gray matter
cell bodies, dendrites
white matter
myelinated axons
white matter tracts - 'highways of the brain"
types of neurons
multipolar
unipolar
bipolar
central nervous system
includes brain and spinal cord
peripheral nervous system
includes everything except the brain and spinal cord
glial cells
glial (glue) cells support neuronal activity
astrocytes
star-shaped glial cells with many processes that receive neuronal input and monitor activity
microglial cells (microglia)
small cells that remove debris from injured cells
oligodendrocyte
myelinates axons in the CNS
cytoplasm of oligodendrocyte wraps around the axon) (Schwann cells in PNS)
cranial nerves
connected directly to the brain
12 total, with sensory and motor functions
spinal (somatic) nerves
connected to the spinal cord
31 pairs
input comes in the dorsal side
output goes out ventral side
superior/inferior
superior up, towards the top of the skull inferior = down, towards the spine *can also use dorsal/ventral
dorsal/ventral
dorsal = up, towards top of skull ventral = down, towards spine *makes more sense if you imagine humans walking on all 4's
means the same as superior/inferior
rostral/caudal
rostral = font, towards the face caudal = back, away from the face *means the same as anterior/posterior
anterior/posterior
anterior = font, towards the face posterior = back, away from the face
can also use rostral/caudal
medial/lateral
medial = inwards, towards the midline lateral = outwards, toward the ears
autonomic nervous system
division of the peripheral nervous system into sympathetic and parasympathetic
primarily controls glands and internal organs
involuntary actions of smooth muscles and heart and glands
sympathetic and parasympathetic nervous system
sympathetic: flight or flight
norepinephrine (adrenaline) parasympathetic: rest and digest
acetylcholine
views of the brain
horizontal
coronal - vertical, front/back view of brain
sagittal - vertical, side view of brain
frontal lobe
part of the cerebral cortex on the anterior part of the brain
borders temporal lobe in the lateral/ventral/posterior side, and the parietal lobe to the posterior sides
lies right behind the forehead
parietal lobe
part of the cerebral cortex on the posterior, dorsal part of the brain -borders frontal lobe in the anterior side, temporal lobe in the lateral/ventral side, and the occipital lobe in the posterior/ventral side
lies below the crown of the head
occipital lobe
part of the cerebral cortex on the posterior part of the head
borders parietal lobe in the dorsal/anterior side, and the temporal lobe in the lateral/anterior side
lies in the back of the head
temporal lobe
part of the cerebral cortex on the lateral sides of the brain
borders the frontal lobe in the dorsal/anterior/medial side, the parietal lobe in the dorsal/posterior/medial side, and the occipital lobe in the posterior side
lies inside the temples of the head
olfactory bulb
one of two enlargements at the terminus of the olfactory nerve at the base of the brain just above the nasal cavities
on the ventral side of the frontal lobes
precentral gyrus
on the posterior edge of the frontal lobe (border w/ parietal lobe), bounded in the back by the central sulcus
contains the motor area
central sulcus
sulcus dividing the frontal and parietal lobes
anterior side: precentral gyrus (frontal lobe)
posterior side: postcentral gyrus (parietal lobe)
postcentral gyrus
on the anterior edge of the parietal lobe (border w/ frontal lobe), bounded in the front by the central sulcus
sylvian fissure
separates the temporal lobe from the frontal and parietal lobes
dorsal to the temporal lobe
gyrus and sulcus
gyri (singular - gyrus): the folds or bumps in the brain sulci (singular - sulcus): the indentations or grooves in the brain
folding of the cortex increases surface are
brain structures
locations of motor, visual, auditory, and somatosensory corteces (and more)
motor cortex: movement
somatosensory cortex: somatic sensation (sense of touch)
visual/striate cortex: vision
auditory cortex: hearing
Brodmann areas
division of the brain based on (cyto)architecture
(cytoarchitecture -cellular composition of the central nervous system's tissues under the microscope)
basal ganglia structures
several motor-related structures
thalamus - sesory processing
tail of caudate, head of caudate (caudate nucleus)
globulus pallidus
nucleus accumbens
putamen -subthalamic nucleus etc. *amygdala is definitely anatomically connected, but not really part of it
limbic system
several structures related to emotional processing
hippocampus - very important for memory
amygdala -olfactory bulbs
cingulate gyrus - reward processing
thalamus etc.
ventricles
protection and supplies
fluid filled
shock absorbers
exchange of nutreints etc. between blood vessels and brain tissue
choroid plexus crucial for producing cerebrospinal fluid
network of blood vessels and cells in the ventricles that are covered by a thin layer of cells that make cerebrospinal fluid -CSF drains out of the bottom of the ventricles and surrounds the brain and spinal cord and it is also gradually recycled into the blood
blood vessels
oxygen supply
internal carotid arteries are connected to many blood vessels in the brain
anterior cerebral artery - feeds the medial, anterior, and dorsal parts of brain
middle cerebral artery - feeds the lateral parts of the brain
posterior cerebral artery - feeds dorsal and posterior parts of the brain
circle of Willis: the joining area of several arteries at the bottom (inferior) side of the brain (forms a 'circle')
brain imaging techniques
MRI (magnetic resonance imaging) - uses strong magnetic fields, magnetic field gradients, and radio waves to generate images of the organs in the body -fMRI (functional MRI) - measures brain activity by detecting changes associated with blood flow
CT (computed tomography) - combines a series of X-ray images taken from different angles around the body and uses computer processing to create cross-sectional images (slices) of the bones, blood vessels and soft tissues inside the body
EEG (electroencephalogram) - records/measures electrical activities through electrodes attached to the scalp
neurophysiology
the study of electrical and chemical processes in neurons
information flow:
within neurons - electrical signals
between neurons - chemical signals
electrical signaling
fast over long distances
neurons contain mostly anions --> inside of a neuron more negatively charged than the outside
ion channels
membrane-spanning transport protein for ions
cell membrane itself is impermeable for water soluble molecules such as ions that are present intra- and extracellularly
selective permeability of a neuron
ex: non-gated potassium (K+) channels selectively allow K+ into the cell
passive transport: does not cost energy
membrane resting potential
difference in electrical potential across the membrane of a cell when it is inactive - about -65mV in neurons
reflects 'balancing act' between opposing forces that drive K+ in and out of the cell
diffusion - movement of molecules from areas of high concentration to low concentration
electrostatic forces - tendency of charged molecules or ions to move towards areas with the opposite charge
ions constantly moving back and forth across membrane through ion channels and pumps (ex. K+ channels, Na+/K+ pumps)
but, at some point, the opposing forces are at equilibrium and there is no net flow
important ions for neural signaling
sodium: Na+
potassium: K+
chloride: Cl-
calcium: CA++ or CA2+
magnesium: Mg++ or Mg2+
at rest: more K+ inside the cell more Na+ and Cl- outside the cell
sodium/potassium pump (Na+/K+)
exchanges 3 Na+ for 2 K+ ions
K+ is pumped in
Na+ is pumped out *active transport: costs energy
can move ions across membrane, creating a large concentration difference (gradient)
equilibrium potential
voltage difference across a permeable membrane needed to counterbalance diffusion forces
The electrical potential at which a given concentration gradient across the membrane is stable, when the membrane is permeable for X.
voltage difference needed to counteract diffusion forces
membrane resting potential of a neuron (value)
about ~65 mV
K+, Cl-, and Na+ are all fighting to reach their equilibrium potential, but there are more passive K+ channels, than Cl- and Na+ channels, so K+ is "winning"
K+ has an EP of -85 mV, but the movement of Cl- and Na+ brings the MRP to about -65mV
there is constant movement of ions passively through channels, since non of the ions are at their EP
hyperpolarization
increasing negativity of membrane potential
depolarization
decreasing negativity of membrane potentail
generating a potential
-potentials/neuronal electrical activity - deviations from the resting potential
caused by temporarily changing, very locally, the permeability for an ion by opening gated ion channels
other ion channels briefly open (ex. Na+), so the membrane potential changes -gets closer to EP of K+, +67 mV ---> depolarization ---> potential
electrotonic conduction
passive propagation of a potential
signals spread along the membrane in all directions extremely fast
but, it also leaks away because of non-gated ion channels that are trying to restore membrane resting potential (it is 'lossy')
passive process, and signals decrease over space
structure of a (multipolar) neuron
dendrites
cell body + nucleus
axon hillock - base of the axon where action potential starts
axon
axon terminal
graded local potentials
spread passively from synapses (dendrites) to axon hillock, and from the tend of the axon to axon terminals
electrotonic conduction
flexible in shape and magnitude
action potential
brief but radical changes in polarization that send an electrical charge down the neuron - threshold: about -40mV
fundamental unit for electrical communication
uniform in shape and magnitude
larger depolarizations produce more action potentials, not bigger or longer ones
information is encoded in the (change in) frequency of action potentials
action potentials propagate actively over the axon
generating an action potential
neurotransmission causes depolarization at the synapse
electrotonic conduction of graded potential (charge flows through the inside of the neuron)
axon hillock: voltage-gated Na+ channels open ---> action potential starts here
absolute vs. relative refractory periods
after an action potential passes through, it is impossible (or difficult) for that section of membrane to fire again
absolute refractory period: Na+ channels already open, or they are INactivated for 1ms
a new action potential absolutely can not be produced
relative refractory period: when Na+ channels DEactivate, the membrane potential is hyperpolarized at -80 mV, so a larger depolarization is needed to trigger a new action potential
Hodgkin-Huxley cycle
Na+ channels open at threshold membrane potential (about -40 mV) --> Na+ rushes into the cell
after about 1 millisecond (at +30 mV) the Na+ channel is inactivated (not closed) --> absolute refractory period
now K+ channels open --> K+ leaves the cell (concentration and electrical gradient)
membrane potential decreases, then becomes negative until about -80 mV, and K+ channels close
Na+ channels are now deactivated (closed) ---> relative refractory period
normal resting potential is restored at -65 mV
action potential propagation
electrotonic conduction not sufficient
the depolarization of an action potential is strong enough to cause threshold depolarization in the next adjacent segment --> the action potential is regenerated along the axon
the action potential cannot flow 'backwards' because the previous segment is in the refractory period
myelin
oligodendrocytes produce myelin that insulate the axon (cytoplasm of oligodendrocyte wraps around the axon)
node of Ranvier - small gaps between myelinated sections
action potential 'jumps' from node to node
action potential can travel farther in a myelinated axon -prevents 'leakage' of ions during electrotonic conduction
very important for communication between neurons
saltatory conduction
action potential 'jumps' from node to node (nodes of ranvier)
electrotonic conduction of AP along myelinated sections, then the AP is regenerated at the node
faster way to travel down an axon than traveling in an axon without myelin.
toxins
some toxins block ion channels and prevent neuronal signaling
ex: tetrodoxin (found in puffer fish) - voltage-gated Na+ channel blocker
multiple sclerosis
autoimmune disease in which the immune system attacks the myelin sheath or the cells that produce and maintain it
particularly the optic nerve, the deep cerebral white matter, the cerebellar peduncles, and particular parts of the brainstem and spinal cord.
how many neurons are there in the brain?
100 billion neurons -10,000 connections each
1 quadrillion (10^15, or 1,000,000,000,000) total synapses in the brain!
2 types of synapses
electrical (gap junction)
chemical
electrical synapse (gap junction)
current just flows between cells - it is 'passive'
bi-directional
fast (no delay)
used for synchronization (ex. heart cells, release of neural hormomes - a bunch of cells need to do the same thing)
about ~2 nanometers of space between neurons
minority in the brain
disadvantage: no computations take place. not doing anything complex, just creating more of the same signal across more cells.
chemical synapse (definition)
new potential created in postsynaptic cell - it is 'active'
one-directional
slow - about ~0.5-1.0 ms of delay between arrival of the action potential at axon terminal and the creation of a postsynaptic action potential.
involves neurotransmitters
used for integration/computation in the postsynaptic neuron
chemical synapse (overview)
presynaptic part:
depolarization from action potential triggers voltage-gated Ca2+ channels -Ca2+ influx leads to vesicles releasing neurotransmitter into the cleft
synaptic cleft:
released neurotransmitter binds to receptor on postsynaptic membrane
neurotransmitter is then either degraded by enzymes or taken up again in the presynaptic part
postsynaptic part:
neurotransmitter activates the receptor to do something, for example to open an ion channel, leading to a postsynaptic potential, either excitatory (EPSP) or inhibitory (IPSP).
neurotransmitter degradation and reuptake
degradation: neurotransmitters are rapidly broken down / deactivated by a special enzyme -NTs may be recycled to make more NT in the axon terminal
reuptake: neurotransmitters are rapidly cleared from the synaptic cleft by being taken up into the presynaptic cell
special receptors (transporters) bring the NT back inside the cell
may be repacked into newly formed synaptic vessicles
excitatory post synaptic potential (EPSP)
local postsynaptic membrane DEpolarization in the postsynaptic neuron
caused by excitatory synapses
pushes the postsynaptic cell a bit closer to threshold membrane potential (Na channels open, Na+ into cell) -EPSPs caused by many neurons that converge on the postsynaptic cell --> action potential
inhibitory postsynaptic potential
local postsynaptic membrane HYPERpolarization in the postsynaptic neuron
caused by inhibitory synapses
pulls the postsynaptic cell further away from threshold membrane potential (Cl channels open, Cl- into cell)
postsynaptic potential (PSP)
neurotransmitters released into the synapse briefly alter the membrane potential of the postsynaptic cell
graded potential: bigger stimulus --> more hyper/depolarization. longer stimulus --> longer lasting hyper/depolarization (no increase in size)
PSPs last much longer than action potentials (more than 10 ms)
(a neuron can receive 100s of synapses from other cells --> 100s or 1000s of PSPs
a balance of excitatory and inhibitory ESPS is vital in neural processing of information (over-excitation --> seizure. under-excitation --> coma/death)
excitatory/inhibitory effects are sometimes caused by which neurotransmitter is present.
action potential generation in the postsynaptic cell is determined by the (im)balance of the number of excitatory and inhibitory signals received.
botox
prevents fusion of vesicles to the presynaptic membrane by splitting SNARE proteins, hence no transmitter release (exocytosis)
botox is a neuromodulator
neurotransmitter
a chemical released from the presynaptic axon terminal that serves as the basis of communication between neurons
generally easy to synthesize from amino acids in diet
amino acids are most common NT in the brain
amines - based on modifications of a single amino acid by enzymes
amino acid neurotransmitters
glutamate: fast excitatory, memory
main excitatory NT in the brain
GABA: fast inhibitory, memory
main inhibitory NT in the brain
subtypes of GABA receptors exhibit quite different properties
GABA A, GABA B, GABA C receptors (gamma-aminobutyric acid)
amine neurotransmitters
dopamine (DA): reward,
involved in schizophrenia and Parkinson's disease norepinephrine (NE) epinephrine (EP) serotonin (5-HT): mood, sleep depression
acetyl choline (ACh)
neurotransmitter: neuromuscular
first NT to be identified
receptors: nicotinic (nACh): ionotropic (muscles) and muscarinic (mACh) metabotropic
Alzheimer's disease: widespread loss of cholinergic neurons
ligand
a molecule that can bind to a receptor protein
can activate or block it
endogenous ligands: neurotransmitters and hormones made inside of the body
agonist exogenous ligands: drugs and toxins from outside the body
receptor agonist
competitive antagonist
non-competitive agonist/antagonist (neuromodulator): does not bind to the same receptor site
antagonist (ligand)
an exogenous ligand that all together stops the receptor from producing a response
ex: poisons can block acetylcholine (ACh) receptors in the brain
agonist (ligand)
molecules (can be drugs) that bind to receptors and mimic the action of a neurotransmitter.
ex: nicotine
types of ion channels
-non-gated -voltage-gated -ligand-gated (also called chemically-gated ion channels or ionotropic receptors) -stretch gated (mechanosensitive)
non-gated ion channels
resting membrane potential
always open
voltage-gated ion channels
triggered by a voltage change
can open and close
mechanosensitive (stretch-gated) ion channels
sensitive to mechanical stress
different chemical synapses
axo-dendritic
axo-somatic
axo-axonic: allows the presynaptic neuron to regulate neurotransmitter release of the postsynaptic neuron
dendro-dendritic - allows coordination of cells' activities
ionotropic receptors
(also called chemically-gated or ligand-gated ion channels) postsynaptic receptor proteins that include an ion channel, which is opened when an agonist binds to it .
fast communication
open when some chemical binds to them (could be a neurotransmitter or some 2nd messenger)
metabotropic receptors
postsynaptic receptor proteins that do not contain an ion channel, but may (when activated) activate a G-protein
G-protein: acts as a '2nd messenger' inside the cell. it amplifies the effect of the 1st messenger (the neurotransmitter) and can initiate processes that affect postsynaptic membrane potential
slower communication
amplify and prolong synaptic signals
different example of postsynaptic receptor: GABA A receptor, Cl- channel (and example of neuromodulation)
alcohol and bind to it (noncompetitive ligand) and modulate the effect of neurotransmitters binding to the receptors
alcohol is a neuromodulator
up-regulation
compensatory increase in receptor availability at the synapse of a neuron
down-regulation
compensatory decrease in receptor availability at the synapse of a neuron
spatial summation
summation of postsynaptic potentials from different synapses (different physical locations across the cell body) that overlap in time
physically closer together --> increased summation (and vice versa)
temporal summation
summation of potentials from one synapse that overlap in time
closer together in time --> increased summation (and vice versa)
information processing
graded postsynaptic potentials spread passively from the dendrites ober the cell body towards the axon hillock (in multi-and bi-polar cells)
if a depolarization is strong enough (exceeds the threshold) reaches the axon hillock --> action potential produced
spatial and temporal summation determine whether an action potential is triggered
optogenetics
inducing EPSPs and IPSPs experimentally
advantage over electrical stimulation: targets specific cells, controlled PSPs
convergence and divergence
convergence: neuronal connections in which many cells send signals to a single cell
range fractionation: information from receptors of different sensitivities is sent to one cell and integrated to code for the intensity of a stimulus
divergence: one cell sends signals to many other cells
allows for an impulse to be amplified in order to produce a response over a widespread area
neural chain
a simple kind of neural circuit in which neurons are attached linearly, end to end
ex: knee jerk reflex: sensory neuron synapses directly onto motor neuron (synapse is in the spinal cord). involves myelinated axons of large diameter.
analog- vs. digital-like signals
analog: vary in strength (ex. graded potential)
digital: all-or-none, vary in frequency (ex. action potential)
event related potentials (ERPs)
(also called evoked potential) gross potential changes evoked by a discrete sensory stimulus, such as light flashes
ex: auditory evoked potentials can be recorded with an EEG, and can diagnose deafness or hearing impairments in infants.
neurochemistry
branch of neuroscience concerned with the fundamental composition and processes OF the nervous system
endogenous processes
neuropharmacology /(psychopharmacology)
the scientific field concerned with the discovery and study of compounds that selectively AFFECT the function of the nervous system
neuropeptide neurotransmitters
endorphins, orexin, oxytocin
four major pathways
Cholinergic (ACh)
Dopaminergic (DA)
Noradrenergic (NE)
Serotonergic (5-HT)
Cholinergic pathways
acetylcholine (ACh) From: basal forebrain, (PPT/LDT - pedunculopontine nucleus and laterodorsal tegmental nucleus) To: hippocampus, amygdala, cortex
Involved in muscle control and memory
Alzheimer's disease: ACh deficiency
nicotinic receptors: ionotropic
important in muscular system
curare (antagonist) --> paralysis
muscarinic receptors: metabotropic
atropine (antagonist) --> confusion, memory problems