Journal of Neuroscience,
Journal Year:
2011,
Volume and Issue:
31(17), P. 6362 - 6370
Published: April 27, 2011
Positive
social
interactions
are
essential
for
emotional
well-being
and
proper
behavioral
development
of
young
individuals.
Here,
we
studied
the
neural
underpinnings
reward
by
investigating
involvement
opioid
neurotransmission
in
nucleus
accumbens
(NAc)
play
behavior,
a
highly
rewarding
interaction
adolescent
rats.
Intra-NAc
infusion
morphine
(0.05–0.1
μg)
increased
pinning
pouncing,
characteristic
elements
behavior
rats,
blockade
NAc
receptors
with
naloxone
(0.5
prevented
play-enhancing
effects
systemic
(1
mg/kg,
s.c.)
administration.
Thus,
stimulation
was
necessary
sufficient
to
increase
play.
treatment
selective
μ-opioid
receptor
agonist
[
d
-Ala
2
,
N
-MePhe
4
,Gly
5
-ol]enkephalin
(DAMGO)
(0.1–10
ng)
antagonist
Cys-Tyr-
-Trp-Arg-Thr-Pen-Thr-NH
(CTAP)
(0.3–3
decreased
play,
respectively.
The
δ-opioid
DPDPE
([
-Pen
]-enkephalin)
had
no
effects,
whereas
κ-opioid
U69593
(
-methyl-2-phenyl-
-[(5
R
,7
S
,8
)-7-(pyrrolidin-1-yl)-1-oxaspiro[4.5]dec-8-yl]acetamide)
(0.01–1
β-endorphin
but
met-enkephalin
(0.1–5
enkephalinase
inhibitor
thiorphan
(0.1–1
were
ineffective.
DAMGO
after
into
both
shell
core
subregions
NAc.
Last,
intra-NAc
CTAP
(3
play-induced
conditioned
place
preference.
These
findings
identify
as
an
important
mechanism
attribution
positive
value
Altered
function
may
underlie
impairments
psychiatric
disorders
such
autism,
schizophrenia,
or
personality
disorders.
Science,
Journal Year:
2009,
Volume and Issue:
324(5930), P. 1080 - 1084
Published: April 24, 2009
Rewarding
Bursts
of
Dopamine
Dopaminergic
neurons
are
thought
to
be
involved
in
the
cognitive
and
hedonic
underpinnings
motivated
behaviors.
However,
it
is
still
unclear
whether
dopaminergic
neuron
activation
sufficient
elicit
reward-related
behavior
which
type
neuronal
activity
pattern
serves
this
purpose.
Tsai
et
al.
(p.
1080;
published
online
23
April)
directly
compared
tonic
versus
phasic
firing
cells
ventral
tegmental
area,
effects
on
both
dopamine
release.
Using
a
transgenic
system
virus
injection
mice,
they
targeted
with
rhodopsin.
Light
stimulation
was
then
used
drive
either
low
level
pulses
or
bursts
high-frequency
pulses,
number
being
equal
across
conditions.
Only
induced
conditioned
place
preference
Physiological Reviews,
Journal Year:
2009,
Volume and Issue:
89(4), P. 1379 - 1412
Published: Sept. 29, 2009
The
opioid
system
consists
of
three
receptors,
mu,
delta,
and
kappa,
which
are
activated
by
endogenous
peptides
processed
from
protein
precursors,
proopiomelanocortin,
proenkephalin,
prodynorphin.
Opioid
receptors
recruited
in
response
to
natural
rewarding
stimuli
drugs
abuse,
both
opioids
their
modified
as
addiction
develops.
Mechanisms
whereby
aberrant
activation
modifications
the
contribute
drug
craving
relapse
remain
be
clarified.
This
review
summarizes
our
present
knowledge
on
brain
sites
where
controls
hedonic
responses
is
abuse
rodent
brain.
We
1)
latest
data
anatomy
system,
2)
consequences
local
intracerebral
pharmacological
manipulation
reinforced
behaviors,
3)
gene
knockout
behaviors
dependence,
4)
chronic
exposure
expression
levels
genes.
Future
studies
will
establish
key
molecular
actors
neural
onset
addictive
disorders.
Combined
with
human
nonhuman
primate
(not
reviewed
here),
research
this
extremely
active
field
has
implications
for
understanding
biology
therapeutic
interventions
treat
disorder.
Physiological Reviews,
Journal Year:
2009,
Volume and Issue:
89(2), P. 649 - 705
Published: April 1, 2009
Alcohol
consumption
is
an
integral
part
of
daily
life
in
many
societies.
The
benefits
associated
with
the
production,
sale,
and
use
alcoholic
beverages
come
at
enormous
cost
to
these
World
Health
Organization
ranks
alcohol
as
one
primary
causes
global
burden
disease
industrialized
countries.
Alcohol-related
diseases,
especially
alcoholism,
are
result
cumulative
responses
exposure,
genetic
make-up
individual,
environmental
perturbations
over
time.
This
complex
gene
×
environment
interaction,
which
has
be
seen
a
life-span
perspective,
leads
large
heterogeneity
among
alcohol-dependent
patients,
terms
both
symptom
dimensions
severity
this
disorder.
Therefore,
reductionistic
approach
not
very
practical
if
better
understanding
pathological
processes
leading
addictive
behavior
achieved.
Instead,
systems-oriented
perspective
interactions
dynamics
all
endogenous
factors
involved
centrally
integrated,
will
lead
further
progress
research.
review
adheres
systems
biology
such
that
interaction
secondary
targets
within
brain
described
relation
behavioral
consequences.
As
targets,
alterations
expression
synaptic
plasticity
take
place
long-lasting
alteration
neuronal
network
activity.
subsequent
consequence,
alcohol-seeking
ensue
can
finally
via
behavior.
British Journal of Pharmacology,
Journal Year:
2008,
Volume and Issue:
154(2), P. 299 - 315
Published: March 3, 2008
Despite
the
generally
held
view
that
alcohol
is
an
unspecific
pharmacological
agent,
recent
molecular
pharmacology
studies
demonstrated
has
only
a
few
known
primary
targets.
These
are
NMDA,
GABA(A),
glycine,
5-hydroxytryptamine
3
(serotonin)
and
nicotinic
ACh
receptors
as
well
L-type
Ca(2+)
channels
G-protein-activated
inwardly
rectifying
K(+)
channels.
Following
this
first
hit
of
on
specific
targets
in
brain,
second
wave
indirect
effects
variety
neurotransmitter/neuropeptide
systems
initiated
leads
subsequently
to
typical
acute
behavioural
alcohol,
ranging
from
disinhibition
sedation
even
hypnosis,
with
increasing
concentrations
alcohol.
Besides
these
pharmacodynamic
aspects
we
discuss
neurochemical
substrates
involved
initiation
maintenance
phase
drinking
behaviour.
Finally,
addictive
behaviour
towards
measured
by
alcohol-seeking
relapse
reviewed
context
their
signalling
pathways.
The
activity
mesolimbic
dopaminergic
system
plays
crucial
role
during
consumption.
long-term,
chronic
consumption
virtually
all
brain
neurotransmission
seems
be
affected,
making
it
difficult
define
which
contributes
most
transition
controlled
compulsive
use.
However,
characterized
decrease
function
reward
neurocircuitry
recruitment
antireward/stress
mechanisms
comes
into
place,
hypertrophic
corticotropin-releasing
factor
hyperfunctional
glutamatergic
being
important
ones.
Disease Models & Mechanisms,
Journal Year:
2016,
Volume and Issue:
9(10), P. 1079 - 1087
Published: Oct. 1, 2016
ABSTRACT
Rodents
(especially
Mus
musculus
and
Rattus
norvegicus)
have
been
the
most
widely
used
models
in
biomedical
research
for
many
years.
A
notable
shift
has
taken
place
over
last
two
decades,
with
mice
taking
a
more
prominent
role
science
compared
to
rats.
This
was
primarily
instigated
by
availability
of
much
larger
genetic
toolbox
mice,
particularly
embryonic-stem-cell-based
targeting
technology
gene
disruption.
With
recent
emergence
tools
altering
rat
genome,
notably
genome-editing
technologies,
technological
gap
between
organisms
is
closing,
it
becoming
important
consider
physiological,
anatomical,
biochemical
pharmacological
differences
rats
when
choosing
right
model
system
specific
biological
question.
The
aim
this
short
review
accompanying
poster
highlight
some
differences,
discuss
their
impact
on
studies
human
diseases,
special
focus
neuropsychiatric
disorders.
Pharmacological Reviews,
Journal Year:
2016,
Volume and Issue:
68(3), P. 816 - 871
Published: June 30, 2016
The
nucleus
accumbens
is
a
major
input
structure
of
the
basal
ganglia
and
integrates
information
from
cortical
limbic
structures
to
mediate
goal-directed
behaviors.
Chronic
exposure
several
classes
drugs
abuse
disrupts
plasticity
in
this
region,
allowing
drug-associated
cues
engender
pathologic
motivation
for
drug
seeking.
A
number
alterations
glutamatergic
transmission
occur
within
after
withdrawal
chronic
exposure.
These
drug-induced
neuroadaptations
serve
as
molecular
basis
relapse
vulnerability.
In
review,
we
focus
on
role
that
glutamate
signal
transduction
plays
addiction-related
First,
explore
accumbens,
including
cell
types
neuronal
populations
present
well
afferent
efferent
connections.
Next
discuss
rodent
models
addiction
assess
viability
these
testing
candidate
pharmacotherapies
prevention
relapse.
Then
provide
review
literature
describing
how
synaptic
altered
also
pharmacological
manipulation
systems
can
inhibit
seeking
laboratory
setting.
Finally,
examine
results
clinical
trials
which
designed
manipulate
have
been
effective
treating
human
patients.
Further
elucidation
alter
will
be
necessary
development
new
therapeutics
treatment
across
all
addictive
substances.