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刺果茜草果实的抗氧化和抗诱变活性。

Antioxidant and antimutagenic activities of Randia echinocarpa fruit.

作者信息

Santos-Cervantes María Elena, Ibarra-Zazueta María Emilia, Loarca-Piña Guadalupe, Paredes-López Octavio, Delgado-Vargas Francisco

机构信息

Maestría en Ciencia y Tecnología de Alimentos, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Sinaloa, Culiacán Sin, Mexico.

出版信息

Plant Foods Hum Nutr. 2007 Jun;62(2):71-7. doi: 10.1007/s11130-007-0044-x. Epub 2007 Jun 19.

Abstract

We report for the first time the antioxidant and antimutagenic activities of fractions from Randia echinocarpa fruit, which is a Rubiaceae plant native to Sinaloa, Mexico. This fruit has been traditionally used in the prevention or treatment of cancer, among other diseases. The pulp of the fruit was sequentially extracted with solvents of different polarity (i.e. hexane, chloroform, methanol and water). A high extraction yield was obtained with methanol (72.17% d.w.). The aqueous extract showed the highest content of phenolics (2.27 mg/g as ferulic acid equivalents) and the highest antioxidant activity based on the beta-carotene bleaching method (486.15). The commercial antioxidant BHT was used as control (835.05). Antimutagenic activity of the aqueous extract (0-500 microg/tube) was evaluated using the Salmonella microsuspension assay (YG1024 strain) and 1-NP as the mutagen (50 and 100 ng/tube). The aqueous extract was neither toxic nor mutagenic and the percentage of inhibition on 1-NP mutagenicity was 32 and 53% at doses of 50 and 100 ng/tube, respectively. The results of the double incubation assay suggest that the extract inhibited the mutagenicity of 1-NP by a combination of desmutagenic and bioantimutagenic effects.

摘要

我们首次报道了来自墨西哥锡那罗亚州的茜草科植物刺果茜草果实提取物的抗氧化和抗诱变活性。这种果实传统上用于预防或治疗癌症及其他疾病。果实果肉依次用不同极性的溶剂(即己烷、氯仿、甲醇和水)进行提取。甲醇提取物的得率较高(干重为72.17%)。水提取物中酚类物质含量最高(以阿魏酸当量计为2.27 mg/g),基于β-胡萝卜素漂白法的抗氧化活性也最高(486.15)。以市售抗氧化剂丁基羟基甲苯作为对照(835.05)。采用沙门氏菌微悬浮试验(YG1024菌株),以1-硝基芘作为诱变剂(50和100 ng/管),评估水提取物(0 - 500 μg/管)的抗诱变活性。水提取物既无毒性也无诱变性,在50和100 ng/管剂量下,对1-硝基芘诱变性的抑制率分别为32%和53%。双温育试验结果表明,该提取物通过去诱变和生物抗诱变作用的组合抑制了1-硝基芘的诱变性。

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