ch.8 neurons Flashcards

(48 cards)

1
Q

factors affecting ion flux across membranes

A

-concentration gradient; ion gradient
-ion membrane permeability

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2
Q

what are the two mechanisms of disruption of membrane potential

A
  1. graded potential
  2. action potential
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3
Q

describe graded potential and the three major characteristics

A

graded potential: change in Vm that caries in size
-found in unexitable membrane
-lacks voltage gated channels but can have ligand gated or mechanically gated channels
1. magnitude of response is directly proportional to magnitude of stimulus
2. does not transmit over long distances
3. effects can be summated, added together

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4
Q

describe action potential and its three characteristics

A

action potential: change in a membrane potential of an excitable membrane
-have voltage gated channels
-found in neurons and non-neuronal tissues like muscles
1. action potentials are all or nothing, magnitude is fixed after threshold
2. capable of transmitting over long distances
3. do not summate

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5
Q

brief summary of how action potentials work

A
  1. start with ligand gated channels
  2. concentration of ions is large enough to reach threshold
  3. transitions to voltage gated channels
  4. depolarizes
  5. reaches max and then repolarizes
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6
Q

threshold

A

minimum stimulus necessary to illicit a response (action potential)
-an above threshold stimulus applied to the membrane can cause a change in voltage resulting in the opening of voltage gated channels
-in the range of 15 mV

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7
Q

voltage gated sodium channels

A

has three conformations:
1. closed but capable of opening, activation gate is closed
2.opened (activated) caused by a change in vM
- activation gate opens when Vm reaches threshold
-does not stay open for long
3. closed and locked (inactivated)
- con only open at -70 mv
-repolarize: K+ leaves the cell and repolarizes the cell

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8
Q

voltage gated potassium channels

A

open in response to changes in vM but are slower than Na+ channels
-increased potassium conductance results in efflux and repolarization. inside becomes (-).
-potassium channels dont inactivate, only close when Vm returns to normal

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9
Q

action potential in depth

A
  • (-70) to threshold: Vm changes caused by Ca+ influx or Na+ influx, from a graded potential (ligand gated channels)
    -Phase 1: Na+ influx to the cell, from a voltage gated sodium channel, becomes activated at threshold.
  • peak point of action potential: VGC sodium channel closes and locks, K+ channel is late in opening: concentration and electrical gradient travel out of the cell.
    -phase 2: potassium efflux repolarizes the cell.
    -(-70): sodium channel is closed but unlocked. potassium channel is slow to close and causes hyperpolarization.
    -cell resets back to normal by a sodium potassium pump.
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10
Q

at rest… the membrane is 6.5 permeable to ___

A

potassium

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11
Q

at rest the gradient is 6.5 times bigger for

A

sodium

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12
Q

describe the permeability of potassium and sodium during a action potential

A
  • sodium permeability: increases during phase 1 and decreases at peak.
  • potassium permeability: increases during phase 1.
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13
Q

components of efferent neuron

A

-nucleus: provides machinery
-dendrites: thin membrane, unexcitable membrane, has no VGC; so it is affected by graded potential
-axon hillock: transition area, gets Vm to threshold. start of VGC, known as the first start of an action potential

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14
Q

local current flow:

A

movement of action potential from one region to neighboring region, relatively slow. used by every muscle cell.

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15
Q

refractory period

A

time period after an action potential in which sodium gates may be inactive and the potassium channels may be open so that a second AP is possible in the future.
-creates one direction flow
-allows membrane to return to resting Vm, “membrane does nothing”

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16
Q

mechanism of local current flow

A

-start at the axon hillock and depolarize to threshold by a graded potential from the dendrites. need more Na going in than K going out
-VGC sodium open: inside of cell receives sodium influx which depolarizes the cell further.
-sodium diffuses to another area of membrane and depolarizes to threshold, opens VGC on that membrane. process continues in one direction down an axon. (positive feedback loop)
-meanwhile potassium VGC channels were also activated but slower to open.
-as the cell is depolarized to about +30mv, VGC sodium close and lock and VGC potassium open
-potassium concentration and electrical gradient travels out of the cell. ( falling phase of AP), which repolarizes the section of membrane. (refractory period)

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17
Q

action potential or graded potentials need _________ to trigger AP

A

disproportionate ion flux, need more sodium coming in than potassium going out.

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18
Q

rates of transmission of signal down a axon depend

A

on the diameter of the axon, wider diameters have less resistance

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19
Q

schwan cells

A

myelin forming cells of the PNS, help prevent leakage of charge
-1:1 ratio

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20
Q

oligodendrocytes

A

myelin forming cells of the CNS
-help prevent leakage of charge
-one oligodendrocyte to several axons

21
Q

astrocytes

A

star shaped cells that surround unmyelinated cells that give structural support

22
Q

what is myelin and its function

A

prevents leakage of charge
-wraps around axon
-made of fat

23
Q

node of ranvier

A

portion of unmyelinated axon, where ions flow through, has VGC

24
Q

saltatory conduction

A

action potential propogation by “jumping” from node to node in myelinated fibers

25
mechanism of saltatory conduction
-axon hillock becomes depolarized and reaches threshold -VGC sodium and potassium channels are triggered. sodium opens first. -first receive Na influx through the node of ranvier, it diffuses and depolarizes the node. -Vm reaches +30 mV: causes sodium VGC to close and unlock, potassium channels open and potassium travels out and repolarizes the Vm (refractory period) -sodium diffuses to the next node and depolarizes it to threshold: causes VGC sodium channels to open and have sodium influx. VGC are also activated but slower to open. process repeats
26
characteristics of a fast neuron
-myelinated -wide neuron
27
loss of myelination
results in the loss of action potential signal -disease multiple sclerosis: immune system destroys myelin
28
synapse:
automically specialized junction between two cells where the electrical activity of one cell influences the excitability of another.
29
two types of synapses
1. electrical (gap junction): ion moves through connexon 2. chemical messenger: NT flows from neuron to neighboring cell
30
presynaptic cell
before the synapse
31
post synaptic cell
after the synapse
32
synaptic cleft
space between the cells, has interstitial fluid
33
synaptic bulb
at the end of a long axon, has vesicles with NT
34
cell body
has nucleus, performs protein synthesis, packages and transports NT via microtubules, stages vesicles in synaptic bulb
35
mechanism of signal transmission
1. AP travels down axon to synaptic bulb and depolarizes via saltatory conduction or local current flow. 2. depolarization of synaptic knob open VGC calcium channels, creating calcium influx inside the cell 3. Calcium influences cytoskeleton and causes fusion of NT filled vesicles with plasma membrane. (triggers exocytosis) 4. NT is released into synpatic cleft and diffuses across it to reach post synaptic membrane 5. NT binds to ligand gated receptors on post synaptic membrane leading to a graded potential: which influences excitability -graded potential can make the cell more or less excited. -receptors on post synaptic membrane can be ligand gated channels, receptor enzymes, GTP coupling receptor, or a intigrine receptor. then trigger a cell response
36
opening a ligand gated channel causes
ion flux, leads to depolarizing or hyperpolarization of 2nd cell. the second cell does not need to be a neuron.
37
fast post synaptic graded potential
occurs when NT binds to a receptor and opens a ligand gated channel and allows ion influx
38
fast post synaptic graded potential a. excitatory post synaptic potential
depolarizing graded potential in post synaptic neuron cell (EPSP), does NOT always reach threshold -can open Na+ or Ca+ to depolarize
39
fast post synaptic graded potential b. inhibitory post synaptic potential
inhibits depolarization in post synaptic neurons (IPSP) -hyperpolarization from K+ efflux, more difficult to reach reach threshold -stabilization by Cl- channels opening. makes it harder to depolarize. Cl has a equilibrium potential of -70
40
grand post synaptic graded potential
the cumulative change in membrane potential -sums EPSP and IPSP -in the post synaptic cell -takes place in the soma and dendrites: unexcitable membrane -graded potential dont diffuse well, so it doesnt reach threshold. needs a large stimulus
41
two methods to enhance GPSP to trigger a action potential
1. temporal summation: summation of two stimuli; from the same neuron that follow eachother in close proximity in time. 2. spatial summation: summation of graded potential from several sources.
42
convergence
one neuron can be influenced by many other neurons
43
divergence
one neuron does not travel to just one place, it can split.
44
common neurotransmitters
1. Acetocholine (Ach) 2. Biogenic amines -primarily catacholamines: epinephrine or nor-epinephrine 3. amino acids 4. misc.
45
post synaptic receptors
1. ligand gated ion channels: (ionotropic) 2. G protein coupled receptor: (metabotropic)
46
post synaptic receptors cholinergic receptors
*respond to Ach a. nicotinic: receptor acts a sodium ligand gated channel ion channel. -found on skeletal muscle (PNS) -ANS CNS -provides excitatory responses with sodium influx b. muscarinic: utlilizes G protein and secon messenger system -found in ANS, CNS -not in skeletal -can be excitatory and inhibitory
47
post synaptic receptors adrenergic receptors
respond to epi or nor epi -alpha 1,2: second messenger system - beta 1,2: utilizes cAMP 2nd messenger system
48
enzymes that degrade NT
-actylcholinesterone (AchE): degrades Ach -monoamino oxidase (MAO) and catechol-o-methyltransferase (CoMT): degrade epi and nor epi -enzymes are always present in the synaptic cleft and are ready to degrade.