Department of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC, USA.
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, USA.
J Crohns Colitis. 2021 Jun 22;15(6):1032-1048. doi: 10.1093/ecco-jcc/jjaa253.
Cannabinoid receptor [CB] activation can attenuate inflammatory bowel disease [IBD] in experimental models and human cohorts. However, the roles of the microbiome, metabolome, and the respective contributions of haematopoietic and non-haematopoietic cells in the anti-colitic effects of cannabinoids have yet to be determined.
Female C57BL/6 mice were treated with either cannabidiol [CBD], Δ 9-tetrahydrocannabinol [THC], a combination of CBD and THC, or vehicle, in several models of chemically induced colitis. Clinical parameters of colitis were assessed by colonoscopy, histology, flow cytometry, and detection of serum biomarkers; single-cell RNA sequencing and qRT-PCR were used to evaluate the effects of cannabinoids on enterocytes. Immune cell transfer from CB2 knockout mice was used to evaluate the contribution of haematopoietic and non-haematopoietic cells to colitis protection.
We found that THC prevented colitis and that CBD, at the dose tested, provided little benefit to the amelioration of colitis, nor when added synergistically with THC. THC increased colonic barrier integrity by stimulating mucus and tight junction and antimicrobial peptide production, and these effects were specific to the large intestine. THC increased colonic Gram-negative bacteria, but the anti-colitic effects of THC were independent of the microbiome. THC acted both on immune cells via CB2 and on enterocytes, to attenuate colitis.
Our findings demonstrate how cannabinoid receptor activation on both immune cells and colonocytes is critical to prevent colonic inflammation. These studies also suggest how cannabinoid receptor activation can be used as a preventive and therapeutic modality against colitis.
大麻素受体 [CB] 的激活可以减轻实验模型和人类队列中的炎症性肠病 [IBD]。然而,微生物组、代谢组以及造血细胞和非造血细胞各自在大麻素的抗结肠炎症作用中的作用尚未确定。
雌性 C57BL/6 小鼠在几种化学诱导的结肠炎模型中接受大麻二酚 [CBD]、Δ 9-四氢大麻酚 [THC]、CBD 和 THC 的组合或载体治疗。通过结肠镜检查、组织学、流式细胞术和血清生物标志物检测评估结肠炎的临床参数;单细胞 RNA 测序和 qRT-PCR 用于评估大麻素对肠细胞的影响。从 CB2 敲除小鼠中转移免疫细胞,用于评估造血细胞和非造血细胞对结肠炎保护的贡献。
我们发现 THC 可预防结肠炎,而 CBD 在测试剂量下对改善结肠炎几乎没有益处,也不能与 THC 协同添加。THC 通过刺激粘液和紧密连接以及抗菌肽的产生来增加结肠屏障完整性,这些作用是大肠特有的。THC 增加了结肠革兰氏阴性菌,但 THC 的抗结肠炎作用与微生物组无关。THC 通过 CB2 作用于免疫细胞和肠细胞,从而减轻结肠炎。
我们的研究结果表明,大麻素受体在免疫细胞和结肠细胞上的激活对于预防结肠炎症至关重要。这些研究还表明,大麻素受体的激活如何可作为预防和治疗结肠炎的一种方式。