Yekhtin Zhanna, Khuja Iman, Meiri David, Or Reuven, Almogi-Hazan Osnat
Laboratory of Immunotherapy and Bone Marrow Transplantation, Hadassah Medical Center, The Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem 91120, Israel.
The Laboratory of Cancer Biology and Cannabinoid Research, Department of Biology, Technion-Israel Institute of Technology, Haifa 320003, Israel.
Biomedicines. 2022 Jul 26;10(8):1793. doi: 10.3390/biomedicines10081793.
Phytocannabinoids possess a wide range of immune regulatory properties, mediated by the endocannabinoid system. Monocyte/macrophage innate immune cells express endocannabinoid receptors. Dysregulation of macrophage function is involved in the pathogenesis of different inflammatory diseases, including inflammatory bowel disease. In our research, we aimed to evaluate the effects of the phytocannabinoids D9 tetrahydrocannabinol (THC) and cannabidiol (CBD) on macrophage activation. Macrophages from young and aged C57BL/6 mice were activated in vitro in the presence of pure cannabinoids or cannabis extracts. The phenotype of the cells, nitric oxide (NO•) secretion, and cytokine secretion were examined. In addition, these treatments were administered to murine colitis model. The clinical statuses of mice, levels of colon infiltrating macrophages, and inflammatory cytokines in the blood, were evaluated. We demonstrated inhibition of macrophage NO• and cytokine secretion and significant effects on expression of cell surface molecules. In the murine model, clinical scores were improved and macrophage colon infiltration reduced following treatment. We identified higher activity of cannabis extracts as compared with pure cannabinoids. Each treatment had a unique effect on cytokine composition. Overall, our results establish that the effects of cannabinoid treatments differ. A better understanding of the reciprocal relationship between cannabinoids and immunity is essential to design targeted treatment strategies.
植物大麻素具有广泛的免疫调节特性,由内源性大麻素系统介导。单核细胞/巨噬细胞先天性免疫细胞表达内源性大麻素受体。巨噬细胞功能失调参与了包括炎症性肠病在内的不同炎症性疾病的发病机制。在我们的研究中,我们旨在评估植物大麻素Δ⁹-四氢大麻酚(THC)和大麻二酚(CBD)对巨噬细胞激活的影响。在纯大麻素或大麻提取物存在的情况下,体外激活来自年轻和老年C57BL/6小鼠的巨噬细胞。检测细胞表型、一氧化氮(NO•)分泌和细胞因子分泌。此外,将这些处理应用于小鼠结肠炎模型。评估小鼠的临床状态、结肠浸润巨噬细胞水平和血液中的炎症细胞因子。我们证明了巨噬细胞NO•和细胞因子分泌受到抑制,并且对细胞表面分子的表达有显著影响。在小鼠模型中,治疗后临床评分改善,巨噬细胞结肠浸润减少。我们发现大麻提取物的活性高于纯大麻素。每种处理对细胞因子组成都有独特的影响。总体而言,我们的结果表明大麻素处理的效果不同。更好地理解大麻素与免疫之间的相互关系对于设计靶向治疗策略至关重要。