. the membrane potential)

Na+ voltage gated channels is closed when at rest; Na+ concentration greater outside cell than inside cell
K+ voltage gated channels is closed when at rest; K+ concentration greater inside cell than outside cell

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13
Q

Describe the Sodium-Potassium pump (active transport pump).

A

Pushes 3 Na+ ions out of the cell where there is a high concentration of Na+
and pulls 2 K+ into cell, where there is a low concentration of Na+
Ensures resting membrane potential
Requires energy (ATP) (active transport) b/c this pump moves ions against their concentration gradient
Role: Regulate ion concentration
Result: Na+ is 10x more concentrated in intracellular space

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14
Q

How does Concentration Gradient (diffusion) and Electrical Gradient (electrostatic pressure) effect Na+? In respect to Activity in the Neuron.

A

Both forces Na+ to enter the cell
Sodium (positive) will want to be pulled into the cell because it is a mostly negative space (mV-70) (electrostatic pressure)
Sodium is more concentrated outside the cell than inside of the cell so sodium will want to be pulled into the cell along its concentration gradient (diffusion) b/c there is less concentration

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15
Q

How does Concentration Gradient (diffusion) and Electrical Gradient (electrostatic pressure) effect K+? In respect to Activity in the Neuron.

A

Competing forces act on K+
Diffusion forces K+ out of the cell where its less concentrated
Electrostatic Pressure forces K+ into the cell, like Na+
Potassium channels are not fully closed so K+ can leak out of cell (Net movement will ensure greater concentration of K+ inside cell at resting)

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16
Q

What is the Action Potential?

A

Electrical charge that runs down the axon from the axon hillock to the terminal buttons

From mV-70 Voltage goes up to mV+40 after depolarization reaching an action potential. After repolarization begins and the mV returns back down to mV-70.
But also going into a refractory period where it hyper-polarizes and becomes more negative than the resting membrane potential.
The sodium potassium pump reinstates the membrane potential go to back to its resting state

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17
Q

What is the Threshold of excitation?

A

the value of the membrane potential that must be reached to produce an action potential

An action potential is all or none, if the charge is not made positive enough an action potential will not be generated

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18
Q

What are the 3 phases of an Action Potential?

A

Depolarization: Reduction (toward zero) of the membrane potential of a cell from its normal resting potential. Less negative
Repolarization: An increase in the membrane potential of a cell toward resting state. More negative
Hyperpolarization: An increase in the membrane potential of a cell, more negative than resting potential

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19
Q

Which respect to an Action Potiential, what is going on with Na+ and K+?

A

Na+ channels open as soon an threshold is met (depolarization)
Na+ begins to enter the cell(depolarization)
K+ channels open and leave the cell(depolarization)
B/c of the rush of Na+ the impact of K+ leaving the cell is minimal
Na+ channels becomes refractory, and shut close no more Na+ can entre(action potential)
K+ continues to leave cell, membrane potential returns to normal(repolarization)
K+ channels close Na+ reset
Extra K+ outside, sodium -potassium pump reestablish resting membrane potential (refractory period)

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20
Q

What is the Absolute refractory Period?

A

brief interval after a successful stimulation (meeting threshold) another action potential can not be generated

Time from opening of the sodium “activation gate” to closing of “inactivation gate”

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21
Q

What is the Relative refractory Period

A

if the cell is stimulated enough then a new action potential may be generated

While the Na+ gates closed, K+ gates open
Only a very strong stimulation can cause an action potential

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22
Q

explain “activation gate” and “inactivation gate”.

A

2 gates “activation gate” activates after threshold and “inactivation gate” closes after a specific period of time

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23
Q

What are the 2 principles for Conduction of the Action Potential ?

A

All-or-none Law

Rate Law

24
Q

Explain the All-or-none Law.

A

The principle that once an action potential is triggered in an axon, it is propagated without growing or diminishing to the end of the fiber (terminal buttons).

25
Q

Explain the Rate Law.

A

The principle that variations in the intensity of a stimulus or other information being transmitted along an axon are represented by variations in the rate at which that axon fires (i.e. number of APs) Has nothing to do with amplitude, whether it’s a +40 or +50, that point of depolarization, it has to do with the frequency of the action potential moving down the axon. Higher rate, stronger stimulus.

26
Q

What does Myelination do?

A

Allows Less time and energy required for the action potential to propagate down the axon

Myelination allow the regeneration process to only take place at the nodes of ranvier(Saltatory conduction). At the nodes of ranvier is where we have our voltage gated channels

27
Q

What disease distrupts myelination

A

In MS(Multiple sclerosis) there are inhibition to movement because the brain can not function because of the loss of myelin and break in the chain of communication. The ions will diffuse and be less likely to generate at the nodes of ranvier.

28
Q

What is a Synapse?

A

specialized space where two neurons communicate

29
Q

What are Sherrington’s Properties of the Synapse?

A
  1. Reflexes are slower than conduction along an axon
  2. Several weak stimuli presented at slightly different times or locations produce a stronger reflex than a single stimulus does. Temporal summation and Spatial summation.
  3. When one set of muscles becomes excited, a different set becomes relaxed.
30
Q

What is Temporal summation and Spatial summation?

A

Temporal summation: (one synapse)timing of firing. Two firings with a pause will not allow an action potential. Three firing in a rapid speed causes the threshold of excitation.

Spatial summation: firing at different areas along this cell membrane. Each location A,B,C (3 synapses) on their own is not strong enough for an action potential. But at the same time it is strong enough

31
Q

What is Law of Reciprocal Innervation?

A

The way inactivation influences the activation of other muscles
As we walk when the muscles involved in the extension of a muscle is activated and the muscles involved in the contraction of that same leg just be inhibited

32
Q

The difference between spatial and temporal summation is ?

A

Temporal summation is when there are firings in rapid succession without a pause which will cause the neuron to reach the threshold of excitation. Spatial summation is simultaneous firing that will create a combined effect for an action potential to be generated

33
Q

What are Presynaptic membrane and Postsynaptic membrane?

A

Presynaptic membrane: The membrane of a terminal button that lies opposite to the postsynaptic membrane, through which the neurotransmitter is released.
Postsynaptic membrane: The cell membrane opposite the terminal button in a synapse, receives the message

34
Q

What is Ligand?

A

Ligand (neurotransmitter) will bind to a specific binding site. Which will produce postsynaptic potential (change potential of the postsynaptic membrane)

35
Q

What is Synaptic cleft and Synaptic vesicle?

A

Synaptic cleft: The space between the presynaptic and postsynaptic membrane.
Synaptic vesicle: A small, spherical hollow organelle; contain molecules of a neurotransmitter.

36
Q

What is the Release zone?

A

Interior of the presynaptic membrane to which vesicles attach and release their neurotransmitter into the synaptic cleft.

37
Q

What is Postsynaptic density?

A

portion of postsynaptic membrane where receptors are located for binding

38
Q

Where can Synapses occur?

A

On dendrites = axodendritic synapse
On the soma = axosomatic synapse
On other axons = axoaxonic synapse (not involved with neural integration(

39
Q

What are the types of Synapses?

A

Axodendritic synapses can occur on the smooth surface of a dendrite or on dendritic spines
Axosomatic synapses occur on somatic membranes.
Axoaxonic synapses consist of synapses between two terminal buttons

40
Q

Explain in-depth how the Axoaxonic Synapses function.

A

Does not contribute to neural integration
Controls amount of chemical release by axon terminal, by either Presynaptic inhibition or Presynaptic facilitation
An Axoaxonic Synapse: The activity of terminal button A can increase or decrease the amount of neurotransmitter released by terminal button B.

41
Q

What is Presynaptic inhibition and Presynaptic facilitation?

A

Presynaptic inhibition: reduces the amount of neurotransmitter released by the postsynaptic terminal button.
Presynaptic facilitation: increases the amount of neurotransmitter released by the postsynaptic terminal button.

42
Q

What are the steps for Communication at the Synapse?

A
  1. Synthesis and Release of neurotransmitter from presynaptic terminals
  2. Activation of postsynaptic receptors
  3. Postsynaptic potential (EPSP or IPSP)
  4. Termination of postsynaptic potential
43
Q

Explain the step of Synthesis and release of Neurotransmitters in the Communication at the Synapse.

A

Synthesis in soma or terminal buttons
Calcium channels open (calcium influx, Ca+). the action potential causes an influx of calcium
Synaptic vesicle fuses with membrane - Exocytosis
Vesicles break open and release neurotransmitters into synaptic cleft

44
Q

Explain the step of Activation of Postsynaptic Receptors in the Communication at the Synapse.

A

A receptor in the postsynaptic membrane of a synapse that contains a binding site for a neurotransmitter (ligand).

Neurotransmitter-dependent ion channel (ligand-gated)
An ion channel that opens when a molecule of a neurotransmitter binds with a postsynaptic receptor

The connection between the ligand and receptor will open a channel, by opening this channel would allow an influx of sodium which would help depolarize the cell, depolarozation is exitiory so this would be exitory postsynaptic potienal

45
Q

What are the 2 ways that neurotransmitters open ion channels?

A

Ionotropic receptor: A receptor that contains a binding site for a neurotransmitter and an ion channel that opens when a molecule of the neurotransmitter attaches to the binding site. Fast acting. (ligand-gated channel, which begin depolarization process)

Metabotropic receptor: A receptor that contains a binding site for a neurotransmitter which then activates an g-protein that begins a series of events that opens an ion channel elsewhere in the membrane of the cell. Slow but amplified. (G-protein-coupled receptors)

46
Q

Explain the step of Postsynaptic Potential: Excitatory or Inhibitory in the Communication at the Synapse.

A

Depends on the ion channels that the receptors open.
3 major types neurotransmitter-dependent ion channels:
Sodium (Na+)
Potassium (K+)
Chloride (Cl-)

47
Q

What are EPSP and IPSP?

A

EPSP = excitatory postsynaptic potentials
Depolarization
Increase Na+ into the cell

IPSP = inhibitory postsynaptic potentials
Hyperpolarization to prevent stimulation of the neuron
Increasing flow of K+ out or influx of Cl- into cell

EPSP and IPSPS are not all or none, they are graded and they can dissipate they can change over time

48
Q

What is Neural integration?

A

The process by which inhibitory and excitatory postsynaptic potentials summate and control the rate of firing of a neuron

The combined effect if EPSPs and IPSPs in one neuron will determine whether that neuron will be depolarized enough to reach that threshold of excitation in order to enable an action potential

49
Q

Explain the step of Termination of Postsynaptic Potential in the Communication at the Synapse.

A

To maintain balance there needs to be termination until a new set of neurotransmitter are released
You don’t want neurotransmitters to linger around

50
Q

What are 2 ways of terminating neurotransmitters?

A

Reuptake: Reuptake protein that allows the reentry of a neurotransmitter just liberated by a terminal button back through its membrane, thus terminating the postsynaptic potential.
Specialized transporter proteins
5HT(serotonin) transporter
DA (dopamine) transporter

Enzymatic deactivation: The destruction (takes apart) of a  neurotransmitter by an enzyme after its release.
Specialized enzyme proteins
Acetylcholinesterase, will break apart acetylcholine, which is a major neural transmitter important for learning and memory
Catechol-O-Methyl transferase (COMT), breaks down catecholamines 
Monoamine Oxidase (MAO)
51
Q

What is a Non-chemical Communication Between Neurons?

A

Electrical synapse
Electrical transmission via gap junctions
Ion channels always open and aligned
Faster transmission than chemical
E.g. Cardiac muscles require fast communication

52
Q

What is a Neurotransmitter

A

Chemicals produced within a neuron
Released by a neuron following depolarization from presynaptic neuron and acts on adjacent post-synaptic neuron
Exogenous administration mimics endogenous release (drugs!)
Does not remain in the postsynaptic cleft for a long period (clearance)

53
Q

What are Neuromodulators/Neuropeptides?

A

Not restricted to the synaptic celf and diffuses through the extracellular fluid, traveling further and more widely dispersed.

54
Q

What are Hormones?

A

A chemical substance that is released by an endocrine gland into the blood that has effects on target cells in other organs (and in the brain).

55
Q

What are some Types of neurotransmitters?

A
  1. Amino acids: glutamate, GABA, glycine
  2. Acetylcholine (Ach)
  3. (Biogenic amines) Monoamines: serotonin (5HT), dopamine (DA), NE, E
  4. Neuropeptides: endorphins, neuropeptide Y
  5. Purines: adenosine
  6. Gases: nitric oxide (NO)
56
Q

What are Amino Acid and Acetylcholine?

A

Amino acids:
Glutamate - excitatory; implicated in Learning and Memory
GABA - inhibitory NT in the brain
Glycine - role in spinal cord, brain stem and retina.

Acetylcholine:
PSP depends on the receptor: nicotinic (excitatory); muscarinic (inhibitory or excitatory)
The primary NT secreted by the efferent axons of the CNS
Implicated in Alzheimer’s disease: 90% drop in Ac

57
Q

What are Monoamines?

A

Indolamine – 5HT(serotonin)
Made from Tryptophan (amino acid)
Important for mood, eating, sleep, arousal, pain, dreaming
Drugs that perturb 5HT: MDMA (ecstasy), LSD, SSRIs

Catecholamines – DA-NE-E
Made from Tyrosine (amino acid)
NE & E (adrenergic NT system): Neurotransmitter and hormone function
Facilitates neural communication and attention
DA: Important for movement, learning, perseveration, motivation, compulsion, emotion
3 main dopaminergic systems: Mesolimbic, Nigrostriatal, Mesocortical DA system