黄连心木黄酮fustin对消炎痛所致大鼠胃溃疡模型的保护作用

A. Georgieva, D. Pavlov, M. Tzaneva, M. Novaković, V. Tešević, M. Reyzov, M. Eftimov, M. Todorova, M. Nikolova, N. Stefanova, S. Valcheva-Kuzmanova
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引用次数: 0

摘要

摘要胃溃疡是常见的健康问题。Cotinus coggygria心木提取物富含黄酮类fustin和硫维素在消炎痛引起的大鼠胃溃疡模型中显示出保护作用。Fustin本身在乙醇诱导的大鼠胃溃疡模型中具有保护作用。本研究旨在研究从黄酮黄丝素中提取的黄酮黄丝素在消炎痛致大鼠胃溃疡模型中的作用。从黄连心材中分离纯化了黄连素。实验选用30只雄性Wistar大鼠,分为Control组、Indo组和F10组。F10组用10 mg/kg b.w.的fustin预处理7 d。处死大鼠,进行胃宏观、组织病理学和免疫组化检查。通过对胃黏膜的宏观、微观和免疫组化检查证实,吲哚美辛对胃粘膜造成了严重的损伤。Fustin预处理对胃损伤的宏观指标(溃疡数量、面积、评分、指数)略有降低,对粘膜糜烂、坏死、出血、炎症等微观指标的严重程度有明显缓解。与吲哚美辛处理的大鼠相比,fustin预处理的大鼠NF-κB表达降低。综上所述,fustin在吲哚美辛诱导的胃溃疡模型中发挥了胃保护作用,可能与其抗炎活性有关。
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Gastroprotective effect of the flavonoid fustin isolated from Cotinus coggygria heartwood in a rat model of indomethacin-induced gastric ulceration
Abstract Gastric ulcer is a common health issue. Cotinus coggygria heartwood extracts rich in the flavonoids fustin and sulfuretin have shown protective effects in a rat model of indomethacin-induced gastric ulceration. Fustin itself has been protective in a rat model of ethanol-induced gastric ulcer. In the present study we aimed to reveal the effect of the flavonoid fustin isolated from Cotinus coggygria heartwood in a rat model of indomethacin-induced gastric ulceration. Fustin was isolated from Cotinus coggygria heartwood and purified. The experiment was performed on 30 male Wistar rats allocated to three groups – Control, Indo and F10. F10 group was pretreated with fustin (10 mg/kg b.w. for 7 days). Rats were sacrificed and macroscopic, histopathological and immunohistochemical investigations of the stomachs were performed. Indomethacin caused severe mucosal damage, proven by the macroscopic, microscopic and immunohistochemical gastric mucosa investigation. Fustin pretreatment slightly reduced the macroscopic indices for gastric damage (ulcer number, area, score and index), and significantly alleviated the severity of the microscopic indices (mucosal erosions, necrosis, hemorrhages and inflammation). In fustin-pretreated rats, the expression of NF-κB was reduced in comparison with indomethacin-treated animals. In conclusion, fustin exerted a gastroprotective action in an indomethacin-induced gastric ulceration model, probably due to its anti-inflammatory activity.
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