百里香精油对甲氨蝶呤引起的肠道损伤的抗炎和抗氧化作用

Yuri de Abreu Gomes-Vasconcelos , Pedro Lucas Martins-Santiago , Dalgimar Beserra de Menezes , José Lima de Carvalho Rocha , Rutyleia Alves-Soares , Maria Diana Moreira-Gomes , Francisco Walber Ferreira-da-Silva , Kerly Shamyra da Silva-Alves , José Henrique Leal-Cardoso , Andrelina Noronha Coelho-de-Souza
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引用次数: 0

摘要

甲氨蝶呤(MTX)是治疗癌症和其他疾病的重要药物。然而,它会诱发许多与胃肠道炎症有关的副作用。百里香精油(EOHc)具有胃肠道保护和抗炎特性。因此,我们旨在研究 EOHc 对 MTX 诱导的大鼠肠道炎症的影响。雄性 Wistar 大鼠先服用 MTX 或生理盐水 3 天,然后再服用 EOHc(300 毫克/千克)或药物 3 天或 7 天。一半动物在 MTX 治疗结束 3 天后(炎症期)安乐死,另一半在 4 天后(炎症后期)安乐死。在粘膜炎炎症相关阶段,MTX 治疗组十二指肠的 MPO 水平是对照组的 284%(对照组:50.9 ± 9.97 U/mg 蛋白),回肠的 MPO 水平是对照组的 231%(对照组:30.4 ± 6.60 U/mg 蛋白)。在 EOHc 组,十二指肠和回肠中的蛋白质水平分别为对照组的 50% 和 113%。在这一阶段,EOHc 阻止了十二指肠和空肠中 TBARs 水平的升高和硫醇水平的降低。在粘膜炎的炎症后阶段,EOHc 可防止胃肠道转运功能的改变,并在总体上增加食物和水的消耗量。总之,观察到的效果,特别是 EOHc 的抗炎和抗氧化作用,以及之前报告的低毒性,使 EOHc 成为减少与使用 MTX 相关的胃肠道副作用的一种有前途的候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-inflammatory and antioxidative effects of essential oil of Hyptis crenata on the intestinal injuries induced by methotrexate
Methotrexate (MTX) is an important drug for the treatment of cancer and other diseases. However, it induces many gastrointestinal inflammation-related side effects. The essential oil of Hyptis crenata (EOHc) has gastrointestinal protective and anti-inflammatory properties. Therefore, we aimed to investigate the effect of EOHc on MTX-induced intestinal inflammation in rats. Male Wistar rats were administered MTX or Saline for 3 days and EOHc (300 mg/kg) or vehicle for an additional 3 or 7 days. Half of the animal was euthanized 3 days after the end of MTX treatment (inflammation phase) and the remaining half euthanized 4 days later (post-inflammation phase). The MPO levels in the mucositis inflammation-related phase of the MTX-treated group were 284 % of the control in the duodenum (cont: 50,9 ± 9,97 U/mg of protein) and 231 % of the control in the ileum (cont: 30,4 ± 6,60 U/mg of protein). In the EOHc group, the levels were 50 % of control in the duodenum and 113 % in the ileum. During this phase, EOHc prevented the increase in TBARs levels and the decrease in thiol levels in the duodenum and jejunum. In the post-inflammation phase of mucositis, EOHc prevented the gastrointestinal transit alteration and, in general, increased food and water consumption. In conclusion, the observed effects, particularly the anti-inflammatory and antioxidant effects of EOHc, as well as its previously reported low toxicity, position EOHc as a promising candidate for reducing gastrointestinal side effects associated with the use of MTX.
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