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The analgesia-addiction interface: Clinical and neurobiological issues

This article discusses the clinical and neurobiological aspects of the analgesia-addiction interface, focusing on the use of opioids and other drugs commonly used for chronic pain. It explores the challenges faced by clinicians in managing pain while minimizing the risk of opioid abuse and addiction. The article also highlights the need for improved pain therapeutics and non-pharmaceutical approaches to pain management.

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The analgesia-addiction interface: Clinical and neurobiological issues

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  1. The analgesia-addiction interface:Clinical and neurobiological issues Howard L. Fields MD PhD NIH March 2007

  2. Drugs Commonly Used for Chronic Pain • Opioids • COX inhibitors • 5HT/NE reuptake inhibitors (TCAs, SNRIs: Venlafaxine, Duloxetine, Tramadol)) • Triptans (5HT1b/d agonists)* • Anticonvulsants (pregabalin, gabapentin, topiramate, etc.)* * ? Broad spectrum analgesics

  3. Many patients have residual pain when non-opioid options are exhausted.Opioids are currently the most potent, and broadest spectrum analgesics.

  4. On the other hand • Opioid efficacy past three months unproven • Side effects (sedation, nausea, constipation, urinary retention) • Tolerance and dependence (hyperalgesia) • Abuse potential

  5. Substance abuse: the scope 2005, SAMSA website ca. 30 million heavy drinkers, 120 million smokers Most individuals are polysubstance users

  6. Question for the clinician: Why is my patient continuing to take opioids? • Effective analgesia • Relieve symptoms of physical dependence • Patient has become addicted • Substance abuse antedated treatment • Patient never had pain

  7. Prescription opioids:two user groups Prescription opioid abuse Pain treatment with opioids Millions of people in both groups

  8. The clinical conundrum • Patient reports inadequate pain relief • Risk of creating drug abuse. • Patient with history of drug abuse • Legitimate pain complaint? • Deception to obtain drugs?

  9. ? The Doctor’s Dilemma:Does pain treatment cause opioid abuse? Prescription opioid abuse Pain treatment with opioids

  10. New abuse rates relatively low when opioids used to treat CNCP • Mark Sullivan—SE area Vets; Edlund et al, Pain in press. 2% ( ca. 300/15000) overall incidence (25% non-opioid Sub Abuse, 67% Mental health Dx)

  11. Prescription drug abuse Some substance abusers become opioid abusers when treated with opioids Drug Abuser +/- pain Treated with opioid analgesics

  12. Know your patient “Doc, only Dilaudid works for me.” “Doctor, John doesn’t like to take drugs”

  13. Patient evaluation and monitoring • Screening instruments (Kirsch, Managed Care 16, Supplement 3, February, 2007) • Urine toxicology • Steve Passik: Aberrant drug taking behaviors—record keeping

  14. The Future • Genetic screens • Endophenotyping, functional imaging

  15. How can we improve pain therapeutics? • Better non-opioid analgesics • Non-pharmaceutical approaches (CBT, etc.) • Opioids with reduced tolerance and dependence (DOR antagonists, adjuvants) • Potent, non-rewarding analgesics

  16. Properties of an Ideal Analgesic The holy grail of pain research • Completely safe & totally effective • Works on all pains • Tolerance does not develop • Non-addicting

  17. What about opioids; can we separate analgesia and reward?

  18. The same receptor mediates both MOP KO Opioid family of 7TMD GPCRs Kieffer TIPS, 1999

  19. Opioid analgesia circuit Leu-enk Tyr-gly-gly-phe-met Tyr-gly-gly-phe-leu Hughes & Kosterlitz, 1975 Basbaum & Fields, 1976

  20. Mesolimbic reward circuit NAc VTA Olds & Milner, 1954 McGill / Hebb lab

  21. Rats self administer drugs directly into the reward circuitry Nucleus Accumbens Cocaine amphetamine Opiates, ETOH, nicotine Dopamine neurons

  22. Reward circuit produces analgesia NAc stimulants VTA Analgesia and drug reward Blocked by NAc DA antagonists opioid Franklin, Neurosci Biobehav. Rev, 1989 Altier & Stewart, JPET, 1998 Schmidt et al, Eur J Neurosci 2002

  23. Psychostimulants potentiate opioid reward NAc AMPH Blocked by Dopamine antagonists in NAc VTA opioid

  24. We need to know how the reward circuitry produces analgesia • If we can uncouple these processes, we may have better analgesics.

  25. Human NAc activity correlates with magnitude of monetary reward Knutson et al, J. Neurosci 2001

  26. Noxious stimuli and pain predictive cues activate human ventral striatum Noxious thermal Stimulus Pain predictive cue Jensen et al, Neuron, 2003 Becerra et al, Neuron, 2001

  27. Expectation of pain relief leads to opioid release in NAc Zubieta et al, J. Neurosci, 2005

  28. Electrodes Hip PF Amyg VTA NA c NAc neurons encode reward value Sharif Taha

  29. How is reward circuit linked to pain modulating pathway? hypothalamus amygdala What are the relevant non-opioid Neurotransmitters? Becerra et al, Neuron, 2001

  30. Summary • Opioids are essential for treating moderate to severe pain • Neurobiologists are making progress in reducing opioid tolerance and dependence • Opioids are rewarding; this has created a growing non-medical demand for prescription opioids • Opioid addiction is a disease • Understanding how opioids produce reward and analgesia will lead to better analgesics and treatments for addiction.

  31. Thanks • NIDA, NINDS and the NIH pain consortium, • The AMA • Allan Basbaum, Jon Levine, Mary Heinricher, Mike Morgan, ZZ Pan, Sharif Taha • State of California Alcoholism and Addiction Research Program, Gallo Research Center, Wheeler Center, University of California

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