Cracking The Neural Code (Week 1) Flashcards

1
Q

2 main types of brain cells

A

neurons and glia

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2
Q

neurons function

A

signal changes in the environment, internal states and plans of action

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3
Q

glia functions

A

regulate chemical context of space between cells (extracellular spaces) and insulate axons of neurons

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4
Q

what are the main cells types representing information

A

neurons

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5
Q

what types of glial cells regulate chemical context of space between cells (extracellular spaces) ?

A

astrocytes

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6
Q

what type of glial cells insulate axons of neurons

A

oligodendrocytes and Schwann Cells

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7
Q

are there more glial cells or neurons in the brain

A

glia

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8
Q

dendrite function

A

connect at synapses with other neurons to receive information from them ; post synaptic part of neuron

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9
Q

what is the cell membrane of a neuron

A

phospholipid bilayer

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10
Q

axon function

A

provide input to other neurons through electrical pulses/ spikes

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11
Q

axon hillock

A

site where action potential is generated

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12
Q

axon terminal

A

part of axon that is part of synapse; pre synaptic part of synapse

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13
Q

cell body (soma) function

A

gene expression (nucleus), protein synthesis (ribosomes, rough ER), protein sorting(smooth er and golgi), cellular respiration (mitochondria)

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14
Q

important ions for neuron signaling

A

K+, Na+, Ca2+, Cl-

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15
Q

electric potential

A

energy needed to move a positive ion towards positive source

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16
Q

when does a positive ion have more stored energy/electric potential?

A

when it is closer to the positive source

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17
Q

what does positive ion have less potential energy/ loose potential energy

A

as it moves towards the negative source of the electric field

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18
Q

what ions are more abundant outside of the cell

A

Na+

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19
Q

what ions are more abundant inside of the cell

A

K+

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20
Q

what allows ions to move through membrane

A

ion channel (peptide subunit) facilitates membrane transport due to selectively permeable membrane

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21
Q

what is resting membrane potential

A

-65 mV; reflects charge separation across cell membrane

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22
Q

why is the resting potential more negative inside of the cell

A

leaky K+ channels move K+ out of the cell which makes the inside of the cell less positive

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23
Q

depolarization

A

membrane potential of cell becomes less negative

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24
Q

hyperpolarization

A

membrane potential of cell becomes more negative

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25
Q

what factors determine ion movement across membrane

A

concentration gradient and electric potential difference/membrane potential

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26
Q

equilibrium potential

A

E ion: electric potential difference that exactly balances ion concentration gradient

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27
Q

what are the 2 classes of ion channels

A

voltage gated ion channels and ligand gated ion channels

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28
Q

ligand gated ion channels

A

ligand binds -> structural change
*GABA receptor: lets in anions
*glutamate receptor: lets in cations

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29
Q

voltage gated ion channels

A

channel opens due to change in membrane potentials (closed at rest)

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30
Q

membrane potential threshold

A

the level at which an action potential is triggered in a cell

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31
Q

what triggers an action potential

A

Na+ moves into the cell and depolarizes it

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32
Q

how how long is channel open during process of firing an action potential

A

about 1 millisecond; after channels closes ->inactivated (absolute refractory period)

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33
Q

stages of firing an action potential

A

1) resting
2) rising phase (depolarization; Na+ into cell)
3) overshoot (spike)
4) falling phase (hyperpolarization; Na+ channels close and K+ channels open)
5) undershoot (refractory period)
6) resting; re establish conc gradient

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34
Q

how is concentration gradient re established in cell

A

sodium potassium pump

35
Q

where does the action potential travel?

A

from axon hillock to axon terminal

36
Q

how is action potential regenerated down axon?

A

Na+ influx of the action potential depolarizes membrane ahead of the threshold -> chain reaction of regenerating action potential

37
Q

2 types of neruons

A

pyramidal neurons (dendrites) and sensory neurons

38
Q

2 types of single neuron/ single unit recordings

A

extracellular and intracellular recordings

39
Q

intracellular recordings

A

intracellular electrode that measure action potentials from targeted cell

40
Q

extracellular recordings

A

electrode in extracellular space pick up spikes from surrounding cell/cells

41
Q

what does a larger amplitude of spike mean in extracellular recordings

A

that spike came from a closer neuron

42
Q

how do you differentiate between neurons in extracellular recording data

A

by shape and amplitude

43
Q

what are local field potentials (LFP)

A

subthreshold fluxuations : how many oscillations in the membrane potential of neurons that occur below the firing threshold

44
Q

how many signals can a classical electrode measure

A

only signals from a few cells

45
Q

matrix electrodes

A

grids of tiny electrodes that can be used to measure or deliver neural signals; measures community of cells

46
Q

laminar probe

A

probe with multiple vertical electrode contacts; can record from all 6 layers of the cerebral cortex

47
Q

can patients feel the electrodes?

A

no because there are no pain receptors in the brain

48
Q

what kind of recordings are used in research more often

A

extracellular recordings; because more recording stability and easier for human behavioral experiment

49
Q

neuropixils probe

A

a new technology that has more electrode contacts in only 1cm

50
Q

impedance

A

a measure of resistant plus electroes ability to store charge (capacitance)

51
Q

how does size impact impedance

A

smaller the electrode contract, the higher the impedance

52
Q

what comes from higher impedance/ resistance

A

harder for currents to flow through, meaning we can isolate certain neurons and get a localized signal

53
Q

consequences of larger exposed metal contact

A

low impedance meaning its harder to isolate individual neurons

54
Q

LFP recordings from extracellular depth electrode

A

reflects ~1,000 cells
*signals derived within 250 microns of electrode tip

55
Q

LFP recordings from ECoG

A

intracranial recordings for epilepsy patients; pre surgery approach to localize seizure/ abnormal vs normal brain activity
*electrodes on exposed brain surface (subdural; invasive)

56
Q

what do EEG signals meausre

A

sum of synchronized activity of neurons with similar spatial orientation

57
Q

how many cells to EEG signals reflect

A

100,000-1,000,000 cells

58
Q

EEG electrode arrangement

A

electrodes above scalp usually on cap; non invasive technique
*good temporal resolution

59
Q

EEG disadvantages

A
  • skull smears signal -> degrade source localization
    -deep brain structures inaccessible
    -poor spatial resolution
60
Q

temporal resolution

A

ability to detect changes in brain activity over time

61
Q

spatial resolution

A

the ability of a neuroimaging technique to distinguish between two closely located points in the brain

  • lower spatial resolution = more blurred image
62
Q

how are FMRI signals produced

A

magnetic field applied to excite H atoms, H atoms align with magnetic field then fall to release energy; emitted radio frequency signal measured
**measures brain activity indirectly by detecting changes in blood flow (the Blood Oxygen Level Dependent, or BOLD signal)

63
Q

FMRI spatial

A

-better spatial resolution than EEG

64
Q

FMRI temporal resolution

A

bad temporal resolution because brain activity measured indirectly by BOLD signal; slower than neuronal activity so only can have a measurement every 2 seconds

65
Q

are FMRI signals more correlated with spikes or LFP’s

66
Q

how are FMRI changes in size of signals measured

A

brain is divided into tiny squares called voxels and percent changes in brain activity graphed

67
Q

single unit recording;
invasive, # of cells, spatial resolution, temporal resolution

A

invasive
1 cell
high spatial resolution (<30um)
high temporal resolution(<1ms)

68
Q

LFP;
invasive, # of cells, spatial resolution, temporal resolution

A

invasive
~1000 cells
less spatial resolution than single unity (250um)
good temporal resolution (<1ms)

69
Q

EEG:
invasive, # of cells, spatial resolution, temporal resolution

A

non invasive
over 1,000,000 cells
bad spatial resolution (>5mm^2)
good temporal resolution (<1ms)

70
Q

FMRI:
invasive, # of cells, spatial resolution, temporal resolution

A

non invasive
500,000 cells
good spatial resolution (2x2x2mm^3)
bad temporal resolution (2s)

71
Q

spike rate code

A

number of brain spikes from 1 cell in a given interval

72
Q

effect of increasing stimulus intensity

A

increasing number of spikes up to a certain point

73
Q

pooled response code

A

number of spikes from multiple cells in a given interval; measures population of neurons

74
Q

why is pooled response code more reliable

A

counteracts variability of single cell response and reduces noise

75
Q

labeled-line code

A

a notion to express which neurons are firing and the number of spikes for each one: vector formed from joint firing of multiple neurons

ex) (cell 1 # of neurons, cell 2 # of neurons)

76
Q

2 types of neural codes

A

spike timing codes and spike rate codes

77
Q

spike pattern codes

A

temporal pattern of spikes in a given time interval; divide each time interval into smaller bits

78
Q

spike rate codes

A

relies on brain’s internal clock (network of neurons that osalate together) to time spikes

79
Q

2 steps in decoding neural activity

A

training step and test step

80
Q

training step: decoding neural activity

A

use subset of data to train classifier to help learn relationship between pattern of neural activity and experimental conditions

*classifier can be linear or nonlinear

81
Q

test step: decoding neural activity

A

predict catagores new data belongs to based on classifier

82
Q

how to increase accuracy in decoding neural activity

A

increase number of sites

83
Q

how do neural prosthese work

A

EEG sends signals to BCI (brain computer interface) which decodes the neural information and feeds it into prostatic to signal muscle activity

84
Q

what neural prosthesis are being developed

A

eeg based models and intracranial implants to record spikes and LFP’s (which would increase decoding accuracy)