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The Neuroscience of Drug Addiction and Therapy
V.Niklesh Rao
Under the guidance of K.Raj Kiran sir
Profile link: http://www.pharmainfo.net/nik
► Introduction► Key Definitions► Reward pathway responsible for
Addictive Changes► Stages of the Addiction Cycle► Neurochemical Changes Associated
with the Drug Use, Dependence and Relapse
► Therapy► Conclusion
Contents
Introduction• Alcohol
– 18 million Americans abuse or are dependent on Alcohol. • Smoking --In US, approximately 440,000 persons die per year of a cigarette smoking & attributable illness
• Opioid Dependency– Dependency has been growing rapidly:
• From 1990 to 2001, the number of people who used prescription painkillers recreationally for the first time grew by 335% to include almost 2.5 million people.
Estimated Prevalence Among 15-54 Year Olds ofNonmedical Use and Dependence Among Users
(1990-1992) (NCS)
Ever UsedPrevalence of Dependence
Dependence Among Users
Tobacco
Alcohol
Illicit Drugs
Cannabis
Cocaine
Drugs
75.6
91.5
51.0
46.3
16.2
24.1
14.1
7.5
4.2
2.7
31.9
15.4
14.7
9.1
16.7
Key Definitions
Drug Addiction — Chronically relapsing disorder that is characterized by a compulsion to seek and take drug, loss of control in limiting intake, and emergence of a negative emotional state (e.g. dysphoria, anxiety, irritability) when access to the drug is prevented (here, defined as the “dark side” of addiction)
Nucleus Accumbens and Extended Amygdala — Forebrain structures involved in the rewarding effects of drugs of abuse. Composed of central nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition zone in the medial part of the nucleus accumbens
Reward pathway responsible for Addictive Changes
Reward pathway responsible for Addictive Changes
Neurochemical Circuitry in Drug Reward
Converging Acute Actions of Drugs of Abuse on the Ventral Tegmental Area and Nucleus Accumbens
Summary- Neurocircuitry of Addiction
• Reward Circuit- nucleus accumbens and extended amygdala (bed nucleus of the stria terminalis and central nucleus of the amygdala)
• “Craving” Circuit- dorsal prefrontal cortex, basolateral amygdala
• “Compulsivity” Circuit- ventral striatum, ventral pallidum,medial thalamic- orbitofrontal cortical loop
Stages of the Addiction Cycle
Stages of the Addiction Cycle
Neurobiological Substrates for the Acute Reinforcing Effects of Drugs of Abuse
Neurotransmitter
Dopamine
Opioid Peptides
GABA
Glutamate
Site
Ventral tegmental area, nucleus accumbens
Nucleus accumbens, amygdala, ventral tegmental area
Amygdala, bed nucleus of stria terminalis
Nucleus accumbens
Neurochemical Changes Associated with the Drug Use, Dependence and Relapse
Neurotransmitters Implicated in the Motivational Effects of Withdrawal from Drug of Abuse
Dopamine … “dysphoria”
Serotonin … “dysphoria”
GABA … anxiety, panic attacks
NPY … anti-stress
Dynorphin … “dysphoria”
CRF … stress
Norepinephrine … stress
Glutamate….hyperexcitability
Common Molecular Changes Associated with Dependence
• Dopamine D-2 receptor binding- decreased in human imaging studies in dependent subjects• CREB ( cyclic adenosine monophosphate response element binding protein) transcription factor-
decreased in nucleus accumbens and extended amygdala during the development of dependence
Reward Transmitters Implicated in the Positive Motivational Effects of Drugs of Abuse
Dopamine
Opioid peptides
GABA
Glutamate
Positive Hedonic Effects
Chronic Use: Hedonic Homeostatic Dysregulation
Hed
onic
Sca
le Normal Affective Responseto Drugs/Alcohol
Altered Dysregulated Set-Pointfollowing chronic drug use
Hedonic Set Point is Altered with Chronic Drug Use
Initially use toget high…
Now use to “get normal”
“Cravings”
“Feel good”
“Feel bad”
Animal Models for the Different Stages of the Addiction Cycle
• Animal Models for the Binge/Intoxication Stage1. Oral or intravenous drug self-administration2. Brain stimulation reward3. Place preference
• Animal models for the Withdrawal/Negative Affect Stage1. Brain stimulation reward2. Place aversion
• Animal Models for the Transition to Addiction1. Dependence-induced drug taking2. Escalation in drug self-administration with prolonged access 3. Drug taking despite aversive consequences
• Animal Models for the Preoccupation/Anticipation (“Craving”) Stage1. Drug- induced reinstatement2. Cue- induced reinstatement3. Alcohol Deprivation Effect4. Stress- induced reinstatement
Mood Changes Associated with Plasma Levels of Cocaine during Coca Paste Smoking
Cocaine Self-Administration
Extracellular DA and 5-HT in the Nucleus Accumbens During Cocaine Self-Administration
and Withdrawal
CNS Actions of Corticotropin Releasing Factor (CRF)
Ethanol Dependence Induction
Extracellular CRF Levels in the CentralAmygdala During Ethanol Withdrawal
Effect of CRF Antagonist D-Phe-CRF12-41
– Central Nucleus of the Amygdala –
Craving-Type 1
• “Craving”- induced by stimuli that have been paired with ethanol self-administration such as environmental cues
• Termed conditioned positive reinforcement in experimental psychology
• An animal model of craving- type 1 is cue induced reinstatement where a cue previously paired with access to ethanol reinstates responding for a lever that has been extinguished.
Reinstatement
Neurobiological Effects of Exposure to Drug-Associated Contextual Stimuli
SA EXT S- S+Daily Sessions of Self-Administration
Common Molecular Changes Associated with Dependence
• Dopamine D-2 receptor binding- decreased in human imaging studies in dependent subjects
• CREB ( cyclic adenosine monophosphate response element binding protein) transcription factor- decreased in nucleus accumbens and extended amygdala during the development of dependence
• Delta-FosB transcription factor-changed during protracted abstinence to drugs of abuse
Key Common Neurocircuitry Elements in Drug Seeking Behavior of Addiction
Craving-Type 1• “Craving”- induced by stimuli that have been paired with ethanol self-administration such as
environmental cues• Termed conditioned positive reinforcement in experimental psychology
Craving-Type 2• State of protracted abstinence in alcoholics weeks after acute withdrawal• Conceptualized as a state change characterized by anxiety and dysphoria or a residual negative
affective state that combines with Craving-Type 1 situations to produce relapse to excessive drinking
Therapy• No single treatment is appropriate for all individualsNo single treatment is appropriate for all individuals• Effective treatment attends to multiple needs of the individual, not just his/her drug useEffective treatment attends to multiple needs of the individual, not just his/her drug use• Treatment must address medical, psychological, social, vocational, and legal problemsTreatment must address medical, psychological, social, vocational, and legal problems
Duration of TreatmentDuration of Treatment
• Depends on patient problems/needsDepends on patient problems/needs• Less than 90 days is of limited/no effectiveness for residential/outpatient settingLess than 90 days is of limited/no effectiveness for residential/outpatient setting• A minimum of 12 months is required for methadone maintenanceA minimum of 12 months is required for methadone maintenance• Longer treatment is often indicatedLonger treatment is often indicated
Medical DetoxificationMedical Detoxification
• Detoxification safely manages the physical symptoms of withdrawaDetoxification safely manages the physical symptoms of withdrawa• lOnly first stage of addiction treatmentlOnly first stage of addiction treatment• Alone, does little to change long-term drug useAlone, does little to change long-term drug use
Medications for Alcohol Dependence
• Disulfiram (Antabuse)- FDA approved 1954
• Naltrexone (ReVia)- FDA approved 1994
• Acamprosate- FDA approved 2004
Therapy
Counseling and Other Behavioral TherapiesCounseling and Other Behavioral Therapies
DrugResistanceSkills
Replace Drug UsingActivities
Motivation
Problem Solving Skills
Interpersonal Relationships
Conclusion• Drug abuse is an issue of global concern especially among the youth and adolescent population.Drug abuse is an issue of global concern especially among the youth and adolescent population.• Drug addiction is the major cause of behavioral disturbances and major cause of criminal Drug addiction is the major cause of behavioral disturbances and major cause of criminal
activity.activity.• The main objective of study of neuroscience of drug addiction is to effectively develop therapy The main objective of study of neuroscience of drug addiction is to effectively develop therapy
for the individuals to rid of their drug seeking behavior and to stabilize their behavior.for the individuals to rid of their drug seeking behavior and to stabilize their behavior.• Based on the studies, newer, more effective pharmacotherapeutic strategies may be developed.Based on the studies, newer, more effective pharmacotherapeutic strategies may be developed.
References • www.nida.nih.gov• www.drugabuse.gov• National Institute on Alcohol Abuse and Alcoholism• National Institute on Drug Abuse• California Society of Addiction Medicine• RANG & DALE'S PHARMACOLOGY • Basic and Clinical Pharmacology by Bertram G. Katzung• Goodman & Gilmann’s Pharmacological Basis of Therapeutics
Acknowledgement I am grateful to our college principal Dr.Y.Srinivasa Rao sir for providing an
opportunity to present this seminar and also all the staff members who have extended their help and valuable suggestions and have provided all the help they could, I would especially like to thank my guide K.Raj Kiran sir for thoroughly supporting me to prepare and present my presentation.
I would like to express my gratitude to pharmainfo.net for giving me an opportunity to present the powerpoint presentation on the chosen topic.
Thank You