Marijuana-based drugs: innovative therapeutics or designer drugs of abuse?

Mol Interv. 2011 Feb;11(1):36-51. doi: 10.1124/mi.11.1.6.

Abstract

The principal psychoactive component of marijuana, Δ(9)-tetrahydrocannabinol (THC), activates CB1 cannabinoid receptors (CB1Rs). Unfortunately, pharmacological research into the design of effective THC analogs has been hampered by psychiatric side effects. THC-based drug design of a less academic nature, however, has led to the marketing of "synthetic marijuana," labeled as K2 or "Spice," among other terms, which elicits psychotropic actions via CB1R activation. Because of structural dissimilarity to THC, the active ingredients of K2/Spice preparations are widely unregulated. The K2/Spice "phenomenon" provides a context for considering whether marijuana-based drugs will truly provide innovative therapeutics or merely perpetuate drug abuse.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Animals
  • Cannabinoids / adverse effects*
  • Cannabinoids / chemistry
  • Cannabinoids / pharmacology
  • Cannabinoids / therapeutic use*
  • Cannabis / adverse effects*
  • Cannabis / chemistry*
  • Clinical Trials as Topic
  • Designer Drugs / adverse effects
  • Designer Drugs / chemistry
  • Designer Drugs / pharmacology
  • Designer Drugs / therapeutic use*
  • Humans
  • Illicit Drugs / adverse effects
  • Illicit Drugs / chemistry
  • Illicit Drugs / pharmacology*
  • Models, Biological

Substances

  • Cannabinoids
  • Designer Drugs
  • Illicit Drugs