Department of Pharmacology, Faculty of Medicine, Minia University, Egypt.
Depatment of Human Anatomy and Embryology, Faculty of Medicine, Minia University, Delegated to Deraya University-New Minia City, Egypt.
Int Immunopharmacol. 2020 Nov;88:106983. doi: 10.1016/j.intimp.2020.106983. Epub 2020 Sep 14.
Intestinal ischemia reperfusion (IR) is a pathophysiologic process that leads to oxidative stress and acute inflammatory responses. Understanding the mechanisms explaining this inflammation is essential to developing therapeutic strategies. Therefore, the purpose of this study was to evaluate the protective outcome of modafinil (Mod) against intestinal damages caused by intestinal IR injury.
METHODS/MATERIALS: Fourty adult Male Wistar rats were randomly divided into four groups: sham control group; intestinal IR group; Mod pre-treated IR group and Mod post-treated IR group. Mod in a dose of 10 mg/kg was injected intraperitoneally once daily for 7 days pre or post IR treatment.
Mod significantly attenuated the IR induced elevations in intestinal malondialdehyde (MDA), nitric oxide (NO), tumor necrosis factor alpha (TNF-α), interleukin 1-β (IL-1β) and P-glycoprotein (P-gp) levels, caspase-3 activity. However, a significant increase in TAC was reported as compared with the IR group but its post-treated IR group was highly protective. Mod post-treatment down-regulated the IR induced cyclo-oxygenase-2 (COX-2) over-expression. Distorted mucosa with loss of surface epithelial cells, epithelial separation oedematous lamina propria and inflammatory cellular infiltration detected by histopathological examination of intestinal tissue, were markedly ameliorated by Mod post-treatment. On the other hand, Mod pre-treatment showed less protection against intestinal IR in rats.
Current study suggests that Mod post-treatment ameliorated intestinal damages, so it can be considered a potential therapeutic agent to protect against the major clinical challenge of intestinal injury resulting from IR.
肠缺血再灌注(IR)是一种导致氧化应激和急性炎症反应的病理生理过程。了解解释这种炎症的机制对于开发治疗策略至关重要。因此,本研究的目的是评估莫达非尼(Mod)对肠 IR 损伤引起的肠道损伤的保护作用。
方法/材料:40 只成年雄性 Wistar 大鼠随机分为四组:假手术对照组;肠 IR 组;Mod 预处理 IR 组和 Mod 后处理 IR 组。Mod 以 10mg/kg 的剂量每天腹腔注射一次,预处理或后处理 IR 治疗 7 天。
Mod 显著减轻了 IR 诱导的肠丙二醛(MDA)、一氧化氮(NO)、肿瘤坏死因子-α(TNF-α)、白细胞介素 1-β(IL-1β)和 P-糖蛋白(P-gp)水平、caspase-3 活性的升高。然而,与 IR 组相比,TAC 显著增加,但后处理 IR 组具有高度的保护作用。Mod 后处理下调了 IR 诱导的环氧化酶-2(COX-2)过表达。通过对肠组织的组织病理学检查发现,莫达非尼后处理明显改善了粘膜扭曲、表面上皮细胞丢失、上皮分离、水肿的固有层和炎症细胞浸润。另一方面,Mod 预处理对大鼠肠 IR 的保护作用较小。
本研究表明,Mod 后处理可改善肠损伤,因此可被认为是一种潜在的治疗药物,可预防由 IR 引起的主要临床挑战:肠损伤。