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Major divisions of the brain
hindbrain
midbrain
forebrain

sulcus
grooves of the brain (wrinkles)

gyrus
folds of the brain

fissure
deep sulcus
Why do we have so many folds in the brain?
More surface area as a result which means more space for neurons leading to increased cognitive capacity
Hindbrain is composed of the following:
Cerebellum
Medulla oblongata
Pons
Cerebellum (functions)
balance, movement, attention (timing)
Medulla oblongata (functions)
extension of spinal cord and vital reflexes (breathing, coughing, sneezing) + opiate receptors
Pons (function)
the “bridge“ for contralateral control
Midbrain is composed of the following:
tectum
inferior and superior colliculus
tegmentum
Tectum (function)
roof of midbrain and some reflexive movements
Inferior and Superior Colliculus (functions)
sensory processing - hearing and vision respectively
Tegmentum (function)
intermediate level + wider range of functions (sleep)
The forebrain is composed of the following:
the lobes (frontal, occipital, parietal, temporal)
the fissures (central, lateral)
subcortical structures (limbic system, cingulate gyrus, basal forebrain, basal ganglia)
ventricles
meninges
Frontal lobe (functions)
behavior, emotion, personality, motor cortex
Parietal lobe (functions)
sensory info and sensory cortex
Occipital lobe
vision
Temporal lobe
auditory info and memory encoding
Limbic system components
amygdala
hippocampus
thalamus
hypothalamus
Amygdala
emotional info
Hippocampus
new memories
Thalamus
working memory + input to cortex
Hypothalamus
direct pituitary gland + homeostasis
Cingulate gyrus (function)
emotion processing + learning/memory
Basal forebrain
nucleus basalis
release acetylcholine to cerebral cortex
linked to arousal
Basal ganglia
movement and skills/habits
Ventricles
4
produce CSF (choroid plexus cells) used as suspension system to aid in swelling
= hydrocephalus- overproduction of CSF leading to learning disabilities
Meninges
membranes surrounding brain and spinal cord
3 of them = pia mater, arachnoid mater, dura mater
swollen blood vessels responsible for pain of headache
no pain receptors in the brain
Gray matter
packed with dendrites/cell bodies
neurons send axons through white matter to the brain and other parts of spinal cord
White matter
made up of axons
connects sections of gray matter
Sensory nerve
sensory info
dorsal root ganglia (cell bodies)
Motor nerve
motor info
cell bodies inside the spinal cord
Ganglia + nuclei
clusters of neuron in PNS + CNS respectively
Autonomic nervous system
things you can’t control
unvoluntary functions (heart and digestive system)
divided into PARASYMAPTHETIC and SYMPATHETIC divisions
Sympathetic Division
“fight or flight“
prep organs for activity burst (increased heart rate // decreased digestive activity)
sweat, adrenal glands, etc.
norepinephrine
Parasympathetic Division
“rest and digest“
opposite of sympathetic activities (decreased heart rate // increased digestive activities)
acetylcholine
many cold remedies have anti-parasympathetic properties (leads to their restriction - anti-runny nose)
Somatic Nervous System
voluntary nervous system
skeletal muscles
sensory nerves
4 categories of research methods
effects of brain damage
stimulation of the brain
recording brain activity
correlating anatomy with behavior
Effects of brain damage (research)
Paul Broca = Broca’s Area = language production
ablation vs. lesion (remove vs. damage)
stereotaxic instrument: placement of electrodes on animal studies
“virtual lesion“: transcranial magnetic stimulation - strong
Stimulation of the brain (research)
Transcranial Magnetic Stimulation - mild
Optogenetics
- using light to control neurons
- Karl Deisseroth
-released for use in 2009
- required 3 steps
1) protein that responds to light
2) develop a virus as a delivery system
3) develop thin fibers to shine light
Recording Brain activity (research)
electrodes to look at individual neurons
Electroencephalograph (EEG)
Magnetoencephalography (MEG)
Positron-emission tomograph (PET) = inject with radioactive substance
Functional Magnetic Resonance Imaging (fMRI); tracking blood flow
Correlating anatomy to behavior (research)
phrenology: using race and skull shape and correlating to behavior(not used anymore)
Computerized Axial Tomography (AT)
Magnetic resonance imaging (MRI)
1800s discovery about us
scientists discovered we are made up of cells
Santiago Ramon y Cajal discovery
used silver salt staining method
used art to show that nerve cells remain separate and do not grow onto each other
Astrocytes
star shaped, wrapped around the synapse
important for rhythms such as breathing
shield synapse from surrounding chemicals
dilate vessels to bring nutrients to active areas
tripartite synapse hypothesis
- chemicals released by the terminal cause astrocytes to release chemicals to magnify/modify message to next neuron
- gliotransmitters
Microglia
act as part of the immune system
removes viruses, fungi, dead/damage neurons, weakest synapses
negative feedback
Oligodendrocytes (CNS) & Schwann Cells (PNS)
build myelin sheath (insulin layer- provides nutrients to cells)
provides nutrients
Radial glia
guide migration during embryonic development
differentiate after embryonic development
most will differentiate into astrocytes (in mammals, mostly)
Molecules that cross the blood-brain barrier
Vitamin A
Vitamin D
drugs meant for the brain
Molecules that cannot cross the blood-brain barrier
glucose
amino acids
purines
iron
choline
Vitamin B
Vitamin C
Most chemotherapy drugs
Alzheimer’s and Blood-Brain Barrier
blood-brain barrier shrinks and lets in harmful chemicals
Charles Scott Sherrington (research)
discovered evidence of synapse using behavioral studies
reflexes are slower than conduction along an axon
several weak stimulus stronger than 1 strong stimuli
when one set becomes excited, another relaxes
delay between stimulus and reflex
thought neuroscience was largely electrical, rather than chemical
TR Elliot
proposed that the sympathetic system stimulated muscles by releasing hormones
prevailing belief was solely in electrical impulses
Otto Loewi
demonstrated the effects of neurotransmitters
Frog Experiment
stimulated vagus nerve of a frog and taking fluid and placing it around the frog’s heart (slowed down heart rate)
stimulated accelerator nerve of a frog and took fluid and placed it around the frog’s heart (accelerated heart rate)
made room for the development of psychiatric drugs!
TYPES OF NEUROTRANSMITTERS: Amino acids
glutamate, GABA, glycine, aspartate
TYPES OF NEUROTRANSMITTERS: Modified Amino Acids
acetylcholine
TYPES OF NEUROTRANSMITTERS: Monoamines
catecholamines= norepinephrine, epinephrine, dopamine
indoleamines= serotonin
TYPES OF NEUROTRANSMITTERS: Neuropeptides
endorphins, substance P
TYPES OF NEUROTRANSMITTERS: Purines
ATP, adenosine
TYPES OF NEUROTRANSMITTERS: Gas
nitric oxide
Ionotropic effects
tend to be excitatory or inhibitory
SHORT AND QUICK EFFECTS
Rapid communication, vision, and hearing
Ex. Glutamate, GABA, glycine, and acetylcholine
Metabotropic effects
neuromodulators that modulate message to other neurotransmitters
SLOW TO START, LONGER LASTING
Taste, emotion
Ex. dopamine, norepinephrine, serotonin
Neurotransmitters vs. Neuromodulators
Neurotransmitters
synthesized from axon terminal
is released from adjacent synaptic knob
lasts milliseconds
Neuromodulators
synthesized from cell body, dendrites, sides of axon
released by spreading out
lasts seconds to minutes
DRUGS: Hallucinogenic
LSD, peyote
resembles receptor (mimics effect of receptor)
distorts perception / inappropriate timing and longer stimulation
DRUGS: Nicotine
increases dopamine release
triggers reward center= more dopamine and wanting more and more
DRUGS: Opiates
derived from or similar to opium (morphine, heroine, methadone)
same receptors as endorphins (pain killers)
Serotonin and Catecholamines
detach from receptor
reuptake into pre synaptic neuron
DRUGS: Stimulants
amphetamine, methylphenidate, cocaine
prevents uptake of serotonin, dopamine, norepinephrine (basis for ADHD meds)
DRUGS: Cannabinoids
tells presynaptic cell to stop even though it never sent a message in the first place
decreases exhibitory/inhibitory messages
can slow reaction time and anxiety
Plato (history)
“sight rays“
theory is not feasible because it would take a long time for a sight ray to travel to the sun
Hasan Ibn-al-Haytham (history)
philosopher
the perception of an object is not in the object itself, but instead in our brain (internal process rather than external process)
Rene Descartes (history)
philosopher
nerves sent a pattern of impulses arranged like the image to the brain
Joannes Miiller
Law of Specific Nerve Energies
modern interpretation: nature of perception is defined by the pathway over which the information travels
Ex. rubbing your eye and seeing little black dots
Miillers interpretation: what excites a nerve establishes a special and unique energy
pupil
opening
iris
eye color, muscles
cornea
outer layer
lens
focus light
ciliary muscle
retina
back of the eye
receptors
fovea (location of cones/rods)
optic nerve
runs to the occipital lobe
Visual info processing in the retina
receptors —> bipolar cells —> ganglion/amacrine cells
receptors are the bottom layer
fovea
center of the retina
1 bipolar cell to 1 cone
midget ganglion cells
Optic nerve
bundle of ganglion axons
blind spot
RECEPTORS: Cones
color vision
bright light
clustered in the fovea
details!
RECEPTORS: Rods
located in the periphery of retina
good in faint light
motion detection
Photopigments
release chemicals when struck by light
Ex. Il-cis-retinal (vitamin A derivative), il-trans-retinal, opsins (proteins)
Trichromatic Theory of Cones
Thomas Young
Hermann von Helmholtz
3 kinds of cones (red/green/blue)
-more red and green
-3 primary color based
Ratio Activity
relative response rates
red = long wavelength
green = middle wavelength
blue = short wavelength
Opponent-Process Theory
Ewald Hering
color perceived in opposites
-red to green, black to white, yellow to blue
-example: bipolar cell with prolonged exposure
still an issue
-afterimage of a green square with a center white circle is red
Retinex Theory
need to explain color constancy
-ability to recognize colors in different lightning
-comparisons
-can trick the brain by removing context
brightness constancy
-brightness perceived as comparison to other objects
Edwin Land
-the cortex compares info from retina to determine color and brightness
Visual Processing Pathway
receptors (cones/rods) —> horizontal cell (inhibitory contact with bipolar cells) —> bipolar cells —> amacrine cells —> ganglion cells (optic nerve) —> lateral geniculate nucleus —> thalamus/visual cortex
Lateral Inhibition
emphasizes borders of objects
bipolar cells
-light decreases inhibitory output (net excitation)
-bipolar cell sends message to horizontal cells
-horizontal cells inhibit nearby bipolar cells
not limited to vision
helps explain certain illusions
-Hermann grid
Parvocellular cells
ganglion cells
small cell bodies, small receptive fields
in fovea - color!
Magnocellular cells
ganglion cells
larger, larger receptive field
even distribution
Koniocellular cells
small cell bodies
occur throughout retina
very difficult to study - have a variety of functions
Primary visual cortex
occipital cortex
-Area V1, striate cortex (striped appearance)
= conscious visual experience
= optical illusions
= “imagining“ seeing = dream, vision
Aphantasia
When you close your eyes and try to picture an object like an apple or a loved one's face, you see nothing instead of a mental picture
Damage to visual cortex
no conscious vision
no visual imagery or dreams
blindsight= ability to respond to visual stimuli without seeing it consciously
Hubel and Wiesal
electrodes to record activity in the occipital cortex of cats and monkeys
Simple cells
receptive field with fixed excitatory/inhibitory zones
more light on inhibitory zones, less of a response
horizontal or vertical
Complex cells
Areas V1 and V2
stimuli moving in a particular direction