Departamento de Fisiologia e Farmacologia/UFC, Coronel Nunes de Melo, 1127 Rodolfo Teófilo, 60430-270, Ceará, Brazil.
Departamento de Morfologia/UFC, Delmiro de Farias S/N, Rodolfo Teófilo, 60416030, Ceará, Brazil.
Phytother Res. 2017 Feb;31(2):312-320. doi: 10.1002/ptr.5752. Epub 2016 Dec 2.
Intestinal mucositis (IM) is the critical side effect of irinotecan (CPT-11), which is the front-line drug used for the treatment of colorectal cancer. This study aimed to evaluate the effectiveness of latex proteins (LP) from Calotropis procera to prevent IM and diarrhea in animals. Swiss mice were treated daily with saline or LP (1, 5, or 50 mg/kg, i.v.) 24 h prior to CTP-11 (75 mg/kg/4 days, i.p) and for additional 6 days. Animal survival, body weight variation, and diarrhea were registered. After animal sacrifice (day 7 post first injection of CPT-11), intestinal samples were collected to study morphology and inflammatory parameters. Animals given LP exhibited improved parameters (survival, body weight, and absence of diarrhea) as compared with the CPT-11 control. The severity of IM observed in animals given CPT-11 was reduced in animals treated with LP. Treatment with LP also prevented the reduction in the villus/crypt ratio promoted by CPT-11. The rise in MPO activity and pro-inflammatory cytokines, over-contractility of the smooth muscle, and diarrhea were all abrogated in LP-treated mice. Markedly reduced immunostaining intensity for COX-2, TNF-α, IL-1β, iNOS, and NF-κB was observed in the intestinal tissue of animals treated with LP. The side-effects of CPT-11 were eliminated by LP treatment in experimental animals and improved clinical parameters characteristic of IM All known biochemical pathogenesis. Copyright © 2016 John Wiley & Sons, Ltd.
肠黏膜炎(IM)是伊立替康(CPT-11)的严重副作用,CPT-11 是治疗结直肠癌的一线药物。本研究旨在评估长春花蛋白(LP)预防 IM 和腹泻的效果。将瑞士小鼠每日用生理盐水或 LP(1、5 或 50mg/kg,iv)处理,于 CPT-11(75mg/kg/4 天,ip)前 24 小时开始,并持续 6 天。记录动物的存活率、体重变化和腹泻情况。在第一次注射 CPT-11 后第 7 天(动物牺牲)时,收集肠组织样本以研究形态学和炎症参数。与 CPT-11 对照组相比,给予 LP 的动物表现出改善的参数(存活率、体重和无腹泻)。与给予 CPT-11 的动物相比,给予 LP 的动物的 IM 严重程度降低。LP 治疗还可预防 CPT-11 引起的绒毛/隐窝比降低。MPO 活性和促炎细胞因子的升高、平滑肌过度收缩和腹泻均在 LP 治疗的小鼠中被消除。在 LP 治疗的动物的肠组织中观察到 COX-2、TNF-α、IL-1β、iNOS 和 NF-κB 的免疫染色强度显著降低。LP 治疗消除了 CPT-11 在实验动物中的副作用,并改善了 IM 的所有已知生化发病机制的临床参数。版权所有©2016 John Wiley & Sons, Ltd.