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Cannabis and the brain

Leslie Iversen
DOI: http://dx.doi.org/10.1093/brain/awg143 1252-1270 First published online: 8 April 2003

Summary

The active compound in herbal cannabis, Δ9‐tetrahydrocannabinol, exerts all of its known central effects through the CB1 cannabinoid receptor. Research on cannabinoid mechanisms has been facilitated by the availability of selective antagonists acting at CB1 receptors and the generation of CB1 receptor knockout mice. Particularly important classes of neurons that express high levels of CB1 receptors are GABAergic interneurons in hippocampus, amygdala and cerebral cortex, which also contain the neuropeptides cholecystokinin. Activation of CB1 receptors leads to inhibition of the release of amino acid and monoamine neurotransmitters. The lipid derivatives anandamide and 2‐arachidonylglycerol act as endogenous ligands for CB1 receptors (endocannabinoids). They may act as retrograde synaptic mediators of the phenomena of depolarization‐induced suppression of inhibition or excitation in hippocampus and cerebellum. Central effects of cannabinoids include disruption of psychomotor behaviour, short‐term memory impairment, intoxication, stimulation of appetite, antinociceptive actions (particularly against pain of neuropathic origin) and anti‐emetic effects. Although there are signs of mild cognitive impairment in chronic cannabis users there is little evidence that such impairments are irreversible, or that they are accompanied by drug‐induced neuropathology. A proportion of regular users of cannabis develop tolerance and dependence on the drug. Some studies have linked chronic use of cannabis with an increased risk of psychiatric illness, but there is little evidence for any causal link. The potential medical applications of cannabis in the treatment of painful muscle spasms and other symptoms of multiple sclerosis are currently being tested in clinical trials. Medicines based on drugs that enhance the function of endocannabinoids may offer novel therapeutic approaches in the future.

  • Keywords: cannabinoid CB1 receptor; Δ9‐tetrahydrocannabinol; rimonabant (SR141716A); anandamide; 2‐arachidonylglycerol
  • Abbreviations: 2‐AG = 2‐arachidonylglycerol; DSI = depolarization‐induced suppression of inhibition; FAAH = fatty acid amide hydrolase; Gi/o = G‐proteins negatively linked to adenylate cyclase or to inositol phosphates; LTD = long‐term depression; LTP = long‐term potentiation; mGlu = metabotropic glutamate; NMDA = N‐methyl‐d‐aspartate; THC = Δ9‐tetrahydrocannabinol
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