PSYC122 weeks 1-3 Flashcards

1
Q

How can we study the brain, behaviour and the mind?

A
  • Ask questions
  • Observe what you are doing
  • Measure your performance on a specific task
  • See how damage to the brain can impact performance
  • Measure activity of healthy brains
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2
Q

Wellington Zoo’s Meerkats, complex social hierarchy, Example: Investigating food preference in meerkats (Brox et al., 2021).

A

controlled how much food they had before, time of day, zookeeper’s outfit
* IV: Food type
* DV: number of meerkats present at each site.
* Tells us about which foods animals prefer when they are given a range of foods to choose from.
The value of observing behaviour, we all observe the world around us, helps us understand processes, teaches us about the world around us

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3
Q

Stroop test

A

a grid filled with names of colours. Your job is to say the names of the colours that the words are printed in from left to right as fast as possible- the colours don’t have to match the word

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4
Q

Automaticity Theory

A

The word interferes with the colour naming when the word and colour do not match because reading is an automatic process and recognising colours is a more controlled process.

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5
Q

Selective Attention process

A

Reading requires less attention compared to identifying a colour, that’s why it takes us longer to identify the colour of words in incongruent trials.

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6
Q

Aphasia

A
  • Language disorder that affects a person’s ability to communicate.
  • The result of a stroke or brain injury.
  • People with aphasia may find the following tasks difficult:
    Talking
    Comprehending spoken, or written language
    Writing
    Using numbers, for example calculating answers to problems.
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7
Q

Broca’s area Aphasia

A
  • Involved in speech production.
  • Difficulty in producing language
  • Comprehension abilities relatively conserved
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8
Q

Wernike’s area Aphasia

A
  • Involved in language comprehension
  • May speak fluently
  • Spoken language often lacks meaning
  • Difficulty with language comprehension
  • Can produce word salad- say a number of words that have no connection to each other
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9
Q

Example: fMRI

A
  • Safe and non-invasive
  • Detects changes in the flow of blood
  • Increases in blood flow are correlated with neuronal activation
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10
Q

Central Nervous System (CNS)

A

made up of the brain and the nerves that go along your spinal cord down your vertebrate

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11
Q

Example 1: Transcranial Magnetic Stimulation (TMS)

A
  • Non-invasive technique that disrupt specific brain activity for a fraction of a second.
  • Allows us to investigate the role of these areas in human functioning.
    Electric currents flow into different parts of the brain as you process different information
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12
Q

Peripheral Nervous System (PNS)

A

made up of all nerves that come out from your spinal cord and goes to fingers, arms, legs, other organs

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13
Q

Neurons

A

Cells that send/receive information

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14
Q

The main structures of a Neuron

A

classic structures to almost every neuron, dendrites= branches that form from round/fat bit, they reach out and expect to receive information from other cells, detect signals, send the information to centre of the cell (round bit) called the cell body or soma, similar to other cells, it contains a lot of organelles which are things that keep the cell alive, creating protein to grow/move, life support system, longer looking tube is called axon, carries information away from the cell body, moves it down towards terminal region/axon terminal they have bulbs at the end, reaching out to send a signal to another cell’s dendrites

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15
Q

How information travels through a Neuron

A

signals always go from the dendrites to the cell body, and then from the cell body down the axon to the axon terminals

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16
Q

When a neuron “fires”

A

the signal may stop or not be allowed to be sent down the rest of the cell, just because the dendrites brings in information from another cell does not mean it is automatically going down the axon, something special happens in the neuron at the very beginning of the axon, called the axon hillock, counting the different signals and keeping a score and there is a threshold where if the signal coming in does not reach this threshold then it does nothing at all, not enough signal to go down the axon- “fires” sends a signal, the axon hillock generates the signal and sends it down- all or nothing principle, either no information or fires

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17
Q

The myelin sheath

A

how signals can move faster down the axon!
Unmyelinated Speed: ~1 metre per second
Myelinated Speed: up to 100 metres per second!
Myelin: a fatty (lipid-rich) substance that insulates the axon, allowing signals to travel faster!- may be myelinated because it is really important for what that information carries for it to get really quickly to your brain
In myelinated neurons, the signal “jumps” from one Node of Ranvier to the next as it moves down that axon. Nodes of ranvier- gaps between the myelin sheath

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18
Q

Other cells in the Nervous system that support Neurons: Glia cells

A

3 kinds- Oligodendrocytes (cell body with arms), Astrocytes (cell body with arms and feet), Schwann Cells

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19
Q

Oligodendrocytes

A
  • Form the myelin sheath around axons in the central nervous system.- form crescent shape from the centre, find an axon that is not myelinated and wrap itself around and around and around and tighten up, can do this on different axons because of multiple arms/form multiple different sections on one axon
  • Help increase speed of information travelling through the axon
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20
Q

Schwann Cells

A
  • Form the myelin sheath around axons in the peripheral nervous system (PNS).- find an axon and wrap their entire cell body around the axon, only forms one part of the myelin sheath
  • Help increase speed of information travelling through the axon
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21
Q

Astrocytes

A

. Helps repair neurons
. Helps bring nutrients from the bloodstream to the neurons using the blood-brain barrier
. Provides structural support for neurons.

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22
Q

Two kinds of signals can travel into the cell body

A
  1. Excitatory signals make the cell more likely to fire
  2. Inhibitory signals make the cell less likely to fire
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23
Q

Summation

A

A process occurs in the Axon Hillock where the sum of all incoming signals (excitatory and inhibitory) determines whether the neuron fires.
Threshold value at which the neuron fires:
-55 mV (millivolts)
Value the neuron starts at (before any signals arrive):
-70 mV (millivolts)
You need 15 more excitatory mV than inhibitory

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24
Q

Resting Membrane Potential

A

below membrane is inside the cell (intracellular), above is outside the cell (extracellular), Inside of the cell is more negatively charged (70 mV more negative) compared to outside the cell, resting membrane potential is achieved when both forces are equally strong and then cell fires

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25
Q

What are these charged particles that reside inside and/or outside the cell?

A

Ions: Molecular clusters with an electrical charge
K+ Na+
Potassium Sodium
These two ions are crucial to sending signal down an axon

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26
Q

How do these charged particles get into the cell (or out of the cell) to make it more positive or more negative?

A

Ion Channels: Doors in the Membrane- openings in the cell that can happen, leaky potassium channel- never closes, potassium can sneak out of the cell

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27
Q

Why don’t these charged particles just stay put where they are?

A

Concentration gradients- Ions move from area of high concentration and toward lower concentration until equilibrium occurs
Electrical gradients- Charged particles will move across membrane until equilibrium occurs (same charge on both sides)

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28
Q

What actually is an Action
Potential?

A

An Action Potential is a change in the voltage (inside is more positive and outside is more negative) inside a cell (relative to outside of the cell) taking place at one section of the cell at a time (not the whole cell at once)- moving change in voltage down the axon

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29
Q

How does an action potential travel down the axon?

A

Action potential propagation- voltage gated sodium channel, only open when it detects certain voltage, -55 mV or greater, opens gates, sodium floods into the cell (less sodium and more negative)
What about potassium- gates open to let potassium in- First not much will happen: Concentration Force (CF) wants to move K+ out; Electrical Force (EF) wants to push K+ in, However, as Na+ flows in, the inside become less negative, leading to a reduction in EF, Now CF is winning and K+ flows out

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30
Q

Action Potentials (change in voltage across time)

A

Depolarization- inside of cell becomes crazy positive, +30 mV threshold closes gates
Repolarization- more negative- goes down lower than it was at beginning -80
Refractory- trying to get back to resting potential -70, can’t fire in the meantime- Voltage gated channels have closed so there’s no way for Sodium to travel down its electrical gradient to leave the cell, This is where the Na+/K+ Pump comes in!- need to get extra sodium out, always need extra potassium since it leaks out the gates

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31
Q

Na+/K+ Pump

A
  1. Throws 3 Na+ out of the cell
  2. Brings in 2 K+ into the cell
  3. Requires energy (NOT passive diffusion!)
32
Q

Is this different for myelinated axons?

A

In myelinated neurons, the action potential jumps from one Node of Ranvier to the next.
This jumping is referred to as Saltatory Conduction (node-to-node conduction of the action potential)
Benefits of Saltatory Conduction:
1. Signal moves faster (increases rate of propagation)
2. Energy efficient (100x less movement of ions!)
the action potentials occurring only at the nodes, not along the whole axon

33
Q

Neuronal Communication is Electrochemical

A
  • action potential= electrical, transmission is chemical process, changes back into electrical in next cell- Takes about ~1 millisecond for chemical transmission to occur- why does it take so long/ slows down the signal so much
34
Q

How signal is transmitted from one neuron to another

A

Pre-Synaptic cell- sending the signal
Synapse- name of the area where one cell meets the next one
Post-synaptic cell- receiving the signal

35
Q

More Ions

A

Cl- Ca2+
Chloride Calcium
Calcium- Essential for allowing chemicals in presynaptic cell to exit the cell and enter the synaptic cleft
Chloride- Essential for understanding how neurons send inhibitory signals.

36
Q

Chemical synapse- steps of synaptic transmission

A
  1. Action potential is travelling down the axon to the presynaptic terminal
  2. Action potential arrives at the presynaptic terminal
  3. Voltage gated Ca2+ channels open, allowing influx of Ca2+
  4. Ca2+ allows vesicles to merge with membrane (fuse) and the neurotransmitter releases out of the other side
  5. Neurotransmitter binds to receptors, causing channels to open (or close)- needs a very specific shape/neurotransmitter to open- ion (just floating around) flows in, neurotransmitters just open the door
  6. Excitatory (or inhibitory) postsynaptic potential is generated
  7. Neurotransmitter is removed by glial uptake (or enzymatic degradation)
37
Q

Excitatory synapse

A

Excitatory postsynaptic potential (EPSP)- have different kinds of neurotransmitters- Glutamate, main kind- shape of doors will differ depending on neurotransmitters- shape of doors only allow in sodium/calcium for excitatory- depolarizes the cell- makes it more positive

38
Q

Inhibitory synapse

A

Inhibitory postsynaptic potential (IPSP) inhibitory neurotransmitter- GABA- doesn’t allow sodium/calcium, only chloride (concentration gradient for reason to flow in, more chloride outside)- hyperpolarizes the cell, makes it more negative- make it harder for the cell to fire

39
Q

Reuptake

A

The pre-synaptic cell membrane has neurotransmitter- specific “transporter” proteins that transport neurotransmitters back into the presynaptic cell- don’t need all the neurotransmitters sent out- pre-synaptic cell wants to recycle it- if they are just hanging out they will open the doors even though there is no action potential- need to empty out- door on pre-synaptic cell has door for neurotransmitters and pumps them back in- doors are called transporters

40
Q

Neurotransmitters

A
  • Chemical messengers that transmit signals across synapses from one neuron to another neuron (or to a muscle cell or gland cell).
  • We do not know how many there are (ongoing subject of study!)
    We have discovered over 100 different kinds so far
  • There are different categories of neurotransmitters:
    Amino Acids (symate, GABA)
    Monoamines (Dopamine, Serotonin, Histamine)
    Peptides (Endorphins, Oxytocin)
  • Neurotransmitters are synthesised inside the neuron (in the cell body or axon terminal)
41
Q

Neurotransmitter: Dopamine

A
  • Can be excitatory or inhibitory (depends on the receptors)- depends on shape of the door
  • Plays diverse roles in the nervous system:
    Involved in thoughts, feelings, motivations, behaviours
  • Associated with the experience of pleasure
  • Learning to associate particular behaviours with reward (“reward pathway”)
  • Attention, mood regulation, emotional responses
  • Coordinating movement (Parkinson’s Disease = progressive loss of dopamine-producing neurons)- producing movement that he shouldn’t produce (tremors)- staying still is a part of coordinating movement
42
Q

Neurotransmitter: Serotonin

A
  • Involved in regulation of mood, sleep, eating, arousal, and pain.
  • Depression associated with reduced serotonin (thus, antidepressants target neurons that produce serotonin)
  • Other ways to increase serotonin levels include sunlight exposure! How?
  • Sunlight exposure stimulates production of Vitamin D in the skin.
  • Vitamin D is involved in Serotonin synthesis
43
Q

The effects of drugs in the Nervous System

A

Agonists- drugs that occupy receptors and activate them
Antagonists- drugs that occupy receptors but do not activate them, block receptor activation by agonists

44
Q

What is the overall structure of the nervous system?
What are the functions of its different branches?

A

Peripheral nervous system- composed of nerves, bundle of axons, held together by connective tissue, other things like blood vessels who provide the axons with oxygen and nutrients- nerves that cause throughout our bodies- somatic nerves, innovate or form synapses on muscles- autonomic

The autonomic nervous system
* Involuntary, automatic activity
* Controls & regulates blood vessels, organs (including the heart) and glands

Sympathetic:
* Increases arousal
* Prepares the body for survival-related action
* Four Fs:
- Fighting
- Fleeing
- Feeding
- Mating

Parasympathetic:
* Reduces arousal
* Returns the body to resting state
- Not separate systems- labels given to nerves who have opposite actions- compliment each other
* The two systems act in a coordinated manner

45
Q

Terminology (CNS)

A

neuraxis (central axis of nervous system), central axis of the spinal cord and brain- different locations relative to neuraxis- with the example of a crocodile- front of nervous system rostral or anterior (front of brain or top of spinal cord)- back end caudal or posterior (bottom end of spinal cord or back of the brain)- anything above neuraxis (top of the brain or back) is known as dorsal, below the neuraxis (bottom of brain or stomach area) is ventral
- in humans the neuraxis is bent (straight through the spinal cord, horizontal through brain), dorsal towards top of the head and ventral below- lateral (towards the side or on the side), medial (in the middle or towards the middle), sagittal- divides the body into right and left sections

46
Q

The spinal cord (CNS)

A

Dorsal horn- going in- sensory neuron outside
Ventral horn- going out- motor neuron inside

47
Q

Somatic nervous system

A

part of perpheral, skeletal muscles, nerves that have synapses with muscles, associated with the voluntary control of body movements

48
Q

The central nervous system: The hindbrain

A
  • Phylogenetically ancient- been with us from very early on in evolution- preserved in the same way in many animals
  • Coordinates information flow to/from the spinal cord
49
Q

The hindbrain: Medulla

A
  • Extension of the spinal cord
  • Controls:
  • Heart rate
  • Circulation
  • Respiration
50
Q

The hindbrain: Reticular formation

A
  • Regulates:
  • sleep/wake
  • Arousal
  • can’t be seen by human eye
51
Q

The hindbrain: Cerebellum

A
  • Controls fine motor activity
  • Doesn’t initiate movements, but refines and smooths them
    Greek for smaller brain
52
Q

The hindbrain: Pons

A
  • Relays info cerebellum between and rest of brain
53
Q

The central nervous system: The midbrain

A
  • two main subdivisions
  • The midbrain coordinates basic functions related to perception and action- deciding what to do and perceiving the world around us in a very basic level/function
  • Tectum (dorsal):
  • Spatial orienting to the environment
  • Superior colliculi – vision- one half of visual space each, two top ones
  • Inferior colliculi - audition- two bottom ones
  • consists of 4 bubble like structures called colliculi
  • Tegmentum (ventral):
  • Movement- not deciding but automatic responses but environmental stimuli
  • Arousal- no single function in the brain ever comes from a single place of the brain the brain operates as a unified whole with different parts of the brain contributing different aspects to a function
  • Pleasure seeking
54
Q

The midbrain: Substantia nigra (part of the tegmentum)

A
  • High level of dopamine gives it dark colour
  • Pale colour in Parkinson’s disease- impaired movement
55
Q

Forebrain

A

Evolutionally the newest, Cortex and sub-cortical structures

56
Q

The Forebrain (Subcortical structures)

A
  • symmetrical one on the left and one on right
57
Q

The Forebrain (Subcortical structures): Basal ganglia

A

(movement, reward)- plan initiation of intentional movement

58
Q

The Forebrain (Subcortical structures): Thalamus

A

(sensory gateway)- relays and filters info from the senses to the cortex

59
Q

The Forebrain (Subcortical structures): Hypothalamus

A

Limbic system, (regulates body function)- regulates internal body functions- temperature, hunger, 4 Fs

60
Q

The Forebrain (Subcortical structures): Hippocampus

A

Limbic system, (memory)- spatial navigation, creates and integrates new memories but not long term memory

61
Q

The Forebrain (Subcortical structures): Amygdala

A

Limbic system, (emotion)- emotional processing and memory- particularly fear

62
Q

The Forebrain (Subcortical structures): Pituitary gland

A

regulates hormones

63
Q

The Forebrain (Cortex)

A

Four lobes per hemisphere

64
Q

Neurosurgery: Brain stimulation- Wilder Penfield

A
  • 1950s: Penfield stimulated exposed cortical surface with an electrode during surgery;
    found this caused sensation/movement/memories/etc…
  • Mapped functions
  • Important:
  • knowledge about the brain
  • knowing what not to cut out
65
Q

The Forebrain (Cortex): Frontal lobe

A

primary motor cortex
* Planning
* Abstract thinking
* Executive control

66
Q

The Forebrain (Cortex): Parietal lobe

A

primary somatosensory cortex
* Spatial attention
* Sensory integration
* Object location
* Numbers/quantities

67
Q

The Forebrain (Cortex): Occipital lobe

A
  • Vision
68
Q

The Forebrain (Cortex): Temporal lobe

A
  • Semantic knowledge
  • Word meanings
  • Object identification
  • Audition
69
Q

What function does the nervous system have?

A
  • Receives sensory information from the environment
  • Integrates and processes information
  • Regulates internal functions
  • Produces motor actions
70
Q

The blind spot in each of our eyes, how?

A

back surface of the eye is lined with a layer of cells called the retina, many different kinds of cells but there are neurons called light receptors, produce an action potential when hit by light, highest concentration is in part of the eye called fovea- corresponds to centre of our vision field, retinas of mammals axons that take information out of the eye all come together and leave the eye together- optic nerve leave the eyes, there are no photoreceptors where the axons leave the eye, bringing light reflected off the paper was falling on blind spot, area is actively filled in, at any given time the brain is receiving information from outside world and doing stuff with it- reconstruct what is out there/filling in missing information, happens under the hood of consciousness

71
Q

Neurons “fire” to carry out specific functions- how neurons know where we are in space- Nobel prize JOhn okeefe, the mosers

A
  • Place cells (O’Keefe, 1971, 1976)- recording activity in single neurons in rat brains, insert electrodes in brains of animals, a particular part of the brain (hippocampus) is involved in spatial navigation so okeefe inserted electrodes into individual neurons in the rat’s hippocampus, neurons that tend to fire when the rat is in a specific location, the way that we represent space happens in these neurons
  • Grid cells (the Mosers, 2004, 2005, 2006)- each red bit forms a triangle with two other red bits, way for the brain to keep track of structure of the place, in combination with place cells knowing where the organism is, compared to the cell and allowing it to be updated, give an idea of where places in space are relative to each other
72
Q

Extra information about sypnatic transmission

A

Synaptic transmission- neurotransmitters that are emitted from presynaptic neurons can be either excitatory or inhibitory, an excitatory neuron will cause the cell body to be less depolarised, an inhibitory will cause the cell body to be more depolarised, analog/digital- analog process the change in voltage is continuous, any number/move smoothly between different values- if an action potential happens, digital process, all or nothing, happens or doest, 0 or 1

Communication between neurons: The patellar (knee-jerk) reflex- doesn’t go through the brain, stays between legs and spinal cords, when the patellar tendon is hit, it stretches, tendon is connected to a muscle, flexor muscles that cause the joint to bend, extensor muscle causes the muscles to unbend to stretch, sensory neuron in muscle, if stretching of the tendon was strong enough it will produce an action potential, axon splits in two, goes into spinal cord, within it forms two synapses, one goes to motor neuron that goes to extensor muscle, excitatory, motor neuron fires an action potential raises our leg, other axon goes to interneuron, connects two neurons, also causes an action potential, but is inhibitory

We have one sensory neuron, one interneuron, two motor neurons. Sensory neuron excites the extensor muscle and through the interneuron it inhibits the flexor muscle. That’s why we have movement in the leg.

The human brain has an estimate:
86 billion neurons
860 trillion synapses
What sorts of operations do they perform?- inhibitory/excitatory

73
Q

How is all this activity organised? Neural computation and modelling

A

connectionism networks, developed in 1980s
Logical operation- fire if both a and b fire, “And”, activation threshold is 1.5
“Or”, fire if a or b or both fire, only needs one, activation threshold is 1
“Xor”, fire if a or b but not both fire, activation threshold is 0.5, interneuron in the middle, strong inhibitory, -2

74
Q

Myth: The brain is (like) a computer

A

Status: It’s complicated
Facts:
* Neurons do perform computations
* But:
- Computer: digital. Brain: analog and digital
- Computer: single CPU (serial). Brain: billions of neurons, trillions of synapses (parallel)
- Computer: fast, accurate, Better at algorithmic tasks. Brain: slow, approximate, better at “fuzzy” tasks (e.g., language, object categorization)

75
Q

Myth: Polygraph machines detect lies

A

Status: Incorrect
Facts:
* Polygraphs measure arousal – i.e., they assess the autonomic system’s activity
* Measures: blood pressure, heart & breathing rates, skin conductance

Facts:
* Assumption: Lying is stressful -> increases arousal
* Is this assumption correct?
- Some people have a high arousal threshold (e.g., psychopaths – just the people we want to catch…)
- Some people get aroused very easily (just being asked about a crime can be enough!)
- So high chance of both misses and false positives

  • Possibility of countermeasures- relaxation techniques/active deception
76
Q

Myth: The right hemisphere is artistic and intuitive, the left hemisphere is logical and rational

A

Status: Distortion, exaggeration, oversimplification
Facts:
* Hemispheric differences do exist
* But it’s not divided by logic/intuition, or art/science, or anything that simplistic; and both sides work together!
* Most prominent lateralization: language
* Also:
- left – details, right – holistic
- left – sequences, right – spatial arrangement

77
Q

Myth: We only use 10% of our brain

A

Status: NOT TRUE
Not even a little bit. Absolutely ridiculous.
Facts.
- We use 100% of our brain
- Different brain regions are more/less active at any time, but none are completely inactive
- All neurons fire, a neuron that does not fire is a dead neuron