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菊科植物L.的黏膜黏附制剂可减轻5-氟尿嘧啶诱导的小鼠肠道黏膜炎所致的肠道损伤。

Mucoadhesive formulation of L. (Asteraceae) reduces intestinal injury from 5-fluorouracil-induced mucositis in mice.

作者信息

de Ávila Paulo Henrique Marcelino, de Ávila Renato Ivan, Dos Santos Filho Edvande Xavier, Cunha Bastos Carla Caroline, Batista Aline Carvalho, Mendonça Elismauro Francisco, Serpa Raphael Caixeta, Marreto Ricardo Neves, da Cruz Andrezza Furquim, Lima Eliana Martins, Valadares Marize Campos

机构信息

Laboratório de Farmacologia e Toxicologia Celular - FarmaTec, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia, GO, Brazil.

Departamento de Estomatologia, Faculdade de Odontologia, Universidade Federal de Goiás, Goiânia, GO, Brazil.

出版信息

Toxicol Rep. 2015 Mar 23;2:563-573. doi: 10.1016/j.toxrep.2015.03.003. eCollection 2015.

Abstract

Gastrointestinal mucositis induced during cancer treatment is considered a serious dose-limiting side effect of chemotherapy and/or radiotherapy. Frequently, interruption of the cancer treatment due to this pathology leads to a reduction in cure rates, increase of treatment costs and decrease life quality of the patient. Natural products such as L. (Asteraceae), represent a potential alternative for the treatment of mucositis given its anti-inflammatory properties. In this study, glycolic extract was formulated (BPF) with poloxamer, a mucoadhesive copolymer, was used for treatment of 5-fluorouracil (5-FU)-induced mucositis in mice. As expected, animals only treated with 5-FU (200 mg/kg) presented marked weight loss, reduction of intestinal villi, crypts and muscular layer, which was associated with severe disruption of crypts, edema, inflammatory infiltrate and vacuolization in the intestinal tissue, as compared to the control group and healthy animals only treated with BPF. On the other hand, the treatment of intestinal mucositis-bearing mice with BPF (75, 100 or 125 mg/kg) managed to mitigate clinical and pathologic changes, noticeably at 100 mg/kg. This dose led to the restoration of intestinal proliferative activity through increasing Ki-67 levels; modulated the expression of Bax, Bcl2 and p53 apoptotic markers protecting intestinal cells from cell death. Moreover, this treatment regulated lipid peroxidation and inflammatory infiltration. No acute toxic effects were observed with this formulation. This work demonstrated that BPF was safe and effective against 5-FU-induced intestinal mucositis in mice. Additional studies are already in progress to further characterize the mechanisms involved in the protective effects of this technological formulation toward the development of a new medicine for the prevention and treatment of intestinal injury in patients undergoing chemotherapy/radiotherapy.

摘要

癌症治疗期间诱发的胃肠道黏膜炎被认为是化疗和/或放疗严重的剂量限制性副作用。由于这种病理状况,癌症治疗常常中断,导致治愈率降低、治疗成本增加以及患者生活质量下降。诸如L.(菊科)等天然产物,因其抗炎特性,是治疗黏膜炎的一种潜在替代物。在本研究中,用泊洛沙姆(一种黏膜黏附共聚物)配制了乙醇提取物(BPF),用于治疗小鼠5-氟尿嘧啶(5-FU)诱发的黏膜炎。正如预期的那样,仅用5-FU(200mg/kg)治疗的动物出现明显体重减轻、肠绒毛、隐窝和肌层减少,与对照组和仅用BPF治疗的健康动物相比,这与肠组织中隐窝严重破坏、水肿、炎性浸润和空泡化有关。另一方面,用BPF(75、100或125mg/kg)治疗患有肠黏膜炎的小鼠能够减轻临床和病理变化,在100mg/kg时尤为明显。该剂量通过增加Ki-67水平导致肠增殖活性恢复;调节Bax、Bcl2和p53凋亡标志物的表达,保护肠细胞免于细胞死亡。此外,该治疗调节脂质过氧化和炎性浸润。该制剂未观察到急性毒性作用。这项工作表明BPF对5-FU诱发的小鼠肠黏膜炎安全有效。进一步的研究正在进行中,以进一步阐明这种技术制剂的保护作用所涉及的机制,从而开发一种预防和治疗接受化疗/放疗患者肠损伤的新药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/007a/5598237/47c0a6855aa9/gr1.jpg

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