Abstract | BACKGROUND AND PURPOSE: Cannabis extracts and several cannabinoids have been shown to exert broad anti-inflammatory activities in experimental models of inflammatory CNS degenerative diseases. Clinical use of many cannabinoids is limited by their psychotropic effects. However, phytocannabinoids like cannabidiol (CBD), devoid of psychoactive activity, are, potentially, safe and effective alternatives for alleviating neuroinflammation and neurodegeneration. EXPERIMENTAL APPROACH: KEY RESULTS: Treatment with CBD during disease onset ameliorated the severity of the clinical signs of EAE. This effect of CBD was accompanied by diminished axonal damage and inflammation as well as microglial activation and T-cell recruitment in the spinal cord of MOG-injected mice. Moreover, CBD inhibited MOG-induced T-cell proliferation in vitro at both low and high concentrations of the myelin antigen. This effect was not mediated via the known cannabinoid CB(1) and CB(2) receptors. CONCLUSIONS AND IMPLICATIONS: CBD, a non-psychoactive cannabinoid, ameliorates clinical signs of EAE in mice, immunized against MOG. Suppression of microglial activity and T-cell proliferation by CBD appeared to contribute to these beneficial effects.
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Authors | Ewa Kozela, Nirit Lev, Nathali Kaushansky, Raya Eilam, Neta Rimmerman, Rivka Levy, Avraham Ben-Nun, Ana Juknat, Zvi Vogel |
Journal | British journal of pharmacology
(Br J Pharmacol)
Vol. 163
Issue 7
Pg. 1507-19
(Aug 2011)
ISSN: 1476-5381 [Electronic] England |
PMID | 21449980
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2011 The Authors. British Journal of Pharmacology © 2011 The British Pharmacological Society. |
Chemical References |
- Mog protein, mouse
- Myelin Proteins
- Myelin-Oligodendrocyte Glycoprotein
- Cannabidiol
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Topics |
- Animals
- Cannabidiol
(pharmacology)
- Diffuse Axonal Injury
(drug therapy)
- Disease Models, Animal
- Disease Progression
- Encephalomyelitis, Autoimmune, Experimental
(chemically induced, drug therapy)
- Female
- Macrophages
(drug effects)
- Mice
- Mice, Inbred C57BL
- Microglia
(drug effects)
- Multiple Sclerosis
(drug therapy, immunology, pathology)
- Myelin Proteins
(pharmacology)
- Myelin-Oligodendrocyte Glycoprotein
- Nerve Degeneration
(drug therapy)
- Spinal Cord
(drug effects)
- T-Lymphocytes
(drug effects, immunology)
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