Thapa Dinesh, Patil Mohan, Warne Leon N, Carlessi Rodrigo, Falasca Marco
Curtin Medical Research Institute, Curtin University, Perth, WA 6102, Australia.
College of Science, Health, Engineering and Education, Murdoch University, Perth, WA 6150, Australia.
Pharmaceuticals (Basel). 2025 Jan 23;18(2):148. doi: 10.3390/ph18020148.
Current inflammatory bowel disease (IBD) treatments focus on symptomatic relief, highlighting the need for innovative approaches. Dysregulation of the cannabinoid 1 (CB1) receptor, part of the endocannabinoid system, is linked to colitis. While tetrahydrocannabinol (THC) alleviates colitis via CB1 activation, its psychotropic effects limit clinical use. ZCZ011, a CB1R allosteric modulator, and cannabidiol (CBD), a non-psychoactive cannabinoid, offer alternatives. This study investigated combining sub-therapeutic THC doses with ZCZ011 or CBD in a murine model of dextran sodium sulphate (DSS)-induced colitis. Acute colitis was induced with 4% DSS for 7 days, followed by 3 days of water. Chronic colitis was modelled over 24 days with alternating DSS concentrations. The combination of 2.5 mg/kg THC with 20 mg/kg ZCZ011 or 10 mg/kg CBD was evaluated. Key markers were assessed to determine efficacy and safety, including disease activity index (DAI), inflammation, cytokine levels, GLP-1, and organ health. DSS-induced colitis resulted in increased DAI scores, cytokines, organ inflammation and dysregulation of GLP-1 and ammonia. THC at 10 mg/kg significantly improved colitis markers but was ineffective at 2.5 and 5 mg/kg. ZCZ011 alone showed transient effects. However, combining 2.5 mg/kg THC with either 20 mg/kg ZCZ011 or 10 mg/kg CBD significantly alleviated colitis markers, restored colon integrity and reestablished GLP-1 homeostasis. This combination also maintained favourable haematological and biochemical profiles, including a notable reduction in colitis-induced elevated ammonia levels. This study demonstrates the synergistic potential of low-dose THC combined with CBD or ZCZ011 as a novel, effective and safer therapeutic strategy for ulcerative colitis.
目前炎症性肠病(IBD)的治疗主要集中在缓解症状上,这凸显了创新治疗方法的必要性。内源性大麻素系统的一部分——大麻素1(CB1)受体失调与结肠炎有关。虽然四氢大麻酚(THC)通过激活CB1减轻结肠炎,但它的精神活性作用限制了其临床应用。CB1R变构调节剂ZCZ011和非精神活性大麻素大麻二酚(CBD)提供了替代方案。本研究在葡聚糖硫酸钠(DSS)诱导的小鼠结肠炎模型中,研究了将低于治疗剂量的THC与ZCZ011或CBD联合使用的效果。用4% DSS诱导急性结肠炎7天,随后3天给予水。通过交替使用不同浓度的DSS,在24天内建立慢性结肠炎模型。评估了2.5 mg/kg THC与20 mg/kg ZCZ011或10 mg/kg CBD联合使用的效果。评估了包括疾病活动指数(DAI)、炎症、细胞因子水平、胰高血糖素样肽-1(GLP-1)和器官健康等关键指标,以确定疗效和安全性。DSS诱导的结肠炎导致DAI评分增加、细胞因子水平升高、器官炎症以及GLP-1和氨的调节异常。10 mg/kg的THC显著改善了结肠炎指标,但2.5 mg/kg和5 mg/kg时无效。单独使用ZCZ011显示出短暂的效果。然而,将2.5 mg/kg THC与20 mg/kg ZCZ011或10 mg/kg CBD联合使用可显著减轻结肠炎指标,恢复结肠完整性并重建GLP-1稳态。这种联合用药还维持了良好的血液学和生化指标,包括显著降低结肠炎诱导的氨水平升高。本研究证明了低剂量THC与CBD或ZCZ011联合使用作为溃疡性结肠炎一种新型、有效且更安全的治疗策略的协同潜力。