喀麦隆蜂胶中的酚类物质及其促慢性胃溃疡愈合作用
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Gastroenterology Research Unit, Animal Physiology Laboratory, Department of Animal Biology & Physiology, Faculty of Science, University of Yaoundé 1, P.O. Box 812, Yaoundé, Cameroon

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Phenolic profile and chronic gastric ulcer healing effects of Cameroonian propolis
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Gastroenterology Research Unit, Animal Physiology Laboratory, Department of Animal Biology & Physiology, Faculty of Science, University of Yaoundé 1, P.O. Box 812, Yaoundé, Cameroon

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    摘要:

    背景:胃溃疡持续影响着全世界数百万人,报告的死亡病例和诊断、预防和治疗对患者构成了负担,特别是在难治性慢性溃疡出现的情况下。蜂胶等天然药物为溃疡的治疗和康复提供了合适的替代疗法。目的:该研究旨在评价喀麦隆蜂胶中酚类物质的特性和对大鼠胃溃疡的促愈合作用。方法:采用HPLC-DAD对蜂胶提取物中的酚类化合物进行了鉴定和定量分析。用乙醇(70%;1 mL/200 g口服)及吲哚美辛(1 mg/kg 口服)分别诱导慢性胃溃疡,并使用醋酸(30%)/消炎痛(1 mg/kg 口服)诱导难愈性胃溃疡。实验动物以赋形剂(吐温20,1 mL/100 g 口服),蜂胶提取物(200 mg/kg、400 mg/kg和600 mg/kg 口服)或硫酸铝糖(50 mg/kg 口服),每天1次,持续10到14天。在每个治疗周期结束时,处死动物,评估溃疡指数、胃黏液重量、组织学和氧化应激参数。结果:在蜂胶中共鉴定出8种酚类化合物,其中最丰富的一种是咖啡酸(45.31 ± 0.25 μg/g)、蜂胶黄素(37.65 ± 0.17 μg/g)和对羟基苯甲酸(34.14 ± 0.21 μg/g)。在两种胃溃疡动物模型中,用200 mg/kg、400 mg/kg和600 mg/kg的蜂胶提取物治疗溃疡大鼠(慢性和难愈性胃溃疡模型)后,与阴性对照组相比,溃疡指数均降低。胃组织病理学观察显示,蜂胶提取物处理导致黏膜的剂量依赖性正常化。在溃疡愈合时,黏液重量显著增加(P < 0.5;P < 0.01和P < 0.001)。此外,200 mg/kg、400 mg/kg和600 mg/kg的蜂胶提取物诱导SOD、过氧化氢酶、亚硝酸盐和谷胱甘肽的含量增加,而MDA浓度均下降。结论:蜂胶提取物的促愈合作用可归因于刺激胃黏液的产生,并改善体内抗氧化状态。这些结果支持蜂胶作为新的治疗消化性溃疡疾病的药物开发策略。

    Abstract:

    Background Gastric ulcers continue to affect millions of people worldwide, with reported cases of fatalities and the diagnosis, prevention and treatment constitute a burden on the patients especially in case of chronic ulcers which are difficult to treat. Natural medicines such as propolis provide suitable therapeutic alternatives in the treatment and curation of ulcers. Objective This work focused on the evaluation of the phenolic profile and healing effect of Cameroonian propolis on gastric ulcers in rats. Methods Identification and quantification of phenolic compounds in the propolis extract was done using HPLC-DAD. Chronic gastric ulcers were induced using ethanol (70%; 1 mL/200 g p.o.)/indomethacin (1 mg/kg p.o.), and “unhealed” gastric ulcerations were induced using acetic acid (30%)/indomethacin (1 mg/kg p.o.). The animals were administered with the vehicle (Tween 20, 1 mL/100 g p.o.), propolis extract (200 mg/kg, 400 mg/kg and 600 mg/kg p.o.) or sucralfate (50 mg/kg p.o.), once daily for ten to fourteen days. At the end of each treatment period, the animals were sacrificed and ulcer indices, gastric mucus weight, histological and oxidative stress parameters were assessed. Results Eight phenolic compounds were identified and quantified and most abundant were Caffeic acid (45.31 ± 0.25 μg/g), Chrysin (37.65 ± 0.17 μg/g) and p-Hydroxy benzoic acid (34.14 ± 0.21 μg/g). The treatment of ulcerated rats (chronic and unhealed gastric ulcer models) with propolis extract at 200 mg/kg, 400 mg/kg and 600 mg/kg resulted in reduction of ulcer index compared to negative controls in both models. Histological observation of stomach tissues showed that treatment with propolis extract led to a dose-dependent normalization of the mucosa. There was a significant increase (P < 0.05; P < 0.01 and P < 0.001) in mucus weight that accompanied the healing of the ulcers. Furthermore, doses of 200 mg/kg, 400 mg/kg and 600 mg/kg of the propolis extract induced an increase in the amounts of SOD, catalase, nitrite and GSH while MDA concentrations decreased in both models. Conclusion The healing effect of propolis extract is due to the stimulation of mucus production followed by an improvement of in vivo antioxidant status. These results support the use of propolis in the development of new pharmacological strategies for the management of peptic ulcers disease.

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  • 在线发布日期: 2024-11-12
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