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Drug Tolerance. A shift in the dose-response curve to the right Cross Tolerance Exposure to one drug can produce tolerance to other similar acting drugs Metabolic Tolerance Reduction in amount of drug which reaches site of action Functional Tolerance
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Drug Tolerance • A shift in the dose-response curve to the right • Cross Tolerance Exposure to one drug can produce tolerance to other similar acting drugs • Metabolic Tolerance Reduction in amount of drug which reaches site of action • Functional Tolerance Reduction in the reactivity of sites of drug action
Withdrawal Syndrome • Sudden drug elimination • Effects are opposite to initial drug effects • Presence indicates physical dependence • Relationship between drug tolerance and drug withdrawal effects
Withdrawal and Tolerance Long Term Drug Use Adaptive (compensatory) neural changes to counteract drug effects Tolerance Drug Withdrawal Unchecked adaptive neural changes opposite to drug effects = Withdrawal Symptoms
Conditioned (Learned) Tolerance Crowell, Hinson and Siegel, 1981 • AlcoholHypothermia • Tolerance to alcohol-induced hypothermia • Tolerance is learned
Crowell, Hinson and Siegel, 1981 • 2 groups of rats: - 20 injections of alcohol - 20 injections of saline (NaCl) • Drug Exposure: Group 1 Group 2 Distinctive Alcohol Saline Room (tolerance devel.) Colony Saline Alcohol Room (tolerance devel.)
Crowell, Hinson and Siegel, 1981Results • Test for tolerance of hypothermia - one injection of alcohol in both rooms Group 1 Group 2 Distinctive Tolerance No Tolerance Room (no hypotherm.) (hypotherm.) Colony No Tolerance Tolerance Room hypotherm.) (no hypotherm.)
Seigel’s Theory After REPEATED pairings of the ROOM with ALCOHOL, the animals learn that the ROOM CUES predict the occurrence of the ALCOHOL effects and the ROOM CUES come to elicit a conditioned (learned)response (hyperthermic) that is opposite to the ALCOHOL hypothermic effects. This is conditioned (learned) tolerance.
Pavlovian Conditioning • Conditioned Stimulus (CS): a NEUTRAL stimulus that predicts the occurrence of an Unconditioned Stimulus (US) - CS = ROOM CUES • Unconditioned Stimulus (US): - US = the primary effects of the drug stimulus (e.g., HYPOthermia) • Unconditioned Response (UR): - UR = the adaptive response to the drug, opposite to the drug effect (HYPERthermia) • Conditioned Response (CR): - CR = the response elicited by the CS after repeated pairings of the CS with the US (e.g., HYPERthermia)
Situational Specificity of Tolerance Implications for drug-related deaths
Heroin in a Familiar Environment Tolerance Develops Increased dosing to achieve effect Increased dose in NEW Environment No learned tolerance exists Lethal consequences
Siegel etal., 1982 • three groups of rats - Groups 1 and 2 made tolerant to heroin with repeated injections of increasing amounts - Group 3 (NAÏVE) received no heroin injections • Tested effects of a HIGH dose of heroin on death rate Group 1: high dose in familiar environment Group 2: high dose in a new environment Group 3: high dose in familiar environment
Siegel etal., 1982-continued Results Group 1 (Familiar environment) - 32% died Group 2 (New Environment) - 64% died Group 3 (Naïve, Familiar environment) - 96% died • An example of learned tolerance. Each incidence of drug administration is a Pavlovian conditioning trial. • May account for drug-related deaths attributed to overdose.
Biopsychological Theories of Addiction • Physical-Dependence Theory • Positive-Incentive Theory
Physical Dependence Theory • Drug addicts take drugs to alleviate withdrawal symptoms Problems: • Detoxified addicts return to drug-taking habits • Some highly addicting drugs (e.g., cocaine) have minimal withdrawal symptoms
Positive-Incentive Theory • The craving for the positive-incentive (i.e., pleasure-producing) properties of the drug is the primary factor in addiction. • The anticipated pleasure of drug-taking is the basis of addiction, not so much the pleasurable effects of the drug per se.
Major Questions • Is addiction to a drug due to its pleasurable or rewarding properties? • What is the brain mechanism(s) by which the drug exerts its pleasurable or rewarding effects
Intracranial Self-Stimulation(ICSS) • Olds and Milner (1954)* • Animals work at high rates to obtain ICSS • ICSS enhances the rewarding properties of food, water, sex • Animals prefer ICSS over food, water, sex • Areas of the brain that best support ICSS are those of the natural reward circuits
The Mesotelencephalic Dopamine System* • The substantia nigra - the nigrostriatal pathway • The ventral tegmental area (VTA) - mesocorticolimbic pathway
What is the evidence for dopamine involvement in ICSS? • Dopamine receptor antagonists and ICSS -Pimozide reduces ICSS* • Destruction of dopamine VTA neurons reduces ICSS*
Fibiger etal., 1987- The VTA, ICSS and Dopamine Right side Left side Forebrain Forebrain Dopamine axons Inject 6-OHDA into left VTA VTA VTA Bilateral stimulation electrodes
Where in the brain does the release of dopamine from VTA neurons contribute to rewarding ICSS? The Nucleus Accumbens (NA)*
The Nucleus Accumbens, Dopamine and ICSS • Spiroperidol = dopamine receptor antagonist • Inject Spiroperidol into markedly reduce nucleus accumbens VTA ICSS • ICSS increases dopamine release in nucleus accumbens* NA VTA Spiroperidol in NA blockes dopamine action on NA neurons DA release
Do Natural Rewards (e.g., food, sex) increase Dopamine Release in the Nucleus Accumbens?
The Nucleus Accumbens, Dopamine and Natural Rewards* Rat lever presses for food or engages in reproductive behavior increase in dopamine release in nucleus accumbens
Neural Mechanisms of Addiction: Behavioral Paradigms* • Drug Self-administration Paradigm • Conditioned place preference
Cocaine and Amphetamine What are the brain mechanisms by which they exert their addictive effects? • Cocaine Blocksdopamine reuptake transport system • Amphetamine Stimulates the release of dopamine Blocks dopamine reuptake
Cocaine, Amphetamine and the Nucleus Accumbens • I.V. Self administration of DA release cocaine or amphetamine in nucleus accumbens in rats* • Rats self-administer cocaine or amphetamine into the nucleus accumbens • DA receptor antagonists injected attenuate i.v. self- into nucleus accumbens of rats administration • 6-OHDA lesions of the nucleus attenuate i.v. self- accumbens of rats* administration
Do other addictive drugs affect the nucleus accumbens? • Nicotine? • Cannabis? • Opiates?
Nicotine • Rats self-administer nicotine i.v. • Systemic nicotine DA release in injections in rats* nucleus accumbens • Mechanism: ACh receptors NA VTA Nicotine stimulates ACh receptors DA release
Evidence for nicotine action on VTA neurons • Nicotine agonist into conditioned place rat VTA preference • Nicotine antagonist into reduces rewarding rat VTA effect of i.v. nicotine • Nicotine antagonist into blocks NA DA rat VTA* release from i.v. nicotine
CANNABISTETRAHYDROCANNABINOL(THC) • Inject rats with THC NA DA release systemically* • Inject THC into NA DA release • Mechanism: NA neuron NA VTA NA DA THC affects receptors on DA boutons
OPIATES • Heroin – - the sap of opium poppy seeds - active ingredients = morphine, codeine • Endogenous opiates - Endorphins enkephalins - brain opiate receptors
Opiates and the VTA-NA Circuit • I.V. self-administration 300% DA increase of heroin in rats in NA • Rats self administer heroin or enkephalin into VTA • Mechanism for VTA effect: Heroin, enkephalin inhibit GABA neuron GABA neuron GABA inhibits VTA Neurons G VTA NA