Pain, pleasure and placebo: the cannabinoids in reward processing and the perception of pain
Maximillian Hugo Brodermann
Mental Health and Addiction Research 2016 DOI: 10.15761/mhar.1000115 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Review Peer reviewed |
|---|---|
| Citations | 3 |
| Key findings | Argues that cannabinoids influence pain, hedonic reward processing, and the placebo effect via cannabinoid type 1 receptors, but that pharmacological targeting of the endocannabinoid system has yielded few licensed drugs with limited applications, partly because endogenous cannabinoid biology remains poorly understood. Proposes that the endocannabinoid system be studied alongside opioid and dopaminergic circuitry, and that the most promising pharmacological opportunities may lie in adjuncts to pre-existing drugs. |
Abstract
Chronic pain poses a complex, widespread problem that remains inadequately resolved by pain medication.Similarly, depression and addiction exist along a spectrum of reward related mood disorders that pose an ever-increasing burden on healthcare services.There is a need for a greater range of drugs to tackle these diverse health conditions and cannabinoid biology offers a unifying line of research that could invigorate the approach to treatment.Cannabinoids are known contributors to the physiological basis and emotional perception of pain, pleasure, and the placebo effect via activation of cannabinoid type 1 receptors widely expressed throughout the central nervous system.Endogenous cannabinoids -arachidonic acid derivatives synthesised on demand -are the primary contributors, but the system is also susceptible to synthetic cannabinoids and plant-derived phytocannabinoids.Targeting the endocannabinoid system pharmacologically has yielded few licenced drugs and with limited applications.The failure to provide a greater range of drugs stems partly from the limited understanding of endogenous cannabinoid biology.This review will critically evaluate current evidence of how cannabinoids influence pain, hedonic reward processing, and the placebo effect.Crucially, the endocannabinoid system must not be considered in isolation, but in the context of opioid and dopaminergic neural circuitry.As such, the most exciting pharmacological opportunities could lie as adjuncts to pre-existing drugs.
Citations in the library
Cites 2
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- Functional tolerance and blockade of long-term depression at synapses in the nucleus accumbens after chronic cannabinoid exposure. Journal of Neuroscience June 15, 2003