AI Article Synopsis

  • Lung inflammation triggers an increase in pro-inflammatory substances, and a treatment called FCBD:std, which contains cannabinoids, effectively reduces inflammation in certain lung cells but not in macrophages.
  • The study examined how FCBD:std interacts with corticosteroids and NSAIDs, revealing that its combination with diclofenac works well to lower inflammation markers in both macrophages and lung epithelial cells.
  • While positive effects were observed from the combination therapies, further pre-clinical and clinical research is necessary to fully understand their potential for treating lung inflammation.

Article Abstract

Lung inflammation is associated with elevated pro-inflammatory cytokines and chemokines. Treatment with FCBD:std (standard mix of cannabidiol [CBD], cannabigerol [CBG] and tetrahydrocannabivarin [THCV]) leads to a marked reduction in the inflammation of alveolar epithelial cells, but not in macrophages. In the present study, the combined anti-inflammatory effect of FCBD:std with two corticosteroids (dexamethasone and budesonide) and two non-steroidal anti-inflammatory drugs (NSAID; ibuprofen and diclofenac), was examined. Enzyme-linked immunosorbent assay (ELISA) was used to determine protein levels. Gene expression was determined by quantitative real-time PCR. Inhibition of cyclo-oxygenase (COX) activity was determined in vitro. FCBD:std and diclofenac act synergistically, reducing IL-8 levels in macrophages and lung epithelial cells. FCBD:std plus diclofenac also reduced , and expression levels in co-cultures of macrophages and lung epithelial cells, in 2D and 3D models. Treatment by FCBD:std and/or NSAID reduced and gene expression but not their enzymatic activity. FCBD:std and diclofenac exhibit synergistic anti-inflammatory effects on macrophages and lung epithelial cells, yet this combined activity needs to be examined in pre-clinical studies and clinical trials.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787964PMC
http://dx.doi.org/10.3390/ph15121559DOI Listing

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