Departamento de Farmacologia, Faculdade de Ciências Médicas, Universidade Estadual de Campinas (Unicamp), 13083-887 Campinas, SP, Brazil.
Departamento de Ciências Biológicas, Universidade Federal de Goiás (UFG), 75704-020 Catalão, GO, Brazil.
Chem Biol Interact. 2014 Feb 25;209:48-55. doi: 10.1016/j.cbi.2013.11.019. Epub 2013 Dec 6.
Isatin, an indole alkaloid has been shown to have anti-microbial, anti-tumor and anti-inflammatory effects. Due to its findings, we evaluated whether this alkaloid would have any effect on TNBS-induced colitis. Animals (male Unib:WH rats, aged 8 weeks old) were induced colitis through a rectal administration of 2,4,6-trinitrobenzene sulphonic acid using a catheter inserted 8 cm into the rectum of the animals. The rats were divided into two major groups: non-colitic and colitic. The colitic group was sub-divided into 6 groups (10 animals per group): colitic non-treated, Isatin 3; 6; 12.5; 18.75 and 25 mg/kg. Our main results showed that the oral treatment with Isatin 6 and 25 mg/kg were capable of avoiding the increase in TNF-α, COX-2 and PGE₂ levels when compared to the colitic non-treated group. Interestingly, the same doses (6 and 25 mg/kg) were also capable of preventing the decrease in IL-10 levels comparing with the colitic non-treated group. The levels of MPO, (an indirect indicator of neutrophil presence), were also maintained lower than those of the colitic non-treated group. Isatin also prevented the decrease of SOD activity and increase of GSH-Px and GSH-Rd activity as well as the depletion of GSH levels. In conclusion, both pre-treatments (6 and 25 mg/kg) were capable of protecting the gut mucosa against the injury caused by TNBS, through the combination of antioxidant and anti-inflammatory properties, which, together, showed a protective activity of the indole alkaloid Isatin.
色胺酮是一种吲哚生物碱,具有抗微生物、抗肿瘤和抗炎作用。由于其发现,我们评估了这种生物碱是否对三硝基苯磺酸诱导的结肠炎有任何影响。动物(雄性 Unib:WH 大鼠,8 周龄)通过直肠内插入导管 8 厘米到动物直肠来诱导结肠炎。这些大鼠被分为两个主要组:非结肠炎和结肠炎。结肠炎组进一步分为 6 个组(每组 10 只动物):未治疗的结肠炎、色胺酮 3、6、12.5、18.75 和 25mg/kg。我们的主要结果表明,与未治疗的结肠炎组相比,口服色胺酮 6 和 25mg/kg 能够避免 TNF-α、COX-2 和 PGE₂水平的增加。有趣的是,相同剂量(6 和 25mg/kg)也能够防止与未治疗的结肠炎组相比,IL-10 水平的下降。髓过氧化物酶(中性粒细胞存在的间接指标)的水平也保持低于未治疗的结肠炎组。色胺酮还防止 SOD 活性的降低、GSH-Px 和 GSH-Rd 活性的增加以及 GSH 水平的消耗。总之,两种预处理(6 和 25mg/kg)都能够通过抗氧化和抗炎特性的结合来保护肠道黏膜免受 TNBS 引起的损伤,共同显示出吲哚生物碱色胺酮的保护活性。