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Fungal biotransformation of cannabinoids: potential for new effective drugs.

Abstract
Phytocannabinoids from the plant Cannabis sativa induce a variety of physiological and pharmacological responses in living systems, including anti-inflammatory, antinociceptive, anti-ulcer and antitumor activities. The discovery of the cannabinoid receptors CB1 and CB2 led to the development of agonists and antagonists of these receptors for the treatment of a variety of diseases. Nabilone, a synthetic derivative of Delta9-tetrahydrocannabinol (Delta9-THC), which is the main natural psychotropic constituent of C sativa, was approved by the US FDA for the treatment of nausea and as an anti-emetic for patients undergoing chemotherapy. Delta9-THC and related cannabinoids are involved in a variety of signal transduction pathways; thus, reducing or removing the psychotropic effects of these compounds would enhance their therapeutic spectra. Compound synthesis and qualitative SAR studies are time-consuming activities; however, microbes are effectively the most inventive synthetic chemists because of their metabolic plasticity. This review discusses the potential of C sativa mycoflora, which is pathogenic as well as endophytic, to remove the psychotropic effects of Delta9-THC and related cannabinoids, and describes the development of a model system for the rapid and cost-effective commercial production of cannabinoids through fermentation pathways.
AuthorsSanjai Saxena
JournalCurrent opinion in drug discovery & development (Curr Opin Drug Discov Devel) Vol. 12 Issue 2 Pg. 305-12 (Mar 2009) ISSN: 2040-3437 [Electronic] England
PMID19333876 (Publication Type: Journal Article, Review)
Chemical References
  • Cannabinoids
  • Plant Preparations
  • Dronabinol
Topics
  • Animals
  • Biotransformation
  • Cannabinoids (adverse effects, chemistry, metabolism, pharmacology)
  • Cannabis (microbiology)
  • Dronabinol (metabolism, pharmacology)
  • Drug Discovery
  • Fermentation
  • Fungi (metabolism)
  • Humans
  • Plant Preparations (adverse effects, chemistry, metabolism)
  • Signal Transduction (drug effects)
  • Structure-Activity Relationship

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