Tung David, Cheung Peter H, Tudor Gregory, Booth Catherine, Saha Saurabh
BioMed Valley Discoveries, Kansas City, Missouri.
Epistem Ltd, Manchester, United Kingdom.
Curr Ther Res Clin Exp. 2011 Dec;72(6):262-72. doi: 10.1016/j.curtheres.2011.11.003.
Fluorouracil (5-FU) is a pyrimidine analogue used as a cancer treatment. Its toxic side effects, including mucositis, are reported to occur in 40% of the treated patients. Because of the inflammatory component of mucositis, we explored the possibility of modulating this condition with an immunomodulatory agent and a tumor necrosis factor-α inhibitor.
The aim of this study was to evaluate the effect of 2 immunosuppressive agents, etanercept and cyclosporine, in a murine model of 5-FU-induced mucositis.
To study the short-term effects of 5-FU on mucositis, cyclosporine and etanercept were administered to mice after an injection of 5-FU. The animals (n = 8) were euthanized at 6 hours post-challenge. Hematoxylin and eosin-stained histologic sections of the small intestine were examined for signs of apoptosis. To further examine the potential of cyclosporine in the treatment of 5-FU-induced mucositis in a longer duration, the animals (N = 15) were given 2 challenges of 5-FU within 6 hours. All mice were dosed daily until day 9 with either cyclosporine (100 mg/kg) or phosphate-buffered saline (PBS).
Six hours after 5-FU challenge, 25 mg/kg etanercept and 50 mg/kg cyclosporine had no effect on 5-FU-induced apoptosis (P > 0.05). However, 100 mg/kg cyclosporine significantly reduced the cumulative level of apoptosis >41.6% of the intestinal crypt surface (P < 0.05). During long-term observation, all mice began to lose weight at a rate of approximately 0.8 g/day after 5-FU exposure. The rates of weight loss and survival were not affected by cyclosporine treatment. The diarrhea onset began on day 4 with 46.7% of the PBS-treated mice showing signs of diarrhea compared with 53.3% in the cyclosporine group. The diarrhea score for both groups plateaued on day 7, with a cumulative score of 41 for the PBS group and 50 for the cyclosporine group. Cyclosporine treatment did not affect the diarrhea onset day or severity compared with the PBS-treated group (P > 0.05).
Our data indicated that etanercept is not a suitable treatment for 5-FU-induced mucositis. Despite decreased apoptosis in the gut, cyclosporine did not affect the severity of the diarrhea or survival. Therefore, we concluded that cyclosporine treatment was only effective in mediating the short-term apoptotic events in the intestines but has no long-term effect on the animals' survival and diarrhea.
氟尿嘧啶(5-FU)是一种用于癌症治疗的嘧啶类似物。据报道,其毒性副作用包括口腔炎,在40%的接受治疗的患者中出现。由于口腔炎的炎症成分,我们探索了用免疫调节剂和肿瘤坏死因子-α抑制剂调节这种情况的可能性。
本研究的目的是评估两种免疫抑制剂依那西普和环孢素在5-FU诱导的口腔炎小鼠模型中的作用。
为了研究5-FU对口腔炎的短期影响,在注射5-FU后给小鼠施用环孢素和依那西普。在攻击后6小时对动物(n = 8)实施安乐死。检查苏木精和伊红染色的小肠组织切片是否有凋亡迹象。为了进一步研究环孢素在更长时间内治疗5-FU诱导的口腔炎的潜力,在6小时内给动物(N = 15)进行两次5-FU攻击。所有小鼠每天给药,直至第9天,给予环孢素(100 mg/kg)或磷酸盐缓冲盐水(PBS)。
5-FU攻击后6小时,25 mg/kg依那西普和50 mg/kg环孢素对5-FU诱导的凋亡没有影响(P > 0.05)。然而,100 mg/kg环孢素显著降低了凋亡累积水平,超过肠隐窝表面的41.6%(P < 0.05)。在长期观察期间,所有小鼠在暴露于5-FU后开始以约0.8 g/天的速度体重减轻。体重减轻率和存活率不受环孢素治疗的影响。腹泻在第4天开始,46.7%的PBS处理小鼠出现腹泻迹象,而环孢素组为53.3%。两组的腹泻评分在第7天趋于平稳,PBS组的累积评分为41,环孢素组为50。与PBS处理组相比,环孢素治疗不影响腹泻开始日期或严重程度(P > 0.05)。
我们的数据表明依那西普不是5-FU诱导的口腔炎的合适治疗方法。尽管肠道凋亡减少,但环孢素不影响腹泻的严重程度或存活率。因此,我们得出结论,环孢素治疗仅在介导肠道短期凋亡事件方面有效,但对动物的存活和腹泻没有长期影响。