Addiction is a Chronic Relapsing Disease of the Brain
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Transcript Addiction is a Chronic Relapsing Disease of the Brain
Addiction is a Brain Disease
Michael L. Johnson, MS
Nancy A. Roget, MS
Brain Disease
Drug addiction is a brain disease
Every type of psychoactive drug
has its own individual mechanism
for changing how the brain
functions
Drug use changes the individual's
brain and its functioning in critical
ways
Leshner, 2001
Addiction is a Brain Disease
Addiction is a Brain Disease
BECAUSE:
Using drugs over time changes brain
structure and function
Some brain changes may persist
after use stops
Long-lasting brain changes effect
cognitive functioning
emotional functioning
Addiction is a Brain Disease
Addiction is a brain disease
addicted brain is different from the nonaddicted brain
Prolonged drug use causes pervasive changes
in brain function
Essence of Addiction
Compulsive craving that
overwhelms all other
motivations (drug use despite
negative and social
consequences)
root cause of health and social
problems
Paradox of Addiction
Initially Voluntary
Addiction’s Similarities with
Other Brain Diseases
Some brain diseases are NOT
simply biological in nature and
expression
Most have social/behavioral aspects
Examples:
Alzheimer's
Schizophrenia
Clinical Depression
The Adult Brain,
and how it works
An Adult
brain
weighs
about 3
pounds and
has billions
of cells
Neurons
Glial cells
The Brain
Organ on thinking, behavior,
homeostasis
Different Areas of the brain regulate
different functions
Complex tasks are split up into
specialized areas
Damage to these areas leads to specific
deficits
“Division of labor” allows for Parallel
Processing
Brain Region & Function
Splits larger tasks into smaller
ones
Component tasks are further
broken into sub component
tasks
Driving
Seeing
Hearing
Moving
Understanding
How
the
Brain
Works
Understanding
How
the
Brain
Works
Function of Brain Regions
Brainstem= basic function
Heart rate, breathing, digestion, sleep
Cerebellum =skilled repetitive
movements, balance
Limbic System=emotions &
motivations
Diencephalon=sensory perception
Function of Brain Regions
Cerebral Cortex = thinking,
perceiving, producing language
Vision, hearing, touch, movement,
smell, thinking & reasoning
Frontal Lobe = social behavior Limbic
System
Uses memories, information about how
the body is working and sensory input
Function and Brain Regions
Phineas Gage
1848 Railroad
worker
Explosion- tamping
rod
Rod entered brain
Temperament
changes
20 years post
accident
Correlated accident
to behavioral
changes
Frontal lobe = social
behavior
Neurons, Brain Chemistry &
Neurotransmission
The
Neuron
Basic signaling unit of
brain
Precise connections allow
for different actions
Neurons
Sensory receptors
Muscles
The
Neuron
Cell
Body
–Nucleus
–Metabolic center
Dendrites
–Input from other
neurons
Axon
–Carry high speed
messages away
from neuron
–Branches into
presynaptic
terminals
The Synapse
The Synapse
N
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R
O
T
R
A
N
S
M
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T
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S
The
End of axon
Typical neuron has 1000 synapses with other
neurons
Intercellular space between neurons
Synaptic cleft
S
y
n
a
p
s
e
Synapses are Dynamic
Neurons can strengthen synaptic
connections
New synapses form (protein
synthesis)
Synapses can be lost
Responses to life experiences
(and aging)
Cellular basis of learning
Synaptic Transmission
Neurons communicate via
electrical and chemical signals
Electrical signal converted to a
chemical signal– a
neurotransmitter
Electrical signal within a
neuron is an action potential
Wave-like flow of ions (electrical
impulse) down axon
Transient depolarization of axon
Synaptic Transmission
At the axon
terminal, the
electrical impulse
leads to release of a
neurotransmitter
Stored in vesicles
which fuse with the
neuronal membrane
and release their
contents into the
cleft
Synaptic Transmission
Neurotransmitters
diffuse into
intercellular space
Bind to receptors on
dendrite of another
cell
Postsynaptic cell
Receptors are
specific
Dopamine receptors
will only bind
dopamine
Synaptic Transmission
Chemical binding
of transmitter
with receptor
leads to changes
in the postsynaptic cell
May generate an
action potential
Post-synaptic cell
may use a
different
neurotransmitter
to communicate
“down stream”
Neurotransmission
Synaptic Transmission
After binding,
neurotransmitters
releases from receptor
and goes back into the
cleft
Removed by enzymes
or reuptake pump/
transporter back into
terminal
quick removal of
transmitters allow for
precise communication
between neurons
Types of Neurotransmitters
A neuron receives many many
messages from connecting neurons
Neuron’s response is the “sum”
Excitatory Transmitters
Lead to (generation of A’s and) stimulate
firing of post-synaptic neuron
Inhibitory Transmitters
Lead to decreased firing in post-synaptic
neuron
Routes of Administration
Inhale
Insuflate
Ingest
Inject
Enema
Contact Absorption (patch)
Drug Ingestion
ORAL
20 to 30 minutes
INHALING
7 to 10 Seconds
INJECTING
3 to 5 minutes- skin popping
15 to 30 seconds- IV
SNORTING
3 to 5 minutes
CONTACT
Limbic System
Reward
System
Nucleus
accumbens
Prefrontal
cortex
Ventral
tegmental
area
Limbic System
Link between higher cortical activity
and the “lower” systems that control
emotional behavior
Limbic Lobe
Deep lying structures
amygdala
hippocampus
mamillary bodies
Limbic System
Specialized brain areas for
producing and regulating
PLEASURE
Ventral Tegmental Area
Nucleus Accumbens
Prefrontal Cortex
Areas of Limbic system– amygdala,
hippocampus, hypothalamus
Limbic System
Generates primitive emotional
responses to situations
Allows for SURVIVAL
Identify danger/ threats
Fear and aggression
Identify pleasure– “natural
rewards”
Eating
Sex
Social Interaction
R
e
w
a
r
d
P
a
t
h
VTA and NA
Primitive brain stem and limbic areas
Activated by drugs of abuse
Activation of these primitive areas can
OVERRIDE more evolved cortical areas
Reward Pathway
Also the site of action for addictions
Drugs activate the pathway with force
and persistence not seen with natural
rewards
Drug Effects On
Neurotransmission
Alcohol, heroin, nicotine excite the
dopamine neurons in the VTA to
increase dopamine release
Drug Effects on Cell
Increased cAMP levels
Activation of transcription factor CREB
and changes in gene expression
Changes in synapses, cell structure and
function
The resulting intracellular changes appear
to be the molecular and cellular basis of
addiction (persistent behavioral
abnormalities)
Nestler Am J Addiction 2001; 201-217
Drug Effects on Cell and Learning
Intracellular changes for
addiction the same as for
learning
Both activities share
intracellular signaling cascades
(cAMP) and depend on activity
of CREB
Drug Effects on Cell and Learning
Learning and addiction show
similar changes in neuron
morphology
Similar changes at the level of the
synapse
Multiple similar changes in the
neuron
Long term changes
Addiction is long term
Nestler 2001 Science 292 (5525) pp 2266-67
Drug Effects
on the Cell
Drugs of abuse all directly or indirectly
increase dopamine binding to post synaptic
receptor with acute behavioral effects
Chronically, this increases cAMP levels and
leads to a cascade of changed cell activity
Other Chronic Drug Effects
Cell Death
Neurons
don’t grow
back
Alcohol,
ecstasy,
meth
Effect
memory,
mood,
learning
Chronic Drug Effects
Persistent Effects of Drug Use
Amygdala
not lit up
Amygdala
activated
Front of Brain
Back of Brain
Nature Video
Cocaine Video
Brain Imaging
PET
Brain Functioning
Radiolabeled glucose for levels of
activity
Effects of Drugs
Distribution in body
Measure local concentration at binding
sites
Spatial Resolution of 4 mm
Positron Emission Tomography (PET)
NIDA Research
Overall goal of NIDA
research to:
Reverse the brain changes
that underlie addiction
Roll back the loss of
cognitive and motor
functions that occur
Develop interventions to
stop brain damage, repair
damage, and retrain the
brain
Restore brain function after
it has been changed by drug
use
PET Scan
Brighter red
indicates
higher levels
of activity
(glucose
utilization)
Your Brain on Drugs
1-2 Min
3-4
6-7
7-8
9-10
10-20
5-6
8-9
20-30
Your Brain After Drugs
Drugs Have
Long-term
Consequences
Stimulant Studies
London et al. (2004)
PET images of brain activity
Patients in acute
methamphetamine withdrawal (4 to
7 days)
Patients
10 year history
4 grams per week
18 days of use out of 30
Stimulant Studies
London et al. (2004)
levels of depression and anxiety
measured
PET Scans
Patient Report
brain- glucose metabolismdepressed mood, sadness, anxiety,
and drug craving
Beck’s Depression Inventory
ratings averaged 9.5 for
methamphetamine patients and 1.1
for control
Examples of Brain Studies
Treatment Application
London et al. (2004)
Treatment of Methamphetamine Users
Mood disorder symptoms
may create an acute
barrier to treatment for
methamphetamine
abusers
Stimulant Studies
Treatment Applications from
London’s Stimulant Studies
Implications for treatment
Expect clients to feel poorly
Treatment engagement strategies should focus
on helping patients to deal with negative
emotional states (Depression and Anxiety)
Avoid counseling techniques that are
confrontational
Relapse potential is high because clients feel
poorly
Be aware of clients’ turning to self medication
activities to relieve the negative feeling states
Cues for Cocaine and Normal
Pleasures Activate Brain Sites
Childress, 1999
Cues for Cocaine
Cocaine abusers may experience a
powerful urge to use when they
encounter environmental cues
associated with use
Limbic regions of the brain are
activated when watching cocainerelated videos
Childress, 1999
Persistent Effects of Drug
As a result of intracellular changes, the
previously cocaine addicted brain has
persistently altered functioning
(craving)
Environmental Cues
Treatment Applications for Childress’
Cue-Induced Cocaine Craving Study
Implications for Treatment
Understand the importance
environmental cues play in initiating the
craving process
Review program educational materials to
ensure that potential environmental cues
for drug use are eliminated
Normalize cue and craving responses for
clients
Teach clients how to “urge surf” and to
identify potential environmental cues
Recovery of Dopamine
Transporters
Pet scan
shows levels of dopamine transporters
Lower levels of dopamine transporters were
associated with poorer performance on tests of
memory and motor skills
Impairments in motor skills and memory continued
Volkow, et al. 2001
Poor Motor & Memory Performance
33 year old male- 80 days post detox
Low Severity- Parkinson Disease
transporter losses may not recover
Volkow, et al. 2001
Simon, et al. 2002
Cognitive Effects of Stimulants
Studied 40 current Methamphetamine
Users
Impairments
memory
abstract thinking
changing points of view
ability to manipulate information
comprehension deficits
Word recall
Simon, et al. 2002
Cognitive Effects of Stimulants
Help clients who are mandated into
treatment deal with cognitive problems
associated comprehension
Ensure that clients understand
what counts as compliance with treatment
services
counselor recommendations
consequences for failure to comply
Give concrete, specific information
Develop methods to help clients
remember treatment recommendations or
medications
Treatment Applications for
Simon, et al.’s study
Treatment Implications:
Drugs’ impact on brain chemistry may
have permanent or long term effects
(impairment 2 years)
Extend length of treatment
Inform/educate client
Structure accessible services
Avoid changing service delivery times
Simplify client paperwork