Cannabidiol, a Major Non‐Psychotropic Cannabis Constituent Enhances Fracture Healing and Stimulates Lysyl Hydroxylase Activity in Osteoblasts. (10th May 2015)
- Record Type:
- Journal Article
- Title:
- Cannabidiol, a Major Non‐Psychotropic Cannabis Constituent Enhances Fracture Healing and Stimulates Lysyl Hydroxylase Activity in Osteoblasts. (10th May 2015)
- Main Title:
- Cannabidiol, a Major Non‐Psychotropic Cannabis Constituent Enhances Fracture Healing and Stimulates Lysyl Hydroxylase Activity in Osteoblasts
- Authors:
- Kogan, Natalya M
Melamed, Eitan
Wasserman, Elad
Raphael, Bitya
Breuer, Aviva
Stok, Kathryn S
Sondergaard, Rachel
Escudero, Ana VVillarreal
Baraghithy, Saja
Attar‐Namdar, Malka
Friedlander‐Barenboim, Silvina
Mathavan, Neashan
Isaksson, Hanna
Mechoulam, Raphael
Müller, Ralph
Bajayo, Alon
Gabet, Yankel
Bab, Itai - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jbmr2513-sec-0001" sec-type="section"> <p>Cannabinoid ligands regulate bone mass, but skeletal effects of cannabis (marijuana and hashish) have not been reported. Bone fractures are highly prevalent, involving prolonged immobilization and discomfort. Here we report that the major non‐psychoactive cannabis constituent, cannabidiol (CBD), enhances the biomechanical properties of healing rat mid‐femoral fractures. The maximal load and work‐to‐failure, but not the stiffness, of femurs from rats given a mixture of CBD and Δ<sup>9</sup>‐tetrahydrocannabinol (THC) for 8 weeks were markedly increased by CBD. This effect is not shared by THC (the psychoactive component of cannabis), but THC potentiates the CBD stimulated work‐to‐failure at 6 weeks postfracture followed by attenuation of the CBD effect at 8 weeks. Using micro–computed tomography (μCT), the fracture callus size was transiently reduced by either CBD or THC 4 weeks after fracture but reached control level after 6 and 8 weeks. The callus material density was unaffected by CBD and/or THC. By contrast, CBD stimulated mRNA expression of <italic>Plod1</italic> in primary osteoblast cultures, encoding an enzyme that catalyzes lysine hydroxylation, which is in turn involved in collagen crosslinking and stabilization. Using Fourier transform infrared (FTIR) spectroscopy we confirmed the increase in collagen crosslink ratio by CBD, which is likely to<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <sec id="jbmr2513-sec-0001" sec-type="section"> <p>Cannabinoid ligands regulate bone mass, but skeletal effects of cannabis (marijuana and hashish) have not been reported. Bone fractures are highly prevalent, involving prolonged immobilization and discomfort. Here we report that the major non‐psychoactive cannabis constituent, cannabidiol (CBD), enhances the biomechanical properties of healing rat mid‐femoral fractures. The maximal load and work‐to‐failure, but not the stiffness, of femurs from rats given a mixture of CBD and Δ<sup>9</sup>‐tetrahydrocannabinol (THC) for 8 weeks were markedly increased by CBD. This effect is not shared by THC (the psychoactive component of cannabis), but THC potentiates the CBD stimulated work‐to‐failure at 6 weeks postfracture followed by attenuation of the CBD effect at 8 weeks. Using micro–computed tomography (μCT), the fracture callus size was transiently reduced by either CBD or THC 4 weeks after fracture but reached control level after 6 and 8 weeks. The callus material density was unaffected by CBD and/or THC. By contrast, CBD stimulated mRNA expression of <italic>Plod1</italic> in primary osteoblast cultures, encoding an enzyme that catalyzes lysine hydroxylation, which is in turn involved in collagen crosslinking and stabilization. Using Fourier transform infrared (FTIR) spectroscopy we confirmed the increase in collagen crosslink ratio by CBD, which is likely to contribute to the improved biomechanical properties of the fracture callus. Taken together, these data show that CBD leads to improvement in fracture healing and demonstrate the critical mechanical role of collagen crosslinking enzymes. © 2015 American Society for Bone and Mineral Research.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of bone and mineral research. Volume 30:Number 10(2015:Oct.)
- Journal:
- Journal of bone and mineral research
- Issue:
- Volume 30:Number 10(2015:Oct.)
- Issue Display:
- Volume 30, Issue 10 (2015)
- Year:
- 2015
- Volume:
- 30
- Issue:
- 10
- Issue Sort Value:
- 2015-0030-0010-0000
- Page Start:
- 1905
- Page End:
- 1913
- Publication Date:
- 2015-05-10
- Subjects:
- Bones -- Metabolism -- Periodicals
Mineral metabolism -- Periodicals
612.392 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1523-4681 ↗
http://www.jbmr-online.com ↗ - DOI:
- 10.1002/jbmr.2513 ↗
- Languages:
- English
- ISSNs:
- 0884-0431
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4954.255530
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4003.xml