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Cannabidiol (CBD): a killer for inflammatory rheumatoid arthritis synovial fibroblasts

Torsten Lowin, Ren Tingting, Julia Zurmahr, Tim Classen, Matthias Schneider, Georg Pongratz
Key takeaways
  1. 01CBD reduces the production of inflammatory markers like IL-6 and IL-8
  2. 02The treatment specifically targets activated cells in an inflammatory environment
  3. 03CBD influences cell survival by altering calcium levels via the TRPA1 receptor
  4. 04Findings suggest CBD has potential anti-arthritic properties in joint cells

CBD may help limit joint destruction in rheumatoid arthritis by targeting and reducing the activity of inflammatory synovial fibroblasts

Abstract

Cannabidiol (CBD) is a non-intoxicating phytocannabinoid from cannabis sativa that has demonstrated anti-inflammatory effects in several inflammatory conditions including arthritis. However, CBD binds to several receptors and enzymes and, therefore, its mode of action remains elusive. In this study, we show that CBD increases intracellular calcium levels, reduces cell viability and IL-6/IL-8/MMP-3 production of rheumatoid arthritis synovial fibroblasts (RASF). These effects were pronounced under inflammatory conditions by activating transient receptor potential ankyrin (TRPA1), and by opening of the mitochondrial permeability transition pore. Changes in intracellular calcium and cell viability were determined by using the fluorescent dyes Cal-520/PoPo3 together with cell titer blue and the luminescent dye RealTime-glo. Cell-based impedance measurements were conducted with the XCELLigence system and TRPA1 protein was detected by flow cytometry. Cytokine production was evaluated by ELISA. CBD reduced cell viability, proliferation, and IL-6/IL-8 production of RASF. Moreover, CBD increased intracellular calcium and uptake of the cationic viability dye PoPo3 in RASF, which was enhanced by pre-treatment with TNF. Concomitant incubation of CBD with the TRPA1 antagonist A967079 but not the TRPV1 antagonist capsazepine reduced the effects of CBD on calcium and PoPo3 uptake. In addition, an inhibitor of the mitochondrial permeability transition pore, cyclosporin A, also blocked the effects of CBD on cell viability and IL-8 production. PoPo3 uptake was inhibited by the voltage-dependent anion-selective channel inhibitor DIDS and Decynium-22, an inhibitor for all organic cation transporter isoforms. CBD increases intracellular calcium levels, reduces cell viability, and IL-6/IL-8/MMP-3 production of RASF by activating TRPA1 and mitochondrial targets. This effect was enhanced by pre-treatment with TNF suggesting that CBD preferentially targets activated, pro-inflammatory RASF. Thus, CBD possesses anti-arthritic activity and might ameliorate arthritis via targeting synovial fibroblasts under inflammatory conditions.

Cite this study
APA
Torsten Lowin, Ren Tingting, Julia Zurmahr, Tim Classen, Matthias Schneider, & Georg Pongratz (2020). Cannabidiol (CBD): a killer for inflammatory rheumatoid arthritis synovial fibroblasts. https://fasciaresearchdatabase.com/cannabidiol-cbd-a-killer-for-inflammatory-rheumatoid-arthritis-synovial-fibroblasts/
MLA
Torsten Lowin, et al. "Cannabidiol (CBD): a killer for inflammatory rheumatoid arthritis synovial fibroblasts." 2020, https://fasciaresearchdatabase.com/cannabidiol-cbd-a-killer-for-inflammatory-rheumatoid-arthritis-synovial-fibroblasts/.
Chicago
Torsten Lowin et al. 2020. "Cannabidiol (CBD): a killer for inflammatory rheumatoid arthritis synovial fibroblasts.". https://fasciaresearchdatabase.com/cannabidiol-cbd-a-killer-for-inflammatory-rheumatoid-arthritis-synovial-fibroblasts/