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生物系统中酚类化合物的生物可及性和生物利用度对Triplaris gardneriana种子乙醇提取物抗氧化活性的影响。

Impact of bioaccessibility and bioavailability of phenolic compounds in biological systems upon the antioxidant activity of the ethanolic extract of Triplaris gardneriana seeds.

作者信息

Neto José Joaquim Lopes, de Almeida Thiago Silva, de Medeiros Jackeline Lima, Vieira Leonardo Rogério, Moreira Thaís Borges, Maia Ana Isabel Vitorino, Ribeiro Paulo Riceli Vasconcelos, de Brito Edy Sousa, Farias Davi Felipe, Carvalho Ana Fontenele Urano

机构信息

Department of Biochemistry and Molecular Biology, Federal University of Ceará, 60020-181, Fortaleza, CE, Brazil.

Embrapa Tropical Agroindustry, 60511-110, Fortaleza, CE, Brazil.

出版信息

Biomed Pharmacother. 2017 Apr;88:999-1007. doi: 10.1016/j.biopha.2017.01.109. Epub 2017 Feb 6.

Abstract

The most studied bioactive potential of phenolic compounds corresponds to antioxidant activity, which in turn, is associated with a reduction in the incidence of various human diseases. However, the total quantity of these bioactive substances in foods and medicinal preparations does not reflect the amount absorbed and metabolized by the body. The present study aimed to investigate the bioaccessibility of Triplaris gardneriana seeds ethanolic extract (EETg) by determination of phenolic composition and antioxidant activities before and after in vitro digestion as well as to estimate its bioavailability by chemical analysis of plasma and urine in animal models after oral administration. The bioaccessibility indexes of phenolic compounds in EETg were 48.65 and 69.28% in the presence and absence of enzymes, respectively. Among the identified phenolics classes, flavonoids, represented by galloylated procyanidins type B, proved to be more bioaccessible, 81.48 and 96.29% in the post-intestinal phase with and without enzymes, respectively. The oral administration in Wistar rats resulted in a significant decrease in plasma of the total antioxidant capacity, TAC, by FRAP assay 4h after beginning the experiment. For urine samples, an increase in TAC by DPPH and FRAP was observed from 1 and 4h after administration, respectively. UPLC-QTOF analysis of urine detected 2 metabolites originated from the degradation of phenolic compounds, i.e. hippuric acid and phenylacetil glycine. These results suggest that phenolic compounds in T. gardneriana are unstable under gastrointestinal conditions, being flavonoids the components with higher bioaccessibility; besides that, they showed limited bioavailability due to their rapid biotransformation and urinary elimination.

摘要

酚类化合物最受研究的生物活性潜力对应于抗氧化活性,而抗氧化活性又与各种人类疾病发病率的降低相关。然而,食品和药物制剂中这些生物活性物质的总量并不能反映身体吸收和代谢的量。本研究旨在通过测定体外消化前后的酚类成分和抗氧化活性来研究加氏刺戟种子乙醇提取物(EETg)的生物可及性,并通过口服给药后动物模型血浆和尿液的化学分析来评估其生物利用度。EETg中酚类化合物在有酶和无酶情况下的生物可及性指数分别为48.65%和69.28%。在已鉴定的酚类类别中,以B型没食子酰化原花青素为代表的黄酮类化合物被证明具有更高的生物可及性,在肠道后期有酶和无酶情况下分别为81.48%和96.29%。在Wistar大鼠中口服给药后,实验开始4小时后通过FRAP法测定发现血浆中总抗氧化能力(TAC)显著降低。对于尿液样本,分别在给药后1小时和4小时观察到通过DPPH和FRAP法测定的TAC增加。尿液的超高效液相色谱-四极杆飞行时间质谱(UPLC-QTOF)分析检测到2种源自酚类化合物降解的代谢物,即马尿酸和苯乙酰甘氨酸。这些结果表明,加氏刺戟中的酚类化合物在胃肠道条件下不稳定,黄酮类是生物可及性较高的成分;此外,由于它们的快速生物转化和经尿液消除,其生物利用度有限。

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