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野生和体外培养的 Castilleja tenuiflora Benth.(列当科)提取物的体内抗炎和抗溃疡活性。

In vivo anti-inflammatory and anti-ulcerogenic activities of extracts from wild growing and in vitro plants of Castilleja tenuiflora Benth. (Orobanchaceae).

机构信息

Departamento de Biotecnología, Centro de Desarrollo de Productos Bióticos, Instituto Politécnico Nacional, PO Box 24, Yautepec, Morelos C.P. 62730, Mexico.

出版信息

J Ethnopharmacol. 2013 Dec 12;150(3):1032-7. doi: 10.1016/j.jep.2013.10.002. Epub 2013 Oct 18.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Castilleja tenuiflora Benth. (Orobanchaceae) is a perennial shrub used since the 16(th) century in Mexican traditional medicine for the treatment of a number of health disorders including inflammation, stomach pain and tumors. The aim of the present study was to evaluate the cytotoxic, anti-inflammatory and anti-ulcerogenic activities of ethyl acetate (EaE), methanol (ME) and aqueous extracts (AE) of Castilleja tenuiflora wild grown (CtW) and in vitro plants (CtIv).

MATERIAL AND METHOD

Phytochemical analysis of the phenylethanoid glycoside (PhG) and iridoid glycoside (IG) components was carried out by chromatographic methods. In vitro cytotoxic activity of the extracts was evaluated in the following four carcinoma cell lines: colon (HF-6), breast (MCF-7), prostate (PC-3), and nasopharyngeal (KB). The topical anti-inflammatory activity was evaluated in mouse ear edema induced by 12-O-tetradecanoylphorbol-13-acetate (TPA). Anti-ulcerogenic activity was evaluated in rats using an absolute ethanol-induced acute gastric ulcer model.

RESULTS

The main compounds in the extracts were isoverbascoside, verbascoside and aucubin and their concentration depended both on the solvent used and on the plant material origin. None of the extracts showed cytotoxicity against the tested cell lines. In contrast, CtWEaE, CtWAE and CtIvEaE (1.6 mg/ear) showed moderate anti-inflammatory activity similar to dexamethasone (1 mg/ear) with a 38.2, 39.3 and 49.1% decrease of inflammation, respectively. CtWEaE and CtIvEaE (100 mg/kg) showed high anti-ulcerogenic activity with 88.3 and 83.1% inhibition, respectively, compared to famotidine (20 mg/kg, 32.8% inhibition).

CONCLUSION

Castilleja tenuiflora extracts provided significant gastric protection in an acute ulcer induction model and topical anti-inflammatory activity in a mouse ear edema model. These activities are related to verbascoside and may explain the traditional use of Castilleja tenuiflora in the treatment of anti-inflammatory and gastrointestinal disorders. Cultured Castilleja tenuiflora plants (in vitro) exhibited pharmacological activities and also have the potential to produce bioactive compounds.

摘要

民族药理学相关性

长管花(Orobanchaceae)是一种多年生灌木,自 16 世纪以来,墨西哥传统医学一直将其用于治疗多种健康疾病,包括炎症、胃痛和肿瘤。本研究的目的是评估野生生长(CtW)和体外植物(CtIv)的长管花乙酸乙酯(EaE)、甲醇(ME)和水提取物(AE)的细胞毒性、抗炎和抗溃疡活性。

材料和方法

通过色谱方法对苯乙醇苷(PhG)和环烯醚萜苷(IG)成分进行了植物化学分析。在以下四种癌细胞系中评估了提取物的体外细胞毒性:结肠(HF-6)、乳腺(MCF-7)、前列腺(PC-3)和鼻咽(KB)。采用 12-O-十四烷酰佛波醇-13-乙酸酯(TPA)诱导的小鼠耳水肿评价局部抗炎活性。采用无水乙醇诱导的急性胃溃疡模型评价抗溃疡活性。

结果

提取物中的主要化合物为异毛蕊花糖苷、毛蕊花糖苷和梓醇,其浓度既取决于所用溶剂,也取决于植物材料的来源。在测试的细胞系中,没有一种提取物表现出细胞毒性。相反,CtWEaE、CtWAE 和 CtIvEaE(1.6mg/耳)表现出适度的抗炎活性,与地塞米松(1mg/耳)相似,炎症分别减少 38.2%、39.3%和 49.1%。CtWEaE 和 CtIvEaE(100mg/kg)表现出高抗溃疡活性,与法莫替丁(20mg/kg,32.8%抑制)相比,分别抑制 88.3%和 83.1%。

结论

长管花提取物在急性溃疡诱导模型中提供了显著的胃保护作用,并在小鼠耳水肿模型中具有局部抗炎活性。这些活性与毛蕊花糖苷有关,可能解释了长管花在治疗抗炎和胃肠道疾病方面的传统用途。培养的长管花植物(体外)表现出药理活性,并且还具有产生生物活性化合物的潜力。

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