Cannabidiol for neurodegenerative disorders: important new clinical applications for this phytocannabinoid?. (10th January 2013)
- Record Type:
- Journal Article
- Title:
- Cannabidiol for neurodegenerative disorders: important new clinical applications for this phytocannabinoid?. (10th January 2013)
- Main Title:
- Cannabidiol for neurodegenerative disorders: important new clinical applications for this phytocannabinoid?
- Authors:
- Fernández‐Ruiz, Javier
Sagredo, Onintza
Pazos, M. Ruth
García, Concepción
Pertwee, Roger
Mechoulam, Raphael
Martínez‐Orgado, José - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Cannabidiol (CBD) is a phytocannabinoid with therapeutic properties for numerous disorders exerted through molecular mechanisms that are yet to be completely identified. CBD acts in some experimental models as an anti‐inflammatory, anticonvulsant, anti‐oxidant, anti‐emetic, anxiolytic and antipsychotic agent, and is therefore a potential medicine for the treatment of neuroinflammation, epilepsy, oxidative injury, vomiting and nausea, anxiety and schizophrenia, respectively. The neuroprotective potential of CBD, based on the combination of its anti‐inflammatory and anti‐oxidant properties, is of particular interest and is presently under intense preclinical research in numerous neurodegenerative disorders. In fact, CBD combined with Δ<sup>9</sup>‐tetrahydrocannabinol is already under clinical evaluation in patients with Huntington's disease to determine its potential as a disease‐modifying therapy. The neuroprotective properties of CBD do not appear to be exerted by the activation of key targets within the endocannabinoid system for plant‐derived cannabinoids like Δ<sup>9</sup>‐tetrahydrocannabinol, i.e. CB<sub>1</sub> and CB<sub>2</sub> receptors, as CBD has negligible activity at these cannabinoid receptors, although certain activity at the CB<sub>2</sub> receptor has been documented in specific pathological conditions (i.e. damage of immature brain). Within the<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Cannabidiol (CBD) is a phytocannabinoid with therapeutic properties for numerous disorders exerted through molecular mechanisms that are yet to be completely identified. CBD acts in some experimental models as an anti‐inflammatory, anticonvulsant, anti‐oxidant, anti‐emetic, anxiolytic and antipsychotic agent, and is therefore a potential medicine for the treatment of neuroinflammation, epilepsy, oxidative injury, vomiting and nausea, anxiety and schizophrenia, respectively. The neuroprotective potential of CBD, based on the combination of its anti‐inflammatory and anti‐oxidant properties, is of particular interest and is presently under intense preclinical research in numerous neurodegenerative disorders. In fact, CBD combined with Δ<sup>9</sup>‐tetrahydrocannabinol is already under clinical evaluation in patients with Huntington's disease to determine its potential as a disease‐modifying therapy. The neuroprotective properties of CBD do not appear to be exerted by the activation of key targets within the endocannabinoid system for plant‐derived cannabinoids like Δ<sup>9</sup>‐tetrahydrocannabinol, i.e. CB<sub>1</sub> and CB<sub>2</sub> receptors, as CBD has negligible activity at these cannabinoid receptors, although certain activity at the CB<sub>2</sub> receptor has been documented in specific pathological conditions (i.e. damage of immature brain). Within the endocannabinoid system, CBD has been shown to have an inhibitory effect on the inactivation of endocannabinoids (i.e. inhibition of FAAH enzyme), thereby enhancing the action of these endogenous molecules on cannabinoid receptors, which is also noted in certain pathological conditions. CBD acts not only through the endocannabinoid system, but also causes direct or indirect activation of metabotropic receptors for serotonin or adenosine, and can target nuclear receptors of the PPAR family and also ion channels.</p> </abstract> … (more)
- Is Part Of:
- British journal of clinical pharmacology. Volume 75:Number 2(2013:Feb.)
- Journal:
- British journal of clinical pharmacology
- Issue:
- Volume 75:Number 2(2013:Feb.)
- Issue Display:
- Volume 75, Issue 2 (2013)
- Year:
- 2013
- Volume:
- 75
- Issue:
- 2
- Issue Sort Value:
- 2013-0075-0002-0000
- Page Start:
- 323
- Page End:
- 333
- Publication Date:
- 2013-01-10
- Subjects:
- Pharmacology -- Periodicals
Drugs -- Periodicals
615.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2125 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/j.1365-2125.2012.04341.x ↗
- Languages:
- English
- ISSNs:
- 0306-5251
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2307.180000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3026.xml