Silvestri Cristoforo, Pagano Ester, Lacroix Sébastien, Venneri Tommaso, Cristiano Claudia, Calignano Antonio, Parisi Olga A, Izzo Angelo A, Di Marzo Vincenzo, Borrelli Francesca
Centre de recherche de l'Institut universitaire de cardiologie et de pneumologie de Québec (IUCPQ), Québec, QC, Canada.
Département de médecine, Faculté de Médecine, Université Laval, Québec, QC, Canada.
Front Pharmacol. 2020 Oct 8;11:585096. doi: 10.3389/fphar.2020.585096. eCollection 2020.
Inflammatory bowel disorders can be associated with alterations in gut microbiota (dysbiosis) and behavioral disturbances. In experimental colitis, administration of fish oil (FO) or cannabinoids, such as cannabidiol (CBD), reduce inflammation. We investigated the effect of combined FO/CBD administration on inflammation and dysbiosis in the dextran sulphate sodium (DSS) model of mouse colitis, which also causes behavioral disturbances. Colitis was induced in CD1 mice by 4% w/v DSS in drinking water for five consecutive days followed by normal drinking water. FO (20-75 mg/mouse) was administered once a day starting two days after DSS, whereas CBD (0.3-30 mg/kg), alone or after FO administration, was administered once a day starting 3 days after DSS, until day 8 (d8) or day 14 (d14). Inflammation was assessed at d8 and d14 (resolution phase; RP) by measuring the Disease Activity Index (DAI) score, change in body weight, colon weight/length ratio, myeloperoxidase activity and colonic interleukin (IL)-1β (IL-1β), IL-10, and IL-6 concentrations. Intestinal permeability was measured with the fluorescein isothiocyanate-dextran. Behavioral tests (novel object recognition (NOR) and light/dark box test) were performed at d8. Fecal microbiota composition was determined by ribosomal 16S DNA sequencing of faecal pellets at d8 and d14. DSS-induced inflammation was stronger at d8 and accompanied by anxiety-like behavior and impaired recognition memory. FO (35, 50, 75 mg/mouse) alone reduced inflammation at d8, whereas CBD alone produced no effect at any of the doses tested; however, when CBD (3, 10 mg/kg) was co-administered with FO (75 mg/mouse) inflammation was attenuated. FO (20 mg/mouse) and CBD (1 mg/kg) were ineffective when given alone, but when co-administered reduced all inflammatory markers and the increased intestinal permeability at both d8 and d14, but not the behavioral impairments. FO, CBD, and their combination affected gut bacteria taxa that were not affected by DSS . , a species suggested to afford anti-inflammatory action in colitis, was increased by DSS only at d14, but its levels were significantly elevated by all treatments at d8. FO and CBD co-administered at ineffective doses reduce colon inflammation, in a manner potentially strengthened by their independent elevation of .
炎症性肠病可能与肠道微生物群改变(生态失调)及行为障碍有关。在实验性结肠炎中,给予鱼油(FO)或大麻素,如大麻二酚(CBD),可减轻炎症。我们研究了联合给予FO/CBD对葡聚糖硫酸钠(DSS)诱导的小鼠结肠炎模型中炎症和生态失调的影响,该模型也会导致行为障碍。通过在饮用水中给予4% w/v DSS连续5天诱导CD1小鼠患结肠炎,随后给予正常饮用水。从DSS处理后两天开始,每天给予FO(20 - 75 mg/小鼠),而CBD(0.3 - 30 mg/kg)单独或在给予FO后,从DSS处理后3天开始,每天给药一次,直至第8天(d8)或第14天(d14)。在第8天和第14天(缓解期;RP)通过测量疾病活动指数(DAI)评分、体重变化、结肠重量/长度比、髓过氧化物酶活性以及结肠白细胞介素(IL)-1β(IL - 1β)、IL - 10和IL - 6浓度来评估炎症。用异硫氰酸荧光素 - 葡聚糖测量肠道通透性。在第8天进行行为测试(新物体识别(NOR)和明暗箱试验)。通过对第8天和第14天粪便颗粒的核糖体16S DNA测序来确定粪便微生物群组成。DSS诱导的炎症在第8天更强,并伴有焦虑样行为和识别记忆受损。单独给予FO(35、50、75 mg/小鼠)可在第8天减轻炎症,而单独给予CBD在任何测试剂量下均无作用;然而,当CBD(3、10 mg/kg)与FO(75 mg/小鼠)联合给药时,炎症减轻。单独给予FO(20 mg/小鼠)和CBD(1 mg/kg)无效,但联合给药可降低第8天和第14天的所有炎症标志物及增加的肠道通透性,但不能改善行为障碍。FO、CBD及其组合影响了不受DSS影响的肠道细菌分类群。 ,一种被认为在结肠炎中具有抗炎作用的物种,仅在第14天被DSS增加,但其水平在第8天被所有处理显著提高到很高水平)。以无效剂量联合给予的FO和CBD可减轻结肠炎症,其方式可能因它们独立提高 水平而得到加强。