Bastos Carla Caroline Cunha, Ávila Paulo Henrique Marcelino de, Filho Edvande Xavier Dos Santos, Ávila Renato Ivan de, Batista Aline Carvalho, Fonseca Simone Gonçalves, Lima Eliana Martins, Marreto Ricardo Neves, Mendonça Elismauro Francisco de, Valadares Marize Campos
Laboratório de Farmacologia e Toxicologia Celular-FarmaTec, Faculdade de Farmácia, Universidade Federal de Goiás (UFG), Goiânia, GO, Brazil.
Laboratório de Patologia Bucal, Faculdade de Odontologia, Universidade Federal de Goiás (UFG), Goiânia, GO, Brazil.
Toxicol Rep. 2015 Oct 30;3:279-287. doi: 10.1016/j.toxrep.2015.10.013. eCollection 2016.
Several studies towards the development of an effective treatment for intestinal mucositis have been reported, since this condition represents a major problem in clinical oncology practice due to cytotoxic effects of chemotherapy. However standardized protocols and universally accepted treatment options are yet to be established.
Given above, this study evaluated the protective effects of a mucoadhesive formulation containing both L. (Asteraceae) (BP) and curcuminoids from L. (Zingiberaceae) (CL) on intestinal mucositis induced by 5-fluoruoacil (5-FU) in mice.
As expected, animals only treated with 5-FU (200 mg/kg) showed a significant reduction of 60.3 and 42.4% in villi and crypts size, respectively, when compared to control. On the other hand, the proposed therapeutic/prophylactic treatment with mucoadhesive formulations managed to reduce histopathologic changes in mice bearing mucositis, especially at 125 mg/kg BP + 15 mg/kg CL dose. The formulation promoted an increase of 275.5% and 148.7% for villi and crypts size, respectively. Moreover, chemotherapy-related weight loss was reduced by 7.4% following the treatment. In addition, an increase of 10 and 30.5% in red and white blood cells was observed when compared to 5-FU group. Furthermore, treatments with the mucoadhesive formulation containing BP/CL up modulated Ki-67 and Bcl-2 expression while reduced pro-apoptotic regulator Bax. The formulation also modulated inflammatory response triggered by 5-FU through reduction of 68% of myeloperoxidase activity and a 4-fold increase in anti-inflammatory IL-10 levels. In parallel, the oxidative stress lipid peroxidation was reduced as indicated by decrease of 63% of malondialdehyde concentrations. Additionally, the new formulation presented low acute oral systemic toxicity, being classified in the category 5 (2000 mg/kg < LD < 5000 mg/kg) of the Globally Harmonized Classification System.
This study showed an interesting potential of the mucoadhesive formulation of BP/CL for the treatment of 5-FU-induced intestinal mucositis. Given the perspectives for the development of a new medicine, clinical studies are in progress to better understand the protective effects of this innovative formulation in treating mucositis.
由于化疗的细胞毒性作用,肠道黏膜炎成为临床肿瘤学实践中的一个主要问题,因此已有多项关于开发有效治疗方法的研究报道。然而,标准化方案和普遍接受的治疗选择尚未确立。
鉴于上述情况,本研究评估了一种同时含有来自菊科植物的滨蒿(BP)和来自姜科植物的姜黄素(CL)的黏膜黏附制剂对5-氟尿嘧啶(5-FU)诱导的小鼠肠道黏膜炎的保护作用。
正如预期的那样,与对照组相比,仅接受5-FU(200 mg/kg)治疗的动物绒毛和隐窝大小分别显著减少了60.3%和42.4%。另一方面,采用黏膜黏附制剂进行的治疗/预防方案成功减轻了患有黏膜炎小鼠的组织病理学变化,尤其是在125 mg/kg BP + 15 mg/kg CL剂量时。该制剂使绒毛和隐窝大小分别增加了275.5%和148.7%。此外,治疗后化疗相关的体重减轻减少了7.4%。此外,与5-FU组相比,红细胞和白细胞分别增加了10%和30.5%。此外,含BP/CL的黏膜黏附制剂治疗上调了Ki-67和Bcl-2表达,同时降低了促凋亡调节因子Bax。该制剂还通过降低68%的髓过氧化物酶活性和使抗炎性白细胞介素-10水平增加4倍来调节由5-FU引发的炎症反应。同时,氧化应激——脂质过氧化作用降低,丙二醛浓度降低了63%表明了这一点。此外,新制剂的急性经口全身毒性较低,在全球统一分类系统中被归类为5类(2000 mg/kg < LD < 5000 mg/kg)。
本研究表明BP/CL黏膜黏附制剂在治疗5-FU诱导的肠道黏膜炎方面具有有趣的潜力。鉴于开发新药的前景,正在进行临床研究以更好地了解这种创新制剂在治疗黏膜炎中的保护作用。