Engel M A, Kellermann C A, Rau T, Burnat G, Hahn E G, Konturek P C
First Department of Medicine, University of Erlangen-Nuremberg, Germany.
J Physiol Pharmacol. 2008 Dec;59(4):673-89.
Anti-inflammatory and anti-nociceptive properties of endocannabinoids and synthetic cannabinoid compounds were described previously. We studied effects of the endogenous cannabinoid anandamide (N-arachidonylethanolamine) in experimental colitis induced by TNBS (2,4,6-trinitrobenzene sulfonic acid) in AKR mice. A scoring system was used to describe clinical and macroscopic changes. Intraperitoneally administered anandamide significantly reduced experimental colitis, quantified by macroscopical and histological scoring systems as well as pro-inflammatory cytokine mRNA expression. We conclude that systemically administered anandamide attenuates TNBS colitis in mice, and that systemically active cannabinoid compounds might have therapeutic potential for the treatment of IBD.
内源性大麻素和合成大麻素化合物的抗炎和抗伤害感受特性先前已有描述。我们研究了内源性大麻素花生四烯酸乙醇胺(N-花生四烯酰乙醇胺)在TNBS(2,4,6-三硝基苯磺酸)诱导的AKR小鼠实验性结肠炎中的作用。采用评分系统来描述临床和宏观变化。腹腔注射花生四烯酸乙醇胺可显著减轻实验性结肠炎,通过宏观和组织学评分系统以及促炎细胞因子mRNA表达进行量化。我们得出结论,全身给药的花生四烯酸乙醇胺可减轻小鼠的TNBS结肠炎,并且具有全身活性的大麻素化合物可能对治疗炎症性肠病具有治疗潜力。