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Brain
Lecture 2
Neurons
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vitalism
refuted by Helmholtz =
neural signal
physical
(electrical) not a
vital
force of nature
specific
to particular
senses
Golgi
invented method of
staining
neurons with silver
nitrate
Cajal
used Golgi's method to produce detailed
drawings
of neural
assemblies
discovered
synapse
& functional
polarity
of neurons -
direction
signals travel -
1
direction
Golgi, Cajal & Neuron
Doctrine
disagree
over whether nervous system composed of
individual
units that
interact
with neighbours (Cajal) or
continuous
mass (Golgi)
Cajal = proved correct
To some extent gap junctions (electrical connections) support Golgi’s ideas
Donald
Hebb
: The
Organization
of Behaviour (1949)
1st comprehensive theory of how complex
psychological
phenomena,
perceptions
,
emotions
,
thoughts
, &
memories
, might be produced by brain activity
alternative to dominant paradigm -
behaviourism
simple
rules on how active cells could form
‘assemblies’
(work
together
+ over
time
) to form elements of
cognition
Sequences
of assemblies (‘synfire chains’) could explain
perception
of
temporal
patterns; i.e. those that unfold in time
Neurons
Cajal - neirons = basic,
distinct
,
units
of
nervous
system
cell
body =
nuclus
,
mitochondria
, other structurers involved in protein
synthesis
&
transport
(e.g. neurotransmitters)
processes -
dentrites
&
axon
(myelin sheath - lipid (fat like) & protein)
terminal
buttons
Membrane
potential
&
Ion
exchange
transmission
in 1 direction -
dendrites
to
terminals
dendrites
&
soma
recieve
input
from
previous
nerurons
input changes
potential
(electrical charge) of neuron
resting
potential = charge across neural membrane at
rest
- membrane
polarized
charge caused by differences in ion
concentrations
& maintained by
diffusive
&
electroststic
pressures &
mechanical
process
membrane potential & Ion exchange -
permeability
regulation
membrane of neuron =
low
permeability to
sodium
ions = restricts
entry
into cell
sodium ions must be kept in
greater
concentration
outside
cell by
low
permeability
Membrabe potential & ion exchange -
sodium-potassium
pump
actively
transports
sodium ions
out
of cell while simultaneously bringing
potassium
ions into cell
operates by
exchanging
3
sodium
ions for every
2
potassium
ions
process helps maintain
concentration
gradient
of sodium ions = ensuring
higher
concentration
outside
cell
Depolarization & Action Potential
Excitation: When neuron
receives
input from other neurons = may become
depolarized
If depolarization reaches
threshold
= action
potential
generated
Voltage-dependent
sodium channels
opened
sodium enters cell - potential
increases
voltage dependent
potassium
chanes opened
sodium
channels close
potassium
leaves
cell - returning potential to
normal
over time sodium potassium pump
restores
concentrations
depolarization
occurs
locally
& spreads down
axon
in an all-or-none fashion
The Synapse – neural transmission
Neurotransmitter
molecule
binds
with a
receptor
(in post synaptic neuron)
causes
opening
of
ion
channels & changes to
polarization
of postsynaptic membrane
effects of transmitter depend on
ion
channel
open
–Na + channels -
depolarization
=
Excitatory
post-synaptic potential (EPSP)
–K + channels -
hyperpolarization
=
Inhibitory
post-synaptic potential (IPSP)
Excitatory & Inhibitory Post synaptic potential
sodium
chanel open →
depolarisation
→
EPSP
= moves potential
closer
to
firing
threshold
potassium
channels open →
hyperpolarization
→
IPSP
= moves potential
away
from
threshold
Neural Processing
ion
channels open
transiently
- PSPs
decay
over time
Seversl EPSPs necessary for
depolarization
to reach threshold
this allows
inputs
from
many
neurons to be added together =
summated
Neural processing -
summation
temporal
summation - PSPs in close
succession
overlap & add together
spatial
summation -
simultaneous
PSPs at different
locations
add
EPSPs & IPSPs can
cancel
each other out
Neurotransmitters
2
primary
transmitters
Glutamate
(
I
effects) &
GABA
(
E
effects)
many
modulatory
transmitters -
regulate
activity of neurons
effect of post-synaptic neuron determined by
receptors
present,
state
of neuron,
presence
of other transmitter substances
= allows complex
modulation
of neural processing
Neurotransmitters - Glutamate
brain's most
common
excitatory
transmitter
increases
membrane potential of
postsynapic
cell - brings closer to threshold
is an
amino
acid prodcued by neuron's
metabolism
activates several types of
receptors
- NMDA, AMPA
AMPA receptor controls
Na+
gate → EPSP
Neurotransmitters: Glutamate p2
NMDA receptor - controls
Na
+ &
Ca2+
gates
Ca2+ = involved in
changes
to AMPA receptors, producing
Long
Term
Potentiation
NMDA receptor
blocked
by Mg+ ion
this removed when membrane
depolarized
other
binding
sites have
modulatory
effects on NMDA receptors
Neurotransmitters - GABA - Gamma-AminoButyric Acid
brain's most
common
inhibitory
transmitter
decreases
membrane
potential
of postsynaptic cell - further from threshold
prevents excessive
excitation
Inhibitory
interneurons
increase
flexibility
of
nervous
system
many
receptor
sites - allowing
drug
action
Neurotransmitters: dopamine
Dopaminergic
projections from
substantia
nigra & ventral
tegmental
area modulate activity in
striate
,
limbic
, &
cortical
areas
effects can be
excitaory
,
inhibitory
or
modulatory
(long lasting effects) depending on receptor
Dopamine - Substania
nigra
modulates
input areas of
basal ganglia
- involved in
action
control
Degeneration
of dopaminergic neurons = associated with
Parkinson’s
disease
Treatment often involves
L-DOPA
-
precursor
of dopamine = compensate for dopamine
deficiency
dopamine -
Ventral
Tegmental area
involved in
reward
,
learning
, and
changing
behaviour to
unexpected
or
highly
salient stimuli
Stimuli associated with VTA activation, particularly nucleus
accumbens
= perceived as
exciting
or
rewarding
(mesolimbic system)