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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >alpha-Mangostin from Cratoxylum arborescens (Vahl) Blume Demonstrates Anti-Ulcerogenic Property: A Mechanistic Study
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alpha-Mangostin from Cratoxylum arborescens (Vahl) Blume Demonstrates Anti-Ulcerogenic Property: A Mechanistic Study

机译:来自Cratoxylum arborescens(Vahl)Blume的α-Mangostin展示了抗致溃疡性:机理研究。

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Cratoxylum arborescens (Vahl) Blume is an Asian herbal medicine with versatile ethnobiological properties including treatment of gastric ulcer. This study evaluated the antiulcerogenic mechanism(s) of a-mangostin (AM) in a rat model of ulcer. AM is a prenylated xanthone derived through biologically guided fractionation of C. arborescens. Rats were orally pretreated with AM and subsequently exposed to acute gastric lesions induced by ethanol. Following treatment, ulcer index, gastric juice acidity, mucus content, histological and immunohistochemical analyses, glutathione (GSH), malondialdehyde (MDA), nitric oxide (NO), and nonprotein sulfhydryl groups (NP-SH) were evaluated. The znti-Helicobacter pylori, cydooxygenase-2 (COX-2) inhibitory effect, and antioxidant activity of AM were also investigated in vitro. AM (10 and 30mg/kg) inhibited significantly (P < 0.05) ethanol-induced gastric lesions by 66.04% and 74.39 %, respectively. The compound induces the expression of Hsp70, restores GSH levels, decreases lipid peroxidation, and inhibits COX-2 activity. The minimum inhibitory concentration (MIC) of AM showed an effective in vitro anti-H. pylori activity. The efficacy of the AM was accomplished safely without presenting any toxicological parameters. The results of the present study indicate that the antioxidant properties and the potent anti-H. pylori, in addition to activation of Hsp70 protein, may contribute to the gastroprotective activity of a-mangostin.
机译:Cratoxylum arborescens(Vahl)Blume是一种具有多种民族生物学特性(包括治疗胃溃疡)的亚洲草药。这项研究评估了大鼠溃疡模型中a-mangostin(AM)的抗溃疡发生机理。 AM是通过生物引导的乔木梭菌分级分离而衍生的异戊烯酮黄酮。大鼠接受AM口服预处理,随后暴露于乙醇诱导的急性胃部损伤。治疗后,评估溃疡指数,胃液酸度,黏液含量,组织学和免疫组化分析,谷胱甘肽(GSH),丙二醛(MDA),一氧化氮(NO)和非蛋白质巯基(NP-SH)。体外还研究了幽门螺杆菌对幽门螺杆菌,环加氧酶-2(COX-2)的抑制作用和抗氧化活性。 AM(10和30mg / kg)分别显着(P <0.05)抑制乙醇诱导的胃部病变,分别为66.04%和74.39%。该化合物诱导Hsp70的表达,恢复GSH水平,减少脂质过氧化,并抑制COX-2活性。 AM的最低抑菌浓度(MIC)显示有效的体外抗H素。幽门螺杆菌活动。安全地完成了AM的功效,没有出现任何毒理学参数。本研究的结果表明,其抗氧化性能和有效的抗H性能。幽门螺杆菌除了激活Hsp70蛋白外,还可能促进a-芒果的胃保护活性。

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